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성함이나 학술지명, PMID로 찾아보십시오.
Ni S에 대해
98건, 그중 18건 표시.
Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer
Ferreiro-Iglesias A,
McKay JD,
Brenner N,
Virani S,
Lesseur C,
Gaborieau V,
Ness AR,
Hung RJ,
Liu G,
Diergaarde B,
Olshan AF,
Hayes N
외 40명 — 모두 보기
Weissler MC,
Schroeder L,
Bender N,
Pawlita M,
Thomas S,
Pring M,
Dudding T,
Kanterewicz B,
Ferris R,
Thomas S,
Brhane Y,
Díez-Obrero V,
Milojevic M,
Smith-Byrne K,
Mariosa D,
Johansson MJ,
Herrero R,
Boccia S,
Cadoni G,
Lacko M,
Holcátová I,
Ahrens W,
Lagiou P,
Lagiou A,
Polesel J,
Simonato L,
Merletti F,
Healy CM,
Hansen BT,
Nygård M,
Conway DI,
Wright S,
Macfarlane TV,
Robinson M,
Alemany L,
Agudo A,
Znaor A,
Amos CI,
Waterboer T,
Brennan P
Nature communications · 2021 · PMID 34642315 · open access
페이지 2개
Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin
Paterson AD,
Lopes-Virella MF,
Waggott D,
Boright AP,
Hosseini SM,
Carter RE,
Shen E,
Mirea L,
Bharaj B,
Sun L,
Bull SB
Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group
Arteriosclerosis, thrombosis, and vascular biology · 2009 · PMID 19729612
페이지 1개
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Haiman CA,
Chen GK,
Vachon CM,
Canzian F,
Dunning A,
Millikan RC,
Wang X,
Ademuyiwa F,
Ahmed S,
Ambrosone CB,
Baglietto L,
Balleine R
외 119명 — 모두 보기
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Blot WJ,
Brauch H,
Buring JE,
Carey LA,
Carpenter JE,
Chang-Claude J,
Chanock SJ,
Chasman DI,
Clarke CL,
Cox A,
Cross SS,
Deming SL,
Diasio RB,
Dimopoulos AM,
Driver WR,
Dünnebier T,
Durcan L,
Eccles D,
Edlund CK,
Ekici AB,
Fasching PA,
Feigelson HS,
Flesch-Janys D,
Fostira F,
Försti A,
Fountzilas G,
Gerty SM,
Giles GG,
Godwin AK,
Goodfellow P,
Graham N,
Greco D,
Hamann U,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Holbrook A,
Hoover RN,
Hu JJ,
Hunter DJ,
Ingles SA,
Irwanto A,
Ivanovich J,
John EM,
Johnson N,
Jukkola-Vuorinen A,
Kaaks R,
Ko YD,
Kolonel LN,
Konstantopoulou I,
Kosma VM,
Kulkarni S,
Lambrechts D,
Lee AM,
Marchand LL,
Lesnick T,
Liu J,
Lindstrom S,
Mannermaa A,
Margolin S,
Martin NG,
Miron P,
Montgomery GW,
Nevanlinna H,
Nickels S,
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Olswold C,
Palmer J,
Pathak H,
Pectasides D,
Perou CM,
Peto J,
Pharoah PD,
Pooler LC,
Press MF,
Pylkäs K,
Rebbeck TR,
Rodriguez-Gil JL,
Rosenberg L,
Ross E,
Rüdiger T,
Silva Idos S,
Sawyer E,
Schmidt MK,
Schulz-Wendtland R,
Schumacher F,
Severi G,
Sheng X,
Signorello LB,
Sinn HP,
Stevens KN,
Southey MC,
Tapper WJ,
Tomlinson I,
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Wauters E,
Weaver J,
Wildiers H,
Winqvist R,
Van Den Berg D,
Wan P,
Xia LY,
Yannoukakos D,
Zheng W,
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Siddiq A,
Slager SL,
Stram DO,
Easton D,
Kraft P,
Henderson BE,
Couch FJ
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
페이지 1개
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer ND,
McDonough CW,
Hicks PJ,
Roh BH,
Wing MR,
An SS,
Hester JM,
Cooke JN,
Bostrom MA,
Rudock ME,
Talbert ME,
Lewis JP
외 379명 — 모두 보기
Ferrara A,
Lu L,
Ziegler JT,
Sale MM,
Divers J,
Shriner D,
Adeyemo A,
Rotimi CN,
Ng MC,
Langefeld CD,
Freedman BI,
Bowden DW,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Morris AP,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Langenberg C,
Hofmann OM,
Dupuis J,
Qi L,
Segrè AV,
van Hoek M,
Navarro P,
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Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
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Charpentier G,
Chines PS,
Cornelis M,
Couper DJ,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
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Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
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Jackson AU,
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Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
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Midthjell K,
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Nilsson P,
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Payne F,
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Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
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Robertson NR,
