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Scott LJ에 대해
33건, 그중 13건 표시.
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
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
외 25명 — 모두 보기
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
페이지 4개
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Lindgren CM,
Heid IM,
Randall JC,
Lamina C,
Steinthorsdottir V,
Qi L,
Speliotes EK,
Thorleifsson G,
Willer CJ,
Herrera BM,
Jackson AU,
Lim N
외 131명 — 모두 보기
Scheet P,
Soranzo N,
Amin N,
Aulchenko YS,
Chambers JC,
Drong A,
Luan J,
Lyon HN,
Rivadeneira F,
Sanna S,
Timpson NJ,
Zillikens MC,
Zhao JH,
Almgren P,
Bandinelli S,
Bennett AJ,
Bergman RN,
Bonnycastle LL,
Bumpstead SJ,
Chanock SJ,
Cherkas L,
Chines P,
Coin L,
Cooper C,
Crawford G,
Doering A,
Dominiczak A,
Doney AS,
Ebrahim S,
Elliott P,
Erdos MR,
Estrada K,
Ferrucci L,
Fischer G,
Forouhi NG,
Gieger C,
Grallert H,
Groves CJ,
Grundy S,
Guiducci C,
Hadley D,
Hamsten A,
Havulinna AS,
Hofman A,
Holle R,
Holloway JW,
Illig T,
Isomaa B,
Jacobs LC,
Jameson K,
Jousilahti P,
Karpe F,
Kuusisto J,
Laitinen J,
Lathrop GM,
Lawlor DA,
Mangino M,
McArdle WL,
Meitinger T,
Morken MA,
Morris AP,
Munroe P,
Narisu N,
Nordström A,
Nordström P,
Oostra BA,
Palmer CN,
Payne F,
Peden JF,
Prokopenko I,
Renström F,
Ruokonen A,
Salomaa V,
Sandhu MS,
Scott LJ,
Scuteri A,
Silander K,
Song K,
Yuan X,
Stringham HM,
Swift AJ,
Tuomi T,
Uda M,
Vollenweider P,
Waeber G,
Wallace C,
Walters GB,
Weedon MN,
Witteman JC,
Zhang C,
Zhang W,
Caulfield MJ,
Collins FS,
Davey Smith G,
Day IN,
Franks PW,
Hattersley AT,
Hu FB,
Jarvelin MR,
Kong A,
Kooner JS,
Laakso M,
Lakatta E,
Mooser V,
Morris AD,
Peltonen L,
Samani NJ,
Spector TD,
Strachan DP,
Tanaka T,
Tuomilehto J,
Uitterlinden AG,
van Duijn CM,
Wareham NJ,
Hugh Watkins,
Waterworth DM,
Boehnke M,
Deloukas P,
Groop L,
Hunter DJ,
Thorsteinsdottir U,
Schlessinger D,
Wichmann HE,
Frayling TM,
Abecasis GR,
Hirschhorn JN,
Loos RJ,
Stefansson K,
Mohlke KL,
Barroso I,
McCarthy MI
Wellcome Trust Case Control Consortium · Procardis Consortia 외 컨소시엄 1곳
PLoS genetics · 2009 · PMID 19557161 · open access
페이지 3개
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
외 290명 — 모두 보기
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
페이지 3개
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Blokland GAM,
Grove J,
Chen CY,
Cotsapas C,
Tobet S,
Handa R,
St Clair D,
Lencz T,
Mowry BJ,
Periyasamy S,
Cairns MJ,
Tooney PA
외 118명 — 모두 보기
Wu JQ,
Kelly B,
Kirov G,
Sullivan PF,
Corvin A,
Riley BP,
Esko T,
Milani L,
Jönsson EG,
Palotie A,
Ehrenreich H,
Begemann M,
Steixner-Kumar A,
Sham PC,
Iwata N,
Weinberger DR,
Gejman PV,
Sanders AR,
Buxbaum JD,
Rujescu D,
Giegling I,
Konte B,
Hartmann AM,
Bramon E,
Murray RM,
Pato MT,
Lee J,
Melle I,
Molden E,
Ophoff RA,
McQuillin A,
Bass NJ,
Adolfsson R,
Malhotra AK,
Martin NG,
Fullerton JM,
Mitchell PB,
Schofield PR,
Forstner AJ,
Degenhardt F,
Schaupp S,
Comes AL,
Kogevinas M,
Guzman-Parra J,
Reif A,
Streit F,
Sirignano L,
Cichon S,
Grigoroiu-Serbanescu M,
Hauser J,
Lissowska J,
Mayoral F,
Müller-Myhsok B,
Świątkowska B,
Schulze TG,
Nöthen MM,
Rietschel M,
Kelsoe J,
Leboyer M,
Jamain S,
Etain B,
Bellivier F,
Vincent JB,
Alda M,
O'Donovan C,
Cervantes P,
Biernacka JM,
Frye M,
McElroy SL,
Scott LJ,
Stahl EA,
Landén M,
Hamshere ML,
Smeland OB,
Djurovic S,
Vaaler AE,
Andreassen OA,
