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성함이나 학술지명, PMID로 찾아보십시오.
O'Mara TA에 대해
10건.
Using human genetics to understand the disease impacts of testosterone in men and women
Ruth KS,
Day FR,
Tyrrell J,
Thompson DJ,
Wood AR,
Mahajan A,
Beaumont RN,
Wittemans L,
Martin S,
Busch AS,
Erzurumluoglu AM,
Hollis B
외 10명 — 모두 보기
Endometrial Cancer Association Consortium
Nature medicine · 2020 · PMID 32042192 · open access
페이지 12개+
Identification of nine new susceptibility loci for endometrial cancer
O'Mara TA,
Glubb DM,
Amant F,
Annibali D,
Ashton K,
Attia J,
Auer PL,
Beckmann MW,
Black A,
Bolla MK,
Brauch H,
Brenner H
외 114명 — 모두 보기
Brinton L,
Buchanan DD,
Burwinkel B,
Chang-Claude J,
Chanock SJ,
Chen C,
Chen MM,
Cheng THT,
Clarke CL,
Clendenning M,
Cook LS,
Couch FJ,
Cox A,
Crous-Bous M,
Czene K,
Day F,
Dennis J,
Depreeuw J,
Doherty JA,
Dörk T,
Dowdy SC,
Dürst M,
Ekici AB,
Fasching PA,
Fridley BL,
Friedenreich CM,
Fritschi L,
Fung J,
García-Closas M,
Gaudet MM,
Giles GG,
Goode EL,
Gorman M,
Haiman CA,
Hall P,
Hankison SE,
Healey CS,
Hein A,
Hillemanns P,
Hodgson S,
Hoivik EA,
Holliday EG,
Hopper JL,
Hunter DJ,
Jones A,
Krakstad C,
Kristensen VN,
Lambrechts D,
Marchand LL,
Liang X,
Lindblom A,
Lissowska J,
Long J,
Lu L,
Magliocco AM,
Martin L,
McEvoy M,
Meindl A,
Michailidou K,
Milne RL,
Mints M,
Montgomery GW,
Nassir R,
Olsson H,
Orlow I,
Otton G,
Palles C,
Perry JRB,
Peto J,
Pooler L,
Prescott J,
Proietto T,
Rebbeck TR,
Risch HA,
Rogers PAW,
Rübner M,
Runnebaum I,
Sacerdote C,
Sarto GE,
Schumacher F,
Scott RJ,
Setiawan VW,
Shah M,
Sheng X,
Shu XO,
Southey MC,
Swerdlow AJ,
Tham E,
Trovik J,
Turman C,
Tyrer JP,
Vachon C,
VanDen Berg D,
Vanderstichele A,
Wang Z,
Webb PM,
Wentzensen N,
Werner HMJ,
Winham SJ,
Wolk A,
Xia L,
Xiang YB,
Yang HP,
Yu H,
Zheng W,
Zheng W,
Pharoah PDP,
Dunning AM,
Kraft P,
De Vivo I,
Tomlinson I,
Easton DF,
Spurdle AB,
Thompson DJ
Nature communications · 2018 · PMID 30093612 · open access
페이지 6개
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Coignard J,
Lush M,
Beesley J,
O'Mara TA,
Dennis J,
Tyrer JP,
Barnes DR,
McGuffog L,
Leslie G,
Bolla MK,
Adank MA,
Agata S
외 207명 — 모두 보기
Ahearn T,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Arnold N,
Aronson KJ,
Arun BK,
Augustinsson A,
Azzollini J,
Barrowdale D,
Baynes C,
Becher H,
Bermisheva M,
Bernstein L,
Białkowska K,
Blomqvist C,
Bojesen SE,
Bonanni B,
Borg A,
Brauch H,
Brenner H,
Burwinkel B,
Buys SS,
Caldés T,
Caligo MA,
Campa D,
Carter BD,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Chung WK,
Claes KBM,
Clarke CL,
Collée JM,
Conroy DM,
Czene K,
Daly MB,
Devilee P,
Diez O,
Ding YC,
Domchek SM,
Dörk T,
Dos-Santos-Silva I,
Dunning AM,
Dwek M,
Eccles DM,
Eliassen AH,
Engel C,
Eriksson M,
Evans DG,
Fasching PA,
Flyger H,
Fostira F,
Friedman E,
Fritschi L,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
Garcia-Barberan V,
García-Closas M,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Gehrig A,
Georgoulias V,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Guénel P,
Haeberle L,
Hahnen E,
