For researchers

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.

108 matches for Eng C, showing the first 20.

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs6667536 rs12540035 rs9819278 rs2491422 rs62391632 rs66819623
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs202219817 rs35499210 rs759831202 rs952170 rs11167778 rs1338668
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
Your height affects your health: genetic determinants and health-related outcomes in Taiwan
BMC medicine · 2022 · PMID 35831902 · open access
12 pages+
rs78899385 rs2008018 rs73780873 rs12606199 rs17032833 rs4463061
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs12566345 rs1921907 rs210280 rs4696931 rs6727028 rs7070947
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs131246 rs4872527 rs10853047 rs1685635 rs2283368 rs572016
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs149780392 rs3794752 rs62233286 rs7095308 rs73048654 rs143445113
Genome-wide association study and polygenic risk prediction of hypothyroidism
DBDS Genomic Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2025 · PMID 41238958 · open access
12 pages+
rs9557207 rs2008260 rs4641716 rs7748169 rs11054900 rs11765986
Genetic landscape and functional exploration of kidney cancer predisposition in cross-ancestral populations
Nature communications · 2026 · PMID 42000752 · open access
12 pages+
rs73113855 rs10015491 rs932826 rs33925946 rs28607501 rs1007934
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
12 pages+
rs736374 rs723291 rs11073337 rs11154825 rs3892710 rs12345171
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
rs112111458 rs10214237 rs6473227 rs6602364 rs7127307 rs2143950
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
NEIGHBOR Consortium
Nature genetics · 2013 · PMID 23291589
10 pages
rs2307121 rs1007000 rs1536482 rs11145951 rs4938174 rs1564892
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
rs10853531 rs11145488 rs12511037 rs1649081 rs16949788 rs10089517
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
10 pages
rs6440008 rs10960765 rs58979150 rs11041426 rs72917317 rs10899501
Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
Nature communications · 2020 · PMID 32139696 · open access
10 pages
rs17268829 rs10760444 rs71559437 rs6964587 rs4496150 rs9833888
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs35200015 rs3133370 rs2206656 rs4784256 rs196807 rs9505301
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
rs79624003 rs55809639 rs4847240 rs4660303 rs7298909 rs56204645
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs5931180 rs12382607 rs4328011 rs139036121 rs5933079 rs181497961

Showing 20 of 108 · page 2 of 6

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.