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7 matches for
Pulit SL.
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Arking DE,
Pulit SL,
Crotti L,
van der Harst P,
Munroe PB,
Koopmann TT,
Sotoodehnia N,
Rossin EJ,
Morley M,
Wang X,
Johnson AD,
Lundby A
and 218 more — show all
Gudbjartsson DF,
Noseworthy PA,
Eijgelsheim M,
Bradford Y,
Tarasov KV,
Dörr M,
Müller-Nurasyid M,
Lahtinen AM,
Nolte IM,
Smith AV,
Bis JC,
Isaacs A,
Newhouse SJ,
Evans DS,
Post WS,
Waggott D,
Lyytikäinen LP,
Hicks AA,
Eisele L,
Ellinghaus D,
Hayward C,
Navarro P,
Ulivi S,
Tanaka T,
Tester DJ,
Chatel S,
Gustafsson S,
Kumari M,
Morris RW,
Naluai ÅT,
Padmanabhan S,
Kluttig A,
Strohmer B,
Panayiotou AG,
Torres M,
Knoflach M,
Hubacek JA,
Slowikowski K,
Raychaudhuri S,
Kumar RD,
Harris TB,
Launer LJ,
Shuldiner AR,
Alonso A,
Bader JS,
Ehret G,
Huang H,
Kao WH,
Strait JB,
Macfarlane PW,
Brown M,
Caulfield MJ,
Samani NJ,
Kronenberg F,
Willeit J,
Smith JG,
Greiser KH,
Meyer Zu Schwabedissen H,
Werdan K,
Carella M,
Zelante L,
Heckbert SR,
Psaty BM,
Rotter JI,
Kolcic I,
Polašek O,
Wright AF,
Griffin M,
Daly MJ,
Arnar DO,
Hólm H,
Thorsteinsdottir U,
Denny JC,
Roden DM,
Zuvich RL,
Emilsson V,
Plump AS,
Larson MG,
O'Donnell CJ,
Yin X,
Bobbo M,
D'Adamo AP,
Iorio A,
Sinagra G,
Carracedo A,
Cummings SR,
Nalls MA,
Jula A,
Kontula KK,
Marjamaa A,
Oikarinen L,
Perola M,
Porthan K,
Erbel R,
Hoffmann P,
Jöckel KH,
Kälsch H,
Nöthen MM,
den Hoed M,
Loos RJ,
Thelle DS,
Gieger C,
Meitinger T,
Perz S,
Peters A,
Prucha H,
Sinner MF,
Waldenberger M,
de Boer RA,
Franke L,
van der Vleuten PA,
Beckmann BM,
Martens E,
Bardai A,
Hofman N,
Wilde AA,
Behr ER,
Dalageorgou C,
Giudicessi JR,
Medeiros-Domingo A,
Barc J,
Kyndt F,
Probst V,
Ghidoni A,
Insolia R,
Hamilton RM,
Scherer SW,
Brandimarto J,
Margulies K,
Moravec CE,
del Greco M F,
Fuchsberger C,
O'Connell JR,
Lee WK,
Watt GC,
Campbell H,
Wild SH,
El Mokhtari NE,
Frey N,
Asselbergs FW,
Mateo Leach I,
Navis G,
van den Berg MP,
van Veldhuisen DJ,
Kellis M,
Krijthe BP,
Franco OH,
Hofman A,
Kors JA,
Uitterlinden AG,
Witteman JC,
Kedenko L,
Lamina C,
Oostra BA,
Abecasis GR,
Lakatta EG,
Mulas A,
Orrú M,
Schlessinger D,
Uda M,
Markus MR,
Völker U,
Snieder H,
Spector TD,
Ärnlöv J,
Lind L,
Sundström J,
Syvänen AC,
Kivimaki M,
Kähönen M,
Mononen N,
Raitakari OT,
Viikari JS,
Adamkova V,
Kiechl S,
Brion M,
Nicolaides AN,
Paulweber B,
Haerting J,
Dominiczak AF,
Nyberg F,
Whincup PH,
Hingorani AD,
Schott JJ,
Bezzina CR,
Ingelsson E,
Ferrucci L,
Gasparini P,
Wilson JF,
Rudan I,
Franke A,