Rocheleau G,
Roden M,
Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
Sparsø T,
Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
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Witteman J,
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Hitman GA,
Hofman A,
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Hveem K,
Laakso M,
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Morris AD,
Palmer CN,
Pramstaller PP,
Rudan I,
Sijbrands E,
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Tuomilehto J,
Uitterlinden A,
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Wareham NJ,
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Abecasis GR,
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Campbell H,
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Hattersley AT,
Hu FB,
Meigs JB,
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Pedersen O,
Wichmann HE,
Barroso I,
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Frayling TM,
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Thorsteinsdottir U,
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Illig T,
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van Duijn CM,
Stefansson K,
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Mägi R,
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Hui J,
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Lecoeur C,
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Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
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Pakyz R,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
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Perola M,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Psaty BM,
Rayner NW,
Rice K,
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Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
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Sharp SJ,
Shields B,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
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Swift A,
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Tanaka T,
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van Dijk KW,
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Walley A,
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Meneton P,
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Nathan DM,
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Salomaa V,
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Schlessinger D,
Uda M,
Ruokonen A,
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Waterworth DM,
Vollenweider P,
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Mooser V,
Sladek R
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
페이지 1개
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
외 190명 — 모두 보기
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
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Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
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Davies G,
de Almeida MA,
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Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
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Mattheisen M,
Meisenzahl E,
Melle I,
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Mühleisen TW,
Nauck M,
Nöthen MM,
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Pandolfo M,
Pike GB,
Puls R,
Reinvang I,
Rentería ME,
Rietschel M,
Roffman JL,
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Rujescu D,
Savitz J,
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Schnell K,
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Smith C,
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Whelan CD,
Agartz I,
Boomsma DI,
Cavalleri GL,
Dale AM,
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Drevets WC,
Hagoort P,
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Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
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Poline JB,
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Wright MJ,
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Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22504417
페이지 1개
