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129 matches for
Smith AV,
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Köttgen A,
Albrecht E,
Teumer A,
Vitart V,
Krumsiek J,
Hundertmark C,
Pistis G,
Ruggiero D,
O'Seaghdha CM,
Haller T,
Yang Q,
Tanaka T
and 214 more — show all
Johnson AD,
Kutalik Z,
Smith AV,
Shi J,
Struchalin M,
Middelberg RP,
Brown MJ,
Gaffo AL,
Pirastu N,
Li G,
Hayward C,
Zemunik T,
Huffman J,
Yengo L,
Zhao JH,
Demirkan A,
Feitosa MF,
Liu X,
Malerba G,
Lopez LM,
van der Harst P,
Li X,
Kleber ME,
Hicks AA,
Nolte IM,
Johansson A,
Murgia F,
Wild SH,
Bakker SJ,
Peden JF,
Dehghan A,
Steri M,
Tenesa A,
Lagou V,
Salo P,
Mangino M,
Rose LM,
Lehtimäki T,
Woodward OM,
Okada Y,
Tin A,
Müller C,
Oldmeadow C,
Putku M,
Czamara D,
Kraft P,
Frogheri L,
Thun GA,
Grotevendt A,
Gislason GK,
Harris TB,
Launer LJ,
McArdle P,
Shuldiner AR,
Boerwinkle E,
Coresh J,
Schmidt H,
Schallert M,
Martin NG,
Montgomery GW,
Kubo M,
Nakamura Y,
Tanaka T,
Munroe PB,
Samani NJ,
Jacobs DR Jr,
Liu K,
D'Adamo P,
Ulivi S,
Rotter JI,
Psaty BM,
Vollenweider P,
Waeber G,
Campbell S,
Devuyst O,
Navarro P,
Kolcic I,
Hastie N,
Balkau B,
Froguel P,
Esko T,
Salumets A,
Khaw KT,
Langenberg C,
Wareham NJ,
Isaacs A,
Kraja A,
Zhang Q,
Wild PS,
Scott RJ,
Holliday EG,
Org E,
Org E,
Viigimaa M,
Bandinelli S,
Metter JE,
Lupo A,
Trabetti E,
Sorice R,
Döring A,
Lattka E,
Strauch K,
Theis F,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Bruinenberg M,
Stolk RP,
Kooner JS,
Zhang W,
Winkelmann BR,
Boehm BO,
Lucae S,
Penninx BW,
Smit JH,
Curhan G,
Mudgal P,
Plenge RM,
Portas L,
Persico I,
Kirin M,
Wilson JF,
Mateo Leach I,
van Gilst WH,
Goel A,
Ongen H,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Imboden M,
von Eckardstein A,
Cucca F,
Nagaraja R,
Piras MG,
Nauck M,
Schurmann C,
Budde K,
Ernst F,
Farrington SM,
Theodoratou E,
Prokopenko I,
Stumvoll M,
Jula A,
Perola M,
Salomaa V,
Shin SY,
Spector TD,
Sala C,
Ridker PM,
Kähönen M,
Viikari J,
Hengstenberg C,
Nelson CP,
Meschia JF,
Nalls MA,
Sharma P,
Singleton AB,
Kamatani N,
Zeller T,
Burnier M,
Attia J,
Laan M,
Klopp N,
Hillege HL,
Kloiber S,
Choi H,
Pirastu M,
Tore S,
Probst-Hensch NM,
Völzke H,
Gudnason V,
Parsa A,
Schmidt R,
Whitfield JB,
Fornage M,
Gasparini P,
Siscovick DS,
Polašek O,
Campbell H,
Rudan I,
Bouatia-Naji N,
Metspalu A,
Loos RJ,
van Duijn CM,
Borecki IB,
Ferrucci L,
Gambaro G,
Deary IJ,
Wolffenbuttel BH,
Chambers JC,
März W,
Pramstaller PP,
Snieder H,
Gyllensten U,
Wright AF,
Navis G,
Watkins H,
Witteman JC,
Sanna S,
Schipf S,
Dunlop MG,
Tönjes A,
Ripatti S,
Soranzo N,
Toniolo D,
Chasman DI,
Raitakari O,
Kao WH,
Ciullo M,
Fox CS,
Caulfield M,
Bochud M,
Gieger C
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
Simino J,
Shi G,
Bis JC,
Chasman DI,
Ehret GB,
Gu X,
