연구자에게
내 논문이 여기 있나요?
논문 2,660편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Van Heel DA에 대해
20건.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
외 98명 — 모두 보기
Manansala R,
Laplante V,
Chen M,
Lo KS,
Qian H,
Lareau CA,
Beaudoin M,
Hunt KA,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala K,
Cho K,
Choquet H,
Correa A,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Lerch MM,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nauck M,
Nikus K,
Ouwehand WH,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Roberts DJ,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Trembath RC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Zonderman AB,
Wilson PWF,
Li Y,
Butterworth AS,
Gauchat JF,
Chiang CWK,
Li B,
Loos RJF,
Astle WJ,
Evangelou E,
van Heel DA,
Sankaran VG,
Okada Y,
Soranzo N,
Johnson AD,
Reiner AP,
Auer PL,
Lettre G
VA Million Veteran Program
Cell · 2020 · PMID 32888493
페이지 12개+
The power of genetic diversity in genome-wide association studies of lipids
Graham SE,
Clarke SL,
Wu KH,
Kanoni S,
Zajac GJM,
Ramdas S,
Surakka I,
Ntalla I,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
외 523명 — 모두 보기
Hwang MY,
Han S,
Narita A,
Choudhury A,
Bentley AR,
Ekoru K,
Verma A,
Trivedi B,
Martin HC,
Hunt KA,
Hui Q,
Klarin D,
Zhu X,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Ruotsalainen SE,
Havulinna AS,
Veturi Y,
Feng Q,
Rosenthal EA,
Lingren T,
Pacheco JA,
Pendergrass SA,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Hindy G,
Rasheed A,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Willemsen G,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Mitchell RE,
Chai JF,
Aadahl M,
Yao J,
Manichaikul A,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Sidore C,
Fiorillo E,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Thuesen BH,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Daw EW,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Feitosa MF,
Wojczynski MK,
Preuss M,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Kember RL,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Leonard HL,
Marten J,
Schmidt B,
Arendt M,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Ahmed M,
Jackson AU,
Yousri NA,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Chai X,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Hung YJ,
Chen S,
Liu F,
Yang J,
Yang J,
Kentistou KA,
Gorski M,
Brumat M,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Lin M,
Xue C,
Zhang J,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
Lee J,
van der Laan SW,
Chitrala KN,
Weiss S,
Zimmermann ME,
Lee JY,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hildalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Schwander K,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Highland HM,
Young KL,
Kawaguchi T,
Thiery J,
Bis JC,
Nadkarni GN,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Kovacs P,
Giardoglou T,
Katsuya T,
Bhatti KF,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Chen YE,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Kato N,
