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67 matches for
Dehghan A,
showing the first 20.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Ganesh SK,
Zakai NA,
van Rooij FJ,
Soranzo N,
Smith AV,
Nalls MA,
Chen MH,
Kottgen A,
Glazer NL,
Dehghan A,
Kuhnel B,
Aspelund T
and 50 more — show all
Yang Q,
Tanaka T,
Jaffe A,
Bis JC,
Verwoert GC,
Teumer A,
Fox CS,
Guralnik JM,
Ehret GB,
Rice K,
Felix JF,
Rendon A,
Eiriksdottir G,
Levy D,
Patel KV,
Boerwinkle E,
Rotter JI,
Hofman A,
Sambrook JG,
Hernandez DG,
Zheng G,
Bandinelli S,
Singleton AB,
Coresh J,
Lumley T,
Uitterlinden AG,
Vangils JM,
Launer LJ,
Cupples LA,
Oostra BA,
Zwaginga JJ,
Ouwehand WH,
Thein SL,
Meisinger C,
Deloukas P,
Nauck M,
Spector TD,
Gieger C,
Gudnason V,
van Duijn CM,
Psaty BM,
Ferrucci L,
Chakravarti A,
Greinacher A,
O'Donnell CJ,
Witteman JC,
Furth S,
Cushman M,
Harris TB,
Lin JP
Nature genetics · 2009 · PMID 19862010 · open access
12 pages+
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
Webb TR,
Zeng L
and 139 more — show all
Dehghan A,
Alver M,
Armasu SM,
Auro K,
Bjonnes A,
Chasman DI,
Chen S,
Ford I,
Franceschini N,
Gieger C,
Grace C,
Gustafsson S,
Huang J,
Hwang SJ,
Kim YK,
Kleber ME,
Lau KW,
Lu X,
Lu Y,
Lyytikäinen LP,
Mihailov E,
Morrison AC,
Pervjakova N,
Qu L,
Rose LM,
Salfati E,
Saxena R,
Scholz M,
Smith AV,
Tikkanen E,
Uitterlinden A,
Yang X,
Zhang W,
Zhao W,
de Andrade M,
de Vries PS,
van Zuydam NR,
Anand SS,
Bertram L,
Beutner F,
Dedoussis G,
Frossard P,
Gauguier D,
Goodall AH,
Gottesman O,
Haber M,
Han BG,
Huang J,
Jalilzadeh S,
Kessler T,
König IR,
Lannfelt L,
Lieb W,
Lind L,
Lindgren CM,
Lokki ML,
Magnusson PK,
Mallick NH,
Mehra N,
Meitinger T,
Memon FU,
Morris AP,
Nieminen MS,
Pedersen NL,
Peters A,
Rallidis LS,
Rasheed A,
Samuel M,
Shah SH,
Sinisalo J,
Stirrups KE,
Trompet S,
Wang L,
Zaman KS,
Ardissino D,
Boerwinkle E,
Borecki IB,
Bottinger EP,
Buring JE,
Chambers JC,
Collins R,
Cupples LA,
Danesh J,
Demuth I,
Elosua R,
Epstein SE,
Esko T,
Feitosa MF,
Franco OH,
Franzosi MG,
Granger CB,
Gu D,
Gudnason V,
Hall AS,
Hamsten A,
Harris TB,
Hazen SL,
Hengstenberg C,
Hofman A,
Ingelsson E,
Iribarren C,
Jukema JW,
Karhunen PJ,
Kim BJ,
Kooner JS,
Kullo IJ,
Lehtimäki T,
Loos RJF,
Melander O,
Metspalu A,
März W,
Palmer CN,
Perola M,
Quertermous T,
Rader DJ,
Ridker PM,
Ripatti S,
Roberts R,
Salomaa V,
Sanghera DK,
Schwartz SM,
Seedorf U,
Stewart AF,
Stott DJ,
Thiery J,
Zalloua PA,
O'Donnell CJ,
Reilly MP,
Assimes TL,
Thompson JR,
Erdmann J,
Clarke R,
Watkins H,
Kathiresan S,
McPherson R,
Deloukas P,
Schunkert H,
Samani NJ,
Farrall M
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
de Vries PS,
Chasman DI,
Sabater-Lleal M,
Chen MH,
Huffman JE,
Steri M,
Tang W,
Teumer A,
Marioni RE,
Grossmann V,
Hottenga JJ,
Trompet S
and 119 more — show all
