For researchers

Is your paper here?

2,671 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.

34 matches for Gelernter J, showing the first 20.

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
Nature neuroscience · 2020 · PMID 32451486 · open access
12 pages+
rs148382129 rs9926289 rs9937709 rs73403005 rs7073987 rs1724429
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals
VA Million Veteran Program
Nature communications · 2020 · PMID 33082346 · open access
12 pages+
rs1385108 rs455650 rs28717373 rs2565060 rs6438208 rs12545053
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+
rs78308718 rs6875495 rs55706012 rs6993953 rs11137399 rs4748468
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+
rs56367474 rs2028269 rs10787738 rs176413 rs332827 rs4659805
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
23andMe Research Team
Nature genetics · 2022 · PMID 35835914
12 pages+
rs10947428 rs10846577 rs61765651 rs8180817 rs55777621 rs9546806
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature medicine · 2023 · PMID 37464041
12 pages+
rs12517438 rs1931388 rs12530388 rs2418449 rs11612312 rs11157241
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs12136984 rs12374612 rs324901 rs534415 rs1526193 rs7415357
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+
rs7243332 rs6032660 rs10487459 rs175086 rs13037326 rs10992779
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
rs1275923 rs371071053 rs74315329 rs6762719 rs115378818 rs3015326
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 1 more consortia
Nature genetics · 2019 · PMID 30478444
8 pages
rs11591402 rs1427829 rs3001723 rs1592757 rs4275621 rs2243517
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder
Molecular psychiatry · 2022 · PMID 35181757 · open access
7 pages
rs10235664 rs931774 rs145108206 rs55770986 rs12699336 rs10105545
Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample
The American journal of psychiatry · 2023 · PMID 37282553
7 pages
rs13146907 rs144228648 rs147759217 rs565298761 rs75438204 rs28470433
Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program
Department of Veterans Affairs Cooperative Studies Program (no. 575B) · VA Million Veteran Program
Nature genetics · 2021 · PMID 33510476 · open access
5 pages
rs251350 rs1496246 rs2314662 rs11760633 rs3800872
Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American populations
VA Million Veteran Program
Cell genomics · 2024 · PMID 38870908 · open access
5 pages
rs146867887 rs4822369 rs9480836 rs9823832 rs7244528
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
Nature communications · 2019 · PMID 30940813 · open access
4 pages
rs11075992 rs540606 rs1229978 Alcohol Use Disorder
Sex-Specific Genetic and Transcriptomic Liability to Neuroticism
Biological psychiatry · 2023 · PMID 36244801
4 pages
rs72995548 rs55955207 rs34216353 rs6722890
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Veterans Affairs Million Veteran Program
Nature genetics · 2023 · PMID 37985822 · open access
4 pages
rs12497569 rs11570190 rs10835372 rs62461186
The genetics of fibromyalgia and its relationships to psychiatric and medical traits
VA Million Veteran Program
Nature communications · 2026 · PMID 42521668 · open access
4 pages
rs72831629 rs75970938 rs186798404 Fibromyalgia
Genome-wide analysis of insomnia disorder
Molecular psychiatry · 2018 · PMID 29520036 · open access
3 pages
rs34670506 rs7138947 Insomnia
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks
JAMA psychiatry · 2016 · PMID 27028160
2 pages
rs77378271 rs146091982

Showing 20 of 34 · page 1 of 2

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.