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48건, 그중 8건 표시.
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Siddiq A,
Couch FJ,
Chen GK,
Lindström S,
Eccles D,
Millikan RC,
Michailidou K,
Stram DO,
Beckmann L,
Rhie SK,
Ambrosone CB,
Aittomäki K
외 129명 — 모두 보기
Amiano P,
Apicella C,
Baglietto L,
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Brauch H,
Brinton L,
Bui QM,
Buring JE,
Buys SS,
Campa D,
Carpenter JE,
Chasman DI,
Chang-Claude J,
Chen C,
Clavel-Chapelon F,
Cox A,
Cross SS,
Czene K,
Deming SL,
Diasio RB,
Diver WR,
Dunning AM,
Durcan L,
Ekici AB,
Fasching PA,
Feigelson HS,
Fejerman L,
Figueroa JD,
Fletcher O,
Flesch-Janys D,
Gaudet MM,
Gerty SM,
Rodriguez-Gil JL,
Giles GG,
van Gils CH,
Godwin AK,
Graham N,
Greco D,
Hall P,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Hoover RN,
Hopper JL,
Hu JJ,
Huntsman S,
Ingles SA,
Irwanto A,
Isaacs C,
Jacobs KB,
John EM,
Justenhoven C,
Kaaks R,
Kolonel LN,
Coetzee GA,
Lathrop M,
Le Marchand L,
Lee AM,
Lee IM,
Lesnick T,
Lichtner P,
Liu J,
Lund E,
Makalic E,
Martin NG,
McLean CA,
Meijers-Heijboer H,
Meindl A,
Miron P,
Monroe KR,
Montgomery GW,
Müller-Myhsok B,
Nickels S,
Nyante SJ,
Olswold C,
Overvad K,
Palli D,
Park DJ,
Palmer JR,
Pathak H,
Peto J,
Pharoah P,
Rahman N,
Rivadeneira F,
Schmidt DF,
Schmutzler RK,
Slager S,
Southey MC,
Stevens KN,
Sinn HP,
Press MF,
Ross E,
Riboli E,
Ridker PM,
Schumacher FR,
Severi G,
Dos Santos Silva I,
Stone J,
Sund M,
Tapper WJ,
Thun MJ,
Travis RC,
Turnbull C,
Uitterlinden AG,
Waisfisz Q,
Wang X,
Wang Z,
Weaver J,
Schulz-Wendtland R,
Wilkens LR,
Van Den Berg D,
Zheng W,
Zheng W,
Ziegler RG,
Ziv E,
Nevanlinna H,
Easton DF,
Hunter DJ,
Henderson BE,
Chanock SJ,
Garcia-Closas M,
Kraft P,
Haiman CA,
Vachon CM
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study 외 컨소시엄 1곳
Human molecular genetics · 2012 · PMID 22976474
페이지 1개
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease
Amin Al Olama A,
Kote-Jarai Z,
Schumacher FR,
Wiklund F,
Berndt SI,
Benlloch S,
Giles GG,
Severi G,
Neal DE,
Hamdy FC,
Donovan JL,
Hunter DJ
외 135명 — 모두 보기
Henderson BE,
Thun MJ,
Gaziano M,
Giovannucci EL,
Siddiq A,
Travis RC,
Cox DG,
Canzian F,
Riboli E,
Key TJ,
Andriole G,
Albanes D,
Hayes RB,
Schleutker J,
Auvinen A,
Tammela TL,
Weischer M,
Stanford JL,
Ostrander EA,
Cybulski C,
Lubinski J,
Thibodeau SN,
Schaid DJ,
Sorensen KD,
Batra J,
Clements JA,
Chambers S,
Aitken J,
Gardiner RA,
Maier C,
Vogel W,
Dörk T,
Brenner H,
Habuchi T,
Ingles S,
John EM,
Dickinson JL,
Cannon-Albright L,
Teixeira MR,
Kaneva R,
Zhang HW,
Lu YJ,
Park JY,
Cooney KA,
Muir KR,
Leongamornlert DA,
Saunders E,
Tymrakiewicz M,
Mahmud N,
Guy M,
Govindasami K,
O'Brien LT,
Wilkinson RA,
Hall AL,
Sawyer EJ,
Dadaev T,
Morrison J,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As N,
Woodhouse CJ,
Thompson A,
Dudderidge T,
Ogden C,
Cooper CS,
Lophatonanon A,
Southey MC,
Hopper JL,
English D,
Virtamo J,
Le Marchand L,
Campa D,
Kaaks R,
Lindstrom S,
Diver WR,
Gapstur S,
Yeager M,
Cox A,
Stern MC,