Guo X,
Hwang SJ,
Sijbrands E,
Smith AV,
Verwoert GC,
Bragg-Gresham JL
and 91 more — show all
Cadby G,
Chen P,
Cheng CY,
Corre T,
de Boer RA,
Goel A,
Johnson T,
Khor CC,
Lluís-Ganella C,
Luan J,
Lyytikäinen LP,
Nolte IM,
Sim X,
Sõber S,
van der Most PJ,
Verweij N,
Zhao JH,
Amin N,
Boerwinkle E,
Bouchard C,
Dehghan A,
Eiriksdottir G,
Elosua R,
Franco OH,
Gieger C,
Harris TB,
Hercberg S,
Hofman A,
James AL,
Johnson AD,
Kähönen M,
Khaw KT,
Kutalik Z,
Larson MG,
Launer LJ,
Li G,
Liu J,
Liu K,
Morrison AC,
Navis G,
Ong RT,
Papanicolau GJ,
Penninx BW,
Psaty BM,
Raffel LJ,
Raitakari OT,
Rice K,
Rivadeneira F,
Rose LM,
Sanna S,
Scott RA,
Siscovick DS,
Stolk RP,
Uitterlinden AG,
Vaidya D,
van der Klauw MM,
Vasan RS,
Vithana EN,
Völker U,
Völzke H,
Watkins H,
Young TL,
Aung T,
Bochud M,
Farrall M,
Hartman CA,
Laan M,
Lakatta EG,
Lehtimäki T,
Loos RJ,
Lucas G,
Meneton P,
Palmer LJ,
Rettig R,
Snieder H,
Tai ES,
Teo YY,
van der Harst P,
Wareham NJ,
Wijmenga C,
Wong TY,
Fornage M,
Gudnason V,
Levy D,
Palmas W,
Ridker PM,
Rotter JI,
van Duijn CM,
Witteman JC,
Chakravarti A,
Rao DC
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
3 pages
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Schumann G,
Liu C,
O'Reilly P,
Gao H,
Song P,
Xu B,
Ruggeri B,
Amin N,
Jia T,
Preis S,
Segura Lepe M,
Akira S
and 115 more — show all
Barbieri C,
Baumeister S,
Cauchi S,
Clarke TK,
Enroth S,
Fischer K,
Hällfors J,
Harris SE,
Hieber S,
Hofer E,
Hottenga JJ,
Johansson Å,
Joshi PK,
Kaartinen N,
Laitinen J,
Lemaitre R,
Loukola A,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Mbarek H,
Milaneschi Y,
Moayyeri A,
Mukamal K,
Nelson C,
Nettleton J,
Partinen E,
Rawal R,
Robino A,
Rose L,
Sala C,
Satoh T,
Schmidt R,
Schraut K,
Scott R,
Smith AV,
Starr JM,
Teumer A,
Trompet S,
Uitterlinden AG,
Venturini C,
Vergnaud AC,
Verweij N,
Vitart V,
Vuckovic D,
Wedenoja J,
Yengo L,
Yu B,
Zhang W,
Zhao JH,
Boomsma DI,
Chambers J,
Chasman DI,
Daniela T,
de Geus E,
Deary I,
Eriksson JG,
Esko T,
Eulenburg V,
Franco OH,
Froguel P,
Gieger C,
Grabe HJ,
Gudnason V,
Gyllensten U,
Harris TB,
Hartikainen AL,
Heath AC,
Hocking L,
Hofman A,
Huth C,
Jarvelin MR,
Jukema JW,
Kaprio J,
Kooner JS,
Kutalik Z,
Lahti J,
Langenberg C,
Lehtimäki T,
Liu Y,
Madden PA,
Martin N,
Morrison A,
Penninx B,
Pirastu N,
Psaty B,
Raitakari O,
Ridker P,
Rose R,
Rotter JI,
Samani NJ,
Schmidt H,
Spector TD,
Stott D,
Strachan D,
Tzoulaki I,
van der Harst P,
van Duijn CM,
Marques-Vidal P,
Vollenweider P,
Wareham NJ,
Whitfield JB,
Wilson J,
Wolffenbuttel B,
Bakalkin G,
Evangelou E,
Liu Y,
Rice KM,
Desrivières S,
Kliewer SA,
Mangelsdorf DJ,
Müller CP,
Levy D,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Franceschini N,
Giambartolomei C,
de Vries PS,
Finan C,
Bis JC,
Huntley RP,
Lovering RC,
