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성함이나 학술지명, PMID로 찾아보십시오.
Vineis P에 대해
18건.
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Law PJ,
Berndt SI,
Speedy HE,
Camp NJ,
Sava GP,
Skibola CF,
Holroyd A,
Joseph V,
Sunter NJ,
Nieters A,
Bea S,
Monnereau A
외 85명 — 모두 보기
Martin-Garcia D,
Goldin LR,
Clot G,
Teras LR,
Quintela I,
Birmann BM,
Jayne S,
Cozen W,
Majid A,
Smedby KE,
Lan Q,
Dearden C,
Brooks-Wilson AR,
Hall AG,
Purdue MP,
Mainou-Fowler T,
Vajdic CM,
Jackson GH,
Cocco P,
Marr H,
Zhang Y,
Zheng T,
Giles GG,
Lawrence C,
Call TG,
Liebow M,
Melbye M,
Glimelius B,
Mansouri L,
Glenn M,
Curtin K,
Diver WR,
Link BK,
Conde L,
Bracci PM,
Holly EA,
Jackson RD,
Tinker LF,
Benavente Y,
Boffetta P,
Brennan P,
Maynadie M,
McKay J,
Albanes D,
Weinstein S,
Wang Z,
Caporaso NE,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Vermeulen RC,
Southey MC,
Milne RL,
Clavel J,
Topka S,
Spinelli JJ,
Kraft P,
Ennas MG,
Summerfield G,
Ferri GM,
Harris RJ,
Miligi L,
Pettitt AR,
North KE,
Allsup DJ,
Fraumeni JF,
Bailey JR,
Offit K,
Pratt G,
Hjalgrim H,
Pepper C,
Chanock SJ,
Fegan C,
Rosenquist R,
de Sanjose S,
Carracedo A,
Dyer MJ,
Catovsky D,
Campo E,
Cerhan JR,
Allan JM,
Rothman N,
Houlston R,
Slager S
Nature communications · 2017 · PMID 28165464 · open access
페이지 12개+
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
McCartney DL,
Min JL,
Richmond RC,
Lu AT,
Sobczyk MK,
Davies G,
Broer L,
Guo X,
Jeong A,
Jung J,
Kasela S,
Katrinli S
외 97명 — 모두 보기
Kuo PL,
Matias-Garcia PR,
Mishra PP,
Nygaard M,
Palviainen T,
Patki A,
Raffield LM,
Ratliff SM,
Richardson TG,
Robinson O,
Soerensen M,
Sun D,
Tsai PC,
van der Zee MD,
Walker RM,
Wang X,
Wang Y,
Xia R,
Xu Z,
Yao J,
Zhao W,
Correa A,
Boerwinkle E,
Dugué PA,
Durda P,
Elliott HR,
Gieger C,
de Geus EJC,
Harris SE,
Hemani G,
Imboden M,
Kähönen M,
Kardia SLR,
Kresovich JK,
Li S,
Lunetta KL,
Mangino M,
Mason D,
McIntosh AM,
Mengel-From J,
Moore AZ,
Murabito JM,
Ollikainen M,
Pankow JS,
Pedersen NL,
Peters A,
Polidoro S,
Porteous DJ,
Raitakari O,
Rich SS,
Sandler DP,
Sillanpää E,
Smith AK,
Southey MC,
Strauch K,
Tiwari H,
Tanaka T,
Tillin T,
Uitterlinden AG,
Van Den Berg DJ,
van Dongen J,
Wilson JG,
Wright J,
Yet I,
Arnett D,
Bandinelli S,
Bell JT,
Binder AM,
Boomsma DI,
Chen W,
Christensen K,
Conneely KN,
Elliott P,
Ferrucci L,
Fornage M,
Hägg S,
Hayward C,
Irvin M,
Kaprio J,
Lawlor DA,
Lehtimäki T,
Lohoff FW,
Milani L,
Milne RL,
Probst-Hensch N,
Reiner AP,
Ritz B,
Rotter JI,
Smith JA,
Taylor JA,
van Meurs JBJ,
Vineis P,
Waldenberger M,
Deary IJ,
Relton CL,
Horvath S,
Marioni RE
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
페이지 12개+
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
외 336명 — 모두 보기
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium 외 컨소시엄 4곳
