For researchers

Is your paper here?

3,070 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.

11 matches for Garrett M.

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+
rs2358483 rs149142 rs78155705 rs62005276 rs639016 rs34322452
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs11662996 rs1857578 rs2668654 rs4863488 rs11078403 rs12641457
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs10865093 rs7431106 rs61946067 rs28986300 rs16948230 rs6801151
Local ancestry-aware genome-wide meta-analysis uncovers novel genetic loci for sickle cell disease nephropathy
Blood advances · 2026 · PMID 42616615
12 pages+
rs35371039 rs149824172 rs28711705 rs77741394 rs13436307 rs75865982
Human genetics implicates a BACH2-NRF2 axis in fetal haemoglobin activation
Nature · 2026 · PMID 42816612
12 pages+
rs2855039 rs9389271 rs13024177 rs12270279 rs7130110 rs10490071
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors
VA Million Veteran Program (MVP) · MVP Suicide Exemplar Workgroup and 6 more consortia
The American journal of psychiatry · 2023 · PMID 37777856
7 pages
rs7649709 rs62404522 rs9525171 rs850261 rs17485141 rs2284000
Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans
Million Veteran Program Suicide Exemplar Workgroup, the International Suicide Genetics Consortium, the Veterans Affairs Mid-Atlantic Mental Illness Research, Education, and Clinical Center Workgroup, and the Veterans Affairs Million Veteran Program
JAMA psychiatry · 2023 · PMID 36515925
6 pages
rs75421528 rs7098086 rs116015815 rs182921948 rs35675346 rs3757323
A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci
VA Million Veteran Program (MVP) · MVP Suicide Exemplar Workgroup and 1 more consortia
Molecular psychiatry · 2022 · PMID 35347246 · open access
4 pages
rs34173987 rs57790277 rs77378519 rs9596440
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Biological psychiatry · 2022 · PMID 34865855 · open access
3 pages
rs7264419 rs6661135 rs10821140
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
3 pages
rs830463 rs111490516 rs62033408
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci
Nature communications · 2019 · PMID 31594949 · open access
1 page
rs115539978

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.