연구자에게
내 논문이 여기 있나요?
논문 2,671편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Uitterlinden AG에 대해
226건, 그중 20건 표시.
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
외 196명 — 모두 보기
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
페이지 12개+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke M,
Li Y,
Li M,
Sieber KB,
Feitosa MF,
Gorski M,
Tin A,
Wang L,
Chu AY,
Hoppmann A,
Kirsten H,
Giri A
외 315명 — 모두 보기
Chai JF,
Sveinbjornsson G,
Tayo BO,
Nutile T,
Fuchsberger C,
Marten J,
Cocca M,
Ghasemi S,
Xu Y,
Horn K,
Noce D,
van der Most PJ,
Sedaghat S,
Yu Z,
Akiyama M,
Afaq S,
Ahluwalia TS,
Almgren P,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boehnke M,
Boerwinkle E,
Boissel M,
Bottinger EP,
Boutin TS,
Brenner H,
Brumat M,
Burkhardt R,
Butterworth AS,
Campana E,
Campbell A,
Campbell H,
Canouil M,
Carroll RJ,
Catamo E,
Chambers JC,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cheng Y,
Christensen K,
Cifkova R,
Ciullo M,
Concas MP,
Cook JP,
Coresh J,
Corre T,
Sala CF,
Cusi D,
Danesh J,
Daw EW,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Delgado G,
Demirkan A,
Di Angelantonio E,
Dittrich K,
Divers J,
Dorajoo R,
Eckardt KU,
Ehret G,
Elliott P,
Endlich K,
Evans MK,
Felix JF,
Foo VHX,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Friedlander Y,
Froguel P,
Gansevoort RT,
Gao H,
Gasparini P,
Gaziano JM,
Giedraitis V,
Gieger C,
Girotto G,
Giulianini F,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hartman CA,
Hayward C,
Hellwege JN,
Heng CK,
Hicks AA,
Hofer E,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Indridason OS,
Ingelsson E,
Ising M,
Jaddoe VWV,
Jakobsdottir J,
Jonas JB,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kammerer CM,
Kanai M,
Kastarinen M,
Kerr SM,
Khor CC,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Kraja AT,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
Kuokkanen M,
Kuusisto J,
La Bianca M,
Laakso M,
Lange LA,
Langefeld CD,
Lee JJ,
Lehne B,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Liu J,
Loeffler M,
Loos RJF,
Lucae S,
Lukas MA,
Lyytikäinen LP,
Mägi R,
Magnusson PKE,
Mahajan A,
Martin NG,
Martins J,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Melander O,
Metspalu A,
Mikaelsdottir EK,
Milaneschi Y,
Miliku K,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell J,
O'Donoghue ML,
Olafsson I,
Oldehinkel AJ,
Orho-Melander M,
Ouwehand WH,
Padmanabhan S,
Palmer ND,
Palsson R,
Penninx BWJH,
Perls T,
Perola M,
Pirastu M,
Pirastu N,
Pistis G,
Podgornaia AI,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Pramstaller PP,
Preuss MH,
Prins BP,
Province MA,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Ridker PM,
Rivadeneira F,
Rizzi F,
Roberts DJ,
Robino A,
Rossing P,
Rudan I,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Sabanayagam C,
Salomaa V,
Salvi E,
Saum KU,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Schupf N,
Shaffer CM,
Shi Y,
Smith AV,
Smith BH,
Soranzo N,
Spracklen CN,
Strauch K,
Stringham HM,
Stumvoll M,
Svensson PO,
Szymczak S,
Tai ES,
Tajuddin SM,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorleifsson G,
Toniolo D,
Tönjes A,
Tremblay J,
Tzoulaki I,
Uitterlinden AG,
Vaccargiu S,
van Dam RM,
van der Harst P,
van Duijn CM,
Velez Edward DR,
Verweij N,
Vogelezang S,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Wallentin L,
Wang YX,
Wang C,
Waterworth DM,
Bin Wei W,
White H,
Whitfield JB,
Wild SH,
Wilson JF,
Wojczynski MK,
Wong C,
Wong TY,
Xu L,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang W,
Zonderman AB,
Rotter JI,
Bochud M,
Psaty BM,
Vitart V,
Wilson JG,
Dehghan A,
Parsa A,
Chasman DI,
Ho K,
Morris AP,
Devuyst O,
Akilesh S,
Pendergrass SA,
Sim X,
Böger CA,
Okada Y,
Edwards TL,
Snieder H,
Stefansson K,
Hung AM,
Heid IM,
Scholz M,
Teumer A,
Köttgen A,
Pattaro C
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
페이지 12개+
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer A,
