For researchers
Is your paper here?
2,645 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.
6 matches for
Zhou K.
Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction
Cheng FF,
Liu X,
Mi H,
Wang L,
Ma R,
Guo Y,
Sidorenko J,
Jiang C,
Islam T,
Meguro A,
Hikino K,
Ishikawa Y
and 15 more — show all
Tang S,
Li T,
Chen R,
Wang L,
Mägi R,
Metspalu A,
Takeuchi M,
Mizuki N,
Choquet H,
Jin ZB,
Chen G,
Zhou K,
Terao C,
Zeng J,
Yang J
Estonian Biobank Research Team · 23andMe Research Team
Nature genetics · 2026 · PMID 42009823 · open access
12 pages+
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Erzurumluoglu AM,
Liu M,
Jackson VE,
Barnes DR,
Datta G,
Melbourne CA,
Young R,
Batini C,
Surendran P,
Jiang T,
Adnan SD,
Afaq S
and 164 more — show all
Agrawal A,
Altmaier E,
Antoniou AC,
Asselbergs FW,
Baumbach C,
Bierut L,
Bertelsen S,
Boehnke M,
Bots ML,
Brazel DM,
Chambers JC,
Chang-Claude J,
Chen C,
Corley J,
Chou YL,
David SP,
de Boer RA,
de Leeuw CA,
Dennis JG,
Dominiczak AF,
Dunning AM,
Easton DF,
Eaton C,
Elliott P,
Evangelou E,
Faul JD,
Foroud T,
Goate A,
Gong J,
Grabe HJ,
Haessler J,
Haiman C,
Hallmans G,
Hammerschlag AR,
Harris SE,
Hattersley A,
Heath A,
Hsu C,
Iacono WG,
Kanoni S,
Kapoor M,
Kaprio J,
Kardia SL,
Karpe F,
Kontto J,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Laakso M,
Lai D,
Langenberg C,
Le N,
Lettre G,
Loukola A,
Luan J,
Madden PAF,
Mangino M,
Marioni RE,
Marouli E,
Marten J,
Martin NG,
McGue M,
Michailidou K,
Mihailov E,
Moayyeri A,
Moitry M,
Müller-Nurasyid M,
Naheed A,
Nauck M,
Neville MJ,
Nielsen SF,
North K,
Perola M,
Pharoah PDP,
Pistis G,
Polderman TJ,
Posthuma D,
Poulter N,
Qaiser B,
Rasheed A,
Reiner A,
Renström F,
Rice J,
Rohde R,
Rolandsson O,
Samani NJ,
Samuel M,
Schlessinger D,
Scholte SH,
Scott RA,
Sever P,
Shao Y,
Shrine N,
Smith JA,
Starr JM,
Stirrups K,
Stram D,
Stringham HM,
Tachmazidou I,
Tardif JC,
Thompson DJ,
Tindle HA,
Tragante V,
Trompet S,
Turcot V,
Tyrrell J,
Vaartjes I,
van der Leij AR,
van der Meer P,
Varga TV,
Verweij N,
Völzke H,
Wareham NJ,
Warren HR,
Weir DR,
Weiss S,
Wetherill L,
Yaghootkar H,
Yavas E,
Jiang Y,
Chen F,
Zhan X,
Zhang W,
Zhao W,
Zhao W,
Zhou K,
Amouyel P,
Blankenberg S,
Caulfield MJ,
Chowdhury R,
Cucca F,
Deary IJ,
Deloukas P,
Di Angelantonio E,
Ferrario M,
Ferrières J,
Franks PW,
Frayling TM,
Frossard P,
Hall IP,
Hayward C,
Jansson JH,
Jukema JW,
Kee F,
Männistö S,
Metspalu A,
Munroe PB,
Nordestgaard BG,
Palmer CNA,
Salomaa V,
Sattar N,
Spector T,
Strachan DP,
van der Harst P,
Zeggini E,
Saleheen D,
Butterworth AS,
Wain LV,
Abecasis GR,
Danesh J,
Tobin MD,
Vrieze S,
Liu DJ,
Howson JMM
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
Zhou K,
Bellenguez C,
Spencer CC,
Bennett AJ,
Coleman RL,
Tavendale R,
Hawley SA,
Donnelly LA,
Schofield C,
Groves CJ,
Burch L,
Carr F
and 38 more — show all
Strange A,
Freeman C,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Gray E,
Hunt S,
Jankowski J,
Langford C,
Markus HS,
Mathew CG,
Plomin R,
Rautanen A,
Sawcer SJ,
Samani NJ,
Trembath R,
Viswanathan AC,
Wood NW,
Harries LW,
Hattersley AT,
Doney AS,
Colhoun H,
Morris AD,
Sutherland C,
Hardie DG,
Peltonen L,
McCarthy MI,
Holman RR,
Palmer CN,
Donnelly P,
Pearson ER
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group · Wellcome Trust Case Control Consortium 2 and 1 more consortia
Nature genetics · 2011 · PMID 21186350 · open access
2 pages
Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin
Zhou K,
Yee SW,
Seiser EL,
van Leeuwen N,
Tavendale R,
Bennett AJ,
Groves CJ,
Coleman RL,
van der Heijden AA,
Beulens JW,
de Keyser CE,
Zaharenko L
and 37 more — show all
Rotroff DM,
Out M,
Jablonski KA,
Chen L,
Javorský M,
Židzik J,
Levin AM,
Williams LK,
Dujic T,
Semiz S,
Kubo M,
Chien HC,
Maeda S,
Witte JS,
Wu L,
Tkáč I,
Kooy A,
van Schaik RHN,
Stehouwer CDA,
Logie L,
Logie L,
Sutherland C,
Klovins J,
Pirags V,
Hofman A,
Stricker BH,
Motsinger-Reif AA,
Wagner MJ,
Innocenti F,
't Hart LM,
Holman RR,
McCarthy MI,
Hedderson MM,
Palmer CNA,
Florez JC,
Giacomini KM,
Pearson ER
MetGen Investigators · DPP Investigators and 1 more consortia
Nature genetics · 2016 · PMID 27500523 · open access
2 pages
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Cousminer DL,
Ahlqvist E,
Mishra R,
Andersen MK,
Chesi A,
Hawa MI,
Davis A,
Hodge KM,
Bradfield JP,
Zhou K,
Guy VC,
Åkerlund M
and 41 more — show all
Wod M,
Fritsche LG,
Vestergaard H,
Snyder J,
Højlund K,
Linneberg A,
Käräjämäki A,
Brandslund I,
Kim CE,
Witte D,
Sørgjerd EP,
Brillon DJ,
Pedersen O,
Beck-Nielsen H,
Grarup N,
Pratley RE,
Rickels MR,
Vella A,
Ovalle F,
Melander O,
Harris RI,
Varvel S,
Grill VER,
Hakonarson H,
Froguel P,
Lonsdale JT,
Mauricio D,
Schloot NC,
Khunti K,
Greenbaum CJ,
Åsvold BO,
Yderstræde KB,
Pearson ER,
Schwartz S,
Voight BF,
Hansen T,
Tuomi T,
Boehm BO,
Groop L,
Leslie RD,
Grant SFA
Bone Mineral Density in Childhood Study
Diabetes care · 2018 · PMID 30254083 · open access
2 pages
Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease
Veluchamy A,
Ballerini L,
Vitart V,
Schraut KE,
Kirin M,
Campbell H,
Joshi PK,
Relan D,
Harris S,
Brown E,
Vaidya SS,
Dhillon B
and 10 more — show all
Arteriosclerosis, thrombosis, and vascular biology · 2019 · PMID 31597446 · 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.