Tajuddin SM,
Winkler TW,
Graff M,
Kavousi M,
Dale C
and 146 more — show all
Smith AV,
Hofer E,
van Leeuwen EM,
Nolte IM,
Lu L,
Scholz M,
Sargurupremraj M,
Pitkänen N,
Franzén O,
Joshi PK,
Noordam R,
Marioni RE,
Hwang SJ,
Musani SK,
Schminke U,
Palmas W,
Isaacs A,
Correa A,
Zonderman AB,
Hofman A,
Teumer A,
Cox AJ,
Uitterlinden AG,
Wong A,
Smit AJ,
Newman AB,
Britton A,
Ruusalepp A,
Sennblad B,
Hedblad B,
Pasaniuc B,
Penninx BW,
Langefeld CD,
Wassel CL,
Tzourio C,
Fava C,
Baldassarre D,
O'Leary DH,
Teupser D,
Kuh D,
Tremoli E,
Mannarino E,
Grossi E,
Boerwinkle E,
Schadt EE,
Ingelsson E,
Veglia F,
Rivadeneira F,
Beutner F,
Chauhan G,
Heiss G,
Snieder H,
Campbell H,
Völzke H,
Markus HS,
Deary IJ,
Jukema JW,
de Graaf J,
Price J,
Pott J,
Hopewell JC,
Liang J,
Thiery J,
Engmann J,
Gertow K,
Rice K,
Taylor KD,
Dhana K,
Kiemeney LALM,
Lind L,
Raffield LM,
Launer LJ,
Holdt LM,
Dörr M,
Dichgans M,
Traylor M,
Sitzer M,
Kumari M,
Kivimaki M,
Nalls MA,
Melander O,
Raitakari O,
Franco OH,
Rueda-Ochoa OL,
Roussos P,
Whincup PH,
Amouyel P,
Giral P,
Anugu P,
Wong Q,
Malik R,
Rauramaa R,
Burkhardt R,
Hardy R,
Schmidt R,
de Mutsert R,
Morris RW,
Strawbridge RJ,
Wannamethee SG,
Hägg S,
Shah S,
McLachlan S,
Trompet S,
Seshadri S,
Kurl S,
Heckbert SR,
Ring S,
Harris TB,
Lehtimäki T,
Galesloot TE,
Shah T,
de Faire U,
Plagnol V,
Rosamond WD,
Post W,
Zhu X,
Zhang X,
Guo X,
Saba Y,
Dehghan A,
Seldenrijk A,
Morrison AC,
Hamsten A,
Psaty BM,
van Duijn CM,
Lawlor DA,
Mook-Kanamori DO,
Bowden DW,
Schmidt H,
Wilson JF,
Wilson JG,
Rotter JI,
Wardlaw JM,
Deanfield J,
Halcox J,
Lyytikäinen LP,
Loeffler M,
Evans MK,
Debette S,
Humphries SE,
Völker U,
Gudnason V,
Hingorani AD,
Björkegren JLM,
Casas JP,
O'Donnell CJ
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
3 pages
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
and 192 more — show all
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
Pedersen NL,
Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
Harris TB,
Navis G,
Harst PV,
Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
Soranzo N,
Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
Siscovick DS,
Watkins H,
Lecoeur C,
Vollenweider P,
Franco-Cereceda A,
Eriksson P,
Jarvelin MR,
Stefansson K,
Hamsten A,
Nicholson G,
Karpe F,
Dermitzakis ET,
Lindgren CM,
McCarthy MI,
Froguel P,
Kaakinen MA,
Lyssenko V,
Watanabe RM,
Ingelsson E,
Florez JC,
Dupuis J,
Barroso I,
Morris AP,
Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Ikram MK,
Sim X,
Jensen RA,
Cotch MF,
Hewitt AW,
Ikram MA,
Wang JJ,
Klein R,
Klein BE,
Breteler MM,
Cheung N,
Liew G
and 45 more — show all
Mitchell P,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
de Jong PT,
van Duijn CM,
Kao L,
Cheng CY,
Smith AV,
Glazer NL,
Lumley T,
McKnight B,
Psaty BM,