Nature · 2011 · PMID 21909115 · open access
페이지 5개
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
Cerhan JR,
Berndt SI,
Vijai J,
Ghesquières H,
McKay J,
Wang SS,
Wang Z,
Yeager M,
Conde L,
de Bakker PI,
Nieters A,
Cox D
외 110명 — 모두 보기
Burdett L,
Monnereau A,
Flowers CR,
De Roos AJ,
Brooks-Wilson AR,
Lan Q,
Severi G,
Melbye M,
Gu J,
Jackson RD,
Kane E,
Teras LR,
Purdue MP,
Vajdic CM,
Spinelli JJ,
Giles GG,
Albanes D,
Kelly RS,
Zucca M,
Bertrand KA,
Zeleniuch-Jacquotte A,
Lawrence C,
Hutchinson A,
Zhi D,
Habermann TM,
Link BK,
Novak AJ,
Dogan A,
Asmann YW,
Liebow M,
Thompson CA,
Ansell SM,
Witzig TE,
Weiner GJ,
Veron AS,
Zelenika D,
Tilly H,
Haioun C,
Molina TJ,
Hjalgrim H,
Glimelius B,
Adami HO,
Bracci PM,
Riby J,
Smith MT,
Holly EA,
Cozen W,
Hartge P,
Morton LM,
Severson RK,
Tinker LF,
North KE,
Becker N,
Benavente Y,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
Staines A,
Lightfoot T,
Crouch S,
Smith A,
Roman E,
Diver WR,
Offit K,
Zelenetz A,
Klein RJ,
Villano DJ,
Zheng T,
Zhang Y,
Holford TR,
Kricker A,
Turner J,
Southey MC,
Clavel J,
Virtamo J,
Weinstein S,
Riboli E,
Vineis P,
Kaaks R,
Trichopoulos D,
Vermeulen RC,
Boeing H,
Tjonneland A,
Angelucci E,
Di Lollo S,
Rais M,
Birmann BM,
Laden F,
Giovannucci E,
Kraft P,
Huang J,
Ma B,
Ye Y,
Chiu BC,
Sampson J,
Liang L,
Park JH,
Chung CC,
Weisenburger DD,
Chatterjee N,
Fraumeni JF Jr,
Slager SL,
Wu X,
de Sanjose S,
Smedby KE,
Salles G,
Skibola CF,
Rothman N,
Chanock SJ
Nature genetics · 2014 · PMID 25261932 · open access
페이지 5개
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
Skibola CF,
Berndt SI,
Vijai J,
Conde L,
Wang Z,
Yeager M,
de Bakker PI,
Birmann BM,
Vajdic CM,
Foo JN,
Bracci PM,
Vermeulen RC
외 100명 — 모두 보기
Slager SL,
de Sanjose S,
Wang SS,
Linet MS,
Salles G,
Lan Q,
Severi G,
Hjalgrim H,
Lightfoot T,
Melbye M,
Gu J,
Ghesquières H,
Link BK,
Morton LM,
Holly EA,
Smith A,
Tinker LF,
Teras LR,
Kricker A,
Becker N,
Purdue MP,
Spinelli JJ,
Zhang Y,
Giles GG,
Vineis P,
Monnereau A,
Bertrand KA,
Albanes D,
Zeleniuch-Jacquotte A,
Gabbas A,
Chung CC,
Burdett L,
Hutchinson A,
Lawrence C,
Montalvan R,
Liang L,
Huang J,
Ma B,
Liu J,
Adami HO,
Glimelius B,
Ye Y,
Nowakowski GS,
Dogan A,
Thompson CA,
Habermann TM,
Novak AJ,
Liebow M,
Witzig TE,
Weiner GJ,
Schenk M,
Hartge P,
De Roos AJ,
Cozen W,
Zhi D,
Akers NK,
Riby J,
Smith MT,
Lacher M,
Villano DJ,
Maria A,
Roman E,
Kane E,
Jackson RD,
North KE,
Diver WR,
Turner J,
Armstrong BK,
Benavente Y,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
Staines A,
McKay J,
Brooks-Wilson AR,
Zheng T,
Holford TR,
Chamosa S,
Kaaks R,
Kelly RS,
Ohlsson B,
Travis RC,
Weiderpass E,
Clavel J,
Giovannucci E,
Kraft P,
Virtamo J,
Mazza P,
Cocco P,
Ennas MG,
Chiu BC,
