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성함이나 학술지명, PMID로 찾아보십시오.
Chen MH에 대해
39건, 그중 19건 표시.
Multiple loci are associated with white blood cell phenotypes
Nalls MA,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Toniolo D,
Zakai NA,
Yang Q,
Greinacher A,
Wood AR,
Garcia M
외 81명 — 모두 보기
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
페이지 3개
Clinical and genetic correlates of growth differentiation factor 15 in the community
Ho JE,
Mahajan A,
Chen MH,
Larson MG,
McCabe EL,
Ghorbani A,
Cheng S,
Johnson AD,
Lindgren CM,
Kempf T,
Lind L,
Ingelsson E
외 5명 — 모두 보기
Clinical chemistry · 2012 · PMID 22997280
페이지 2개
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
외 52명 — 모두 보기
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
페이지 2개
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Huang J,
Huffman JE,
Yamakuchi M,
Trompet S,
Asselbergs FW,
Sabater-Lleal M,
Trégouët DA,
Chen WM,
Smith NL,
Kleber ME,
Shin SY,
Becker DM
외 81명 — 모두 보기
Tang W,
Dehghan A,
Johnson AD,
Truong V,
Folkersen L,
Yang Q,
Oudot-Mellkah T,
Buckley BM,
Moore JH,
Williams FM,
Campbell H,
Silbernagel G,
Vitart V,
Rudan I,
Tofler GH,
Navis GJ,
Destefano A,
Wright AF,
Chen MH,
de Craen AJ,
Worrall BB,
Rudnicka AR,
Rumley A,
Bookman EB,
Psaty BM,
Chen F,
Keene KL,
Franco OH,
Böhm BO,
Uitterlinden AG,
Carter AM,
Jukema JW,
Sattar N,
Bis JC,
Bis JC,
Ikram MA,
Sale MM,
McKnight B,
Fornage M,
Ford I,
Taylor K,
Slagboom PE,
McArdle WL,
Hsu FC,
Franco-Cereceda A,
Goodall AH,
Yanek LR,
Furie KL,
Cushman M,
Hofman A,
Witteman JC,
Folsom AR,
Basu S,
Matijevic N,
van Gilst WH,
Wilson JF,
Westendorp RG,
Kathiresan S,
Reilly MP,
Tracy RP,
Polasek O,
Winkelmann BR,
Grant PJ,
Hillege HL,
Cambien F,
Stott DJ,
Lowe GD,
Spector TD,
Meigs JB,
Marz W,
Eriksson P,
Becker LC,
Morange PE,
Soranzo N,
Williams SM,
Hayward C,
van der Harst P,
Hamsten A,
Lowenstein CJ,
Strachan DP,
O'Donnell CJ
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium 외 컨소시엄 1곳
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
페이지 2개
Identification of new susceptibility loci for IgA nephropathy in Han Chinese
Li M,
Foo JN,
Wang JQ,
Low HQ,
Tang XQ,
Toh KY,
Yin PR,
Khor CC,
Goh YF,
Irwan ID,
Xu RC,
Andiappan AK
외 29명 — 모두 보기
Bei JX,
Rotzschke O,
Chen MH,
Cheng CY,
Sun LD,
Jiang GR,
Wong TY,
Lin HL,
Aung T,
Liao YH,
Saw SM,
Ye K,
Ebstein RP,
Chen QK,
Shi W,
Chew SH,
Chen J,
Zhang FR,
Li SP,
Xu G,
Shyong Tai E,
Wang L,
Chen N,
Zhang XJ,
Zeng YX,
Zhang H,
Liu ZH,
Yu XQ,
Liu JJ
Nature communications · 2015 · PMID 26028593 · open access
페이지 2개
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Lindström S,
