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13 matches for
Longstreth WT Jr.
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+
Cerebral small vessel disease genomics and its implications across the lifespan
Sargurupremraj M,
Suzuki H,
Jian X,
Sarnowski C,
Evans TE,
Bis JC,
Eiriksdottir G,
Sakaue S,
Terzikhan N,
Habes M,
Zhao W,
Zhao W
and 105 more — show all
Armstrong NJ,
Hofer E,
Yanek LR,
Hagenaars SP,
Kumar RB,
van den Akker EB,
McWhirter RE,
Trompet S,
Mishra A,
Saba Y,
Satizabal CL,
Beaudet G,
Petit L,
Tsuchida A,
Zago L,
Schilling S,
Sigurdsson S,
Gottesman RF,
Lewis CE,
Aggarwal NT,
Lopez OL,
Smith JA,
Valdés Hernández MC,
van der Grond J,
Wright MJ,
Knol MJ,
Dörr M,
Thomson RJ,
Bordes C,
Le Grand Q,
Duperron MG,
Smith AV,
Knopman DS,
Schreiner PJ,
Evans DA,
Rotter JI,
Beiser AS,
Maniega SM,
Beekman M,
Trollor J,
Stott DJ,
Vernooij MW,
Wittfeld K,
Niessen WJ,
Soumaré A,
Boerwinkle E,
Sidney S,
Turner ST,
Davies G,
Thalamuthu A,
Völker U,
van Buchem MA,
Bryan RN,
Dupuis J,
Bastin ME,
Ames D,
Teumer A,
Amouyel P,
Kwok JB,
Bülow R,
Deary IJ,
Schofield PR,
Brodaty H,
Jiang J,
Tabara Y,
Setoh K,
Miyamoto S,
Yoshida K,
Nagata M,
Kamatani Y,
Matsuda F,
Psaty BM,
Bennett DA,
De Jager PL,
Mosley TH,
Sachdev PS,
Schmidt R,
Warren HR,
Evangelou E,
Trégouët DA,
Ikram MA,
Wen W,
DeCarli C,
Srikanth VK,
Jukema JW,
Slagboom EP,
Kardia SLR,
Okada Y,
Mazoyer B,
Wardlaw JM,
Nyquist PA,
Mather KA,
Grabe HJ,
Schmidt H,
Van Duijn CM,
Gudnason V,
Longstreth WT Jr,
Launer LJ,
Lathrop M,
Seshadri S,
Tzourio C,
Adams HH,
Matthews PM,
Fornage M,
Debette S
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal CL,
Adams HHH,
Hibar DP,
White CC,
Knol MJ,
Stein JL,
Scholz M,
Sargurupremraj M,
Jahanshad N,
Roshchupkin GV,
Smith AV,
Bis JC
and 277 more — show all
Jian X,
Luciano M,
Hofer E,
Teumer A,
van der Lee SJ,
Yang J,
Yanek LR,
Lee TV,
Li S,
Hu Y,
Koh JY,
Eicher JD,
Desrivières S,
Arias-Vasquez A,
Chauhan G,
Athanasiu L,
Rentería ME,
Kim S,
Hoehn D,
Armstrong NJ,
Chen Q,
Holmes AJ,
den Braber A,
Kloszewska I,
Andersson M,
Espeseth T,
Grimm O,
Abramovic L,
Alhusaini S,
Milaneschi Y,
Papmeyer M,
Axelsson T,
Ehrlich S,
Roiz-Santiañez R,
Kraemer B,
Håberg AK,
Jones HJ,
Pike GB,
Stein DJ,
Stevens A,
Bralten J,
Vernooij MW,
Harris TB,
Filippi I,
Witte AV,
Guadalupe T,
Wittfeld K,
Mosley TH,
Becker JT,
Doan NT,
Hagenaars SP,
Saba Y,
Cuellar-Partida G,
Amin N,
Hilal S,
Nho K,
Mirza-Schreiber N,
Arfanakis K,
Becker DM,
Ames D,
Goldman AL,
Lee PH,
Boomsma DI,
Lovestone S,
Giddaluru S,
Le Hellard S,
Mattheisen M,
Bohlken MM,
Kasperaviciute D,
Schmaal L,
Lawrie SM,
Agartz I,
Walton E,
Tordesillas-Gutierrez D,
Davies GE,
Shin J,
Ipser JC,
Vinke LN,
Hoogman M,
Jia T,
Burkhardt R,
Klein M,
Crivello F,
Janowitz D,
Carmichael O,
Haukvik UK,
Aribisala BS,
Schmidt H,
Strike LT,
Cheng CY,
Risacher SL,
Pütz B,
Fleischman DA,
Assareh AA,
Mattay VS,
Buckner RL,
Mecocci P,
Dale AM,
Cichon S,
Boks MP,
Matarin M,
Penninx BWJH,
Calhoun VD,
Chakravarty MM,
Marquand AF,
Macare C,
Kharabian Masouleh S,
Oosterlaan J,
Amouyel P,
Hegenscheid K,
Rotter JI,
Schork AJ,
Liewald DCM,
de Zubicaray GI,
Wong TY,
Shen L,
Sämann PG,
Brodaty H,
Roffman JL,
de Geus EJC,
Tsolaki M,
Erk S,
van Eijk KR,
Cavalleri GL,
van der Wee NJA,
McIntosh AM,
Gollub RL,
Bulayeva KB,
Bernard M,
Richards JS,
Himali JJ,
Loeffler M,
Rommelse N,
Hoffmann W,
Westlye LT,
Valdés Hernández MC,
Hansell NK,
van Erp TGM,
Wolf C,
Kwok JBJ,
Vellas B,
Heinz A,
Olde Loohuis LM,
Delanty N,
Ho BC,
Ching CRK,
Shumskaya E,
Singh B,
Hofman A,
