For researchers

Is your paper here?

2,663 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.

29 matches for Li A, showing the first 20.

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Cell · 2016 · PMID 27863252 · open access
12 pages+
rs17563683 rs11579220 rs144670711 rs6782812 rs7439923 rs56390363
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors
American journal of human genetics · 2017 · PMID 27989323
12 pages+
rs113831257 rs141053179 rs2070074 rs28637706 rs3748034 rs4656236
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs62037363 rs5758605 rs75477016 rs77418166 rs113714691 rs77482156
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Profile Study · Australian Prostate Cancer BioResource (APCB) and 7 more consortia
Nature genetics · 2018 · PMID 29892016
12 pages+
rs684232 rs182314334 rs2121875 rs17021918 rs11859370 rs2788524
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
rs3800406 rs75393320 rs71559014 rs2362529 rs10275712 rs10177080
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs2028900 rs339351 rs9306894 rs28441558 rs76765083 rs4714485
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs79210963 rs7933981 rs7900775 rs7575796 rs140365013 rs302317
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs1160545 rs3759344 rs7067170 rs7615206 rs1691471 rs4483592
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs78416326 rs17804499 rs72725734 rs11228580 rs7336001 rs77541621
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs12113633 rs62169409 rs4140952 rs7629500 rs61758556 rs240471
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
BSTOP study group · Estonian Biobank research team
Nature communications · 2025 · PMID 40021644 · open access
9 pages
rs7108441 rs74688172 rs4728141 rs7171410 rs8107351 rs13137072
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Nature communications · 2018 · PMID 29374233 · open access
6 pages
rs2736099 rs143093668 rs6915893 rs78781855 rs1005277 Telomere Length and Epigenetic Age Acceleration
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Cell · 2019 · PMID 31675503
6 pages
rs151330263 rs115231893 rs569795903 rs7564935 rs148228241 rs1088639
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Nature genetics · 2014 · PMID 25086665 · open access
5 pages
rs9581943 rs2736098 rs6971499 rs7190458 Pancreatic Cancer
Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study
Nature genetics · 2024 · PMID 39294497
5 pages
rs10171148 rs17408393 rs2510682 rs10138360 rs4870060
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
NIDDK IBD Genetics Consortium
Nature genetics · 2010 · PMID 20228799
4 pages
rs13003464 rs11190140 rs2836878 rs2395185
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns
Journal of medical genetics · 2019 · PMID 31217265 · open access
4 pages
rs117960796 rs117238625 rs192716315 rs6917603
Genomic loci and molecular genetic mechanisms for hidradenitis suppurativa
The British journal of dermatology · 2025 · PMID 40650879 · open access
4 pages
rs981625 rs10146136 rs12100281 rs2681502
Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder
Frontiers in psychiatry · 2018 · PMID 29559929 · open access
3 pages
rs35792458 rs4761545 rs144733372
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
European Scleroderma Group† · Australian Scleroderma Interest Group (ASIG)
Nature communications · 2019 · PMID 31672989 · open access
3 pages
rs4076852 rs3792783 rs36073657

Showing 20 of 29 · 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.