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.

24 matches for Thorgeirsson TE, showing the first 20.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs2004038 rs34878803 rs13213986 rs7383287 rs11632038 rs116826541
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
rs7841320 rs10028756 rs9557376 rs3846449 rs4650206 rs8192726
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+
rs2336147 rs10866641 rs67712855 rs748455 rs78308718 rs6875495
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
International Headache Genetics Consortium · HUNT All-in Headache and 1 more consortia
Nature genetics · 2022 · PMID 35115687 · open access
12 pages+
rs12057629 rs6057599 rs1019990 rs7506921 rs1285294 rs75002882
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
12 pages+
rs9722048 rs12762780 rs12539945 rs73978133 rs56214011 rs57822625
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs11949611 rs2099016 rs2241470 rs1913311 rs231046 rs11237456
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
11 pages
rs73005873 rs9927389 rs183821586 rs41282145 rs17300770 rs9621
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
eQTLGen · 23andMe and 1 more consortia
Nature genetics · 2018 · PMID 29700475 · open access
10 pages
rs10950398 rs11643192 rs7430565 rs116755193 rs4904738 rs62099069
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
9 pages
rs751450 rs3135842 rs4757353 rs28487989 rs16934882 rs3010044
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
7 pages
rs17649684 rs13128363 rs11749692 rs955007 rs9843219 rs9980363
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
rs111444407 rs10950456 rs57957974 rs17183814 rs10896090 rs10035291
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
rs61914392 rs17099617 rs73217448 rs60147627
The genetic architecture of fibromyalgia across 2.5 million individuals
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
rs62194170 rs2734833 rs34683740 Fibromyalgia
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
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
A genetic risk factor for periodic limb movements in sleep
The New England journal of medicine · 2007 · PMID 17634447
1 page
rs3923809
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Nature · 2008 · PMID 18385739
1 page
Lung Cancer
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium
Biological psychiatry · 2017 · PMID 27519822 · open access
1 page
rs7647854
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Nature genetics · 2017 · PMID 27918536
1 page
rs6481128

Showing 20 of 24 · 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.