Jonasson F,
Eiriksdottir G,
Aspelund T,
Harris TB,
Launer LJ,
Taylor KD,
Li X,
Iyengar SK,
Xi Q,
Sivakumaran TA,
Mackey DA,
Macgregor S,
Martin NG,
Young TL,
Bis JC,
Wiggins KL,
Heckbert SR,
Hammond CJ,
Andrew T,
Fahy S,
Attia J,
Holliday EG,
Scott RJ,
Islam FM,
Rotter JI,
McAuley AK,
Boerwinkle E,
Tai ES,
Gudnason V,
Siscovick DS,
Vingerling JR,
Wong TY
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
2 pages
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
Bis JC,
Kavousi M,
Franceschini N,
Isaacs A,
Abecasis GR,
Schminke U,
Post WS,
Smith AV,
Cupples LA,
Markus HS,
Schmidt R,
Huffman JE
and 81 more — show all
Lehtimäki T,
Baumert J,
Münzel T,
Heckbert SR,
Dehghan A,
North K,
Oostra B,
Bevan S,
Stoegerer EM,
Hayward C,
Raitakari O,
Meisinger C,
Schillert A,
Sanna S,
Völzke H,
Cheng YC,
Thorsson B,
Fox CS,
Rice K,
Rivadeneira F,
Nambi V,
Halperin E,
Petrovic KE,
Peltonen L,
Wichmann HE,
Schnabel RB,
Dörr M,
Parsa A,
Aspelund T,
Demissie S,
Kathiresan S,
Reilly MP,
Taylor K,
Uitterlinden A,
Couper DJ,
Sitzer M,
Kähönen M,
Illig T,
Wild PS,
Orru M,
Lüdemann J,
Shuldiner AR,
Eiriksdottir G,
White CC,
Rotter JI,
Hofman A,
Seissler J,
Zeller T,
Usala G,
Ernst F,
Launer LJ,
D'Agostino RB Sr,
O'Leary DH,
Ballantyne C,
Thiery J,
Ziegler A,
Lakatta EG,
Chilukoti RK,
Harris TB,
Wolf PA,
Psaty BM,
Polak JF,
Li X,
Rathmann W,
Uda M,
Boerwinkle E,
Klopp N,
Schmidt H,
Wilson JF,
Viikari J,
Koenig W,
Blankenberg S,
Newman AB,
Witteman J,
Heiss G,
Duijn Cv,
Scuteri A,
Homuth G,
Mitchell BD,
Gudnason V,
O'Donnell CJ
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
2 pages
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Bis JC,
DeCarli C,
Smith AV,
van der Lijn F,
Crivello F,
Fornage M,
Debette S,
Shulman JM,
Schmidt H,
Srikanth V,
Schuur M,
Yu L
and 71 more — show all
Choi SH,
Sigurdsson S,
Verhaaren BF,
DeStefano AL,
Lambert JC,
Jack CR Jr,
Struchalin M,
Stankovich J,
Ibrahim-Verbaas CA,
Fleischman D,
Zijdenbos A,
den Heijer T,
Mazoyer B,
Coker LH,
Enzinger C,
Danoy P,
Amin N,
Arfanakis K,
van Buchem MA,
de Bruijn RF,
Beiser A,
Dufouil C,
Huang J,
Cavalieri M,
Thomson R,
Niessen WJ,
Chibnik LB,
Gislason GK,
Hofman A,
Pikula A,
Pikula A,
Amouyel P,
Freeman KB,
Phan TG,
Oostra BA,
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Wright MJ,
Franke B,
Martin NG,
Thompson PM,
Nalls MA,
Uitterlinden AG,
Au R,
Elbaz A,
Beare RJ,
van Swieten JC,
Lopez OL,
Harris TB,
Chouraki V,
Breteler MM,
De Jager PL,
Becker JT,
Vernooij MW,
Knopman D,
Fazekas F,
Wolf PA,
van der Lugt A,
Gudnason V,
Longstreth WT Jr,
Brown MA,
Bennett DA,
van Duijn CM,
Mosley TH,
Schmidt R,
Tzourio C,
Launer LJ,
Ikram MA,
Seshadri S
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women
Fox CS,
Liu Y,
White CC,
Feitosa M,
Smith AV,
Heard-Costa N,