Fraumeni JF Jr,
Nieters A,
Offit K,
Wu X,
Cerhan JR,
Smedby KE,
Chanock SJ,
Rothman N
American journal of human genetics · 2014 · PMID 25279986
페이지 5개
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
외 147명 — 모두 보기
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
페이지 4개
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Berndt SI,
Skibola CF,
Joseph V,
Camp NJ,
Nieters A,
Wang Z,
Cozen W,
Monnereau A,
Wang SS,
Kelly RS,
Lan Q,
Teras LR
외 118명 — 모두 보기
Chatterjee N,
Chung CC,
Yeager M,
Brooks-Wilson AR,
Hartge P,
Purdue MP,
Birmann BM,
Armstrong BK,
Cocco P,
Zhang Y,
Severi G,
Zeleniuch-Jacquotte A,
Lawrence C,
Burdette L,
Yuenger J,
Hutchinson A,
Jacobs KB,
Call TG,
Shanafelt TD,
Novak AJ,
Kay NE,
Liebow M,
Wang AH,
Smedby KE,
Adami HO,
Melbye M,
Glimelius B,
Chang ET,
Glenn M,
Curtin K,
Cannon-Albright LA,
Jones B,
Diver WR,
Link BK,
Weiner GJ,
Conde L,
Bracci PM,
Riby J,
Holly EA,
Smith MT,
Jackson RD,
Tinker LF,
Benavente Y,
Becker N,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
McKay J,
Staines A,
Rabe KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Lanasa MC,
Spector LG,
Leis JF,
Cunningham JM,
Weinberg JB,
Morrison VA,
Caporaso NE,
Norman AD,
Linet MS,
De Roos AJ,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Kaaks R,
Trichopoulos D,
Masala G,
Weiderpass E,
Chirlaque MD,
Vermeulen RC,
Travis RC,
Giles GG,
Albanes D,
Virtamo J,
Weinstein S,
Clavel J,
Zheng T,
Holford TR,
Offit K,
Zelenetz A,
Klein RJ,
Spinelli JJ,
Bertrand KA,
Laden F,
Giovannucci E,
Kraft P,
Kricker A,
Turner J,
Vajdic CM,
Ennas MG,
Ferri GM,
Miligi L,
Liang L,
Sampson J,
Crouch S,
Park JH,
North KE,
Cox A,
Snowden JA,
Wright J,
Carracedo A,
Lopez-Otin C,
Bea S,
Salaverria I,
Martin-Garcia D,
Campo E,
Fraumeni JF Jr,
de Sanjose S,
Hjalgrim H,
Cerhan JR,
Chanock SJ,
Rothman N,
Slager SL
Nature genetics · 2013 · PMID 23770605 · open access
페이지 3개
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Hung RJ,
McKay JD,
Gaborieau V,
Boffetta P,
Hashibe M,
Zaridze D,
Mukeria A,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D
외 53명 — 모두 보기
Bencko V,
Foretova L,
Janout V,
Chen C,
Goodman G,
Field JK,
Liloglou T,
Xinarianos G,
Cassidy A,
McLaughlin J,
Liu G,
Narod S,
Krokan HE,
Skorpen F,
Elvestad MB,
Hveem K,
Vatten L,
Linseisen J,
Clavel-Chapelon F,
Vineis P,
Bueno-de-Mesquita HB,
Lund E,
Martinez C,
Bingham S,
Rasmuson T,
Hainaut P,
Riboli E,
Ahrens W,
Benhamou S,
Lagiou P,
Trichopoulos D,
Holcátová I,
Merletti F,
Kjaerheim K,
Agudo A,
Macfarlane G,
Talamini R,
Simonato L,
Lowry R,
Conway DI,
Znaor A,
Healy C,
Zelenika D,
Boland A,
Delepine M,
Foglio M,
Lechner D,
Matsuda F,
Blanche H,
Gut I,
Heath S,
Lathrop M,
Brennan P
Nature · 2008 · PMID 18385738
페이지 2개
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Wu X,