Schulze MB,
Girotto G,
Jung B,
Böger CA,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
den Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Yajnik CS,
Mercader JM,
Tusié-Luna T,
Aguilar-Salinas CA,
Villalpando CG,
Orozco L,
Fornage M,
Tai ES,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Lu F,
Qu J,
Hishigaki H,
Lin X,
März W,
Parra EJ,
Parra EJ,
Cruz M,
Gudnason V,
Tardif JC,
Lettre G,
't Hart LM,
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Province MA,
Psaty BM,
Brandslund I,
Pramstaller PP,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Cucca F,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Rotter JI,
Dantoft TM,
Karpe F,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
de Geus EJC,
Cupples LA,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Justice AE,
Baras A,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Thorsteinsdottir U,
Stefansson K,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson P,
Rotimi CN,
Hazelhurst S,
Ramsay M,
Trembath RC,
van Heel DA,
Tamiya G,
Yamamoto M,
Kim BJ,
Mohlke KL,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Boehnke M,
Natarajan P,
Peloso GM,
Brown CD,
Morris AP,
Assimes TL,
Deloukas P,
Sun YV,
Willer CJ
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
페이지 12개+
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Zhou W,
Kanai M,
Wu KH,
Rasheed H,
Tsuo K,
Hirbo JB,
Wang Y,
Bhattacharya A,
Zhao H,
Namba S,
Surakka I,
Wolford BN
외 140명 — 모두 보기
Lo Faro V,
Lopera-Maya EA,
Läll K,
Favé MJ,
Partanen JJ,
Chapman SB,
Karjalainen J,
Kurki M,
Maasha M,
Brumpton BM,
Chavan S,
Chen TT,
Daya M,
Ding Y,
Feng YA,
Guare LA,
Gignoux CR,
Graham SE,
Hornsby WE,
Ingold N,
Ismail SI,
Johnson R,
Laisk T,
Lin K,
Lv J,
Millwood IY,
Moreno-Grau S,
Nam K,
Palta P,
Pandit A,
Preuss MH,
Saad C,
Setia-Verma S,
Thorsteinsdottir U,
Uzunovic J,
Verma A,
Zawistowski M,
Zhong X,
Afifi N,
Al-Dabhani KM,
Al Thani A,
Bradford Y,
Campbell A,
Crooks K,
de Bock GH,
Damrauer SM,
Douville NJ,
Finer S,
Fritsche LG,
Fthenou E,
Gonzalez-Arroyo G,
Griffiths CJ,
Guo Y,
Hunt KA,
Ioannidis A,
Jansonius NM,
Konuma T,
Lee MTM,
Lopez-Pineda A,
Matsuda Y,
Marioni RE,
Moatamed B,
Nava-Aguilar MA,
Numakura K,
Patil S,
Rafaels N,
Richmond A,
Rojas-Muñoz A,
Shortt JA,
Straub P,
Tao R,
Vanderwerff B,
Vernekar M,
Veturi Y,
Barnes KC,
Boezen M,
Chen Z,
Chen CY,
Cho J,
Smith GD,
Finucane HK,
Franke L,
Gamazon ER,
Ganna A,
Gaunt TR,
Ge T,
Huang H,
Huffman J,
Katsanis N,
Koskela JT,
Lajonchere C,
Law MH,
Li L,
Lindgren CM,
Loos RJF,
MacGregor S,
Matsuda K,
Olsen CM,
Porteous DJ,
Shavit JA,
Snieder H,
Takano T,
Trembath RC,
Vonk JM,
Whiteman DC,
Wicks SJ,
Wijmenga C,
Wright J,
Zheng J,
Zhou X,
Awadalla P,
Boehnke M,
Bustamante CD,
Cox NJ,
Fatumo S,
Geschwind DH,
Hayward C,
Hveem K,
Kenny EE,
Lee S,
Lin YF,
Mbarek H,
Mägi R,
Martin HC,
Medland SE,
Okada Y,
Palotie AV,
Pasaniuc B,
Rader DJ,
Ritchie MD,
Sanna S,
Smoller JW,
Stefansson K,
van Heel DA,
Walters RG,
Zöllner S,
Martin AR,
Willer CJ,
Daly MJ,
Neale BM
Biobank of the Americas · Biobank Japan Project 외 컨소시엄 22곳