Haiman CA,
Håkansson N,
Hall P,
Hamann U,
Harrington PA,
Hart SN,
He W,
Hogervorst FBL,
Hollestelle A,
Hopper JL,
Horcasitas DJ,
Hulick PJ,
Hunter DJ,
Imyanitov EN,
Jager A,
Jakubowska A,
James PA,
Jensen UB,
John EM,
Jones ME,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khusnutdinova E,
Kiiski JI,
Ko YD,
Kosma VM,
Kraft P,
Kurian AW,
Laitman Y,
Lambrechts D,
Le Marchand L,
Lester J,
Lesueur F,
Lindstrom T,
Lopez-Fernández A,
Loud JT,
Luccarini C,
Mannermaa A,
Manoukian S,
Margolin S,
Martens JWM,
Mebirouk N,
Meindl A,
Miller A,
Milne RL,
Montagna M,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Nielsen FC,
O'Brien KM,
Olopade OI,
Olson JE,
Olsson H,
Osorio A,
Ottini L,
Park-Simon TW,
Parsons MT,
Pedersen IS,
Peshkin B,
Peterlongo P,
Peto J,
Pharoah PDP,
Phillips KA,
Polley EC,
Poppe B,
Presneau N,
Pujana MA,
Punie K,
Radice P,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Robson M,
Romero A,
Rossing M,
Saloustros E,
Sandler DP,
Santella R,
Scheuner MT,
Schmidt MK,
Schmidt G,
Scott C,
Sharma P,
Soucy P,
Southey MC,
Spinelli JJ,
Steinsnyder Z,
Stone J,
Stoppa-Lyonnet D,
Swerdlow A,
Tamimi RM,
Tapper WJ,
Taylor JA,
Terry MB,
Teulé A,
Thull DL,
Tischkowitz M,
Toland AE,
Torres D,
Trainer AH,
Truong T,
Tung N,
Vachon CM,
Vega A,
Vijai J,
Wang Q,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wendt C,
Wolk A,
Yadav S,
Yang XR,
Yannoukakos D,
Zheng W,
Ziogas A,
Zorn KK,
Park SK,
Thomassen M,
Offit K,
Schmutzler RK,
Couch FJ,
Simard J,
Chenevix-Trench G,
Easton DF,
Andrieu N,
Antoniou AC
GEMO Study Collaborators · EMBRACE Collaborators 외 컨소시엄 3곳
Nature communications · 2021 · PMID 33597508 · open access
페이지 5개
Five endometrial cancer risk loci identified through genome-wide association analysis
Cheng TH,
Thompson DJ,
O'Mara TA,
Painter JN,
Glubb DM,
Flach S,
Lewis A,
French JD,
Freeman-Mills L,
Church D,
Gorman M,
Martin L
외 76명 — 모두 보기
Hodgson S,
Webb PM,
Attia J,
Holliday EG,
McEvoy M,
Scott RJ,
Henders AK,
Martin NG,
Montgomery GW,
Nyholt DR,
Ahmed S,
Healey CS,
Shah M,
Dennis J,
Fasching PA,
Beckmann MW,
Hein A,
Ekici AB,
Hall P,
Czene K,
Darabi H,
Li J,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Amant F,
Schrauwen S,
Zhao H,
Lambrechts D,
Depreeuw J,
Dowdy SC,
Goode EL,
Fridley BL,
Winham SJ,
Njølstad TS,
Salvesen HB,
Trovik J,
Werner HM,
Ashton K,
Otton G,
Proietto T,
Liu T,
Mints M,
Tham E,
Consortium C,
Jun Li M,
Yip SH,
Wang J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Dunlop M,
Houlston R,
Palles C,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Cunningham JM,
Pharoah PDP,
Dunning AM,
Edwards SL,
Easton DF,
Tomlinson I,
Spurdle AB
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) 외 컨소시엄 2곳
Nature genetics · 2016 · PMID 27135401 · open access
페이지 3개
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Painter JN,
O'Mara TA,
Morris AP,
Cheng THT,
Gorman M,
Martin L,
Hodson S,
Jones A,
Martin NG,
Gordon S,
Henders AK,
Attia J
외 65명 — 모두 보기
McEvoy M,
Holliday EG,
Scott RJ,
Webb PM,
Fasching PA,
Beckmann MW,
Ekici AB,
Hein A,
Rübner M,
Hall P,
