연구자에게
내 논문이 여기 있나요?
논문 2,682편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Ng A에 대해
320건, 그중 20건 표시.
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Brito Nunes C,
Rukins V,
Cisse AH,
White F,
McBride N,
Kuang A,
Allard C,
Ronkainen J,
Hughes A,
Elliott A,
Thorleifsson G,
Vaudel M
외 67명 — 모두 보기
Laisk T,
Gu Y,
Lamri A,
Chen L,
Tuhkanen J,
Lahti J,
Calas L,
Muntaner M,
Karhunen V,
Choi J,
Heiskala A,
Hatem G,
Fragoso-Bargas N,
Rifas-Shiman SL,
Paz-Lopez G,
Stinson SE,
Bhowmik B,
Ahlqvist E,
Deleuze JF,
Eriksson JG,
Park J,
Teo K,
Räikkönen K,
Stefansson K,
Molina-Vega M,
Subbarao P,
Beaumont RN,
Johansson S,
Tuomi T,
Hansen T,
Engelbrechtsen L,
Morcillo S,
Oken E,
Quigstad E,
Birkeland KI,
Vääräsmäki M,
Hattersley AT,
Sebert S,
Hitman GA,
Kwak SH,
Järvelin MR,
Prasad RB,
Heude B,
Meirhaeghe A,
Bouchard L,
Jacques PÉ,
Laivuori H,
Tan KH,
Anand SS,
van Heel DA,
Liu S,
Njølstad PR,
Steinthorsdottir V,
Widén E,
Keikkala E,
Scholtens DM,
Lowe WL,
Finer S,
Morris AP,
Mägi R,
Zöllner J,
Borges MC,
Lawlor DA,
Hivert MF,
Freathy RM,
Evans DM,
Moen GH
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
페이지 5개
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Aulchenko YS,
Ripatti S,
Lindqvist I,
Boomsma D,
Heid IM,
Pramstaller PP,
Penninx BW,
Janssens AC,
Wilson JF,
Spector T,
Martin NG,
Pedersen NL
외 45명 — 모두 보기
Kyvik KO,
Kaprio J,
Hofman A,
Freimer NB,
Jarvelin MR,
Gyllensten U,
Campbell H,
Rudan I,
Johansson A,
Marroni F,
Hayward C,
Vitart V,
Jonasson I,
Pattaro C,
Wright A,
Hastie N,
Pichler I,
Hicks AA,
Falchi M,
Willemsen G,
Hottenga JJ,
de Geus EJ,
Montgomery GW,
Whitfield J,
Magnusson P,
Saharinen J,
Perola M,
Silander K,
Isaacs A,
Sijbrands EJ,
Uitterlinden AG,
Witteman JC,
Oostra BA,
Elliott P,
Ruokonen A,
Sabatti C,
Gieger C,
Meitinger T,
Kronenberg F,
Döring A,
Wichmann HE,
Smit JH,
McCarthy MI,
van Duijn CM,
Peltonen L
ENGAGE Consortium
Nature genetics · 2009 · PMID 19060911
페이지 4개
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
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Rivadeneira F,
Styrkársdottir U,
Estrada K,
Halldórsson BV,
Hsu YH,
Richards JB,
Zillikens MC,
Kavvoura FK,
Amin N,
Aulchenko YS,
Cupples LA,
Deloukas P
외 23명 — 모두 보기
Demissie S,
Grundberg E,
Hofman A,
Kong A,
Karasik D,
van Meurs JB,
Oostra B,
Pastinen T,
Pols HA,
Sigurdsson G,
Soranzo N,
Thorleifsson G,
Thorsteinsdottir U,
Williams FM,
Wilson SG,
Zhou Y,
Ralston SH,
van Duijn CM,
Spector T,
Kiel DP,
Stefansson K,
Ioannidis JP,
Uitterlinden AG
Genetic Factors for Osteoporosis (GEFOS) Consortium
Nature genetics · 2009 · PMID 19801982 · open access
페이지 4개
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Dupuis J,
Langenberg C,
Prokopenko I,
Saxena R,
Soranzo N,
Jackson AU,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Gloyn AL,
Lindgren CM,
Mägi R
외 292명 — 모두 보기
Morris AP,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Thorleifsson G,
Steinthorsdottir V,
Henneman P,
Grallert H,
Dehghan A,
Hottenga JJ,
Franklin CS,
Navarro P,