Baune BT,
Air T,
Preisig M,
Uher R,
Levinson DF,
Weissman MM,
Potash JB,
Shi J,
Knowles JA,
Perlis RH,
Lucae S,
Boomsma DI,
Penninx BWJH,
Hottenga JJ,
de Geus EJC,
Willemsen G,
Milaneschi Y,
Tiemeier H,
Grabe HJ,
Teumer A,
Van der Auwera S,
Völker U,
Hamilton SP,
Magnusson PKE,
Viktorin A,
Mehta D,
Mullins N,
Adams MJ,
Breen G,
McIntosh AM,
Lewis CM,
Hougaard DM,
Nordentoft M,
Mors O,
Mortensen PB,
Werge T,
Als TD,
Børglum AD,
Petryshen TL,
Smoller JW,
Goldstein JM
Schizophrenia Working Group of the Psychiatric Genomics Consortium · Bipolar Disorder Working Group of the Psychiatric Genomics Consortium 외 컨소시엄 3곳
Biological psychiatry · 2022 · PMID 34099189
페이지 3개
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
Huyghe JR,
Jackson AU,
Fogarty MP,
Buchkovich ML,
Stančáková A,
Stringham HM,
Sim X,
Yang L,
Fuchsberger C,
Cederberg H,
Chines PS,
Teslovich TM
외 17명 — 모두 보기
Romm JM,
Ling H,
McMullen I,
Ingersoll R,
Pugh EW,
Doheny KF,
Neale BM,
Daly MJ,
Kuusisto J,
Scott LJ,
Kang HM,
Collins FS,
Abecasis GR,
Watanabe RM,
Boehnke M,
Laakso M,
Mohlke KL
Nature genetics · 2013 · PMID 23263489
페이지 2개
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
외 152명 — 모두 보기
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration 외 컨소시엄 8곳
Nature · 2019 · PMID 31118516 · open access
페이지 2개
Variants in MTNR1B influence fasting glucose levels
Prokopenko I,
Langenberg C,
Florez JC,
Saxena R,
Soranzo N,
Thorleifsson G,
Loos RJ,
Manning AK,
Jackson AU,
Aulchenko Y,
Potter SC,
Erdos MR
외 96명 — 모두 보기
Sanna S,
Hottenga JJ,
Wheeler E,
Kaakinen M,
Lyssenko V,
Chen WM,
Ahmadi K,
Beckmann JS,
Bergman RN,
Bochud M,
Bonnycastle LL,
Buchanan TA,
Cao A,
Cervino A,
Coin L,
Collins FS,
Crisponi L,
de Geus EJ,
Dehghan A,
Deloukas P,
Doney AS,
Elliott P,
Freimer N,
Gateva V,
Herder C,
Hofman A,
Hughes TE,
Hunt S,
Illig T,
Inouye M,
Isomaa B,
Johnson T,
Kong A,
Krestyaninova M,
Kuusisto J,
Laakso M,
Lim N,
Lindblad U,
Lindgren CM,
McCann OT,
Mohlke KL,
Morris AD,
Naitza S,
Orrù M,
Palmer CN,
Pouta A,
Randall J,
Rathmann W,
Saramies J,
Scheet P,
Scott LJ,
Scuteri A,
Sharp S,
Sijbrands E,
Smit JH,
Song K,
Steinthorsdottir V,
Stringham HM,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Voight BF,
Waterworth D,
Wichmann HE,
Willemsen G,
Witteman JC,
Yuan X,
Zhao JH,
Zeggini E,
Schlessinger D,
Sandhu M,
Boomsma DI,
Uda M,
Spector TD,
Penninx BW,
Altshuler D,
Vollenweider P,
Jarvelin MR,
Lakatta E,
Waeber G,
Fox CS,
Peltonen L,
Groop LC,
Mooser V,
Cupples LA,
Thorsteinsdottir U,
Boehnke M,
Barroso I,
Van Duijn C,
Dupuis J,
Watanabe RM,
Stefansson K,
McCarthy MI,
Wareham NJ,
Meigs JB,
Abecasis GR
Nature genetics · 2009 · PMID 19060907
페이지 1개
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Willer CJ,
Speliotes EK,
Loos RJ,
Li S,
Lindgren CM,
Heid IM,
Berndt SI,
Elliott AL,
Jackson AU,
Lamina C,
Lettre G,
Lim N
외 133명 — 모두 보기
Lyon HN,
McCarroll SA,
Papadakis K,
Qi L,
Randall JC,
Roccasecca RM,
Sanna S,
Scheet P,
Weedon MN,
Wheeler E,
Zhao JH,
Jacobs LC,
Prokopenko I,
Soranzo N,
Tanaka T,
Timpson NJ,
Almgren P,
Bennett A,
Bergman RN,
Bingham SA,
Bonnycastle LL,
Brown M,
Burtt NP,
Chines P,
Coin L,
Collins FS,
Connell JM,
Cooper C,
Smith GD,
Dennison EM,
Deodhar P,
Elliott P,
Erdos MR,
Estrada K,
Evans DM,
Gianniny L,
Gieger C,
Gillson CJ,
Guiducci C,
Hackett R,
Hadley D,
Hall AS,
Havulinna AS,
