Acknowledgment. Distinguished Visiting Scholar Committee United College

Size: px
Start display at page:

Download "Acknowledgment. Distinguished Visiting Scholar Committee United College"

Transcription

1 Acknowledgment The United College Distinguished Visiting Scholar Committee acknowledges with thanks the generous grant from the United College Endowment Fund which has made possible the visit of Professor Paul Pharoah, Professor of Cancer Epidemiology, Department of Public Health and Primary Care and Department of Oncology, University of Cambridge, United Kingdom, to United College as our Distinguished Visiting Scholar in Distinguished Visiting Scholar Committee United College 1

2 2 UNITED COLLEGE THE CHINESE UNIVERSITY OF HONG KONG Distinguished Visiting Scholar Lectures Understanding why cancer tends to run in families? Tuesday, 6 November 2018, 4:30 pm 為甚麼癌症會在一些家族中流行? 2018 年 11 月 6 日 ( 星期二 ) 下午 4 時 30 分 Professor Paul Pharoah 保祿 費羅教授 Professor of Cancer Epidemiology Department of Public Health and Primary Care Department of Oncology University of Cambridge 劍橋大學公共衛生及基層醫療學系腫瘤學系癌症流行病學講座教授 Are we ready for genetic testing in population? Thursday, 8 November 2018, 4:30 pm 癌症基因測試 市民大眾準備好未? 2018 年 11 月 8 日 ( 星期四 ) 下午 4 時 30 分 Venue: Lau Chor Tak Lecture Theatre, Ground Floor Yasumoto International Academic Park, CUHK 地點 : 香港中文大學康本國際學術園地下劉佐德演講廳 Lectures in English 英語主講 Enquiries: /

3 4 A Warm Welcome to Professor Paul Pharoah Professor Pharoah obtained his medical degree from the University of Oxford in He started his research in the genetic basis of Cancer at the University of Cambridge since He advanced through appointments from Senior Clinical Research Fellow to Reader in Cancer Epidemiology and then promoted to Chair Professor in He has been the key persons in numerous cancer study projects in UK, across Europe and around the World. Professor Pharoah and his colleagues painstakingly established large cohorts of cancer patients across UK and Europe and later around the World to answer these questions. Nowadays the genetic landscape of cancer is made clear, thanks to his works and that of many other researchers. It enables proper use of genetic testing in suitable patients to inform their genetic conditions, to inform their family relatives about their risk, to predict the future risk of cancer in persons who carry such mutations and so on. These clinical use and applications are not possible without the hard work of Professor Pharoah and colleagues in the past 20 years. To set the stage for Professor Pharoah s lectures, please allow me to go back to the 90s and see what was known about genetics then. At that time, we knew very little about the human genome. The plan to sequence the human genome was announced just in 1990 which was scheduled to take 15 years (to be completed in 2005). Complete automation of DNA sequencing which was used to decoding the A,C,T,G code from people samples was only possible in And only about 100 human genetic diseases had their causative genes revealed. Among them was the gene known as BRCA1 causing a form of breast cancer that ran in families which was just discovered in However, we have little idea how many cancer patients had familial genetic diseases. Furthermore, does genetics play a role in the great majority patients without BRCA1 mutations and to what extent? His contribution is self-evident on reading this long list of publications. Majority of them appears in high tier Journals, like Nature, Nature series, Science, New England Journal of Medicine, JAMA, JNCI, so on. He has published over 500 papers and his H-index is over 100. He also masterminded important tools that we now used in everyday clinical work. For example, the probability of having a gene mutation can be assessed by his web based program. Professor Pharoah also serves in various UK and International organizations and advisory bodies, such as the National Cancer Institute s PDQ Cancer Genetics Advisory Board which sets guidelines on how to manage patients with familial cancers. 5

4 Poster of Professor Paul Pharoah 6 United College has the privilege and honor to invite Professor Pharoah to speak to us this time as the Distinguished Visiting Scholar, on behalf of the staff and students of United College and The Chinese University of Hong Kong, I would like to express our warmest welcome to Professor Paul Pharoah and wish him a very memorable stay in Hong Kong. Nelson TANG Department of Chemical Pathology 7

5 8 Lecture One Lecture Two Understanding why cancer tends to run in families? Are we ready for genetic testing in the population? Many research studies have shown that cancer tends to run in families. Sometimes it is the same type of cancer in the family, and sometimes it is different types of cancer. This may happen because related individuals in families tend to have a similar genetic make-up as we all inherit our genes from our families. Another explanation is that people in families tend to have similar lifestyles and share the same environment. Studies of twins have shown that it is our inherited genetic make-up that is the most important of these two alternatives but shared lifestyle/ environment is important too. In the past twenty years many of the genetic differences between individuals that are responsible for familial cancer have been identified. Genetic differences (genetic variation) between individuals are responsible for many of the physical differences between individuals such as eye colour and height. Some genetic differences (or variants) are also associated with differences in disease risks and for particular variants the disease risks can be high. For example, some rare variants in the gene BRCA1 are associated with a lifetime risk of approximately 60 per cent for breast cancer and 40% for ovarian cancer. These high-risk variants are sometimes called mutations or faults. In the past genetic testing to find BRCA1 mutations was labor intensive and expensive and only available to individuals with a strong family history of disease. However, the cost of genetic testing is now much less and so it would be possible to test whole populations for genetic mutations. However, this raises scientific, clinical and ethical issues that need to be addressed before population testing could be recommended. 9

6 10 Selected Research Projects and Publications (recent 5 years) of Professor Paul Pharoah Latest Papers Amos CI, Dennis J, Wang Z, Byun J, Schumacher FR, Gayther SA, Casey G, Hunter DJ, Sellers TA, Gruber SB, Dunning AM, Michailidou K, Fachal L, Doheny K, Spurdle AB, Li Y, Xiao X, Romm J, Pugh E, Coetzee GA, Hazelett DJ, Bojesen SE, Caga-Anan C, Haiman CA, Kamal A, Luccarini C, Tessier D, Vincent D, Bacot F, Van Den Berg DJ, Nelson S, Demetriades S, Goldgar DE, Couch FJ, Forman JL, Giles GG, Conti DV, Bickeboller H, Risch A, Waldenberger M, Bruske-Hohlfeld I, Hicks BD, Ling H, McGuffog L, Lee A, Kuchenbaecker K, Soucy P, Manz J, Cunningham JM, Butterbach K, Kote- Jarai Z, Kraft P, FitzGerald L, Lindstrom S, Adams M, McKay JD, Phelan CM, Benlloch S, Kelemen LE, Brennan P, Riggan M, O Mara TA, Shen H, Shi Y, Thompson DJ, Goodman MT, Nielsen SF, Berchuck A, Laboissiere S, Schmit SL, Shelford T, Edlund CK, Taylor JA, Field JK, Park SK, Offit K, Thomassen M,Schmutzler R, Ottini L, Hung RJ, Marchini J, Amin Al Olama A, Peters U, Eeles RA, Seldin MF, Gillanders E, Seminara D, Antoniou AC, Pharoah PD, Chenevix-Trench G, Chanock SJ, Simard J, Easton DF. The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers. Cancer Epidemiol Biomarkers Prev Blows FM, Ali HR, Dawson SJ, Le Quesne J, Provenzano E, Caldas C, Pharoah PD. Decline in Antigenicity of Tumor Markers by Storage Time Using Pathology Sections Cut From Tissue Microarrays. Appl Immunohistochem Mol Morphol 2016;24(3): Dorling L, Barnett GC, Michailidou K, Coles CE, Burnet NG, Yarnold J, Elliott RM, Dunning AM, Pharoah PD, West CM. Patients with a High Polygenic Risk of Breast Cancer do not have An Increased Risk of Radiotherapy Toxicity. Clin Cancer Res 2016;22(6): Dorling L, Kar S, Michailidou K, Hiller L, Vallier AL, Ingle S, Hardy R, Bowden SJ, Dunn JA, Twelves C, Poole CJ, Caldas C, Earl HM, Pharoah PD, Abraham JE. The Relationship between Common Genetic Markers of Breast Cancer Risk and Chemotherapy-Induced Toxicity: A Case- Control Study. PLoS One 2016;11(7):e Guo Y, Warren Andersen S, Shu XO, Michailidou K, Bolla MK, Wang Q, Garcia-Closas M, Milne RL, Schmidt MK, Chang-Claude J, Dunning A, Bojesen SE, Ahsan H, Aittomaki K, Andrulis IL, Anton-Culver H, Arndt V, Beckmann MW, Beeghly-Fadiel A, Benitez J, Bogdanova NV, Bonanni B, Borresen-Dale AL, Brand J, Brauch H, Brenner H, Bruning T, Burwinkel B, Casey G, Chenevix-Trench G, Couch FJ, Cox A, Cross SS, Czene K, Devilee P, Dork T, Dumont M, Fasching PA, Figueroa J, Flesch-Janys D, Fletcher O, Flyger H, Fostira F, Gammon M, Giles GG, Guenel P, Haiman CA, Hamann U, Hooning MJ, Hopper JL, Jakubowska A, Jasmine F, Jenkins M, John EM, Johnson N, Jones ME, Kabisch M, Kibriya M, Knight JA, Koppert LB, Kosma VM, Kristensen V, Le Marchand L, Lee E, Li J, Lindblom A, Luben R, Lubinski J, Malone KE, Mannermaa A, Margolin S, Marme F, McLean C, Meijers-Heijboer H, Meindl A, Neuhausen SL, Nevanlinna H, Neven P, Olson JE, Perez JI, Perkins B, Peterlongo P, Phillips KA, Pylkas K, Rudolph A, Santella R, Sawyer EJ, Schmutzler RK, Seynaeve C, Shah M, Shrubsole MJ, Southey MC, Swerdlow AJ, Toland AE, Tomlinson I, Torres D, Truong T, Ursin G, Van Der Luijt RB, Verhoef S, Whittemore AS, Winqvist R, Zhao H, Zhao S, Hall P, Simard J, Kraft P, Pharoah P, Hunter D, Easton DF, Zheng W. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent. PLoS Med 2016; 13(8):e