Czene K,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Lambrechts D,
Lambrechts D,
Amant F,
Annibali D,
Depreeuw J,
Vanderstichele A,
Goode EL,
Cunningham JM,
Dowdy SC,
Winham SJ,
Trovik J,
Hoivik E,
Werner HMJ,
Krakstad C,
Ashton K,
Otton G,
Proietto T,
Tham E,
Mints M,
Ahmed S,
Healey CS,
Shah M,
Pharoah PDP,
Dunning AM,
Dennis J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Zondervan KT,
Nyholt DR,
MacGregor S,
Montgomery GW,
Tomlinson I,
Easton DF,
Thompson DJ,
Spurdle AB
Cancer medicine · 2018 · PMID 29608257 · open access
페이지 3개
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang H,
Ahearn TU,
Lecarpentier J,
Barnes D,
Beesley J,
Qi G,
Jiang X,
O'Mara TA,
Zhao N,
Bolla MK,
Dunning AM,
Dennis J
외 261명 — 모두 보기
Wang Q,
Ful ZA,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Aronson KJ,
Arun BK,
Auer PL,
Azzollini J,
Barrowdale D,
Becher H,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bialkowska K,
Blanco A,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Bondavalli D,
Borg A,
Brauch H,
Brenner H,
Briceno I,
Broeks A,
Brucker SY,
Brüning T,
Burwinkel B,
Buys SS,
Byers H,
Caldés T,
Caligo MA,
Calvello M,
Campa D,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Christiaens M,
Christiansen H,
Chung WK,
Claes KBM,
Clarke CL,
Cornelissen S,
Couch FJ,
Cox A,
Cross SS,
Czene K,
Daly MB,
Devilee P,
Diez O,
Domchek SM,
Dörk T,
Dwek M,
Eccles DM,
Ekici AB,
Evans DG,
Fasching PA,
Figueroa J,
Foretova L,
Fostira F,
Friedman E,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Gronwald J,
Guénel P,
Häberle L,
Hahnen E,
Haiman CA,
Hake CR,
Hall P,
Hamann U,
Harkness EF,
Heemskerk-Gerritsen BAM,
Hillemanns P,
Hogervorst FBL,
Holleczek B,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Howell A,
Huebner H,
Hulick PJ,
Imyanitov EN,
Isaacs C,
Izatt L,
Jager A,
Jakimovska M,
Jakubowska A,
James P,
Janavicius R,
Janni W,
John EM,
Jones ME,
Jung A,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khan S,
Khusnutdinova E,
Kitahara CM,
Ko YD,
Konstantopoulou I,
Koppert LB,
Koutros S,
Kristensen VN,
Laenkholm AV,
Lambrechts D,
Larsson SC,
Laurent-Puig P,
Lazaro C,
Lazarova E,
Lejbkowicz F,
Leslie G,
Lesueur F,
Lindblom A,
Lissowska J,
Lo WY,
Loud JT,
Lubinski J,
Lukomska A,
MacInnis RJ,
Mannermaa A,
Manoochehri M,
Manoukian S,
Margolin S,
Martinez ME,
Matricardi L,
McGuffog L,
McLean C,
Mebirouk N,
Meindl A,
Menon U,
Miller A,
Mingazheva E,
Montagna M,
Mulligan AM,
Mulot C,
Muranen TA,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Neven P,
Newman WG,
Nielsen FC,
Nikitina-Zake L,
Nodora J,
Offit K,
Olah E,
Olopade OI,
Olsson H,
Orr N,
Papi L,
Papp J,
Park-Simon TW,
Parsons MT,
Peissel B,
Peixoto A,
Peshkin B,
Peterlongo P,
Peto J,
Phillips KA,
Piedmonte M,
Plaseska-Karanfilska D,
Prajzendanc K,
Prentice R,
Prokofyeva D,
Rack B,
Radice P,
Ramus SJ,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Risch HA,
Romero A,
Rookus MA,
Rübner M,
Rüdiger T,
Saloustros E,
Sampson S,
Sandler DP,
Sawyer EJ,
Scheuner MT,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schöttker B,
