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성함이나 학술지명, PMID로 찾아보십시오.
Wright A에 대해
70건, 그중 10건 표시.
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Hou L,
Bergen SE,
Akula N,
Song J,
Hultman CM,
Landén M,
Adli M,
Alda M,
Ardau R,
Arias B,
Aubry JM,
Backlund L
외 127명 — 모두 보기
Badner JA,
Barrett TB,
Bauer M,
Baune BT,
Bellivier F,
Benabarre A,
Bengesser S,
Berrettini WH,
Bhattacharjee AK,
Biernacka JM,
Birner A,
Bloss CS,
Brichant-Petitjean C,
Bui ET,
Byerley W,
Cervantes P,
Chillotti C,
Cichon S,
Colom F,
Coryell W,
Craig DW,
Cruceanu C,
Czerski PM,
Davis T,
Dayer A,
Degenhardt F,
Del Zompo M,
DePaulo JR,
Edenberg HJ,
Étain B,
Falkai P,
Foroud T,
Forstner AJ,
Frisén L,
Frye MA,
Fullerton JM,
Gard S,
Garnham JS,
Gershon ES,
Goes FS,
Greenwood TA,
Grigoroiu-Serbanescu M,
Hauser J,
Heilbronner U,
Heilmann-Heimbach S,
Herms S,
Hipolito M,
Hitturlingappa S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kelsoe JR,
Kittel-Schneider S,
Kliwicki S,
Koller DL,
König B,
Lackner N,
Laje G,
Lang M,
Lavebratt C,
Lawson WB,
Leboyer M,
Leckband SG,
Liu C,
Maaser A,
Mahon PB,
Maier W,
Maj M,
Manchia M,
Martinsson L,
McCarthy MJ,
McElroy SL,
McInnis MG,
McKinney R,
Mitchell PB,
Mitjans M,
Mondimore FM,
Monteleone P,
Mühleisen TW,
Nievergelt CM,
Nöthen MM,
Novák T,
Nurnberger JI Jr,
Nwulia EA,
Ösby U,
Pfennig A,
Potash JB,
Propping P,
Reif A,
Reininghaus E,
Rice J,
Rietschel M,
Rouleau GA,
Rybakowski JK,
Schalling M,
Scheftner WA,
Schofield PR,
Schork NJ,
Schulze TG,
Schumacher J,
Schweizer BW,
Severino G,
Shekhtman T,
Shilling PD,
Simhandl C,
Slaney CM,
Smith EN,
Squassina A,
Stamm T,
Stopkova P,
Streit F,
Strohmaier J,
Szelinger S,
Tighe SK,
Tortorella A,
Turecki G,
Vieta E,
Volkert J,
Witt SH,
Wright A,
Zandi PP,
Zhang P,
Zollner S,
McMahon FJ
Human molecular genetics · 2016 · PMID 27329760
페이지 2개
Genome-wide association analysis identifies multiple loci related to resting heart rate
Eijgelsheim M,
Newton-Cheh C,
Sotoodehnia N,
de Bakker PI,
Müller M,
Morrison AC,
Smith AV,
Isaacs A,
Sanna S,
Dörr M,
Navarro P,
Fuchsberger C
외 62명 — 모두 보기
Nolte IM,
de Geus EJ,
Estrada K,
Hwang SJ,
Bis JC,
Rückert IM,
Alonso A,
Launer LJ,
Hottenga JJ,
Rivadeneira F,
Noseworthy PA,
Rice KM,
Perz S,
Arking DE,
Spector TD,
Kors JA,
Aulchenko YS,
Tarasov KV,
Homuth G,
Wild SH,
Marroni F,
Gieger C,
Licht CM,
Prineas RJ,
Hofman A,
Rotter JI,
Hicks AA,
Ernst F,
Najjar SS,
Wright AF,
Peters A,
Fox ER,
Oostra BA,
Kroemer HK,
Couper D,
Völzke H,
Campbell H,
Meitinger T,
Uda M,
Witteman JC,
Psaty BM,
Wichmann HE,
Harris TB,
Kääb S,
Siscovick DS,
Jamshidi Y,
Uitterlinden AG,
Folsom AR,
Larson MG,
Wilson JF,
Penninx BW,
Snieder H,
Pramstaller PP,
van Duijn CM,
Lakatta EG,
Felix SB,
Gudnason V,
Pfeufer A,
Heckbert SR,
Stricker BH,
Boerwinkle E,
O'Donnell CJ
Human molecular genetics · 2010 · PMID 20639392
페이지 1개
Genetic predictors of fibrin D-dimer levels in healthy adults
Smith NL,
Huffman JE,
Strachan DP,
Huang J,
Dehghan A,
