For researchers

Is your paper here?

2,646 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.

9 matches for Lu Q.

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
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank
The Journal of allergy and clinical immunology · 2020 · PMID 31669095
6 pages
rs12493005 rs73086541 rs73084574 rs1787663 rs9275570 rs8089834
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
American journal of human genetics · 2013 · PMID 23273568
5 pages
rs6705628 rs4852324 rs6804441 rs34330 rs729302
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans
Consortium on the Genetics of Schizophrenia (COGS) · Genomic Psychiatry Cohort (GPC) Investigators and 1 more consortia
Schizophrenia bulletin · 2021 · PMID 33169155
4 pages
rs11742527 rs2143757 rs156089 rs11226509
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
The Journal of investigative dermatology · 2023 · PMID 35933036
3 pages
rs61986182 rs117754460 rs434124
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations
GIANT consortium
Nature genetics · 2012 · PMID 22344221
2 pages
rs12149832 rs11671664
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
Nature communications · 2014 · PMID 24399259
2 pages
rs7531806 Severe Acne
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations
Communications biology · 2021 · PMID 33437055 · open access
2 pages
rs6546857 rs11253995
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Nature genetics · 2009 · PMID 19838193
1 page
rs1167796

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.