For researchers

Is your paper here?

2,677 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.

580 matches for An J, showing the first 20.

The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs35513223 rs4808566 rs5744168 rs62006258 rs62246445 rs6588417
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
American journal of human genetics · 2020 · PMID 33031748
12 pages+
rs7964228 rs74882993 rs11607853 rs363334 rs11245064 rs324420
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+
rs184289122 rs149165710 rs145441283 rs187207161 rs767105335 rs77357563
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs2018336 rs2038542 rs10412482 rs7618603 rs2074840 rs2672843
A cross-platform approach identifies genetic regulators of human metabolism and health
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
rs1165167 rs10024263 rs2234633 rs2608920 rs4253272 rs731165
Genetics of 35 blood and urine biomarkers in the UK Biobank
FinnGen
Nature genetics · 2021 · PMID 33462484 · open access
12 pages+
rs17553750 rs17736453 rs1892510 rs35634464 rs72700826 rs75360998
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+
rs2491422 rs62391632 rs66819623 rs8141610 rs56233426 rs11710845
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10180829 rs672769 rs10071837 rs4899520 rs75823898 rs112226333
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
12 pages+
rs17708090 rs10821130 rs1554269 rs10193760 rs72813408 rs7567451
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
rs61047863 rs189305788 rs781930992 rs968218067 rs114310641 rs890565237
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs2336147 rs10866641 rs67712855 rs748455 rs10917509 rs78308718
Interpreting type 1 diabetes risk with genetics and single-cell epigenomics
Nature · 2021 · PMID 34012112
12 pages+
rs541856133 rs855330 rs1493696 rs12128789 rs1881146 rs13018977
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 rs182859029 rs7063597 rs3752435 rs4317621 rs4731113
Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
American journal of human genetics · 2021 · PMID 34077760 · open access
12 pages+
rs4849203 rs4964616 rs35424590 rs6117259 rs11746859 rs10998137
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · open access
12 pages+
rs6688826 rs1051861 rs12375898 rs72944387 rs76887862 rs2023553
Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia
American journal of human genetics · 2021 · PMID 34469753
12 pages+
rs60756694 rs112901136 rs6479286 rs16941541 rs34635139 rs9792678
Mapping the proteo-genomic convergence of human diseases
Science (New York, N.Y.) · 2021 · PMID 34648354
12 pages+
rs200903 rs34827868 rs3796867 rs6589441 rs7085715 rs7798138
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+
rs2003892 rs56299595 rs7212325 rs11183212 rs577703186 rs184980867
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs68002929 rs12541 rs61833239 rs13016542 rs11711948 rs9674103

Showing 20 of 580 · page 5 of 29

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.