For researchers

Is your paper here?

2,673 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.

28 matches for Foroud T, showing the first 20.

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and 10 more consortia
Nature genetics · 2014 · PMID 25064009 · open access
12 pages+
rs1555399 rs2414739 rs14235 rs35749011 rs10797576 rs1474055
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
rs2274465 rs6747380 rs6758290 rs4369815 rs17236969 rs17233066
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs2469933 rs1727284 rs442467 rs11135030 rs11210887 rs12053870
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+
rs28455634 rs12672003 rs35306827 rs2336147 rs10866641 rs67712855
Genome-wide meta-analyses of cross substance use disorders in diverse populations
Molecular psychiatry · 2026 · PMID 41057643 · open access
12 pages+
rs62135525 rs3774611 rs12495571 rs7103679 rs2509377 rs13196692
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
rs1364063 rs4840086 rs9939609 rs10980926 rs7642134 rs17188434
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs10217651 rs35200015 rs3133370 rs2206656 rs4784256 rs196807
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
9 pages
rs60755019 rs3848143 rs62374257 rs3851179 rs6605556 rs7767350
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment
PLoS genetics · 2014 · PMID 24945404 · open access
7 pages
rs2450083 rs3920498 rs7776725 rs17536328 rs2235529 rs798943
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs10896090 rs10035291 rs111444407 rs10950456 rs57957974 rs17183814
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Lancet (London, England) · 2010 · PMID 20541252
3 pages
rs2282679 Vitamin D Deficiency and the GC Gene Vitamin D
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 and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
2 pages
rs6943555 Alcohol Consumption
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Human molecular genetics · 2016 · PMID 27329760
2 pages
rs2517959 rs4236274
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23
Journal of the American Society of Nephrology : JASN · 2018 · PMID 30217807
2 pages
rs11741640 rs2769071
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
Identification of common variants associated with human hippocampal and intracranial volumes
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
rs10784502
Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6
Genes, brain, and behavior · 2012 · PMID 22554406
1 page
rs2835872
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

Showing 20 of 28 · 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.