7 12 6. Hollestelle A, van der Baan FH, Berchuck A, Johnatty SE, Aben KK, Agnarsson BA, Aittomaki K, Alducci E, Andrulis IL, Anton-Culver H, Antonenkova NN, Antoniou AC, Apicella C, Arndt V, Arnold N, Arun BK, Arver B, Ashworth A, Australian Ovarian Cancer Study G, Baglietto L, Balleine R, Bandera EV, Barrowdale D, Bean YT, Beckmann L, Beckmann MW, Benitez J, Berger A, Berger R, Beuselinck B, Bisogna M, Bjorge L, Blomqvist C, Bogdanova NV, Bojesen A, Bojesen SE, Bolla MK, Bonanni B, Brand JS, Brauch H, Breast Cancer Family R, Brenner H, Brinton L, Brooks-Wilson A, Bruinsma F, Brunet J, Bruning T, Budzilowska A, Bunker CH, Burwinkel B, Butzow R, Buys SS, Caligo MA,Campbell I, Carter J, Chang-Claude J, Chanock SJ, Claes KB, Collee JM, Cook LS, Couch FJ, Cox A, Cramer D, Cross SS, Cunningham JM, Cybulski C, Czene K, Damiola F, Dansonka-Mieszkowska A, Darabi H, de la Hoya M, defazio A, Dennis J, Devilee P, Dicks EM, Diez O, Doherty JA, Domchek SM, Dorfling CM, Dork T, Silva Idos S, du Bois A, Dumont M, Dunning AM, Duran M, Easton DF, Eccles D, Edwards RP, Ehrencrona H, Ejlertsen B, Ekici AB, Ellis SD, Embrace, Engel C, Eriksson M, Fasching PA, Feliubadalo L, Figueroa J, Flesch-Janys D, Fletcher O, Fontaine A, Fortuzzi S, Fostira F, Fridley BL, Friebel T, Friedman E, Friel G, Frost D, Garber J, Garcia-Closas M, Gayther SA, Collaborators GS, Network G, Gentry-Maharaj A, Gerdes AM, Giles GG, Glasspool R, Glendon G, Godwin AK,Goodman MT, Gore M, Greene MH, Grip M, Gronwald J, Gschwantler Kaulich D, Guenel P, Guzman SR, Haeberle L, Haiman CA, Hall P, Halverson SL, Hamann U, Hansen TV, Harter P, Hartikainen JM, Healey S, Hebon, Hein A, Heitz F, Henderson BE, Herzog J, MA TH, Hogdall CK, Hogdall E, Hogervorst FB, Hopper JL, Humphreys K, Huzarski T, Imyanitov EN, Isaacs C, Jakubowska A, Janavicius R, Jaworska K, Jensen A, Jensen UB, Johnson N, Jukkola- Vuorinen A, Kabisch M, Karlan BY, Kataja V, Kauff N, Investigators KC, Kelemen LE, Kerin MJ, Kiemeney LA, Kjaer SK, Knight JA, Knol-Bout JP, Konstantopoulou I, Kosma VM, Krakstad C, Kristensen V, Kuchenbaecker KB, Kupryjanczyk J,Laitman Y, Lambrechts D, Lambrechts S, Larson MC, Lasa A, Laurent-Puig P, Lazaro C, Le ND, Le Marchand L, Leminen A, Lester J, Levine DA, Li J, Liang D, Lindblom A, Lindor N, Lissowska J, Long J, Lu KH, Lubinski J, Lundvall L, Lurie G, Mai PL, Mannermaa A, Margolin S, Mariette F, Marme F, Martens JW, Massuger LF, Maugard C, Mazoyer S, McGuffog L, McGuire V, McLean C, McNeish I, Meindl A, Menegaux F, Menendez P, Menkiszak J, Menon U, Mensenkamp AR, Miller N, Milne RL, Modugno F, Montagna M, Moysich KB, Muller H, Mulligan AM, Muranen TA, Narod SA, Nathanson KL, Ness RB, Neuhausen SL, Nevanlinna H, Neven P, Nielsen FC, Nielsen SF, Nordestgaard BG, Nussbaum RL, Odunsi K, Offit K, Olah E, Olopade OI, Olson JE, Olson SH, Oosterwijk JC, Orlow I, Orr N, Orsulic S, Osorio A, Ottini L, Paul J, Pearce CL, Pedersen IS, Peissel B, Pejovic T, Pelttari LM, Perkins J, Permuth-Wey J, Peterlongo P, Peto J, Phelan CM, Phillips KA, Piedmonte M, Pike MC, Platte R, Plisiecka-Halasa J, Poole EM, Poppe B, Pylkas K, Radice P, Ramus SJ, Rebbeck TR, Reed MW, Rennert G, Risch HA, Robson M, Rodriguez GC, Romero A, Rossing MA, Rothstein JH, Rudolph A, Runnebaum I, Salani R, Salvesen HB, Sawyer EJ, Schildkraut JM, Schmidt MK, Schmutzler RK, Schneeweiss A, Schoemaker MJ, Schrauder MG, Schumacher F, Schwaab I, Scuvera G, Sellers TA, Severi G, Seynaeve CM, Shah M, Shrubsole M, Siddiqui N, Sieh W, Simard J, Singer CF, Sinilnikova OM, Smeets D, Sohn C, Soller M, Song H, Soucy P, Southey MC, Stegmaier C, Stoppa-Lyonnet D, Sucheston L, Swe B, Swerdlow A, Tangen IL, Tea MK, Teixeira MR, Terry KL, Terry MB, Thomassen M, Thompson PJ, Tihomirova L, Tischkowitz M, Toland AE, Tollenaar RA, Tomlinson I, Torres D,Truong T, Tsimiklis H, Tung N, Tworoger SS, Tyrer JP, Vachon CM, Van t Veer LJ, van Altena AM, Van Asperen CJ, van den Berg D, van den Ouweland AM, van Doorn HC, Van Nieuwenhuysen E, van Rensburg EJ, Vergote I, Verhoef S, Vierkant RA, Vijai J, Vitonis AF, von Wachenfeldt A, Walsh C,Wang Q, Wang-Gohrke S, Wappenschmidt B, Weischer M, Weitzel JN, Weltens 13

8 14 7. C, Wentzensen N, Whittemore AS, Wilkens LR, Winqvist R, Wu AH, Wu X, Yang HP, Zaffaroni D, Pilar Zamora M, Zheng W, Ziogas A, Chenevix- Trench G, Pharoah PD, Rookus MA, Hooning MJ, Goode EL. No clinical utility of KRAS variant rs for ovarian or breast cancer. Gynecol Oncol 2016;141(2): Kar SP, Beesley J, Amin Al Olama A, Michailidou K, Tyrer J, Kote-Jarai Z, Lawrenson K, Lindstrom S, Ramus SJ, Thompson DJ, Investigators A, Kibel AS, Dansonka-Mieszkowska A, Michael A, Dieffenbach AK, Gentry- Maharaj A, Whittemore AS, Wolk A, Monteiro A, Peixoto A, Kierzek A, Cox A, Rudolph A, Gonzalez-Neira A, Wu AH, Lindblom A, Swerdlow A, Group AS, Australian Cancer S, BioResource A, Ziogas A, Ekici AB, Burwinkel B, Karlan BY, Nordestgaard BG, Blomqvist C, Phelan C, McLean C, Pearce CL, Vachon C, Cybulski C, Slavov C, Stegmaier C, Maier C, Ambrosone CB, Hogdall CK,Teerlink CC, Kang D, Tessier DC, Schaid DJ, Stram DO, Cramer DW, Neal DE, Eccles D, Flesch-Janys D, Edwards DR, Wokozorczyk D, Levine DA, Yannoukakos D, Sawyer EJ, Bandera EV, Poole EM, Goode EL, Khusnutdinova E, Hogdall E, Song F, Bruinsma F, Heitz F, Modugno F, Hamdy FC, Wiklund F, Giles GG, Olsson H, Wildiers H, Ulmer HU, Pandha H, Risch HA, Darabi H, Salvesen HB, Nevanlinna H, Gronberg H, Brenner H, Brauch H, Anton-Culver H, Song H, Lim HY, McNeish I, Campbell I, Vergote I,Gronwald J, Lubinski J, Stanford JL, Benitez J, Doherty JA, Permuth JB, Chang-Claude J, Donovan JL, Dennis J, Schildkraut JM, Schleutker J, Hopper JL, Kupryjanczyk J, Park JY, Figueroa J, Clements JA, Knight JA, Peto J, Cunningham JM, Pow-Sang J, Batra J, Czene K, Lu KH, Herkommer K, Khaw KT, kconfab I, Matsuo K, Muir K, Offitt K, Chen K, Moysich KB, Aittomaki K, Odunsi K, Kiemeney LA, Massuger LF, Fitzgerald LM, Cook LS, Cannon-Albright L, Hooning MJ, Pike MC, Bolla MK, Luedeke M, Teixeira MR, Goodman MT, Schmidt MK, Riggan M, Aly M, Rossing MA, Beckmann 8. MW, Moisse M, Sanderson M, Southey MC, Jones M, Lush M, Hildebrandt MA, Hou MF, Schoemaker MJ, Garcia- Closas M, Bogdanova N, Rahman N, Investigators N, Le ND, Orr N, Wentzensen N, Pashayan N, Peterlongo P, Guenel P, Brennan P, Paulo P, Webb PM, Broberg P, Fasching PA, Devilee P, Wang Q, Cai Q, Li Q, Kaneva R, Butzow R, Kopperud RK, Schmutzler RK, Stephenson RA, MacInnis RJ, Hoover RN, Winqvist R, Ness R, Milne RL, Travis RC, Benlloch S, Olson SH, McDonnell SK, Tworoger SS, Maia S, Berndt S, Lee SC, Teo SH, Thibodeau SN, Bojesen SE, Gapstur SM, Kjaer SK, Pejovic T, Tammela TL,Network G, consortium P, Dork T, Bruning T, Wahlfors T, Key TJ, Edwards TL, Menon U, Hamann U, Mitev V, Kosma VM, Setiawan VW, Kristensen V, Arndt V, Vogel W, Zheng W, Sieh W, Blot WJ, Kluzniak W, Shu XO, Gao YT, Schumacher F, Freedman ML, Berchuck A, Dunning AM, Simard J, Haiman CA, Spurdle A, Sellers TA, Hunter DJ, Henderson BE, Kraft P, Chanock SJ, Couch FJ, Hall P, Gayther SA, Easton DF, Chenevix-Trench G, Eeles R, Pharoah PD, Lambrechts D. Genome- Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types. Cancer Discov Kerns SL, Dorling L, Fachal L, Bentzen S, Pharoah PD, Barnes DR, Gomez-Caamano A, Carballo AM, Dearnaley DP, Peleteiro P, Gulliford SL, Hall E, Michailidou K, Carracedo A, Sia M, Stock R, Stone NN, Sydes MR, Tyrer JP, Ahmed S, Parliament M, Ostrer H, Rosenstein BS, Vega A, Burnet NG, Dunning AM, Barnett GC, West CM, Radiogenomics C. Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer. EBioMedicine

9 16 9. Lawrenson K, Kar S, McCue K, Kuchenbaeker K, Michailidou K, Tyrer J, Beesley J. Ramus SJ, Li Q, Delgado MK, Lee JM, Aittomaki K, Andrulis IL, Anton- Culver H, Arndt V, Arun BK, Arver B, Bandera EV, Barile M, Barkardottir RB, Barrowdale D, Beckmann MW, Benitez J, Berchuck A, Bisogna M, Bjorge L, Blomqvist C, Blot W, Bogdanova N, Bojesen A, Bojesen SE, Bolla MK, Bonanni B, Borresen-Dale AL, Brauch H, Brennan P, Brenner H, Bruinsma F, Brunet J, Buhari SA, Burwinkel B, Butzow R, Buys SS, Cai Q, Caldes T, Campbell I, Canniotto R, Chang-Claude J, Chiquette J, Choi JY, Claes KB, Collaborators GS, Cook LS, Cox A, Cramer DW, Cross SS, Cybulski C, Czene K, Daly MB, Damiola F, Dansonka-Mieszkowska A, Darabi H, Dennis J, Devilee P, Diez O, Doherty JA, Domchek SM, Dorfling CM, Dork T, Dumont M, Ehrencrona H, Ejlertsen B, Ellis S, Embrace, Engel C, Lee E, Evans DG, Fasching PA, Feliubadalo L, Figueroa J, Flesch-Janys D, Fletcher O, Flyger H, Foretova L, Fostira F, Foulkes WD, Fridley BL, Friedman E, Frost D, Gambino G, Ganz PA, Garber J, Garcia-Closas M, Gentry-Maharaj A, Ghoussaini M, Giles GG, Glasspool R, Godwin AK, Goldberg MS, Goldgar DE, Gonzalez-Neira A, Goode EL, Goodman MT, Greene MH, Gronwald J, Guenel P, Haiman CA, Hall P, Hallberg E, Hamann U, Hansen TV, Harrington PA, Hartman M, Hassan N, Healey S, Hereditary B, Ovarian Cancer Research Group N, Heitz F, Herzog J, Hogdall E, Hogdall CK, Hogervorst FB, Hollestelle A, Hopper JL, Hulick PJ, Huzarski T, Imyanitov EN, Investigators KC, Australian Ovarian Cancer Study G, Isaacs C, Ito H, Jakubowska A, Janavicius R, Jensen A, John EM, Johnson N, Kabisch M, Kang D, Kapuscinski M, Karlan BY, Khan S, Kiemeney LA, Kjaer SK, Knight JA, Konstantopoulou I,Kosma VM, Kristensen V, Kupryjanczyk J, Kwong A, de la Hoya M, Laitman Y, Lambrechts D, Le N, De Leeneer K, Lester J, Levine DA, Li J, Lindblom A, Long J, Lophatananon A, Loud JT, Lu K, Lubinski J, Mannermaa A, Manoukian S, Le Marchand L, Margolin S, Marme F, Massuger LF, Matsuo K,Mazoyer S, McGuffog L, McLean C, McNeish I, Meindl A, Menon U, Mensenkamp AR, Milne 10. RL,Montagna M, Moysich KB, Muir K, Mulligan AM, Nathanson KL, Ness RB, Neuhausen SL, Nevanlinna H, Nord S, Nussbaum RL, Odunsi K, Offit K, Olah E, Olopade OI, Olson JE, Olswold C, O Malley D, Orlow I, Orr N, Osorio A, Park SK, Pearce CL, Pejovic T, Peterlongo P, Pfeiler G, Phelan CM, PooleEM, Pylkas K, Radice P, Rantala J, Rashid MU, Rennert G, Rhenius V, Rhiem K, Risch HA, Rodriguez G, Rossing MA, Rudolph A, Salvesen HB, Sangrajrang S, Sawyer EJ, Schildkraut JM, Schmidt MK, Schmutzler RK, Sellers TA, Seynaeve C, Shah M, Shen CY, Shu XO, Sieh W, Singer CF, Sinilnikova OM, Slager S, Song H, Soucy P, Southey MC, Stenmark-Askmalm M, Stoppa- Lyonnet D, Sutter C, Swerdlow A, Tchatchou S, Teixeira MR, Teo SH, Terry KL, Terry MB, Thomassen M, Tibiletti MG, Tihomirova L, Tognazzo S, Toland AE, Tomlinson I, Torres D, Truong T, Tseng CC, Tung N, Tworoger SS, Vachon C, van den Ouweland AM, van Doorn HC, van Rensburg EJ, Van t Veer LJ, Vanderstichele A, Vergote I, Vijai J, Wang Q, Wang-Gohrke S, Weitzel JN, Wentzensen N, Whittemore AS, Wildiers H, Winqvist R, Wu AH, Yannoukakos D, Yoon SY, Yu JC, Zheng W, Zheng Y, Khanna KK, Simard J, Monteiro AN, French JD, Couch FJ, Freedman ML, Easton DF, Dunning AM, Pharoah PD, Edwards SL, Chenevix-Trench G, Antoniou AC, Gayther SA. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus. Nat Commun 2016;7: Pharoah PD, Song H, Dicks E, Intermaggio MP, Harrington P, Baynes C, Alsop K, Australian Ovarian Cancer Study G, Bogdanova N, Cicek MS, Cunningham JM, Fridley BL, Gentry-Maharaj A, Hillemanns P, Lele S, Lester J, McGuire V, Moysich KB, Poblete S, Sieh W, Sucheston-Campbell L, Widschwendter M, Ovarian Cancer Association C, Whittemore AS, Dork T, Menon U, Odunsi K, Goode EL, Karlan BY, Bowtell DD, Gayther SA, Ramus SJ. PPM1D Mosaic Truncating Variants in Ovarian Cancer Cases May Be Treatment-Related Somatic Mutations. J Natl Cancer Inst 2016;108(3). 17