Mühleisen TW,
Pramstaller PP,
Lehtimäki TJ,
Paterson AD,
Parsa A,
Liu Y,
van Duijn CM,
Siscovick DS,
Gudnason V,
Jamshidi Y,
Salomaa V,
Felix SB,
Sanna S,
Ritchie MD,
Stricker BH,
Stefansson K,
Boyer LA,
Cappola TP,
Olsen JV,
Lage K,
Schwartz PJ,
Kääb S,
Chakravarti A,
Ackerman MJ,
Pfeufer A,
de Bakker PI,
Newton-Cheh C
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
Multi-ethnic genome-wide association study for atrial fibrillation
Roselli C,
Chaffin MD,
Weng LC,
Aeschbacher S,
Ahlberg G,
Albert CM,
Almgren P,
Alonso A,
Anderson CD,
Aragam KG,
Arking DE,
Barnard J
and 206 more — show all
Bartz TM,
Benjamin EJ,
Bihlmeyer NA,
Bis JC,
Bloom HL,
Boerwinkle E,
Bottinger EB,
Brody JA,
Calkins H,
Campbell A,
Cappola TP,
Carlquist J,
Chasman DI,
Chen LY,
Chen YI,
Choi EK,
Choi SH,
Christophersen IE,
Chung MK,
Cole JW,
Conen D,
Cook J,
Crijns HJ,
Cutler MJ,
Damrauer SM,
Daniels BR,
Darbar D,
Delgado G,
Denny JC,
Dichgans M,
Dörr M,
Dudink EA,
Dudley SC,
Esa N,
Esko T,
Eskola M,
Fatkin D,
Felix SB,
Ford I,
Franco OH,
Geelhoed B,
Grewal RP,
Gudnason V,
Guo X,
Gupta N,
Gustafsson S,
Gutmann R,
Hamsten A,
Harris TB,
Hayward C,
Heckbert SR,
Hernesniemi J,
Hocking LJ,
Hofman A,
Horimoto ARVR,
Huang J,
Huang PL,
Huffman J,
Ingelsson E,
Ipek EG,
Ito K,
Jimenez-Conde J,
Johnson R,
Jukema JW,
Kääb S,
Kähönen M,
Kamatani Y,
Kane JP,
Kastrati A,
Kathiresan S,
Katschnig-Winter P,
Kavousi M,
Kessler T,
Kietselaer BL,
Kirchhof P,
Kleber ME,
Knight S,
Krieger JE,
Kubo M,
Launer LJ,
Laurikka J,
Lehtimäki T,
Leineweber K,
Lemaitre RN,
Li M,
Lim HE,
Lin HJ,
Lin H,
Lind L,
Lindgren CM,
Lokki ML,
London B,
Loos RJF,
Low SK,
Lu Y,
Lyytikäinen LP,
Macfarlane PW,
Magnusson PK,
Mahajan A,
Malik R,
Mansur AJ,
Marcus GM,
Margolin L,
Margulies KB,
März W,
McManus DD,
Melander O,
Mohanty S,
Montgomery JA,
Morley MP,
Morris AP,
Müller-Nurasyid M,
Natale A,
Nazarian S,
Neumann B,
Newton-Cheh C,
Niemeijer MN,
Nikus K,
Nilsson P,
Noordam R,
Oellers H,
Olesen MS,
Orho-Melander M,
Padmanabhan S,
Pak HN,
Paré G,
Pedersen NL,
Pera J,
Pereira A,
Porteous D,
Psaty BM,
Pulit SL,
Pullinger CR,
Rader DJ,
Refsgaard L,
Ribasés M,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rosand J,
Rosenberg MA,
Rost N,
Rotter JI,
Saba S,
Sandhu RK,
Schnabel RB,
Schramm K,
Schunkert H,
Schurman C,
Scott SA,
Seppälä I,
Shaffer C,
Shah S,
Shalaby AA,
Shim J,
Shoemaker MB,
Siland JE,
Sinisalo J,
Sinner MF,
Slowik A,
Smith AV,
Smith BH,
Smith JG,
Smith JD,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Stricker BH,
Sun A,
Sun H,