Li Y,
Ghasemi S,
Prins BP,
Wuttke M,
Hermle T,
Giri A,
Sieber KB,
Qiu C,
Kirsten H,
Tin A,
Chu AY
외 174명 — 모두 보기
Bansal N,
Feitosa MF,
Wang L,
Chai JF,
Cocca M,
Fuchsberger C,
Gorski M,
Hoppmann A,
Horn K,
Li M,
Marten J,
Noce D,
Nutile T,
Sedaghat S,
Sveinbjornsson G,
Tayo BO,
van der Most PJ,
Xu Y,
Yu Z,
Gerstner L,
Ärnlöv J,
Bakker SJL,
Baptista D,
Biggs ML,
Boerwinkle E,
Brenner H,
Burkhardt R,
Carroll RJ,
Chee ML,
Chee ML,
Chen M,
Cheng CY,
Cook JP,
Coresh J,
Corre T,
Danesh J,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Dittrich K,
Divers J,
Eckardt KU,
Ehret G,
Endlich K,
Felix JF,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Gansevoort RT,
Giedraitis V,
Gögele M,
Grundner-Culemann F,
Gudbjartsson DF,
Gudnason V,
Hamet P,
Harris TB,
Hicks AA,
Holm H,
Foo VHX,
Hwang SJ,
Ikram MA,
Ingelsson E,
Jaddoe VWV,
Jakobsdottir J,
Josyula NS,
Jung B,
Kähönen M,
Khor CC,
Kiess W,
Koenig W,
Körner A,
Kovacs P,
Kramer H,
Krämer BK,
Kronenberg F,
Lange LA,
Langefeld CD,
Lee JJ,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
Meisinger C,
Meitinger T,
Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
Mychaleckyj JC,
Nauck M,
Nikus K,
Ning B,
Noordam R,
Connell JO,
Olafsson I,
Palmer ND,
Peters A,
Podgornaia AI,
Ponte B,
Poulain T,
Pramstaller PP,
Rabelink TJ,
Raffield LM,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Rivadeneira F,
Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
Shaffer CM,
Shi Y,
Smith AV,
Strauch K,
Stumvoll M,
Sun BB,
Szymczak S,
Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
Tremblay J,
Uitterlinden AG,
van der Harst P,
Verweij N,
Vogelezang S,
Völker U,
Waldenberger M,
Wang C,
Wilson OD,
Wong C,
Wong TY,
Yang Q,
Yasuda M,
Akilesh S,
Bochud M,
Böger CA,
Devuyst O,
Edwards TL,
Ho K,
Morris AP,
Parsa A,
Pendergrass SA,
Psaty BM,
Rotter JI,
Stefansson K,
Wilson JG,
Susztak K,
Snieder H,
Heid IM,
Scholz M,
Butterworth AS,
Hung AM,
Pattaro C,
Köttgen A
Nature communications · 2019 · PMID 31511532 · open access
페이지 12개+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
외 213명 — 모두 보기
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
Teumer A,
Pattaro C,
Woodward OM,
Vitart V,
Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31578528 · open access
페이지 12개+
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Pazoki R,
Vujkovic M,
Elliott J,
Evangelou E,
Gill D,
Ghanbari M,
van der Most PJ,
Pinto RC,
Wielscher M,
Farlik M,
Zuber V,
de Knegt RJ
외 23명 — 모두 보기
Snieder H,
Uitterlinden AG,
Lynch JA,
Jiang X,
Said S,
Kaplan DE,
Lee KM,
Serper M,
Carr RM,
Tsao PS,
Atkinson SR,
Dehghan A,
Tzoulaki I,
Ikram MA,
Herzig KH,
Järvelin MR,
Alizadeh BZ,
O'Donnell CJ,
Saleheen D,
Voight BF,
Chang KM,
Thursz MR,
Elliott P
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · 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 insights into biological mechanisms governing human ovarian ageing
Ruth KS,
Day FR,
Hussain J,
Martínez-Marchal A,
Aiken CE,
Azad A,
Thompson DJ,
Knoblochova L,
Abe H,
Tarry-Adkins JL,
Gonzalez JM,
Fontanillas P
외 256명 — 모두 보기
Claringbould A,
Bakker OB,
Sulem P,
Walters RG,
Terao C,
Turon S,
Horikoshi M,
Lin K,
Onland-Moret NC,
Sankar A,
Hertz EPT,
Timshel PN,
Shukla V,
Borup R,
Olsen KW,
Aguilera P,
Ferrer-Roda M,
Huang Y,
Stankovic S,
Timmers PRHJ,
Ahearn TU,
Alizadeh BZ,
Naderi E,
Andrulis IL,
Arnold AM,
Aronson KJ,
Augustinsson A,
Bandinelli S,
Barbieri CM,
Beaumont RN,
Becher H,
Beckmann MW,
Benonisdottir S,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Boomsma DI,
Bowker N,
Brody JA,
Broer L,
Buring JE,
Campbell A,
Campbell H,
Castelao JE,
Catamo E,
Chanock SJ,
Chenevix-Trench G,
Ciullo M,
Corre T,
Couch FJ,
Cox A,
Crisponi L,
Cross SS,
Cucca F,
Czene K,
Smith GD,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Demerath EW,
Dennis J,
Dunning AM,
Dwek M,
Eriksson M,
Esko T,
Fasching PA,
Faul JD,
Ferrucci L,
Franceschini N,
Frayling TM,
Gago-Dominguez M,
