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3 matches for
Sehmi JS.
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
den Hoed M,
Eijgelsheim M,
Esko T,
Brundel BJ,
Peal DS,
Evans DM,
Nolte IM,
Segrè AV,
Holm H,
Handsaker RE,
Westra HJ,
Johnson T
and 256 more — show all
Isaacs A,
Yang J,
Lundby A,
Zhao JH,
Kim YJ,
Go MJ,
Almgren P,
Bochud M,
Boucher G,
Cornelis MC,
Gudbjartsson D,
Hadley D,
van der Harst P,
Hayward C,
den Heijer M,
Igl W,
Jackson AU,
Kutalik Z,
Luan J,
Kemp JP,
Kristiansson K,
Ladenvall C,
Lorentzon M,
Montasser ME,
Njajou OT,
O'Reilly PF,
Padmanabhan S,
St Pourcain B,
Rankinen T,
Salo P,
Tanaka T,
Timpson NJ,
Vitart V,
Waite L,
Wheeler W,
Zhang W,
Draisma HH,
Feitosa MF,
Kerr KF,
Lind PA,
Mihailov E,
Onland-Moret NC,
Song C,
Weedon MN,
Xie W,
Yengo L,
Absher D,
Albert CM,
Alonso A,
Arking DE,
de Bakker PI,
Balkau B,
Barlassina C,
Benaglio P,
Bis JC,
Bouatia-Naji N,
Brage S,
Chanock SJ,
Chines PS,
Chung M,
Darbar D,
Dina C,
Dörr M,
Elliott P,
Felix SB,
Fischer K,
Fuchsberger C,
de Geus EJ,
Goyette P,
Gudnason V,
Harris TB,
Hartikainen AL,
Havulinna AS,
Heckbert SR,
Hicks AA,
Hofman A,
Holewijn S,
Hoogstra-Berends F,
Hottenga JJ,
Jensen MK,
Johansson A,
Junttila J,
Kääb S,
Kanon B,
Ketkar S,
Khaw KT,
Knowles JW,
Kooner AS,
Kors JA,
Kumari M,
Milani L,
Laiho P,
Lakatta EG,
Langenberg C,
Leusink M,
Liu Y,
Luben RN,
Lunetta KL,
Lynch SN,
Markus MR,
Marques-Vidal P,
Mateo Leach I,
McArdle WL,
McCarroll SA,
Medland SE,
Miller KA,
Montgomery GW,
Morrison AC,
Müller-Nurasyid M,
Navarro P,
Nelis M,
O'Connell JR,
O'Donnell CJ,
Ong KK,
Newman AB,
Peters A,
Polasek O,
Pouta A,
Pramstaller PP,
Psaty BM,
Rao DC,
Ring SM,
Rossin EJ,
Rudan D,
Sanna S,
Scott RA,
Sehmi JS,
Sharp S,
Shin JT,
Singleton AB,
Smith AV,
Soranzo N,
Spector TD,
Stewart C,
Stringham HM,
Tarasov KV,
Uitterlinden AG,
Vandenput L,
Hwang SJ,
Whitfield JB,
Wijmenga C,
Wild SH,
Willemsen G,
Wilson JF,
Witteman JC,
Wong A,
Wong Q,
Jamshidi Y,
Zitting P,
Boer JM,
Boomsma DI,
Borecki IB,
van Duijn CM,
Ekelund U,
Forouhi NG,
Froguel P,
Hingorani A,
Ingelsson E,
Kivimaki M,
Kronmal RA,
Kuh D,
Lind L,
Martin NG,
Oostra BA,
Pedersen NL,
Quertermous T,
Rotter JI,
van der Schouw YT,
Verschuren WM,
Walker M,
Albanes D,
Arnar DO,
Assimes TL,
Bandinelli S,
Boehnke M,
de Boer RA,
Bouchard C,
Caulfield WL,
Chambers JC,
Curhan G,
Cusi D,
Eriksson J,
Ferrucci L,
van Gilst WH,
Glorioso N,
de Graaf J,
Groop L,
Gyllensten U,
Hsueh WC,
Hu FB,
Huikuri HV,
Hunter DJ,
Iribarren C,
Isomaa B,
Jarvelin MR,
Jula A,
Kähönen M,
Kiemeney LA,
van der Klauw MM,
Kooner JS,
Kraft P,
Iacoviello L,
Lehtimäki T,
Lokki ML,
Mitchell BD,
Navis G,
Nieminen MS,
Ohlsson C,
Poulter NR,
Qi L,
Raitakari OT,
Rimm EB,
Rioux JD,
Rizzi F,
Rudan I,
Salomaa V,
Sever PS,
Shields DC,
Shuldiner AR,
Sinisalo J,
Stanton AV,
Stolk RP,
Strachan DP,
Tardif JC,
Thorsteinsdottir U,
Tuomilehto J,
van Veldhuisen DJ,
Virtamo J,
Viikari J,
Vollenweider P,
Waeber G,
Widen E,
Cho YS,
Olsen JV,
Visscher PM,
Willer C,
Franke L,
Erdmann J,
Thompson JR,
Pfeufer A,
Sotoodehnia N,
Newton-Cheh C,
Ellinor PT,
Stricker BH,
Metspalu A,
Perola M,
Beckmann JS,
Smith GD,
Stefansson K,
Wareham NJ,
Munroe PB,
Sibon OC,
Milan DJ,
Snieder H,
Samani NJ,
Loos RJ
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 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
Genetic loci influencing kidney function and chronic kidney disease
Chambers JC,
Zhang W,
Lord GM,
van der Harst P,
Lawlor DA,
Sehmi JS,
Gale DP,
Wass MN,
Ahmadi KR,
Bakker SJ,
Beckmann J,
Bilo HJ
and 82 more — show all
Bochud M,
Brown MJ,
Caulfield MJ,
Connell JM,
Cook HT,
Cotlarciuc I,
Davey Smith G,
de Silva R,
Deng G,
Devuyst O,
Dikkeschei LD,
Dimkovic N,
Dockrell M,
Dominiczak A,
Ebrahim S,
Eggermann T,
Farrall M,
Ferrucci L,
Floege J,
Forouhi NG,
Gansevoort RT,
Han X,
Hedblad B,
Homan van der Heide JJ,
Hepkema BG,
Hernandez-Fuentes M,
Hypponen E,
Johnson T,
de Jong PE,
Kleefstra N,
Lagou V,
Lapsley M,
Li Y,
Loos RJ,
Luan J,
Luttropp K,
Maréchal C,
Melander O,
Munroe PB,
Nordfors L,
Parsa A,
Peltonen L,
Penninx BW,
Perucha E,
Pouta A,
Prokopenko I,
Roderick PJ,
Ruokonen A,
Samani NJ,
Sanna S,
Schalling M,
Schlessinger D,
Schlieper G,
Seelen MA,
Shuldiner AR,
Sjögren M,
Smit JH,
Snieder H,
Soranzo N,
Spector TD,
Stenvinkel P,
Sternberg MJ,
Swaminathan R,
Tanaka T,
Ubink-Veltmaat LJ,
Uda M,
Vollenweider P,
Wallace C,
Waterworth D,
Zerres K,
Waeber G,
Wareham NJ,
Maxwell PH,
McCarthy MI,
Jarvelin MR,
Mooser V,
Abecasis GR,
Lightstone L,
Scott J,
Navis G,
Elliott P,
Kooner JS
Nature genetics · 2010 · PMID 20383145
1 page
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Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
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Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
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