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189 matches for
Psaty B,
showing the first 20.
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
and 68 more — show all
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
Wilk JB,
Shrine NR,
Loehr LR,
Zhao JH,
Manichaikul A,
Lopez LM,
Smith AV,
Heckbert SR,
Smolonska J,
Tang W,
Loth DW,
Curjuric I
and 67 more — show all
Hui J,
Cho MH,
Latourelle JC,
Henry AP,
Aldrich M,
Bakke P,
Beaty TH,
Bentley AR,
Borecki IB,
Brusselle GG,
Burkart KM,
Chen TH,
Couper D,
Crapo JD,
Davies G,
Dupuis J,
Franceschini N,
Gulsvik A,
Hancock DB,
Harris TB,
Hofman A,
Imboden M,
James AL,
Khaw KT,
Lahousse L,
Launer LJ,
Litonjua A,
Liu Y,
Lohman KK,
Lomas DA,
Lumley T,
Marciante KD,
McArdle WL,
Meibohm B,
Morrison AC,
Musk AW,
Myers RH,
North KE,
Postma DS,
Psaty BM,
Rich SS,
Rivadeneira F,
Rochat T,
Rotter JI,
Soler Artigas M,
Starr JM,
Uitterlinden AG,
Wareham NJ,
Wijmenga C,
Zanen P,
Province MA,
Silverman EK,
Deary IJ,
Palmer LJ,
Cassano PA,
Gudnason V,
Barr RG,
Loos RJ,
Strachan DP,
London SJ,
Boezen HM,
Probst-Hensch N,
Gharib SA,
Hall IP,
O'Connor GT,
Tobin MD,
Stricker BH
American journal of respiratory and critical care medicine · 2012 · PMID 22837378
1 page
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
Loos RJ,
Powell JE,
Medland SE,
Speliotes EK,
Chasman DI,
Rose LM,
Thorleifsson G,
Steinthorsdottir V,
Mägi R,
Waite L,
Smith AV
and 160 more — show all
Yerges-Armstrong LM,
Monda KL,
Hadley D,
Mahajan A,
Li G,
Kapur K,
Vitart V,
Huffman JE,
Wang SR,
Palmer C,
Esko T,
Fischer K,
Zhao JH,
Demirkan A,
Isaacs A,
Feitosa MF,
Luan J,
Heard-Costa NL,
White C,
Jackson AU,
Preuss M,
Ziegler A,
Eriksson J,
Kutalik Z,
Frau F,
Nolte IM,
Van Vliet-Ostaptchouk JV,
Hottenga JJ,
Jacobs KB,
Verweij N,
Goel A,
Medina-Gomez C,
Estrada K,
Bragg-Gresham JL,
Sanna S,
Sidore C,
Tyrer J,
Teumer A,
Prokopenko I,
Mangino M,
Lindgren CM,
Assimes TL,
Shuldiner AR,
Hui J,
Beilby JP,
McArdle WL,
Hall P,
Haritunians T,
Zgaga L,
Kolcic I,
Polasek O,
Zemunik T,
Oostra BA,
Junttila MJ,
Grönberg H,
Schreiber S,
Peters A,
Hicks AA,
Stephens J,
Foad NS,
Laitinen J,
Pouta A,
Kaakinen M,
Willemsen G,
Vink JM,
Wild SH,
Navis G,
Asselbergs FW,
Homuth G,
John U,
Iribarren C,
Harris T,
Launer L,
Gudnason V,
O'Connell JR,
Boerwinkle E,
Cadby G,
Palmer LJ,
James AL,
Musk AW,
Ingelsson E,
Psaty BM,
Beckmann JS,
Waeber G,
Vollenweider P,
Hayward C,
Wright AF,
Rudan I,
Groop LC,
Metspalu A,
Khaw KT,
van Duijn CM,
Borecki IB,
Province MA,
Wareham NJ,
Tardif JC,
Huikuri HV,
Cupples LA,
Atwood LD,
Fox CS,
Boehnke M,
Collins FS,
Mohlke KL,
Erdmann J,
Schunkert H,
Hengstenberg C,
Stark K,
Lorentzon M,
Ohlsson C,
Cusi D,
Staessen JA,
Van der Klauw MM,
Pramstaller PP,
Kathiresan S,
Jolley JD,
Ripatti S,
Jarvelin MR,
de Geus EJ,
Boomsma DI,
Penninx B,
Wilson JF,
Campbell H,
Chanock SJ,
van der Harst P,
Hamsten A,
Watkins H,
Hofman A,
Witteman JC,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Zillikens MC,
Kiemeney LA,
Vermeulen SH,
Abecasis GR,
Schlessinger D,
Schipf S,
Stumvoll M,
Tönjes A,
Spector TD,
North KE,
Lettre G,
McCarthy MI,
Berndt SI,
Heath AC,
Madden PA,
Nyholt DR,
Montgomery GW,
Martin NG,
McKnight B,
Strachan DP,
Hill WG,
Snieder H,
Ridker PM,
Thorsteinsdottir U,
Stefansson K,
Frayling TM,
Hirschhorn JN,
Goddard ME,
Visscher PM
Nature · 2012 · PMID 22982992
1 page
Impact of ancestry and common genetic variants on QT interval in African Americans
Smith JG,
Avery CL,
Evans DS,
Nalls MA,
Meng YA,
Smith EN,
Palmer C,
Tanaka T,
Mehra R,
Butler AM,
Young T,
Buxbaum SG
and 39 more — show all
