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39 matches for
Ehret G,
showing the first 19.
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior
Cornelis MC,
Kacprowski T,
Menni C,
Gustafsson S,
Pivin E,
Adamski J,
Artati A,
Eap CB,
Ehret G,
Friedrich N,
Ganna A,
Guessous I
and 12 more — show all
Homuth G,
Lind L,
Magnusson PK,
Mangino M,
Pedersen NL,
Pietzner M,
Suhre K,
Völzke H,
Bochud M,
Spector TD,
Grabe HJ,
Ingelsson E
Swiss Kidney Project on Genes in Hypertension (SKIPOGH) team
Human molecular genetics · 2016 · PMID 27702941
7 pages
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Sung YJ,
Winkler TW,
de las Fuentes L,
Bentley AR,
Brown MR,
Kraja AT,
Schwander K,
Ntalla I,
Guo X,
Franceschini N,
Lu Y,
Cheng CY
and 286 more — show all
Sim X,
Vojinovic D,
Marten J,
Musani SK,
Li C,
Feitosa MF,
Kilpeläinen TO,
Richard MA,
Noordam R,
Aslibekyan S,
Aschard H,
Bartz TM,
Dorajoo R,
Liu Y,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Tayo BO,
Warren HR,
Zhao W,
Zhou Y,
Matoba N,
Sofer T,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Giulianini F,
Goel A,
Harris SE,
Hartwig FP,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kähönen M,
Kasturiratne A,
Kühnel B,
Leander K,
Lee WJ,
Lin KH,
'an Luan J,
McKenzie CA,
Meian H,
Nelson CP,
Rauramaa R,
Schupf N,
Scott RA,
Sheu WHH,
Stančáková A,
Takeuchi F,
van der Most PJ,
Varga TV,
Wang H,
Wang Y,
Ware EB,
Weiss S,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Alfred T,
Amin N,
Arking D,
Aung T,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Braund PS,
Brody JA,
Broeckel U,
Cabrera CP,
Cade B,
Caizheng Y,
Campbell A,
Canouil M,
Chakravarti A,
Chauhan G,
Christensen K,
Cocca M,
Collins FS,
Connell JM,
de Mutsert R,
de Silva HJ,
Debette S,
Dörr M,
Duan Q,
Eaton CB,
Ehret G,
Evangelou E,
Faul JD,
Fisher VA,
Forouhi NG,
Franco OH,
Friedlander Y,
Gao H,
Gigante B,
Graff M,
Gu CC,
Gu D,
Gupta P,
Hagenaars SP,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hirata M,
Hofman A,
Howard BV,
Hunt S,
Irvin MR,
Jia Y,
Joehanes R,
Justice AE,
Katsuya T,
Kaufman J,
Kerrison ND,
Khor CC,
Koh WP,
Koistinen HA,
Komulainen P,
Kooperberg C,
Krieger JE,
Kubo M,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Lim SH,
Lin S,
Liu CT,
Liu J,
Liu J,
Liu K,
Liu Y,
Loh M,
Lohman KK,
Long J,
Louie T,
Mägi R,
Mahajan A,
Meitinger T,
Metspalu A,
Milani L,
Momozawa Y,
Morris AP,
Mosley TH Jr,
Munson P,
Murray AD,
Nalls MA,
Nasri U,
Norris JM,
North K,
Ogunniyi A,
Padmanabhan S,
Palmas WR,
Palmer ND,
Pankow JS,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Raitakari OT,
Renström F,
Rice TK,
Ridker PM,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Sabanayagam C,