Müller-Nurasyid M,
Zhao JH,
Brody JA,
Kleber ME,
Guo X,
Wang JJ,
Auer PL,
Attia JR,
Yanek LR,
Ahluwalia TS,
Lahti J,
Venturini C,
Tanaka T,
Bielak LF,
Joshi PK,
Rocanin-Arjo A,
Kolcic I,
Navarro P,
Rose LM,
Oldmeadow C,
Riess H,
Mazur J,
Basu S,
Goel A,
Yang Q,
Ghanbari M,
Willemsen G,
Rumley A,
Fiorillo E,
de Craen AJ,
Grotevendt A,
Scott R,
Taylor KD,
Delgado GE,
Yao J,
Kifley A,
Kooperberg C,
Qayyum R,
Lopez LM,
Berentzen TL,
Räikkönen K,
Mangino M,
Bandinelli S,
Peyser PA,
Wild S,
Trégouët DA,
Wright AF,
Marten J,
Zemunik T,
Morrison AC,
Sennblad B,
Tofler G,
de Maat MP,
de Geus EJ,
Lowe GD,
Zoledziewska M,
Sattar N,
Binder H,
Völker U,
Waldenberger M,
Khaw KT,
Mcknight B,
Huang J,
Jenny NS,
Holliday EG,
Qi L,
Mcevoy MG,
Becker DM,
Starr JM,
Sarin AP,
Hysi PG,
Hernandez DG,
Jhun MA,
Campbell H,
Hamsten A,
Rivadeneira F,
Mcardle WL,
Slagboom PE,
Zeller T,
Koenig W,
Psaty BM,
Haritunians T,
Liu J,
Palotie A,
Uitterlinden AG,
Stott DJ,
Hofman A,
Franco OH,
Polasek O,
Rudan I,
Morange PE,
Wilson JF,
Kardia SL,
Ferrucci L,
Spector TD,
Eriksson JG,
Hansen T,
Deary IJ,
Becker LC,
Scott RJ,
Mitchell P,
März W,
Wareham NJ,
Peters A,
Greinacher A,
Wild PS,
Jukema JW,
Boomsma DI,
Hayward C,
Cucca F,
Tracy R,
Watkins H,
Reiner AP,
Folsom AR,
Ridker PM,
O'Donnell CJ,
Smith NL,
Strachan DP,
Dehghan A
Human molecular genetics · 2016 · PMID 26561523
12 pages+
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Pattaro C,
Teumer A,
Gorski M,
Chu AY,
Li M,
Mijatovic V,
Garnaas M,
Tin A,
Sorice R,
Li Y,
Taliun D,
Olden M
and 240 more — show all
Foster M,
Yang Q,
Chen MH,
Pers TH,
Johnson AD,
Ko YA,
Fuchsberger C,
Tayo B,
Nalls M,
Feitosa MF,
Isaacs A,
Dehghan A,
d'Adamo P,
Adeyemo A,
Dieffenbach AK,
Zonderman AB,
Nolte IM,
van der Most PJ,
Wright AF,
Shuldiner AR,
Morrison AC,
Hofman A,
Smith AV,
Dreisbach AW,
Franke A,
Uitterlinden AG,
Metspalu A,
Tonjes A,
Lupo A,
Robino A,
Johansson Å,
Demirkan A,
Kollerits B,
Freedman BI,
Ponte B,
Oostra BA,
Paulweber B,
Krämer BK,
Mitchell BD,
Buckley BM,
Peralta CA,
Hayward C,
Helmer C,
Rotimi CN,
Shaffer CM,
Müller C,
Sala C,
van Duijn CM,
Saint-Pierre A,
Ackermann D,
Shriner D,
Ruggiero D,
Toniolo D,
Lu Y,
Cusi D,
Czamara D,
Ellinghaus D,
Siscovick DS,
Ruderfer D,
Gieger C,
Grallert H,
Rochtchina E,
Atkinson EJ,
Holliday EG,
Boerwinkle E,
Salvi E,
Bottinger EP,
Murgia F,
Rivadeneira F,
Ernst F,
Kronenberg F,
Hu FB,
Navis GJ,
Curhan GC,
Ehret GB,
Homuth G,
Coassin S,
Thun GA,
Pistis G,
Gambaro G,
Malerba G,
Montgomery GW,
Eiriksdottir G,
Jacobs G,
Li G,
Wichmann HE,
Campbell H,
Schmidt H,
Wallaschofski H,
Völzke H,
Brenner H,
Kroemer HK,
Kramer H,
Lin H,
Leach IM,
Ford I,
Guessous I,
Rudan I,
Prokopenko I,
Borecki I,
Heid IM,
Kolcic I,
Persico I,
Jukema JW,
Wilson JF,
Felix JF,
Divers J,
Lambert JC,
Stafford JM,