Cell genomics · 2022 · PMID 36777996 · open access
페이지 12개+
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
Williams AT,
Chen J,
Coley K,
Batini C,
Izquierdo A,
Packer R,
Abner E,
Kanoni S,
Shepherd DJ,
Free RC,
Hollox EJ,
Brunskill NJ
외 20명 — 모두 보기
Ntalla I,
Reeve N,
Brightling CE,
Venn L,
Adams E,
Bee C,
Wallace SE,
Pareek M,
Hansell AL,
Esko T,
Stow D,
Jacobs BM,
van Heel DA,
Hennah W,
Rao BS,
Dudbridge F,
Wain LV,
Shrine N,
Tobin MD,
John C
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2023 · PMID 37872160 · open access
페이지 12개+
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Meng X,
Navoly G,
Giannakopoulou O,
Levey DF,
Koller D,
Pathak GA,
Koen N,
Lin K,
Adams MJ,
Rentería ME,
Feng Y,
Gaziano JM
외 66명 — 모두 보기
Stein DJ,
Zar HJ,
Campbell ML,
van Heel DA,
Trivedi B,
Finer S,
McQuillin A,
Bass N,
Chundru VK,
Martin HC,
Huang QQ,
Valkovskaya M,
Chu CY,
Kanjira S,
Kuo PH,
Chen HC,
Tsai SJ,
Liu YL,
Kendler KS,
Peterson RE,
Cai N,
Fang Y,
Sen S,
Scott LJ,
Burmeister M,
Loos RJF,
Preuss MH,
Actkins KV,
Davis LK,
Uddin M,
Wani AH,
Wildman DE,
Aiello AE,
Ursano RJ,
Kessler RC,
Kanai M,
Okada Y,
Sakaue S,
Rabinowitz JA,
Maher BS,
Uhl G,
Eaton W,
Cruz-Fuentes CS,
Martinez-Levy GA,
Campos AI,
Millwood IY,
Chen Z,
Li L,
Wassertheil-Smoller S,
Jiang Y,
Tian C,
Martin NG,
Mitchell BL,
Byrne EM,
Awasthi S,
Coleman JRI,
Ripke S,
Sofer T,
Walters RG,
McIntosh AM,
Polimanti R,
Dunn EC,
Stein MB,
Gelernter J,
Lewis CM,
Kuchenbaecker K
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group 외 컨소시엄 3곳
Nature genetics · 2024 · PMID 38177345 · open access
페이지 12개+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
외 351명 — 모두 보기
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Broadaway KA,
Williamson A,
Kamali Z,
Cui J,
Thangam M,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
Bertoni A,
Bork-Jensen J,
Brandslund I,
Buchanan TA,
Burant CF,
Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Danesh J,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Franco OH,
Frayling TM,
Freedman BI,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Gordon-Larsen P,
Gross M,
Guare LA,
Hackinger S,
Hakaste L,
Han S,
Hattersley AT,
Herder C,
Horikoshi M,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen T,
Kamanu FK,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee KM,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lynch JA,
Lyssenko V,
Maeda S,
Mamakou V,
Mansuri SR,
Matsuda K,
Meitinger T,
Melander O,
Metspalu A,
Mo H,
Morris AD,
Moura FA,
Nadler JL,
Nalls MA,
Nayak U,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Patil S,
Pei P,
Pereira MA,
Peters A,
Pirie FJ,
Polikowsky HG,
Porneala B,
Prasad G,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sandow K,
Sankareswaran A,
Sattar N,
Schönherr S,
Shahriar M,
Shen B,
Shi J,
Shin DM,
Shojima N,
Smith JA,
So WY,
Stančáková A,
Steinthorsdottir V,
Stilp AM,
Strauch K,
Taylor KD,
Thorand B,
Thorsteinsdottir U,
Tomlinson B,
Tran TC,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Wacher-Rodarte N,
