For researchers

Is your paper here?

3,095 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.

26 matches for Pericak-Vance M, showing the first 20.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International Multiple Sclerosis Genetics Consortium (IMSGC) · Wellcome Trust Case Control Consortium 2 (WTCCC2) and 1 more consortia
Nature genetics · 2013 · PMID 24076602 · open access
12 pages+
rs35967351 rs2726518 rs1843938 rs7120737 rs12296430 rs4772201
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
12 pages+
rs10947943 rs6489896 rs7908662 rs9304690 rs16941239 rs16824536
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
11 pages
rs11154801 rs12212193 rs7522462 rs9282641 rs10466829 rs2119704
Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023 · PMID 35770850
11 pages
rs7155666 rs896559 rs116668122 rs372758 rs6978419 rs2345589
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
rs1864163 rs920915 rs8135665 rs8017304 rs9542236 rs13081855
Stratification by a polygenic risk score of common variation aids in Alzheimer's disease rare variant discovery
Alzheimer's Disease Sequencing Project
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026 · PMID 42557982 · open access
5 pages
rs960000673 rs539602997 rs17086376 rs895919483 rs140189521
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
International MS Genetics Consortium
Nature genetics · 2009 · PMID 19525953
3 pages
rs2300747 rs17445836 Multiple Sclerosis
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Complications of Age-Related Macular Degeneration Prevention Trial Research Group
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385819
3 pages
rs9380272 rs429608 Age-Related Macular Degeneration
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
rs7561528 rs9349407 Alzheimer's Disease
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias
Alzheimer's Disease Genetics Consortium (ADGC)
PLoS genetics · 2014 · PMID 25188341 · open access
3 pages
rs6857 rs62341097 rs429358
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
2 pages
rs10838725 rs10498633
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
2 pages
rs284491 rs1333037
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers
Alzheimer’s Disease Neuroimaging Initiative (ADNI) · Alzheimer Disease Genetic Consortium (ADGC)
Acta neuropathologica · 2017 · PMID 28247064
2 pages
rs769449 rs9527039
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Alzheimer Disease Genetics Consortium (ADGC), · European Alzheimer’s Disease Initiative (EADI), and 2 more consortia
Nature genetics · 2019 · PMID 30820047
2 pages
rs138190086 rs7185636
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
rs111486601 rs1898895
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities
PLoS genetics · 2010 · PMID 20885792 · open access
1 page
rs2075650
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans
Alzheimer Disease Genetics Consortium
JAMA · 2013 · PMID 23571587
1 page
rs115550680
A novel Alzheimer disease locus located near the gene encoding tau protein
IGAP Consortium
Molecular psychiatry · 2016 · PMID 25778476 · open access
1 page
rs2732703
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

Showing 20 of 26 · 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.