Gaspoz JM,
Smith JA,
Faul JD,
Wang JJ,
Ding J,
Hirschhorn JN,
Attia J,
Whitfield JB,
Chalmers J,
Viikari J,
Coresh J,
Denny JC,
Karjalainen J,
Fernandes JK,
Endlich K,
Butterbach K,
Keene KL,
Lohman K,
Portas L,
Launer LJ,
Lyytikäinen LP,
Yengo L,
Franke L,
Ferrucci L,
Rose LM,
Kedenko L,
Rao M,
Struchalin M,
Kleber ME,
Cavalieri M,
Haun M,
Cornelis MC,
Ciullo M,
Pirastu M,
de Andrade M,
McEvoy MA,
Woodward M,
Adam M,
Cocca M,
Nauck M,
Imboden M,
Waldenberger M,
Pruijm M,
Metzger M,
Stumvoll M,
Evans MK,
Sale MM,
Kähönen M,
Boban M,
Bochud M,
Rheinberger M,
Verweij N,
Bouatia-Naji N,
Martin NG,
Hastie N,
Probst-Hensch N,
Soranzo N,
Devuyst O,
Raitakari O,
Gottesman O,
Franco OH,
Polasek O,
Gasparini P,
Munroe PB,
Ridker PM,
Mitchell P,
Muntner P,
Meisinger C,
Smit JH,
Kovacs P,
Wild PS,
Froguel P,
Rettig R,
Mägi R,
Biffar R,
Schmidt R,
Middelberg RP,
Carroll RJ,
Penninx BW,
Scott RJ,
Katz R,
Sedaghat S,
Wild SH,
Kardia SL,
Ulivi S,
Hwang SJ,
Enroth S,
Kloiber S,
Trompet S,
Stengel B,
Hancock SJ,
Turner ST,
Rosas SE,
Stracke S,
Harris TB,
Zeller T,
Zemunik T,
Lehtimäki T,
Illig T,
Aspelund T,
Nikopensius T,
Esko T,
Tanaka T,
Gyllensten U,
Völker U,
Emilsson V,
Vitart V,
Aalto V,
Gudnason V,
Chouraki V,
Chen WM,
Igl W,
März W,
Koenig W,
Lieb W,
Loos RJ,
Liu Y,
Snieder H,
Pramstaller PP,
Parsa A,
O'Connell JR,
Susztak K,
Hamet P,
Tremblay J,
de Boer IH,
Böger CA,
Goessling W,
Chasman DI,
Köttgen A,
Kao WH,
Fox CS
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Davies G,
Lam M,
Harris SE,
Trampush JW,
Luciano M,
Hill WD,
Hagenaars SP,
Ritchie SJ,
Marioni RE,
Fawns-Ritchie C,
Liewald DCM,
Okely JA
and 212 more — show all
Ahola-Olli AV,
Barnes CLK,
Bertram L,
Bis JC,
Burdick KE,
Christoforou A,
DeRosse P,
Djurovic S,
Espeseth T,
Giakoumaki S,
Giddaluru S,
Gustavson DE,
Hayward C,
Hofer E,
Ikram MA,
Karlsson R,
Knowles E,
Lahti J,
Leber M,
Li S,
Mather KA,
Melle I,
Morris D,
Oldmeadow C,
Palviainen T,
Payton A,
Pazoki R,
Petrovic K,
Reynolds CA,
Sargurupremraj M,
Scholz M,
Smith JA,
Smith AV,
Terzikhan N,
Thalamuthu A,
Trompet S,
van der Lee SJ,
Ware EB,
Windham BG,
Wright MJ,
Yang J,
Yu J,
Ames D,
Amin N,
Amouyel P,
Andreassen OA,
Armstrong NJ,
Assareh AA,
Attia JR,
Attix D,
Avramopoulos D,
Bennett DA,
Böhmer AC,
Boyle PA,
Brodaty H,
Campbell H,
Cannon TD,
Cirulli ET,
Congdon E,
Conley ED,
Corley J,
Cox SR,
Dale AM,
Dehghan A,
Dick D,
Dickinson D,
Eriksson JG,
Evangelou E,
Faul JD,
Ford I,
Freimer NA,
Gao H,
Giegling I,
Gillespie NA,
Gordon SD,
Gottesman RF,
Griswold ME,
Gudnason V,
Harris TB,
Hartmann AM,
Hatzimanolis A,
Heiss G,
Holliday EG,
Joshi PK,
Kähönen M,
Kardia SLR,
Karlsson I,
Kleineidam L,
Knopman DS,
Kochan NA,
Konte B,
Kwok JB,
Le Hellard S,
Lee T,
Lehtimäki T,
Li SC,
Lill CM,
Liu T,
Koini M,
London E,
Longstreth WT Jr,