Kerr KF,
Berenson GS,
Schnabel RB,
Li G,
Ellinor PT,
Magnani JW,
Chen W,
Bis JC,
Curb JD,
Hsueh WC,
Rotter JI,
Liu Y,
Newman AB,
Limacher MC,
North KE,
Reiner AP,
Quibrera PM,
Schork NJ,
Singleton AB,
Psaty BM,
Soliman EZ,
Solomon AJ,
Srinivasan SR,
Alonso A,
Wallace R,
Redline S,
Zhang ZM,
Post WS,
Zonderman AB,
Taylor HA,
Murray SS,
Ferrucci L,
Arking DE,
Evans MK,
Fox ER,
Sotoodehnia N,
Heckbert SR,
Whitsel EA,
Newton-Cheh C
CARe and COGENT consortia
Circulation. Cardiovascular genetics · 2012 · PMID 23166209
1 page
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies
Yu B,
Barbalic M,
Brautbar A,
Nambi V,
Hoogeveen RC,
Tang W,
Mosley TH,
Rotter JI,
deFilippi CR,
O'Donnell CJ,
Kathiresan S,
Rice K
and 4 more — show all
CARDIoGRAM Consortium
Circulation. Cardiovascular genetics · 2013 · PMID 23247143
1 page
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
Tang W,
Teichert M,
Chasman DI,
Heit JA,
Morange PE,
Li G,
Pankratz N,
Leebeek FW,
Paré G,
de Andrade M,
Tzourio C,
Psaty BM
and 28 more — show all
Basu S,
Ruiter R,
Rose L,
Armasu SM,
Lumley T,
Heckbert SR,
Uitterlinden AG,
Lathrop M,
Rice KM,
Cushman M,
Hofman A,
Lambert JC,
Glazer NL,
Pankow JS,
Witteman JC,
Amouyel P,
Bis JC,
Bovill EG,
Kong X,
Tracy RP,
Boerwinkle E,
Rotter JI,
Trégouët DA,
Loth DW,
Stricker BHC,
Ridker PM,
Folsom AR,
Smith NL
Genetic epidemiology · 2013 · PMID 23650146
1 page
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Lambert JC,
Ibrahim-Verbaas CA,
Harold D,
Naj AC,
Sims R,
Bellenguez C,
DeStafano AL,
Bis JC,
Beecham GW,
Grenier-Boley B,
Russo G,
Thorton-Wells TA
and 160 more — show all
Jones N,
Smith AV,
Chouraki V,
Thomas C,
Ikram MA,
Zelenika D,
Vardarajan BN,
Kamatani Y,
Lin CF,
Gerrish A,
Gerrish A,
Schmidt H,
Kunkle B,
Dunstan ML,
Ruiz A,
Bihoreau MT,
Choi SH,
Reitz C,
Pasquier F,
Cruchaga C,
Craig D,
Amin N,
Berr C,
Lopez OL,
De Jager PL,
Deramecourt V,
Johnston JA,
Evans D,
Lovestone S,
Letenneur L,
Morón FJ,
Rubinsztein DC,
Eiriksdottir G,
Sleegers K,
Goate AM,
Fiévet N,
Huentelman MW,
Gill M,
Brown K,
Kamboh MI,
Keller L,
Barberger-Gateau P,
McGuiness B,
Larson EB,
Green R,
Myers AJ,
Dufouil C,
Todd S,
Wallon D,
Love S,
Rogaeva E,
Gallacher J,
St George-Hyslop P,
Clarimon J,
Lleo A,
Bayer A,
Tsuang DW,
Yu L,
Tsolaki M,
Bossù P,
Spalletta G,
Proitsi P,
Collinge J,
Sorbi S,
Sanchez-Garcia F,
Fox NC,
Hardy J,
Deniz Naranjo MC,
Bosco P,
Clarke R,
Brayne C,
Galimberti D,
Mancuso M,
Matthews F,
Moebus S,
Mecocci P,
Del Zompo M,
Maier W,
Hampel H,
Pilotto A,
Bullido M,
Panza F,
Caffarra P,
Nacmias B,
Gilbert JR,
Mayhaus M,
Lannefelt L,
Hakonarson H,
Pichler S,
Carrasquillo MM,
Ingelsson M,
Beekly D,
Alvarez V,
Zou F,
Valladares O,
Younkin SG,
Coto E,
Hamilton-Nelson KL,
Gu W,
Razquin C,
Pastor P,
Mateo I,
Owen MJ,
Faber KM,
Jonsson PV,
Combarros O,
O'Donovan MC,
Cantwell LB,
Soininen H,
Blacker D,
Mead S,
Mosley TH Jr,
Bennett DA,
Harris TB,
Fratiglioni L,
Holmes C,
de Bruijn RF,
Passmore P,
Montine TJ,
Bettens K,
Rotter JI,
Brice A,
Morgan K,
Foroud TM,
Kukull WA,
Hannequin D,
Powell JF,
Nalls MA,
Ritchie K,
Lunetta KL,
Kauwe JS,
Boerwinkle E,
Riemenschneider M,
Boada M,
Hiltuenen M,
Martin ER,
Schmidt R,
Rujescu D,
Wang LS,
Dartigues JF,
Mayeux R,
Tzourio C,
Hofman A,
Nöthen MM,
Graff C,
Psaty BM,
Jones L,
Haines JL,
Holmans PA,
Lathrop M,
Pericak-Vance MA,
Launer LJ,
Farrer LA,
van Duijn CM,
Van Broeckhoven C,
Moskvina V,
Seshadri S,
Williams J,
Schellenberg GD,
Amouyel P
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
Dichgans M,
Malik R,
König IR,
Rosand J,
Clarke R,
Gretarsdottir S,
Thorleifsson G,
