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12 matches for
Hung AM.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Evangelou E,
Warren HR,
Mosen-Ansorena D,
Mifsud B,
Pazoki R,
Gao H,
Ntritsos G,
Dimou N,
Cabrera CP,
Karaman I,
Ng FL,
Evangelou M
and 268 more — show all
Witkowska K,
Tzanis E,
Hellwege JN,
Giri A,
Velez Edwards DR,
Sun YV,
Cho K,
Gaziano JM,
Wilson PWF,
Tsao PS,
Kovesdy CP,
Esko T,
Mägi R,
Milani L,
Almgren P,
Boutin T,
Debette S,
Ding J,
Giulianini F,
Holliday EG,
Jackson AU,
Li-Gao R,
Lin WY,
Luan J,
Mangino M,
Oldmeadow C,
Prins BP,
Qian Y,
Sargurupremraj M,
Shah N,
Surendran P,
Thériault S,
Verweij N,
Willems SM,
Zhao JH,
Amouyel P,
Connell J,
de Mutsert R,
Doney ASF,
Farrall M,
Menni C,
Morris AD,
Noordam R,
Paré G,
Poulter NR,
Shields DC,
Stanton A,
Thom S,
Abecasis G,
Amin N,
Arking DE,
Ayers KL,
Barbieri CM,
Batini C,
Bis JC,
Blake T,
Bochud M,
Boehnke M,
Boerwinkle E,
Boomsma DI,
Bottinger EP,
Braund PS,
Brumat M,
Campbell A,
Campbell H,
Chakravarti A,
Chambers JC,
Chauhan G,
Ciullo M,
Cocca M,
Collins F,
Cordell HJ,
Davies G,
de Borst MH,
de Geus EJ,
Deary IJ,
Deelen J,
Del Greco M F,
Demirkale CY,
Dörr M,
Ehret GB,
Elosua R,
Enroth S,
Erzurumluoglu AM,
Ferreira T,
Frånberg M,
Franco OH,
Gandin I,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Goel A,
Gow AJ,
Gudnason V,
Guo X,
Gyllensten U,
Hamsten A,
Harris TB,
Harris SE,
Hartman CA,
Havulinna AS,
Hicks AA,
Hofer E,
Hofman A,
Hottenga JJ,
Huffman JE,
Hwang SJ,
Ingelsson E,
James A,
Jansen R,
Jarvelin MR,
Joehanes R,
Johansson Å,
Johnson AD,
Joshi PK,
Jousilahti P,
Jukema JW,
Jula A,
Kähönen M,
Kathiresan S,
Keavney BD,
Khaw KT,
Knekt P,
Knight J,
Kolcic I,
Kooner JS,
Koskinen S,
Kristiansson K,
Kutalik Z,
Laan M,
Larson M,
Launer LJ,
Lehne B,
Lehtimäki T,
Liewald DCM,
Lin L,
Lind L,
Lindgren CM,
Liu Y,
Loos RJF,
Lopez LM,
Lu Y,
Lyytikäinen LP,
Mahajan A,
Mamasoula C,
Marrugat J,
Marten J,
Milaneschi Y,
Morgan A,
Morris AP,
Morrison AC,
Munson PJ,
Nalls MA,
Nandakumar P,
Nelson CP,
Niiranen T,
Nolte IM,
Nutile T,
Oldehinkel AJ,
Oostra BA,
O'Reilly PF,
Org E,
Padmanabhan S,
Palmas W,
Palotie A,
Pattie A,
Penninx BWJH,
Perola M,
Peters A,
Polasek O,
Pramstaller PP,
Nguyen QT,
Raitakari OT,
Ren M,
Rettig R,
Rice K,
Ridker PM,
Ried JS,
Riese H,
Ripatti S,
Robino A,
Rose LM,
Rotter JI,
Rudan I,
Ruggiero D,
Saba Y,
Sala CF,
Salomaa V,
Samani NJ,
Sarin AP,
Schmidt R,
Schmidt H,
Shrine N,
Siscovick D,
Smith AV,
Snieder H,
Sõber S,
Sorice R,
Starr JM,
Stott DJ,
Strachan DP,
Strawbridge RJ,
Sundström J,
Swertz MA,
Taylor KD,
Teumer A,
Tobin MD,
Tomaszewski M,
Toniolo D,
Traglia M,
Trompet S,
Tuomilehto J,
Tzourio C,
Uitterlinden AG,
Vaez A,
van der Most PJ,
van Duijn CM,
Vergnaud AC,
Verwoert GC,
Vitart V,
Völker U,
Vollenweider P,
Vuckovic D,
Watkins H,
Wild SH,
Willemsen G,
Wilson JF,
Wright AF,
Yao J,
Zemunik T,
Zhang W,
Attia JR,
Butterworth AS,