10 Radice P, Pharoah PD, Peterlongo P. Personalized testing based on polygenic risk score is promising for more efficient population-based screening programs for common oncological diseases. Ann Oncol Ali HR, Glont SE, Blows FM, Provenzano E, Dawson SJ, Liu B, Hiller L, Dunn J, Poole CJ, Bowden S, Earl HM, Pharoah PD, Caldas C. PD- L1 protein expression in breast cancer is rare, enriched in basal-like tumours and associated with infiltrating lymphocytes. Ann Oncol 2015;26(7): Blows FM, Ali HR, Dawson SJ, Le Quesne J, Provenzano E, Caldas C, Pharoah PD. Decline in Antigenicity of Tumor Markers by Storage Time Using Pathology Sections Cut From Tissue Microarrays. Appl Immunohistochem Mol Morphol Candido Dos Reis FJ, Song H, Goode EL, Cunningham JM, Fridley BL, Larson MC, Alsop K, Dicks E, Harrington P, Ramus SJ, de Fazio A, Mitchell G, Fereday S, Bolton KL, Gourley C, Michie C, Karlan BY, Lester J, Walsh C, Cass I, Olsson H, Gore M, Benitez J, Garcia MJ, Andrulis IL, Mulligan AM, Glendon G, Blanco I, Lazaro C, Whittemore AS, McGuire V, Sieh W, Montagna M, Alducci E, Sadetzki S, Chetrit A, Kwong A, Kjaer SK, Jensen A, Hogdall E, Neuhausen SL, Nussbaum RL, Daly M, Greene MH, Mai PL, Loud JT, Moysich KB, Toland AE, Lambrechts D, Ellis S, Frost D, Brenton JD, Tischkowitz M, Easton DF, Antoniou AC, Chenevix-Trench G, Gayther SA, Bowtell DD, Pharoah PD. Germline mutation in BRCA1 or BRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer. Clin Cancer Res 2015;21(3): Candido Dos Reis FJ, Lynn S, Ali HR, Eccles D, Hanby A, Provenzano E, Caldas C, Howat WJ, McDuffus LA, Liu B, Daley F, Coulson P, Vyas RJ, Harris LM, Owens JM, Carton AF, McQuillan JP, Paterson AM, Hirji Z, Christie SK, Holmes AR, Schmidt MK, Garcia-Closas M, Easton DF, Bolla MK, Wang Q, Benitez J, Milne RL, Mannermaa A, Couch F, Devilee P, Tollenaar RA, Seynaeve C, Cox A, Cross SS, Blows FM, Sanders J, de Groot R, Figueroa J, Sherman M, Hooning M, Brenner H, Holleczek B, Stegmaier C, Lintott C, Pharoah PD. Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in Cancer. EBioMedicine 2015;2(7): Dorling L, Barnett GC, Michailidou K, Coles CE, Burnet NG, Yarnold JR, Elliott RM, Dunning AM, Pharoah PD, West CM. Patients with a high polygenic risk of breast cancer do not have an increased risk of radiotherapy toxicity. Clin Cancer Res Easton DF, Pharoah PD, Antoniou AC, Tischkowitz M, Tavtigian SV, Nathanson KL, Devilee P, Meindl A, Couch FJ, Southey M, Goldgar DE, Evans DG, Chenevix-Trench G, Rahman N, Robson M, Domchek SM, Foulkes WD. Gene-panel sequencing and the prediction of breastcancer risk. N Engl J Med 2015;372(23): Guo Q, Abraham JE, Caldas C, Earl HM, Pharoah PP, investigators P. Replication of Genetic Polymorphisms Reported to Be Associated with Taxane-Related Sensory Neuropathy in Patients with Early Breast Cancer Treated with Paclitaxel-Response. Clin Cancer Res 2015;21(13):

11 Guo Q, Schmidt MK, Kraft P, Canisius S, Chen C, Khan S, Tyrer J, Bolla MK, Wang Q, Dennis J, Michailidou K, Lush M, Kar S, Beesley J, Dunning AM, Shah M, Czene K, Darabi H, Eriksson M, Lambrechts D, Weltens C, Leunen K, Bojesen SE, Nordestgaard BG, Nielsen SF, Flyger H, Chang- Claude J, Rudolph A, Seibold P, Flesch-Janys D, Blomqvist C, Aittomaki K, Fagerholm R, Muranen TA, Couch FJ, Olson JE, Vachon C, Andrulis IL, Knight JA, Glendon G, Mulligan AM, Broeks A, Hogervorst FB, Haiman CA, Henderson BE, Schumacher F, Le Marchand L, Hopper JL, Tsimiklis H, Apicella C, Southey MC, Cox A, Cross SS, Reed MW, Giles GG, Milne RL, McLean C, Winqvist R, Pylkas K, Jukkola-Vuorinen A, Grip M, Hooning MJ, Hollestelle A, Martens JW, van den Ouweland AM, Marme F, Schneeweiss A, Yang R, Burwinkel B, Figueroa J, Chanock SJ, Lissowska J, Sawyer EJ, Tomlinson I, Kerin MJ, Miller N, Brenner H, Dieffenbach AK, Arndt V, Holleczek B, Mannermaa A, Kataja V, Kosma VM, Hartikainen JM, Li J, Brand JS, Humphreys K, Devilee P, Tollenaar RA, Seynaeve C, Radice P, Peterlongo P, Bonanni B, Mariani P, Fasching PA, Beckmann MW, Hein A, Ekici AB, Chenevix-Trench G, Balleine R, kconfab I, Phillips KA, Benitez J, Zamora MP, Arias Perez JI, Menendez P, Jakubowska A, Lubinski J, Jaworska-Bieniek K, Durda K, Hamann U, Kabisch M, Ulmer HU, Rudiger T, Margolin S, Kristensen V, Nord S, Evans DG, Abraham JE, Earl HM, Hiller L, Dunn JA, Bowden S, Berg C, Campa D, Diver WR, Gapstur SM, Gaudet MM, Hankinson SE, Hoover RN, Husing A, Kaaks R, Machiela MJ, Willett W, Barrdahl M, Canzian F, Chin SF, Caldas C, Hunter DJ, Lindstrom S, Garcia-Closas M, Hall P, Easton DF, Eccles DM, Rahman N, Nevanlinna H, Pharoah PD. Identification of novel genetic markers of breast cancer survival. J Natl Cancer Inst 2015;107(5). Johnatty S, Tyrer JP, Kar SP, Beesley J, Lu Y, Gao B, Fasching PA, Hein A, Ekici AB, Beckmann MW, Lambrechts D, Van Nieuwenhuysen E, 21. Vergote I, Lambrechts S, Rossing MA, Doherty JA, Chang- Claude J, Modugno F, Ness RB, Moysich KB, Levine DA, Kiemeney LA, Massuger L, Gronwald J, Lubinski J, Brinton LA, Lissowska J, Wentzensen N, Song H, Rhenius V, Campbell I, Eccles D, Sieh W, Whittemore AS, McGuire V, Rothstein JH, Sutphen R, Anton-Culver H, Ziogas A, Gayther SA, Gentry- Maharaj A, Menon U, Ramus SJ, Pearce CL, Pike MC, Stram D, Wu AH, Kupryjanczyk J, Dansonka- Mieszkowska A, Rzepecka IK, Spiewankiewicz B, Goodman MT, Wilkens LR, Carney ME, Thompson PJ, Heitz F, du Bois A, Schwaab I, Harter P, Pisterer J, Hillemanns P, Karlan BY, Walsh C, Lester J, Orsulic S, Winham SJ, Earp M, Larson MC, Fogarty Z, Hogdall E, Jensen A, Kruger Kjaer S, Fridley BL, Cunningham J, Vierkant RA, Schildkraut JM, Iversen E, Terry KL, Cramer D, Bandera E, Orlow I, Pejovic T, Bean YT, Hogdall C, Lundvall L, McNeish IA, Paul J, Carty K, Siddiqui N, Glasspool R, Sellers TA, Kennedy C, Chiew YE, Berchuck A, Macgregor S, Pharoah P, Goode EL, defazio A, Webb P, Chenevix-Trench G. Genome-wide analysis identifies novel loci associated with ovarian cancer outcomes: findings from the Ovarian Cancer Association Consortium. Clin Cancer Res Kar SP, Tyrer JP, Li Q, Lawrenson K, Aben KK, Anton-Culver H, Antonenkova N, Chenevix-Trench G, Baker H, Bandera E, Bean YT, Beckmann MW, Berchuck A, Bisogna M, Bjorge L, Bogdanova N, Brinton LA, Brooks-Wilson A, Butzow R, Campbell I, Carty K, Chang- Claude J, Chen YA, Chen Z, Cook LS, Cramer D, Cunningham J, Cybulski C, Dansonka-Mieszkowska A, Dennis J, Dicks E, Doherty JA, Dork T, du Bois A, Durst M, Eccles D, Easton DF, Edwards RP, Ekici AB, Fasching PA, Fridley BL, Gao YT, Gentry- Maharaj A, Giles GG, Glasspool R, Goode EL, Goodman MT, Grownwald J, Harrington P, Harter P, Hein A, Heitz F, Hildebrandt MA, Hillemanns P, Hogdall E, Hogdall CK, 21

12 Hosono S, Iversen ES, Jakubowska A, Paul J, Jensen A, Ji BT, Karlan BY, Kjaer SK, Kelemen LE, Kellar M, Kelley J, Kiemeney LA, Krakstad C, Kupryjanczyk J, Lambrechts D, Lambrechts S, Le ND, Lee AW, Lele S, Leminen A, Lester J, Levine DA, Liang D, Lissowska J, Lu K, Lubinski J, Lundvall L, Massuger L, Matsuo K, McGuire V, McLaughlin JR, McNeish IA, Menon U, Modugno F, Moysich KB, Narod SA, Nedergaard L, Ness RB, Nevanlinna H, Odunsi K, Olson SH, Orlow I, Orsulic S, Weber RP, Pearce CL, Pejovic T, Pelttari LM, Permuth-Wey J, Phelan CM, Pike MC, Poole EM, Ramus SJ, Risch HA, Rosen B, Rossing MA, Rothstein JH, Rudolph A, Runnebaum IB, Rzepecka IK, Salvesen HB, Schildkraut JM, Schwaab I, Shu XO, Shvetsov YB, Siddiqui N, Sieh W, Song H, Southey MC, Sucheston-Campbell LE, Tangen IL, Teo SH, Terry KL, Thompson PJ, Timorek A, Tsai YY, Tworoger SS, van Altena AM, Nieuwenhuysen EV, Vergote I, Vierkant RA, Wang-Gohrke S, Walsh C, Wentzensen N, Whittemore AS, Wicklund KG, Wilkens LR, Woo YL, Wu X, Wu A, Yang H, Zheng W, Ziogas A, Sellers TA, Monteiro AN, Freedman ML, Gayther SA, Pharoah PD. Network-based integration of GWAS and gene expression identifies a HOX-centric network associated with serous ovarian cancer risk. Cancer Epidemiol Biomarkers Prev Kuchenbaecker KB, Ramus SJ, Tyrer J, Lee A, Shen HC, Beesley J, Lawrenson K, McGuffog L, Healey S, Lee JM, Spindler TJ, Lin YG, Pejovic T, Bean Y, Li Q, Coetzee S, Hazelett D, Miron A, Southey M, Terry MB, Goldgar DE, Buys SS, Janavicius R, Dorfling CM, van Rensburg EJ, Neuhausen SL, Ding YC, Hansen TV, Jonson L, Gerdes AM, Ejlertsen B, Barrowdale D, Dennis J, Benitez J, Osorio A, Garcia MJ, Komenaka I, Weitzel JN, Ganschow P, Peterlongo P, Bernard L, Viel A, Bonanni B, Peissel B, Manoukian S, Radice P, Papi L, Ottini L, Fostira F, Konstantopoulou I, Garber J, Frost D, Perkins J, Platte R, Ellis S, Embrace, Godwin AK, Schmutzler RK, Meindl A, Engel C, Sutter C, Sinilnikova OM, Collaborators GS, Damiola F, Mazoyer S, Stoppa- Lyonnet D, Claes K, De Leeneer K, Kirk J, Rodriguez GC, Piedmonte M, O Malley DM, de la Hoya M, Caldes T, Aittomaki K, Nevanlinna H, Collee JM, Rookus MA, Oosterwijk JC, Breast Cancer Family R, Tihomirova L, Tung N, Hamann U, Isaccs C,Tischkowitz M, Imyanitov EN, Caligo MA, Campbell IG, Hogervorst FB, Hebon, Olah E, Diez O, Blanco I, Brunet J, Lazaro C, Pujana MA, Jakubowska A, Gronwald J, Lubinski J, Sukiennicki G, Barkardottir RB, Plante M, Simard J, Soucy P, Montagna M, Tognazzo S, Teixeira MR, Investigators KC, Pankratz VS, Wang X, Lindor N, Szabo CI, Kauff N, Vijai J, Aghajanian CA, Pfeiler G, Berger A, Singer CF, Tea MK, Phelan CM, Greene MH, Mai PL, Rennert G, Mulligan AM, Tchatchou S, Andrulis IL, Glendon G, Toland AE, Jensen UB, Kruse TA, Thomassen M, Bojesen A, Zidan J, Friedman E, Laitman Y, Soller M, Liljegren A, Arver B, Einbeigi Z, Stenmark-Askmalm M, Olopade OI, Nussbaum RL, Rebbeck TR, Nathanson KL, Domchek SM, Lu KH, Karlan BY, Walsh C, Lester J, Australian Cancer S, Australian Ovarian Cancer Study G, Hein A, Ekici AB, Beckmann MW, Fasching PA, Lambrechts D, Van Nieuwenhuysen E, Vergote I, Lambrechts S, Dicks E, Doherty JA, Wicklund KG, Rossing MA, Rudolph A, Chang-Claude J, Wang- Gohrke S, Eilber U, Moysich KB, Odunsi K, Sucheston L, Lele S, Wilkens LR, Goodman MT, Thompson PJ, Shvetsov YB, Runnebaum IB, Durst M, Hillemanns P, Dork T, Antonenkova N, Bogdanova N, Leminen A, Pelttari LM, Butzow R, Modugno F, Kelley JL, Edwards RP, Ness RB, du Bois A, Heitz F, Schwaab I, Harter P, Matsuo K, Hosono S, Orsulic S, Jensen A, Kjaer SK, Hogdall E, Hasmad HN, Azmi MA, Teo SH, Woo YL, Fridley BL, Goode EL, Cunningham JM, Vierkant RA, Bruinsma F, Giles GG, Liang D, Hildebrandt MA, Wu X, Levine DA, Bisogna M, Berchuck A, Iversen ES, Schildkraut JM, Concannon P, Weber RP, Cramer DW, Terry 23

