For researchers

Is your paper here?

2,657 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.

30 matches for Lin A, showing the first 20.

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
23and Me Research Team · eQTLgen Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30643258
12 pages+
rs9815332 rs9992704 rs198535 rs4576809 rs73047488 rs9967799
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+
rs7552830 rs75199129 rs13024996 rs13077520 rs13288470 rs61741649
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
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
NeuroImage · 2021 · PMID 34560273
12 pages+
rs73234874 rs10508465 rs12621130 rs12666168 rs4272702 rs56192920
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+
rs6057599 rs1019990 rs7506921 rs1285294 rs75002882 rs28756401
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs72974238 rs6538539 rs708228 rs17571951 rs79210963 rs7933981
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+
rs199929 rs2008551 rs60172152 rs12136984 rs12374612 rs324901
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
rs6866323 rs6899343 rs144988974 rs9583095 rs58472573 rs739846
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+
rs6801151 rs78201023 rs7243332 rs6032660 rs10487459 rs175086
A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform
Nature genetics · 2025 · PMID 41310232 · open access
12 pages+
rs288296 rs73143813 rs7604812 rs9442970 rs8101725 rs12151742
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
rs2506142 rs4081947 rs6791480 rs6693567 rs10155855 rs10218452
Genome-Wide Association and Two-Sample Mendelian Randomization Analyses of Plasma Ghrelin and Gastrointestinal Cancer Risk
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023 · PMID 37791980 · open access
9 pages
rs143729751 rs56284847 rs17032621 rs715827 rs55821288 rs73026596
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature genetics · 2025 · PMID 40962958
8 pages
rs4462678 rs9959583 rs4131786 rs1435746 rs7100410 rs71428363
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
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
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
rs2798641 rs12447804 rs6903823 rs1036429
Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1
Hypertension (Dallas, Tex. : 1979) · 2013 · PMID 23381795
4 pages
rs2731672 rs5370 rs4253238 rs2957692
Genome-wide association study reveals two new risk loci for bipolar disorder
Nature communications · 2014 · PMID 24618891
4 pages
rs12290811 rs17826816 rs12202969 rs6550435
Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases
JCI insight · 2022 · PMID 35446786 · open access
4 pages
rs9646256 rs7224888 rs73338360 rs10738906
Genome-wide association study identifies five loci associated with lung function
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
rs12899618 rs10516526 rs12504628

Showing 20 of 30 · 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.