Salako BL,
Sandow K,
Schmidt CO,
Schreiner PJ,
Scott WR,
Seshadri S,
Sever P,
Sitlani CM,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yuan JM,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Chen YI,
de Faire U,
Deary IJ,
Esko T,
Farrall M,
Forrester T,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Hung YJ,
Jonas JB,
Kato N,
Kooner JS,
Laakso M,
Lehtimäki T,
Liang KW,
Magnusson PKE,
Newman AB,
Oldehinkel AJ,
Pereira AC,
Redline S,
Rettig R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zheng W,
Zheng W,
Kamatani Y,
Laurie CC,
Bouchard C,
Cooper RS,
Evans MK,
Gudnason V,
Kardia SLR,
Kritchevsky SB,
Levy D,
O'Connell JR,
Psaty BM,
van Dam RM,
Sims M,
Arnett DK,
Mook-Kanamori DO,
Kelly TN,
Fox ER,
Hayward C,
Fornage M,
Rotimi CN,
Province MA,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Reiner AP,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Caulfield MJ,
Elliott P,
Rice K,
Munroe PB,
Morrison AC,
Cupples LA,
Rao DC,
Chasman DI
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
Genome-wide association study of PR interval
Pfeufer A,
van Noord C,
Marciante KD,
Arking DE,
Larson MG,
Smith AV,
Tarasov KV,
Müller M,
Sotoodehnia N,
Sinner MF,
Verwoert GC,
Li M
and 53 more — show all
Kao WH,
Köttgen A,
Coresh J,
Bis JC,
Psaty BM,
Rice K,
Rotter JI,
Rivadeneira F,
Hofman A,
Kors JA,
Stricker BH,
Uitterlinden AG,
van Duijn CM,
Beckmann BM,
Sauter W,
Gieger C,
Lubitz SA,
Newton-Cheh C,
Wang TJ,
Magnani JW,
Schnabel RB,
Chung MK,
Barnard J,
Smith JD,
Van Wagoner DR,
Vasan RS,
Aspelund T,
Eiriksdottir G,
Harris TB,
Launer LJ,
Najjar SS,
Lakatta E,
Schlessinger D,
Uda M,
Abecasis GR,
Müller-Myhsok B,
Ehret GB,
Boerwinkle E,
Chakravarti A,
Soliman EZ,
Lunetta KL,
Perz S,
Wichmann HE,
Meitinger T,
Levy D,
Gudnason V,
Ellinor PT,
Sanna S,
Kääb S,
Witteman JC,
Alonso A,
Benjamin EJ,
Heckbert SR
Nature genetics · 2010 · PMID 20062060 · open access
6 pages
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Wain LV,
Verwoert GC,
O'Reilly PF,
Shi G,
Johnson T,
Johnson AD,
Bochud M,
Rice KM,
Henneman P,
Smith AV,
Ehret GB,
Amin N
and 214 more — show all
Larson MG,
Mooser V,
Hadley D,
Dörr M,
Bis JC,
Aspelund T,
Esko T,
Janssens AC,
Zhao JH,
Heath S,
Laan M,
Fu J,
Pistis G,
Luan J,
Arora P,
Lucas G,
Pirastu N,
Pichler I,
Jackson AU,
Webster RJ,
Zhang F,
Peden JF,
Schmidt H,
Tanaka T,
Campbell H,
Igl W,
Milaneschi Y,
Hottenga JJ,
Vitart V,
Chasman DI,
Trompet S,
Bragg-Gresham JL,
Alizadeh BZ,
Chambers JC,
Guo X,
Lehtimäki T,
Kühnel B,
Lopez LM,
Polašek O,
Boban M,
Nelson CP,
Morrison AC,
Pihur V,
Ganesh SK,
Hofman A,
Kundu S,
Mattace-Raso FU,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Hwang SJ,
