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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.
94 matches for
He C,
showing the first 20.
Genome-wide association analysis of left ventricular imaging-derived phenotypes identifies 72 risk loci and yields genetic insights into hypertrophic cardiomyopathy
Ning C,
Fan L,
Jin M,
Wang W,
Hu Z,
Cai Y,
Chen L,
Lu Z,
Zhang M,
Chen C,
Li Y,
Zhang F
and 23 more — show all
Wang W,
Liu Y,
Chen S,
Jiang Y,
He C,
Wang Z,
Chen X,
Li H,
Li G,
Ma Q,
Geng H,
Tian W,
Zhang H,
Liu B,
Xia Q,
Yang X,
Liu Z,
Li B,
Zhu Y,
Li X,
Zhang S,
Tian J,
Miao X
Nature communications · 2023 · PMID 38036550 · open access
8 pages
Assessing the causal association of glycine with risk of cardio-metabolic diseases
Wittemans LBL,
Lotta LA,
Oliver-Williams C,
Stewart ID,
Surendran P,
Karthikeyan S,
Day FR,
Koulman A,
Imamura F,
Zeng L,
Erdmann J,
Schunkert H
and 11 more — show all
Khaw KT,
Griffin JL,
Forouhi NG,
Scott RA,
Wood AM,
Burgess S,
Howson JMM,
Danesh J,
Wareham NJ,
Butterworth AS,
Langenberg C
Nature communications · 2019 · PMID 30837465 · open access
7 pages
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
Gorman BR,
Francis M,
Nealon CL,
Halladay CW,
Duro N,
Markianos K,
Genovese G,
Hysi PG,
Choquet H,
Afshari NA,
Li YJ,
Gaziano JM
and 7 more — show all
VA Million Veteran Program
Communications biology · 2024 · PMID 38582945 · open access
7 pages
Polygenic risk score for atopic dermatitis in the Canadian population
Simard M,
Madore AM,
Girard S,
Waserman S,
Duan Q,
Subbarao P,
Sears MR,
Moraes TJ,
Becker AB,
Turvey SE,
Mandhane PJ,
Morin C
and 2 more — show all
The Journal of allergy and clinical immunology · 2021 · PMID 32439431
6 pages
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium
Guan W,
Steffen BT,
Lemaitre RN,
Wu JHY,
Tanaka T,
Manichaikul A,
Foy M,
Rich SS,
Wang L,
Nettleton JA,
Tang W,
Gu X
and 12 more — show all
Bandinelli S,
King IB,
McKnight B,
Psaty BM,
Siscovick D,
Djousse L,
Chen YI,
Ferrucci L,
Fornage M,
Mozafarrian D,
Tsai MY,
Steffen LM
Circulation. Cardiovascular genetics · 2014 · PMID 24823311
5 pages
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality
Soler Artigas M,
Sánchez-Mora C,
Rovira P,
Richarte V,
Garcia-Martínez I,
Pagerols M,
Demontis D,
Stringer S,
Vink JM,
Børglum AD,
Neale BM,
Franke B
and 4 more — show all
ADHD Group of the Psychiatric Genomics Consortium, International Cannabis Consortium
Molecular psychiatry · 2020 · PMID 30610198
5 pages
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study
Greenwood TA,
Lazzeroni LC,
Maihofer AX,
Swerdlow NR,
Calkins ME,
Freedman R,
Green MF,
Light GA,
Nievergelt CM,
Nuechterlein KH,
Radant AD,
Siever LJ
and 9 more — show all
JAMA psychiatry · 2019 · PMID 31596458
5 pages
Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway
Hällfors J,
Palviainen T,
Surakka I,
Gupta R,
Buchwald J,
Raevuori A,
Ripatti S,
Korhonen T,
Jousilahti P,
Madden PAF,
Kaprio J,
Loukola A
Addiction biology · 2019 · PMID 29532581 · open access
4 pages
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey
Spracklen CN,
Shi J,
Vadlamudi S,
Wu Y,
Zou M,
Raulerson CK,
Davis JP,
Zeynalzadeh M,
Jackson K,
Yuan W,
Wang H,
Shou W
and 9 more — show all
PLoS genetics · 2018 · PMID 29621232 · open access
4 pages
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
Day F,
Karaderi T,
Jones MR,
Meun C,
He C,
Drong A,
Kraft P,
Lin N,
Huang H,
Broer L,
Magi R,
Saxena R
and 37 more — show all
Laisk T,
Urbanek M,
Hayes MG,
Thorleifsson G,
Fernandez-Tajes J,
Mahajan A,
Mullin BH,
Stuckey BGA,
Spector TD,
Wilson SG,
Goodarzi MO,
Davis L,
Obermayer-Pietsch B,
Uitterlinden AG,
Anttila V,
Neale BM,
Jarvelin MR,
Fauser B,
Kowalska I,