Song K,
Goel A,
Perry JR,
Egan JM,
Lajunen T,
Grarup N,
Sparsø T,
Doney A,
Voight BF,
Stringham HM,
Li M,
Kanoni S,
Shrader P,
Cavalcanti-Proença C,
Kumari M,
Qi L,
Timpson NJ,
Gieger C,
Zabena C,
Rocheleau G,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Payne F,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ardlie K,
Ariyurek Y,
Balkau B,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Benediktsson R,
Bennett AJ,
Bergmann S,
Bochud M,
Boerwinkle E,
Bonnefond A,
Bonnycastle LL,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Charpentier G,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Cornelis M,
Crawford G,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Dina C,
Erdos MR,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Fox CS,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Groves CJ,
Grundy S,
Gwilliam R,
Gyllensten U,
Hadjadj S,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hassanali N,
Hayward C,
Heath SC,
Hercberg S,
Herder C,
Hicks AA,
Hillman DR,
Hingorani AD,
Hofman A,
Hui J,
Hung J,
Isomaa B,
Johnson PR,
Jørgensen T,
Jula A,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Lyssenko V,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McCulloch LJ,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Morken MA,
Mukherjee S,
Naitza S,
Narisu N,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
Palmer CN,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Perola M,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Psaty BM,
Rathmann W,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Roden M,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Scott LJ,
Seedorf U,
Sharp SJ,
Shields B,
Sigurethsson G,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Thorand B,
Tichet J,
Tönjes A,
Tuomi T,
Uitterlinden AG,
van Dijk KW,
van Hoek M,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Walters GB,
Ward KL,
Watkins H,
Weedon MN,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zeggini E,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Hattersley AT,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Morris AD,
Lind L,
Palmer LJ,
Hu FB,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pankow JS,
Sampson MJ,
Kuusisto J,
Laakso M,
Hansen T,
Pedersen O,
Pramstaller PP,
Wichmann HE,
Illig T,
Rudan I,
Wright AF,
Stumvoll M,
Campbell H,
Wilson JF,
Bergman RN,
Buchanan TA,
Collins FS,
Mohlke KL,
Tuomilehto J,
Valle TT,
Altshuler D,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Frayling TM,
Ferrucci L,
Kong A,
Thorsteinsdottir U,
Stefansson K,
van Duijn CM,
Aulchenko YS,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Abecasis GR,
Wareham NJ,
Sladek R,
Froguel P,
Watanabe RM,
Meigs JB,
Groop L,
Boehnke M,
McCarthy MI,
Florez JC,
Barroso I
DIAGRAM Consortium · GIANT Consortium 외 컨소시엄 3곳
Nature genetics · 2010 · PMID 20081858 · open access
페이지 4개
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Chen ZJ,
Zhao H,
He L,
Shi Y,
Qin Y,
Shi Y,
Li Z,
You L,
Zhao J,
