For researchers
Is your paper here?
2,681 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.
145 matches for
He G,
showing the first 20.
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
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Qiu F,
Tang R,
Zuo X,
Shi X,
Wei Y,
Zheng X,
Dai Y,
Gong Y,
Wang L,
Xu P,
Zhu X,
Wu J
and 78 more — show all
Han C,
Gao Y,
Zhang K,
Jiang Y,
Zhou J,
Shao Y,
Hu Z,
Tian Y,
Zhang H,
Dai N,
Liu L,
Wu X,
Zhao W,
Zhang X,
Zang Z,
Nie J,
Sun W,
Zhao Y,
Mao Y,
Jiang P,
Ji H,
Dong Q,
Li J,
Li Z,
Bai X,
Li L,
Lin M,
Dong M,
Li J,
Zhu P,
Wang C,
Zhang Y,
Jiang P,
Wang Y,
Jawed R,
Xu J,
Zhang Y,
Wang Q,
Yang Y,
Yang F,
Lian M,
Jiang X,
Xiao X,
Li Y,
Fang J,
Qiu D,
Zhu Z,
Qiu H,
Zhang J,
Tian W,
Chen S,
Jiang L,
Ji B,
Li P,
Chen G,
Wu T,
Sun Y,
Yu J,
Tang H,
He M,
Xia M,
Pei H,
Huang L,
Qing Z,
Wu J,
Huang Q,
Han J,
Xie W,
Sun Z,
Guo J,
He G,
Eric Gershwin M,
Lian Z,
Liu X,
Seldin MF,
Liu X,
Chen W,
Ma X
Nature communications · 2017 · PMID 28425483 · open access
2 pages
New variants near RHOJ and C2, HLA-DRA region and susceptibility to endometriosis in the Polish population-The genome-wide association study
Sobalska-Kwapis M,
Smolarz B,
Słomka M,
Szaflik T,
Kępka E,
Kulig B,
Siewierska-Górska A,
Polak G,
Romanowicz H,
Strapagiel D,
Szyłło K
European journal of obstetrics, gynecology, and reproductive biology · 2017 · PMID 28881265
2 pages
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Jiang X,
O'Reilly PF,
Aschard H,
Aschard H,
Hsu YH,
Richards JB,
Dupuis J,
Ingelsson E,
Karasik D,
Pilz S,
Berry D,
Kestenbaum B
and 93 more — show all
Zheng J,
Luan J,
Sofianopoulou E,
Streeten EA,
Albanes D,
Lutsey PL,
Yao L,
Tang W,
Econs MJ,
Wallaschofski H,
Völzke H,
Zhou A,
Power C,
McCarthy MI,
Michos ED,
Boerwinkle E,
Weinstein SJ,
Freedman ND,
Huang WY,
Van Schoor NM,
van der Velde N,
Groot LCPGM,
Enneman A,
Cupples LA,
Booth SL,
Vasan RS,
Liu CT,
Zhou Y,
Ripatti S,
Ohlsson C,
Vandenput L,
Lorentzon M,
Eriksson JG,
Shea MK,
Houston DK,
Kritchevsky SB,
Liu Y,
Lohman KK,
Ferrucci L,
Peacock M,
Gieger C,
Beekman M,
Slagboom E,
Deelen J,
Heemst DV,
Kleber ME,
März W,
de Boer IH,
Wood AC,
Rotter JI,
Rich SS,
Robinson-Cohen C,
den Heijer M,
Jarvelin MR,
Cavadino A,
Joshi PK,
Wilson JF,
Hayward C,
Lind L,
Michaëlsson K,
Trompet S,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Broer L,
Zgaga L,
Campbell H,
Theodoratou E,
Farrington SM,
Timofeeva M,
Dunlop MG,
Valdes AM,
Tikkanen E,
Lehtimäki T,
Lyytikäinen LP,
Kähönen M,
Raitakari OT,
Mikkilä V,
Ikram MA,
Sattar N,
Jukema JW,
Wareham NJ,
Langenberg C,
Forouhi NG,
Gundersen TE,
Khaw KT,
Butterworth AS,
Danesh J,
Spector T,
Wang TJ,
Hyppönen E,
Kraft P,
Kiel DP
Nature communications · 2018 · PMID 29343764 · open access
2 pages
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort
Galván-Femenía I,
Obón-Santacana M,
Piñeyro D,
Guindo-Martinez M,
Duran X,
Carreras A,
Pluvinet R,
Velasco J,
Ramos L,
Aussó S,
Mercader JM,
Puig L
and 5 more — show all
Journal of medical genetics · 2018 · PMID 30166351 · open access
2 pages
Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project
Lopera-Maya EA,
Kurilshikov A,
van der Graaf A,
Hu S,
Andreu-Sánchez S,
Chen L,
Vila AV,
Gacesa R,
Sinha T,
Collij V,
Klaassen MAY,
Bolte LA
and 9 more — show all
LifeLines Cohort Study
Nature genetics · 2022 · PMID 35115690
2 pages
Genome-wide association study provides insights into the genetic basis of Lewy body dementia
Zhu P,
Jin Z,
Wu S,
Gao S,
He Y,
Hu S,
Liu F,
Chen Y,
Wang M,
Wang K,
Liu G
Molecular psychiatry · 2025 · PMID 41068259
2 pages
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis
Peters U,
Jiao S,
Schumacher FR,
Hutter CM,
Aragaki AK,
Baron JA,
Berndt SI,
Bézieau S,
Brenner H,
Butterbach K,
Caan BJ,
Campbell PT
and 65 more — show all
Carlson CS,
Casey G,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chen LS,
Coetzee GA,
Coetzee SG,
Conti DV,
Curtis KR,
Duggan D,
Edwards T,
Fuchs CS,
Gallinger S,
Giovannucci EL,
Gogarten SM,
Gruber SB,
Haile RW,
Harrison TA,
Hayes RB,
Henderson BE,
Hoffmeister M,
Hopper JL,
Hudson TJ,
Hunter DJ,
Jackson RD,
Jee SH,
Jenkins MA,
Jia WH,
Kolonel LN,
Kooperberg C,
Küry S,
Lacroix AZ,
Laurie CC,
Laurie CA,
Le Marchand L,
Lemire M,
Levine D,
Lindor NM,
Liu Y,
Ma J,
Makar KW,
Matsuo K,
Newcomb PA,
Potter JD,
Prentice RL,
Qu C,
Rohan T,
Rosse SA,
Schoen RE,
Seminara D,
Shrubsole M,
Shu XO,
Slattery ML,
Taverna D,
Thibodeau SN,
Ulrich CM,
White E,
Xiang Y,
Zanke BW,
Zeng YX,
Zhang B,
Zheng W,
Zheng W,
Hsu L
Colon Cancer Family Registry and the Genetics and Epidemiology of Colorectal Cancer Consortium
Gastroenterology · 2013 · PMID 23266556
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.