Mezzavilla M,
García-Closas M,
Gieger C,
Giles GG,
Grallert H,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Haiman CA,
Håkansson N,
Hall P,
Hayward C,
He C,
He W,
Heiss G,
Høffding MK,
Hopper JL,
Hottenga JJ,
Hu F,
Hunter D,
Ikram MA,
Jackson RD,
Joaquim MDR,
John EM,
Joshi PK,
Karasik D,
Kardia SLR,
Kartsonaki C,
Karlsson R,
Kitahara CM,
Kolcic I,
Kooperberg C,
Kraft P,
Kurian AW,
Kutalik Z,
La Bianca M,
LaChance G,
Langenberg C,
Launer LJ,
Laven JSE,
Lawlor DA,
Le Marchand L,
Li J,
Lindblom A,
Lindstrom S,
Lindstrom T,
Linet M,
Liu Y,
Liu S,
Luan J,
Mägi R,
Magnusson PKE,
Mangino M,
Mannermaa A,
Marco B,
Marten J,
Martin NG,
Mbarek H,
McKnight B,
Medland SE,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Milani L,
Milne RL,
Montgomery GW,
Mook-Kanamori DO,
Mulas A,
Mulligan AM,
Murray A,
Nalls MA,
Newman A,
Noordam R,
Nutile T,
Nyholt DR,
Olshan AF,
Olsson H,
Painter JN,
Patel AV,
Pedersen NL,
Perjakova N,
Peters A,
Peters U,
Pharoah PDP,
Polasek O,
Porcu E,
Psaty BM,
Rahman I,
Rennert G,
Rennert HS,
Ridker PM,
Ring SM,
Robino A,
Rose LM,
Rosendaal FR,
Rossouw J,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Saloustros E,
Sandler DP,
Sanna S,
Sawyer EJ,
Sarnowski C,
Schlessinger D,
Schmidt MK,
Schoemaker MJ,
Schraut KE,
Scott C,
Shekari S,
Shrikhande A,
Smith AV,
Smith BH,
Smith JA,
Sorice R,
Southey MC,
Spector TD,
Spinelli JJ,
Stampfer M,
Stöckl D,
van Meurs JBJ,
Strauch K,
Styrkarsdottir U,
Swerdlow AJ,
Tanaka T,
Teras LR,
Teumer A,
Þorsteinsdottir U,
Timpson NJ,
Toniolo D,
Traglia M,
Troester MA,
Truong T,
Tyrrell J,
Uitterlinden AG,
Ulivi S,
Vachon CM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wang Q,
Wareham NJ,
Weinberg CR,
Weir DR,
Wilcox AN,
van Dijk KW,
Willemsen G,
Wilson JF,
Wolffenbuttel BHR,
Wolk A,
Wood AR,
Zhao W,
Zygmunt M,
Chen Z,
Li L,
Franke L,
Burgess S,
Deelen P,
Pers TH,
Grøndahl ML,
Andersen CY,
Pujol A,
Lopez-Contreras AJ,
Daniel JA,
Stefansson K,
Chang-Claude J,
van der Schouw YT,
Lunetta KL,
Chasman DI,
Easton DF,
Visser JA,
Ozanne SE,
Namekawa SH,
Solc P,
Murabito JM,
Ong KK,
Hoffmann ER,
Murray A,
Roig I,
Perry JRB
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium 외 컨소시엄 6곳
Nature · 2021 · PMID 34349265
페이지 12개+
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Boer CG,
Hatzikotoulas K,
Southam L,
Stefánsdóttir L,
Zhang Y,
Coutinho de Almeida R,
Wu TT,
Zheng J,
Hartley A,
Teder-Laving M,
Skogholt AH,
Terao C
외 50명 — 모두 보기
Zengini E,
Alexiadis G,
Barysenka A,
Bjornsdottir G,
Gabrielsen ME,
Gilly A,
Ingvarsson T,
Johnsen MB,
Jonsson H,
Kloppenburg M,
Luetge A,
Lund SH,
Mägi R,
Mangino M,
Nelissen RRGHH,
Shivakumar M,
Steinberg J,
Takuwa H,
Thomas LF,
Tuerlings M,
Babis GC,
Cheung JPY,
Kang JH,
Kraft P,
Lietman SA,
Samartzis D,
Slagboom PE,
Stefansson K,
Thorsteinsdottir U,
Tobias JH,
Uitterlinden AG,
Winsvold B,
Zwart JA,
Davey Smith G,
Sham PC,
Thorleifsson G,
Gaunt TR,
Morris AP,
Valdes AM,
Tsezou A,
Cheah KSE,
Ikegawa S,
Hveem K,
Esko T,
Wilkinson JM,
Meulenbelt I,
Lee MTM,
van Meurs JBJ,
Styrkársdóttir U,
Zeggini E
arcOGEN Consortium · HUNT All-In Pain 외 컨소시엄 2곳
Cell · 2021 · PMID 34450027 · open access
페이지 12개+
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Wang Z,
Emmerich A,
Pillon NJ,
Moore T,
Hemerich D,
Cornelis MC,
Mazzaferro E,
Broos S,
Ahluwalia TS,
Bartz TM,
Bentley AR,
Bielak LF
외 206명 — 모두 보기
Chong M,
Chu AY,
Berry D,
Dorajoo R,
Dueker ND,
Kasbohm E,
Feenstra B,
Feitosa MF,
Gieger C,
Graff M,
Hall LM,
Haller T,
Hartwig FP,
Hillis DA,
Huikari V,
Heard-Costa N,
Holzapfel C,
Jackson AU,
Johansson Å,
Jørgensen AM,
Kaakinen MA,
Karlsson R,
Kerr KF,
Kim B,
Koolhaas CM,
Kutalik Z,
Lagou V,
Lind PA,
Lorentzon M,
Lyytikäinen LP,
Mangino M,
Metzendorf C,
Monroe KR,
Pacolet A,
Pérusse L,
Pool R,
Richmond RC,
Rivera NV,
Robiou-du-Pont S,
Schraut KE,
Schulz CA,
Stringham HM,
Tanaka T,
Teumer A,
Turman C,
van der Most PJ,
Vanmunster M,
van Rooij FJA,