Svendsen JH,
Tanaka T,
Tanriverdi K,
Taylor KD,
Teder-Laving M,
Teumer A,
Thériault S,
Trompet S,
Tucker NR,
Tveit A,
Uitterlinden AG,
Van Der Harst P,
Van Gelder IC,
Van Wagoner DR,
Verweij N,
Vlachopoulou E,
Völker U,
Wang B,
Weeke PE,
Weijs B,
Weiss R,
Weiss S,
Wells QS,
Wiggins KL,
Wong JA,
Woo D,
Worrall BB,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Lubitz SA,
Lunetta KL,
Ellinor PT
Nature genetics · 2018 · PMID 29892015
12 pages+
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry
Pulit SL,
Stoneman C,
Morris AP,
Wood AR,
Glastonbury CA,
Tyrrell J,
Yengo L,
Ferreira T,
Marouli E,
Ji Y,
Yang J,
Jones S
and 10 more — show all
GIANT Consortium
Human molecular genetics · 2019 · PMID 30239722 · open access
12 pages+
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
Pereyra F,
Jia X,
McLaren PJ,
Telenti A,
de Bakker PI,
Walker BD,
Ripke S,
Brumme CJ,
Pulit SL,
Carrington M,
Kadie CM,
Carlson JM
and 326 more — show all
Heckerman D,
Graham RR,
Plenge RM,
Deeks SG,
Gianniny L,
Crawford G,
Sullivan J,
Gonzalez E,
Davies L,
Camargo A,
Moore JM,
Beattie N,
Gupta S,
Crenshaw A,
Burtt NP,
Guiducci C,
Gupta N,
Gao X,
Qi Y,
Yuki Y,
Piechocka-Trocha A,
Cutrell E,
Rosenberg R,
Moss KL,
Lemay P,
O'Leary J,
Schaefer T,
Verma P,
Toth I,
Block B,
Baker B,
Rothchild A,
Lian J,
Proudfoot J,
Alvino DM,
Vine S,
Addo MM,
Allen TM,
Altfeld M,
Henn MR,
Le Gall S,
Streeck H,
Haas DW,
Kuritzkes DR,
Robbins GK,
Shafer RW,
Gulick RM,
Shikuma CM,
Haubrich R,
Riddler S,
Sax PE,
Daar ES,
Ribaudo HJ,
Agan B,
Agarwal S,
Ahern RL,
Allen BL,
Altidor S,
Altschuler EL,
Ambardar S,
Anastos K,
Anderson B,
Anderson V,
Andrady U,
Antoniskis D,
Bangsberg D,
Barbaro D,
Barrie W,
Bartczak J,
Barton S,
Basden P,
Basgoz N,
Bazner S,
Bellos NC,
Benson AM,
Berger J,
Bernard NF,
Bernard AM,
Birch C,
Bodner SJ,
Bolan RK,
Boudreaux ET,
Bradley M,
Braun JF,
Brndjar JE,
Brown SJ,
Brown K,
Brown ST,
Burack J,
Bush LM,
Cafaro V,
Campbell O,
Campbell J,
Carlson RH,
Carmichael JK,
Casey KK,
Cavacuiti C,
Celestin G,
Chambers ST,
Chez N,
Chirch LM,
Cimoch PJ,
Cohen D,
Cohn LE,
Conway B,
Cooper DA,
Cornelson B,
Cox DT,
Cristofano MV,
Cuchural G Jr,
Czartoski JL,
Dahman JM,
Daly JS,
Davis BT,
Davis K,
Davod SM,
DeJesus E,
Dietz CA,
Dunham E,
Dunn ME,
Ellerin TB,
Eron JJ,
Fangman JJ,
Farel CE,
Ferlazzo H,
Fidler S,
Fleenor-Ford A,
Frankel R,
Freedberg KA,
French NK,
Fuchs JD,
Fuller JD,
Gaberman J,
Gallant JE,
Gandhi RT,
Garcia E,
Garmon D,
Gathe JC Jr,
Gaultier CR,
Gebre W,
Gilman FD,
Gilson I,
Goepfert PA,
Gottlieb MS,
