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26 matches for
Paré G,
showing the first 20.
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Lango Allen H,
Estrada K,
Lettre G,
Berndt SI,
Weedon MN,
Rivadeneira F,
Willer CJ,
Jackson AU,
Vedantam S,
Raychaudhuri S,
Ferreira T,
Wood AR
and 281 more — show all
Weyant RJ,
Segrè AV,
Speliotes EK,
Wheeler E,
Soranzo N,
Park JH,
Yang J,
Gudbjartsson D,
Heard-Costa NL,
Randall JC,
Qi L,
Vernon Smith A,
Mägi R,
Pastinen T,
Liang L,
Heid IM,
Luan J,
Thorleifsson G,
Winkler TW,
Goddard ME,
Sin Lo K,
Palmer C,
Workalemahu T,
Aulchenko YS,
Johansson A,
Zillikens MC,
Feitosa MF,
Esko T,
Johnson T,
Ketkar S,
Kraft P,
Mangino M,
Prokopenko I,
Absher D,
Albrecht E,
Ernst F,
Glazer NL,
Hayward C,
Hottenga JJ,
Jacobs KB,
Knowles JW,
Kutalik Z,
Monda KL,
Polasek O,
Preuss M,
Rayner NW,
Robertson NR,
Steinthorsdottir V,
Tyrer JP,
Voight BF,
Wiklund F,
Xu J,
Zhao JH,
Nyholt DR,
Pellikka N,
Perola M,
Perry JR,
Surakka I,
Tammesoo ML,
Altmaier EL,
Amin N,
Aspelund T,
Bhangale T,
Boucher G,
Chasman DI,
Chen C,
Coin L,
Cooper MN,
Dixon AL,
Gibson Q,
Grundberg E,
Hao K,
Juhani Junttila M,
Kaplan LM,
Kettunen J,
König IR,
Kwan T,
Lawrence RW,
Levinson DF,
Lorentzon M,
McKnight B,
Morris AP,
Müller M,
Suh Ngwa J,
Purcell S,
Rafelt S,
Salem RM,
Salvi E,
Sanna S,
Shi J,
Sovio U,
Thompson JR,
Turchin MC,
Vandenput L,
Verlaan DJ,
Vitart V,
White CC,
Ziegler A,
Almgren P,
Balmforth AJ,
Campbell H,
Citterio L,
De Grandi A,
Dominiczak A,
Duan J,
Elliott P,
Elosua R,
Eriksson JG,
Freimer NB,
Geus EJ,
Glorioso N,
Haiqing S,
Hartikainen AL,
Havulinna AS,
Hicks AA,
Hui J,
Igl W,
Illig T,
Jula A,
Kajantie E,
Kilpeläinen TO,
Koiranen M,
Kolcic I,
Koskinen S,
Kovacs P,
Laitinen J,
Liu J,
Lokki ML,
Marusic A,
Maschio A,
Meitinger T,
Mulas A,
Paré G,
Parker AN,
Peden JF,
Petersmann A,
Pichler I,
Pietiläinen KH,
Pouta A,
Ridderstråle M,
Rotter JI,
Sambrook JG,
Sanders AR,
Schmidt CO,
Sinisalo J,
Smit JH,
Stringham HM,
Bragi Walters G,
Widen E,
Wild SH,
Willemsen G,
Zagato L,
Zgaga L,
Zitting P,
Alavere H,
Farrall M,
McArdle WL,
Nelis M,
Peters MJ,
Ripatti S,
van Meurs JB,
Aben KK,
Ardlie KG,
Beckmann JS,
Beilby JP,
Bergman RN,
Bergmann S,
Collins FS,
Cusi D,
den Heijer M,
Eiriksdottir G,
Gejman PV,
Hall AS,
Hamsten A,
Huikuri HV,
Iribarren C,
Kähönen M,
Kaprio J,
Kathiresan S,
Kiemeney L,
Kocher T,
Launer LJ,
Lehtimäki T,
Melander O,
Mosley TH Jr,
Musk AW,
Nieminen MS,
O'Donnell CJ,
Ohlsson C,
Oostra B,
Palmer LJ,
Raitakari O,
Ridker PM,
Rioux JD,
Rissanen A,
Rivolta C,