Schürmann P,
Senter L,
Sharma P,
Sherman ME,
Shu XO,
Singer CF,
Smichkoska S,
Soucy P,
Southey MC,
Spinelli JJ,
Stone J,
Stoppa-Lyonnet D,
Swerdlow AJ,
Szabo CI,
Tamimi RM,
Tapper WJ,
Taylor JA,
Teixeira MR,
Terry M,
Thomassen M,
Thull DL,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Torres D,
Troester MA,
Truong T,
Tung N,
Untch M,
Vachon CM,
van den Ouweland AMW,
van der Kolk LE,
van Veen EM,
vanRensburg EJ,
Vega A,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wildiers H,
Winqvist R,
Wolk A,
Yang XR,
Yannoukakos D,
Zheng W,
Zheng W,
Zorn KK,
Milne RL,
Kraft P,
Simard J,
Pharoah PDP,
Michailidou K,
Antoniou AC,
Schmidt MK,
Chenevix-Trench G,
Easton DF,
Chatterjee N,
García-Closas M
kConFab Investigators · ABCTB Investigators 외 컨소시엄 2곳
Nature genetics · 2020 · PMID 32424353 · open access
페이지 2개
GWAS meta-analysis identifies five susceptibility loci for endometrial cancer
Ramachandran D,
Wang X,
Laisk T,
Zheng Y,
Ingold N,
Canson DM,
Kho PF,
Naumann BJ,
Chapman CJ,
Bousset K,
Krause AV,
Schürmann P
외 62명 — 모두 보기
Wieland B,
Hanel P,
Hülse F,
Häfner N,
Runnebaum I,
Dubrowinskaja N,
Turmanov N,
Yugay T,
Yessimsiitova ZB,
Amant F,
Annibali D,
Beckmann MW,
Bodelon C,
Buchanan DD,
Chen C,
Clarke MA,
Cook LS,
De Vivo I,
De Wispelaere W,
Du M,
Easton DF,
Emons J,
Fasching PA,
Friedenreich CM,
Gallagher G,
Giles GG,
Goode EL,
Harris HR,
Hunter DJ,
Kolin DL,
Kraft P,
Lacey JV,
Lambrechts D,
Lu L,
Mutter GL,
Naduparambil J,
O'Connell K,
Patel AV,
Pharoah PDP,
Rebbeck TR,
Ricceri F,
Risch HA,
Ruebner M,
Sacerdote C,
Scott RJ,
Setiawan VW,
Shu XO,
Southey MC,
Tham E,
Tomlinson I,
Turman C,
Wentzensen N,
Xu W,
Yu H,
Zheng W,
Spurdle AB,
Yarden Y,
Mägi R,
Hillemanns P,
Glubb DM,
Dörk T,
O'Mara TA
Estonian Biobank Research Team
EBioMedicine · 2025 · PMID 40633141 · open access
페이지 2개
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
외 204명 — 모두 보기
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28436984
페이지 1개
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions
Lindström S,
Wang L,
Feng H,
Majumdar A,
Huo S,
Macdonald J,
Harrison T,
Turman C,
Chen H,
Mancuso N,
Bammler T,
Gallinger S
외 49명 — 모두 보기
Gruber SB,
Gunter MJ,
Le Marchand L,
Moreno V,
Offit K,
De Vivo I,
O'Mara TA,
Spurdle AB,
Tomlinson I,
Fitzgerald R,
Gharahkhani P,
Gockel I,
Jankowski J,
Macgregor S,
Schumacher J,
Barnholtz-Sloan J,
Bondy ML,
Houlston RS,
Jenkins RB,
Melin B,
Wrensch M,
Brennan P,
Christiani DC,
Johansson M,
Mckay J,
Aldrich MC,
Amos CI,
Landi MT,
Tardon A,
Bishop DT,
Demenais F,
Goldstein AM,
Iles MM,
Kanetsky PA,
Law MH,
Amundadottir LT,
Stolzenberg-Solomon R,
Wolpin BM,
Klein A,
Petersen G,
Risch H,
Chanock SJ,
Purdue MP,
Scelo G,
Pharoah P,
Kar S,
Hung RJ,
Pasaniuc B,
Kraft P
Breast Cancer Association Consortium (BCAC) · Colorectal Transdisciplinary Study (CORECT), Colon Cancer Family Registry Study (CCFR), Genetics And Epidemiology Of Colorectal Cancer Consortium (GECCO) 외 컨소시엄 5곳
Journal of the National Cancer Institute · 2023 · PMID 36929942
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