13 KL, Poole EM, Tworoger SS, Bandera EV, Orlow I, Olson SH, Krakstad C, Salvesen HB, Tangen IL, Bjorge L, van Altena AM, Aben KK, Kiemeney LA, Massuger LF, Kellar M, Brooks-Wilson A, Kelemen LE, Cook LS, Le ND, Cybulski C, Yang H, Lissowska J, Brinton LA, Wentzensen N, Hogdall C, Lundvall L, Nedergaard L, Baker H, Song H, Eccles D, McNeish I, Paul J, Carty K, Siddiqui N, Glasspool R, Whittemore AS, Rothstein JH, McGuire V, Sieh W, Ji BT, Zheng W, Shu XO, Gao YT, Rosen B, Risch HA, McLaughlin JR, Narod SA, Monteiro AN, Chen A, Lin HY, Permuth-Wey J, Sellers TA, Tsai YY, Chen Z, Ziogas A,Anton-Culver H, Gentry-Maharaj A, Menon U, Harrington P, Lee AW, Wu AH, Pearce CL, Coetzee G, Pike MC, Dansonka-Mieszkowska A, Timorek A, Rzepecka IK, Kupryjanczyk J, Freedman M, Noushmehr H, Easton DF, Offit K, Couch FJ, Gayther S, Pharoah PP, Antoniou AC, Chenevix-Trench G, Consortium of Investigators of Modifiers of B, Brca. Identification of six new susceptibility loci for invasive epithelial ovarian cancer. Nat Genet 2015;47(2): Pashayan N, Duffy SW, Neal DE, Hamdy FC, Donovan JL, Martin RM, Harrington P, Benlloch S, Amin Al Olama A, Shah M, Kote-Jarai Z, Easton DF, Eeles R, Pharoah PD. Implications of polygenic risk- stratified screening for prostate cancer on overdiagnosis. Genet Med Pashayan N, Pharoah PD, Schleutker J, Talala K, Tammela T, Maattanen L, Harrington P, Tyrer J, Eeles R, Duffy SW, Auvinen A. Reducing overdiagnosis by polygenic risk-stratified screening: findings from the Finnish section of the ERSPC. Br J Cancer 2015;113(7): Pirie A, Guo Q, Kraft P, Canisius S, Eccles DM, Rahman N, Nevanlinna H, Chen C, Khan S, Tyrer J, Bolla MK, Wang Q, Dennis J, Michailidou 26. K, Lush M, Dunning AM, Shah M, Czene K, Darabi H, Eriksson M, Lambrechts D, Weltens C, Leunen K, van Ongeval C, Nordestgaard BG, Nielsen SF, Flyger H, Rudolph A, Seibold P, Flesch-Janys D, Blomqvist C, Aittomaki K, Fagerholm R, Muranen TA, Olsen JE, Hallberg E, Vachon C, Knight JA, Glendon G, Mulligan AM, Broeks A, Cornelissen S, Haiman CA, Henderson BE, Schumacher F, Le Marchand L, Hopper JL, Tsimiklis H, Apicella C, Southey MC, Cross SS, Reed MW, Giles GG, Milne RL, McLean C, Winqvist R, Pylkas K, Jukkola-Vuorinen A, Grip M, Hooning MJ, Hollestelle A, Martens JW, van den Ouweland AM, Marme F, Schneeweiss A, Yang R, Burwinkel B, Figueroa J, Chanock SJ, Lissowska J, Sawyer EJ, Tomlinson I, Kerin MJ, Miller N, Brenner H, Butterbach K, Holleczek B, Kataja V, Kosma VM, Hartikainen JM, Li J, Brand JS, Humphreys K, Devilee P, Tollenaar RA, Seynaeve C, Radice P, Peterlongo P, Manoukian S, Ficarazzi F, Beckmann MW, Hein A, Ekici AB, Balleine R, Phillips KA, kconfab I, Benitez J, Zamora MP, Perez JI, Menendez P, Jakubowska A, Lubinski J, Gronwald J, Durda K, Hamann U, Kabisch M, Ulmer HU, Rudiger T, Margolin S, Kristensen V, Nord S, Investigators N, Evans DG, Abraham J, Earl H, Poole CJ, Hiller L, Dunn JA, Bowden S, Yang R, Campa D, Diver WR, Gapstur SM, Gaudet MM, Hankinson S, Hoover RN, Husing A, Kaaks R, Machiela MJ, Willett W, Barrdahl M, Canzian F, Chin SF, Caldas C, Hunter DJ, Lindstrom S, Garcia- Closas M, Couch FJ, Chenevix-Trench G, Mannermaa A, Andrulis IL, Hall P, Chang-Claude J, Easton DF, Bojesen SE, Cox A, Fasching PA, Pharoah PD, Schmidt MK. Common germline polymorphisms associated with breast cancer specific survival. Breast Cancer Res 2015;17(1):58. Pirie A, Wood A, Lush M, Tyrer J, Pharoah PD. The effect of rare variants on inflation of the test statistics in case-control analyses. BMC Bioinformatics 2015;16(1):53. 25

14 Ramus SJ, Song H, Dicks E, Tyrer JP, Rosenthal AN, Intermaggio MP, Fraser L, Gentry-Maharaj A, Hayward J, Philpott S, Anderson C, Edlund CK, Conti D, Harrington P, Barrowdale D, Bowtell DD, Alsop K, Mitchell G, Group AS, Cicek MS, Cunningham JM, Fridley BL, Alsop J, Jimenez- Linan M, Poblete S, Lele S, Sucheston-Campbell L, Moysich KB, Sieh W, McGuire V, Lester J, Bogdanova N, Durst M, Hillemanns P, Ovarian Cancer Association C, Odunsi K, Whittemore AS, Karlan BY, Dork T, Goode EL, Menon U, Jacobs IJ, Antoniou AC, Pharoah PD, Gayther SA. Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women with Ovarian Cancer. J Natl Cancer Inst 2015;107(11). Song H, Dicks E, Ramus SJ, Tyrer JP, Intermaggio MP, Hayward J, Edlund CK, Conti D, Harrington P, Fraser L, Philpott S, Anderson C, Rosenthal A, Gentry-Maharaj A, Bowtell DD, Alsop K, Cicek MS, Cunningham JM, Fridley BL, Alsop J, Jimenez-Linan M, Hogdall E, Hogdall CK, Jensen A, Kjaer SK, Lubinski J, Huzarski T, Jakubowska A, Gronwald J, Poblete S, Lele S, Sucheston-Campbell L, Moysich KB, Odunsi K, Goode EL, Menon U, Jacobs IJ, Gayther SA, Pharoah PD. Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. J Clin Oncol Abraham JE, Guo Q, Dorling L, Tyrer J, Ingle S, Hardy R, Vallier AL, Hiller L, Burns R, Jones L, Bowden SJ, Dunn JA, Poole CJ, Caldas C, Pharoah PP, Earl HM. Replication of genetic polymorphisms reported to be associated with taxane-related sensory neuropathy in patients with early breast cancer treated with Paclitaxel. Clin Cancer Res 2014;20(9): Ali AM, Schmidt MK, Bolla MK, Wang Q, Gago-Dominguez M, Castelao JE, Carracedo A, Garzon VM, Bojesen SE, Nordestgaard BG, Flyger H, Chang-Claude J, Vrieling A, Rudolph A, Seibold P, Nevanlinna H, Muranen TA, Aaltonen K, Blomqvist C, Matsuo K, Ito H, Iwata H, Horio A, John EM, Sherman M, Lissowska J, Figueroa J, Garcia-Closas M, Anton- Culver H, Shah M, Hopper JL, Trichopoulou A, Bueno-de-Mesquita B, Krogh V, Weiderpass E, Andersson A, Clavel-Chapelon F, Dossus L, Fagherazzi G, Peeters PH, Olsen A, Wishart GC, Easton DF, Borgquist S, Overvad K, Barricarte A, Gonzalez CA, Sanchez MJ, Amiano P, Riboli E, Key T, Pharoah PD. Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases. Cancer Epidemiol Biomarkers Prev 2014;23(6): Ali HR, Provenzano E, Dawson SJ, Blows FM, Liu B, Shah M, Earl HM, Poole CJ, Hiller L, Dunn JA, Bowden SJ, Twelves C, Bartlett JM, Mahmoud SM, Rakha E, Ellis IO, Liu S, Gao D, Nielsen TO, Pharoah PD, Caldas C. Association between CD8+ T-cell infiltration and breast cancer survival in patients. Ann Oncol 2014;25(8): Hall AE, Chowdhury S, Hallowell N, Pashayan N, Dent T, Pharoah P, Burton H. Implementing risk- stratified screening for common cancers: a review of potential ethical, legal and social issues. J Public Health (Oxf) 2014;36(2): Hall AE, Chowdhury S, Pashayan N, Hallowell N, Pharoah P, Burton H. What ethical and legal principles should guide the genotyping of children as part of a personalised screening programme for common cancer? J Med Ethics 2014;40(3):

