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Hellwege JN에 대해
14건.
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
외 268명 — 모두 보기
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
페이지 12개+
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
외 86명 — 모두 보기
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 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30578418 · open access
페이지 12개+
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
외 315명 — 모두 보기
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
페이지 12개+
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
외 18명 — 모두 보기
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
페이지 12개+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
외 269명 — 모두 보기
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Wang A,
Shen J,
Rodriguez AA,
Saunders EJ,
Chen F,
Janivara R,
Darst BF,
Sheng X,
Xu Y,
Chou AJ,
Benlloch S,
Dadaev T
외 279명 — 모두 보기
Brook MN,
Plym A,
Sahimi A,
Hoffman TJ,
Takahashi A,
Matsuda K,
Momozawa Y,
Fujita M,
Laisk T,
Figuerêdo J,
Muir K,
Ito S,
Liu X,
Uchio Y,
Kubo M,
Kamatani Y,
Lophatananon A,
Wan P,
Andrews C,
Lori A,
Choudhury PP,
Schleutker J,
Tammela TLJ,
Sipeky C,
Auvinen A,
Giles GG,
Southey MC,
MacInnis RJ,
Cybulski C,
Wokolorczyk D,
Lubinski J,
Rentsch CT,
Cho K,
Mcmahon BH,
Neal DE,
Donovan JL,
Hamdy FC,
Martin RM,
Nordestgaard BG,
Nielsen SF,
Weischer M,
Bojesen SE,
Røder A,
Stroomberg HV,
Batra J,
Chambers S,
Horvath L,
Clements JA,
Tilly W,
Risbridger GP,
Gronberg H,
Aly M,
Szulkin R,
Eklund M,
Nordstrom T,
Pashayan N,
Dunning AM,
Ghoussaini M,
Travis RC,
Key TJ,
Riboli E,
Park JY,
Sellers TA,
Lin HY,
Albanes D,
Weinstein S,
Cook MB,
Mucci LA,
Giovannucci E,
Lindstrom S,
Kraft P,
Hunter DJ,
Penney KL,
Turman C,
Tangen CM,
Goodman PJ,
Thompson IM Jr,
Hamilton RJ,
Fleshner NE,
Finelli A,
Parent MÉ,
Stanford JL,
Ostrander EA,
Koutros S,
Beane Freeman LE,
Stampfer M,
Wolk A,
Håkansson N,
Andriole GL,
Hoover RN,
Machiela MJ,
Sørensen KD,
Borre M,
Blot WJ,
Zheng W,
Yeboah ED,
Mensah JE,
Lu YJ,
Zhang HW,
Feng N,
Mao X,
Wu Y,
Zhao SC,
Sun Z,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
West CML,
Barnett G,
Maier C,
Schnoeller T,
Luedeke M,
Kibel AS,
Drake BF,
Cussenot O,
Cancel-Tassin G,
Menegaux F,
Truong T,
Koudou YA,
John EM,
Grindedal EM,
Maehle L,
Khaw KT,
Ingles SA,
Stern MC,
Vega A,
Gómez-Caamaño A,
Fachal L,
Rosenstein BS,
Kerns SL,
Ostrer H,
Teixeira MR,
Paulo P,
Brandão A,
Watya S,
Lubwama A,
Bensen JT,
Butler EN,
Mohler JL,
Taylor JA,
Kogevinas M,
Dierssen-Sotos T,
Castaño-Vinyals G,
Cannon-Albright L,
Teerlink CC,
Huff CD,
Pilie P,
Yu Y,
Bohlender RJ,
Gu J,
Strom SS,
Multigner L,
Blanchet P,
Brureau L,
Kaneva R,
Slavov C,
Mitev V,
Leach RJ,
Brenner H,
Chen X,
Holleczek B,
Schöttker B,
Klein EA,
Hsing AW,
Kittles RA,
Murphy AB,
Logothetis CJ,
Kim J,
Neuhausen SL,
Steele L,
Ding YC,
Isaacs WB,
Nemesure B,
Hennis AJM,
Carpten J,
Pandha H,
Michael A,
De Ruyck K,
De Meerleer G,
Ost P,
Xu J,
Razack A,
Lim J,
Teo SH,
Newcomb LF,
Lin DW,
Fowke JH,
Neslund-Dudas CM,
Rybicki BA,
Gamulin M,
Lessel D,
Kulis T,
Usmani N,
Abraham A,
Singhal S,
