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99 matches for
Launer LJ,
showing the first 19.
Genome-wide association analysis identifies multiple loci related to resting heart rate
Eijgelsheim M,
Newton-Cheh C,
Sotoodehnia N,
de Bakker PI,
Müller M,
Morrison AC,
Smith AV,
Isaacs A,
Sanna S,
Dörr M,
Navarro P,
Fuchsberger C
and 62 more — show all
Nolte IM,
de Geus EJ,
Estrada K,
Hwang SJ,
Bis JC,
Rückert IM,
Alonso A,
Launer LJ,
Hottenga JJ,
Rivadeneira F,
Noseworthy PA,
Rice KM,
Perz S,
Arking DE,
Spector TD,
Kors JA,
Aulchenko YS,
Tarasov KV,
Homuth G,
Wild SH,
Marroni F,
Gieger C,
Licht CM,
Prineas RJ,
Hofman A,
Rotter JI,
Hicks AA,
Ernst F,
Najjar SS,
Wright AF,
Peters A,
Fox ER,
Oostra BA,
Kroemer HK,
Couper D,
Völzke H,
Campbell H,
Meitinger T,
Uda M,
Witteman JC,
Psaty BM,
Wichmann HE,
Harris TB,
Kääb S,
Siscovick DS,
Jamshidi Y,
Uitterlinden AG,
Folsom AR,
Larson MG,
Wilson JF,
Penninx BW,
Snieder H,
Pramstaller PP,
van Duijn CM,
Lakatta EG,
Felix SB,
Gudnason V,
Pfeufer A,
Heckbert SR,
Stricker BH,
Boerwinkle E,
O'Donnell CJ
Human molecular genetics · 2010 · PMID 20639392
1 page
CUBN is a gene locus for albuminuria
Böger CA,
Chen MH,
Tin A,
Olden M,
Köttgen A,
de Boer IH,
Fuchsberger C,
O'Seaghdha CM,
Pattaro C,
Teumer A,
Liu CT,
Glazer NL
and 103 more — show all
Li M,
O'Connell JR,
Tanaka T,
Peralta CA,
Kutalik Z,
Luan J,
Zhao JH,
Hwang SJ,
Akylbekova E,
Kramer H,
van der Harst P,
Smith AV,
Lohman K,
de Andrade M,
Hayward C,
Kollerits B,
Tönjes A,
Aspelund T,
Ingelsson E,
Eiriksdottir G,
Launer LJ,
Harris TB,
Shuldiner AR,
Mitchell BD,
Arking DE,
Franceschini N,
Boerwinkle E,
Egan J,
Hernandez D,
Reilly M,
Townsend RR,
Lumley T,
Siscovick DS,
Psaty BM,
Kestenbaum B,
Haritunians T,
Bergmann S,
Vollenweider P,
Waeber G,
Mooser V,
Waterworth D,
Johnson AD,
Florez JC,
Meigs JB,
Lu X,
Turner ST,
Atkinson EJ,
Leak TS,
Aasarød K,
Skorpen F,
Syvänen AC,
Illig T,
Baumert J,
Koenig W,
Krämer BK,
Devuyst O,
Mychaleckyj JC,
Minelli C,
Bakker SJ,
Kedenko L,
Paulweber B,
Coassin S,
Endlich K,
Kroemer HK,
Biffar R,
Stracke S,
Völzke H,
Stumvoll M,
Mägi R,
Campbell H,
Vitart V,
Hastie ND,
Gudnason V,
Kardia SL,
Liu Y,
Polasek O,
Curhan G,
Kronenberg F,
Prokopenko I,
Rudan I,
Arnlöv J,
Hallan S,
Navis G,
Parsa A,
Ferrucci L,
Coresh J,
Shlipak MG,
Bull SB,
Paterson NJ,
Wichmann HE,
Wareham NJ,
Loos RJ,
Rotter JI,
Pramstaller PP,
Cupples LA,
Beckmann JS,
Yang Q,
Heid IM,
Rettig R,
Dreisbach AW,
Bochud M,
Fox CS,
Kao WH
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Fornage M,
Debette S,
Bis JC,
Schmidt H,
Ikram MA,
Dufouil C,
Sigurdsson S,
Lumley T,
DeStefano AL,
Fazekas F,
Vrooman HA,
Shibata DK
and 51 more — show all
Maillard P,
Zijdenbos A,
Smith AV,
Gudnason H,
de Boer R,
Cushman M,
Mazoyer B,
Heiss G,
Vernooij MW,
Enzinger C,
Glazer NL,
Beiser A,
Knopman DS,
Cavalieri M,
Niessen WJ,
Harris TB,
Petrovic K,
Lopez OL,
Au R,
Lambert JC,
Hofman A,
Gottesman RF,
Garcia M,
Heckbert SR,
Atwood LD,
Catellier DJ,
Uitterlinden AG,
Yang Q,
Smith NL,
Aspelund T,
Romero JR,
Rice K,
Taylor KD,
Nalls MA,
Rotter JI,
Sharrett R,
van Duijn CM,
Amouyel P,
Wolf PA,
Gudnason V,
van der Lugt A,
Boerwinkle E,
Psaty BM,
Seshadri S,
Tzourio C,
Breteler MM,
Mosley TH,
Schmidt R,
Longstreth WT,
DeCarli C,
Launer LJ