15 Jervis S, Song H, Lee A, Dicks E, Tyrer J, Harrington P, Easton DF, Jacobs IJ, Pharoah PP, Antoniou AC.Ovarian cancer familial relative risks by tumour subtypes and by known ovarian cancer genetic susceptibility variants. J Med Genet 2014;51(2): Song H, Cicek MS, Dicks E, Harrington P, Ramus SJ, Cunningham JM, Fridley BL, Tyrer JP, Alsop J, Jimenez-Linan M, Gayther SA, Goode EL, Pharoah PD. The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population. Hum Mol Genet 2014;23(17): Wishart GC, Rakha E, Green A, Ellis I, Ali HR, Provenzano E, Blows FM, Caldas C, Pharoah PD. Inclusion of KI67 significantly improves performance of the PREDICT prognostication and prediction model for early breast cancer. BMC Cancer 2014;14:908. Ali AM, Provenzano E, Bartlett JM, Abraham J, Driver K, Munro AF, Twelves C, Poole CJ, Hiller L, Dunn JA, Earl HM, Caldas C, Pharoah PD. Prognosis of early breast cancer by immunohistochemistry defined intrinsic sub-types in patients treated with adjuvant chemotherapy in the NEAT/BR9601 trial. Int J Cancer 2013;133(6): Ali HR, Irwin M, Morris L, Dawson SJ, Blows FM, Provenzano E, Mahler- Araujo B, Pharoah PD, Walton NA, Brenton JD, Caldas C. Astronomical algorithms for automated analysis of tissue protein expression in breast cancer. Br J Cancer 2013;108(3): Burton H, Chowdhury S, Dent T, Hall A, Pashayan N, Pharoah P. Public health implications from COGS and potential for risk stratification and screening. Nat Genet 2013;45(4): Dent T, Jbilou J, Rafi I, Segnan N, Tornberg S, Chowdhury S, Hall A, Lyratzopoulos G, Eeles R, Eccles D, Hallowell N, Pashayan N, Pharoah P, Burton H. Stratified cancer screening: the practicalities of implementation. Public Health Genomics 2013;16(3):94-9. Pashayan N, Hall A, Chowdhury S, Dent T, Pharoah PD, Burton H. Public health genomics and personalized prevention: lessons from the COGS project. J Intern Med 2013;274(5): Permuth-Wey J, Lawrenson K, Shen HC, Velkova A, Tyrer JP, Chen Z, Lin HY, Ann Chen Y, Tsai YY, Qu X, Ramus SJ, Karevan R, Lee J, Lee N, Larson MC, Aben KK, Anton-Culver H, Antonenkova N, Antoniou AC, Armasu SM, Bacot F, Baglietto L, Bandera EV, Barnholtz-Sloan J, Beckmann MW, Birrer MJ, Bloom G, Bogdanova N, Brinton LA, Brooks-Wilson A, Brown R, Butzow R, Cai Q, Campbell I, Chang- Claude J, Chanock S, Chenevix-Trench G, Cheng JQ, Cicek MS, Coetzee GA, Cook LS, Couch FJ,Cramer DW, Cunningham JM, Dansonka-Mieszkowska A, Despierre E, Doherty JA, Dork T, du Bois A, Durst M, Easton DF, Eccles D, Edwards R, Ekici AB, Fasching PA, Fenstermacher DA, Flanagan JM, Garcia-Closas M, Gentry-Maharaj A, Giles GG, Glasspool RM, Gonzalez-Bosquet J, Goodman MT,Gore M, Gorski B, Gronwald J, Hall P, Halle MK, Harter P, Heitz F, Hillemanns P, Hoatlin M, Hogdall CK, Hogdall E, Hosono S, Jakubowska A, Jensen A, Jim H, Kalli KR, Karlan BY, Kaye SB, Kelemen LE, Kiemeney LA, Kikkawa F, Konecny GE, Krakstad C, Kruger Kjaer S, Kupryjanczyk J, Lambrechts D, Lambrechts S, Lancaster JM, Le ND, Leminen A, Levine DA, Liang D, Kiong Lim B, Lin J, Lissowska J,Lu KH, Lubinski J, Lurie G, Massuger LF, Matsuo K, McGuire V, McLaughlin JR, Menon U, Modugno F,Moysich KB, Nakanishi T, Narod SA, Nedergaard L, Ness RB, Nevanlinna H, Nickels S, Noushmehr H, Odunsi K, Olson SH, Orlow I, Paul J, Pearce CL, Pejovic T, Pelttari LM, Pike MC, Poole EM, Raska P, Renner SP, Risch HA, Rodriguez-Rodriguez L, Anne Rossing M, Rudolph A, Runnebaum IB, Rzepecka IK, Salvesen HB, Schwaab I, Severi G, Shridhar V, Shu XO, 29

16 Shvetsov YB, Sieh W, Song H, Southey MC, Spiewankiewicz B, Stram D, Sutphen R, Teo SH, Terry KL, Tessier DC, Thompson PJ, Tworoger SS,van Altena AM, Vergote I, Vierkant RA, Vincent D, Vitonis AF, Wang-Gohrke S, Palmieri Weber R, Wentzensen N, Whittemore AS, Wik E, Wilkens LR, Winterhoff B, Ling Woo Y, Wu AH, Xiang YB, Yang HP, Zheng W, Ziogas A, Zulkifli F, Phelan CM, Iversen E, Schildkraut JM, Berchuck A, Fridley BL, Goode EL, Pharoah PD, Monteiro AN, Sellers TA, Gayther SA. Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q Nat Commun 2013;4:1627. Pharoah PD, Sewell B, Fitzsimmons D, Bennett HS, Pashayan N. Cost effectiveness of the NHS breast screening programme: life table model. BMJ 2013;346:f2618. Pharoah PD, Tsai YY, Ramus SJ, Phelan CM, Goode EL, Lawrenson K, Buckley M, Fridley BL, Tyrer JP, Shen H, Weber R, Karevan R, Larson MC, Song H, Tessier DC, Bacot F, Vincent D, Cunningham JM, Dennis J, Dicks E, Aben KK, Anton-Culver H, Antonenkova N, Armasu SM, Baglietto L, Bandera EV, Beckmann MW, Birrer MJ, Bloom G, Bogdanova N, Brenton JD, Brinton LA, Brooks-Wilson A, Brown R, Butzow R, Campbell I, Carney ME, Carvalho RS, Chang-Claude J, Chen YA, Chen Z, Chow WH,Cicek MS, Coetzee G, Cook LS, Cramer DW, Cybulski C, Dansonka- Mieszkowska A, Despierre E, Doherty JA, Dork T, du Bois A, Durst M, Eccles D, Edwards R, Ekici AB, Fasching PA, Fenstermacher D, Flanagan J, Gao YT, Garcia- Closas M, Gentry-Maharaj A, Giles G, Gjyshi A, Gore M, Gronwald J, Guo Q, Halle MK, Harter P, Hein A, Heitz F, Hillemanns P, Hoatlin M, Hogdall E, Hogdall CK, Hosono S, Jakubowska A, Jensen A, Kalli KR, Karlan BY, Kelemen LE, Kiemeney LA, Kjaer SK, Konecny GE, Krakstad C, Kupryjanczyk J, Lambrechts D, Lambrechts S, Le ND, Lee N, Lee J, Leminen A, Lim BK, Lissowska J, Lubinski J, Lundvall L, Lurie G, Massuger LF, Matsuo K, McGuire V, McLaughlin JR, Menon U, Modugno F, Moysich KB, Nakanishi T, Narod SA, Ness RB, Nevanlinna H, Nickels S, Noushmehr H, Odunsi 45. K, Olson S, Orlow I, Paul J, Pejovic T, Pelttari LM, Permuth-Wey J, Pike MC, Poole EM, Qu X, Risch HA, Rodriguez-Rodriguez L, Rossing MA, Rudolph A, Runnebaum I, Rzepecka IK, Salvesen HB, Schwaab I, Severi G, Shen H, Shridhar V, Shu XO, Sieh W, Southey MC, Spellman P, Tajima K, Teo SH, Terry KL, Thompson PJ, Timorek A, Tworoger SS, van Altena AM, van den Berg D, Vergote I, Vierkant RA, Vitonis AF, Wang-Gohrke S, Wentzensen N, Whittemore AS, Wik E, Winterhoff B, Woo YL, Wu AH, Yang HP, Zheng W, Ziogas A, Zulkifli F, Goodman MT, Hall P, Easton DF, Pearce CL, Berchuck A, Chenevix-Trench G, Iversen E, Monteiro AN, Gayther SA, Schildkraut JM, Sellers TA. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. Nat Genet 2013;45(4): Shen H, Fridley BL, Song H, Lawrenson K, Cunningham JM, Ramus SJ, Cicek MS, Tyrer J, Stram D, Larson MC, Kobel M, Ziogas A, Zheng W, Yang HP, Wu AH, Wozniak EL, Woo YL, Winterhoff B, Wik E, Whittemore AS, Wentzensen N, Weber RP, Vitonis AF, Vincent D, Vierkant RA, Vergote I, Van Den Berg D, Van Altena AM, Tworoger SS, Thompson PJ, Tessier DC, Terry KL, Teo SH, Templeman C, Stram DO, Southey MC, Sieh W, Siddiqui N, Shvetsov YB, Shu XO, Shridhar V, Wang-Gohrke S, Severi G, Schwaab I, Salvesen HB, Rzepecka IK, Runnebaum IB, Rossing MA, Rodriguez- Rodriguez L, Risch HA, Renner SP, Poole EM, Pike MC, Phelan CM, Pelttari LM, Pejovic T, Paul J, Orlow I, Omar SZ, Olson SH, Odunsi K, Nickels S, Nevanlinna H, Ness RB, Narod SA, Nakanishi T, Moysich KB, Monteiro AN, Moes-Sosnowska J, Modugno F, Menon U, McLaughlin JR, McGuire V, Matsuo K, Adenan NA, Massuger LF, Lurie G, Lundvall L, Lubinski J, Lissowska J, Levine DA, Leminen A, Lee AW, Le ND, Lambrechts S, Lambrechts D, Kupryjanczyk J, Krakstad C, Konecny GE, Kjaer SK, Kiemeney LA, Kelemen LE, Keeney GL, Karlan BY, Karevan R, Kalli KR, Kajiyama H, Ji BT, Jensen A, Jakubowska A, Iversen E, Hosono S, Hogdall CK, Hogdall E, Hoatlin M, Hillemanns P, Heitz F, Hein R, Harter P, Halle MK, Hall P, Gronwald J, Gore M, Goodman MT, Giles GG, Gentry-Maharaj A, Garcia-Closas M, Flanagan JM, Fasching PA, Ekici AB, Edwards R, Eccles D, Easton DF, Durst M, du Bois A, Dork T, Doherty 31

17 JA, Despierre E, Dansonka-Mieszkowska A, Cybulski C, Cramer DW, Cook LS, Chen X, Charbonneau B, Chang-Claude J, Campbell I, Butzow R, Bunker CH, Brueggmann D, Brown R, Brooks-Wilson A, Brinton LA, Bogdanova N, Block MS, Benjamin E, Beesley J, Beckmann MW, Bandera EV, Baglietto L, Bacot F, Armasu SM, Antonenkova N, Anton- Culver H, Aben KK, Liang D, Wu X, Lu K, Hildebrandt MA, Schildkraut JM, Sellers TA, Huntsman D, Berchuck A, Chenevix-Trench G, Gayther SA, Pharoah PD, Laird PW, Goode EL, Pearce CL. Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer. Nat Commun 2013;4:1628. Sieh W, Kobel M, Longacre TA, Bowtell DD, Defazio A, Goodman MT, Hogdall E, Deen S, Wentzensen N, Moysich KB, Brenton JD, Clarke BA, Menon U, Gilks CB, Kim A, Madore J, Fereday S, George J, Galletta L, Lurie G, Wilkens LR, Carney ME, Thompson PJ, Matsuno RK, Kjaer SK, Jensen A, Hogdall C, Kalli KR, Fridley BL, Keeney GL, Vierkant RA, Cunningham JM, Brinton LA, Yang HP, Sherman ME, Garcia-Closas M, Lissowska J, Odunsi K, Morrison C, Lele S, Bshara W, Sucheston L, Jimenez-Linan M, Driver K, Alsop J, Mack M, McGuire V, Rothstein JH, Rosen BP, Bernardini MQ, Mackay H, Oza A, Wozniak EL, Benjamin E, Gentry-Maharaj A, Gayther SA, Tinker AV, Prentice LM, Chow C, Anglesio MS, Johnatty SE, Chenevix- Trench G, Whittemore AS, Pharoah PD, Goode EL, Huntsman DG, Ramus SJ. Hormone-receptor expression and ovarian cancer survival: an Ovarian Tumor Tissue Analysis consortium study. Lancet Oncol 2013;14(9): Tyrer JP, Guo Q, Easton DF, Pharoah PD. The admixture maximum likelihood test to test for association between rare variants and disease phenotypes. BMC Bioinformatics 2013;14(1): Reviews Ghoussaini M, Pharoah PD, Easton DF. Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning? Am J Pathol 2013;183(4): Eccles SA, Aboagye EO, Ali S, Anderson AS, Armes J, Berditchevski F, Blaydes JP, Brennan K, Brown NJ, Bryant HE, Bundred NJ, Burchell JM, Campbell AM, Carroll JS, Clarke RB, Coles CE, Cook GJ, Cox A, Curtin NJ, Dekker LV, Dos Santos Silva I, Duffy SW, Easton DF, Eccles DM, Edwards DR, Edwards J, Evans D, Fenlon DF, Flanagan JM, Foster C, Gallagher WM, Garcia-Closas M, Gee JM, Gescher AJ, Goh V, Groves AM, Harvey AJ, Harvie M, Hennessy BT, Hiscox S, Holen I, Howell SJ, Howell A, Hubbard G, Hulbert-Williams N, Hunter MS, Jasani B, Jones LI, Key TJ, Kirwan CC, Kong A, Kunkler IH, Langdon SP, Leach MO, Mann DJ, Marshall JF, Martin L, Martin SG, Macdougall JE, Miles DW, Miller WR, Morris JR, Moss SM, Mullan P, Natrajan R, O Connor JP, O Connor R, Palmieri C, Pharoah PD, Rakha EA, Reed E, Robinson SP, Sshai E, Saxton JM, Schmid P, Smalley MJ, Speirs V, Stein R, Stingl J, Streuli CH, Tutt AN, Velikova G, Walker RA, Watson CJ, Williams KJ, Young LS, Thompson AM. Critical research gaps and translational priorities for the successful prevention and treatment of breast cancer. Breast Cancer Res 2013; 15(5): R92. Latest Reports National Institute for Health and Clinical Excellence. Familial breast cancer: Classification and care of people at risk of familial breast cancer and management of breast cancer and related risks in people with a family history of breast cancer, 2013 Advisory Group on Ionising Radiation. Human Radiosensitivity: Health Protection Agency,

CURRICULUM VITAE. University of California, Los Angeles Department of Ecology and Evolutionary Biology B.S. (Biology), June 2006

CURRICULUM VITAE. University of California, Los Angeles Department of Ecology and Evolutionary Biology B.S. (Biology), June 2006 July 2016 CURRICULUM VITAE Personal Information Name Work Address Alice Wen-Ron Lee, PhD, MPH 800 N. State College Blvd, KHS-127 Fullerton, CA 92831 Phone (657) 278-8104 E-mail Address alicelee@fullerton.edu

More information

Curriculum Vitae Edwin Severin Iversen, Jr.