Lohman K,
Johnson AD,
Foster MC,
Greenawalt DM,
Griffin P,
Ding J
and 12 more — show all
Newman AB,
Tylavsky F,
Miljkovic I,
Kritchevsky SB,
Launer L,
Garcia M,
Eiriksdottir G,
Carr JJ,
Gudnason V,
Harris TB,
Cupples LA,
Borecki IB
GIANT Consortium · MAGIC Consortium and 1 more consortia
PLoS genetics · 2012 · PMID 22589738 · open access
2 pages
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
Hancock DB,
Soler Artigas M,
Gharib SA,
Henry A,
Manichaikul A,
Ramasamy A,
Loth DW,
Imboden M,
Koch B,
McArdle WL,
Smith AV,
Smolonska J
and 78 more — show all
Sood A,
Tang W,
Wilk JB,
Zhai G,
Zhao JH,
Aschard H,
Burkart KM,
Curjuric I,
Eijgelsheim M,
Elliott P,
Gu X,
Harris TB,
Janson C,
Homuth G,
Hysi PG,
Liu JZ,
Loehr LR,
Lohman K,
Loos RJ,
Manning AK,
Marciante KD,
Obeidat M,
Postma DS,
Aldrich MC,
Brusselle GG,
Chen TH,
Eiriksdottir G,
Franceschini N,
Heinrich J,
Rotter JI,
Wijmenga C,
Williams OD,
Bentley AR,
Hofman A,
Laurie CC,
Lumley T,
Morrison AC,
Joubert BR,
Rivadeneira F,
Couper DJ,
Kritchevsky SB,
Liu Y,
Wjst M,
Wain LV,
Vonk JM,
Uitterlinden AG,
Rochat T,
Rich SS,
Psaty BM,
O'Connor GT,
North KE,
Mirel DB,
Meibohm B,
Launer LJ,
Khaw KT,
Hartikainen AL,
Hammond CJ,
Gläser S,
Marchini J,
Kraft P,
Wareham NJ,
Völzke H,
Stricker BH,
Spector TD,
Probst-Hensch NM,
Jarvis D,
Jarvelin MR,
Heckbert SR,
Gudnason V,
Boezen HM,
Barr RG,
Cassano PA,
Strachan DP,
Fornage M,
Hall IP,
Dupuis J,
Tobin MD,
London SJ
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
and 52 more — show all
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
O'Seaghdha CM,
Wu H,
Yang Q,
Kapur K,
Guessous I,
Zuber AM,
Köttgen A,
Stoudmann C,
Teumer A,
Kutalik Z,
Mangino M,
Dehghan A
and 97 more — show all
Zhang W,
Eiriksdottir G,
Li G,
Tanaka T,
Portas L,
Lopez LM,
Hayward C,
Lohman K,
Matsuda K,
Padmanabhan S,
Firsov D,
Sorice R,
Ulivi S,
Brockhaus AC,
Kleber ME,
Mahajan A,
Ernst FD,
Gudnason V,
Launer LJ,
Mace A,
Boerwinckle E,
Arking DE,
Tanikawa C,
Nakamura Y,
Brown MJ,
Gaspoz JM,
Theler JM,
Siscovick DS,
Psaty BM,
Bergmann S,
Vollenweider P,
Vitart V,
Wright AF,
Zemunik T,
Boban M,
Kolcic I,
Navarro P,
Brown EM,
Estrada K,
Ding J,
Harris TB,
Bandinelli S,
Hernandez D,
Singleton AB,
Girotto G,
Ruggiero D,
d'Adamo AP,
Robino A,
Meitinger T,
Meisinger C,
Davies G,
Starr JM,
Chambers JC,
Boehm BO,
Winkelmann BR,
Huang J,
Murgia F,
Wild SH,
Campbell H,
Morris AP,
Franco OH,
Hofman A,
Uitterlinden AG,
Rivadeneira F,
Völker U,
Hannemann A,
Biffar R,
Hoffmann W,
Shin SY,
Lescuyer P,
Henry H,
Schurmann C,
Munroe PB,
Gasparini P,
Pirastu N,
Ciullo M,
Gieger C,
März W,
Lind L,
Spector TD,
Smith AV,
Rudan I,
Wilson JF,
Polasek O,
Deary IJ,
Pirastu M,
Ferrucci L,
Liu Y,
Kestenbaum B,
Kooner JS,
Witteman JC,
Nauck M,
Kao WH,
Wallaschofski H,
Bonny O,