Schunkert H,
Shuldiner AR,
Siscovick DS,
Stumvoll M,
Tönjes A,
Tuomilehto J,
van Ommen GJ,
Viikari J,
Heath AC,
Martin NG,
Montgomery GW,
Province MA,
Kayser M,
Arnold AM,
Atwood LD,
Boerwinkle E,
Chanock SJ,
Deloukas P,
Gieger C,
Grönberg H,
Hall P,
Hattersley AT,
Hengstenberg C,
Hoffman W,
Lathrop GM,
Salomaa V,
Schreiber S,
Uda M,
Waterworth D,
Wright AF,
Assimes TL,
Barroso I,
Hofman A,
Mohlke KL,
Boomsma DI,
Caulfield MJ,
Cupples LA,
Erdmann J,
Fox CS,
Gudnason V,
Gyllensten U,
Harris TB,
Hayes RB,
Jarvelin MR,
Mooser V,
Munroe PB,
Ouwehand WH,
Penninx BW,
Pramstaller PP,
Quertermous T,
Rudan I,
Samani NJ,
Spector TD,
Völzke H,
Watkins H,
Wilson JF,
Groop LC,
Haritunians T,
Hu FB,
Kaplan RC,
Metspalu A,
North KE,
Schlessinger D,
Wareham NJ,
Hunter DJ,
O'Connell JR,
Strachan DP,
Wichmann HE,
Borecki IB,
van Duijn CM,
Schadt EE,
Thorsteinsdottir U,
Peltonen L,
Uitterlinden AG,
Visscher PM,
Chatterjee N,
Loos RJ,
Boehnke M,
McCarthy MI,
Ingelsson E,
Lindgren CM,
Abecasis GR,
Stefansson K,
Frayling TM,
Hirschhorn JN
Nature · 2010 · PMID 20881960 · open access
12 pages+
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
and 150 more — show all
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Wain LV,
Vaez A,
Jansen R,
Joehanes R,
van der Most PJ,
Erzurumluoglu AM,
O'Reilly PF,
Cabrera CP,
Warren HR,
Rose LM,
Verwoert GC,
Hottenga JJ
and 239 more — show all
Strawbridge RJ,
Esko T,
Arking DE,
Hwang SJ,
Guo X,
Kutalik Z,
Trompet S,
Shrine N,
Teumer A,
Ried JS,
Bis JC,
Smith AV,
Amin N,
Nolte IM,
Lyytikäinen LP,
Mahajan A,
Wareham NJ,
Hofer E,
Joshi PK,
Kristiansson K,
Traglia M,
Havulinna AS,
Goel A,
Nalls MA,
Sõber S,
Vuckovic D,
Luan J,
Del Greco M F,
Ayers KL,
Marrugat J,
Ruggiero D,
Lopez LM,
Niiranen T,
Enroth S,
Jackson AU,
Nelson CP,
Huffman JE,
Zhang W,
Marten J,
Gandin I,
Harris SE,
Zemunik T,
Lu Y,
Evangelou E,
Shah N,
de Borst MH,
Mangino M,
Prins BP,
Campbell A,
Li-Gao R,
Chauhan G,
Oldmeadow C,
Abecasis G,
Abedi M,
Barbieri CM,
Barnes MR,
Batini C,
Beilby J,
Blake T,
Boehnke M,
Bottinger EP,
Braund PS,
Brown M,
Brumat M,
Campbell H,
Chambers JC,
Cocca M,
Collins F,
Connell J,
Cordell HJ,
Damman JJ,
Davies G,
de Geus EJ,
de Mutsert R,
Deelen J,
Demirkale Y,
Doney ASF,
Doney ASF,
Dörr M,
Farrall M,
Ferreira T,
Frånberg M,
Gao H,
Giedraitis V,
Gieger C,
Giulianini F,
Gow AJ,
Hamsten A,
Harris TB,
Hofman A,
Holliday EG,
Hui J,
Jarvelin MR,
Johansson Å,
Johnson AD,
Jousilahti P,
Jula A,
Kähönen M,
Kathiresan S,
Khaw KT,
Kolcic I,
Koskinen S,
Langenberg C,
Larson M,
Launer LJ,
Lehne B,