Hebebrand J,
Hofman A,
Isomaa B,
Jacobs KB,
Johnson T,
Jousilahti P,
Jovanovic Z,
Khaw KT,
Kraft P,
Kuokkanen M,
Kuusisto J,
Laitinen J,
Lakatta EG,
Luan J,
Luben RN,
Mangino M,
McArdle WL,
Meitinger T,
Mulas A,
Munroe PB,
Narisu N,
Ness AR,
Northstone K,
O'Rahilly S,
Purmann C,
Rees MG,
Ridderstråle M,
Ring SM,
Rivadeneira F,
Ruokonen A,
Sandhu MS,
Saramies J,
Scott LJ,
Scuteri A,
Silander K,
Sims MA,
Song K,
Stephens J,
Stevens S,
Stringham HM,
Tung YC,
Valle TT,
Van Duijn CM,
Vimaleswaran KS,
Vollenweider P,
Waeber G,
Wallace C,
Watanabe RM,
Waterworth DM,
Watkins N,
Witteman JC,
Zeggini E,
Zhai G,
Zillikens MC,
Altshuler D,
Caulfield MJ,
Chanock SJ,
Farooqi IS,
Ferrucci L,
Guralnik JM,
Hattersley AT,
Hu FB,
Jarvelin MR,
Laakso M,
Mooser V,
Ong KK,
Ouwehand WH,
Salomaa V,
Samani NJ,
Spector TD,
Tuomi T,
Tuomilehto J,
Uda M,
Uitterlinden AG,
Wareham NJ,
Deloukas P,
Frayling TM,
Groop LC,
Hayes RB,
Hunter DJ,
Mohlke KL,
Peltonen L,
Schlessinger D,
Strachan DP,
Wichmann HE,
McCarthy MI,
Boehnke M,
Barroso I,
Abecasis GR,
Hirschhorn JN
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
페이지 1개
A genome-wide association search for type 2 diabetes genes in African Americans
Palmer ND,
McDonough CW,
Hicks PJ,
Roh BH,
Wing MR,
An SS,
Hester JM,
Cooke JN,
Bostrom MA,
Rudock ME,
Talbert ME,
Lewis JP
외 379명 — 모두 보기
Ferrara A,
Lu L,
Ziegler JT,
Sale MM,
Divers J,
Shriner D,
Adeyemo A,
Rotimi CN,
Ng MC,
Langefeld CD,
Freedman BI,
Bowden DW,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Morris AP,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Langenberg C,
Hofmann OM,
Dupuis J,
Qi L,
Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
Balkau B,
Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
Burtt NP,
Charpentier G,
Chines PS,
Cornelis M,
Couper DJ,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
Green T,
Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
Herder C,
Isomaa B,
Jackson AU,
Johnson PR,
Jørgensen T,
Kao WH,
Klopp N,
Kong A,
Kraft P,
Kuusisto J,
Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
Marre M,
Meitinger T,
Midthjell K,
Morken MA,
Narisu N,
Nilsson P,
Owen KR,
Payne F,
Perry JR,
Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
Rayner NW,
Robertson NR,
Rocheleau G,
Roden M,
Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
Sparsø T,
Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
Wijmenga C,
Witteman J,
Bergman RN,
Cauchi S,
Collins FS,
Gloyn AL,
Gyllensten U,
Hansen T,
Hide WA,
Hitman GA,
Hofman A,
Hunter DJ,
Hveem K,
Laakso M,
Mohlke KL,
Morris AD,
Palmer CN,
Pramstaller PP,
Rudan I,
Sijbrands E,
Stein LD,
Tuomilehto J,
Uitterlinden A,
Walker M,
Wareham NJ,
Watanabe RM,
Abecasis GR,
Boehm BO,
Campbell H,
Daly MJ,
Hattersley AT,
Hu FB,
Meigs JB,
Pankow JS,
Pedersen O,
Wichmann HE,
Barroso I,
Florez JC,
Frayling TM,
Groop L,
Sladek R,
Thorsteinsdottir U,
Wilson JF,
Illig T,
Froguel P,
van Duijn CM,
Stefansson K,
Altshuler D,
Boehnke M,
McCarthy MI,
Soranzo N,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Mägi R,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Henneman P,
Dehghan A,
Hottenga JJ,
Song K,
Goel A,
Egan JM,
Lajunen T,
Doney A,
Kanoni S,
Cavalcanti-Proença C,
Kumari M,
Timpson NJ,
Zabena C,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ariyurek Y,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Bergmann S,
