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.

10 matches for Sherva R.

Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages
Alzheimer's Disease Neuroimaging Initiative
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2018 · PMID 29274321
8 pages
rs55644114 rs74442473 rs2378873 rs10775009 rs2819438 rs118130881
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks
JAMA psychiatry · 2016 · PMID 27028160
2 pages
rs77378271 rs146091982
Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression
JAMA psychiatry · 2017 · PMID 29071344
2 pages
rs139438618 Major Depression and Alcohol Dependence (Comorbid)
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs1898895 rs111486601
Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci
Molecular psychiatry · 2014 · PMID 24166409
1 page
rs2066702
Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans
Biological psychiatry · 2015 · PMID 25555482
1 page
rs144667340
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans
Alzheimer's Disease Genetics Consortium
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2017 · PMID 27770636
1 page
rs16961023
Transethnic genome-wide scan identifies novel Alzheimer's disease loci
Alzheimer's Disease Genetics Consortium
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2017 · PMID 28183528
1 page
rs11257238
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020 · PMID 31294817
1 page
rs16969968
African ancestry GWAS of dementia in a large military cohort identifies significant risk loci
Molecular psychiatry · 2023 · PMID 36543923
1 page
rs73505251

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.