For researchers
Is your paper here?
2,661 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
7 matches for
Patel K.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Ganesh SK,
Zakai NA,
van Rooij FJ,
Soranzo N,
Smith AV,
Nalls MA,
Chen MH,
Kottgen A,
Glazer NL,
Dehghan A,
Kuhnel B,
Aspelund T
and 50 more — show all
Yang Q,
Tanaka T,
Jaffe A,
Bis JC,
Verwoert GC,
Teumer A,
Fox CS,
Guralnik JM,
Ehret GB,
Rice K,
Felix JF,
Rendon A,
Eiriksdottir G,
Levy D,
Patel KV,
Boerwinkle E,
Rotter JI,
Hofman A,
Sambrook JG,
Hernandez DG,
Zheng G,
Bandinelli S,
Singleton AB,
Coresh J,
Lumley T,
Uitterlinden AG,
Vangils JM,
Launer LJ,
Cupples LA,
Oostra BA,
Zwaginga JJ,
Ouwehand WH,
Thein SL,
Meisinger C,
Deloukas P,
Nauck M,
Spector TD,
Gieger C,
Gudnason V,
van Duijn CM,
Psaty BM,
Ferrucci L,
Chakravarti A,
Greinacher A,
O'Donnell CJ,
Witteman JC,
Furth S,
Cushman M,
Harris TB,
Lin JP
Nature genetics · 2009 · PMID 19862010 · open access
12 pages+
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates
Dashti HS,
Jones SE,
Wood AR,
Lane JM,
van Hees VT,
Wang H,
Rhodes JA,
Song Y,
Patel K,
Anderson SG,
Beaumont RN,
Bechtold DA
and 20 more — show all
Bowden J,
Cade BE,
Garaulet M,
Kyle SD,
Little MA,
Loudon AS,
Luik AI,
Scheer FAJL,
Spiegelhalder K,
Tyrrell J,
Gottlieb DJ,
Tiemeier H,
Ray DW,
Purcell SM,
Frayling TM,
Redline S,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
Nature communications · 2019 · PMID 30846698 · open access
12 pages+
Biological and clinical insights from genetics of insomnia symptoms
Lane JM,
Jones SE,
Dashti HS,
Wood AR,
Aragam KG,
van Hees VT,
Strand LB,
Winsvold BS,
Wang H,
Bowden J,
Song Y,
Patel K
and 31 more — show all
Anderson SG,
Beaumont RN,
Bechtold DA,
Cade BE,
Haas M,
Kathiresan S,
Little MA,
Luik AI,
Loudon AS,
Purcell S,
Richmond RC,
Scheer FAJL,
Schormair B,
Tyrrell J,
Winkelman JW,
Winkelmann J,
Hveem K,
Zhao C,
Nielsen JB,
Willer CJ,
Redline S,
Spiegelhalder K,
Kyle SD,
Ray DW,
Zwart JA,
Brumpton B,
Frayling TM,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij FJA,
Qayyum R,
Smith AV,
Zhou Y,
Trompet S,
Tanaka T,
Keller MF,
Chang LC,
Schmidt H,
Yang ML,
Chen MH,
Hayes J
and 88 more — show all
Johnson AD,
Yanek LR,
Mueller C,
Lange L,
Floyd JS,
Ghanbari M,
Zonderman AB,
Jukema JW,
Hofman A,
van Duijn CM,
Desch KC,
Saba Y,
Ozel AB,
Snively BM,
Wu JY,
Schmidt R,
Fornage M,
Klein RJ,
Fox CS,
Matsuda K,
Kamatani N,
Wild PS,
Stott DJ,
Ford I,
Slagboom PE,
Yang J,
Chu AY,
Lambert AJ,
Uitterlinden AG,
Franco OH,
Hofer E,
Ginsburg D,
Hu B,
Keating B,
Schick UM,
Brody JA,
Li JZ,
Chen Z,
Zeller T,
Guralnik JM,
Chasman DI,
Peters LL,
Kubo M,
Becker DM,
Li J,
Eiriksdottir G,
Rotter JI,
Levy D,
Grossmann V,
Patel KV,
Chen CH,
Ridker PM,
Tang H,
Launer LJ,
Rice KM,
Li-Gao R,
Ferrucci L,
Evans MK,
Choudhuri A,
Trompouki E,
Abraham BJ,
Yang S,
Takahashi A,
Kamatani Y,
Kooperberg C,
Harris TB,
Jee SH,
Coresh J,
Tsai FJ,
Longo DL,
Chen YT,
Felix JF,
Yang Q,
Psaty BM,
Boerwinkle E,
Becker LC,
Mook-Kanamori DO,
Wilson JG,
Gudnason V,
O'Donnell CJ,
Dehghan A,
Cupples LA,
Nalls MA,
Morris AP,
Okada Y,
Reiner AP,
Zon LI,
Ganesh SK
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome
Lessard CJ,
Li H,
Adrianto I,
Ice JA,
Rasmussen A,
Grundahl KM,
Kelly JA,
Dozmorov MG,
Miceli-Richard C,
Bowman S,
Lester S,
Eriksson P
and 48 more — show all
Eloranta ML,
Brun JG,
Gøransson LG,
Harboe E,
Guthridge JM,
Kaufman KM,
Kvarnström M,
Jazebi H,
Cunninghame Graham DS,
Grandits ME,
Nazmul-Hossain AN,
Patel K,
Adler AJ,
Maier-Moore JS,
Farris AD,
Brennan MT,
Lessard JA,
Chodosh J,
Gopalakrishnan R,
Hefner KS,
Houston GD,
Huang AJ,
Hughes PJ,
Lewis DM,
Radfar L,
Rohrer MD,
Stone DU,
Wren JD,
Vyse TJ,
Gaffney PM,
James JA,
Omdal R,
Wahren-Herlenius M,
Illei GG,
Witte T,
Jonsson R,
Rischmueller M,
Rönnblom L,
Nordmark G,
Ng WF,
Mariette X,
Anaya JM,
Rhodus NL,
Segal BM,
Scofield RH,
Montgomery CG,
Harley JB,
Sivils KL
UK Primary Sjögren's Syndrome Registry
Nature genetics · 2013 · PMID 24097067 · open access
4 pages
Multiple loci are associated with white blood cell phenotypes
Nalls MA,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Toniolo D,
Zakai NA,
Yang Q,
Greinacher A,
Wood AR,
Garcia M
and 81 more — show all
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations
Hawkes G,
Wright HIW,
Beaumont RN,
Chundru K,
Hanson A,
Jackson L,
Murray A,
Patel K,
Frayling TM,
Wright CF,
Wood AR,
Weedon MN
Nature communications · 2026 · PMID 41651857 · 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.