Liu J,
Liang X,
Zhao X
외 22명 — 모두 보기
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
Bian Y,
Gao X,
Geng L,
Li Y,
Zhu D,
Sun X,
Xu JE,
Hao C,
Ren CE,
Zhang Y,
Chen S,
Zhang W,
Yang A,
Yan J,
Li Y,
Ma J,
Zhao Y
Nature genetics · 2011 · PMID 21151128
페이지 4개
Genetic correction of PSA values using sequence variants associated with PSA levels
Gudmundsson J,
Besenbacher S,
Sulem P,
Gudbjartsson DF,
Olafsson I,
Arinbjarnarson S,
Agnarsson BA,
Benediktsdottir KR,
Isaksson HJ,
Kostic JP,
Gudjonsson SA,
Stacey SN
외 37명 — 모두 보기
Gylfason A,
Sigurdsson A,
Holm H,
Bjornsdottir US,
Eyjolfsson GI,
Navarrete S,
Fuertes F,
Garcia-Prats MD,
Polo E,
Checherita IA,
Jinga M,
Badea P,
Aben KK,
Schalken JA,
van Oort IM,
Sweep FC,
Helfand BT,
Davis M,
Donovan JL,
Hamdy FC,
Kristjansson K,
Gulcher JR,
Masson G,
Kong A,
Catalona WJ,
Mayordomo JI,
Geirsson G,
Einarsson GV,
Barkardottir RB,
Jonsson E,
Jinga V,
Mates D,
Kiemeney LA,
Neal DE,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Science translational medicine · 2010 · PMID 21160077
페이지 4개
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
Soler Artigas M,
Loth DW,
Wain LV,
Gharib SA,
Obeidat M,
Tang W,
Zhai G,
Zhao JH,
Smith AV,
Huffman JE,
Albrecht E,
Jackson CM
외 158명 — 모두 보기
Evans DM,
Cadby G,
Fornage M,
Manichaikul A,
Lopez LM,
Johnson T,
Aldrich MC,
Aspelund T,
Barroso I,
Campbell H,
Cassano PA,
Couper DJ,
Eiriksdottir G,
Franceschini N,
Garcia M,
Gieger C,
Gislason GK,
Grkovic I,
Hammond CJ,
Hancock DB,
Harris TB,
Ramasamy A,
Heckbert SR,
Heliövaara M,
Homuth G,
Hysi PG,
James AL,
James AL,
Jankovic S,
Joubert BR,
Karrasch S,
Klopp N,
Koch B,
Kritchevsky SB,
Launer LJ,
Liu Y,
Loehr LR,
Lohman K,
Loos RJ,
Lumley T,
Al Balushi KA,
Ang WQ,
Barr RG,
Beilby J,
Blakey JD,
Boban M,
Boraska V,
Brisman J,
Britton JR,
Brusselle GG,
Cooper C,
Curjuric I,
Dahgam S,
Deary IJ,
Ebrahim S,
Eijgelsheim M,
Francks C,
Gaysina D,
Granell R,
Gu X,
Hankinson JL,
Hardy R,
Harris SE,
Henderson J,
Henry A,
Hingorani AD,
Hofman A,
Holt PG,
Hui J,
Hunter ML,
Imboden M,
Jameson KA,
Kerr SM,
Kolcic I,
Kronenberg F,
Liu JZ,
Marchini J,
McKeever T,
Morris AD,
Olin AC,
Porteous DJ,
Postma DS,
Rich SS,
Ring SM,
Rivadeneira F,
Rochat T,
Sayer AA,
Sayers I,
Sly PD,
Smith GD,
Sood A,
Starr JM,
Uitterlinden AG,
Vonk JM,
Wannamethee SG,
Whincup PH,
Wijmenga C,
Williams OD,
Wong A,
Mangino M,
Marciante KD,
McArdle WL,
Meibohm B,
Morrison AC,
North KE,
Omenaas E,
Palmer LJ,
Pietiläinen KH,
Pin I,
Pola Sbreve Ek O,
Pouta A,
Psaty BM,
Hartikainen AL,
Rantanen T,
Ripatti S,
Rotter JI,
Rudan I,
Rudnicka AR,
Schulz H,
Shin SY,
Spector TD,
Surakka I,
Vitart V,
Völzke H,
Wareham NJ,
Warrington NM,
Wichmann HE,
Wild SH,
Wilk JB,
Wjst M,
Wright AF,
Zgaga L,
Zemunik T,
Pennell CE,
Nyberg F,
Kuh D,
Holloway JW,
Boezen HM,
Lawlor DA,
Morris RW,
Probst-Hensch N,
Kaprio J,
Wilson JF,
Hayward C,
Kähönen M,
Heinrich J,
Musk AW,
Jarvis DL,
Gläser S,
Järvelin MR,
Ch Stricker BH,
Elliott P,
O'Connor GT,
Strachan DP,
London SJ,
Hall IP,
Gudnason V,