Trompet S,
Lopez LM,
Shin SY,
Baumert J,
Vitart V,
Bis JC,
Wild SH
외 54명 — 모두 보기
Rumley A,
Yang Q,
Uitterlinden AG,
Stott DJ,
Davies G,
Carter AM,
Thorand B,
Polašek O,
McKnight B,
Campbell H,
Rudnicka AR,
Chen MH,
Buckley BM,
Harris SE,
Peters A,
Pulanic D,
Lumley T,
de Craen AJ,
Liewald DC,
Gieger C,
Campbell S,
Ford I,
Gow AJ,
Luciano M,
Porteous DJ,
Guo X,
Sattar N,
Tenesa A,
Cushman M,
Slagboom PE,
Visscher PM,
Spector TD,
Illig T,
Rudan I,
Bovill EG,
Wright AF,
McArdle WL,
Tofler G,
Hofman A,
Westendorp RG,
Starr JM,
Grant PJ,
Karakas M,
Hastie ND,
Psaty BM,
Wilson JF,
Lowe GD,
O'Donnell CJ,
Witteman JC,
Jukema JW,
Deary IJ,
Soranzo N,
Koenig W,
Hayward C
Circulation · 2011 · PMID 21502573
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
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
Loos RJ,
Powell JE,
Medland SE,
Speliotes EK,
Chasman DI,
Rose LM,
Thorleifsson G,
Steinthorsdottir V,
Mägi R,
Waite L,
Smith AV
외 160명 — 모두 보기
Yerges-Armstrong LM,
Monda KL,
Hadley D,
Mahajan A,
Li G,
Kapur K,
Vitart V,
Huffman JE,
Wang SR,
Palmer C,
Esko T,
Fischer K,
Zhao JH,
Demirkan A,
Isaacs A,
Feitosa MF,
Luan J,
Heard-Costa NL,
White C,
Jackson AU,
Preuss M,
Ziegler A,
Eriksson J,
Kutalik Z,
Frau F,
Nolte IM,
Van Vliet-Ostaptchouk JV,
Hottenga JJ,
Jacobs KB,
Verweij N,
Goel A,
Medina-Gomez C,
Estrada K,
Bragg-Gresham JL,
Sanna S,
Sidore C,
Tyrer J,
Teumer A,
Prokopenko I,
Mangino M,
Lindgren CM,
Assimes TL,
Shuldiner AR,
Hui J,
Beilby JP,
McArdle WL,
Hall P,
Haritunians T,
Zgaga L,
Kolcic I,
Polasek O,
Zemunik T,
Oostra BA,
Junttila MJ,
Grönberg H,
Schreiber S,
Peters A,
Hicks AA,
Stephens J,
Foad NS,
Laitinen J,
Pouta A,
Kaakinen M,
Willemsen G,
Vink JM,
Wild SH,
Navis G,
Asselbergs FW,
Homuth G,
John U,
Iribarren C,
Harris T,
Launer L,
Gudnason V,
O'Connell JR,
Boerwinkle E,
Cadby G,
Palmer LJ,
James AL,
Musk AW,
Ingelsson E,
Psaty BM,
Beckmann JS,
Waeber G,
Vollenweider P,
Hayward C,
Wright AF,
Rudan I,
Groop LC,
Metspalu A,
Khaw KT,
van Duijn CM,
Borecki IB,
Province MA,
Wareham NJ,
Tardif JC,
Huikuri HV,
Cupples LA,
Atwood LD,
Fox CS,
Boehnke M,
Collins FS,
Mohlke KL,
Erdmann J,
Schunkert H,
Hengstenberg C,
Stark K,
Lorentzon M,
Ohlsson C,
Cusi D,
Staessen JA,
Van der Klauw MM,
Pramstaller PP,
Kathiresan S,
Jolley JD,
Ripatti S,
Jarvelin MR,
de Geus EJ,
Boomsma DI,
Penninx B,
Wilson JF,
Campbell H,
Chanock SJ,
van der Harst P,
Hamsten A,
Watkins H,
Hofman A,
Witteman JC,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Zillikens MC,
Kiemeney LA,
Vermeulen SH,
Abecasis GR,
Schlessinger D,
Schipf S,
Stumvoll M,
Tönjes A,
Spector TD,
North KE,
Lettre G,
McCarthy MI,
Berndt SI,
Heath AC,
Madden PA,
Nyholt DR,
Montgomery GW,
Martin NG,
McKnight B,
Strachan DP,
Hill WG,
Snieder H,
Ridker PM,
Thorsteinsdottir U,
Stefansson K,
Frayling TM,
Hirschhorn JN,
Goddard ME,
Visscher PM
Nature · 2012 · PMID 22982992
페이지 1개
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Huffman JE,
Albrecht E,