Parliament M,
Claessens F,
Joniau S,
Van den Broeck T,
Gago-Dominguez M,
Castelao JE,
Martinez ME,
Larkin S,
Townsend PA,
Aukim-Hastie C,
Bush WS,
Aldrich MC,
Crawford DC,
Srivastava S,
Cullen J,
Petrovics G,
Casey G,
Wang Y,
Tettey Y,
Lachance J,
Tang W,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Yamoah K,
Govindasami K,
Chokkalingam AP,
Keaton JM,
Hellwege JN,
Clark PE,
Jalloh M,
Gueye SM,
Niang L,
Ogunbiyi O,
Shittu O,
Amodu O,
Adebiyi AO,
Aisuodionoe-Shadrach OI,
Ajibola HO,
Jamda MA,
Oluwole OP,
Nwegbu M,
Adusei B,
Mante S,
Darkwa-Abrahams A,
Diop H,
Gundell SM,
Roobol MJ,
Jenster G,
van Schaik RHN,
Hu JJ,
Sanderson M,
Kachuri L,
Varma R,
McKean-Cowdin R,
Torres M,
Preuss MH,
Loos RJF,
Zawistowski M,
Zöllner S,
Lu Z,
Van Den Eeden SK,
Easton DF,
Ambs S,
Edwards TL,
Mägi R,
Rebbeck TR,
Fritsche L,
Chanock SJ,
Berndt SI,
Wiklund F,
Nakagawa H,
Witte JS,
Gaziano JM,
Justice AC,
Mancuso N,
Terao C,
Eeles RA,
Kote-Jarai Z,
Madduri RK,
Conti DV,
Haiman CA
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
페이지 12개+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
외 135명 — 모두 보기
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38689001 · open access
페이지 12개+
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups
Kim J,
Williams A,
Noh H,
Jasper EA,
Jones SH,
Jaworski JA,
Shuey MM,
Ruiz-Narváez EA,
Wise LA,
Palmer JR,
Connolly J,
Keaton JM
외 11명 — 모두 보기
Denny JC,
Khan A,
Abbass MA,
Rasmussen-Torvik LJ,
Kottyan LC,
Madhivanan P,
Krupp K,
Wei WQ,
Edwards TL,
Velez Edwards DR,
Hellwege JN
Nature communications · 2025 · PMID 40050615 · open access
페이지 12개+
Multi-ancestry meta-analysis of keloids uncovers novel susceptibility loci in diverse populations
Greene CA,
Hampton G,
Jaworski J,
Shuey MM,
Khan A,
Luo Y,
Jarvik GP,
Namjou-Khales B,
Edwards TL,
Velez Edwards DR,
Hellwege JN
Nature communications · 2025 · PMID 40835838 · open access
페이지 11개
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
Scholz M,
Horn K,
Pott J,
Wuttke M,
Kühnapfel A,
Nasr MK,
Kirsten H,
Li Y,
Hoppmann A,
Gorski M,
Ghasemi S,
Li M
외 147명 — 모두 보기
Tin A,
Chai JF,
Cocca M,
Wang J,
Nutile T,
Akiyama M,
Åsvold BO,
Bansal N,
Biggs ML,
Boutin T,
Brenner H,
Brumpton B,
Burkhardt R,
Cai J,
Campbell A,
Campbell H,
Chalmers J,
Chasman DI,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cifkova R,
Daviglus M,
Delgado G,
Dittrich K,
Edwards TL,
Endlich K,
Michael Gaziano J,
Giri A,
Giulianini F,
Gordon SD,
Gudbjartsson DF,
Hallan S,
Hamet P,
Hartman CA,
Hayward C,
Heid IM,
Hellwege JN,
Holleczek B,
Holm H,
Hutri-Kähönen N,
Hveem K,
Isermann B,
Jonas JB,
Joshi PK,
Kamatani Y,
Kanai M,
Kastarinen M,
Khor CC,
Kiess W,
Kleber ME,
Körner A,
Kovacs P,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kuokkanen M,
Kähönen M,
Lange LA,
Lash JP,
Lehtimäki T,
Li H,
Lin BM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Magnusson PKE,
Martin NG,
Matsuda K,
Milaneschi Y,
Mishra PP,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
März W,
Nauck M,
Nikus K,
Nolte IM,
Noordam R,
Okada Y,
Olafsson I,
Oldehinkel AJ,
Penninx BWJH,
Perola M,
Pirastu N,
Polasek O,
Porteous DJ,
