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2,663 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
28 matches for
Rice KM,
showing the first 8.
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
Dehghan A,
Bis JC,
White CC,
Smith AV,
Morrison AC,
Cupples LA,
Trompet S,
Chasman DI,
Lumley T,
Völker U,
Buckley BM,
Ding J
and 55 more — show all
Jensen MK,
Folsom AR,
Kritchevsky SB,
Girman CJ,
Ford I,
Dörr M,
Salomaa V,
Uitterlinden AG,
Eiriksdottir G,
Vasan RS,
Franceschini N,
Carty CL,
Virtamo J,
Demissie S,
Amouyel P,
Arveiler D,
Heckbert SR,
Ferrières J,
Ducimetière P,
Smith NL,
Wang YA,
Siscovick DS,
Rice KM,
Wiklund PG,
Taylor KD,
Evans A,
Kee F,
Rotter JI,
Karvanen J,
Kuulasmaa K,
Heiss G,
Kraft P,
Launer LJ,
Hofman A,
Markus MR,
Rose LM,
Silander K,
Wagner P,
Benjamin EJ,
Lohman K,
Stott DJ,
Rivadeneira F,
Harris TB,
Levy D,
Liu Y,
Rimm EB,
Jukema JW,
Völzke H,
Ridker PM,
Blankenberg S,
Franco OH,
Gudnason V,
Psaty BM,
Boerwinkle E,
O'Donnell CJ
PloS one · 2016 · PMID 26950853 · open access
2 pages
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
van Leeuwen EM,
Sabo A,
Bis JC,
Huffman JE,
Manichaikul A,
Smith AV,
Feitosa MF,
Demissie S,
Joshi PK,
Duan Q,
Marten J,
van Klinken JB
and 86 more — show all
Surakka I,
Nolte IM,
Zhang W,
Mbarek H,
Li-Gao R,
Trompet S,
Verweij N,
Evangelou E,
Lyytikäinen LP,
Tayo BO,
Deelen J,
van der Most PJ,
van der Laan SW,
Arking DE,
Morrison A,
Dehghan A,
Franco OH,
Hofman A,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Mychaleckyj JC,
Campbell A,
Hocking LJ,
Padmanabhan S,
Brody JA,
Rice KM,
White CC,
Harris T,
Isaacs A,
Campbell H,
Lange LA,
Rudan I,
Kolcic I,
Navarro P,
Zemunik T,
Salomaa V,
Kooner AS,
Kooner JS,
Lehne B,
Scott WR,
Tan ST,
de Geus EJ,
Milaneschi Y,
Penninx BW,
Willemsen G,
de Mutsert R,
Ford I,
Gansevoort RT,
Segura-Lepe MP,
Raitakari OT,
Viikari JS,
Nikus K,
Forrester T,
McKenzie CA,
de Craen AJ,
de Ruijter HM,
Pasterkamp G,
Snieder H,
Oldehinkel AJ,
Slagboom PE,
Cooper RS,
Kähönen M,
Lehtimäki T,
Elliott P,
van der Harst P,
Jukema JW,
Mook-Kanamori DO,
Boomsma DI,
Chambers JC,
Swertz M,
Ripatti S,
Willems van Dijk K,
Vitart V,
Polasek O,
Hayward C,
Wilson JG,
Wilson JF,
Gudnason V,
Rich SS,
Psaty BM,
Borecki IB,
Boerwinkle E,
Rotter JI,
Cupples LA,
van Duijn CM
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
2 pages
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
and 119 more — show all
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
2 pages
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Benjamin EJ,
Rice KM,
Arking DE,
Pfeufer A,
van Noord C,
Smith AV,
Schnabel RB,
Bis JC,
Boerwinkle E,
Sinner MF,
Dehghan A,
Lubitz SA
and 44 more — show all
D'Agostino RB Sr,
Lumley T,
Ehret GB,
Heeringa J,
Aspelund T,
Newton-Cheh C,
Larson MG,
Marciante KD,
Soliman EZ,
Rivadeneira F,
Wang TJ,
Eiríksdottir G,
Levy D,
Psaty BM,
Li M,
Chamberlain AM,
Hofman A,
Vasan RS,
Harris TB,
Rotter JI,
Kao WH,
Agarwal SK,
Stricker BH,
Wang K,
Launer LJ,
Smith NL,
Chakravarti A,
Uitterlinden AG,
Wolf PA,
Sotoodehnia N,
Köttgen A,
van Duijn CM,
Meitinger T,
Mueller M,
Perz S,
Steinbeck G,
Wichmann HE,
Lunetta KL,
Heckbert SR,
Gudnason V,
Alonso A,
Kääb S,
Ellinor PT,
Witteman JC
Nature genetics · 2009 · PMID 19597492 · open access
1 page
Common variants in KCNN3 are associated with lone atrial fibrillation
Ellinor PT,
Lunetta KL,
Glazer NL,
Pfeufer A,
Alonso A,
Chung MK,
Sinner MF,
de Bakker PI,
Mueller M,
Lubitz SA,
Fox E,
Darbar D
and 50 more — show all
Smith NL,
Smith JD,
Schnabel RB,
Soliman EZ,
Rice KM,
Van Wagoner DR,
Beckmann BM,
van Noord C,
Wang K,
Ehret GB,
Rotter JI,
Hazen SL,
Steinbeck G,
Smith AV,
Launer LJ,
Harris TB,
Makino S,
Nelis M,
Milan DJ,
Perz S,
Esko T,
Köttgen A,
Moebus S,
Newton-Cheh C,
Li M,
Möhlenkamp S,
Wang TJ,
Kao WH,
Vasan RS,
Nöthen MM,
MacRae CA,
Stricker BH,
Hofman A,
Uitterlinden AG,
Levy D,
Boerwinkle E,
Metspalu A,
Topol EJ,
Chakravarti A,
Gudnason V,
Psaty BM,
Roden DM,
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
Common genetic variants associate with serum phosphorus concentration
Kestenbaum B,
Glazer NL,
Köttgen A,
Felix JF,
Hwang SJ,
Liu Y,
Lohman K,
Kritchevsky SB,
Hausman DB,
Petersen AK,
Gieger C,
Ried JS
and 27 more — show all
Meitinger T,
Strom TM,
Wichmann HE,
Campbell H,
Hayward C,
Rudan I,
de Boer IH,
Psaty BM,
Rice KM,
Chen YD,
Li M,
Arking DE,
Boerwinkle E,
Coresh J,
Yang Q,
Levy D,
van Rooij FJ,
Dehghan A,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Shlipak MG,
Kao WH,
Witteman JC,
Siscovick DS,
Fox CS
Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
1 page
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
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
Tang W,
Teichert M,
Chasman DI,
Heit JA,
Morange PE,
Li G,
Pankratz N,
Leebeek FW,
Paré G,
de Andrade M,
Tzourio C,
Psaty BM
and 28 more — show all
Basu S,
Ruiter R,
Rose L,
Armasu SM,
Lumley T,
Heckbert SR,
Uitterlinden AG,
Lathrop M,
Rice KM,
Cushman M,
Hofman A,
Lambert JC,
Glazer NL,
Pankow JS,
Witteman JC,
Amouyel P,
Bis JC,
Bovill EG,
Kong X,
Tracy RP,
Boerwinkle E,
Rotter JI,
Trégouët DA,
Loth DW,
Stricker BHC,
Ridker PM,
Folsom AR,
Smith NL
Genetic epidemiology · 2013 · PMID 23650146
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.