Teumer A,
Mangino M,
Kapur K,
Johnson T,
Kutalik Z,
Pirastu N,
Pistis G,
Lopez LM,
Haller T,
Salo P
외 108명 — 모두 보기
Goel A,
Li M,
Tanaka T,
Dehghan A,
Ruggiero D,
Malerba G,
Smith AV,
Nolte IM,
Portas L,
Phipps-Green A,
Boteva L,
Navarro P,
Johansson A,
Hicks AA,
Polasek O,
Esko T,
Peden JF,
Harris SE,
Murgia F,
Wild SH,
Tenesa A,
Tin A,
Mihailov E,
Grotevendt A,
Gislason GK,
Coresh J,
D'Adamo P,
Ulivi S,
Vollenweider P,
Waeber G,
Campbell S,
Kolcic I,
Fisher K,
Viigimaa M,
Metter JE,
Masciullo C,
Trabetti E,
Bombieri C,
Sorice R,
Döring A,
Reischl E,
Strauch K,
Hofman A,
Uitterlinden AG,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Dalbeth N,
Stamp L,
Smit JH,
Kirin M,
Nagaraja R,
Nauck M,
Schurmann C,
Budde K,
Farrington SM,
Theodoratou E,
Jula A,
Salomaa V,
Sala C,
Hengstenberg C,
Burnier M,
Mägi R,
Klopp N,
Kloiber S,
Schipf S,
Ripatti S,
Cabras S,
Soranzo N,
Homuth G,
Nutile T,
Munroe PB,
Hastie N,
Campbell H,
Rudan I,
Cabrera C,
Haley C,
Franco OH,
Merriman TR,
Gudnason V,
Pirastu M,
Penninx BW,
Snieder H,
Metspalu A,
Ciullo M,
Pramstaller PP,
van Duijn CM,
Ferrucci L,
Gambaro G,
Deary IJ,
Dunlop MG,
Wilson JF,
Gasparini P,
Gyllensten U,
Spector TD,
Wright AF,
Hayward C,
Watkins H,
Perola M,
Bochud M,
Kao WH,
Caulfield M,
Toniolo D,
Völzke H,
Gieger C,
Köttgen A,
Vitart V
PloS one · 2015 · PMID 25811787 · open access
페이지 1개
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study
Hou L,
Heilbronner U,
Degenhardt F,
Adli M,
Akiyama K,
Akula N,
Ardau R,
Arias B,
Backlund L,
Banzato CEM,
Benabarre A,
Bengesser S
외 111명 — 모두 보기
Bhattacharjee AK,
Biernacka JM,
Birner A,
Brichant-Petitjean C,
Bui ET,
Cervantes P,
Chen GB,
Chen HC,
Chillotti C,
Cichon S,
Clark SR,
Colom F,
Cousins DA,
Cruceanu C,
Czerski PM,
Dantas CR,
Dayer A,
Étain B,
Falkai P,
Forstner AJ,
Frisén L,
Fullerton JM,
Gard S,
Garnham JS,
Goes FS,
Grof P,
Gruber O,
Hashimoto R,
Hauser J,
Herms S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kittel-Schneider S,
Kliwicki S,
König B,
Kusumi I,
Lackner N,
Laje G,
Landén M,
Lavebratt C,
Leboyer M,
Leckband SG,
Jaramillo CAL,
MacQueen G,
Manchia M,
Martinsson L,
Mattheisen M,
McCarthy MJ,
McElroy SL,
Mitjans M,
Mondimore FM,
Monteleone P,
Nievergelt CM,
Nöthen MM,
Ösby U,
Ozaki N,
Perlis RH,
Pfennig A,
Reich-Erkelenz D,
Rouleau GA,
Schofield PR,
Schubert KO,
Schweizer BW,
Seemüller F,
Severino G,
Shekhtman T,
Shilling PD,
Shimoda K,
Simhandl C,
Slaney CM,
Smoller JW,
Squassina A,
Stamm T,
Stopkova P,
Tighe SK,
Tortorella A,
Turecki G,
Volkert J,
Witt S,
Wright A,
Young LT,
Zandi PP,
Potash JB,
DePaulo JR,
Bauer M,
Reininghaus EZ,
Novák T,
Aubry JM,
Maj M,
Baune BT,
Mitchell PB,
Vieta E,
Frye MA,
Rybakowski JK,
Kuo PH,
Kato T,
Grigoroiu-Serbanescu M,
Reif A,
Del Zompo M,
Bellivier F,
Schalling M,
Wray NR,
Kelsoe JR,
Alda M,
Rietschel M,
McMahon FJ,
Schulze TG
Lancet (London, England) · 2016 · PMID 26806518 · open access
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