For researchers

Is your paper here?

2,673 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.

47 matches for Zhang L, showing the first 20.

Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy
Nature genetics · 2011 · PMID 22019778
4 pages
rs16948876 rs2275606 rs3762318 Leprosy
Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus
Rheumatology (Oxford, England) · 2021 · PMID 33493351
4 pages
rs4807205 rs12153670 rs73366469 rs2362475
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
rs117754460 rs434124 rs61986182 rs73075571
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
rs7447717 rs2905432 rs2532363
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis
PLoS genetics · 2010 · PMID 20072603 · open access
2 pages
rs13182402 Osteoporosis
Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies
PLoS genetics · 2013 · PMID 23349640 · open access
2 pages
rs4530903 rs12289961
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs12525220 rs1854853
Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene
Bone · 2016 · PMID 27424934
2 pages
rs9371538 Spine Bone Mineral Density
Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans
PLoS genetics · 2018 · PMID 30248107 · open access
2 pages
rs1866188 rs12651896
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese
Nature communications · 2018 · PMID 30287856 · open access
2 pages
rs6114027 Tuberculosis
Identification of new susceptibility loci associated with rheumatoid arthritis
Annals of the rheumatic diseases · 2020 · PMID 32868391
2 pages
rs770667 rs2201584
A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers
iScience · 2023 · PMID 37636041 · open access
2 pages
rs71238846 rs9620778
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
2 pages
rs55718051 HBV-Related Hepatocellular Carcinoma
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
PLoS genetics · 2012 · PMID 22383897 · open access
1 page
rs9485372
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
rs9268402
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Human molecular genetics · 2014 · PMID 24064335
1 page
rs62033400
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
Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016 · PMID 27311723
1 page
rs7839059
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci
PLoS genetics · 2019 · PMID 30807572 · open access
1 page
rs61948108
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
1 page
rs12451295

Showing 20 of 47 · page 2 of 3

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.