Wang L,
Smith EN,
Gordon W,
van Hylckama Vlieg A,
de Andrade M,
Brody JA,
Pattee JW,
Haessler J,
Brumpton BM,
Chasman DI,
Suchon P
외 45명 — 모두 보기
Chen MH,
Turman C,
Germain M,
Wiggins KL,
MacDonald J,
Braekkan SK,
Armasu SM,
Pankratz N,
Jackson RD,
Nielsen JB,
Giulianini F,
Puurunen MK,
Ibrahim M,
Heckbert SR,
Damrauer SM,
Natarajan P,
Klarin D,
de Vries PS,
Sabater-Lleal M,
Huffman JE,
Bammler TK,
Frazer KA,
McCauley BM,
Taylor K,
Pankow JS,
Reiner AP,
Gabrielsen ME,
Deleuze JF,
O'Donnell CJ,
Kim J,
McKnight B,
Kraft P,
Hansen JB,
Rosendaal FR,
Heit JA,
Psaty BM,
Tang W,
Kooperberg C,
Hveem K,
Ridker PM,
Morange PE,
Johnson AD,
Kabrhel C,
Trégouët DA,
Smith NL
Million Veteran Program · CHARGE Hemostasis Working Group
Blood · 2019 · PMID 31420334
페이지 2개
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
Hu Y,
Sun Q,
Jain D,
Broome J,
Chen MH,
Thibord F,
McHugh C,
Surendran P,
Blackwell TW,
Brody JA,
Bhan A
외 55명 — 모두 보기
Chami N,
de Vries PS,
Ekunwe L,
Heard-Costa N,
Hobbs BD,
Manichaikul A,
Moon JY,
Preuss MH,
Ryan K,
Wang Z,
Wheeler M,
Yanek LR,
Abecasis GR,
Almasy L,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Choquet H,
Correa A,
Curran JE,
Faraday N,
Fornage M,
Glahn DC,
Hou L,
Jorgenson E,
Kooperberg C,
Lewis JP,
Lloyd-Jones DM,
Loos RJF,
Min YI,
Mitchell BD,
Morrison AC,
Nickerson DA,
North KE,
O'Connell JR,
Pankratz N,
Psaty BM,
Vasan RS,
Rich SS,
Rotter JI,
Smith AV,
Smith NL,
Tang H,
Tracy RP,
Conomos MP,
Laurie CA,
Mathias RA,
Li Y,
Auer PL,
Thornton T,
Reiner AP,
Johnson AD,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
페이지 2개
Genome-wide association meta-analysis for total serum bilirubin levels
Johnson AD,
Kavousi M,
Smith AV,
Chen MH,
Dehghan A,
Aspelund T,
Lin JP,
van Duijn CM,
Harris TB,
Cupples LA,
Uitterlinden AG,
Launer L
외 7명 — 모두 보기
Human molecular genetics · 2009 · PMID 19414484
페이지 1개
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts
Dehghan A,
Yang Q,
Peters A,
Basu S,
Bis JC,
Rudnicka AR,
Kavousi M,
Chen MH,
Baumert J,
Lowe GD,
McKnight B,
Tang W
외 29명 — 모두 보기
de Maat M,
Larson MG,
Eyhermendy S,
McArdle WL,
Lumley T,
Pankow JS,
Hofman A,
Massaro JM,
Rivadeneira F,
Kolz M,
Taylor KD,
van Duijn CM,
Kathiresan S,
Illig T,
Aulchenko YS,
Volcik KA,
Johnson AD,
Uitterlinden AG,
Tofler GH,
Gieger C,
Psaty BM,
Couper DJ,
Boerwinkle E,
Koenig W,
O'Donnell CJ,
Witteman JC,
Strachan DP,
Smith NL,
Folsom AR
Wellcome Trust Case Control Consortium
Circulation. Cardiovascular genetics · 2009 · PMID 20031576
페이지 1개
Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists
Johnson AD,
Yanek LR,
Chen MH,
Faraday N,
Larson MG,