Tobin MD
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
페이지 4개
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Shi Y,
Zhao H,
Shi Y,
Cao Y,
Yang D,
Li Z,
Zhang B,
Liang X,
Li T,
Chen J,
Shen J,
Zhao J
외 41명 — 모두 보기
You L,
Gao X,
Zhu D,
Zhao X,
Yan Y,
Qin Y,
Li W,
Yan J,
Wang Q,
Zhao J,
Geng L,
Ma J,
Zhao Y,
He G,
Zhang A,
Zou S,
Yang A,
Liu J,
Li W,
Li B,
Wan C,
Qin Y,
Shi J,
Yang J,
Jiang H,
Xu JE,
Qi X,
Sun Y,
Zhang Y,
Hao C,
Ju X,
Zhao D,
Ren CE,
Li X,
Zhang W,
Zhang Y,
Zhang J,
Wu D,
Zhang C,
He L,
Chen ZJ
Nature genetics · 2012 · PMID 22885925
페이지 4개
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome
Lessard CJ,
Li H,
Adrianto I,
Ice JA,
Rasmussen A,
Grundahl KM,
Kelly JA,
Dozmorov MG,
Miceli-Richard C,
Bowman S,
Lester S,
Eriksson P
외 48명 — 모두 보기
Eloranta ML,
Brun JG,
Gøransson LG,
Harboe E,
Guthridge JM,
Kaufman KM,
Kvarnström M,
Jazebi H,
Cunninghame Graham DS,
Grandits ME,
Nazmul-Hossain AN,
Patel K,
Adler AJ,
Maier-Moore JS,
Farris AD,
Brennan MT,
Lessard JA,
Chodosh J,
Gopalakrishnan R,
Hefner KS,
Houston GD,
Huang AJ,
Hughes PJ,
Lewis DM,
Radfar L,
Rohrer MD,
Stone DU,
Wren JD,
Vyse TJ,
Gaffney PM,
James JA,
Omdal R,
Wahren-Herlenius M,
Illei GG,
Witte T,
Jonsson R,
Rischmueller M,
Rönnblom L,
Nordmark G,
Ng WF,
Mariette X,
Anaya JM,
Rhodus NL,
Segal BM,
Scofield RH,
Montgomery CG,
Harley JB,
Sivils KL
UK Primary Sjögren's Syndrome Registry
Nature genetics · 2013 · PMID 24097067 · open access
페이지 4개
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Moayyeri A,
Hsu YH,
Karasik D,
Estrada K,
Xiao SM,
Nielson C,
Srikanth P,
Giroux S,
Wilson SG,
Zheng HF,
Smith AV,
Pye SR
외 118명 — 모두 보기
Leo PJ,
Teumer A,
Hwang JY,
Ohlsson C,
McGuigan F,
Minster RL,
Hayward C,
Olmos JM,
Lyytikäinen LP,
Lewis JR,
Swart KM,
Masi L,
Oldmeadow C,
Holliday EG,
Cheng S,
van Schoor NM,
Harvey NC,
Kruk M,
del Greco M F,
Igl W,
Trummer O,
Grigoriou E,
Luben R,
Liu CT,
Zhou Y,
Oei L,
Medina-Gomez C,
Zmuda J,
Tranah G,
Brown SJ,
Williams FM,
Soranzo N,
Jakobsdottir J,
Siggeirsdottir K,
Holliday KL,
Hannemann A,
Go MJ,
Garcia M,
Polasek O,
Laaksonen M,
Zhu K,
Enneman AW,
McEvoy M,
Peel R,
Sham PC,
Jaworski M,
Johansson Å,
Hicks AA,
Pludowski P,
Scott R,
Dhonukshe-Rutten RA,
van der Velde N,
Kähönen M,
Viikari JS,
Sievänen H,
Raitakari OT,
González-Macías J,
Hernández JL,
Mellström D,
Ljunggren O,
Cho YS,
Völker U,
Nauck M,
Homuth G,
Völzke H,
Haring R,
Brown MA,
McCloskey E,
Nicholson GC,
Eastell R,
Eisman JA,
Jones G,
Reid IR,
Dennison EM,
Wark J,
Boonen S,
Vanderschueren D,
Wu FC,
Aspelund T,
Richards JB,
Bauer D,
Hofman A,
Khaw KT,
Dedoussis G,
Obermayer-Pietsch B,
Gyllensten U,
Pramstaller PP,
Lorenc RS,
Cooper C,
Kung AW,
Lips P,
Alen M,
Attia J,
Brandi ML,
de Groot LC,
Lehtimäki T,
Riancho JA,
Campbell H,
Liu Y,
Harris TB,
Akesson K,
Karlsson M,
Lee JY,
Wallaschofski H,
Duncan EL,
O'Neill TW,
Gudnason V,
Spector TD,
Rousseau F,
Orwoll E,
Cummings SR,
Wareham NJ,
Rivadeneira F,
Uitterlinden AG,
Prince RL,
Kiel DP,
Reeve J,
Kaptoge SK