van Vliet-Ostaptchouk JV,
Zhang X,
Zhao JH,
Zhao W,
Balkhiyarova Z,
Balslev-Harder MN,
Baumeister SE,
Beilby J,
Blangero J,
Boomsma DI,
Brage S,
Braund PS,
Brody JA,
Bruinenberg M,
Ekelund U,
Liu CT,
Cole JW,
Collins FS,
Cupples LA,
Esko T,
Enroth S,
Faul JD,
Fernandez-Rhodes L,
Fohner AE,
Franco OH,
Galesloot TE,
Gordon SD,
Grarup N,
Hartman CA,
Heiss G,
Hui J,
Illig T,
Jago R,
James A,
Joshi PK,
Jung T,
Kähönen M,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kraft PP,
Kuusisto J,
Launer LJ,
Li A,
Linneberg A,
Luan J,
Vidal PM,
Medland SE,
Milaneschi Y,
Moscati A,
Musk B,
Nelson CP,
Nolte IM,
Pedersen NL,
Peters A,
Peyser PA,
Power C,
Raitakari OT,
Reedik M,
Reiner AP,
Ridker PM,
Rudan I,
Ryan K,
Sarzynski MA,
Scott LJ,
Scott RA,
Sidney S,
Siggeirsdottir K,
Smith AV,
Smith JA,
Sonestedt E,
Strøm M,
Tai ES,
Teo KK,
Thorand B,
Tönjes A,
Tremblay A,
Uitterlinden AG,
Vangipurapu J,
van Schoor N,
Völker U,
Willemsen G,
Williams K,
Wong Q,
Xu H,
Young KL,
Yuan JM,
Zillikens MC,
Zonderman AB,
Ameur A,
Bandinelli S,
Bis JC,
Boehnke M,
Bouchard C,
Chasman DI,
Smith GD,
de Geus EJC,
Deldicque L,
Dörr M,
Evans MK,
Ferrucci L,
Fornage M,
Fox C,
Garland T Jr,
Gudnason V,
Gyllensten U,
Hansen T,
Hayward C,
Horta BL,
Hyppönen E,
Jarvelin MR,
Johnson WC,
Kardia SLR,
Kiemeney LA,
Laakso M,
Langenberg C,
Lehtimäki T,
Marchand LL,
Magnusson PKE,
Martin NG,
Melbye M,
Metspalu A,
Meyre D,
North KE,
Ohlsson C,
Oldehinkel AJ,
Orho-Melander M,
Pare G,
Park T,
Pedersen O,
Penninx BWJH,
Pers TH,
Polasek O,
Prokopenko I,
Rotimi CN,
Samani NJ,
Sim X,
Snieder H,
Sørensen TIA,
Spector TD,
Timpson NJ,
van Dam RM,
van der Velde N,
van Duijn CM,
Vollenweider P,
Völzke H,
Voortman T,
Waeber G,
Wareham NJ,
Weir DR,
Wichmann HE,
Wilson JF,
Hevener AL,
Krook A,
Zierath JR,
Thomis MAI,
Loos RJF,
Hoed MD
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
페이지 12개+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
외 610명 — 모두 보기
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger S,
Sim X,
Vrieze S,
Ahluwalia TS,
Akiyama M,
Allison MA,
Alvarez M,
Andersen MK,
Ani A,
Appadurai V,
Arbeeva L,
Bhaskar S,
Bielak LF,
Bollepalli S,
Bonnycastle LL,
Bork-Jensen J,
Bradfield JP,
Bradford Y,
Braund PS,
Brody JA,
Burgdorf KS,
Cade BE,
Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
Delgado GE,
Delitala A,
Demirkan A,
Deng X,
Devineni P,
Dietl A,
Dimitriou M,
Dimitrov L,
Dorajoo R,
Ekici AB,
Engmann JE,
Fairhurst-Hunter Z,
Farmaki AE,
Faul JD,
Fernandez-Lopez JC,
Forer L,
Francescatto M,
Freitag-Wolf S,
Fuchsberger C,
Galesloot TE,
Gao Y,
Gao Z,
Geller F,
Giannakopoulou O,
Giulianini F,
Gjesing AP,
Goel A,
Gordon SD,
Gorski M,
Grove J,
Guo X,
Gustafsson S,
Haessler J,
Hansen TF,
Havulinna AS,
Haworth SJ,
He J,
Heard-Costa N,
Hebbar P,
Hindy G,
Ho YA,
Hofer E,
Holliday E,
Horn K,
Hornsby WE,
Hottenga JJ,
Huang H,
Huang J,
Huerta-Chagoya A,
Huffman JE,
Hung YJ,
Huo S,
Hwang MY,
Iha H,
Ikeda DD,
Isono M,
Jackson AU,
Jäger S,
Jansen IE,
Johansson I,
Jonas JB,
Jonsson A,
Jørgensen T,
Kalafati IP,
Kanai M,
Kanoni S,
Kårhus LL,
Kasturiratne A,
Katsuya T,
Kawaguchi T,
Kember RL,
Kentistou KA,
Kim HN,
Kim YJ,
Kleber ME,
Knol MJ,
Kurbasic A,
Lauzon M,
Le P,
Lea R,
Lee JY,
Leonard HL,
Li SA,
Li X,
Li X,
Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
Lyytikäinen LP,
Mahajan A,
Mamakou V,
Mangino M,
Manichaikul A,
Marten J,
Mattheisen M,
Mavarani L,
McDaid AF,
Meidtner K,
Melendez TL,
Mercader JM,
Milaneschi Y,
Miller JE,
Millwood IY,
Mishra PP,
Mitchell RE,
Møllehave LT,
Morgan A,
Mucha S,
Munz M,
Nakatochi M,
Nelson CP,
Nethander M,
Nho CW,
Nielsen AA,
Nolte IM,
Nongmaithem SS,
Noordam R,
Ntalla I,
Nutile T,
Pandit A,
Christofidou P,
Pärna K,
Pauper M,
Petersen ERB,
Petersen LV,
Pitkänen N,
Polašek O,
Poveda A,
Preuss MH,
Pyarajan S,
Raffield LM,
Rakugi H,
Ramirez J,
Rasheed A,
Raven D,
Rayner NW,
Riveros C,
Rohde R,
Ruggiero D,
Ruotsalainen SE,
Ryan KA,
Sabater-Lleal M,