Ye Y,
Kiemeney LA,
Sulem P,
Rafnar T,
Matullo G,
Seminara D,
Yoshida T,
Saeki N,
Andrew AS,
Dinney CP,
Czerniak B
외 36명 — 모두 보기
Zhang ZF,
Kiltie AE,
Bishop DT,
Vineis P,
Porru S,
Buntinx F,
Kellen E,
Zeegers MP,
Kumar R,
Rudnai P,
Gurzau E,
Koppova K,
Mayordomo JI,
Sanchez M,
Saez B,
Lindblom A,
de Verdier P,
Steineck G,
Mills GB,
Schned A,
Guarrera S,
Polidoro S,
Chang SC,
Lin J,
Chang DW,
Hale KS,
Majewski T,
Grossman HB,
Thorlacius S,
Thorsteinsdottir U,
Aben KK,
Witjes JA,
Stefansson K,
Amos CI,
Karagas MR,
Gu J
Nature genetics · 2009 · PMID 19648920
페이지 2개
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Rothman N,
Garcia-Closas M,
Chatterjee N,
Malats N,
Wu X,
Figueroa JD,
Real FX,
Van Den Berg D,
Matullo G,
Baris D,
Thun M,
Kiemeney LA
외 98명 — 모두 보기
Vineis P,
De Vivo I,
Albanes D,
Purdue MP,
Rafnar T,
Hildebrandt MA,
Kiltie AE,
Cussenot O,
Golka K,
Kumar R,
Taylor JA,
Mayordomo JI,
Jacobs KB,
Kogevinas M,
Hutchinson A,
Wang Z,
Fu YP,
Prokunina-Olsson L,
Burdett L,
Yeager M,
Wheeler W,
Tardón A,
Serra C,
Carrato A,
García-Closas R,
Lloreta J,
Johnson A,
Schwenn M,
Karagas MR,
Schned A,
Andriole G Jr,
Grubb R 3rd,
Black A,
Jacobs EJ,
Diver WR,
Gapstur SM,
Weinstein SJ,
Virtamo J,
Cortessis VK,
Gago-Dominguez M,
Pike MC,
Stern MC,
Yuan JM,
Hunter DJ,
McGrath M,
Dinney CP,
Czerniak B,
Chen M,
Yang H,
Vermeulen SH,
Aben KK,
Witjes JA,
Makkinje RR,
Sulem P,
Besenbacher S,
Stefansson K,
Riboli E,
Brennan P,
Panico S,
Navarro C,
Allen NE,
Bueno-de-Mesquita HB,
Trichopoulos D,
Caporaso N,
Landi MT,
Canzian F,
Ljungberg B,
Tjonneland A,
Clavel-Chapelon F,
Bishop DT,
Teo MT,
Knowles MA,
Guarrera S,
Polidoro S,
Ricceri F,
Sacerdote C,
Allione A,
Cancel-Tassin G,
Selinski S,
Hengstler JG,
Dietrich H,
Fletcher T,
Rudnai P,
Gurzau E,
Koppova K,
Bolick SC,
Godfrey A,
Xu Z,
Sanz-Velez JI,
D García-Prats M,
Sanchez M,
Valdivia G,
Porru S,
Benhamou S,
Hoover RN,
Fraumeni JF Jr,
Silverman DT,
Chanock SJ
Nature genetics · 2010 · PMID 20972438 · open access
페이지 2개
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Schumann G,
Coin LJ,
Lourdusamy A,
Charoen P,
Berger KH,
Stacey D,
Desrivières S,
Aliev FA,
Khan AA,
Amin N,
Aulchenko YS,
Bakalkin G
외 104명 — 모두 보기
Bakker SJ,
Balkau B,
Beulens JW,
Bilbao A,
de Boer RA,
Beury D,
Bots ML,
Breetvelt EJ,
Cauchi S,
Cavalcanti-Proença C,
Chambers JC,
Clarke TK,
Dahmen N,
de Geus EJ,
Dick D,
Ducci F,
Easton A,
Edenberg HJ,
Esko T,
Fernández-Medarde A,
Foroud T,
Freimer NB,
Girault JA,
Grobbee DE,
Guarrera S,
Gudbjartsson DF,
Hartikainen AL,
Heath AC,
Hesselbrock V,
Hofman A,
Hottenga JJ,
Isohanni MK,
Kaprio J,
Khaw KT,
Kuehnel B,
Laitinen J,
Lobbens S,
Luan J,
Mangino M,
Maroteaux M,
Matullo G,
McCarthy MI,
Mueller C,
Navis G,
Numans ME,
