For researchers

Is your paper here?

2,657 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.

15 matches for Seldin MF.

An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
9 pages
rs589446 rs11742270 rs859767 rs6550965 rs12419634 rs742108
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
International Consortium for Systemic Lupus Erythematosus Genetics (SLEGEN)
Nature genetics · 2008 · PMID 18204446
3 pages
rs9888739 rs3131379 rs12537284
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
Nature genetics · 2009 · PMID 19838195
3 pages
rs3135394 rs2070197 rs11860650
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
Canadian-US PBC Consortium · Italian PBC Genetics Study Group and 1 more consortia
Nature communications · 2015 · PMID 26394269 · open access
3 pages
rs526231 rs6933404 Primary Biliary Cholangitis
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Nature genetics · 2007 · PMID 17982456
2 pages
rs10499194 Rheumatoid Arthritis
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
BIRAC Consortium · YEAR Consortium
Nature genetics · 2010 · PMID 20453842
2 pages
rs874040 rs6910071
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
Nature genetics · 2010 · PMID 20639880
2 pages
rs6441286 Primary Biliary Cholangitis
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
Annals of neurology · 2012 · PMID 23055271
2 pages
rs3130544 Myasthenia Gravis
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of <i>TNFRSF11A</i> and Identification of <i>ZBTB10</i> and Three Distinct HLA Associations
Molecular medicine (Cambridge, Mass.) · 2016 · PMID 26562150
2 pages
rs111945767 Myasthenia Gravis
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency
Nature genetics · 2016 · PMID 27723758 · open access
2 pages
rs4565870 Selective IgA Deficiency
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Nature communications · 2017 · PMID 28425483 · open access
2 pages
rs9501251 Primary Biliary Cholangitis
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX
The New England journal of medicine · 2008 · PMID 18204098
1 page
rs11574637
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis
Nature genetics · 2009 · PMID 19503088 · open access
1 page
rs13017599
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
Italian PBC Genetics Study Group
Human molecular genetics · 2012 · PMID 22936693
1 page
rs7775055
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280

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.