For researchers

Is your paper here?

2,676 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.

13 matches for Wen J.

Multi-omic spatial effects on high-resolution AI-derived retinal thickness
Nature communications · 2025 · PMID 39904976 · open access
12 pages+
rs16926921 rs10771345 rs17095953 rs12531825 rs17507554 rs7191242
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Cell genomics · 2024 · PMID 38190104 · open access
6 pages
rs13392691 rs35790011 rs11753349 rs73392143 rs10993435 rs2016708
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Dihydropyrimidine Dehydrogenase Genotype and Fluoropyrimidine Dosing: 2017 Update
Clinical pharmacology and therapeutics · 2018 · PMID 29152729
5 pages
rs3918290 rs67376798 rs75017182 Colorectal Cancer Fluoropyrimidine Dosing (DPYD)
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
rs7561528 rs9349407 Alzheimer's Disease
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans
DIAGRAM Consortium · AGEN-T2D Consortium
Diabetes · 2013 · PMID 22961080 · open access
3 pages
rs10886471 rs10814916 rs12010175
Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants
Clinical Pharmacogenetics Implementation Consortium
Clinical pharmacology and therapeutics · 2013 · PMID 23486447
2 pages
Migraine Major Depressive Disorder
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for CYP3A5 Genotype and Tacrolimus Dosing
Clinical pharmacology and therapeutics · 2015 · PMID 25801146
2 pages
rs776746 CYP3A5 Metaboliser Status
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies
Journal of human genetics · 2022 · PMID 34376796 · open access
2 pages
rs556126054 rs112902560
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients
American journal of respiratory and critical care medicine · 2023 · PMID 36921087
2 pages
rs56108664 rs12009976
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs111486601 rs1898895
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Nature genetics · 2013 · PMID 23708190
1 page
rs1531070
New loci associated with chronic hepatitis B virus infection in Han Chinese
Nature genetics · 2013 · PMID 24162738
1 page
rs3130542
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528

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.