Poulain T,
Psaty BM,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rasheed H,
Reilly DF,
Rice KM,
Richmond A,
Ridker PM,
Rotter JI,
Rudan I,
Sabanayagam C,
Salomaa V,
Schneiderman N,
Schöttker B,
Sims M,
Snieder H,
Stark KJ,
Stefansson K,
Stocker H,
Stumvoll M,
Sulem P,
Sveinbjornsson G,
Svensson PO,
Tai ES,
Taylor KD,
Tayo BO,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomas LF,
Tremblay J,
Tönjes A,
van der Most PJ,
Vitart V,
Völker U,
Wang YX,
Wang C,
Wei WB,
Whitfield JB,
Wild SH,
Wilson JF,
Winkler TW,
Wong TY,
Woodward M,
Sim X,
Chu AY,
Feitosa MF,
Thorsteinsdottir U,
Hung AM,
Teumer A,
Franceschini N,
Parsa A,
Köttgen A,
Schlosser P,
Pattaro C
Nature communications · 2024 · PMID 38233393 · open access
페이지 8개
Genetic analysis in African ancestry populations reveals genetic contributors to lung cancer susceptibility
Betti MJ,
Jaworski J,
Zhao S,
Rao JS,
Ryan BM,
Schwartz AG,
Lusk CM,
McCoy L,
Wiencke JK,
Bruce MA,
Chanock S,
Gamazon ER
외 2명 — 모두 보기
American journal of human genetics · 2025 · PMID 40829600
페이지 2개
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,
Correa A,
Stott DJ,
Ford I,
Jukema JW,
Gudnason V,
Mook-Kanamori DO,
Trompet S,
Palmas W,
Warren HR,
Hellwege JN,
Giri A,
O'donnell C,
Hung AM,
Edwards TL,
Ahluwalia TS,
Arnett DK,
Avery CL
American journal of hypertension · 2019 · PMID 31545351
페이지 1개
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry
Chen F,
Madduri RK,
Rodriguez AA,
Darst BF,
Chou A,
Sheng X,
Wang A,
Shen J,
Saunders EJ,
Rhie SK,
Bensen JT,
Ingles SA
외 106명 — 모두 보기
Kittles RA,
Strom SS,
Rybicki BA,
Nemesure B,
Isaacs WB,
Stanford JL,
Zheng W,
Sanderson M,
John EM,
Park JY,
Xu J,
Wang Y,
Berndt SI,
Huff CD,
Yeboah ED,
Tettey Y,
Lachance J,
Tang W,
Rentsch CT,
Cho K,
Mcmahon BH,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Sellers TA,
Yamoah K,
Murphy AB,
Crawford DC,
Patel AV,
Bush WS,
Aldrich MC,
Cussenot O,
Petrovics G,
Cullen J,
Neslund-Dudas CM,
Stern MC,
Kote-Jarai Z,
Govindasami K,
Cook MB,
Chokkalingam AP,
Hsing AW,
Goodman PJ,
Hoffmann TJ,
Drake BF,
Hu JJ,
Keaton JM,
Hellwege JN,
Clark PE,
Jalloh M,
Gueye SM,
Niang L,
Ogunbiyi O,
Idowu MO,
Popoola O,
Adebiyi AO,
Aisuodionoe-Shadrach OI,
Ajibola HO,
Jamda MA,
Oluwole OP,
Nwegbu M,
Adusei B,
Mante S,
Darkwa-Abrahams A,
Mensah JE,
Diop H,
Van Den Eeden SK,
Blanchet P,
Fowke JH,
Casey G,
Hennis AJ,
Lubwama A,
Thompson IM Jr,
Leach R,
Easton DF,
Preuss MH,
Loos RJ,
Gundell SM,
Wan P,
Mohler JL,
Fontham ET,
Smith GJ,
Taylor JA,
Srivastava S,
Eeles RA,
Carpten JD,
Kibel AS,
Multigner L,
Parent MÉ,
Menegaux F,
Cancel-Tassin G,
Klein EA,
Andrews C,
Rebbeck TR,
Brureau L,
Ambs S,
Edwards TL,
Watya S,
Chanock SJ,
Witte JS,
Blot WJ,
Michael Gaziano J,
Justice AC,
Conti DV,
Haiman CA
European urology · 2023 · PMID 36872133
페이지 1개
Genome-Wide Association Study of CKD Progression
Robinson-Cohen C,
Triozzi JL,
Rowan B,
He J,
Chen HC,
Zheng NS,
Wei WQ,
Wei WQ,
Wilson OD,
Hellwege JN,
Tsao PS,
Gaziano JM
외 8명 — 모두 보기
Journal of the American Society of Nephrology : JASN · 2023 · PMID 37261792
페이지 1개
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