Visser JA,
Andersen M,
Ong K,
Stener-Victorin E,
Ehrmann D,
Legro RS,
Salumets A,
McCarthy MI,
Morin-Papunen L,
Thorsteinsdottir U,
Stefansson K,
Styrkarsdottir U,
Perry JRB,
Dunaif A,
Laven J,
Franks S,
Lindgren CM,
Welt CK
23andMe Research Team
PLoS genetics · 2018 · PMID 30566500 · open access
4 pages
Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration
Lorés-Motta L,
van Beek AE,
Willems E,
Zandstra J,
van Mierlo G,
Einhaus A,
Mary JL,
Stucki C,
Bakker B,
Hoyng CB,
Fauser S,
Clark SJ
and 6 more — show all
American journal of human genetics · 2021 · PMID 34260947 · open access
4 pages
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
Zhang L,
Qiu L,
Wu J,
Qi Y,
Gao X,
He C,
Qi R,
Wang H,
Yao X,
Zhu H,
Li Y,
Hao S
and 33 more — show all
Lu Q,
Long H,
Lian S,
Zhu W,
Zhang H,
Lai W,
Su X,
Lu R,
Guo Z,
Li J,
Li M,
Liu Q,
Wang H,
He L,
Nong X,
Li F,
Li Y,
Yao C,
Xu J,
Tang H,
Wang D,
Li Z,
Yu H,
Xiao S,
An J,
Pu X,
Yu S,
Zhang J,
Chen X,
Wang H,
Huang W,
Chen H,
Xiao T
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape
Goovaerts S,
Hoskens H,
Eller RJ,
Herrick N,
Musolf AM,
Justice CM,
Yuan M,
Naqvi S,
Lee MK,
Vandermeulen D,
Szabo-Rogers HL,
Romitti PA
and 8 more — show all
Nature communications · 2023 · PMID 37973980 · open access
4 pages
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
Chen Z,
Tang H,
Qayyum R,
Schick UM,
Nalls MA,
Handsaker R,
Li J,
Lu Y,
Yanek LR,
Keating B,
Meng Y,
van Rooij FJ
and 24 more — show all
Okada Y,
Kubo M,
Rasmussen-Torvik L,
Keller MF,
Lange L,
Evans M,
Bottinger EP,
Linderman MD,
Ruderfer DM,
Hakonarson H,
Papanicolaou G,
Zonderman AB,
Gottesman O,
Thomson C,
Ziv E,
Singleton AB,
Loos RJ,
Sleiman PM,
Ganesh S,
McCarroll S,
Becker DM,
Wilson JG,
Lettre G,
Reiner AP
BioBank Japan Project · CHARGE Consortium
Human molecular genetics · 2013 · PMID 23446634
3 pages
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia
Reiner AP,
Hartiala J,
Zeller T,
Bis JC,
Dupuis J,
Fornage M,
Baumert J,
Kleber ME,
Wild PS,
Baldus S,
Bielinski SJ,
Fontes JD
and 23 more — show all
Illig T,
Keating BJ,
Lange LA,
Ojeda F,
Müller-Nurasyid M,
Munzel TF,
Psaty BM,
Rice K,
Rotter JI,
Schnabel RB,
Tang WH,
Thorand B,
Erdmann J,
Jacobs DR Jr,
Wilson JG,
Koenig W,
Tracy RP,
Blankenberg S,
März W,
Gross MD,
Benjamin EJ,
Hazen SL,
Allayee H
CARDIoGRAM Consortium
Human molecular genetics · 2013 · PMID 23620142
3 pages
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
Simino J,
Shi G,
Bis JC,
Chasman DI,
Ehret GB,
Gu X,
Guo X,
Hwang SJ,
Sijbrands E,
Smith AV,
Verwoert GC,
Bragg-Gresham JL
and 91 more — show all
Cadby G,
Chen P,
Cheng CY,
Corre T,
de Boer RA,
Goel A,
Johnson T,
Khor CC,
Lluís-Ganella C,
Luan J,
Lyytikäinen LP,
Nolte IM,
Sim X,
Sõber S,
van der Most PJ,
Verweij N,
Zhao JH,
Amin N,
Boerwinkle E,
Bouchard C,
Dehghan A,
Eiriksdottir G,
Elosua R,
Franco OH,
Gieger C,
Harris TB,
Hercberg S,
Hofman A,
James AL,
Johnson AD,
Kähönen M,
Khaw KT,
Kutalik Z,
Larson MG,
Launer LJ,
Li G,
Liu J,
Liu K,
Morrison AC,
Navis G,
Ong RT,
Papanicolau GJ,
Penninx BW,
Psaty BM,
Raffel LJ,
Raitakari OT,
Rice K,
Rivadeneira F,
Rose LM,
Sanna S,
Scott RA,
Siscovick DS,
Stolk RP,
Uitterlinden AG,
Vaidya D,
van der Klauw MM,
Vasan RS,
Vithana EN,
Völker U,
Völzke H,
Watkins H,
Young TL,
Aung T,
Bochud M,
Farrall M,
Hartman CA,
Laan M,
Lakatta EG,
Lehtimäki T,
Loos RJ,
Lucas G,
Meneton P,
Palmer LJ,
Rettig R,
Snieder H,
Tai ES,
Teo YY,
van der Harst P,
Wareham NJ,
Wijmenga C,
Wong TY,
Fornage M,
Gudnason V,
Levy D,
Palmas W,
Ridker PM,
Rotter JI,
van Duijn CM,
Witteman JC,
Chakravarti A,
Rao DC
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
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.