Wheeler E,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamamoto K,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zawistowski M,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Fornage M,
Hanis CL,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Yokota M,
Kardia SLR,
Peyser PA,
Pankow JS,
Engert JC,
Bonnefond A,
Froguel P,
Wilson JG,
Sheu WHH,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Mook-Kanamori DO,
Tuomi T,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
Chen YI,
Rich SS,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Ghanbari M,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Bowden DW,
Palmer CNA,
Kooner JS,
Kooperberg C,
Liu S,
North KE,
Saleheen D,
Hansen T,
Pedersen O,
Wareham NJ,
Lee J,
Kim BJ,
Millwood IY,
Walters RG,
Stefansson K,
Ahlqvist E,
Goodarzi MO,
Mohlke KL,
Langenberg C,
Haiman CA,
Loos RJF,
Florez JC,
Rader DJ,
Ritchie MD,
Zöllner S,
Mägi R,
Marston NA,
Ruff CT,
van Heel DA,
Finer S,
Denny JC,
Yamauchi T,
Kadowaki T,
Chambers JC,
Ng MCY,
Sim X,
Below JE,
Tsao PS,
Chang KM,
McCarthy MI,
Meigs JB,
Mahajan A,
Spracklen CN,
Mercader JM,
Boehnke M,
Rotter JI,
Vujkovic M,
Voight BF,
Morris AP,
Zeggini E
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
Jacobs BM,
Stow D,
Hodgson S,
Zöllner J,
Samuel M,
Kanoni S,
Bidi S,
Walter K,
Langenberg C,
Dobson R,
Finer S,
Morton C
외 5명 — 모두 보기
Genes & Health Research Team
Nature communications · 2024 · PMID 39414775 · open access
페이지 12개+
Translational genomics of osteoarthritis in 1,962,069 individuals
Hatzikotoulas K,
Southam L,
Stefansdottir L,
Boer CG,
McDonald ML,
Pett JP,
Park YC,
Tuerlings M,
Mulders R,
Barysenka A,
Arruda AL,
Tragante V
외 162명 — 모두 보기
Rocco A,
Bittner N,
Chen S,
Horn S,
Srinivasasainagendra V,
To K,
Katsoula G,
Kreitmaier P,
Tenghe AMM,
Gilly A,
Arbeeva L,
Chen LG,
de Pins AM,
Dochtermann D,
Henkel C,
Höijer J,
Ito S,
Lind PA,
Lukusa-Sawalena B,
Minn AKK,
Mola-Caminal M,
Narita A,
Nguyen C,
Reimann E,
Silberstein MD,
Skogholt AH,
Tiwari HK,
Yau MS,
Yue M,
Zhao W,
Zhao W,
Zhou JJ,
Alexiadis G,
Banasik K,
Brunak S,
Campbell A,
Cheung JTS,
Dowsett J,
Faquih T,
Faul JD,
Fei L,
Fenstad AM,
Funayama T,
Gabrielsen ME,
Gocho C,
Gromov K,
Hansen T,
Hudjashov G,
Ingvarsson T,
Johnson JS,
Jonsson H,
Kakehi S,
Karjalainen J,
Kasbohm E,
Lemmelä S,
Lin K,
Liu X,
Loef M,
Mangino M,
McCartney D,
Millwood IY,
Richman J,
Roberts MB,
Ryan KA,
Samartzis D,
Shivakumar M,
Skou ST,
Sugimoto S,
Suzuki K,
Takuwa H,
Teder-Laving M,
Thomas L,
Tomizuka K,
Turman C,
Weiss S,
Wu TT,
Zengini E,
Zhang Y,
Ferreira MAR,
Babis G,
Baras A,
Barker T,
Carey DJ,
Cheah KSE,
Chen Z,
Cheung JP,
Daly M,
de Mutsert R,
Eaton CB,
Erikstrup C,
Furnes ON,
Golightly YM,
Gudbjartsson DF,
Hailer NP,
Hayward C,
Hochberg MC,
Homuth G,
Huckins LM,
Hveem K,
Ikegawa S,
Ishijima M,
Isomura M,
Jones M,
Kang JH,
Kardia SLR,
Kloppenburg M,
Kraft P,
Kumahashi N,
Kuwata S,
Lee MTM,
Lee PH,
Lerner R,
Li L,
Lietman SA,
Lotta L,
Lupton MK,
Mägi R,
Martin NG,
McAlindon TE,
Medland SE,
Michaëlsson K,
Mitchell BD,
Mook-Kanamori DO,
Morris AP,