Mitchell BD,
Assimes TL,
Levi C,
O'Donnell CJ,
Fornage M
and 27 more — show all
Thorsteinsdottir U,
Psaty BM,
Hengstenberg C,
Seshadri S,
Erdmann J,
Bis JC,
Peters A,
Boncoraglio GB,
März W,
Meschia JF,
Kathiresan S,
Ikram MA,
McPherson R,
Stefansson K,
Sudlow C,
Reilly MP,
Thompson JR,
Sharma P,
Hopewell JC,
Chambers JC,
Watkins H,
Rothwell PM,
Roberts R,
Markus HS,
Samani NJ,
Farrall M,
Schunkert H
METASTROKE Consortium · CARDIoGRAM Consortium and 2 more consortia
Stroke · 2014 · PMID 24262325
1 page
Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine
Lüneburg N,
Lieb W,
Zeller T,
Chen MH,
Maas R,
Carter AM,
Xanthakis V,
Glazer NL,
Schwedhelm E,
Seshadri S,
Ikram MA,
Longstreth WT Jr
and 32 more — show all
Fornage M,
König IR,
Loley C,
Ojeda FM,
Schillert A,
Wang TJ,
Sticht H,
Kittel A,
König J,
Benjamin EJ,
Sullivan LM,
Bernges I,
Anderssohn M,
Ziegler A,
Gieger C,
Illig T,
Meisinger C,
Wichmann HE,
Wild PS,
Schunkert H,
Psaty BM,
Wiggins KL,
Heckbert SR,
Smith N,
Lackner K,
Lunetta KL,
Blankenberg S,
Erdmann J,
Munzel T,
Grant PJ,
Vasan RS,
Böger RH
Circulation. Cardiovascular genetics · 2014 · PMID 25245031
1 page
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Gottlieb DJ,
Hek K,
Chen TH,
Watson NF,
Eiriksdottir G,
Byrne EM,
Cornelis M,
Warby SC,
Bandinelli S,
Cherkas L,
Evans DS,
Grabe HJ
and 74 more — show all
Lahti J,
Li M,
Lehtimäki T,
Lumley T,
Marciante KD,
Pérusse L,
Psaty BM,
Robbins J,
Tranah GJ,
Vink JM,
Wilk JB,
Stafford JM,
Bellis C,
Biffar R,
Bouchard C,
Cade B,
Curhan GC,
Eriksson JG,
Ewert R,
Ferrucci L,
Fülöp T,
Gehrman PR,
Goodloe R,
Harris TB,
Heath AC,
Hernandez D,
Hofman A,
Hottenga JJ,
Hunter DJ,
Jensen MK,
Johnson AD,
Kähönen M,
Kao L,
Kraft P,
Larkin EK,
Lauderdale DS,
Luik AI,
Medici M,
Montgomery GW,
Palotie A,
Patel SR,
Pistis G,
Porcu E,
Quaye L,
Raitakari O,
Redline S,
Rimm EB,
Rotter JI,
Smith AV,
Spector TD,
Teumer A,
Uitterlinden AG,
Vohl MC,
Widen E,
Willemsen G,
Young T,
Zhang X,
Liu Y,
Blangero J,
Boomsma DI,
Gudnason V,
Hu F,
Mangino M,
Martin NG,
O'Connor GT,
Stone KL,
Tanaka T,
Viikari J,
Gharib SA,
Punjabi NM,
Räikkönen K,
Völzke H,
Mignot E,
Tiemeier H
Molecular psychiatry · 2015 · PMID 25469926 · open access
1 page
Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Mozaffarian D,
Kabagambe EK,
Johnson CO,
Lemaitre RN,
Manichaikul A,
Sun Q,
Foy M,
Wang L,
Wiener H,
Irvin MR,
Rich SS,
Wu H
and 17 more — show all
Jensen MK,
Chasman DI,
Chu AY,
Fornage M,
Steffen L,
King IB,
McKnight B,
Psaty BM,
Djoussé L,
Chen IY,
Wu JH,
Siscovick DS,
Ridker PM,
Tsai MY,
Rimm EB,
Hu FB,
Arnett DK
The American journal of clinical nutrition · 2015 · PMID 25646338
1 page
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
Khera AV,
Won HH,
Peloso GM,
Lawson KS,
Bartz TM,
Deng X,
van Leeuwen EM,
Natarajan P,
Emdin CA,
Bick AG,
Morrison AC,
Brody JA
and 23 more — show all
Gupta N,
Nomura A,
Kessler T,
Duga S,
Bis JC,
van Duijn CM,
Cupples LA,
Psaty B,
Rader DJ,
Danesh J,
Schunkert H,
McPherson R,
Farrall M,
Watkins H,
Lander E,
Wilson JG,
Correa A,
Boerwinkle E,
Merlini PA,
Ardissino D,
Saleheen D,
Gabriel S,
Kathiresan S
Journal of the American College of Cardiology · 2016 · PMID 27050191
1 page
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations
Hu Y,
Tanaka T,
Zhu J,
Guan W,
Wu JHY,
Psaty BM,
McKnight B,
King IB,
Sun Q,
Richard M,
Manichaikul A,
Frazier-Wood AC
and 21 more — show all
Kabagambe EK,
Hopkins PN,
Ordovas JM,
Ferrucci L,
Bandinelli S,
Arnett DK,
Chen YI,
Liang S,
Siscovick DS,
Tsai MY,
Rich SS,
Fornage M,
Hu FB,
Rimm EB,
Jensen MK,
Lemaitre RN,