Liewald DCM,
Lin L,
Lind L,
Mach F,
Mamasoula C,
Menni C,
Menni C,
Mifsud B,
Milaneschi Y,
Morgan A,
Morris AD,
Morrison AC,
Munson PJ,
Nandakumar P,
Nguyen QT,
Nutile T,
Oldehinkel AJ,
Oostra BA,
Org E,
Org E,
Padmanabhan S,
Palotie A,
Paré G,
Pattie A,
Penninx BWJH,
Poulter N,
Pramstaller PP,
Raitakari OT,
Ren M,
Rice K,
Ridker PM,
Riese H,
Ripatti S,
Robino A,
Rotter JI,
Rudan I,
Saba Y,
Saint Pierre A,
Sala CF,
Sarin AP,
Schmidt R,
Scott R,
Seelen MA,
Shields DC,
Siscovick D,
Sorice R,
Stanton A,
Stott DJ,
Sundström J,
Swertz M,
Taylor KD,
Thom S,
Tzoulaki I,
Tzourio C,
Uitterlinden AG,
Uitterlinden AG,
Völker U,
Vollenweider P,
Wild S,
Willemsen G,
Wright AF,
Yao J,
Thériault S,
Conen D,
Attia J,
Sever P,
Debette S,
Mook-Kanamori DO,
Zeggini E,
Spector TD,
van der Harst P,
Palmer CNA,
Vergnaud AC,
Loos RJF,
Polasek O,
Polasek O,
Starr JM,
Girotto G,
Hayward C,
Kooner JS,
Lindgren CM,
Vitart V,
Samani NJ,
Tuomilehto J,
Gyllensten U,
Knekt P,
Deary IJ,
Ciullo M,
Elosua R,
Elosua R,
Keavney BD,
Hicks AA,
Scott RA,
Gasparini P,
Laan M,
Liu Y,
Watkins H,
Hartman CA,
Salomaa V,
Toniolo D,
Perola M,
Wilson JF,
Schmidt H,
Zhao JH,
Lehtimäki T,
Lehtimäki T,
van Duijn CM,
Gudnason V,
Psaty BM,
Peters A,
Rettig R,
James A,
Jukema JW,
Strachan DP,
Palmas W,
Metspalu A,
Ingelsson E,
Boomsma DI,
Franco OH,
Bochud M,
Newton-Cheh C,
Munroe PB,
Elliott P,
Chasman DI,
Chakravarti A,
Knight J,
Knight J,
Morris AP,
Levy D,
Tobin MD,
Snieder H,
Caulfield MJ,
Ehret GB
BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
12 pages+
Multi-ethnic genome-wide association study for atrial fibrillation
Roselli C,
Chaffin MD,
Weng LC,
Aeschbacher S,
Ahlberg G,
Albert CM,
Almgren P,
Alonso A,
Anderson CD,
Aragam KG,
Arking DE,
Barnard J
and 206 more — show all
Bartz TM,
Benjamin EJ,
Bihlmeyer NA,
Bis JC,
Bloom HL,
Boerwinkle E,
Bottinger EB,
Brody JA,
Calkins H,
Campbell A,
Cappola TP,
Carlquist J,
Chasman DI,
Chen LY,
Chen YI,
Choi EK,
Choi SH,
Christophersen IE,
Chung MK,
Cole JW,
Conen D,
Cook J,
Crijns HJ,
Cutler MJ,
Damrauer SM,
Daniels BR,
Darbar D,
Delgado G,
Denny JC,
Dichgans M,
Dörr M,
Dudink EA,
Dudley SC,
Esa N,
Esko T,
Eskola M,
Fatkin D,
Felix SB,
Ford I,
Franco OH,
Geelhoed B,
Grewal RP,
Gudnason V,
Guo X,
Gupta N,
Gustafsson S,
Gutmann R,
Hamsten A,
Harris TB,
Hayward C,
Heckbert SR,
Hernesniemi J,
Hocking LJ,
Hofman A,
Horimoto ARVR,
Huang J,
Huang PL,
Huffman J,
Ingelsson E,
Ipek EG,
Ito K,
Jimenez-Conde J,
Johnson R,
Jukema JW,
Kääb S,
Kähönen M,
Kamatani Y,
Kane JP,
Kastrati A,
Kathiresan S,