Bochud M,
Bonnefond A,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Grundy S,
Gwilliam R,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hayward C,
Heath SC,
Hercberg S,
Hicks AA,
Hillman DR,
Hingorani AD,
Hui J,
Hung J,
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,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
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,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Seedorf U,
Sharp SJ,
Shields B,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Tönjes A,
Uitterlinden AG,
van Dijk KW,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Ward KL,
Watkins H,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Lind L,
Palmer LJ,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pramstaller PP,
Wright AF,
Stumvoll M,
Hamsten A,
Buchanan TA,
Valle TT,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Ferrucci L,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Sladek R
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
페이지 1개
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
Perry JR,
Voight BF,
Yengo L,
Amin N,
Dupuis J,
Ganser M,
Grallert H,
Navarro P,
Li M,
Qi L,
Steinthorsdottir V,
Scott RA
외 63명 — 모두 보기
Almgren P,
Arking DE,
Aulchenko Y,
Balkau B,
Benediktsson R,
Bergman RN,
Boerwinkle E,
Bonnycastle L,
Burtt NP,
Campbell H,
Charpentier G,
Collins FS,
Gieger C,
Green T,
Hadjadj S,
Hattersley AT,
Herder C,
Hofman A,
Johnson AD,
Kottgen A,
Kraft P,
Labrune Y,
Langenberg C,
Manning AK,
Mohlke KL,
Morris AP,
Oostra B,
Pankow J,
Petersen AK,
Pramstaller PP,
Prokopenko I,
Rathmann W,
Rayner W,
Roden M,
Rudan I,
Rybin D,
Scott LJ,
Sigurdsson G,
Sladek R,
Thorleifsson G,
Thorsteinsdottir U,
Tuomilehto J,
Uitterlinden AG,
Vivequin S,
Weedon MN,
Wright AF,
Hu FB,
Illig T,
Kao L,
Meigs JB,
Wilson JF,
Stefansson K,
van Duijn C,
Altschuler D,
Morris AD,
Boehnke M,
McCarthy MI,
Froguel P,
Palmer CN,
Wareham NJ,
Groop L,
Frayling TM,
Cauchi S
MAGIC · DIAGRAM Consortium 외 컨소시엄 1곳
PLoS genetics · 2012 · PMID 22693455 · open access
페이지 1개
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
Jackson AU,
Ferreira T
외 163명 — 모두 보기
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
Baldassarre D,
Gertow K,
Humphries SE,
Tremoli E,
Klopp N,
Meyer J,
Steinbach G,
Wennauer R,
Eriksson JG,
Mӓnnistö S,
Peltonen L,
Tikkanen E,
Charpentier G,
Eury E,
Lobbens S,
Gigante B,
Leander K,
McLeod O,
Bottinger EP,
Gottesman O,
Ruderfer D,
Blüher M,
Kovacs P,
Tonjes A,
Maruthur NM,
Scapoli C,
Erbel R,
Jöckel KH,
Moebus S,
de Faire U,
Hamsten A,
Stumvoll M,
Deloukas P,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Ripatti S,
Salomaa V,
Pedersen NL,
Boehm BO,
Bergman RN,
Collins FS,
Mohlke KL,
Tuomilehto J,
Hansen T,
Pedersen O,
Barroso I,
Lannfelt L,
Ingelsson E,
Lind L,
Lindgren CM,
Cauchi S,
Froguel P,
Loos RJF,
Balkau B,
Boeing H,
Franks PW,
Barricarte Gurrea A,
Palli D,
van der Schouw YT,
Altshuler D,
Groop LC,
Langenberg C,
Wareham NJ,
Sijbrands E,
van Duijn CM,
Florez JC,
Meigs JB,
Boerwinkle E,
Gieger C,
Strauch K,
Metspalu A,
Morris AD,
Palmer CNA,
Hu FB,
Thorsteinsdottir U,
Stefansson K,
Dupuis J,
Morris AP,
Boehnke M,
McCarthy MI,
Prokopenko I
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
페이지 1개
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