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Is your paper here?
2,662 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
Zheng Z.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
and 65 more — show all
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Xue A,
Wu Y,
Zhu Z,
Zhang F,
Kemper KE,
Zheng Z,
Yengo L,
Lloyd-Jones LR,
Sidorenko J,
Wu Y,
McRae AF,
Visscher PM
and 2 more — show all
eQTLGen Consortium
Nature communications · 2018 · PMID 30054458 · open access
12 pages+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
and 135 more — show all
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
Genetic signatures of high-altitude adaptation in Tibetans
Yang J,
Jin ZB,
Chen J,
Huang XF,
Li XM,
Liang YB,
Mao JY,
Chen X,
Zheng Z,
Bakshi A,
Zheng DD,
Zheng MQ
and 4 more — show all
Proceedings of the National Academy of Sciences of the United States of America · 2017 · PMID 28373541
3 pages
Trans-ethnic genome-wide association study of blood metabolites in the Chronic Renal Insufficiency Cohort (CRIC) study
Rhee EP,
Surapaneni A,
Zheng Z,
Zhou L,
Dutta D,
Arking DE,
Zhang J,
Duong T,
Chatterjee N,
Luo S,
Schlosser P,
Mehta R
and 14 more — show all
Waikar SS,
Saraf SL,
Kelly TN,
Hamm LL,
Rao PS,
Mathew AV,
Hsu CY,
Parsa A,
Vasan RS,
Kimmel PL,
Clish CB,
Coresh J,
Feldman HI,
Grams ME
CKD Biomarkers Consortium and the Chronic Renal Insufficiency Cohort (CRIC) Study Investigators
Kidney international · 2022 · PMID 35120996
3 pages
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.