van der Meer D,
Homuth G,
Psaty BM,
Bastin ME,
Montgomery GW,
Foroud TM,
Reppermund S,
Hottenga JJ,
Simmons A,
Meyer-Lindenberg A,
Cahn W,
Whelan CD,
van Donkelaar MMJ,
Yang Q,
Hosten N,
Green RC,
Thalamuthu A,
Mohnke S,
Hulshoff Pol HE,
Lin H,
Jack CR Jr,
Schofield PR,
Mühleisen TW,
Maillard P,
Potkin SG,
Wen W,
Fletcher E,
Toga AW,
Gruber O,
Huentelman M,
Davey Smith G,
Launer LJ,
Nyberg L,
Jönsson EG,
Crespo-Facorro B,
Koen N,
Greve DN,
Uitterlinden AG,
Weinberger DR,
Steen VM,
Fedko IO,
Groenewold NA,
Niessen WJ,
Toro R,
Tzourio C,
Longstreth WT Jr,
Ikram MK,
Smoller JW,
van Tol MJ,
Sussmann JE,
Paus T,
Lemaître H,
Schroeter ML,
Mazoyer B,
Andreassen OA,
Holsboer F,
Depondt C,
Veltman DJ,
Turner JA,
Pausova Z,
Schumann G,
van Rooij D,
Djurovic S,
Deary IJ,
McMahon KL,
Müller-Myhsok B,
Brouwer RM,
Soininen H,
Pandolfo M,
Wassink TH,
Cheung JW,
Wolfers T,
Martinot JL,
Zwiers MP,
Nauck M,
Melle I,
Martin NG,
Kanai R,
Westman E,
Kahn RS,
Sisodiya SM,
White T,
Saremi A,
van Bokhoven H,
Brunner HG,
Völzke H,
Wright MJ,
van 't Ent D,
Nöthen MM,
Ophoff RA,
Buitelaar JK,
Fernández G,
Sachdev PS,
Rietschel M,
van Haren NEM,
Fisher SE,
Beiser AS,
Francks C,
Saykin AJ,
Mather KA,
Romanczuk-Seiferth N,
Hartman CA,
DeStefano AL,
Heslenfeld DJ,
Weiner MW,
Walter H,
Hoekstra PJ,
Nyquist PA,
Franke B,
Bennett DA,
Grabe HJ,
Johnson AD,
Chen C,
van Duijn CM,
Lopez OL,
Fornage M,
Wardlaw JM,
Schmidt R,
DeCarli C,
De Jager PL,
Villringer A,
Debette S,
Gudnason V,
Medland SE,
Shulman JM,
Thompson PM,
Seshadri S,
Ikram MA
Nature genetics · 2019 · PMID 31636452
9 pages
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Verhaaren BF,
Debette S,
Bis JC,
Smith JA,
Ikram MK,
Adams HH,
Beecham AH,
Rajan KB,
Lopez LM,
Barral S,
van Buchem MA,
van der Grond J
and 90 more — show all
Smith AV,
Hegenscheid K,
Aggarwal NT,
de Andrade M,
Atkinson EJ,
Beekman M,
Beiser AS,
Blanton SH,
Boerwinkle E,
Brickman AM,
Bryan RN,
Chauhan G,
Chen CP,
Chouraki V,
de Craen AJ,
Crivello F,
Deary IJ,
Deelen J,
De Jager PL,
Dufouil C,
Elkind MS,
Evans DA,
Freudenberger P,
Gottesman RF,
Guðnason V,
Habes M,
Heckbert SR,
Heiss G,
Hilal S,
Hofer E,
Hofman A,
Ibrahim-Verbaas CA,
Knopman DS,
Lewis CE,
Liao J,
Liewald DC,
Luciano M,
van der Lugt A,
Martinez OO,
Mayeux R,
Mazoyer B,
Nalls M,
Nauck M,
Niessen WJ,
Oostra BA,
Psaty BM,
Rice KM,
Rotter JI,
von Sarnowski B,
Schmidt H,
Schreiner PJ,
Schuur M,
Sidney SS,
Sigurdsson S,
Slagboom PE,
Stott DJ,
van Swieten JC,
Teumer A,
Töglhofer AM,
Traylor M,
Trompet S,
Turner ST,
Tzourio C,
Uh HW,
Uitterlinden AG,
Vernooij MW,
Wang JJ,
Wong TY,
Wardlaw JM,
Windham BG,
Wittfeld K,
Wolf C,
Wright CB,
Yang Q,
Zhao W,
Zijdenbos A,
Jukema JW,
Sacco RL,
Kardia SL,
Amouyel P,
Mosley TH,
Longstreth WT Jr,
DeCarli CC,
van Duijn CM,
Schmidt R,
Launer LJ,
Grabe HJ,
Seshadri SS,
Ikram MA,
Fornage M
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 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,
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Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
1 page
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METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
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ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
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Scientific reports · 2019 · PMID 31645637 · open access
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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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