Lopez OL,
Loukola A,
Luck T,
Lundervold AJ,
Lundquist A,
Lyytikäinen LP,
Martin NG,
Montgomery GW,
Murray AD,
Need AC,
Noordam R,
Nyberg L,
Ollier W,
Papenberg G,
Pattie A,
Polasek O,
Poldrack RA,
Psaty BM,
Reppermund S,
Riedel-Heller SG,
Rose RJ,
Rotter JI,
Roussos P,
Rovio SP,
Saba Y,
Sabb FW,
Sachdev PS,
Satizabal CL,
Satizabal CL,
Schmid M,
Scott RJ,
Scult MA,
Simino J,
Slagboom PE,
Smyrnis N,
Soumaré A,
Stefanis NC,
Stott DJ,
Straub RE,
Sundet K,
Taylor AM,
Taylor KD,
Tzoulaki I,
Tzourio C,
Uitterlinden A,
Vitart V,
Voineskos AN,
Kaprio J,
Wagner M,
Wagner H,
Weinhold L,
Wen KH,
Widen E,
Yang Q,
Zhao W,
Adams HHH,
Arking DE,
Bilder RM,
Bitsios P,
Boerwinkle E,
Chiba-Falek O,
Corvin A,
De Jager PL,
Debette S,
Donohoe G,
Elliott P,
Fitzpatrick AL,
Gill M,
Glahn DC,
Hägg S,
Hansell NK,
Hariri AR,
Ikram MK,
Jukema JW,
Jukema JW,
Vuoksimaa E,
Keller MC,
Kremen WS,
Launer L,
Lindenberger U,
Palotie A,
Pedersen NL,
Pendleton N,
Porteous DJ,
Räikkönen K,
Raitakari OT,
Ramirez A,
Reinvang I,
Rudan I,
Dan Rujescu,
Schmidt R,
Schmidt H,
Schofield PW,
Schofield PR,
Starr JM,
Steen VM,
Trollor JN,
Turner ST,
Van Duijn CM,
Villringer A,
Weinberger DR,
Weir DR,
Wilson JF,
Malhotra A,
McIntosh AM,
Gale CR,
Seshadri S,
Mosley TH Jr,
Bressler J,
Lencz T,
Deary IJ
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Mahajan A,
Taliun D,
Thurner M,
Robertson NR,
Torres JM,
Rayner NW,
Payne AJ,
Steinthorsdottir V,
Scott RA,
Grarup N,
Cook JP,
Schmidt EM
and 103 more — show all
Wuttke M,
Sarnowski C,
Mägi R,
Nano J,
Gieger C,
Trompet S,
Lecoeur C,
Preuss MH,
Prins BP,
Guo X,
Bielak LF,
Below JE,
Bowden DW,
Chambers JC,
Kim YJ,
Ng MCY,
Petty LE,
Sim X,
Zhang W,
Bennett AJ,
Bork-Jensen J,
Brummett CM,
Canouil M,
Ec Kardt KU,
Fischer K,
Kardia SLR,
Kronenberg F,
Läll K,
Liu CT,
Locke AE,
Luan J,
Ntalla I,
Nylander V,
Schönherr S,
Schurmann C,
Yengo L,
Bottinger EP,
Brandslund I,
Christensen C,
Dedoussis G,
Florez JC,
Ford I,
Franco OH,
Frayling TM,
Giedraitis V,
Hackinger S,
Hattersley AT,
Herder C,
Ikram MA,
Ingelsson M,
Jørgensen ME,
Jørgensen T,
Kriebel J,
Kuusisto J,
Ligthart S,
Lindgren CM,
Linneberg A,
Lyssenko V,
Mamakou V,
Meitinger T,
Mohlke KL,
Morris AD,
Nadkarni G,
Pankow JS,
Peters A,
Sattar N,
Stančáková A,
Strauch K,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tuomilehto J,
Witte DR,
Dupuis J,
Peyser PA,
Zeggini E,
Loos RJF,
Froguel P,
Ingelsson E,
Lind L,
Groop L,
Laakso M,
Collins FS,
Jukema JW,
Palmer CNA,
Grallert H,
Metspalu A,
Dehghan A,
Köttgen A,
Abecasis GR,
Meigs JB,
Rotter JI,
Marchini J,
Pedersen O,
Hansen T,
Langenberg C,
Wareham NJ,
Stefansson K,
Gloyn AL,
Morris AP,
Boehnke M,
McCarthy MI
Nature genetics · 2018 · PMID 30297969
12 pages+
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Ligthart S,
Vaez A,
Võsa U,