Saxena R,
Scholz M,
Sendamarai A,
Shen B,
Shi J,
Shin JH,
Sidore C,
Sitlani CM,
Slieker RC,
Smit RAJ,
Smith AV,
Smith JA,
Smyth LJ,
Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu C,
Terzikhan N,
Tesolin P,
Teumer A,
Theusch E,
Thompson DJ,
Thorleifsson G,
Timmers PRHJ,
Trompet S,
Turman C,
Vaccargiu S,
van der Laan SW,
van der Most PJ,
van Klinken JB,
van Setten J,
Verma SS,
Verweij N,
Veturi Y,
Wang CA,
Wang C,
Wang L,
Wang Z,
Warren HR,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
Wu Y,
Wuttke M,
Xia R,
Xie T,
Yamamoto K,
Yang J,
Yao J,
Young H,
Yousri NA,
Yu L,
Zeng L,
Zhang W,
Zhang X,
Zhao JH,
Zhao W,
Zhou W,
Zimmermann ME,
Zoledziewska M,
Adair LS,
Adams HHH,
Aguilar-Salinas CA,
Al-Mulla F,
Arnett DK,
Asselbergs FW,
Åsvold BO,
Attia J,
Banas B,
Bandinelli S,
Bennett DA,
Bergler T,
Bharadwaj D,
Biino G,
Bisgaard H,
Boerwinkle E,
Böger CA,
Bønnelykke K,
Boomsma DI,
Børglum AD,
Borja JB,
Bouchard C,
Bowden DW,
Brandslund I,
Brumpton B,
Buring JE,
Caulfield MJ,
Chambers JC,
Chandak GR,
Chanock SJ,
Chaturvedi N,
Chen YI,
Chen Z,
Cheng CY,
Christophersen IE,
Ciullo M,
Cole JW,
Collins FS,
Cooper RS,
Cruz M,
Cucca F,
Cupples LA,
Cutler MJ,
Damrauer SM,
Dantoft TM,
de Borst GJ,
de Groot LCPGM,
De Jager PL,
de Kleijn DPV,
Janaka de Silva H,
Dedoussis GV,
den Hollander AI,
Du S,
Easton DF,
Elders PJM,
Eliassen AH,
Ellinor PT,
Elmståhl S,
Erdmann J,
Evans MK,
Fatkin D,
Feenstra B,
Feitosa MF,
Ferrucci L,
Ford I,
Fornage M,
Franke A,
Franks PW,
Freedman BI,
Gasparini P,
Gieger C,
Girotto G,
Goddard ME,
Golightly YM,
Gonzalez-Villalpando C,
Gordon-Larsen P,
Grallert H,
Grant SFA,
Grarup N,
Griffiths L,
Gudnason V,
Haiman C,
Hakonarson H,
Hansen T,
Hartman CA,
Hattersley AT,
Hayward C,
Heckbert SR,
Heng CK,
Hengstenberg C,
Hewitt AW,
Hishigaki H,
Hoyng CB,
Huang PL,
Huang W,
Hunt SC,
Hveem K,
Hyppönen E,
Iacono WG,
Ichihara S,
Ikram MA,
Isasi CR,
Jackson RD,
Jarvelin MR,
Jin ZB,
Jöckel KH,
Joshi PK,
Jousilahti P,
Jukema JW,
Kähönen M,
Kamatani Y,
Kang KD,
Kaprio J,
Kardia SLR,
Karpe F,
Kato N,
Kee F,
Kessler T,
Khera AV,
Khor CC,
Kiemeney LALM,
Kim BJ,
Kim EK,
Kim HL,
Kirchhof P,
Kivimaki M,
Koh WP,
Koistinen HA,
Kolovou GD,
Kooner JS,
Kooperberg C,
Köttgen A,
Kovacs P,
Kraaijeveld A,
Kraft P,
Krauss RM,
Kumari M,
Kutalik Z,
Laakso M,
Lange LA,
Langenberg C,
Launer LJ,
Le Marchand L,
Lee H,
Lee NR,
Lehtimäki T,
Li H,
Li L,
Lieb W,
Lin X,
Lind L,
Linneberg A,
Liu CT,
Liu J,
Loeffler M,
London B,
Lubitz SA,
Lye SJ,
Mackey DA,
Mägi R,
Magnusson PKE,
Marcus GM,
Vidal PM,
Martin NG,
März W,
Matsuda F,
McGarrah RW,
McGue M,
McKnight AJ,
Medland SE,
Mellström D,
Metspalu A,
Mitchell BD,
Mitchell P,
Mook-Kanamori DO,
Morris AD,
Mucci LA,
Munroe PB,
Nalls MA,
Nazarian S,
Nelson AE,
Neville MJ,
Newton-Cheh C,
Nielsen CS,
Nöthen MM,
Ohlsson C,
Oldehinkel AJ,
Orozco L,
Pahkala K,
Pajukanta P,
Palmer CNA,
Parra EJ,
Pattaro C,
Pedersen O,
Pennell CE,
Penninx BWJH,
Perusse L,
Peters A,
Peyser PA,
Porteous DJ,
Posthuma D,
Power C,
Pramstaller PP,
Province MA,
Qi Q,
Qu J,
Rader DJ,
Raitakari OT,
Ralhan S,
Rallidis LS,
Rao DC,
Redline S,
Reilly DF,
Reiner AP,
Rhee SY,
Ridker PM,
Rienstra M,
Ripatti S,
Ritchie MD,
Roden DM,
Rosendaal FR,
Rotter JI,
Rudan I,
Rutters F,
Sabanayagam C,
Saleheen D,
Salomaa V,
Samani NJ,
Sanghera DK,
Sattar N,
Schmidt B,
Schmidt H,
Schmidt R,
Schulze MB,
Schunkert H,
Scott LJ,
Scott RJ,
Sever P,
Shiroma EJ,
Shoemaker MB,
Shu XO,
Simonsick EM,
Sims M,
Singh JR,
Singleton AB,
Sinner MF,
Smith JG,
Snieder H,
Spector TD,
Stampfer MJ,
Stark KJ,
Strachan DP,
't Hart LM,
Tabara Y,
Tang H,
Tardif JC,
Thanaraj TA,
Timpson NJ,
Tönjes A,
Tremblay A,
Tuomi T,
Tuomilehto J,
Tusié-Luna MT,
Uitterlinden AG,
van Dam RM,
van der Harst P,
Van der Velde N,
van Duijn CM,
van Schoor NM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wacher-Rodarte NH,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Weir DR,
Werge TM,
