For researchers

Is your paper here?

2,673 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.

184 matches for Ell C, showing the first 20.

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Understanding Society Scientific Group · International Consortium for Blood Pressure and 2 more consortia
Nature genetics · 2019 · PMID 30578418 · open access
12 pages+
rs2009598 rs9708177 rs139055942 rs6848906 rs533030436 rs181718607
An atlas of genetic influences on osteoporosis in humans and mice
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
12 pages+
rs6421572 rs143290532 rs35717986 rs73066226 rs194608 rs9606138
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs754868 rs3746448 rs4809731 rs62023486 rs75034466 rs7285579
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program
Nature communications · 2019 · PMID 31451708 · open access
12 pages+
rs755631 rs3132374 rs71559067 rs11621061 rs3101823 rs68137036
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs11781985 rs72782806 rs861536 rs10438961 rs6707386 rs98270
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs170239 rs2358483 rs149142 rs78155705 rs62005276 rs639016
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · open access
12 pages+
rs9806595 rs1548942 rs11740254 rs7959830 rs4083463 rs13050142
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
rs9370243 rs9900074 rs73121277 rs1470560 rs7538321 rs11114650
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs10025456 rs8032301 rs1624825 rs145502455 rs273592 rs11937432
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction
Nature genetics · 2021 · PMID 33414549 · open access
12 pages+
rs10996426 rs9630631 rs6577356 rs1492057 rs62009152 rs6718450
Genetic and functional interaction network analysis reveals global enrichment of regulatory T cell genes influencing basal cell carcinoma susceptibility
Genome medicine · 2021 · PMID 33549134 · open access
12 pages+
rs41271951 rs801108 rs2882274 rs79522206 rs340797 rs6707137
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
12 pages+
rs62463430 rs187345738 rs202155306 rs5747734 rs529876271 rs17710
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+
rs17256082 rs12784552 rs142484519 rs118164457 rs7063597 rs3752435
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
rs74117915 rs182462345 rs886816 rs6693965 rs12145394 rs376671198
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals
VA Million Veteran Program
Nature communications · 2021 · PMID 34272381 · open access
12 pages+
rs3119304 rs2960455 rs17256228 rs35289683 rs4970765 rs164747
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+
rs10928512 rs187479321 rs6493583 rs72729623 rs115726216 rs144242131
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs340009 rs2726950 rs6632109 rs8049403 rs2048528 rs1518760
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+
rs1887200 rs11904581 rs6139109 rs1442883 rs973730 rs6020177
A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma
23andMe Research Team
Nature communications · 2022 · PMID 36496446 · open access
12 pages+
rs10830255 rs6989943 rs502803 rs2849695 rs11961808 rs10102592

Showing 20 of 184 · page 2 of 10

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.