Núñez A,
Nyholt DR,
Onland-Moret CN,
Oostra BA,
O'Reilly PF,
Palkovits M,
Penninx BW,
Polidoro S,
Pouta A,
Prokopenko I,
Ricceri F,
Santos E,
Smit JH,
Soranzo N,
Song K,
Sovio U,
Stumvoll M,
Surakk I,
Thorgeirsson TE,
Thorsteinsdottir U,
Troakes C,
Tyrfingsson T,
Tönjes A,
Uiterwaal CS,
Uitterlinden AG,
van der Harst P,
van der Schouw YT,
Staehlin O,
Vogelzangs N,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Whitfield JB,
Wichmann EH,
Willemsen G,
Witteman JC,
Yuan X,
Zhai G,
Zhao JH,
Zhang W,
Martin NG,
Metspalu A,
Doering A,
Scott J,
Spector TD,
Loos RJ,
Boomsma DI,
Mooser V,
Peltonen L,
Stefansson K,
van Duijn CM,
Vineis P,
Sommer WH,
Kooner JS,
Spanagel R,
Heberlein UA,
Jarvelin MR,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
페이지 2개
Genome-wide association study identifies new prostate cancer susceptibility loci
Schumacher FR,
Berndt SI,
Siddiq A,
Jacobs KB,
Wang Z,
Lindstrom S,
Stevens VL,
Chen C,
Mondul AM,
Travis RC,
Stram DO,
Eeles RA
외 49명 — 모두 보기
Easton DF,
Giles G,
Hopper JL,
Neal DE,
Hamdy FC,
Donovan JL,
Muir K,
Al Olama AA,
Kote-Jarai Z,
Guy M,
Severi G,
Grönberg H,
Isaacs WB,
Karlsson R,
Wiklund F,
Xu J,
Allen NE,
Andriole GL,
Barricarte A,
Boeing H,
Bueno-de-Mesquita HB,
Crawford ED,
Diver WR,
Gonzalez CA,
Gaziano JM,
Giovannucci EL,
Johansson M,
Le Marchand L,
Ma J,
Sieri S,
Stattin P,
Stampfer MJ,
Tjonneland A,
Vineis P,
Virtamo J,
Vogel U,
Weinstein SJ,
Yeager M,
Thun MJ,
Kolonel LN,
Henderson BE,
Albanes D,
Hayes RB,
Feigelson HS,
Riboli E,
Hunter DJ,
Chanock SJ,
Haiman CA,
Kraft P
Human molecular genetics · 2011 · PMID 21743057
페이지 2개
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
외 233명 — 모두 보기
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD 외 컨소시엄 2곳
Nature genetics · 2015 · PMID 26390057
페이지 2개
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Berndt SI,
Camp NJ,
Skibola CF,
Vijai J,
Wang Z,
Gu J,
Nieters A,
Kelly RS,
Smedby KE,
Monnereau A,
Cozen W,
Cox A
외 115명 — 모두 보기
Wang SS,
Lan Q,
Teras LR,
Machado M,
Yeager M,
Brooks-Wilson AR,
Hartge P,
Purdue MP,
Birmann BM,
Vajdic CM,
Cocco P,
Zhang Y,
Giles GG,
Zeleniuch-Jacquotte A,
Lawrence C,
Montalvan R,
Burdett L,
Hutchinson A,
Ye Y,
Call TG,
Shanafelt TD,
Novak AJ,
Kay NE,
Liebow M,
Cunningham JM,
Allmer C,
Hjalgrim H,
Adami HO,
Melbye M,
Glimelius B,
Chang ET,
Glenn M,
Curtin K,
Cannon-Albright LA,
Diver WR,
Link BK,
Weiner GJ,
Conde L,
Bracci PM,
Riby J,
Arnett DK,
Zhi D,
Leach JM,
Holly EA,
Jackson RD,
Tinker LF,
Benavente Y,
Sala N,
Casabonne D,
Becker N,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
McKay J,
Staines A,
Chaffee KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Leis JF,
Weinberg JB,
Caporaso NE,
Norman AD,
De Roos AJ,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Kaaks R,
