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Ma J에 대해
101건, 그중 20건 표시.
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
Dehghan A,
Bis JC,
White CC,
Smith AV,
Morrison AC,
Cupples LA,
Trompet S,
Chasman DI,
Lumley T,
Völker U,
Buckley BM,
Ding J
외 55명 — 모두 보기
Jensen MK,
Folsom AR,
Kritchevsky SB,
Girman CJ,
Ford I,
Dörr M,
Salomaa V,
Uitterlinden AG,
Eiriksdottir G,
Vasan RS,
Franceschini N,
Carty CL,
Virtamo J,
Demissie S,
Amouyel P,
Arveiler D,
Heckbert SR,
Ferrières J,
Ducimetière P,
Smith NL,
Wang YA,
Siscovick DS,
Rice KM,
Wiklund PG,
Taylor KD,
Evans A,
Kee F,
Rotter JI,
Karvanen J,
Kuulasmaa K,
Heiss G,
Kraft P,
Launer LJ,
Hofman A,
Markus MR,
Rose LM,
Silander K,
Wagner P,
Benjamin EJ,
Lohman K,
Stott DJ,
Rivadeneira F,
Harris TB,
Levy D,
Liu Y,
Rimm EB,
Jukema JW,
Völzke H,
Ridker PM,
Blankenberg S,
Franco OH,
Gudnason V,
Psaty BM,
Boerwinkle E,
O'Donnell CJ
PloS one · 2016 · PMID 26950853 · open access
페이지 2개
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
van Leeuwen EM,
Sabo A,
Bis JC,
Huffman JE,
Manichaikul A,
Smith AV,
Feitosa MF,
Demissie S,
Joshi PK,
Duan Q,
Marten J,
van Klinken JB
외 86명 — 모두 보기
Surakka I,
Nolte IM,
Zhang W,
Mbarek H,
Li-Gao R,
Trompet S,
Verweij N,
Evangelou E,
Lyytikäinen LP,
Tayo BO,
Deelen J,
van der Most PJ,
van der Laan SW,
Arking DE,
Morrison A,
Dehghan A,
Franco OH,
Hofman A,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Mychaleckyj JC,
Campbell A,
Hocking LJ,
Padmanabhan S,
Brody JA,
Rice KM,
White CC,
Harris T,
Isaacs A,
Campbell H,
Lange LA,
Rudan I,
Kolcic I,
Navarro P,
Zemunik T,
Salomaa V,
Kooner AS,
Kooner JS,
Lehne B,
Scott WR,
Tan ST,
de Geus EJ,
Milaneschi Y,
Penninx BW,
Willemsen G,
de Mutsert R,
Ford I,
Gansevoort RT,
Segura-Lepe MP,
Raitakari OT,
Viikari JS,
Nikus K,
Forrester T,
McKenzie CA,
de Craen AJ,
de Ruijter HM,
Pasterkamp G,
Snieder H,
Oldehinkel AJ,
Slagboom PE,
Cooper RS,
Kähönen M,
Lehtimäki T,
Elliott P,
van der Harst P,
Jukema JW,
Mook-Kanamori DO,
Boomsma DI,
Chambers JC,
Swertz M,
Ripatti S,
Willems van Dijk K,
Vitart V,
Polasek O,
Hayward C,
Wilson JG,
Wilson JF,
Gudnason V,
Rich SS,
Psaty BM,
Borecki IB,
Boerwinkle E,
Rotter JI,
Cupples LA,
van Duijn CM
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
페이지 2개
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
외 76명 — 모두 보기
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
페이지 2개
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Jiang X,
O'Reilly PF,
Aschard H,
Aschard H,
Hsu YH,
Richards JB,
Dupuis J,
Ingelsson E,
Karasik D,
Pilz S,
Berry D,
Kestenbaum B
외 93명 — 모두 보기
Zheng J,
Luan J,
Sofianopoulou E,
Streeten EA,
Albanes D,
Lutsey PL,
Yao L,
Tang W,
Econs MJ,
Wallaschofski H,
Völzke H,
Zhou A,
Power C,
McCarthy MI,
Michos ED,
Boerwinkle E,
Weinstein SJ,
Freedman ND,
Huang WY,
Van Schoor NM,
van der Velde N,
Groot LCPGM,