Vasan RS,
Wang TJ,
Bergmann S,
Vollenweider P,
Waeber G,
Laitinen J,
Pouta A,
Zitting P,
McArdle WL,
Kroemer HK,
Völker U,
Völzke H,
Glazer NL,
Taylor KD,
Harris TB,
Alavere H,
Haller T,
Keis A,
Tammesoo ML,
Aulchenko Y,
Barroso I,
Khaw KT,
Galan P,
Hercberg S,
Lathrop M,
Eyheramendy S,
Org E,
Org E,
Sõber S,
Lu X,
Nolte IM,
Penninx BW,
Corre T,
Masciullo C,
Sala C,
Groop L,
Voight BF,
Melander O,
O'Donnell CJ,
Salomaa V,
d'Adamo AP,
Fabretto A,
Faletra F,
Ulivi S,
Del Greco F,
Facheris M,
Collins FS,
Bergman RN,
Beilby JP,
Hung J,
Musk AW,
Mangino M,
Shin SY,
Soranzo N,
Watkins H,
Goel A,
Hamsten A,
Gider P,
Loitfelder M,
Zeginigg M,
Hernandez D,
Najjar SS,
Navarro P,
Wild SH,
Corsi AM,
Singleton A,
de Geus EJ,
Willemsen G,
Willemsen G,
Parker AN,
Rose LM,
Buckley B,
Stott D,
Orru M,
Uda M,
van der Klauw MM,
Zhang W,
Li X,
Scott J,
Chen YD,
Burke GL,
Kähönen M,
Viikari J,
Döring A,
Meitinger T,
Davies G,
Starr JM,
Emilsson V,
Plump A,
Lindeman JH,
Hoen PA,
König IR,
Felix JF,
Clarke R,
Hopewell JC,
Ongen H,
Breteler M,
Debette S,
Destefano AL,
Fornage M,
Mitchell GF,
Smith NL,
Holm H,
Stefansson K,
Thorleifsson G,
Thorsteinsdottir U,
Samani NJ,
Preuss M,
Rudan I,
Hayward C,
Deary IJ,
Wichmann HE,
Raitakari OT,
Palmas W,
Kooner JS,
Stolk RP,
Jukema JW,
Wright AF,
Boomsma DI,
Bandinelli S,
Gyllensten UB,
Wilson JF,
Ferrucci L,
Schmidt R,
Farrall M,
Spector TD,
Palmer LJ,
Tuomilehto J,
Pfeufer A,
Gasparini P,
Siscovick D,
Altshuler D,
Loos RJ,
Toniolo D,
Snieder H,
Gieger C,
Meneton P,
Wareham NJ,
Oostra BA,
Metspalu A,
Launer L,
Rettig R,
Strachan DP,
Beckmann JS,
Witteman JC,
Erdmann J,
van Dijk KW,
Boerwinkle E,
Boehnke M,
Ridker PM,
Jarvelin MR,
Chakravarti A,
Abecasis GR,
Gudnason V,
Newton-Cheh C,
Levy D,
Munroe PB,
Psaty BM,
Caulfield MJ,
Rao DC,
Tobin MD,
Elliott P,
van Duijn CM
LifeLines Cohort Study · EchoGen consortium and 6 more consortia
Nature genetics · 2011 · PMID 21909110 · open access
6 pages
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nolte IM,
Munoz ML,
Tragante V,
Amare AT,
Jansen R,
Vaez A,
von der Heyde B,
Avery CL,
Bis JC,
Dierckx B,
van Dongen J,
Gogarten SM
and 153 more — show all
Goyette P,
Hernesniemi J,
Huikari V,
Hwang SJ,
Jaju D,
Kerr KF,
Kluttig A,
Krijthe BP,
Kumar J,
van der Laan SW,
Lyytikäinen LP,
Maihofer AX,
Minassian A,
van der Most PJ,
Müller-Nurasyid M,
Nivard M,
Salvi E,
Stewart JD,
Thayer JF,
Verweij N,
Wong A,
Zabaneh D,
Zafarmand MH,
Abdellaoui A,
Albarwani S,
Albert C,
Alonso A,
Ashar F,
Auvinen J,
Axelsson T,
Baker DG,
de Bakker PIW,
Barcella M,
Bayoumi R,
Bieringa RJ,
Boomsma D,
Boucher G,
Britton AR,
Christophersen I,
Dietrich A,