Widen E,
Wilkens LR,
Willemsen G,
Willett WC,
Wilson JF,
Wong TY,
Woo JT,
Wright AF,
Wu JY,
Xu H,
Yajnik CS,
Yokota M,
Yuan JM,
Zeggini E,
Zemel BS,
Zheng W,
Zhu X,
Zmuda JM,
Zonderman AB,
Zwart JA,
Chasman DI,
Cho YS,
Heid IM,
McCarthy MI,
Ng MCY,
O'Donnell CJ,
Rivadeneira F,
Thorsteinsdottir U,
Sun YV,
Tai ES,
Boehnke M,
Deloukas P,
Justice AE,
Lindgren CM,
Loos RJF,
Mohlke KL,
North KE,
Stefansson K,
Walters RG,
Winkler TW,
Young KL,
Loh PR,
Yang J,
Esko T,
Assimes TL,
Auton A,
Abecasis GR,
Willer CJ,
Locke AE,
Berndt SI,
Lettre G,
Frayling TM,
Okada Y,
Wood AR,
Visscher PM,
Hirschhorn JN
23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
페이지 12개+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
외 136명 — 모두 보기
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
페이지 12개+
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
Lagou V,
Jiang L,
Ulrich A,
Zudina L,
González KSG,
Balkhiyarova Z,
Faggian A,
Maina JG,
Chen S,
Todorov PV,
Sharapov S,
David A
외 84명 — 모두 보기
Marullo L,
Mägi R,
Rujan RM,
Ahlqvist E,
Thorleifsson G,
Gao Η,
Εvangelou Ε,
Benyamin B,
Scott RA,
Isaacs A,
Zhao JH,
Willems SM,
Johnson T,
Gieger C,
Grallert H,
Meisinger C,
Müller-Nurasyid M,
Strawbridge RJ,
Goel A,
Rybin D,
Albrecht E,
Jackson AU,
Stringham HM,
Corrêa IR Jr,
Farber-Eger E,
Steinthorsdottir V,
Uitterlinden AG,
Munroe PB,
Brown MJ,
Schmidberger J,
Holmen O,
Thorand B,
Hveem K,
Wilsgaard T,
Mohlke KL,
Wang Z,
Shmeliov A,
den Hoed M,
Loos RJF,
Kratzer W,
Haenle M,
Koenig W,
Boehm BO,
Tan TM,
Tomas A,
Salem V,
Barroso I,
Tuomilehto J,
Boehnke M,
Florez JC,
Hamsten A,
Watkins H,
Njølstad I,
Wichmann HE,
Caulfield MJ,
Khaw KT,
van Duijn CM,
Hofman A,
Wareham NJ,
Langenberg C,
Whitfield JB,
Martin NG,
Montgomery G,
Scapoli C,
Tzoulaki I,
Elliott P,
Thorsteinsdottir U,
Stefansson K,
Brittain EL,
McCarthy MI,
Froguel P,
Sexton PM,
Wootten D,
Groop L,
Dupuis J,
Meigs JB,
Deganutti G,
Demirkan A,
Pers TH,
Reynolds CA,
Aulchenko YS,
Kaakinen MA,
Jones B,
Prokopenko I
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
페이지 12개+
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Henry A,
Mo X,
Finan C,
Chaffin MD,
Speed D,
Issa H,
Denaxas S,
Ware JS,
Zheng SL,
Malarstig A,
Gratton J,
Bond I
외 169명 — 모두 보기
Roselli C,
Miller D,
Chopade S,
Schmidt AF,
Abner E,
Adams L,
Andersson C,
Aragam KG,
Ärnlöv J,
Asselin G,
Raja AA,
Backman JD,
Bartz TM,
Biddinger KJ,
Biggs ML,
Bloom HL,
Boersma E,
Brandimarto J,
Brown MR,
Brunak S,
Bruun MT,
Buckbinder L,
Bundgaard H,
Carey DJ,
Chasman DI,
Chen X,
Cook JP,
Czuba T,
de Denus S,
Dehghan A,
Delgado GE,
Doney AS,
Dörr M,
Dowsett J,
Dudley SC,
Engström G,
Erikstrup C,
Esko T,
Farber-Eger EH,
Felix SB,
Finer S,
Ford I,
Ghanbari M,
Ghasemi S,
Ghouse J,
Giedraitis V,
Giulianini F,
Gottdiener JS,
Gross S,
Guðbjartsson DF,
Gui H,
Gutmann R,
Hägg S,
Haggerty CM,
Hedman ÅK,
Helgadottir A,
Hemingway H,
Hillege H,
Hyde CL,
Aagaard Jensen B,
Jukema JW,
Kardys I,
Karra R,
Kavousi M,
Kizer JR,
Kleber ME,
Køber L,
Koekemoer A,
Kuchenbaecker K,
Lai YP,
Lanfear D,
Langenberg C,
Lin H,
Lind L,
Lindgren CM,
Liu PP,
London B,
Lowery BD,
Luan J,
Lubitz SA,
Magnusson P,
Margulies KB,
Marston NA,
Martin H,
März W,
Melander O,
Mordi IR,
Morley MP,
Morris AP,
Morrison AC,
Morton L,
Nagle MW,
Nelson CP,
Niessner A,
Niiranen T,
Noordam R,
Nowak C,
O'Donoghue ML,
Ostrowski SR,
Owens AT,
Palmer CNA,
Paré G,
Pedersen OB,
Perola M,
Pigeyre M,
Psaty BM,
Rice KM,
Ridker PM,
Romaine SPR,
Rotter JI,
Ruff CT,
Sabatine MS,
Sallah N,
Salomaa V,
Sattar N,
Shalaby AA,
Shekhar A,
Smelser DT,
Smith NL,
Sørensen E,
Srinivasan S,
Stefansson K,
Sveinbjörnsson G,
Svensson P,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teumer A,
Thorgeirsson G,
Thorsteinsdottir U,
Torp-Pedersen C,
Tragante V,
Trompet S,
Uitterlinden AG,
Ullum H,
van der Harst P,
van Heel D,
van Setten J,
van Vugt M,
Veluchamy A,
Verschuuren M,
Verweij N,
Vissing CR,
Völker U,
Voors AA,
