For researchers

Is your paper here?

2,682 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 Li Q, showing the first 20.

Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level
Alzheimer’s Disease Neuroimaging Initiative
PloS one · 2015 · PMID 26252872 · open access
12 pages+
rs1503351 rs75638798 rs7581969 rs76744071 rs78649275 rs79158673
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+
rs10917509 rs78308718 rs6875495 rs55706012 rs6993953 rs11137399
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs6538539 rs708228 rs17571951 rs61828917 rs815609 rs16940992
Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus
Nature communications · 2023 · PMID 36750564 · open access
12 pages+
rs9911688 rs11200927 rs4599150 rs13014122 rs12490565 rs906868
Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women
mSystems · 2021 · PMID 34282934 · open access
11 pages
rs75042393 rs78166340 rs58520434 rs117290187 rs12204265 rs12205331
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Breast and Prostate Cancer Cohort Consortium (BPC3) · PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25217961 · open access
10 pages
rs1041449 rs17599629 rs9287719 rs56232506 rs17694493 rs76934034
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
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
rs2628317 rs17762342 rs739704 rs3802173 rs1469713 rs9657608
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
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Nature communications · 2026 · PMID 42014397 · open access
4 pages
rs4843552 rs798560 rs35327527 rs7928895
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
International Consortium for Systemic Lupus Erythematosus Genetics (SLEGEN)
Nature genetics · 2008 · PMID 18204446
3 pages
rs9888739 rs3131379 rs12537284
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Cancer discovery · 2015 · PMID 26034056
3 pages
rs116041037 rs72725879 rs10896449
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Nature genetics · 2011 · PMID 22138694
2 pages
rs17095830 Ankylosing Spondylitis
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
PLoS genetics · 2013 · PMID 24204295 · open access
2 pages
rs17212223 rs7744020
Shared genetic risk factors and causal association between psoriasis and coronary artery disease
Nature communications · 2022 · PMID 36323703 · open access
2 pages
rs76151170 rs12979495
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
American journal of human genetics · 2009 · PMID 19836008
1 page
rs31489
Genome-wide association study of circulating vitamin D levels
Human molecular genetics · 2010 · PMID 20418485 · open access
1 page
rs3829251
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Nature genetics · 2013 · PMID 24097066
1 page
rs4282438

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.