Human molecular genetics · 2014 · PMID 24430505
페이지 4개
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban N,
Jansen R,
de Vlaming R,
Vaez A,
Mandemakers JJ,
Tropf FC,
Shen X,
Wilson JF,
Chasman DI,
Nolte IM,
Tragante V,
van der Laan SW
외 241명 — 모두 보기
Perry JR,
Kong A,
Ahluwalia TS,
Albrecht E,
Yerges-Armstrong L,
Atzmon G,
Auro K,
Ayers K,
Bakshi A,
Ben-Avraham D,
Berger K,
Bergman A,
Bertram L,
Bielak LF,
Bjornsdottir G,
Bonder MJ,
Broer L,
Bui M,
Barbieri C,
Cavadino A,
Chavarro JE,
Turman C,
Concas MP,
Cordell HJ,
Davies G,
Eibich P,
Eriksson N,
Esko T,
Eriksson J,
Falahi F,
Felix JF,
Fontana MA,
Franke L,
Gandin I,
Gaskins AJ,
Gieger C,
Gunderson EP,
Guo X,
Hayward C,
He C,
Hofer E,
Huang H,
Joshi PK,
Kanoni S,
Karlsson R,
Kiechl S,
Kifley A,
Kluttig A,
Kraft P,
Lagou V,
Lecoeur C,
Lahti J,
Li-Gao R,
Lind PA,
Liu T,
Makalic E,
Mamasoula C,
Matteson L,
Mbarek H,
McArdle PF,
McMahon G,
Meddens SF,
Mihailov E,
Miller M,
Missmer SA,
Monnereau C,
van der Most PJ,
Myhre R,
Nalls MA,
Nutile T,
Kalafati IP,
Porcu E,
Prokopenko I,
Rajan KB,
Rich-Edwards J,
Rietveld CA,
Robino A,
Rose LM,
Rueedi R,
Ryan KA,
Saba Y,
Schmidt D,
Smith JA,
Stolk L,
Streeten E,
Tönjes A,
Thorleifsson G,
Ulivi S,
Wedenoja J,
Wellmann J,
Willeit P,
Yao J,
Yengo L,
Zhao JH,
Zhao W,
Zhernakova DV,
Amin N,
Andrews H,
Balkau B,
Barzilai N,
Bergmann S,
Biino G,
Bisgaard H,
Bønnelykke K,
Boomsma DI,
Buring JE,
Campbell H,
Cappellani S,
Ciullo M,
Cox SR,
Cucca F,
Toniolo D,
Davey-Smith G,
Deary IJ,
Dedoussis G,
Deloukas P,
van Duijn CM,
de Geus EJ,
Eriksson JG,
Evans DA,
Faul JD,
Sala CF,
Froguel P,
Gasparini P,
Girotto G,
Grabe HJ,
Greiser KH,
Groenen PJ,
de Haan HG,
Haerting J,
Harris TB,
Heath AC,
Heikkilä K,
Hofman A,
Homuth G,
Holliday EG,
Hopper J,
Hyppönen E,
Jacobsson B,
Jaddoe VW,
Johannesson M,
Jugessur A,
Kähönen M,
Kajantie E,
Kardia SL,
Keavney B,
Kolcic I,
Koponen P,
Kovacs P,
Kronenberg F,
Kutalik Z,
La Bianca M,
Lachance G,
Iacono WG,
Lai S,
Lehtimäki T,
Liewald DC,
Lindgren CM,
Liu Y,
Luben R,
Lucht M,
Luoto R,
Magnus P,
Magnusson PK,
Martin NG,
McGue M,
McQuillan R,
Medland SE,
Meisinger C,
Mellström D,
Metspalu A,
Traglia M,
Milani L,
Mitchell P,
Montgomery GW,
Mook-Kanamori D,
de Mutsert R,
Nohr EA,
Ohlsson C,
Olsen J,
Ong KK,
Paternoster L,
Pattie A,
Penninx BW,
Perola M,
Peyser PA,
Pirastu M,
Polasek O,
Power C,
Kaprio J,
Raffel LJ,
Räikkönen K,
Raitakari O,
Ridker PM,
Ring SM,
Roll K,
Rudan I,
Ruggiero D,
Rujescu D,
Salomaa V,
Schlessinger D,
Schmidt H,
Schmidt R,
Schupf N,
Smit J,
Sorice R,
Spector TD,
Starr JM,
Stöckl D,
Strauch K,
Stumvoll M,
Swertz MA,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tung JY,
Uitterlinden AG,
Vaccargiu S,
Viikari J,
Vitart V,
Völzke H,
Vollenweider P,
Vuckovic D,
Waage J,
Wagner GG,
Wang JJ,
Wareham NJ,
Weir DR,
Willemsen G,
Willeit J,
Wright AF,
Zondervan KT,
Stefansson K,
Krueger RF,
Lee JJ,
Benjamin DJ,
Cesarini D,
Koellinger PD,
den Hoed M,
Snieder H,
Mills MC
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