Fox CS,
Bochud M
SUNLIGHT Consortium · GEFOS Consortium
PLoS genetics · 2013 · PMID 24068962 · open access
2 pages
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
and 470 more — show all
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
Dehghan A,
Bis JC,
White CC,
Smith AV,
Morrison AC,
Cupples LA,
Trompet S,
Chasman DI,
Lumley T,
Völker U,
Buckley BM,
Ding J
and 55 more — show all
Jensen MK,
Folsom AR,
Kritchevsky SB,
Girman CJ,
Ford I,
Dörr M,
Salomaa V,
Uitterlinden AG,
Eiriksdottir G,
Vasan RS,
Franceschini N,
Carty CL,
Virtamo J,
Demissie S,
Amouyel P,
Arveiler D,
Heckbert SR,
Ferrières J,
Ducimetière P,
Smith NL,
Wang YA,
Siscovick DS,
Rice KM,
Wiklund PG,
Taylor KD,
Evans A,
Kee F,
Rotter JI,
Karvanen J,
Kuulasmaa K,
Heiss G,
Kraft P,
Launer LJ,
Hofman A,
Markus MR,
Rose LM,
Silander K,
Wagner P,
Benjamin EJ,
Lohman K,
Stott DJ,
Rivadeneira F,
Harris TB,
Levy D,
Liu Y,
Rimm EB,
Jukema JW,
Völzke H,
Ridker PM,
Blankenberg S,
Franco OH,
Gudnason V,
Psaty BM,
Boerwinkle E,
O'Donnell CJ
PloS one · 2016 · PMID 26950853 · open access
2 pages
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
van Leeuwen EM,
Sabo A,
Bis JC,
Huffman JE,
Manichaikul A,
Smith AV,
Feitosa MF,
Demissie S,
Joshi PK,
Duan Q,
Marten J,
van Klinken JB
and 86 more — show all
Surakka I,
Nolte IM,
Zhang W,
Mbarek H,
Li-Gao R,
Trompet S,
Verweij N,
Evangelou E,
Lyytikäinen LP,
Tayo BO,
Deelen J,
van der Most PJ,
van der Laan SW,
Arking DE,
Morrison A,
Dehghan A,
Franco OH,
Hofman A,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Mychaleckyj JC,
Campbell A,
Hocking LJ,
Padmanabhan S,
Brody JA,
Rice KM,
White CC,
Harris T,
Isaacs A,
Campbell H,
Lange LA,
Rudan I,
Kolcic I,
Navarro P,
Zemunik T,
Salomaa V,
Kooner AS,
Kooner JS,
Lehne B,
Scott WR,
Tan ST,
de Geus EJ,
Milaneschi Y,
Penninx BW,
Willemsen G,
de Mutsert R,
Ford I,
Gansevoort RT,
Segura-Lepe MP,
Raitakari OT,
Viikari JS,
Nikus K,
Forrester T,
McKenzie CA,
de Craen AJ,
de Ruijter HM,
Pasterkamp G,
Snieder H,
Oldehinkel AJ,
Slagboom PE,
Cooper RS,
Kähönen M,
Lehtimäki T,
Elliott P,
van der Harst P,
Jukema JW,
Mook-Kanamori DO,
Boomsma DI,
Chambers JC,
Swertz M,
Ripatti S,
Willems van Dijk K,
Vitart V,
Polasek O,
Hayward C,
Wilson JG,
Wilson JF,
Gudnason V,
Rich SS,
Psaty BM,
Borecki IB,
Boerwinkle E,
Rotter JI,
Cupples LA,
van Duijn CM
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
2 pages
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Matteini AM,
Tanaka T,
Karasik D,
Atzmon G,
Chou WC,
Eicher JD,
Johnson AD,
Arnold AM,
Callisaya ML,
Davies G,
Evans DS,
Holtfreter B
and 55 more — show all
Lohman K,
Lunetta KL,
Mangino M,
Smith AV,
Smith JA,
Teumer A,
Yu L,
Arking DE,
Buchman AS,
Chibinik LB,
De Jager PL,
Evans DA,
Faul JD,
Garcia ME,
Gillham-Nasenya I,