Stathopoulou MG,
de Vries PS,
Prins BP,
Van der Most PJ,
Tanaka T,
Naderi E,
Rose LM,
Wu Y,
Karlsson R
and 274 more — show all
Barbalic M,
Lin H,
Pool R,
Zhu G,
Macé A,
Sidore C,
Trompet S,
Mangino M,
Sabater-Lleal M,
Kemp JP,
Abbasi A,
Kacprowski T,
Verweij N,
Smith AV,
Huang T,
Marzi C,
Feitosa MF,
Lohman KK,
Kleber ME,
Milaneschi Y,
Mueller C,
Huq M,
Vlachopoulou E,
Lyytikäinen LP,
Oldmeadow C,
Deelen J,
Perola M,
Zhao JH,
Feenstra B,
Amini M,
Lahti J,
Schraut KE,
Fornage M,
Suktitipat B,
Chen WM,
Li X,
Nutile T,
Malerba G,
Luan J,
Bak T,
Schork N,
Del Greco M F,
Thiering E,
Mahajan A,
Marioni RE,
Mihailov E,
Eriksson J,
Ozel AB,
Zhang W,
Nethander M,
Cheng YC,
Aslibekyan S,
Ang W,
Gandin I,
Yengo L,
Portas L,
Kooperberg C,
Hofer E,
Rajan KB,
Schurmann C,
den Hollander W,
Ahluwalia TS,
Zhao J,
Draisma HHM,
Ford I,
Timpson N,
Teumer A,
Huang H,
Wahl S,
Liu Y,
Huang J,
Uh HW,
Geller F,
Joshi PK,
Yanek LR,
Trabetti E,
Lehne B,
Vozzi D,
Verbanck M,
Biino G,
Saba Y,
Meulenbelt I,
O'Connell JR,
Laakso M,
Giulianini F,
Magnusson PKE,
Ballantyne CM,
Hottenga JJ,
Montgomery GW,
Rivadineira F,
Rueedi R,
Steri M,
Herzig KH,
Stott DJ,
Menni C,
Frånberg M,
St Pourcain B,
Felix SB,
Pers TH,
Bakker SJL,
Kraft P,
Peters A,
Vaidya D,
Delgado G,
Smit JH,
Großmann V,
Sinisalo J,
Seppälä I,
Williams SR,
Holliday EG,
Moed M,
Langenberg C,
Räikkönen K,
Ding J,
Campbell H,
Sale MM,
Chen YI,
James AL,
Ruggiero D,
Soranzo N,
Hartman CA,
Smith EN,
Berenson GS,
Fuchsberger C,
Hernandez D,
Tiesler CMT,
Giedraitis V,
Liewald D,
Fischer K,
Mellström D,
Larsson A,
Wang Y,
Scott WR,
Lorentzon M,
Beilby J,
Ryan KA,
Pennell CE,
Vuckovic D,
Balkau B,
Concas MP,
Schmidt R,
Mendes de Leon CF,
Bottinger EP,
Kloppenburg M,
Paternoster L,
Boehnke M,
Musk AW,
Willemsen G,
Evans DM,
Madden PAF,
Kähönen M,
Kutalik Z,
Zoledziewska M,
Karhunen V,
Kritchevsky SB,
Sattar N,
Lachance G,
Clarke R,
Harris TB,
Raitakari OT,
Attia JR,
van Heemst D,
Kajantie E,
Sorice R,
Gambaro G,
Scott RA,
Hicks AA,
Ferrucci L,
Standl M,
Lindgren CM,
Starr JM,
Karlsson M,
Lind L,
Li JZ,
Chambers JC,
Mori TA,
de Geus EJCN,
Heath AC,
Martin NG,
Auvinen J,
Buckley BM,
de Craen AJM,
Waldenberger M,
Strauch K,
Meitinger T,
Scott RJ,
McEvoy M,
Beekman M,
Bombieri C,
Ridker PM,
Mohlke KL,
Pedersen NL,
Morrison AC,
Boomsma DI,
Whitfield JB,
Strachan DP,
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FinnGen · eMERGE Consortium
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Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
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Nature communications · 2022 · PMID 35922433 · open access
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Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
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