Annals of neurology · 2011 · PMID 21681796
1 page
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
and 190 more — show all
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
Lopez LM,
Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
Curran JE,
Davies G,
de Almeida MA,
Delanty N,
Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
Matarin M,
Mattheisen M,
Meisenzahl E,
Melle I,
Moses EK,
Mühleisen TW,
Nauck M,
Nöthen MM,
Olvera RL,
Pandolfo M,
Pike GB,
Puls R,
Reinvang I,
Rentería ME,
Rietschel M,
Roffman JL,
Royle NA,
Rujescu D,
Savitz J,
Schnack HG,
Schnell K,
Seiferth N,
Smith C,
Steen VM,
Valdés Hernández MC,
Van den Heuvel M,
van der Wee NJ,
Van Haren NE,
Veltman JA,
Völzke H,
Walker R,
Westlye LT,
Whelan CD,
Agartz I,
Boomsma DI,
Cavalleri GL,
Dale AM,
Djurovic S,
Drevets WC,
Hagoort P,
Hall J,
Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
Montgomery GW,
Poline JB,
Porteous DJ,
Sisodiya SM,
Starr JM,
Sussmann J,
Toga AW,
Veltman DJ,
Walter H,
Weiner MW,
Bis JC,
Ikram MA,
Smith AV,
Gudnason V,
Tzourio C,
Vernooij MW,
Launer LJ,
DeCarli C,
Seshadri S,
Andreassen OA,
Apostolova LG,
Bastin ME,
Blangero J,
Brunner HG,
Buckner RL,
Cichon S,
Coppola G,
de Zubicaray GI,
Deary IJ,
Donohoe G,
de Geus EJ,
Espeseth T,
Fernández G,
Glahn DC,
Grabe HJ,
Hardy J,
Hulshoff Pol HE,
Jenkinson M,
Kahn RS,
McDonald C,
McIntosh AM,
McMahon FJ,
McMahon KL,
Meyer-Lindenberg A,
Morris DW,
Müller-Myhsok B,
Nichols TE,
Ophoff RA,
Paus T,
Pausova Z,
Penninx BW,
Potkin SG,
Sämann PG,
Saykin AJ,
Schumann G,
Smoller JW,
Wardlaw JM,
Weale ME,
Martin NG,
Franke B,
Wright MJ,
Thompson PM
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
Common variants at 6q22 and 17q21 are associated with intracranial volume
Ikram MA,
Fornage M,
Smith AV,
Seshadri S,
Schmidt R,
Debette S,
Vrooman HA,
Sigurdsson S,
Ropele S,
Taal HR,
Mook-Kanamori DO,
Coker LH
and 44 more — show all
Longstreth WT Jr,
Niessen WJ,
DeStefano AL,
Beiser A,
Zijdenbos AP,
Struchalin M,
Jack CR Jr,
Rivadeneira F,
Uitterlinden AG,
Knopman DS,
Hartikainen AL,
Pennell CE,
Thiering E,
Steegers EA,
Hakonarson H,
Heinrich J,
Palmer LJ,
Jarvelin MR,
McCarthy MI,
Grant SF,
St Pourcain B,
Timpson NJ,
Smith GD,
Sovio U,
Nalls MA,
Au R,
Hofman A,
Gudnason H,
van der Lugt A,
Harris TB,
Meeks WM,
Vernooij MW,
van Buchem MA,
Catellier D,
Jaddoe VW,
Gudnason V,
Windham BG,
Wolf PA,
van Duijn CM,
Mosley TH Jr,
Schmidt H,
Launer LJ,
Breteler MM,
DeCarli C
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
1 page
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
and 74 more — show all
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
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
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
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
and 55 more — show all
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
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Campbell A,
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Molecular psychiatry · 2022 · PMID 35974141 · open access
1 page
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
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Communications biology · 2024 · PMID 39251807 · open access
1 page
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