Mozaffarian D,
Steffen LM,
Morris AP,
Li H,
Lin X
Journal of lipid research · 2017 · PMID 28298293 · open access
1 page
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Sims R,
van der Lee SJ,
Naj AC,
Bellenguez C,
Badarinarayan N,
Jakobsdottir J,
Kunkle BW,
Boland A,
Raybould R,
Bis JC,
Martin ER,
Grenier-Boley B
and 437 more — show all
Heilmann-Heimbach S,
Chouraki V,
Kuzma AB,
Sleegers K,
Vronskaya M,
Ruiz A,
Graham RR,
Olaso R,
Hoffmann P,
Grove ML,
Vardarajan BN,
Hiltunen M,
Nöthen MM,
White CC,
Hamilton-Nelson KL,
Epelbaum J,
Maier W,
Choi SH,
Beecham GW,
Dulary C,
Herms S,
Smith AV,
Funk CC,
Derbois C,
Forstner AJ,
Ahmad S,
Li H,
Bacq D,
Harold D,
Satizabal CL,
Valladares O,
Squassina A,
Thomas R,
Brody JA,
Qu L,
Sánchez-Juan P,
Morgan T,
Wolters FJ,
Zhao Y,
Garcia FS,
Denning N,
Fornage M,
Malamon J,
Naranjo MCD,
Majounie E,
Mosley TH,
Dombroski B,
Wallon D,
Lupton MK,
Dupuis J,
Whitehead P,
Fratiglioni L,
Medway C,
Jian X,
Mukherjee S,
Keller L,
Brown K,
Lin H,
Cantwell LB,
Panza F,
McGuinness B,
Moreno-Grau S,
Burgess JD,
Solfrizzi V,
Proitsi P,
Adams HH,
Allen M,
Seripa D,
Pastor P,
Cupples LA,
Price ND,
Hannequin D,
Frank-García A,
Levy D,
Chakrabarty P,
Caffarra P,
Giegling I,
Beiser AS,
Giedraitis V,
Hampel H,
Garcia ME,
Wang X,
Lannfelt L,
Mecocci P,
Eiriksdottir G,
Crane PK,
Pasquier F,
Boccardi V,
Henández I,
Barber RC,
Scherer M,
Tarraga L,
Adams PM,
Leber M,
Chen Y,
Albert MS,
Riedel-Heller S,
Emilsson V,
Beekly D,
Braae A,
Schmidt R,
Blacker D,
Masullo C,
Schmidt H,
Doody RS,
Spalletta G,
Longstreth WT Jr,
Fairchild TJ,
Bossù P,
Lopez OL,
Frosch MP,
Sacchinelli E,
Ghetti B,
Yang Q,
Huebinger RM,
Jessen F,
Li S,
Kamboh MI,
Morris J,
Sotolongo-Grau O,
Katz MJ,
Corcoran C,
Dunstan M,
Braddel A,
Thomas C,
Meggy A,
Marshall R,
Gerrish A,
Chapman J,
Aguilar M,
Taylor S,
Hill M,
Fairén MD,
Hodges A,
Vellas B,
Soininen H,
Kloszewska I,
Daniilidou M,
Uphill J,
Patel Y,
Hughes JT,
Lord J,
Turton J,
Hartmann AM,
Cecchetti R,
Fenoglio C,
Serpente M,
Arcaro M,
Caltagirone C,
Orfei MD,
Ciaramella A,
Pichler S,
Mayhaus M,
Gu W,
Lleó A,
Fortea J,
Blesa R,
Barber IS,
Brookes K,
Cupidi C,
Maletta RG,
Carrell D,
Sorbi S,
Moebus S,
Urbano M,
Pilotto A,
Kornhuber J,
Bosco P,
Todd S,
Craig D,
Johnston J,
Gill M,
Lawlor B,
Lynch A,
Fox NC,
Hardy J,
Albin RL,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Baldwin CT,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Bigio EH,
Bird TD,
Boeve BF,
Bowen JD,
Boxer A,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Carroll SL,
Diaz CC,
Chui HC,
Clark DG,
Cribbs DH,
Crocco EA,
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ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy
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Yan S,
Duan Q
and 21 more — show all
Roach J,
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Whitsel EA
Scientific reports · 2018 · PMID 29618737 · open access
1 page
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Bihlmeyer NA,
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Radmanesh F,
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Li M,
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Circulation. Genomic and precision medicine · 2018 · PMID 29874175 · open access
1 page
Meta-analysis of exome array data identifies six novel genetic loci for lung function
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Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
1 page
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
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Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