Gudnason V,
Hofman A,
Hsu YH,
Ittermann T,
Lahousse L,
Liewald DC,
Liu Y,
Lopez L,
Rivadeneira F,
Rotter JI,
Siggeirsdottir K,
Starr JM,
Thomson R,
Tranah GJ,
Uitterlinden AG,
Völker U,
Völzke H,
Weir DR,
Yaffe K,
Zhao W,
Zhuang WV,
Zmuda JM,
Bennett DA,
Cummings SR,
Deary IJ,
Ferrucci L,
Harris TB,
Kardia SL,
Kocher T,
Kritchevsky SB,
Psaty BM,
Seshadri S,
Spector TD,
Srikanth VK,
Windham BG,
Zillikens MC,
Newman AB,
Walston JD,
Kiel DP,
Murabito JM
Aging cell · 2016 · PMID 27325353 · open access
2 pages
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
and 76 more — show all
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
2 pages
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Armstrong NJ,
Mather KA,
Sargurupremraj M,
Knol MJ,
Malik R,
Satizabal CL,
Yanek LR,
Wen W,
Gudnason VG,
Dueker ND,
Elliott LT,
Hofer E
and 74 more — show all
Bis J,
Jahanshad N,
Li S,
Logue MA,
Luciano M,
Scholz M,
Smith AV,
Trompet S,
Vojinovic D,
Xia R,
Alfaro-Almagro F,
Ames D,
Amin N,
Amouyel P,
Beiser AS,
Brodaty H,
Deary IJ,
Fennema-Notestine C,
Gampawar PG,
Gottesman R,
Griffanti L,
Jack CR Jr,
Jenkinson M,
Jiang J,
Kral BG,
Kwok JB,
Lampe L,
C M Liewald D,
Maillard P,
Marchini J,
Bastin ME,
Mazoyer B,
Pirpamer L,
Rafael Romero J,
Roshchupkin GV,
Schofield PR,
Schroeter ML,
Stott DJ,
Thalamuthu A,
Trollor J,
Tzourio C,
van der Grond J,
Vernooij MW,
Witte VA,
Wright MJ,
Yang Q,
Morris Z,
Siggurdsson S,
Psaty B,
Villringer A,
Schmidt H,
Haberg AK,
van Duijn CM,
Jukema JW,
Dichgans M,
Sacco RL,
Wright CB,
Kremen WS,
Becker LC,
Thompson PM,
Mosley TH,
Wardlaw JM,
Ikram MA,
Adams HHH,
Seshadri S,
Sachdev PS,
Smith SM,
Launer L,
Longstreth W,
DeCarli C,
Schmidt R,
Fornage M,
Debette S,
Nyquist PA
Stroke · 2020 · PMID 32517579
2 pages
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
Hu Y,
Sun Q,
Jain D,
Broome J,
Chen MH,
Thibord F,
McHugh C,
Surendran P,
Blackwell TW,
Brody JA,
Bhan A
and 55 more — show all
Chami N,
de Vries PS,
Ekunwe L,
Heard-Costa N,
Hobbs BD,
Manichaikul A,
Moon JY,
Preuss MH,
Ryan K,
Wang Z,
Wheeler M,
Yanek LR,
Abecasis GR,
Almasy L,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Choquet H,
Correa A,
Curran JE,
Faraday N,
Fornage M,
Glahn DC,
Hou L,
Jorgenson E,
Kooperberg C,
Lewis JP,
Lloyd-Jones DM,
Loos RJF,
Min YI,
Mitchell BD,
Morrison AC,
Nickerson DA,
North KE,
O'Connell JR,
Pankratz N,
Psaty BM,
Vasan RS,
Rich SS,
Rotter JI,
Smith AV,
Smith NL,
Tang H,
Tracy RP,
Conomos MP,
Laurie CA,
Mathias RA,
Li Y,
Auer PL,
Thornton T,
Reiner AP,
Johnson AD,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
2 pages
Questions about this list
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My paper is not here. Does that mean you rejected it?
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