Curriculum Vitae Edwin Severin Iversen, Jr. Curriculum Vitae Edwin Severin Iversen, Jr. March 5, 2019 2529 Perkins Rd. Dept. Statistical Science, Box 90251 Durham, NC 27705 Duke University (919) 419 1487 Durham, NC 27708 0251 (919) 681 8442 iversen@duke.edu

More information

Prof Kelly-Anne Phillips, Publications List

Prof Kelly-Anne Phillips, Publications List Prof Kelly-Anne Phillips, Publications List 2018: 1. Butow P, Price M, Coll J, Tucker K, Meiser B, Milne R, Wilson J, Heiniger L, Baylock B, Bullen T, Weideman P, Phillips KA; kconfab investigators; kconfab

More information

Supplementary Figure S1A

Supplementary Figure S1A Supplementary Figure S1A-G. LocusZoom regional association plots for the seven new cross-cancer loci that were > 1 Mb from known index SNPs. Genes up to 500 kb on either side of each new index SNP are

More information

Professor of Epidemiology Yale School of Public Health, Yale School of Medicine

Professor of Epidemiology Yale School of Public Health, Yale School of Medicine Curriculum Vitae for: HARVEY A. RISCH, M.D., PH.D. Professor of Epidemiology Yale School of Public Health, Yale School of Medicine Business Address: Yale School of Public Health 60 College Street, LEPH

More information

Professor of Epidemiology Yale School of Public Health Yale School of Medicine Yale Cancer Center

Professor of Epidemiology Yale School of Public Health Yale School of Medicine Yale Cancer Center Curriculum Vitae for: HARVEY A. RISCH, M.D., PH.D. Professor of Epidemiology Yale School of Public Health Yale School of Medicine Yale Cancer Center Business Address: Yale School of Public Health 60 College

More information

PREPARED FOR: U.S. Army Medical Research and Materiel Command Fort Detrick, Maryland

PREPARED FOR: U.S. Army Medical Research and Materiel Command Fort Detrick, Maryland AD Award Number: W81XWH-10-1-0341 TITLE: Genetic Modifiers of Ovarian Cancer PRINCIPAL INVESTIGATOR: Fergus Couch CONTRACTING ORGANIZATION: Mayo Clinic Rochester, MN 55905 REPORT DATE: June 2011 TYPE OF

More information

Hui-Yi Lin, PhD Date: Jun. 2016

Hui-Yi Lin, PhD Date: Jun. 2016 , PhD Date: Current Position: Associate Professor Biostatistics Program School of Public Health Louisiana State University Health Sciences Center (LSUHSC) 2020 Gravier Street, Room 265 New Orleans, LA

More information

Hui-Yi Lin, PhD Date: Dec. 2017

Hui-Yi Lin, PhD Date: Dec. 2017 , PhD Date: Current Position: Associate Professor Biostatistics Program School of Public Health Louisiana State University Health Sciences Center (LSUHSC) 2020 Gravier Street, Room 265 New Orleans, LA

More information

Use of multiple Single Nucleotide Polymorphism (SNP) testing to predict breast cancer risk in a familial screening clinic

Use of multiple Single Nucleotide Polymorphism (SNP) testing to predict breast cancer risk in a familial screening clinic Use of multiple Single Nucleotide Polymorphism (SNP) testing to predict breast cancer risk in a familial screening clinic Running title: SNP testing in familial breast cancer Evans D Gareth MD, *1,2 Brentnall

More information

Supplementary webappendix

Supplementary webappendix Supplementary webappendix This webappendix formed part of the original submission and has been peer reviewed. We post it as supplied by the authors. Supplement to: Hartman M, Loy EY, Ku CS, Chia KS. Molecular

More information

Specifying the ovarian cancer risk threshold of premenopausal risk reducing salpingooophorectomy

Specifying the ovarian cancer risk threshold of premenopausal risk reducing salpingooophorectomy Specifying the ovarian cancer risk threshold of premenopausal risk reducing salpingooophorectomy for ovarian cancer prevention: a cost-effectiveness analysis 1,2,3 Ranjit Manchanda, 4 Rosa Legood, 5 Antonis

More information

Original Article Impact of gene polymorphisms located near ADAM17 and additional SNP-SNP interaction on ovarian cancer risk in Chinese women

Original Article Impact of gene polymorphisms located near ADAM17 and additional SNP-SNP interaction on ovarian cancer risk in Chinese women Int J Clin Exp Med 2018;11(9):9941-9949 www.ijcem.com /ISSN:1940-5901/IJCEM0073417 Original Article Impact of gene polymorphisms located near ADAM17 and additional SNP-SNP interaction on ovarian cancer

More information

Original Article Loss of expression of EphB1 protein in serous carcinoma of ovary associated with metastasis and poor survival

Original Article Loss of expression of EphB1 protein in serous carcinoma of ovary associated with metastasis and poor survival Int J Clin Exp Pathol 2014;7(1):313-321 www.ijcep.com /ISSN:1936-2625/IJCEP1308075 Original Article Loss of expression of EphB1 protein in serous carcinoma of ovary associated with metastasis and poor

More information

Cancer risk prediction via algorithms: identifying individuals at high-risk of breast and ovarian cancer

Cancer risk prediction via algorithms: identifying individuals at high-risk of breast and ovarian cancer Cancer risk prediction via algorithms: identifying individuals at high-risk of breast and ovarian cancer Antonis C. Antoniou Department of Public Health and Primary Care University of Cambridge, U.K. No

More information

committee of the International Agency for Research on Cancer (IARC), the University of

committee of the International Agency for Research on Cancer (IARC), the University of Supplemental Methods Ethics Statement The mutation screening and analyses described here were approved by the Ethics committee of the International Agency for Research on Cancer (IARC), the University

More information

General Introduction and outline

General Introduction and outline Chapter 1 General Introduction and outline Breast cancer outcome some facts and figures Breast cancer is the most common cancer in women worldwide (Ferlay et al, 2010b; Ferlay et al, 2013). Although the

More information

2016 Publications by members of the Vanderbilt Epidemiology Center Jain NB Raskin L Vermund SH Vermund SH Rebeiro PF Andersen SW Blot WJ Shu X-O

2016 Publications by members of the Vanderbilt Epidemiology Center Jain NB Raskin L Vermund SH Vermund SH Rebeiro PF Andersen SW Blot WJ Shu X-O 2016 Publications by members of the Vanderbilt Epidemiology Center (Bold names are VEC members) 1. Abdul-Wahab TA, Betancourt JP, Hassan F, Thani SA, Choueiri H, Jain NB, Malanga GA, Murrell WD, Prasad

More information

Publikationsverzeichnis Prof. Dr. Y. Ko Stand 05/2018

Publikationsverzeichnis Prof. Dr. Y. Ko Stand 05/2018 1 1. Frank R, Scheffler M, Merkelbach-Bruse S, Ihle MA, Kron A, Rauer M, Ueckeroth F, Koenig K, Michels S, Fischer R, Eisert A, Fassunke J, Heydt C, Serke M, Ko, Y.D., Gerigk U, Geist T, Kaminsky B, Heukamp

More information

WISSENSCHAFTLICHE PUBLIKATIONEN 2016

WISSENSCHAFTLICHE PUBLIKATIONEN 2016 WISSENSCHAFTLICHE PUBLIKATIONEN 2016 Universitätsklinik für Frauenheilkunde 215 Auer K, Bachmayr-Heyda A, Aust S, Grunt TW, Pils D Comparative transcriptome analysis links distinct peritoneal tumor spread

More information

TITLE: Aurora-A as a Modifier of Breast Cancer Risk in BRCA1/2 Mutation Carriers

TITLE: Aurora-A as a Modifier of Breast Cancer Risk in BRCA1/2 Mutation Carriers AD Award Number: W81XWH-04-1-0588 TITLE: Aurora-A as a Modifier of Breast Cancer Risk in BRCA1/2 Mutation Carriers PRINCIPAL INVESTIGATOR: Fergus J. Couch, Ph.D. CONTRACTING ORGANIZATION: Mayo Clinic Rochester,

More information

PREPARED FOR: U.S. Army Medical Research and Materiel Command Fort Detrick, Maryland

PREPARED FOR: U.S. Army Medical Research and Materiel Command Fort Detrick, Maryland AD Award Number: W81XWH-11-1-0342 TITLE: Identification of Genes and Genetic Variants Associated with Poor Treatment Response in Patients with Prostate Cancer PRINCIPAL INVESTIGATOR: Lisa A. Cannon-Albright

More information

Accepted Preprint first posted on 15 August 2016 as Manuscript ERC

Accepted Preprint first posted on 15 August 2016 as Manuscript ERC Page 1 of 28 Accepted Preprint first posted on 15 August 2016 as Manuscript ERC-16-0277 1 Modifiers of breast and ovarian cancer risks for BRCA1 and BRCA2 mutation carriers. 2 3 Roger L. Milne 1,2 and

More information

Managing Moderate Penetrance

Managing Moderate Penetrance Managing Moderate Penetrance Thomas Slavin, MD, FACMG Assistant Clinical Professor, Department of Medical Oncology, Division of Clinical Cancer Genetics Program Member, Cancer Control and Population Sciences

More information

Breast and ovarian cancer risk assessment using multigene panel tests Prof Antonis Antoniou

Breast and ovarian cancer risk assessment using multigene panel tests Prof Antonis Antoniou Breast and ovarian cancer risk assessment using multigene panel tests Prof Antonis Antoniou Department of Public Health and Primary Care University of Cambridge, U.K. Cancer risk prediction in the era

More information

EMMANOUIL SALOUSTROS MD, DSc Biosketch July -2018

EMMANOUIL SALOUSTROS MD, DSc Biosketch July -2018 EMMANOUIL SALOUSTROS MD, DSc Biosketch July -2018 DATE OF BIRTH 19 August 1975 CITIZENSHIP LANGUAGES Work Address: E-mail Skype ID Greek Greek: Native English: Fluent Department of Oncology, University

More information

Genetic Testing For Ovarian Cancer: When, How And Who? Judith Balmaña, MD, PhD University Hospital Vall d Hebron Barcelona, Spain

Genetic Testing For Ovarian Cancer: When, How And Who? Judith Balmaña, MD, PhD University Hospital Vall d Hebron Barcelona, Spain Genetic Testing For Ovarian Cancer: When, How And Who? Judith Balmaña, MD, PhD University Hospital Vall d Hebron Barcelona, Spain Why Would We Consider Genetic Testing in Patients With Ovarian Cancer?