Chasman DI,
Conen D,
Cucca F,
Danesh J,
Hayward C,
Howson JMM,
Laakso M,
Lakatta EG,
Langenberg C,
Melander O,
Mook-Kanamori DO,
Palmer CNA,
Risch L,
Scott RA,
Scott RJ,
Sever P,
Spector TD,
van der Harst P,
Wareham NJ,
Zeggini E,
Levy D,
Munroe PB,
Newton-Cheh C,
Brown MJ,
Metspalu A,
Hung AM,
O'Donnell CJ,
Edwards TL,
Psaty BM,
Tzoulaki I,
Barnes MR,
Wain LV,
Elliott P,
Caulfield MJ
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Giri A,
Hellwege JN,
Keaton JM,
Park J,
Qiu C,
Warren HR,
Torstenson ES,
Kovesdy CP,
Sun YV,
Wilson OD,
Robinson-Cohen C,
Roumie CL
and 86 more — show all
Chung CP,
Birdwell KA,
Damrauer SM,
DuVall SL,
Klarin D,
Cho K,
Wang Y,
Evangelou E,
Cabrera CP,
Wain LV,
Shrestha R,
Mautz BS,
Akwo EA,
Sargurupremraj M,
Debette S,
Boehnke M,
Scott LJ,
Luan J,
Zhao JH,
Willems SM,
Thériault S,
Shah N,
Oldmeadow C,
Almgren P,
Li-Gao R,
Verweij N,
Boutin TS,
Mangino M,
Ntalla I,
Feofanova E,
Surendran P,
Cook JP,
Karthikeyan S,
Lahrouchi N,
Liu C,
Sepúlveda N,
Richardson TG,
Kraja A,
Amouyel P,
Farrall M,
Poulter NR,
Laakso M,
Zeggini E,
Sever P,
Scott RA,
Langenberg C,
Wareham NJ,
Conen D,
Palmer CNA,
Attia J,
Chasman DI,
Ridker PM,
Melander O,
Mook-Kanamori DO,
Harst PV,
Cucca F,
Schlessinger D,
Hayward C,
Spector TD,
Jarvelin MR,
Hennig BJ,
Timpson NJ,
Wei WQ,
Smith JC,
Xu Y,
Matheny ME,
Siew EE,
Lindgren C,
Herzig KH,
Dedoussis G,
Denny JC,
Psaty BM,
Howson JMM,
Munroe PB,
Newton-Cheh C,
Caulfield MJ,
Elliott P,
Gaziano JM,
Concato J,
Wilson PWF,
Tsao PS,
Velez Edwards DR,
Susztak K,
O'Donnell CJ,
Hung AM,
Edwards TL
Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke M,
Li Y,
Li M,
Sieber KB,
Feitosa MF,
Gorski M,
Tin A,
Wang L,
Chu AY,
Hoppmann A,
Kirsten H,
Giri A
and 315 more — show all
Chai JF,
Sveinbjornsson G,
Tayo BO,
Nutile T,
Fuchsberger C,
Marten J,
Cocca M,
Ghasemi S,
Xu Y,
Horn K,
Noce D,
van der Most PJ,
Sedaghat S,
Yu Z,
Akiyama M,
Afaq S,
Ahluwalia TS,
Almgren P,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boehnke M,
Boerwinkle E,
Boissel M,
Bottinger EP,
Boutin TS,
Brenner H,
Brumat M,
Burkhardt R,
Butterworth AS,
Campana E,
Campbell A,
Campbell H,
Canouil M,
Carroll RJ,
Catamo E,
Chambers JC,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cheng Y,
Christensen K,
Cifkova R,
Ciullo M,
Concas MP,
Cook JP,
Coresh J,
Corre T,
Sala CF,
Cusi D,
Danesh J,
Daw EW,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Delgado G,
Demirkan A,
Di Angelantonio E,
Dittrich K,
Divers J,
Dorajoo R,
Eckardt KU,
Ehret G,
Elliott P,
Endlich K,
Evans MK,
Felix JF,
Foo VHX,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Friedlander Y,
Froguel P,
Gansevoort RT,
Gao H,
Gasparini P,
Gaziano JM,
Giedraitis V,
Gieger C,
Girotto G,
Giulianini F,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hartman CA,
Hayward C,
Hellwege JN,
Heng CK,
Hicks AA,
Hofer E,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Indridason OS,