Goulston C,
Groger RK,
Gurley TD,
Haber S,
Hardwicke R,
Hardy WD,
Harrigan PR,
Hawkins TN,
Heath S,
Hecht FM,
Henry WK,
Hladek M,
Hoffman RP,
Horton JM,
Hsu RK,
Huhn GD,
Hunt P,
Hupert MJ,
Illeman ML,
Jaeger H,
Jellinger RM,
John M,
Johnson JA,
Johnson KL,
Johnson H,
Johnson K,
Joly J,
Jordan WC,
Kauffman CA,
Khanlou H,
Killian RK,
Kim AY,
Kim DD,
Kinder CA,
Kirchner JT,
Kogelman L,
Kojic EM,
Korthuis PT,
Kurisu W,
Kwon DS,
LaMar M,
Lampiris H,
Lanzafame M,
Lederman MM,
Lee DM,
Lee JM,
Lee MJ,
Lee ET,
Lemoine J,
Levy JA,
Llibre JM,
Liguori MA,
Little SJ,
Liu AY,
Lopez AJ,
Loutfy MR,
Loy D,
Mohammed DY,
Man A,
Mansour MK,
Marconi VC,
Markowitz M,
Marques R,
Martin JN,
Martin HL Jr,
Mayer KH,
McElrath MJ,
McGhee TA,
McGovern BH,
McGowan K,
McIntyre D,
Mcleod GX,
Menezes P,
Mesa G,
Metroka CE,
Meyer-Olson D,
Miller AO,
Montgomery K,
Mounzer KC,
Nagami EH,
Nagin I,
Nahass RG,
Nelson MO,
Nielsen C,
Norene DL,
O'Connor DH,
Ojikutu BO,
Okulicz J,
Oladehin OO,
Oldfield EC 3rd,
Olender SA,
Ostrowski M,
Owen WF Jr,
Pae E,
Parsonnet J,
Pavlatos AM,
Perlmutter AM,
Pierce MN,
Pincus JM,
Pisani L,
Price LJ,
Proia L,
Prokesch RC,
Pujet HC,
Ramgopal M,
Rathod A,
Rausch M,
Ravishankar J,
Rhame FS,
Richards CS,
Richman DD,
Rodes B,
Rodriguez M,
Rose RC 3rd,
Rosenberg ES,
Rosenthal D,
Ross PE,
Rubin DS,
Rumbaugh E,
Saenz L,
Salvaggio MR,
Sanchez WC,
Sanjana VM,
Santiago S,
Schmidt W,
Schuitemaker H,
Sestak PM,
Shalit P,
Shay W,
Shirvani VN,
Silebi VI,
Sizemore JM Jr,
Skolnik PR,
Sokol-Anderson M,
Sosman JM,
Stabile P,
Stapleton JT,
Starrett S,
Stein F,
Stellbrink HJ,
Sterman FL,
Stone VE,
Stone DR,
Tambussi G,
Taplitz RA,
Tedaldi EM,
Telenti A,
Theisen W,
Torres R,
Tosiello L,
Tremblay C,
Tribble MA,
Trinh PD,
Tsao A,
Ueda P,
Vaccaro A,
Valadas E,
Vanig TJ,
Vecino I,
Vega VM,
Veikley W,
Wade BH,
Walworth C,
Wanidworanun C,
Ward DJ,
Warner DA,
Weber RD,
Webster D,
Weis S,
Wheeler DA,
White DJ,
Wilkins E,
Winston A,
Wlodaver CG,
van't Wout A,
Wright DP,
Yang OO,
Yurdin DL,
Zabukovic BW,
Zachary KC,
Zeeman B,
Zhao M
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease
Huertas-Vazquez A,
Nelson CP,
Guo X,
Reinier K,
Uy-Evanado A,
Teodorescu C,
Ayala J,
Jerger K,
Chugh H,
Braund PS,
Deloukas P,
Hall AS
and 11 more — show all
Balmforth AJ,
Jones M,
Taylor KD,
Pulit SL,
Newton-Cheh C,
Gunson K,
Jui J,
Rotter JI,
Albert CM,
Samani NJ,
Chugh SS
WTCCC+
PloS one · 2013 · PMID 23593153 · open access
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
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