Wallentin L,
Wang Y,
Weeke PE,
Wiggins KL,
Williams LK,
Yang Y,
Yu B,
Zannad F,
Zheng C,
Asselbergs FW,
Cappola TP,
Dubé MP,
Dunn ME,
Lang CC,
Samani NJ,
Shah S,
Vasan RS,
Smith JG,
Holm H,
Shah S,
Ellinor PT,
Hingorani AD,
Wells Q,
Lumbers RT
Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 2곳
Nature genetics · 2025 · PMID 40038546 · 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+
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks CE,
Perry JR,
Sulem P,
Chasman DI,
Franceschini N,
He C,
Lunetta KL,
Visser JA,
Byrne EM,
Cousminer DL,
Gudbjartsson DF,
Esko T
외 162명 — 모두 보기
Feenstra B,
Hottenga JJ,
Koller DL,
Kutalik Z,
Lin P,
Mangino M,
Marongiu M,
McArdle PF,
Smith AV,
Stolk L,
van Wingerden SH,
Zhao JH,
Albrecht E,
Corre T,
Ingelsson E,
Hayward C,
Magnusson PK,
Smith EN,
Ulivi S,
Warrington NM,
Zgaga L,
Alavere H,
Amin N,
Aspelund T,
Bandinelli S,
Barroso I,
Berenson GS,
Bergmann S,
Blackburn H,
Boerwinkle E,
Buring JE,
Busonero F,
Campbell H,
Chanock SJ,
Chen W,
Cornelis MC,
Couper D,
Coviello AD,
d'Adamo P,
de Faire U,
de Geus EJ,
Deloukas P,
Döring A,
Smith GD,
Easton DF,
Eiriksdottir G,
Emilsson V,
Eriksson J,
Ferrucci L,
Folsom AR,
Foroud T,
Garcia M,
Gasparini P,
Geller F,
Gieger C,
Gudnason V,
Hall P,
Hankinson SE,
Ferreli L,
Heath AC,
Hernandez DG,
Hofman A,
Hu FB,
Illig T,
Järvelin MR,
Johnson AD,
Karasik D,
Khaw KT,
Kiel DP,
Kilpeläinen TO,
Kolcic I,
Kraft P,
Launer LJ,
Laven JS,
Li S,
Liu J,
Levy D,
Martin NG,
McArdle WL,
Melbye M,
Mooser V,
Murray JC,
Murray SS,
Nalls MA,
Navarro P,
Nelis M,
Ness AR,
Northstone K,
Oostra BA,
Peacock M,
Palmer LJ,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peltonen L,
Pennell CE,
Pharoah P,
Polasek O,
Plump AS,
Pouta A,
Porcu E,
Rafnar T,
Rice JP,
Ring SM,
Rivadeneira F,
Rudan I,
Sala C,
Salomaa V,
Sanna S,
Schlessinger D,
Schork NJ,
Scuteri A,
Segrè AV,
Shuldiner AR,
Soranzo N,
Sovio U,
Srinivasan SR,
Strachan DP,
Tammesoo ML,
Tikkanen E,
Toniolo D,
Tsui K,
Tryggvadottir L,
Tyrer J,
Uda M,
van Dam RM,
van Meurs JB,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Weedon MN,
Wichmann HE,
Willemsen G,
Wilson JF,
Wright AF,
Young L,
Zhai G,
Zhuang WV,
Bierut LJ,
Boomsma DI,
Boyd HA,
Crisponi L,
Demerath EW,
van Duijn CM,
Econs MJ,
Harris TB,
Hunter DJ,
Loos RJ,
Metspalu A,
Montgomery GW,
Ridker PM,
Spector TD,
Streeten EA,
Stefansson K,
Thorsteinsdottir U,
Uitterlinden AG,
Widen E,
Murabito JM,
Ong KK,
Murray A
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
페이지 11개
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
외 140명 — 모두 보기
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
페이지 11개
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Medina-Gomez C,
Kemp JP,
Dimou NL,
Kreiner E,
Chesi A,
Zemel BS,
Bønnelykke K,
Boer CG,
Ahluwalia TS,
Bisgaard H,
Evangelou E,
Heppe DHM
외 22명 — 모두 보기
Bonewald LF,
Gorski JP,
Ghanbari M,
Demissie S,
Duque G,
Maurano MT,
Kiel DP,
Hsu YH,
C J van der Eerden B,
Ackert-Bicknell C,
Reppe S,
Gautvik KM,
Raastad T,
Karasik D,
van de Peppel J,
Jaddoe VWV,
Uitterlinden AG,
Tobias JH,
Grant SFA,
Bagos PG,
Evans DM,
Rivadeneira F
Nature communications · 2017 · PMID 28743860 · open access
페이지 11개
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Medina-Gomez C,
Mullin BH,
Chesi A,
Prijatelj V,
Kemp JP,
Shochat-Carvalho C,
Trajanoska K,
Wang C,
Joro R,
Evans TE,
Schraut KE,
Li-Gao R
외 46명 — 모두 보기
Ahluwalia TS,
Zillikens MC,
Zhu K,
Mook-Kanamori DO,
Evans DS,
Nethander M,
Knol MJ,
Thorleifsson G,
Prokic I,
Zemel B,
Broer L,
McGuigan FE,
van Schoor NM,
Reppe S,
Pawlak MA,
Ralston SH,
van der Velde N,
Lorentzon M,
Stefansson K,
Adams HHH,
Wilson SG,
Ikram MA,
Walsh JP,
Lakka TA,
Gautvik KM,
Wilson JF,
Orwoll ES,
van Duijn CM,
Bønnelykke K,
Uitterlinden AG,
Styrkársdóttir U,
Akesson KE,
Spector TD,
Tobias JH,
Ohlsson C,
Felix JF,
Bisgaard H,
Grant SFA,
Richards JB,
Evans DM,
van der Eerden B,
van de Peppel J,
Ackert-Bicknell C,