페이지 4개
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
Sud A,
Thomsen H,
Law PJ,
Försti A,
Filho MIDS,
Holroyd A,
Broderick P,
Orlando G,
Lenive O,
Wright L,
Cooke R,
Easton D
외 23명 — 모두 보기
Pharoah P,
Dunning A,
Peto J,
Canzian F,
Eeles R,
Kote-Jarai Z,
Muir K,
Pashayan N,
Hoffmann P,
Nöthen MM,
Jöckel KH,
Strandmann EPV,
Lightfoot T,
Kane E,
Roman E,
Lake A,
Montgomery D,
Jarrett RF,
Swerdlow AJ,
Engert A,
Orr N,
Hemminki K,
Houlston RS
PRACTICAL consortium
Nature communications · 2017 · PMID 29196614 · open access
페이지 4개
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Bonàs-Guarch S,
Guindo-Martínez M,
Miguel-Escalada I,
Grarup N,
Sebastian D,
Rodriguez-Fos E,
Sánchez F,
Planas-Fèlix M,
Cortes-Sánchez P,
González S,
Timshel P,
Pers TH
외 31명 — 모두 보기
Morgan CC,
Moran I,
Atla G,
González JR,
Puiggros M,
Martí J,
Andersson EA,
Díaz C,
Badia RM,
Udler M,
Leong A,
Kaur V,
Flannick J,
Jørgensen T,
Linneberg A,
Jørgensen ME,
Witte DR,
Christensen C,
Brandslund I,
Appel EV,
Scott RA,
Luan J,
Langenberg C,
Wareham NJ,
Pedersen O,
Zorzano A,
Florez JC,
Hansen T,
Ferrer J,
Mercader JM,
Torrents D
Nature communications · 2018 · PMID 29358691 · open access
페이지 4개
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Prins BP,
Mead TJ,
Brody JA,
Sveinbjornsson G,
Ntalla I,
Bihlmeyer NA,
van den Berg M,
Bork-Jensen J,
Cappellani S,
Van Duijvenboden S,
Klena NT,
Gabriel GC
외 101명 — 모두 보기
Liu X,
Gulec C,
Grarup N,
Haessler J,
Hall LM,
Iorio A,
Isaacs A,
Li-Gao R,
Lin H,
Liu CT,
Lyytikäinen LP,
Marten J,
Mei H,
Müller-Nurasyid M,
Orini M,
Padmanabhan S,
Radmanesh F,
Ramirez J,
Robino A,
Schwartz M,
van Setten J,
Smith AV,
Verweij N,
Warren HR,
Weiss S,
Alonso A,
Arnar DO,
Bots ML,
de Boer RA,
Dominiczak AF,
Eijgelsheim M,
Ellinor PT,
Guo X,
Felix SB,
Harris TB,
Hayward C,
Heckbert SR,
Huang PL,
Jukema JW,
Kähönen M,
Kors JA,
Lambiase PD,
Launer LJ,
Li M,
Linneberg A,
Nelson CP,
Pedersen O,
Perez M,
Peters A,
Polasek O,
Psaty BM,
Raitakari OT,
Rice KM,
Rotter JI,
Sinner MF,
Soliman EZ,
Spector TD,
Strauch K,
Thorsteinsdottir U,
Tinker A,
Trompet S,
Uitterlinden A,
Vaartjes I,
van der Meer P,
Völker U,
Völzke H,
Waldenberger M,
Wilson JG,
Xie Z,
Asselbergs FW,
Dörr M,
van Duijn CM,
Gasparini P,
Gudbjartsson DF,
Gudnason V,
Hansen T,
Kääb S,
Kanters JK,
Kooperberg C,
Lehtimäki T,
Lin HJ,
Lubitz SA,
Mook-Kanamori DO,
Conti FJ,
Newton-Cheh CH,
Rosand J,
Rudan I,
Samani NJ,
Sinagra G,
Smith BH,
Holm H,
Stricker BH,
Ulivi S,
Sotoodehnia N,
Apte SS,
van der Harst P,
Stefansson K,
Munroe PB,
Arking DE,
Lo CW,
Jamshidi Y
Genome biology · 2018 · PMID 30012220 · open access
페이지 4개
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Rhodes CJ,
Batai K,
Bleda M,
Haimel M,
Southgate L,
Germain M,
Pauciulo MW,
Hadinnapola C,
Aman J,
Girerd B,
Arora A,
Knight J
외 106명 — 모두 보기
Hanscombe KB,
Karnes JH,
Kaakinen M,
Gall H,
Ulrich A,
Harbaum L,
Cebola I,
Ferrer J,
Lutz K,
Swietlik EM,
Ahmad F,
Amouyel P,
Archer SL,
Argula R,
Austin ED,
Badesch D,