Tofler G,
Lin SJ,
Kraja AT,
Province MA,
Yang Q,
Becker DM,
O'Donnell CJ
외 1명 — 모두 보기
Nature genetics · 2010 · PMID 20526338 · open access
페이지 1개
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3
Kaplan RC,
Petersen AK,
Chen MH,
Teumer A,
Glazer NL,
Döring A,
Lam CS,
Friedrich N,
Newman A,
Müller M,
Yang Q,
Homuth G
외 25명 — 모두 보기
Cappola A,
Klopp N,
Smith H,
Ernst F,
Psaty BM,
Wichmann HE,
Sawyer DB,
Biffar R,
Rotter JI,
Gieger C,
Sullivan LS,
Völzke H,
Rice K,
Spyroglou A,
Kroemer HK,
Ida Chen YD,
Manolopoulou J,
Nauck M,
Strickler HD,
Goodarzi MO,
Reincke M,
Pollak MN,
Bidlingmaier M,
Vasan RS,
Wallaschofski H
Human molecular genetics · 2011 · PMID 21216879
페이지 1개
CUBN is a gene locus for albuminuria
Böger CA,
Chen MH,
Tin A,
Olden M,
Köttgen A,
de Boer IH,
Fuchsberger C,
O'Seaghdha CM,
Pattaro C,
Teumer A,
Liu CT,
Glazer NL
외 103명 — 모두 보기
Li M,
O'Connell JR,
Tanaka T,
Peralta CA,
Kutalik Z,
Luan J,
Zhao JH,
Hwang SJ,
Akylbekova E,
Kramer H,
van der Harst P,
Smith AV,
Lohman K,
de Andrade M,
Hayward C,
Kollerits B,
Tönjes A,
Aspelund T,
Ingelsson E,
Eiriksdottir G,
Launer LJ,
Harris TB,
Shuldiner AR,
Mitchell BD,
Arking DE,
Franceschini N,
Boerwinkle E,
Egan J,
Hernandez D,
Reilly M,
Townsend RR,
Lumley T,
Siscovick DS,
Psaty BM,
Kestenbaum B,
Haritunians T,
Bergmann S,
Vollenweider P,
Waeber G,
Mooser V,
Waterworth D,
Johnson AD,
Florez JC,
Meigs JB,
Lu X,
Turner ST,
Atkinson EJ,
Leak TS,
Aasarød K,
Skorpen F,
Syvänen AC,
Illig T,
Baumert J,
Koenig W,
Krämer BK,
Devuyst O,
Mychaleckyj JC,
Minelli C,
Bakker SJ,
Kedenko L,
Paulweber B,
Coassin S,
Endlich K,
Kroemer HK,
Biffar R,
Stracke S,
Völzke H,
Stumvoll M,
Mägi R,
Campbell H,
Vitart V,
Hastie ND,
Gudnason V,
Kardia SL,
Liu Y,
Polasek O,
Curhan G,
Kronenberg F,
Prokopenko I,
Rudan I,
Arnlöv J,
Hallan S,
Navis G,
Parsa A,
Ferrucci L,
Coresh J,
Shlipak MG,
Bull SB,
Paterson NJ,
Wichmann HE,
Wareham NJ,
Loos RJ,
Rotter JI,
Pramstaller PP,
Cupples LA,
Beckmann JS,
Yang Q,
Heid IM,
Rettig R,
Dreisbach AW,
Bochud M,
Fox CS,
Kao WH
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
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
Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine
Lüneburg N,
Lieb W,
Zeller T,
Chen MH,
Maas R,
Carter AM,
Xanthakis V,
Glazer NL,
Schwedhelm E,
Seshadri S,
Ikram MA,
Longstreth WT Jr
외 32명 — 모두 보기
Fornage M,
König IR,
Loley C,
Ojeda FM,
Schillert A,
Wang TJ,
Sticht H,
Kittel A,
König J,
Benjamin EJ,
Sullivan LM,
Bernges I,
Anderssohn M,
Ziegler A,
Gieger C,
Illig T,
Meisinger C,
Wichmann HE,
Wild PS,
Schunkert H,
Psaty BM,
Wiggins KL,
Heckbert SR,
Smith N,
Lackner K,
