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.

11 matches for Sidorenko J.

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
rs11732160 rs12967010 rs13099165 rs1335482 rs142344547 rs1570926
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
eQTLGen Consortium
Nature communications · 2018 · PMID 30054458 · open access
12 pages+
rs12088739 rs2493394 rs17334919 rs12617659 rs7561798 rs2292662
Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
Nature communications · 2018 · PMID 30573740 · open access
12 pages+
rs10185460 rs11138885 rs59277927 rs10778623 rs6597371 rs180807105
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Nature communications · 2020 · PMID 32242144 · open access
12 pages+
rs12794714 rs8121940 rs10832254 rs12278461 rs59536295 rs7784802
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
23andMe Research Team · Social Science Genetic Association Consortium
Nature genetics · 2022 · PMID 35361970 · open access
12 pages+
rs11607466 rs11897647 rs11942352 rs12034740 rs12709063 rs13025467
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs9674103 rs11619756 rs1399551 rs2278515 rs56282503 rs12363019
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs11570441 rs11656344 rs11030613 rs11769128 rs11955611 rs11991223
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Cell genomics · 2023 · PMID 38116117 · open access
12 pages+
rs10414623 rs7769158 rs3130321 rs9469058 rs2535300 rs11751198
Genetic architecture reconciles linkage and association studies of complex traits
Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
12 pages+
rs16932761 rs2504674 rs6504165 rs11610621 rs11656076 rs17609347
Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction
Estonian Biobank Research Team · 23andMe Research Team
Nature genetics · 2026 · PMID 42009823 · open access
12 pages+
rs1729948 rs72773791 rs113329317 rs4674113 rs77541496 rs757747
GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression
Nature communications · 2021 · PMID 33608531 · open access
8 pages
rs35788599 rs10500661 rs34074411 rs9581957 rs200964 rs967823

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.