Nabika T,
Nagami F,
Nelson AE,
Ostrowski SR,
Palotie A,
Pedersen OB,
Rosendaal FR,
Sakurai-Yageta M,
Schmidt CO,
Sham PC,
Singh JA,
Smelser DT,
Smith JA,
Song YQ,
Sørensen E,
Tamiya G,
Tamura Y,
Terao C,
Thorleifsson G,
Troelsen A,
Tsezou A,
Uchio Y,
Uitterlinden AG,
Ullum H,
Valdes AM,
van Heel DA,
Walters RG,
Weir DR,
Wilkinson JM,
Winsvold BS,
Yamamoto M,
Zwart JA,
Stefansson K,
Meulenbelt I,
Teichmann SA,
van Meurs JBJ,
Styrkarsdottir U,
Zeggini E
arcOGEN Consortium · ARGO Consortium 외 컨소시엄 7곳
Nature · 2025 · PMID 40205036 · open access
페이지 12개+
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Venkatesh SS,
Wittemans LBL,
Palmer DS,
Baya NA,
Ferreira T,
Hill B,
Lassen FH,
Parker MJ,
Reibe S,
Elhakeem A,
Banasik K,
Bruun MT
외 39명 — 모두 보기
Erikstrup C,
Aagard Jensen B,
Juul A,
Mikkelsen C,
Nielsen HS,
Ostrowski SR,
Pedersen OB,
Rohde PD,
Sørensen E,
Ullum H,
Westergaard D,
Haraldsson A,
Holm H,
Jonsdottir I,
Olafsson I,
Steingrimsdottir T,
Steinthorsdottir V,
Thorleifsson G,
Figueredo J,
Karjalainen MK,
Pasanen A,
Jacobs BM,
Kalantzis G,
Hubers N,
Lippincott M,
Fraser A,
Lawlor DA,
Timpson NJ,
Nyegaard M,
Stefansson K,
Magi R,
Laivuori H,
van Heel DA,
Boomsma DI,
Balasubramanian R,
Seminara SB,
Chan YM,
Laisk T,
Lindgren CM
Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 3곳
Nature genetics · 2025 · PMID 40229599 · open access
페이지 12개+
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small AM,
Yang TY,
Itoh S,
Thériault S,
Dufresne L,
Kurosawa R,
Komuro I,
Matsuda K,
Vy HMT,
Farber-Eger EH,
Shaffer LL,
Boulier KM
외 89명 — 모두 보기
Corey KM,
Ramaker ME,
Laporte F,
Schott JJ,
Le Scouarnec S,
Singh SA,
Sonawane AR,
Smith HA,
Rafaels N,
Ghouse J,
Raja AA,
Ostrowski SR,
Sørensen E,
Mikkelsen C,
Pedersen OB,
Erikstrup C,
Ullum H,
Sveinbjornsson G,
Gudbjartsson DF,
Abner E,
Lee J,
Ganna A,
Nowak-Göttl U,
Finer S,
Schumacher J,
Maj C,
Al-Kassou B,
Nickenig G,
Trenkwalder T,
Dreβen M,
Krane M,
Nöthen MM,
Moksnes MR,
Brumpton BM,
Knight S,
Knowlton KU,
Nadauld L,
Debiec R,
Musameh MD,
Braund PS,
Nelson CP,
Czuba T,
Melander O,
Selvaraj MS,
Koyama S,
Bhukar R,
Ruan Y,
Ljungberg J,
Damrauer SM,
Levin MG,
Franke A,
Berger K,
Ruff CT,
Melloni GEM,
Kamanu FK,
Ito K,
Do R,
Loos RJF,
Schunkert H,
Wells QS,
Shah SH,
Le Tourneau T,
Messika-Zeitoun D,
Gignoux C,
Bundgaard H,
Larsson SC,
Michaëlsson K,
Holm H,
Helgadottir A,
Esko T,
van Heel DA,
Mathieu P,
Samani NJ,
Smith JG,
Söderberg S,
Rader DJ,
Marston NA,
Sabatine MS,
Pasaniuc B,
Cho K,
Wilson PWF,
O'Donnell CJ,
Stefansson K,
Bossé Y,
Aikawa E,
Engert JC,
Peloso GM,
Natarajan P,
Thanassoulis G
Colorado Center for Personalized Medicine · DBDS Genomic Consortium 외 컨소시엄 2곳
Nature genetics · 2026 · PMID 41419686 · open access
페이지 12개+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
외 73명 — 모두 보기
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium 외 컨소시엄 4곳
Nature genetics · 2026 · PMID 41644669 · open access
페이지 12개+
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Soranzo N,
Spector TD,
Mangino M,
Kühnel B,
Rendon A,
Teumer A,
Willenborg C,