Ingelsson E,
Ising M,
Jaddoe VWV,
Jakobsdottir J,
Jonas JB,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kammerer CM,
Kanai M,
Kastarinen M,
Kerr SM,
Khor CC,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Kraja AT,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
Kuokkanen M,
Kuusisto J,
La Bianca M,
Laakso M,
Lange LA,
Langefeld CD,
Lee JJ,
Lehne B,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Liu J,
Loeffler M,
Loos RJF,
Lucae S,
Lukas MA,
Lyytikäinen LP,
Mägi R,
Magnusson PKE,
Mahajan A,
Martin NG,
Martins J,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Melander O,
Metspalu A,
Mikaelsdottir EK,
Milaneschi Y,
Miliku K,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell J,
O'Donoghue ML,
Olafsson I,
Oldehinkel AJ,
Orho-Melander M,
Ouwehand WH,
Padmanabhan S,
Palmer ND,
Palsson R,
Penninx BWJH,
Perls T,
Perola M,
Pirastu M,
Pirastu N,
Pistis G,
Podgornaia AI,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Pramstaller PP,
Preuss MH,
Prins BP,
Province MA,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Ridker PM,
Rivadeneira F,
Rizzi F,
Roberts DJ,
Robino A,
Rossing P,
Rudan I,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Sabanayagam C,
Salomaa V,
Salvi E,
Saum KU,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Schupf N,
Shaffer CM,
Shi Y,
Smith AV,
Smith BH,
Soranzo N,
Spracklen CN,
Strauch K,
Stringham HM,
Stumvoll M,
Svensson PO,
Szymczak S,
Tai ES,
Tajuddin SM,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorleifsson G,
Toniolo D,
Tönjes A,
Tremblay J,
Tzoulaki I,
Uitterlinden AG,
Vaccargiu S,
van Dam RM,
van der Harst P,
van Duijn CM,
Velez Edward DR,
Verweij N,
Vogelezang S,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Wallentin L,
Wang YX,
Wang C,
Waterworth DM,
Bin Wei W,
White H,
Whitfield JB,
Wild SH,
Wilson JF,
Wojczynski MK,
Wong C,
Wong TY,
Xu L,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang W,
Zonderman AB,
Rotter JI,
Bochud M,
Psaty BM,
Vitart V,
Wilson JG,
Dehghan A,
Parsa A,
Chasman DI,
Ho K,
Morris AP,
Devuyst O,
Akilesh S,
Pendergrass SA,
Sim X,
Böger CA,
Okada Y,
Edwards TL,
Snieder H,
Stefansson K,
Hung AM,
Heid IM,
Scholz M,
Teumer A,
Köttgen A,
Pattaro C
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program
Hellwege JN,
Velez Edwards DR,
Giri A,
Qiu C,
Park J,
Torstenson ES,
Keaton JM,
Wilson OD,
Robinson-Cohen C,
Chung CP,
Roumie CL,
Klarin D
and 18 more — show all
Damrauer SM,
DuVall SL,
Siew E,
Akwo EA,
Wuttke M,
Gorski M,
Li M,
Li Y,
Gaziano JM,
Wilson PWF,
Tsao PS,
O'Donnell CJ,
Kovesdy CP,
Pattaro C,
Köttgen A,
Susztak K,
Edwards TL,
Hung AM
Nature communications · 2019 · PMID 31451708 · open access
12 pages+
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer A,
Li Y,
Ghasemi S,
Prins BP,
Wuttke M,
Hermle T,
Giri A,
Sieber KB,
Qiu C,
Kirsten H,
Tin A,
Chu AY
and 174 more — show all