Bakshi S,
Barnett C,
Benza R,
Bhatt N,
Bogaard HJ,
Burger CD,
Chakinala M,
Church C,
Coghlan JG,
Condliffe R,
Corris PA,
Danesino C,
Debette S,
Elliott CG,
Elwing J,
Eyries M,
Fortin T,
Franke A,
Frantz RP,
Frost A,
Garcia JGN,
Ghio S,
Ghofrani HA,
Gibbs JSR,
Harley J,
He H,
Hill NS,
Hirsch R,
Houweling AC,
Howard LS,
Ivy D,
Kiely DG,
Klinger J,
Kovacs G,
Lahm T,
Laudes M,
Machado RD,
MacKenzie Ross RV,
Marsolo K,
Martin LJ,
Moledina S,
Montani D,
Nathan SD,
Newnham M,
Olschewski A,
Olschewski H,
Oudiz RJ,
Ouwehand WH,
Peacock AJ,
Pepke-Zaba J,
Rehman Z,
Robbins I,
Roden DM,
Rosenzweig EB,
Saydain G,
Scelsi L,
Schilz R,
Seeger W,
Shaffer CM,
Simms RW,
Simon M,
Sitbon O,
Suntharalingam J,
Tang H,
Tchourbanov AY,
Thenappan T,
Torres F,
Toshner MR,
Treacy CM,
Vonk Noordegraaf A,
Waisfisz Q,
Walsworth AK,
Walter RE,
Wharton J,
White RJ,
Wilt J,
Wort SJ,
Yung D,
Lawrie A,
Humbert M,
Soubrier F,
Trégouët DA,
Prokopenko I,
Kittles R,
Gräf S,
Nichols WC,
Trembath RC,
Desai AA,
Morrell NW,
Wilkins MR
UK NIHR BioResource Rare Diseases Consortium · UK PAH Cohort Study Consortium 외 컨소시엄 1곳
The Lancet. Respiratory medicine · 2019 · PMID 30527956 · open access
페이지 4개
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Day F,
Karaderi T,
Jones MR,
Meun C,
He C,
Drong A,
Kraft P,
Lin N,
Huang H,
Broer L,
Magi R,
Saxena R
외 37명 — 모두 보기
Laisk T,
Urbanek M,
Hayes MG,
Thorleifsson G,
Fernandez-Tajes J,
Mahajan A,
Mullin BH,
Stuckey BGA,
Spector TD,
Wilson SG,
Goodarzi MO,
Davis L,
Obermayer-Pietsch B,
Uitterlinden AG,
Anttila V,
Neale BM,
Jarvelin MR,
Fauser B,
Kowalska I,
Visser JA,
Andersen M,
Ong K,
Stener-Victorin E,
Ehrmann D,
Legro RS,
Salumets A,
McCarthy MI,
Morin-Papunen L,
Thorsteinsdottir U,
Stefansson K,
Styrkarsdottir U,
Perry JRB,
Dunaif A,
Laven J,
Franks S,
Lindgren CM,
Welt CK
23andMe Research Team
PLoS genetics · 2018 · PMID 30566500 · open access
페이지 4개
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
de las Fuentes L,
Sung YJ,
Noordam R,
Winkler T,
Feitosa MF,
Schwander K,
Bentley AR,
Brown MR,
Guo X,
Manning A,
Chasman DI,
Aschard H
외 211명 — 모두 보기
Bartz TM,
Bielak LF,
Campbell A,
Cheng CY,
Dorajoo R,
Hartwig FP,
Horimoto ARVR,
Li C,
Li-Gao R,
Liu Y,
Marten J,
Musani SK,
Ntalla I,
Rankinen T,
Richard M,
Sim X,
Smith AV,
Tajuddin SM,
Tayo BO,
Vojinovic D,
Warren HR,
Xuan D,
Alver M,
Boissel M,
Chai JF,
Chen X,
Christensen K,
Divers J,
Evangelou E,
Gao C,
Girotto G,
Harris SE,
He M,
Hsu FC,
Kühnel B,
Laguzzi F,
Li X,
Lyytikäinen LP,
Nolte IM,
Poveda A,
Rauramaa R,
Riaz M,
Rueedi R,
Shu XO,
Snieder H,
Sofer T,
Takeuchi F,
Verweij N,
Ware EB,
Weiss S,
Yanek LR,
Amin N,
Arking DE,
Arnett DK,
Bergmann S,
Boerwinkle E,
Brody JA,
Broeckel U,
Brumat M,
Burke G,
Cabrera CP,
Canouil M,
Chee ML,
Chen YI,
Cocca M,
Connell J,
de Silva HJ,
de Vries PS,
Eiriksdottir G,
Faul JD,
Fisher V,
Forrester T,
Fox EF,
Friedlander Y,
Gao H,
Gigante B,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt S,
Ikram MA,
Irvin MR,
Kähönen M,
Kavousi M,