Katschnig-Winter P,
Kavousi M,
Kessler T,
Kietselaer BL,
Kirchhof P,
Kleber ME,
Knight S,
Krieger JE,
Kubo M,
Launer LJ,
Laurikka J,
Lehtimäki T,
Leineweber K,
Lemaitre RN,
Li M,
Lim HE,
Lin HJ,
Lin H,
Lind L,
Lindgren CM,
Lokki ML,
London B,
Loos RJF,
Low SK,
Lu Y,
Lyytikäinen LP,
Macfarlane PW,
Magnusson PK,
Mahajan A,
Malik R,
Mansur AJ,
Marcus GM,
Margolin L,
Margulies KB,
März W,
McManus DD,
Melander O,
Mohanty S,
Montgomery JA,
Morley MP,
Morris AP,
Müller-Nurasyid M,
Natale A,
Nazarian S,
Neumann B,
Newton-Cheh C,
Niemeijer MN,
Nikus K,
Nilsson P,
Noordam R,
Oellers H,
Olesen MS,
Orho-Melander M,
Padmanabhan S,
Pak HN,
Paré G,
Pedersen NL,
Pera J,
Pereira A,
Porteous D,
Psaty BM,
Pulit SL,
Pullinger CR,
Rader DJ,
Refsgaard L,
Ribasés M,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rosand J,
Rosenberg MA,
Rost N,
Rotter JI,
Saba S,
Sandhu RK,
Schnabel RB,
Schramm K,
Schunkert H,
Schurman C,
Scott SA,
Seppälä I,
Shaffer C,
Shah S,
Shalaby AA,
Shim J,
Shoemaker MB,
Siland JE,
Sinisalo J,
Sinner MF,
Slowik A,
Smith AV,
Smith BH,
Smith JG,
Smith JD,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Stricker BH,
Sun A,
Sun H,
Svendsen JH,
Tanaka T,
Tanriverdi K,
Taylor KD,
Teder-Laving M,
Teumer A,
Thériault S,
Trompet S,
Tucker NR,
Tveit A,
Uitterlinden AG,
Van Der Harst P,
Van Gelder IC,
Van Wagoner DR,
Verweij N,
Vlachopoulou E,
Völker U,
Wang B,
Weeke PE,
Weijs B,
Weiss R,
Weiss S,
Wells QS,
Wiggins KL,
Wong JA,
Woo D,
Worrall BB,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Lubitz SA,
Lunetta KL,
Ellinor PT
Nature genetics · 2018 · PMID 29892015
12 pages+
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,
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Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Hughes O,
Bentley AR,
Breeze CE,
Aguet F,
Xu X,
Nadkarni G,
Sun Q,
Lin BM,
Gilliland T,
Meyer MC,
Du J,
Raffield LM
and 62 more — show all
Kramer H,
Morton RW,
Gouveia MH,
Atkinson EG,
Valladares-Salgado A,
Wacher-Rodarte N,
Dueker ND,
Guo X,
Hai Y,
Adeyemo A,
Best LG,
Cai J,
Chen G,
Chong M,
Doumatey A,
Eales J,
Goodarzi MO,
Ipp E,
Irvin MR,
Jiang M,
Jones AC,
Kooperberg C,
Krieger JE,
Lange EM,
Lanktree MB,
Lash JP,
Lotufo PA,
Loos RJF,
Ha My VT,
Peralta-Romero J,
Qi L,
Raffel LJ,
Rich SS,
Rodriquez EJ,
Tarazona-Santos E,
Taylor KD,
Umans JG,
Wen J,
Young BA,
Yu Z,
Zhang Y,
Ida Chen YD,
Rundek T,
Rotter JI,
Cruz M,
Fornage M,
Lima-Costa MF,
Pereira AC,
Paré G,
Natarajan P,
Cole SA,
Carson AP,
Lange LA,
Li Y,
Perez-Stable EJ,
Do R,
Charchar FJ,
Tomaszewski M,
