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31 matches for
Tang H,
showing the first 20.
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Feitosa MF,
Kraja AT,
Chasman DI,
Sung YJ,
Winkler TW,
Ntalla I,
Guo X,
Franceschini N,
Cheng CY,
Sim X,
Vojinovic D,
Marten J
and 261 more — show all
Musani SK,
Li C,
Bentley AR,
Brown MR,
Schwander K,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Wojczynski MK,
Alver M,
Boissel M,
Cai Q,
Campbell A,
Chai JF,
Chen X,
Divers J,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Kähönen M,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Luan J,
Matoba N,
Nolte IM,
Padmanabhan S,
Riaz M,
Rueedi R,
Robino A,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Vitart V,
Wang Y,
Ware EB,
Warren HR,
Weiss S,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Boerwinkle E,
Borecki I,
Broeckel U,
Brown M,
Brumat M,
Burke GL,
Canouil M,
Chakravarti A,
Charumathi S,
Ida Chen YD,
Connell JM,
Correa A,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Deng X,
Ding J,
Duan Q,
Eaton CB,
Ehret G,
Eppinga RN,
Evangelou E,
Faul JD,
Felix SB,
Forouhi NG,
Forrester T,
Franco OH,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gigante B,
Gu CC,
Gu D,
Hagenaars SP,
Hallmans G,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hirata M,
Howard BV,
Ikram MA,
John U,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Lin S,
Liu J,
Liu J,
Loh M,
Louie T,
Mägi R,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Nalls MA,
Nelson CP,
Sotoodehnia N,
Norris JM,
O'Connell JR,
Palmer ND,
Perls T,
Pedersen NL,
Peters A,
Peyser PA,
Poulter N,
Raffel LJ,
Raitakari OT,
Roll K,
Rose LM,
Rosendaal FR,
Rotter JI,
Schmidt CO,
Schreiner PJ,
Schupf N,
Scott WR,
Sever PS,
Shi Y,
Sidney S,
Sims M,
Sitlani CM,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Turner ST,
Uitterlinden AG,
Vollenweider P,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Williams C,
Yao J,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Jonas JB,
Kamatani Y,
Kato N,
Kooner JS,
Kutalik Z,
Laakso M,
Laurie CC,
Leander K,
Lehtimäki T,
Study LC,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Polasek O,
Porteous DJ,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zheng W,
Bouchard C,
Christensen K,
Evans MK,
Gudnason V,
Horta BL,
Kardia SLR,
Liu Y,
Pereira AC,
Psaty BM,
Ridker PM,
van Dam RM,
Gauderman WJ,
Zhu X,
Mook-Kanamori DO,
Fornage M,
Rotimi CN,
Cupples LA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Kooperberg C,
Palmas W,
Rice K,
Morrison AC,
Elliott P,
Caulfield MJ,
Munroe PB,
Rao DC,
Province MA,
Levy D
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Klarin D,
Damrauer SM,
Cho K,
Sun YV,
Teslovich TM,
Honerlaw J,
Gagnon DR,
DuVall SL,
Li J,
Peloso GM,
Chaffin M,
Small AM
and 33 more — show all
Huang J,
Tang H,
Lynch JA,
Ho YL,
Liu DJ,
Emdin CA,
Li AH,
Huffman JE,
Lee JS,
Natarajan P,
Chowdhury R,
Saleheen D,
Vujkovic M,
Baras A,
Pyarajan S,
Di Angelantonio E,
Neale BM,
Naheed A,
Khera AV,
Danesh J,
Chang KM,
Abecasis G,
Willer C,
Dewey FE,
Carey DJ,
Concato J,
Gaziano JM,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Rader DJ,
Wilson PWF,
Assimes TL
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Kilpeläinen TO,
Bentley AR,
Noordam R,
Sung YJ,
Schwander K,
Winkler TW,
Jakupović H,
Chasman DI,
Manning A,
Ntalla I,
Aschard H,
Brown MR
and 217 more — show all
de las Fuentes L,
Franceschini N,
Guo X,
Vojinovic D,
Aslibekyan S,
Feitosa MF,
Kho M,
Musani SK,
Richard M,
Wang H,
Wang Z,
Bartz TM,
Bielak LF,
Campbell A,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Li C,
Lohman KK,
Marten J,
Sim X,
Smith AV,
Tajuddin SM,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Graff M,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Zhao JH,
Kraja AT,
Kühnel B,
Laguzzi F,
Lyytikäinen LP,
Nolte IM,
Rauramaa R,
Riaz M,
Robino A,
Rueedi R,
Stringham HM,
Takeuchi F,
van der Most PJ,
Varga TV,
Verweij N,
Ware EB,
Wen W,
Li X,
Yanek LR,
Amin N,
Arnett DK,
Boerwinkle E,
Brumat M,
Cade B,
Canouil M,
Chen YI,
Concas MP,
Connell J,
de Mutsert R,
de Silva HJ,
de Vries PS,
Demirkan A,
Ding J,
Eaton CB,
Faul JD,
Friedlander Y,
Gabriel KP,
Ghanbari M,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt SC,
Ikram MA,
Jonas JB,
Koh WP,
Komulainen P,
Krieger JE,
Kritchevsky SB,
Kutalik Z,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Leander K,
Lemaitre RN,
Lewis CE,
Liang J,
Liu J,
Mägi R,
Manichaikul A,
Meitinger T,