Bansal N,
Feitosa MF,
Wang L,
Chai JF,
Cocca M,
Fuchsberger C,
Gorski M,
Hoppmann A,
Horn K,
Li M,
Marten J,
Noce D,
Nutile T,
Sedaghat S,
Sveinbjornsson G,
Tayo BO,
van der Most PJ,
Xu Y,
Yu Z,
Gerstner L,
Ärnlöv J,
Bakker SJL,
Baptista D,
Biggs ML,
Boerwinkle E,
Brenner H,
Burkhardt R,
Carroll RJ,
Chee ML,
Chee ML,
Chen M,
Cheng CY,
Cook JP,
Coresh J,
Corre T,
Danesh J,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Dittrich K,
Divers J,
Eckardt KU,
Ehret G,
Endlich K,
Felix JF,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Gansevoort RT,
Giedraitis V,
Gögele M,
Grundner-Culemann F,
Gudbjartsson DF,
Gudnason V,
Hamet P,
Harris TB,
Hicks AA,
Holm H,
Foo VHX,
Hwang SJ,
Ikram MA,
Ingelsson E,
Jaddoe VWV,
Jakobsdottir J,
Josyula NS,
Jung B,
Kähönen M,
Khor CC,
Kiess W,
Koenig W,
Körner A,
Kovacs P,
Kramer H,
Krämer BK,
Kronenberg F,
Lange LA,
Langefeld CD,
Lee JJ,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
Meisinger C,
Meitinger T,
Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
Mychaleckyj JC,
Nauck M,
Nikus K,
Ning B,
Noordam R,
Connell JO,
Olafsson I,
Palmer ND,
Peters A,
Podgornaia AI,
Ponte B,
Poulain T,
Pramstaller PP,
Rabelink TJ,
Raffield LM,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Rivadeneira F,
Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
Shaffer CM,
Shi Y,
Smith AV,
Strauch K,
Stumvoll M,
Sun BB,
Szymczak S,
Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
Tremblay J,
Uitterlinden AG,
van der Harst P,
Verweij N,
Vogelezang S,
Völker U,
Waldenberger M,
Wang C,
Wilson OD,
Wong C,
Wong TY,
Yang Q,
Yasuda M,
Akilesh S,
Bochud M,
Böger CA,
Devuyst O,
Edwards TL,
Ho K,
Morris AP,
Parsa A,
Pendergrass SA,
Psaty BM,
Rotter JI,
Stefansson K,
Wilson JG,
Susztak K,
Snieder H,
Heid IM,
Scholz M,
Butterworth AS,
Hung AM,
Pattaro C,
Köttgen A
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
and 213 more — show all
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
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LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
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Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals
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Gaziano JM,
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VA Million Veteran Program
Nature communications · 2021 · PMID 34272381 · open access
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X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
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Tin A,
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Nature communications · 2024 · PMID 38233393 · open access
8 pages
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
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Genome-Wide Association Study of CKD Progression
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