Wright B,
Chen L,
Li M,
Salo P,
Voight BF
외 68명 — 모두 보기
Burns P,
Laskowski RA,
Xue Y,
Menzel S,
Altshuler D,
Bradley JR,
Bumpstead S,
Burnett MS,
Devaney J,
Döring A,
Elosua R,
Epstein SE,
Erber W,
Falchi M,
Garner SF,
Ghori MJ,
Goodall AH,
Gwilliam R,
Hakonarson HH,
Hall AS,
Hammond N,
Hengstenberg C,
Illig T,
König IR,
Knouff CW,
McPherson R,
Melander O,
Mooser V,
Nauck M,
Nieminen MS,
O'Donnell CJ,
Peltonen L,
Potter SC,
Prokisch H,
Rader DJ,
Rice CM,
Roberts R,
Salomaa V,
Sambrook J,
Schreiber S,
Schunkert H,
Schwartz SM,
Serbanovic-Canic J,
Sinisalo J,
Siscovick DS,
Stark K,
Surakka I,
Stephens J,
Thompson JR,
Völker U,
Völzke H,
Watkins NA,
Wells GA,
Wichmann HE,
Van Heel DA,
Tyler-Smith C,
Thein SL,
Kathiresan S,
Perola M,
Reilly MP,
Stewart AF,
Erdmann J,
Samani NJ,
Meisinger C,
Greinacher A,
Deloukas P,
Ouwehand WH,
Gieger C
Nature genetics · 2009 · PMID 19820697
페이지 8개
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Trynka G,
Hunt KA,
Bockett NA,
Romanos J,
Mistry V,
Szperl A,
Bakker SF,
Bardella MT,
Bhaw-Rosun L,
Castillejo G,
de la Concha EG,
de Almeida RC
외 52명 — 모두 보기
Dias KR,
van Diemen CC,
Dubois PC,
Duerr RH,
Edkins S,
Franke L,
Fransen K,
Gutierrez J,
Heap GA,
Hrdlickova B,
Hunt S,
Plaza Izurieta L,
Izzo V,
Joosten LA,
Langford C,
Mazzilli MC,
Mein CA,
Midah V,
Mitrovic M,
Mora B,
Morelli M,
Nutland S,
Núñez C,
Onengut-Gumuscu S,
Pearce K,
Platteel M,
Polanco I,
Potter S,
Ribes-Koninckx C,
Ricaño-Ponce I,
Rich SS,
Rybak A,
Santiago JL,
Senapati S,
Sood A,
Szajewska H,
Troncone R,
Varadé J,
Wallace C,
Wolters VM,
Zhernakova A,
Thelma BK,
Cukrowska B,
Urcelay E,
Bilbao JR,
Mearin ML,
Barisani D,
Barrett JC,
Plagnol V,
Deloukas P,
Wijmenga C,
van Heel DA
Spanish Consortium on the Genetics of Coeliac Disease (CEGEC) · PreventCD Study Group 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 22057235 · open access
페이지 7개
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
외 527명 — 모두 보기
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Francesco C,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Chuang LM,
Rotter JI,
Dantoft TM,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Li H,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
Willemsen AHM,
Cupples L,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
Hazelhurst S,
Ramsay M,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Baras A,
Justice AE,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Tamiya G,
Yamamoto M,
van Heel DA,
Trembath RC,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson PWF,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Mohlke KL,
Sun YV,
Morris AP,
Boehnke M,
Brown CD,
Natarajan P,
Deloukas P,
Willer CJ,
Assimes TL,
Peloso GM
Genome biology · 2022 · PMID 36575460 · open access
페이지 7개
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
Genomics of chronic dry cough unravels neurological pathways
Coley K,
John C,
Ghouse J,
Shepherd DJ,
Shrine N,
Izquierdo AG,
Kanoni S,
Magavern EF,
Packer R,
McGarvey L,
Smith JA,
Bundgaard H
외 11명 — 모두 보기
Ostrowski SR,
Erikstrup C,