Ehret GB,
Ellinor PT,
Eskola M,
Felix JF,
Floras JS,
Franco OH,
Friberg P,
Gademan MGJ,
Geyer MA,
Giedraitis V,
Hartman CA,
Hemerich D,
Hofman A,
Hottenga JJ,
Huikuri H,
Hutri-Kähönen N,
Jouven X,
Junttila J,
Juonala M,
Kiviniemi AM,
Kors JA,
Kumari M,
Kuznetsova T,
Kuznetsova T,
Laurie CC,
Lefrandt JD,
Li Y,
Li Y,
Liao D,
Limacher MC,
Lin HJ,
Lindgren CM,
Lubitz SA,
Mahajan A,
McKnight B,
Zu Schwabedissen HM,
Milaneschi Y,
Mononen N,
Morris AP,
Nalls MA,
Navis G,
Neijts M,
Nikus K,
North KE,
O'Connor DT,
Ormel J,
Perz S,
Peters A,
Psaty BM,
Raitakari OT,
Risbrough VB,
Sinner MF,
Siscovick D,
Smit JH,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Staessen JA,
Stein PK,
Stilp AM,
Stolarz-Skrzypek K,
Strauch K,
Sundström J,
Swenne CA,
Syvänen AC,
Tardif JC,
Taylor KD,
Teumer A,
Thornton TA,
Tinker LE,
Uitterlinden AG,
van Setten J,
Voss A,
Waldenberger M,
Wilhelmsen KC,
Willemsen G,
Wong Q,
Zhang ZM,
Zonderman AB,
Cusi D,
Evans MK,
Greiser HK,
van der Harst P,
Hassan M,
Ingelsson E,
Järvelin MR,
Kääb S,
Kähönen M,
Kivimaki M,
Kooperberg C,
Kuh D,
Lehtimäki T,
Lind L,
Nievergelt CM,
O'Donnell CJ,
Oldehinkel AJ,
Penninx B,
Reiner AP,
Riese H,
van Roon AM,
Rioux JD,
Rotter JI,
Sofer T,
Stricker BH,
Tiemeier H,
Vrijkotte TGM,
Asselbergs FW,
Brundel BJJM,
Heckbert SR,
Whitsel EA,
den Hoed M,
Snieder H,
de Geus EJC
Nature communications · 2017 · PMID 28613276 · open access
6 pages
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Gurdasani D,
Carstensen T,
Fatumo S,
Chen G,
Franklin CS,
Prado-Martinez J,
Bouman H,
Abascal F,
Haber M,
Tachmazidou I,
Mathieson I,
Ekoru K
and 45 more — show all
DeGorter MK,
Nsubuga RN,
Finan C,
Wheeler E,
Chen L,
Cooper DN,
Schiffels S,
Chen Y,
Ritchie GRS,
Pollard MO,
Fortune MD,
Mentzer AJ,
Garrison E,
Bergström A,
Hatzikotoulas K,
Adeyemo A,
Doumatey A,
Elding H,
Wain LV,
Ehret G,
Auer PL,
Kooperberg CL,
Reiner AP,
Franceschini N,
Maher D,
Montgomery SB,
Kadie C,
Widmer C,
Xue Y,
Seeley J,
Asiki G,
Kamali A,
Young EH,
Pomilla C,
Soranzo N,
Zeggini E,
Pirie F,
Morris AP,
Heckerman D,
Tyler-Smith C,
Motala AA,
Rotimi C,
Kaleebu P,
Barroso I,
Sandhu MS
Cell · 2019 · PMID 31675503
6 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,
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Meitinger T,
Wichmann HE,
Witteman JC,
Barnard J,
Arking DE,
Benjamin EJ,
Heckbert SR,
Kääb S
Nature genetics · 2010 · PMID 20173747 · open access
1 page
Questions about this list
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.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
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.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.