More information

2015 Publications by members of the Vanderbilt Epidemiology Center (Bold names are VEC members)

2015 Publications by members of the Vanderbilt Epidemiology Center (Bold names are VEC members) 1. Ahn A, Edwards KM, Grijalva CG, Self WH, Zhu Y, Chappell JD, Arnold SR, McCullers JA, Ampofo K, Pavia AT, Bramley AM, Jain S, Williams DJ. Secondhand Smoke Exposure and Illness Severity among Children

More information

Original Article Increased expression of SOX4 contributes to ovarian cancer progression

Original Article Increased expression of SOX4 contributes to ovarian cancer progression Int J Clin Exp Pathol 2016;9(10):9879-9888 www.ijcep.com /ISSN:1936-2625/IJCEP0026011 Original Article Increased expression of SOX4 contributes to ovarian cancer progression Yue Qian 1, Yan Chen 2 1 Department

More information

AMY TRENTHAM-DIETZ, PhD, MS

AMY TRENTHAM-DIETZ, PhD, MS AMY TRENTHAM-DIETZ, PhD, MS PERSONAL DATA WARF Room 307 610 Walnut Street Madison, WI 53726 Telephone: (608) 265-4175 Fax: (608) 265-5330 Email: trentham@wisc.edu EDUCATION 1997 PhD, Epidemiology University

More information

Original Article HOXB5 mrna is upregulated in osteosarcoma tissues and promotes osteosarcoma cell line proliferation in vitro

Original Article HOXB5 mrna is upregulated in osteosarcoma tissues and promotes osteosarcoma cell line proliferation in vitro Int J Clin Exp Med 2018;11(3):1750-1757 www.ijcem.com /ISSN:1940-5901/IJCEM0071706 Original Article HOXB5 mrna is upregulated in osteosarcoma tissues and promotes osteosarcoma cell line proliferation in

More information

Edinburgh Research Explorer

Edinburgh Research Explorer Edinburgh Research Explorer Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers Citation for published version: Schmidt, MK, Hogervorst, F, van Hien, R, Cornelissen,

More information

Drakoulis Yannoukakos PhD Director of Research European registered Clinical Laboratory Geneticist (ErCLG) Molecular Diagnostics Laboratory

Drakoulis Yannoukakos PhD Director of Research European registered Clinical Laboratory Geneticist (ErCLG) Molecular Diagnostics Laboratory Drakoulis Yannoukakos PhD Director of Research European registered Clinical Laboratory Geneticist (ErCLG) Molecular Diagnostics Laboratory Address Molecular Diagnostics Laboratory Institute of Nuclear

More information

FULL TITLE: Incorporating Truncating. Variants in PALB2, CHEK2 and ATM into. the BOADICEA Breast Cancer Risk. SHORT TITLE: Rare Variants in the

FULL TITLE: Incorporating Truncating. Variants in PALB2, CHEK2 and ATM into. the BOADICEA Breast Cancer Risk. SHORT TITLE: Rare Variants in the FULL TITLE: Incorporating Truncating Variants in PALB, CHEK and ATM into the BOADICEA Breast Cancer Risk Model SHORT TITLE: Rare Variants in the BOADICEA Breast Cancer Risk Model Authorship Andrew J. Lee

More information

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk https://helda.helsinki.fi Genetic modifiers of CHEK2*1100delC-associated breast cancer risk Muranen, Taru A. 2017-05 Muranen, T A, Greco, D, Blomqvist, C, Aittomäki, K, Khan, S, Hogervorst, F, Verhoef,

More information

Aalborg Universitet. DOI (link to publication from Publisher): /JCO Creative Commons License CC BY 4.0. Publication date: 2017

Aalborg Universitet. DOI (link to publication from Publisher): /JCO Creative Commons License CC BY 4.0. Publication date: 2017 Aalborg Universitet Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores Lecarpentier, Julie; Silvestri, Valentina; Kuchenbaecker, Karoline

More information

Curriculum vitae: Brooke L. Fridley Page 1. UNIVERSITY OF KANSAS SCHOOL OF MEDICINE Faculty Curriculum Vitae

Curriculum vitae: Brooke L. Fridley Page 1. UNIVERSITY OF KANSAS SCHOOL OF MEDICINE Faculty Curriculum Vitae Curriculum vitae: Brooke L. Fridley Page 1 Date: August 24, 2015 UNIVERSITY OF KANSAS SCHOOL OF MEDICINE Faculty Curriculum Vitae I. PERSONAL DATA: 1. Applicant Information: First Name: Brooke Middle Initial:

More information

Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks

Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks JMG Online First, published on August 4, 2017 as 10.1136/jmedgenet-2017-104588 Cancer genetics Additional material is published online only. To view please visit the journal online (http:// dx. doi. org/

More information

Large-Scale Evaluation of Common Variation in Regulatory T Cell Related Genes and Ovarian Cancer Outcome

Large-Scale Evaluation of Common Variation in Regulatory T Cell Related Genes and Ovarian Cancer Outcome Research Article Cancer Immunology Research Large-Scale Evaluation of Common Variation in Regulatory T Cell Related Genes and Ovarian Cancer Outcome Bridget Charbonneau 1, Kirsten B. Moysich 7,KimberlyR.Kalli

More information

Universities of Leeds, Sheffield and York

Universities of Leeds, Sheffield and York promoting access to White Rose research papers Universities of Leeds, Sheffield and York http://eprints.whiterose.ac.uk/ This is a copy of the final published version of a paper published via gold open

More information

Effect of Prior Bilateral Oophorectomy on the Presentation of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers

Effect of Prior Bilateral Oophorectomy on the Presentation of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers Hereditary Cancer in Clinical Practice 2005; 3(2) pp. 53-57 Effect of Prior Bilateral Oophorectomy on the Presentation of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers Kelly A. Metcalfe 1, 2, William

More information

Original Article Association between genetic polymorphisms of antioxidant enzyme genes and susceptibility to hepatocellular carcinoma: a meta-analysis

Original Article Association between genetic polymorphisms of antioxidant enzyme genes and susceptibility to hepatocellular carcinoma: a meta-analysis Int J Clin Exp Med 2016;9(8):15645-15655 www.ijcem.com /ISSN:1940-5901/IJCEM0027573 Original Article Association between genetic polymorphisms of antioxidant enzyme genes and susceptibility to hepatocellular

More information

Polygenic susceptibility to prostate and breast cancer: implications for personalised screening

Polygenic susceptibility to prostate and breast cancer: implications for personalised screening British Journal of Cancer (2011), 1 8 All rights reserved 0007 0920/11 www.bjcancer.com Full Paper Polygenic susceptibility to prostate and breast cancer: implications for personalised screening N Pashayan*,1,

More information

The lymphoma-associated NPM-ALK oncogene elicits a p16ink4a/prb-dependent tumor-suppressive pathway. Blood Jun 16;117(24):

The lymphoma-associated NPM-ALK oncogene elicits a p16ink4a/prb-dependent tumor-suppressive pathway. Blood Jun 16;117(24): DNA Sequencing Publications Standard Sequencing 1 Carro MS et al. DEK Expression is controlled by E2F and deregulated in diverse tumor types. Cell Cycle. 2006 Jun;5(11) 2 Lassandro L et al. The DNA sequence

More information

Downloaded from:

Downloaded from: Schmidt, MK; Hogervorst, F; van Hien, R; Cornelissen, S; Broeks, A; Adank, MA; Meijers, H; Waisfisz, Q; Hollestelle, A; Schutte, M; van den Ouweland, A; Hooning, M; Andrulis, IL; Anton-Culver, H; Antonenkova,

More information

Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations British Journal of Cancer (2004) 91, 1911 1915 All rights reserved 0007 0920/04 $30.00 www.bjcancer.com Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations AS Whittemore*,1,

More information

A genetic risk score to guide age-specific, personalized prostate cancer screening. Tyler M. Seibert, MD, PhD

A genetic risk score to guide age-specific, personalized prostate cancer screening. Tyler M. Seibert, MD, PhD A genetic risk score to guide age-specific, personalized prostate cancer screening Tyler M. Seibert, MD, PhD Center for Multimodal Imaging and Genetics Dept. of Radiation Medicine and Applied Sciences

More information

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer Research Article Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer Stacey J. Winham 1, Ailith Pirie 2, Yian Ann Chen 3, Melissa C. Larson 1, Zachary C. Fogarty 1, Madalene

More information

MOLECULAR GENETICS OF BREAST AND OVARIAN CANCER: RECENT ADVANCES AND CLINICAL IMPLICATIONS

MOLECULAR GENETICS OF BREAST AND OVARIAN CANCER: RECENT ADVANCES AND CLINICAL IMPLICATIONS BJMG,Supplement 15 (2012) 75-80 10.2478/v10034 012 0024 9 Proceedings of the MACPROGEN Final Conference held at Ohrid, Republic of Macedonia, March 29-April 1 2012 MOLECULAR GENETICS OF BREAST AND OVARIAN

More information

Downloaded from:

Downloaded from: Warren, H; Dudbridge, F; Fletcher, O; Orr, N; Johnson, N; Hopper, JL; Apicella, C; Southey, MC; Mahmoodi, M; Schmidt, MK; Broeks, A; Cornelissen, S; Braaf, LM; Muir, KR; Lophatananon, A; Chaiwerawattana,

More information

No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers

No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers Hereditary Cancer in Clinical Practice 2007; 5(2) pp. 67-71 No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers Pål Møller 1, Lovise Mºhle 1, Neal Clark 1, Jaran Apold 2 1 Section

More information

TITLE: Genetic Association Study of Ancestry-Matched African American Prostate Cancer Cases and Controls

TITLE: Genetic Association Study of Ancestry-Matched African American Prostate Cancer Cases and Controls AD Award Number: W81XWH-07-1-0122 TITLE: Genetic Association Study of Ancestry-Matched African American Prostate Cancer Cases and Controls PRINCIPAL INVESTIGATOR: William B. Isaacs, Ph.D. CONTRACTING ORGANIZATION:

More information

C. H. H. Kerkhofs 1, A. B. Spurdle 2, P. J. Lindsey 1, D. E. Goldgar 3 and E. B. Gómez-García 1*

C. H. H. Kerkhofs 1, A. B. Spurdle 2, P. J. Lindsey 1, D. E. Goldgar 3 and E. B. Gómez-García 1* Kerkhofs et al. Hereditary Cancer in Clinical Practice (2016) 14:10 DOI 10.1186/s13053-016-0050-9 RESEARCH Assessing biases of information contained in pedigrees for the classification of BRCAgenetic variants:

More information

Cancer risks among BRCA1 and BRCA2 mutation carriers

Cancer risks among BRCA1 and BRCA2 mutation carriers British Journal of Cancer (2007) 96, 11 15 All rights reserved 0007 0920/07 $30.00 www.bjcancer.com Minireview Cancer risks among BRCA1 and BRCA2 mutation carriers E Levy-Lahad*,1 and E Friedman 2 1 Institute

More information

Int J Clin Exp Pathol 2016;9(10): /ISSN: /IJCEP

Int J Clin Exp Pathol 2016;9(10): /ISSN: /IJCEP Int J Clin Exp Pathol 2016;9(10):10398-10405 www.ijcep.com /ISSN:1936-2625/IJCEP0031061 Original Article TOX3 rs3803662 C > T polymorphism contributes to breast cancer susceptibility in the Chinese population:

More information

Original Article Associations of TERT polymorphisms with hepatocellular carcinoma risk in a Han Chinese population

Original Article Associations of TERT polymorphisms with hepatocellular carcinoma risk in a Han Chinese population Int J Clin Exp Pathol 2017;10(7):7776-7783 www.ijcep.com /ISSN:1936-2625/IJCEP0055787 Original Article Associations of TERT polymorphisms with hepatocellular carcinoma risk in a Han Chinese population

More information

Gerald Bronfman Department of Oncology Annual Report 2016 Publications

Gerald Bronfman Department of Oncology Annual Report 2016 Publications Bassam Abdulkarim 1. Ayman Oweida, Abdulkarim B. Ablative versus fractionated radiation therapy: A controversial role in cancer invasion and metastasis. Oncogene. 2016 Apr 25. doi: 10.1038/onc.2016.130.

More information

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA The Harvard community has made this article openly available. Please share how this access benefits

More information

Prostate Cancer in a Patient with a Family History of BRCA Mutation: a Case Report and Literature Review

Prostate Cancer in a Patient with a Family History of BRCA Mutation: a Case Report and Literature Review CASE REPORT Oncology & Hematology https://doi.org/10.3346/jkms.2017.32.2.377 J Korean Med Sci 2017; 32: 377-381 Prostate Cancer in a Patient with a Family History of BRCA Mutation: a Case Report and Literature

More information

2013 Publication List Vanderbilt Epidemiology Center

2013 Publication List Vanderbilt Epidemiology Center 2013 Publication List Vanderbilt Epidemiology Center 1. Akard TF, Gilmer MJ, Friedman DL, Given B, Hendricks-Ferguson VL, Hinds PS.From qualitative work to intervention development in pediatric oncology

More information

Conflicts of Interest

Conflicts of Interest This is great information, but how do I use it?: Information needs of genetic counselors related to reclassification of Variants of Uncertain Significance Courtney Scherr, PhD Moffitt Cancer Center Teri

More information

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions British Journal of Cancer (2008) 98, 1457 1466 All rights reserved 0007 0920/08 $30.00 www.bjcancer.com The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

More information

Assessing the Genetic Architecture of Epithelial Ovarian Cancer Histological Subtypes

Assessing the Genetic Architecture of Epithelial Ovarian Cancer Histological Subtypes Assessing the Genetic Architecture of Epithelial Ovarian Cancer Histological Subtypes Gabriel Cuellar 1; 2, Yi Lu 1, Suzanne C Dixon 3, Australian Ovarian Cancer Study 4; 5, Peter A. Fasching 7; 8, Alexander

More information

A systematic analysis of the association studies between CASP8 D302H polymorphisms and breast cancer risk

A systematic analysis of the association studies between CASP8 D302H polymorphisms and breast cancer risk Indian Academy of Sciences RESEARCH ARTICLE A systematic analysis of the association studies between CASP8 D302H polymorphisms and breast cancer risk YINLIANG ZHANG 1, WEI LI 1,2,YIHONG 1,2, GUOYING WU

More information

Twenty-One Gene Recurrence Score Assay in BRCA-Associated Versus Sporadic Breast Cancers: Differences Based on Germline Mutation Status

Twenty-One Gene Recurrence Score Assay in BRCA-Associated Versus Sporadic Breast Cancers: Differences Based on Germline Mutation Status Twenty-One Gene Recurrence Score Assay in BRCA-Associated Versus Sporadic Breast Cancers: Differences Based on Germline Mutation Status Payal D. Shah, MD 1 ; Sujata Patil, PhD 2 ; Maura N. Dickler, MD

More information

Spherical Bearings Heavy Duty Equipments

Spherical Bearings Heavy Duty Equipments Spherical Bearings Heavy Duty Equipments Highlights Quality Service Price Wbf Replacement Parts adaptableto > Caterpillar >Komatsu >Volvo 1 WBF SPHERICAL BEARINGS adaptable to Caterpillar Part No. Description

More information

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters.