Genome-wide association study of age at menarche in African-American women
Demerath EW,
Liu CT,
Franceschini N,
Chen G,
Palmer JR,
Smith EN,
Chen CT,
Ambrosone CB,
Arnold AM,
Bandera EV,
Berenson GS,
Bernstein L
외 45명 — 모두 보기
Britton A,
Cappola AR,
Carlson CS,
Chanock SJ,
Chen W,
Chen Z,
Deming SL,
Elks CE,
Evans MK,
Gajdos Z,
Henderson BE,
Hu JJ,
Ingles S,
John EM,
Kerr KF,
Kolonel LN,
Le Marchand L,
Lu X,
Millikan RC,
Musani SK,
Nock NL,
North K,
Nyante S,
Press MF,
Rodriquez-Gil JL,
Ruiz-Narvaez EA,
Schork NJ,
Srinivasan SR,
Woods NF,
Zheng W,
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Ziegler RG,
Zonderman A,
Heiss G,
Gwen Windham B,
Wellons M,
Murray SS,
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Pastinen T,
Rajkovic A,
Hirschhorn J,
Adrienne Cupples L,
Kooperberg C,
Murabito JM,
Haiman CA
Human molecular genetics · 2013 · PMID 23599027
페이지 1개
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
Nudel R,
Simpson NH,
Baird G,
O'Hare A,
Conti-Ramsden G,
Bolton PF,
Hennessy ER,
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Davey Smith G,
Francks C,
Paracchini S,
Monaco AP
외 2명 — 모두 보기
SLI Consortium
Genes, brain, and behavior · 2014 · PMID 24571439 · open access
페이지 1개
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study
Musani SK,
Fox ER,
Kraja A,
Bidulescu A,
Lieb W,
Lin H,
Beecham A,
Chen MH,
Felix JF,
Fox CS,
Kao WH,
Kardia SL
외 11명 — 모두 보기
Liu CT,
Nalls MA,
Rundek T,
Sacco RL,
Smith J,
Sun YV,
Wilson G,
Zhang Z,
Mosley TH,
Taylor HA,
Vasan RS
Circulation. Cardiovascular genetics · 2015 · PMID 25561047
페이지 1개
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Khor CC,
Do T,
Jia H,
Nakano M,
George R,
Abu-Amero K,
Duvesh R,
Chen LJ,
Li Z,
Nongpiur ME,
Perera SA,
Qiao C
외 217명 — 모두 보기
Wong HT,
Sakai H,
Barbosa de Melo M,
Lee MC,
Chan AS,
Azhany Y,
Dao TL,
Ikeda Y,
Perez-Grossmann RA,
Zarnowski T,
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Jonas JB,
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Jap A,
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Goh D,
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Wang H,
Yong VK,
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Trinh TB,
Makornwattana M,
Nguyen TT,
Leuenberger EU,
Park KH,
Wiyogo WA,
Kumar RS,
Tello C,
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Thapa SS,
Pathanapitoon K,
Salmon JF,
Sohn YH,
Fea A,
Ozaki M,
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Tantisevi V,
Khaing CC,
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Tang G,
Fan S,
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Meng H,
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Tran TD,
Ueno M,
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Ramli N,
Aung YM,
Reyes RD,
Vernon SA,
Fang SK,
Xie Z,
Chen XY,
Foo JN,
Sim KS,
Wong TT,
Quek DT,
Venkatesh R,
Kavitha S,
Krishnadas SR,
Soumittra N,
Shantha B,
Lim BA,
Ogle J,
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Costa VP,
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Low S,
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Craven ER,
Khan MI,
Dada R,
Mohanty K,
Faiq MA,
Hewitt AW,
Burdon KP,
Gan EH,
Prutthipongsit A,
Patthanathamrongkasem T,
Catacutan MA,
Felarca IR,
Liao CS,
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Istiantoro VW,
Consolandi G,
Pignata G,
Lavia C,
Rojanapongpun P,
Mangkornkanokpong L,
Chansangpetch S,
Chan JC,
Choy BN,
Shum JW,
Than HM,
Oo KT,
Han AT,
Yong VH,
Ng XY,
Goh SR,
Chong YF,
Hibberd ML,
Seielstad M,
Png E,
Dunstan SJ,
Chau NV,
Bei J,
Zeng YX,
Karkey A,
Basnyat B,
Pasutto F,
Paoli D,
Frezzotti P,
Wang JJ,
Mitchell P,
Fingert JH,
Allingham RR,
Hauser MA,
Lim ST,
Chew SH,
Ebstein RP,
Sakuntabhai A,
Park KH,
Ahn J,
Boland G,
Snippe H,
Stead R,
Quino R,
Zaw SN,
Lukasik U,
Shetty R,
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Bae HW,
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Hwang YH,
Kiire CA,
Kuroda M,
Djamal ZE,
Peregrino JI,
Ghosh A,
Jeoung JW,
Hoan TS,
Srisamran N,
Sandragasu T,
Set SH,
Doan VH,
Bhattacharya SS,
Ho CL,
Tan DT,
Sihota R,
Loon SC,
Mori K,
Kinoshita S,
Hollander AI,
Qamar R,
Wang YX,
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Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
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