Enneman A,
Cupples LA,
Booth SL,
Vasan RS,
Liu CT,
Zhou Y,
Ripatti S,
Ohlsson C,
Vandenput L,
Lorentzon M,
Eriksson JG,
Shea MK,
Houston DK,
Kritchevsky SB,
Liu Y,
Lohman KK,
Ferrucci L,
Peacock M,
Gieger C,
Beekman M,
Slagboom E,
Deelen J,
Heemst DV,
Kleber ME,
März W,
de Boer IH,
Wood AC,
Rotter JI,
Rich SS,
Robinson-Cohen C,
den Heijer M,
Jarvelin MR,
Cavadino A,
Joshi PK,
Wilson JF,
Hayward C,
Lind L,
Michaëlsson K,
Trompet S,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Broer L,
Zgaga L,
Campbell H,
Theodoratou E,
Farrington SM,
Timofeeva M,
Dunlop MG,
Valdes AM,
Tikkanen E,
Lehtimäki T,
Lyytikäinen LP,
Kähönen M,
Raitakari OT,
Mikkilä V,
Ikram MA,
Sattar N,
Jukema JW,
Wareham NJ,
Langenberg C,
Forouhi NG,
Gundersen TE,
Khaw KT,
Butterworth AS,
Danesh J,
Spector T,
Wang TJ,
Hyppönen E,
Kraft P,
Kiel DP
Nature communications · 2018 · PMID 29343764 · open access
페이지 2개
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Armstrong NJ,
Mather KA,
Sargurupremraj M,
Knol MJ,
Malik R,
Satizabal CL,
Yanek LR,
Wen W,
Gudnason VG,
Dueker ND,
Elliott LT,
Hofer E
외 74명 — 모두 보기
Bis J,
Jahanshad N,
Li S,
Logue MA,
Luciano M,
Scholz M,
Smith AV,
Trompet S,
Vojinovic D,
Xia R,
Alfaro-Almagro F,
Ames D,
Amin N,
Amouyel P,
Beiser AS,
Brodaty H,
Deary IJ,
Fennema-Notestine C,
Gampawar PG,
Gottesman R,
Griffanti L,
Jack CR Jr,
Jenkinson M,
Jiang J,
Kral BG,
Kwok JB,
Lampe L,
C M Liewald D,
Maillard P,
Marchini J,
Bastin ME,
Mazoyer B,
Pirpamer L,
Rafael Romero J,
Roshchupkin GV,
Schofield PR,
Schroeter ML,
Stott DJ,
Thalamuthu A,
Trollor J,
Tzourio C,
van der Grond J,
Vernooij MW,
Witte VA,
Wright MJ,
Yang Q,
Morris Z,
Siggurdsson S,
Psaty B,
Villringer A,
Schmidt H,
Haberg AK,
van Duijn CM,
Jukema JW,
Dichgans M,
Sacco RL,
Wright CB,
Kremen WS,
Becker LC,
Thompson PM,
Mosley TH,
Wardlaw JM,
Ikram MA,
Adams HHH,
Seshadri S,
Sachdev PS,
Smith SM,
Launer L,
Longstreth W,
DeCarli C,
Schmidt R,
Fornage M,
Debette S,
Nyquist PA
Stroke · 2020 · PMID 32517579
페이지 2개
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 study identifies two new risk loci for Graves' disease
Chu X,
Pan CM,
Zhao SX,
Liang J,
Gao GQ,
Zhang XM,
Yuan GY,
Li CG,
Xue LQ,
Shen M,
Liu W,
Xie F
외 36명 — 모두 보기
Yang SY,
Wang HF,
Shi JY,
Sun WW,
Du WH,
Zuo CL,
Shi JX,
Liu BL,
Guo CC,
Zhan M,
Gu ZH,
Zhang XN,
Sun F,
Wang ZQ,
Song ZY,
Zou CY,
Sun WH,
Guo T,
Cao HM,
Ma JH,
Han B,
Li P,
Jiang H,
Huang QH,
Liang L,
Liu LB,
Chen G,
Su Q,
Peng YD,
Zhao JJ,
Ning G,
Chen Z,
Chen JL,
Chen SJ,
Huang W,
Song HD
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
페이지 1개
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis
Peters U,
Jiao S,
Schumacher FR,
Hutter CM,
Aragaki AK,
Baron JA,
Berndt SI,
Bézieau S,
Brenner H,
Butterbach K,
Caan BJ,
Campbell PT
외 65명 — 모두 보기
Carlson CS,
Casey G,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chen LS,