Khor CC,
Kilpeläinen TO,
Koh WP,
Komulainen P,
Kraja AT,
Krieger JE,
Langefeld CD,
Li Y,
Liang J,
Liewald DCM,
Liu CT,
Liu J,
Lohman KK,
Mägi R,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mook-Kanamori DO,
Nalls MA,
Nelson CP,
Norris JM,
O'Connell J,
Ogunniyi A,
Padmanabhan S,
Palmer ND,
Pedersen NL,
Perls T,
Peters A,
Petersmann A,
Peyser PA,
Polasek O,
Porteous DJ,
Raffel LJ,
Rice TK,
Rotter JI,
Rudan I,
Rueda-Ochoa OL,
Sabanayagam C,
Salako BL,
Schreiner PJ,
Shikany JM,
Sidney SS,
Sims M,
Sitlani CM,
Smith JA,
Starr JM,
Strauch K,
Swertz MA,
Teumer A,
Tham YC,
Uitterlinden AG,
Vaidya D,
van der Ende MY,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Weir DR,
Wen W,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zhao W,
Zonderman AB,
Becker DM,
Bowden DW,
Deary IJ,
Dörr M,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Jonas JB,
Kammerer CM,
Kato N,
Lakka TA,
Leander K,
Lehtimäki T,
Magnusson PKE,
Marques-Vidal P,
Penninx BWJH,
Samani NJ,
van der Harst P,
Wagenknecht LE,
Wu T,
Zheng W,
Zhu X,
Bouchard C,
Cooper RS,
Correa A,
Evans MK,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Kritchevsky SB,
Levy D,
Palmas WR,
Pereira AC,
Province MM,
Psaty BM,
Ridker PM,
Rotimi CN,
Tai ES,
van Dam RM,
van Duijn CM,
Wong TY,
Rice K,
Gauderman WJ,
Morrison AC,
North KE,
Kardia SLR,
Caulfield MJ,
Elliott P,
Munroe PB,
Franks PW,
Rao DC,
Fornage M
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
페이지 4개
Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa
Janivara R,
Chen WC,
Hazra U,
Baichoo S,
Agalliu I,
Kachambwa P,
Simonti CN,
Brown LM,
Tambe SP,
Kim MS,
Harlemon M,
Jalloh M
외 48명 — 모두 보기
Muzondiwa D,
Naidoo D,
Ajayi OO,
Snyper NY,
Niang L,
Diop H,
Ndoye M,
Mensah JE,
Abrahams AOD,
Biritwum R,
Adjei AA,
Adebiyi AO,
Shittu O,
Ogunbiyi O,
Adebayo S,
Nwegbu MM,
Ajibola HO,
Oluwole OP,
Jamda MA,
Pentz A,
Haiman CA,
Spies PV,
van der Merwe A,
Cook MB,
Chanock SJ,
Berndt SI,
Watya S,
Lubwama A,
Muchengeti M,
Doherty S,
Smyth N,
Lounsbury D,
Fortier B,
Rohan TE,
Jacobson JS,
Neugut AI,
Hsing AW,
Gusev A,
Aisuodionoe-Shadrach OI,
Joffe M,
Adusei B,
Gueye SM,
Fernandez PW,
McBride J,
Andrews C,
Petersen LN,
Lachance J,
Rebbeck TR
Nature genetics · 2024 · PMID 39358599
페이지 4개
Identifying expression and DNA methylation biomarkers for lung adenocarcinoma risk in East Asia
Chen TY,
Chien LH,
Jiang SS,
Choi J,
Hung HH,
Hsiao CF,
Shi J,
Blechter B,
Breeze CE,
Chang GC,
Chen KY,
Tsai YH
외 19명 — 모두 보기
Su WC,
Huang MS,
Chen YM,
Wen YF,
Chen CY,
Wang CL,
Tsai FY,
Chen HL,
Hsieh WS,
Lin HC,
Wang LH,
Chen CJ,
Yang PC,
Chen CY,
Rothman N,
Chanock SJ,
Lan Q,
Chang IS,
Hsiung CA
Journal of the National Cancer Institute · 2026 · PMID 41581221 · open access
페이지 4개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
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
보다 지적을 받는 편이 낫습니다.
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
인용하는 페이지가 모두 몇 개인지입니다.
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
하는 페이지에 붙어 있어야 하기 때문입니다.