Corral R,
Aly M,
Isaacs W,
Adolfsson J,
Xu J,
Zheng SL,
Wahlfors T,
Taari K,
Kujala P,
Klarskov P,
Nordestgaard BG,
Røder MA,
Frikke-Schmidt R,
Bojesen SE,
FitzGerald LM,
Kolb S,
Kwon EM,
Karyadi DM,
Orntoft TF,
Borre M,
Rinckleb A,
Luedeke M,
Herkommer K,
Meyer A,
Serth J,
Marthick JR,
Patterson B,
Wokolorczyk D,
Spurdle A,
Lose F,
McDonnell SK,
Joshi AD,
Shahabi A,
Pinto P,
Santos J,
Ray A,
Sellers TA,
Lin HY,
Stephenson RA,
Teerlink C,
Muller H,
Rothenbacher D,
Tsuchiya N,
Narita S,
Cao GW,
Slavov C,
Mitev V,
Chanock S,
Gronberg H,
Haiman CA,
Kraft P,
Easton DF,
Eeles RA
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators 외 컨소시엄 2곳
Human molecular genetics · 2013 · PMID 23065704
페이지 1개
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk
Lindström S,
Thompson DJ,
Paterson AD,
Li J,
Gierach GL,
Scott C,
Stone J,
Douglas JA,
dos-Santos-Silva I,
Fernandez-Navarro P,
Verghase J,
Smith P
외 33명 — 모두 보기
Brown J,
Luben R,
Wareham NJ,
Loos RJ,
Heit JA,
Pankratz VS,
Norman A,
Goode EL,
Cunningham JM,
deAndrade M,
Vierkant RA,
Czene K,
Fasching PA,
Baglietto L,
Southey MC,
Giles GG,
Shah KP,
Chan HP,
Helvie MA,
Beck AH,
Knoblauch NW,
Hazra A,
Hunter DJ,
Kraft P,
Pollan M,
Figueroa JD,
Couch FJ,
Hopper JL,
Hall P,
Easton DF,
Boyd NF,
Vachon CM,
Tamimi RM
Nature communications · 2014 · PMID 25342443 · open access
페이지 1개
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
Sex specific associations in genome wide association analysis of renal cell carcinoma
Laskar RS,
Muller DC,
Li P,
Machiela MJ,
Ye Y,
Gaborieau V,
Foll M,
Hofmann JN,
Colli L,
Sampson JN,
Wang Z,
Bacq-Daian D
외 96명 — 모두 보기
Boland A,
Abedi-Ardekani B,
Durand G,
Le Calvez-Kelm F,
Robinot N,
Blanche H,
Prokhortchouk E,
Skryabin KG,
Burdett L,
Yeager M,
Radojevic-Skodric S,
Savic S,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Rascu S,
Mukeria A,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Świątkowska B,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Trichopoulou A,
Riboli E,
Overvad K,
Panico S,
Ljungberg B,
Sitaram RT,
Giles GG,
Milne RL,
Severi G,
Bruinsma F,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Beane Freeman LE,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Chow WH,
Moore LE,
Choueiri TK,
Wood C,
Johansson M,
McKay JD,
Brown KM,
Rothman N,
Lathrop MG,
Deleuze JF,
Wu X,
Brennan P,
Chanock SJ,
Purdue MP,
Scelo G
European journal of human genetics : EJHG · 2019 · PMID 31231134
페이지 1개
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Din L,
Sheikh M,
Kosaraju N,
Smedby KE,
Bernatsky S,
Berndt SI,
Skibola CF,
Nieters A,
Wang S,
McKay JD,
Cocco P,
Maynadié M
외 80명 — 모두 보기
Foretová L,
Staines A,
Mack TM,
de Sanjosé S,
Vyse TJ,
Padyukov L,
Monnereau A,
Arslan AA,
Moore A,
Brooks-Wilson AR,
Novak AJ,
Glimelius B,
Birmann BM,
Link BK,
Stewart C,
Vajdic CM,
Haioun C,
Magnani C,
Conti DV,
Cox DG,
Casabonne D,
Albanes D,
Kane E,
Roman E,
Muzi G,
Salles G,
Giles GG,
Adami HO,
Ghesquières H,
De Vivo I,
Clavel J,
Cerhan JR,
Spinelli JJ,
Hofmann J,
