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.

8 matches for Wang YF.

Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups
Nature communications · 2021 · PMID 33536424 · open access
12 pages+
rs1016140 rs7815944 rs405858 rs9630991 rs9899849 rs12093154
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
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus
Nature genetics · 2016 · PMID 27399966
3 pages
rs17321999 rs6762714 rs494003
Shared genetic study gives insights into the shared and distinct pathogenic immunity components of IgA nephropathy and SLE
Molecular genetics and genomics : MGG · 2021 · PMID 34076728
3 pages
rs9270539 rs16869875 rs10847697
A genome-wide association study identifies novel loci of vertigo in an Asian population-based cohort
Communications biology · 2024 · PMID 39174713 · open access
3 pages
rs428549 rs612969 rs10862089
Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population
Arthritis research & therapy · 2020 · PMID 32771030 · open access
2 pages
rs74989671 rs117522574
Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population
Cephalalgia : an international journal of headache · 2022 · PMID 34404248
1 page
rs10493859
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

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.