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 He D, showing the first 9.

Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Nature genetics · 2012 · PMID 23023329
1 page
rs103294
Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries
Clinical chemistry · 2015 · PMID 25414277
1 page
Cholesterol (LDL, HDL and Total)
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials
BEYOND and BENEFIT Study Groups
Multiple sclerosis (Houndmills, Basingstoke, England) · 2019 · PMID 29521573
1 page
rs2454138
A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia
Molecular psychiatry · 2019 · PMID 30647433
1 page
rs77198048
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Nature communications · 2019 · PMID 31413261 · open access
1 page
Human Lifespan and Longevity
Identification of Shared and Asian-Specific Loci for Systemic Lupus Erythematosus and Evidence for Roles of Type III Interferon Signaling and Lysosomal Function in the Disease: A Multi-Ancestral Genome-Wide Association Study
Arthritis & rheumatology (Hoboken, N.J.) · 2022 · PMID 34783190
1 page
rs76596471
Comparative Genetic Analysis of Psoriatic Arthritis and Psoriasis for the Discovery of Genetic Risk Factors and Risk Prediction Modeling
BADBIR Study Group · BSTOP study group
Arthritis & rheumatology (Hoboken, N.J.) · 2022 · PMID 35507331 · open access
1 page
rs1395621
Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees
Journal of blood medicine · 2026 · PMID 42732403 · open access
1 page
Research roundup — September 2026
Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals
Nature genetics · 1995 · PMID 7663520
1 page
Duffy-Null Phenotype and Benign Ethnic Neutropenia

Showing 9 of 29 · page 2 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.