Coetzee GA,
Coetzee SG,
Conti DV,
Curtis KR,
Duggan D,
Edwards T,
Fuchs CS,
Gallinger S,
Giovannucci EL,
Gogarten SM,
Gruber SB,
Haile RW,
Harrison TA,
Hayes RB,
Henderson BE,
Hoffmeister M,
Hopper JL,
Hudson TJ,
Hunter DJ,
Jackson RD,
Jee SH,
Jenkins MA,
Jia WH,
Kolonel LN,
Kooperberg C,
Küry S,
Lacroix AZ,
Laurie CC,
Laurie CA,
Le Marchand L,
Lemire M,
Levine D,
Lindor NM,
Liu Y,
Ma J,
Makar KW,
Matsuo K,
Newcomb PA,
Potter JD,
Prentice RL,
Qu C,
Rohan T,
Rosse SA,
Schoen RE,
Seminara D,
Shrubsole M,
Shu XO,
Slattery ML,
Taverna D,
Thibodeau SN,
Ulrich CM,
White E,
Xiang Y,
Zanke BW,
Zeng YX,
Zhang B,
Zheng W,
Zheng W,
Hsu L
Colon Cancer Family Registry and the Genetics and Epidemiology of Colorectal Cancer Consortium
Gastroenterology · 2013 · PMID 23266556
페이지 1개
Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics
Wu AC,
Himes BE,
Lasky-Su J,
Litonjua A,
Peters SP,
Lima J,
Kubo M,
Tamari M,
Nakamura Y,
Qiu W,
Weiss ST,
Tantisira K
The Journal of allergy and clinical immunology · 2014 · PMID 24280104
페이지 1개
CETP (Cholesteryl Ester Transfer Protein) Concentration: A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease
Blauw LL,
Li-Gao R,
Noordam R,
de Mutsert R,
Trompet S,
Berbée JFP,
Wang Y,
van Klinken JB,
Christen T,
van Heemst D,
Mook-Kanamori DO,
Rosendaal FR
외 3명 — 모두 보기
Circulation. Genomic and precision medicine · 2018 · PMID 29728394
페이지 1개
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Bihlmeyer NA,
Brody JA,
Smith AV,
Warren HR,
Lin H,
Isaacs A,
Liu CT,
Marten J,
Radmanesh F,
Hall LM,
Grarup N,
Mei H
외 88명 — 모두 보기
Müller-Nurasyid M,
Huffman JE,
Verweij N,
Guo X,
Yao J,
Li-Gao R,
van den Berg M,
Weiss S,
Prins BP,
van Setten J,
Haessler J,
Lyytikäinen LP,
Li M,
Alonso A,
Soliman EZ,
Bis JC,
Austin T,
Chen YI,
Psaty BM,
Harrris TB,
Launer LJ,
Padmanabhan S,
Dominiczak A,
Huang PL,
Xie Z,
Ellinor PT,
Kors JA,
Campbell A,
Murray AD,
Nelson CP,
Tobin MD,
Bork-Jensen J,
Hansen T,
Pedersen O,
Linneberg A,
Sinner MF,
Peters A,
Waldenberger M,
Meitinger T,
Perz S,
Kolcic I,
Rudan I,
de Boer RA,
van der Meer P,
Lin HJ,
Taylor KD,
de Mutsert R,
Trompet S,
Jukema JW,
Maan AC,
Stricker BHC,
Rivadeneira F,
Uitterlinden A,
Völker U,
Homuth G,
Völzke H,
Felix SB,
Mangino M,
Spector TD,
Bots ML,
Perez M,
Raitakari OT,
Kähönen M,
Mononen N,
Gudnason V,
Munroe PB,
Lubitz SA,
van Duijn CM,
Newton-Cheh CH,
Hayward C,
Rosand J,
Samani NJ,
Kanters JK,
Wilson JG,
Kääb S,
Polasek O,
van der Harst P,
Heckbert SR,
Rotter JI,
Mook-Kanamori DO,
Eijgelsheim M,
Dörr M,
Jamshidi Y,
Asselbergs FW,
Kooperberg C,
Lehtimäki T,
Arking DE,
Sotoodehnia N
Circulation. Genomic and precision medicine · 2018 · PMID 29874175 · open access
페이지 1개
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
Bis JC,
Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
Saba Y,
Luciano M