Pedersen OBV,
van Heel DA,
Hennah W,
Marttila M,
Free RC,
Hollox EJ,
Wain LV,
Tobin MD,
Batini C
Genes and Health Research Team
The European respiratory journal · 2025 · PMID 40675770 · open access
페이지 4개
Multiple common variants for celiac disease influencing immune gene expression
Dubois PC,
Trynka G,
Franke L,
Hunt KA,
Romanos J,
Curtotti A,
Zhernakova A,
Heap GA,
Adány R,
Aromaa A,
Bardella MT,
van den Berg LH
외 55명 — 모두 보기
Bockett NA,
de la Concha EG,
Dema B,
Fehrmann RS,
Fernández-Arquero M,
Fiatal S,
Grandone E,
Green PM,
Groen HJ,
Gwilliam R,
Houwen RH,
Hunt SE,
Kaukinen K,
Kelleher D,
Korponay-Szabo I,
Kurppa K,
MacMathuna P,
Mäki M,
Mazzilli MC,
McCann OT,
Mearin ML,
Mein CA,
Mirza MM,
Mistry V,
Mora B,
Morley KI,
Mulder CJ,
Murray JA,
Núñez C,
Oosterom E,
Ophoff RA,
Polanco I,
Peltonen L,
Platteel M,
Rybak A,
Salomaa V,
Schweizer JJ,
Sperandeo MP,
Tack GJ,
Turner G,
Veldink JH,
Verbeek WH,
Weersma RK,
Wolters VM,
Urcelay E,
Cukrowska B,
Greco L,
Neuhausen SL,
McManus R,
Barisani D,
Deloukas P,
Barrett JC,
Saavalainen P,
Wijmenga C,
van Heel DA
Nature genetics · 2010 · PMID 20190752 · open access
페이지 3개
Newly identified genetic risk variants for celiac disease related to the immune response
Hunt KA,
Zhernakova A,
Turner G,
Heap GA,
Franke L,
Bruinenberg M,
Romanos J,
Dinesen LC,
Ryan AW,
Panesar D,
Gwilliam R,
Takeuchi F
외 25명 — 모두 보기
McLaren WM,
Holmes GK,
Howdle PD,
Walters JR,
Sanders DS,
Playford RJ,
Trynka G,
Mulder CJ,
Mearin ML,
Verbeek WH,
Trimble V,
Stevens FM,
O'Morain C,
Kennedy NP,
Kelleher D,
Pennington DJ,
Strachan DP,
McArdle WL,
Mein CA,
Wapenaar MC,
Deloukas P,
McGinnis R,
McManus R,
Wijmenga C,
van Heel DA
Nature genetics · 2008 · PMID 18311140
페이지 2개
Polygenic prediction of preeclampsia and gestational hypertension
Honigberg MC,
Truong B,
Khan RR,
Xiao B,
Bhatta L,
Vy HMT,
Guerrero RF,
Schuermans A,
Selvaraj MS,
Patel AP,
Koyama S,
Cho SMJ
외 20명 — 모두 보기
Vellarikkal SK,
Trinder M,
Urbut SM,
Gray KJ,
Brumpton BM,
Patil S,
Zöllner S,
Antopia MC,
Saxena R,
Nadkarni GN,
Do R,
Yan Q,
Pe'er I,
Verma SS,
Gupta RM,
Haas DM,
Martin HC,
van Heel DA,
Laisk T,
Natarajan P
Nature medicine · 2023 · PMID 37248299
페이지 2개
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Heap GA,
Weedon MN,
Bewshea CM,
Singh A,
Chen M,
Satchwell JB,
Vivian JP,
So K,
Dubois PC,
Andrews JM,
Annese V,
Bampton P
외 44명 — 모두 보기
Barnardo M,
Bell S,
Cole A,
Connor SJ,
Creed T,
Cummings FR,
D'Amato M,
Daneshmend TK,
Fedorak RN,
Florin TH,
Gaya DR,
Greig E,
Halfvarson J,
Hart A,
Irving PM,
Jones G,
Karban A,
Lawrance IC,
Lee JC,
Lees C,
Lev-Tzion R,
Lindsay JO,
Mansfield J,
Mawdsley J,
Mazhar Z,
Parkes M,
Parnell K,
Orchard TR,
Radford-Smith G,
Russell RK,
Reffitt D,
Satsangi J,
Silverberg MS,
Sturniolo GC,
Tremelling M,
Tsianos EV,
van Heel DA,
Walsh A,
Watermeyer G,
Weersma RK,
Zeissig S,
Rossjohn J,
Holden AL,
Ahmad T
International Serious Adverse Events Consortium · IBD Pharmacogenetics Study Group
Nature genetics · 2014 · PMID 25217962
페이지 1개
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.