Lunetta KL,
Blankenberg S,
Erdmann J,
Munzel T,
Grant PJ,
Vasan RS,
Böger RH
Circulation. Cardiovascular genetics · 2014 · PMID 25245031
페이지 1개
Genome-wide association study for endothelial growth factors
Lieb W,
Chen MH,
Larson MG,
Safa R,
Teumer A,
Baumeister SE,
Lin H,
Smith HM,
Koch M,
Lorbeer R,
Völker U,
Nauck M
외 4명 — 모두 보기
Circulation. Cardiovascular genetics · 2015 · PMID 25552591
페이지 1개
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study
Musani SK,
Fox ER,
Kraja A,
Bidulescu A,
Lieb W,
Lin H,
Beecham A,
Chen MH,
Felix JF,
Fox CS,
Kao WH,
Kardia SL
외 11명 — 모두 보기
Liu CT,
Nalls MA,
Rundek T,
Sacco RL,
Smith J,
Sun YV,
Wilson G,
Zhang Z,
Mosley TH,
Taylor HA,
Vasan RS
Circulation. Cardiovascular genetics · 2015 · PMID 25561047
페이지 1개
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels
Zhang W,
Jernerén F,
Lehne BC,
Chen MH,
Luben RN,
Johnston C,
Elshorbagy A,
Eppinga RN,
Scott WR,
Adeyeye E,
Scott J,
Böger RH
외 7명 — 모두 보기
Thrombosis and haemostasis · 2016 · PMID 27656708
페이지 1개
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy
Li M,
Wang L,
Shi DC,
Foo JN,
Zhong Z,
Khor CC,
Lanzani C,
Citterio L,
Salvi E,
Yin PR,
Bei JX,
Wang L
외 13명 — 모두 보기
Liao YH,
Chen J,
Chen QK,
Xu G,
Jiang GR,
Wan JX,
Chen MH,
Chen N,
Zhang H,
Zeng YX,
Liu ZH,
Liu JJ,
Yu XQ
Journal of the American Society of Nephrology : JASN · 2020 · PMID 32912934
페이지 1개
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Mikhaylova AV,
McHugh CP,
Polfus LM,
Raffield LM,
Boorgula MP,
Blackwell TW,
Brody JA,
Broome J,
Chami N,
Chen MH,
Conomos MP,
Cox C
외 81명 — 모두 보기
Curran JE,
Daya M,
Ekunwe L,
Glahn DC,
Heard-Costa N,
Highland HM,
Hobbs BD,
Ilboudo Y,
Jain D,
Lange LA,
Miller-Fleming TW,
Min N,
Moon JY,
Preuss MH,
Rosen J,
Ryan K,
Smith AV,
Sun Q,
Surendran P,
de Vries PS,
Walter K,
Wang Z,
Wheeler M,
Yanek LR,
Zhong X,
Abecasis GR,
Almasy L,
Barnes KC,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Chavan S,
Cho MH,
Choquet H,
Correa A,
Cox N,
DeMeo DL,
Faraday N,
Fornage M,
Gerszten RE,
Hou L,
Johnson AD,
Jorgenson E,
Kaplan R,
Kooperberg C,
Kundu K,
Laurie CA,
Lettre G,
Lewis JP,
Li B,
Li Y,
Lloyd-Jones DM,
Loos RJF,
Manichaikul A,
Meyers DA,
Mitchell BD,
Morrison AC,
Ngo D,
Nickerson DA,
Nongmaithem S,
North KE,
O'Connell JR,
Ortega VE,
Pankratz N,
Perry JA,
Psaty BM,
Rich SS,
Soranzo N,
Rotter JI,
Silverman EK,
Smith NL,
Tang H,
Tracy RP,
Thornton TA,
Vasan RS,
Zein J,
Mathias RA,
Reiner AP,
Auer PL
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
페이지 1개
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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.