외 79명 — 모두 보기
Bernard M,
Trompet S,
Yang J,
Gillespie NA,
van der Lee SJ,
Neumann A,
Ahmad S,
Andreassen OA,
Ames D,
Amin N,
Arfanakis K,
Bastin ME,
Becker DM,
Beiser AS,
Beyer F,
Brodaty H,
Bryan RN,
Bülow R,
Dale AM,
De Jager PL,
Deary IJ,
DeCarli C,
Fleischman DA,
Gottesman RF,
van der Grond J,
Gudnason V,
Harris TB,
Homuth G,
Knopman DS,
Kwok JB,
Lewis CE,
Li S,
Loeffler M,
Lopez OL,
Maillard P,
El Marroun H,
Mather KA,
Mosley TH,
Muetzel RL,
Nauck M,
Nyquist PA,
Panizzon MS,
Pausova Z,
Psaty BM,
Rice K,
Rotter JI,
Royle N,
Satizabal CL,
Schmidt R,
Schofield PR,
Schreiner PJ,
Sidney S,
Stott DJ,
Thalamuthu A,
Uitterlinden AG,
Valdés Hernández MC,
Vernooij MW,
Wen W,
White T,
Witte AV,
Wittfeld K,
Wright MJ,
Yanek LR,
Tiemeier H,
Kremen WS,
Bennett DA,
Jukema JW,
Paus T,
Wardlaw JM,
Schmidt H,
Sachdev PS,
Villringer A,
Grabe HJ,
Longstreth WT,
van Duijn CM,
Launer LJ,
Seshadri S,
Ikram MA,
Fornage M
Nature communications · 2018 · PMID 30258056 · open access
페이지 1개
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
Zhao SX,
Liu W,
Liang J,
Gao GQ,
Zhang XM,
Yao Y,
Wang HN,
Yuan FF,
Xue LQ,
Ma YR,
Zhang LL,
Ye XP
외 25명 — 모두 보기
Zhang QY,
Sun F,
Zhang RJ,
Yang SY,
Zhan M,
Du WH,
Liu BL,
Chen X,
Song ZY,
Li XS,
Li P,
Ru Y,
Zuo CL,
Li SX,
Han B,
Zhu H,
Qiao J,
Xuan M,
Su B,
Sun F,
Ma JH,
Chen JL,
Tian HM,
Chen SJ,
Song HD
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
페이지 1개
Sex specific associations in genome wide association analysis of renal cell carcinoma
Laskar RS,
Muller DC,
Li P,
Machiela MJ,
Ye Y,
Gaborieau V,
Foll M,
Hofmann JN,
Colli L,
Sampson JN,
Wang Z,
Bacq-Daian D
외 96명 — 모두 보기
Boland A,
Abedi-Ardekani B,
Durand G,
Le Calvez-Kelm F,
Robinot N,
Blanche H,
Prokhortchouk E,
Skryabin KG,
Burdett L,
Yeager M,
Radojevic-Skodric S,
Savic S,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Rascu S,
Mukeria A,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Świątkowska B,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Trichopoulou A,
Riboli E,
Overvad K,
Panico S,
Ljungberg B,
Sitaram RT,
Giles GG,
Milne RL,
Severi G,
Bruinsma F,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Beane Freeman LE,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Chow WH,
Moore LE,
Choueiri TK,
Wood C,
Johansson M,
McKay JD,
Brown KM,
Rothman N,
Lathrop MG,
Deleuze JF,
Wu X,
Brennan P,
Chanock SJ,
Purdue MP,
Scelo G
European journal of human genetics : EJHG · 2019 · PMID 31231134
페이지 1개
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
Irvin MR,
Sitlani CM,
Floyd JS,
Psaty BM,
Bis JC,
Wiggins KL,
Whitsel EA,
Sturmer T,
Stewart J,
Raffield L,
Sun F,
Liu CT
외 32명 — 모두 보기
Xu H,
Cupples AL,
Tanner RM,
Rossing P,
Smith A,
Zilhão NR,
Launer LJ,
Noordam R,
Rotter JI,
Yao J,
Li X,
Guo X,
Limdi N,
Sundaresan A,
Lange L,
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