Vijai J,
Curtin K,
Costenbader KH,
Onel K,
Offit K,
Teras LR,
Morton L,
Conde L,
Miligi L,
Melbye M,
Ennas MG,
Liebow M,
Purdue MP,
Glenn M,
Southey MC,
Din M,
Rothman N,
Camp NJ,
Wong Doo N,
Becker N,
Pradhan N,
Bracci PM,
Boffetta P,
Vineis P,
Brennan P,
Kraft P,
Lan Q,
Severson RK,
Vermeulen RCH,
Milne RL,
Kaaks R,
Travis RC,
Weinstein SJ,
Chanock SJ,
Ansell SM,
Slager SL,
Zheng T,
Zhang Y,
Benavente Y,
Taub Z,
Madireddy L,
Gourraud PA,
Oksenberg JR,
Cozen W,
Hjalgrim H,
Khankhanian P
Genetic epidemiology · 2019 · PMID 31407831
페이지 1개
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
외 128명 — 모두 보기
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
페이지 1개
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
Dareng EO,
Coetzee SG,
Tyrer JP,
Peng PC,
Rosenow W,
Chen S,
Davis BD,
Dezem FS,
Seo JH,
Nameki R,
Reyes AL,
Aben KKH
외 141명 — 모두 보기
Anton-Culver H,
Antonenkova NN,
Aravantinos G,
Bandera EV,
Beane Freeman LE,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernardini MQ,
Bjorge L,
Black A,
Bogdanova NV,
Bolton KL,
Brenton JD,
Budzilowska A,
Butzow R,
Cai H,
Campbell I,
Cannioto R,
Chang-Claude J,
Chanock SJ,
Chen K,
Chenevix-Trench G,
Chiew YE,
Cook LS,
DeFazio A,
Dennis J,
Doherty JA,
Dörk T,
du Bois A,
Dürst M,
Eccles DM,
Ene G,
Fasching PA,
Flanagan JM,
Fortner RT,
Fostira F,
Gentry-Maharaj A,
Giles GG,
Goodman MT,
Gronwald J,
Haiman CA,
Håkansson N,
Heitz F,
Hildebrandt MAT,
Høgdall E,
Høgdall CK,
Huang RY,
Jensen A,
Jones ME,
Kang D,
Karlan BY,
Karnezis AN,
Kelemen LE,
Kennedy CJ,
Khusnutdinova EK,
Kiemeney LA,
Kjaer SK,
Kupryjanczyk J,
Labrie M,
Lambrechts D,
Larson MC,
Le ND,
Lester J,
Li L,
Lubiński J,
Lush M,
Marks JR,
Matsuo K,
May T,
McLaughlin JR,
McNeish IA,
Menon U,
Missmer S,
Modugno F,
Moffitt M,
Monteiro AN,
Moysich KB,
Narod SA,
Nguyen-Dumont T,
Odunsi K,
Olsson H,
Onland-Moret NC,
Park SK,
Pejovic T,
Permuth JB,
Piskorz A,
Prokofyeva D,
Riggan MJ,
Risch HA,
Rodríguez-Antona C,
Rossing MA,
Sandler DP,
Setiawan VW,
Shan K,
Song H,
Southey MC,
Steed H,
Sutphen R,
Swerdlow AJ,
Teo SH,
Terry KL,
Thompson PJ,
Vestrheim Thomsen LC,
Titus L,
Trabert B,
Travis R,
Tworoger SS,
Valen E,
Van Nieuwenhuysen E,
Edwards DV,
Vierkant RA,
Webb PM,
Weinberg CR,
Weise RM,
Wentzensen N,
White E,
Winham SJ,
Wolk A,
Woo YL,
Wu AH,
Yan L,
Yannoukakos D,
Zeinomar N,
Zheng W,
Ziogas A,
Berchuck A,
Goode EL,
Huntsman DG,
Pearce CL,
Ramus SJ,
Sellers TA,
Freedman ML,
Lawrenson K,
Schildkraut JM,
Hazelett D,
Plummer JT,
Kar S,
Jones MR,
Pharoah PDP,
Gayther SA
AOCS Group · OPAL Study Group 외 컨소시엄 1곳
American journal of human genetics · 2024 · PMID 38723632
페이지 1개
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인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
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제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
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얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
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