Masala G,
Weiderpass E,
Chirlaque MD,
Vermeulen RCH,
Travis RC,
Southey MC,
Milne RL,
Albanes D,
Virtamo J,
Weinstein S,
Clavel J,
Zheng T,
Holford TR,
Villano DJ,
Maria A,
Spinelli JJ,
Gascoyne RD,
Connors JM,
Bertrand KA,
Giovannucci E,
Kraft P,
Kricker A,
Turner J,
Ennas MG,
Ferri GM,
Miligi L,
Liang L,
Ma B,
Huang J,
Huang J,
Crouch S,
Park JH,
Chatterjee N,
North KE,
Snowden JA,
Wright J,
Fraumeni JF,
Offit K,
Wu X,
de Sanjose S,
Cerhan JR,
Chanock SJ,
Rothman N,
Slager SL
Nature communications · 2016 · PMID 26956414 · open access
페이지 2개
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Wang Y,
McKay JD,
Rafnar T,
Wang Z,
Timofeeva MN,
Broderick P,
Zong X,
Laplana M,
Wei Y,
Han Y,
Lloyd A,
Delahaye-Sourdeix M
외 71명 — 모두 보기
Chubb D,
Gaborieau V,
Wheeler W,
Chatterjee N,
Thorleifsson G,
Sulem P,
Liu G,
Kaaks R,
Henrion M,
Kinnersley B,
Vallée M,
LeCalvez-Kelm F,
Stevens VL,
Gapstur SM,
Chen WV,
Zaridze D,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D,
Bencko V,
Foretova L,
Janout V,
Krokan HE,
Gabrielsen ME,
Skorpen F,
Vatten L,
Njølstad I,
Chen C,
Goodman G,
Benhamou S,
Vooder T,
Välk K,
Nelis M,
Metspalu A,
Lener M,
Lubiński J,
Johansson M,
Vineis P,
Agudo A,
Clavel-Chapelon F,
Bueno-de-Mesquita HB,
Trichopoulos D,
Khaw KT,
Johansson M,
Weiderpass E,
Tjønneland A,
Riboli E,
Lathrop M,
Scelo G,
Albanes D,
Caporaso NE,
Ye Y,
Gu J,
Wu X,
Spitz MR,
Dienemann H,
Rosenberger A,
Su L,
Matakidou A,
Eisen T,
Stefansson K,
Risch A,
Chanock SJ,
Christiani DC,
Hung RJ,
Brennan P,
Landi MT,
Houlston RS,
Amos CI
Nature genetics · 2014 · PMID 24880342 · open access
페이지 1개
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
McMaster ML,
Berndt SI,
Zhang J,
Slager SL,
Li SA,
Vajdic CM,
Smedby KE,
Yan H,
Birmann BM,
Brown EE,
Smith A,
Kleinstern G
외 69명 — 모두 보기
Fansler MM,
Mayr C,
Zhu B,
Chung CC,
Park JH,
Burdette L,
Hicks BD,
Hutchinson A,
Teras LR,
Adami HO,
Bracci PM,
McKay J,
Monnereau A,
Link BK,
Vermeulen RCH,
Ansell SM,
Maria A,
Diver WR,
Melbye M,
Ojesina AI,
Kraft P,
Boffetta P,
Clavel J,
Giovannucci E,
Besson CM,
Canzian F,
Travis RC,
Vineis P,
Weiderpass E,
Montalvan R,
Wang Z,
Yeager M,
Becker N,
Benavente Y,
Brennan P,
Foretova L,
Maynadie M,
Nieters A,
de Sanjose S,
Staines A,
Conde L,
Riby J,
Glimelius B,
Hjalgrim H,
Pradhan N,
Feldman AL,
Novak AJ,
Lawrence C,
Bassig BA,
Lan Q,
Zheng T,
North KE,
Tinker LF,
Cozen W,
Severson RK,
Hofmann JN,
Zhang Y,
Jackson RD,
Morton LM,
Purdue MP,
Chatterjee N,
Offit K,
Cerhan JR,
Chanock SJ,
Rothman N,
Vijai J,
Goldin LR,
Skibola CF,
Caporaso NE
Nature communications · 2018 · PMID 30305637 · open access
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
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