Mychaleckyj JC,
Rotimi C,
Morris AP,
Franceschini N
Cell genomics · 2024 · PMID 38190104 · open access
5 pages
New loci associated with kidney function and chronic kidney disease
Köttgen A,
Pattaro C,
Böger CA,
Fuchsberger C,
Olden M,
Glazer NL,
Parsa A,
Gao X,
Yang Q,
Smith AV,
O'Connell JR,
Li M
and 120 more — show all
Schmidt H,
Tanaka T,
Isaacs A,
Ketkar S,
Hwang SJ,
Johnson AD,
Dehghan A,
Teumer A,
Paré G,
Atkinson EJ,
Zeller T,
Lohman K,
Cornelis MC,
Probst-Hensch NM,
Kronenberg F,
Tönjes A,
Hayward C,
Aspelund T,
Eiriksdottir G,
Launer LJ,
Harris TB,
Rampersaud E,
Mitchell BD,
Arking DE,
Boerwinkle E,
Struchalin M,
Cavalieri M,
Singleton A,
Giallauria F,
Metter J,
de Boer IH,
Haritunians T,
Lumley T,
Siscovick D,
Psaty BM,
Zillikens MC,
Oostra BA,
Feitosa M,
Province M,
de Andrade M,
Turner ST,
Schillert A,
Ziegler A,
Wild PS,
Schnabel RB,
Wilde S,
Munzel TF,
Leak TS,
Illig T,
Klopp N,
Meisinger C,
Wichmann HE,
Koenig W,
Zgaga L,
Zemunik T,
Kolcic I,
Minelli C,
Hu FB,
Johansson A,
Igl W,
Zaboli G,
Wild SH,
Wright AF,
Campbell H,
Ellinghaus D,
Schreiber S,
Aulchenko YS,
Felix JF,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
Imboden M,
Nitsch D,
Brandstätter A,
Kollerits B,
Kedenko L,
Mägi R,
Stumvoll M,
Kovacs P,
Boban M,
Campbell S,
Endlich K,
Völzke H,
Kroemer HK,
Nauck M,
Völker U,
Polasek O,
Vitart V,
Badola S,
Parker AN,
Ridker PM,
Kardia SL,
Blankenberg S,
Liu Y,
Curhan GC,
Franke A,
Rochat T,
Paulweber B,
Prokopenko I,
Wang W,
Gudnason V,
Shuldiner AR,
Coresh J,
Schmidt R,
Ferrucci L,
Shlipak MG,
van Duijn CM,
Borecki I,
Krämer BK,
Rudan I,
Gyllensten U,
Wilson JF,
Witteman JC,
Pramstaller PP,
Rettig R,
Hastie N,
Chasman DI,
Kao WH,
Heid IM,
Fox CS
Nature genetics · 2010 · PMID 20383146
4 pages
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors
Yang Q,
Köttgen A,
Dehghan A,
Smith AV,
Glazer NL,
Chen MH,
Chasman DI,
Aspelund T,
Eiriksdottir G,
Harris TB,
Launer L,
Nalls M
and 29 more — show all
Hernandez D,
Arking DE,
Boerwinkle E,
Grove ML,
Li M,
Linda Kao WH,
Chonchol M,
Haritunians T,
Li G,
Lumley T,
Psaty BM,
Shlipak M,
Hwang SJ,
Larson MG,
O'Donnell CJ,
Upadhyay A,
van Duijn CM,
Hofman A,
Rivadeneira F,
Stricker B,
Uitterlinden AG,
Paré G,
Parker AN,
Ridker PM,
Siscovick DS,
Gudnason V,
Witteman JC,
Fox CS,
Coresh J
Circulation. Cardiovascular genetics · 2010 · PMID 20884846
4 pages
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
and 70 more — show all
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
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