Metspalu A,
Milaneschi Y,
Mohlke KL,
Mosley TH Jr,
Murray AD,
Nalls MA,
Nang EK,
Nelson CP,
Nona S,
Norris JM,
Nwuba CV,
O'Connell J,
Palmer ND,
Papanicolau GJ,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Porteous DJ,
Poveda A,
Raitakari OT,
Rich SS,
Risch N,
Robinson JG,
Rose LM,
Rudan I,
Schreiner PJ,
Scott RA,
Sidney SS,
Sims M,
Smith JA,
Snieder H,
Sofer T,
Starr JM,
Sternfeld B,
Strauch K,
Tang H,
Taylor KD,
Tsai MY,
Tuomilehto J,
Uitterlinden AG,
van der Ende MY,
van Heemst D,
Voortman T,
Waldenberger M,
Wennberg P,
Wilson G,
Xiang YB,
Yao J,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Kato N,
Laakso M,
Lakka TA,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Samani NJ,
Shu XO,
van der Harst P,
Van Vliet-Ostaptchouk JV,
Vollenweider P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Weir DR,
Wu T,
Zheng W,
Zhu X,
Evans MK,
Franks PW,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Liu Y,
North KE,
Pereira AC,
Ridker PM,
Tai ES,
van Dam RM,
Fox ER,
Kardia SLR,
Liu CT,
Mook-Kanamori DO,
Province MA,
Redline S,
van Duijn CM,
Rotter JI,
Kooperberg CB,
Gauderman WJ,
Psaty BM,
Rice K,
Munroe PB,
Fornage M,
Cupples LA,
Rotimi CN,
Morrison AC,
Rao DC,
Loos RJF
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
and 98 more — show all
Manansala R,
Laplante V,
Chen M,
Lo KS,
Qian H,
Lareau CA,
Beaudoin M,
Hunt KA,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala K,
Cho K,
Choquet H,
Correa A,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Lerch MM,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nauck M,
Nikus K,
Ouwehand WH,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Roberts DJ,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Trembath RC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Zonderman AB,
Wilson PWF,
Li Y,
Butterworth AS,
Gauchat JF,
Chiang CWK,
Li B,
Loos RJF,
Astle WJ,
Evangelou E,
van Heel DA,
Sankaran VG,
Okada Y,
Soranzo N,
Johnson AD,
Reiner AP,
Auer PL,
Lettre G
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
Megy K
and 100 more — show all
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
Lo KS,
Qian H,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala KN,
Wilson PWF,
Choquet H,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Felix SB,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Guo Q,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nikus K,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Weiss S,
Cai N,
Kundu K,
Watt SB,
Walter K,
Zonderman AB,
Cho K,
Li Y,
Loos RJF,
Knight JC,
Georges M,
Stegle O,
Evangelou E,
Okada Y,
Roberts DJ,
Inouye M,
Johnson AD,
Auer PL,
Astle WJ,
Reiner AP,
Butterworth AS,
Ouwehand WH,
Lettre G,
Sankaran VG,
Soranzo N
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Hu Y,
Stilp AM,
McHugh CP,
Rao S,
Jain D,
Zheng X,
Lane J,
Méric de Bellefon S,
Raffield LM,
Chen MH,
Yanek LR,
Wheeler M
and 67 more — show all
Yao Y,
Ren C,
Broome J,
Moon JY,
de Vries PS,
Hobbs BD,
Sun Q,
Surendran P,
Brody JA,
Blackwell TW,
Choquet H,
Ryan K,
Duggirala R,
Heard-Costa N,
Wang Z,
Chami N,
Preuss MH,
Min N,
Ekunwe L,
Lange LA,
Cushman M,
Faraday N,
Curran JE,
Almasy L,
Kundu K,
Smith AV,
Gabriel S,
Rotter JI,
Fornage M,
Lloyd-Jones DM,
Vasan RS,
Smith NL,
North KE,
Boerwinkle E,
Becker LC,
Lewis JP,
Abecasis GR,
Hou L,
O'Connell JR,
Morrison AC,
Beaty TH,
Kaplan R,
Correa A,
Blangero J,
Jorgenson E,
Psaty BM,
Kooperberg C,
Walton RT,
Kleinstiver BP,
Tang H,
Loos RJF,
Soranzo N,
Butterworth AS,
Nickerson D,
Rich SS,
Mitchell BD,
Johnson AD,
Auer PL,
Li Y,
Mathias RA,
Lettre G,
Pankratz N,
Laurie CC,
Laurie CA,
Bauer DE,
Conomos MP,
Reiner AP
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
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
and 610 more — show all
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,
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Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
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Pan HF,
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American journal of human genetics · 2013 · PMID 23273568
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American journal of human genetics · 2013 · PMID 23726366
5 pages
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
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The Journal of investigative dermatology · 2023 · PMID 35933036
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