Karasik D,
Kague E,
Rivadeneira F
Communications biology · 2023 · PMID 37402774 · open access
페이지 11개
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Morris AP,
Voight BF,
Teslovich TM,
Ferreira T,
Segrè AV,
Steinthorsdottir V,
Strawbridge RJ,
Khan H,
Grallert H,
Mahajan A,
Prokopenko I,
Kang HM
외 192명 — 모두 보기
Dina C,
Esko T,
Fraser RM,
Kanoni S,
Kumar A,
Lagou V,
Langenberg C,
Luan J,
Lindgren CM,
Müller-Nurasyid M,
Pechlivanis S,
Rayner NW,
Scott LJ,
Wiltshire S,
Yengo L,
Kinnunen L,
Rossin EJ,
Raychaudhuri S,
Johnson AD,
Dimas AS,
Loos RJ,
Vedantam S,
Chen H,
Florez JC,
Fox C,
Liu CT,
Rybin D,
Couper DJ,
Kao WH,
Li M,
Cornelis MC,
Kraft P,
Sun Q,
van Dam RM,
Stringham HM,
Chines PS,
Fischer K,
Fontanillas P,
Holmen OL,
Hunt SE,
Jackson AU,
Kong A,
Lawrence R,
Meyer J,
Perry JR,
Platou CG,
Potter S,
Rehnberg E,
Robertson N,
Sivapalaratnam S,
Stančáková A,
Stirrups K,
Thorleifsson G,
Tikkanen E,
Wood AR,
Almgren P,
Atalay M,
Benediktsson R,
Bonnycastle LL,
Burtt N,
Carey J,
Charpentier G,
Crenshaw AT,
Doney AS,
Dorkhan M,
Edkins S,
Emilsson V,
Eury E,
Forsen T,
Gertow K,
Gigante B,
Grant GB,
Groves CJ,
Guiducci C,
Herder C,
Hreidarsson AB,
Hui J,
James A,
Jonsson A,
Rathmann W,
Klopp N,
Kravic J,
Krjutškov K,
Langford C,
Leander K,
Lindholm E,
Lobbens S,
Männistö S,
Mirza G,
Mühleisen TW,
Musk B,
Parkin M,
Rallidis L,
Saramies J,
Sennblad B,
Shah S,
Sigurðsson G,
Silveira A,
Steinbach G,
Thorand B,
Trakalo J,
Veglia F,
Wennauer R,
Winckler W,
Zabaneh D,
Campbell H,
van Duijn C,
Uitterlinden AG,
Hofman A,
Sijbrands E,
Abecasis GR,
Owen KR,
Zeggini E,
Trip MD,
Forouhi NG,
Syvänen AC,
Eriksson JG,
Peltonen L,
Nöthen MM,
Balkau B,
Palmer CN,
Lyssenko V,
Tuomi T,
Isomaa B,
Hunter DJ,
Qi L,
Shuldiner AR,
Roden M,
Barroso I,
Wilsgaard T,
Beilby J,
Hovingh K,
Price JF,
Wilson JF,
Rauramaa R,
Lakka TA,
Lind L,
Dedoussis G,
Njølstad I,
Pedersen NL,
Khaw KT,
Wareham NJ,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Korpi-Hyövälti E,
Saltevo J,
Laakso M,
Kuusisto J,
Metspalu A,
Collins FS,
Mohlke KL,
Bergman RN,
Tuomilehto J,
Boehm BO,
Gieger C,
Hveem K,
Cauchi S,
Froguel P,
Baldassarre D,
Tremoli E,
Humphries SE,
Saleheen D,
Danesh J,
Ingelsson E,
Ripatti S,
Salomaa V,
Erbel R,
Jöckel KH,
Moebus S,
Peters A,
Illig T,
de Faire U,
Hamsten A,
Morris AD,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Boerwinkle E,
Melander O,
Kathiresan S,
Nilsson PM,
Deloukas P,
Thorsteinsdottir U,
Groop LC,
Stefansson K,
Hu F,
Pankow JS,
Dupuis J,
Meigs JB,
Altshuler D,
Boehnke M,
McCarthy MI
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22885922 · open access
페이지 10개
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
Porcu E,
Medici M,
Pistis G,
Volpato CB,
Wilson SG,
Cappola AR,
Bos SD,
Deelen J,
den Heijer M,
Freathy RM,
Lahti J,
Liu C
외 82명 — 모두 보기
Lopez LM,
Nolte IM,
O'Connell JR,
Tanaka T,
Trompet S,
Arnold A,
Bandinelli S,
Beekman M,
Böhringer S,
Brown SJ,
Buckley BM,
Camaschella C,
de Craen AJ,
Davies G,
de Visser MC,
Ford I,
Forsen T,
Frayling TM,
Fugazzola L,
Gögele M,
Hattersley AT,
Hermus AR,
Hofman A,
Houwing-Duistermaat JJ,
Jensen RA,
Kajantie E,
Kloppenburg M,
Lim EM,
Masciullo C,
Mariotti S,
Minelli C,
Mitchell BD,
Nagaraja R,
Netea-Maier RT,
Palotie A,
Persani L,
Piras MG,
Psaty BM,
Räikkönen K,
Richards JB,
Rivadeneira F,
Sala C,
Sabra MM,
Sattar N,
Shields BM,
Soranzo N,
Starr JM,
Stott DJ,
Sweep FC,
Usala G,
van der Klauw MM,
van Heemst D,
van Mullem A,
Vermeulen SH,
Visser WE,
Walsh JP,
Westendorp RG,
Widen E,
Zhai G,
Cucca F,
Deary IJ,
Eriksson JG,
Ferrucci L,
Fox CS,
Jukema JW,
Kiemeney LA,
Pramstaller PP,
Schlessinger D,
Shuldiner AR,
Slagboom EP,
Uitterlinden AG,
Vaidya B,
Visser TJ,
Wolffenbuttel BH,
Meulenbelt I,
Rotter JI,
Spector TD,
Hicks AA,
Toniolo D,
Sanna S,
Peeters RP,
Naitza S
PLoS genetics · 2013 · PMID 23408906 · open access
페이지 10개
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.