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Bernard M,
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Neumann A,
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Ames D,
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Rice K,
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Satizabal CL,
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Sidney S,
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Jukema JW,
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Nature communications · 2018 · PMID 30258056 · open access
1 page
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
Suri P,
Palmer MR,
Tsepilov YA,
Freidin MB,
Boer CG,
Yau MS,
Evans DS,
Gelemanovic A,
Bartz TM,
Nethander M,
Arbeeva L,
Karssen L
and 25 more — show all
Neogi T,
Campbell A,
Mellstrom D,
Ohlsson C,
Marshall LM,
Orwoll E,
Uitterlinden A,
Rotter JI,
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Karlsson MK,
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Polasek O,
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Van Meurs JBJ,
Jackson R,
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Hayward C,
Smith NL,
Aulchenko YS,
Williams FMK
PLoS genetics · 2018 · PMID 30261039 · open access
1 page
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
and 290 more — show all
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
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Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
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Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
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Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
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Boerwinkle E,
Bottinger EP,
Broeckel U,
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Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
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Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
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Forouhi NG,
Forrester T,
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Gandin I,
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Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
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Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
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Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
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Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
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Bowden DW,
Chambers JC,
Cooper RS,
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Elliott P,
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Juang JJ,
Kamatani Y,
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Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
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Redline S,
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van der Harst P,
Wagenknecht LE,
Wang JS,
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Watkins H,
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Wickremasinghe AR,
Wu T,
Zeggini E,
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Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
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Hayward C,
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COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
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