More information

The diagnostic value of determination of serum GOLPH3 associated with CA125, CA19.9 in patients with ovarian cancer

The diagnostic value of determination of serum GOLPH3 associated with CA125, CA19.9 in patients with ovarian cancer European Review for Medical and Pharmacological Sciences 2017; 21: 4039-4044 The diagnostic value of determination of serum GOLPH3 associated with CA125, CA19.9 in patients with ovarian cancer H.-Y. FAN

More information

Genetic testing for hereditary cancer

Genetic testing for hereditary cancer Genetic testing for hereditary cancer THE GENETICS OF HEREDITARY CANCER About half of all men and one-third of all women in the US will develop cancer during their lifetimes. Approximately 5% to 10% of

More information

Original Article Correlation between LSP1 polymorphisms and the susceptibility to breast cancer

Original Article Correlation between LSP1 polymorphisms and the susceptibility to breast cancer Int J Clin Exp Pathol 2015;8(5):5798-5802 www.ijcep.com /ISSN:1936-2625/IJCEP0005835 Original Article Correlation between LSP1 polymorphisms and the susceptibility to breast cancer Hai Chen, Xiaodong Qi,

More information

Correlations between the COMT gene rs4680 polymorphism and susceptibility to ovarian cancer

Correlations between the COMT gene rs4680 polymorphism and susceptibility to ovarian cancer Correlations between the COMT gene rs4680 polymorphism and susceptibility to ovarian cancer W. Pan 1 and H. Liao 2 1 Department of Obstetrics and Gynecology, Huangshi Central Hospital of Hubei Province

More information

Publication list; Keith Humphreys

Publication list; Keith Humphreys Publication list; Keith Humphreys 1. Li J, Humphreys K, Darabi H, Rosin G, Hannelius U, Heikkinen T, Aittomäki K, Blomqvist C, Pharoah PDP, Dunning AM, Ahmed S, Hooning MJ, Hollestelle A, Oldenburg RA,

More information

The risk of ovarian cancer after breast cancer in BRCA1 and BRCA2 carriers

The risk of ovarian cancer after breast cancer in BRCA1 and BRCA2 carriers Gynecologic Oncology 96 (2005) 222 226 www.elsevier.com/locate/ygyno The risk of ovarian cancer after breast cancer in BRCA1 and BRCA2 carriers Kelly A. Metcalfe a,b, *, Henry T. Lynch c, Parviz Ghadirian

More information

Breast cancer risk prediction using a polygenic risk score in the familial setting: a

Breast cancer risk prediction using a polygenic risk score in the familial setting: a Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kconfab Hongyan Li 1 MSc, Bingjian Feng 2 PhD, Alexander

More information

Histologic Types of Endometrial Cancer:

Histologic Types of Endometrial Cancer: Histologic Types of Endometrial Cancer: Have They Different Risk Factors? Advances in Endometrial Cancer Epidemiology and Biology Boston, MA March 17-18, 2014 V. Wendy Setiawan, Ph.D. Department of Preventive

More information

A follow-up study of breast and other cancers in families of an unselected series of breast cancer patients

A follow-up study of breast and other cancers in families of an unselected series of breast cancer patients British Journal of Cancer (2002) 86, 718 722 All rights reserved 0007 0920/02 $25.00 www.bjcancer.com A follow-up study of breast and other cancers in families of an unselected series of breast cancer

More information

Association between ERCC1 and ERCC2 polymorphisms and breast cancer risk in a Chinese population

Association between ERCC1 and ERCC2 polymorphisms and breast cancer risk in a Chinese population Association between ERCC1 and ERCC2 polymorphisms and breast cancer risk in a Chinese population R. Zhao and M.F. Ying Department of Pharmacy, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University,

More information

IJC International Journal of Cancer

IJC International Journal of Cancer IJC International Journal of Cancer Short Report Oncotype Dx recurrence score among BRCA1/2 germline mutation carriers with hormone receptors positive breast cancer Naama Halpern 1, Amir Sonnenblick 2,

More information

Medicina de precisión en cáncer de ovario: Determinación de BRCA germinal y somático

Medicina de precisión en cáncer de ovario: Determinación de BRCA germinal y somático Medicina de precisión en cáncer de ovario: Determinación de BRCA germinal y somático Dra. Cristina Martin Lorente Hospital de la Santa Creu i Sant Pau. Barcelona Introduction Ovarian cancer is the fifth

More information

Towards Evidence-Based Management of Inherited Breast and Breast-Ovarian Cancer

Towards Evidence-Based Management of Inherited Breast and Breast-Ovarian Cancer Hereditary Cancer in Clinical Practice 2004; 2(1) pp. 11-16 Towards Evidence-Based Management of Inherited Breast and Breast-Ovarian Cancer Pål Møller Section of Genetic Counseling, Department of Cancer

More information

Accuracy of the BRCAPRO Model Among Women With Bilateral Breast Cancer

Accuracy of the BRCAPRO Model Among Women With Bilateral Breast Cancer Accuracy of the BRCAPRO Model Among Women With Bilateral Breast Cancer Kaylene J. Ready, MS 1, Kristen J. Vogel, MS 2, Deann P. Atchley, PhD 1, Kristine R. Broglio, MS 1, Kimberly K. Solomon, MBA 1, Christopher

More information

Global Breast Cancer Conference 2015 & 4th International Breast Cancer Symposium April 24 th, 2015 The Shilla Jeju Hotel, Jeju Island, Korea

Global Breast Cancer Conference 2015 & 4th International Breast Cancer Symposium April 24 th, 2015 The Shilla Jeju Hotel, Jeju Island, Korea Global Breast Cancer Conference 2015 & 4th International Breast Cancer Symposium April 24 th, 2015 The Shilla Jeju Hotel, Jeju Island, Korea Dr. Steven A. Narod MD, FRCPC Canada Research Chair in Breast

More information

Germline Testing for Hereditary Cancer with Multigene Panel

Germline Testing for Hereditary Cancer with Multigene Panel Germline Testing for Hereditary Cancer with Multigene Panel Po-Han Lin, MD Department of Medical Genetics National Taiwan University Hospital 2017-04-20 Disclosure No relevant financial relationships with

More information

GENETIC STUDIES IN FAMILIAL NON-BRCA BREAST CANCER

GENETIC STUDIES IN FAMILIAL NON-BRCA BREAST CANCER From the Department of Oncology-Pathology Karolinska Institutet and the Department of Oncology, Södersjukhuset, Stockholm, Sweden GENETIC STUDIES IN FAMILIAL NON-BRCA BREAST CANCER Camilla Wendt Stockholm

More information

Common genetic variation associated with increased susceptibility to prostate cancer does not increase risk of radiotherapy toxicity

Common genetic variation associated with increased susceptibility to prostate cancer does not increase risk of radiotherapy toxicity FULL PAPER British Journal of Cancer (216), 1 1 doi: 1.138/bjc.216.94 Keywords: prostate cancer; genetic variants; radiotherapy; late toxicity Common genetic variation associated with increased susceptibility

More information

1. Collaborative Group on Epidemiological Studies of Ovarian Cancer. Ovarian cancer and oral contraceptives: collaborative reanalysis of data from 45

1. Collaborative Group on Epidemiological Studies of Ovarian Cancer. Ovarian cancer and oral contraceptives: collaborative reanalysis of data from 45 1 2 3 1. Collaborative Group on Epidemiological Studies of Ovarian Cancer. Ovarian cancer and oral contraceptives: collaborative reanalysis of data from 45 epidemiological studies including 23,257 women

More information

Evaluation of the need for routine clinical testing of PALB2 c.1592delt mutation in BRCA negative Northern Finnish breast cancer families

Evaluation of the need for routine clinical testing of PALB2 c.1592delt mutation in BRCA negative Northern Finnish breast cancer families Haanpää et al. BMC Medical Genetics 2013, 14:82 RESEARCH ARTICLE Open Access Evaluation of the need for routine clinical testing of PALB2 c.1592delt mutation in BRCA negative Northern Finnish breast cancer

More information

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer JAMA. 2012;307(4):

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer JAMA. 2012;307(4): ORIGINAL CONTRIBUTION Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer Kelly L. Bolton, PhD, Georgia Chenevix- Trench, PhD, Cindy Goh, BA, Siegal

More information

Supplementary Table 1. Summary characteristics of the 37 participating BCAC studies

Supplementary Table 1. Summary characteristics of the 37 participating BCAC studies Supplementary Table 1. Summary characteristics of the 37 participating BCAC studies Study (ref. no.) Study acronym Country Study design Specifically selected genetically-enriched cases No. Cases No. Controls

More information

Inferring causality in observational epidemiology: Breast Cancer Risk as an Example

Inferring causality in observational epidemiology: Breast Cancer Risk as an Example Inferring causality in observational epidemiology: Breast Cancer Risk as an Example Mary Beth Terry, PhD Department of Epidemiology and Environmental Sciences Cancer Genes vs Environmental Risk Factors

More information

Obesity and Breast Cancer in a Multiethnic Population. Gertraud Maskarinec, MD, PhD University of Hawaii Cancer Center, Honolulu, HI

Obesity and Breast Cancer in a Multiethnic Population. Gertraud Maskarinec, MD, PhD University of Hawaii Cancer Center, Honolulu, HI Obesity and Breast Cancer in a Multiethnic Population Gertraud Maskarinec, MD, PhD University of Hawaii Cancer Center, Honolulu, HI Background Breast cancer incidence remains lower in many Asian than Western

More information

Clinical, Molecular and Geographical Features of Hereditary Breast/Ovarian Cancer in Latvia

Clinical, Molecular and Geographical Features of Hereditary Breast/Ovarian Cancer in Latvia Hereditary Cancer in Clinical Practice 2005; 3(2) pp. 71-76 Clinical, Molecular and Geographical Features of Hereditary Breast/Ovarian Cancer in Latvia Andris Gardovskis 1, Arvids Irmejs 1, Edvins Miklasevics

More information

RESULTS. rs and rs are associated with survival after adjuvant chemotherapy

RESULTS. rs and rs are associated with survival after adjuvant chemotherapy www.impactjournals.com/oncotarget/ Oncotarget, Vol. 6, No. 10 The SNP rs6500843 in 16p13.3 is associated with survival V S H F L F D O O \ D P R Q J F K H P R W K H U D S \ W U H D W H G E U H D V W F

More information

Polymorphic Variations in 5 HT2A, 5 HTT and DISC 1 in first episode schizophrenia patients

Polymorphic Variations in 5 HT2A, 5 HTT and DISC 1 in first episode schizophrenia patients PolymorphicVariationsin5 HT2A,5 HTTandDISC1infirst episodeschizophreniapatients L.MedinaGonzález,DepartmentofClinicalChemistry,RamónyCajalHospital,Madrid. PhD.MJArranz,SectionofClinicalNeuropharmacologyattheInstituteofPsychiatry,

More information

Tumour morphology predicts PALB2 germline mutation status

Tumour morphology predicts PALB2 germline mutation status FULL PAPER British Journal of Cancer (2013) 109, 154 163 doi: 10.1038/bjc.2013.295 Keywords: PALB2; hereditary; breast cancer; tumour morphology Tumour morphology predicts PALB2 germline mutation status

More information

Ovarian cancer variant rs is associated with HOXD1 and HOXD3 gene expression

Ovarian cancer variant rs is associated with HOXD1 and HOXD3 gene expression /, 2017, Vol. 8, (No. 61), pp: 103410-103414 Ovarian cancer variant rs2072590 is associated with HOXD1 and HOXD3 gene expression Liyuan Guo 1,*, Yan Peng 2,*, Lei Sun 3,*, Xia Han 4, Juan Xu 4 and Dongwei

More information

BRECT collaborative publications 2010-present Original research publications (131) 2015

BRECT collaborative publications 2010-present Original research publications (131) 2015 BRECT collaborative publications 2010-present Original research publications (131) 2015 1. Brand, Judith S., Jingmei Li, Keith Humphreys, Robert Karlsson, Mikael Eriksson, Emma Ivansson, Per Hall, and

More information

Original Article Lysyl oxidase single-nucleotide polymorphism (SNP) (G473A) is negatively associated with ovarian cancer prognosis

Original Article Lysyl oxidase single-nucleotide polymorphism (SNP) (G473A) is negatively associated with ovarian cancer prognosis Int J Clin Exp Med 2017;10(12):16595-16602 www.ijcem.com /ISSN:1940-5901/IJCEM0057707 Original Article Lysyl oxidase single-nucleotide polymorphism (SNP) (G473A) is negatively associated with ovarian cancer

More information

Supplementary Table 4. Study characteristics and association between OC use and endometrial cancer incidence

Supplementary Table 4. Study characteristics and association between OC use and endometrial cancer incidence Supplementary Table 4. characteristics and association between OC use and endometrial cancer incidence a Details OR b 95% CI Covariates Region Case-control Parslov, 2000 (1) Danish women aged 25 49 yr

More information