For researchers

Is your paper here?

2,661 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 Sidore C.

Discovery and refinement of loci associated with lipid levels
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
rs7248104 rs4883201 rs11603023 rs11136341 rs4253772 rs13315871
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
SpiroMeta Consortium · GoT2D Consortium and 3 more consortia
American journal of human genetics · 2017 · PMID 28552196 · open access
12 pages+
rs28376121 rs3116614 rs2061456 rs42377 rs1975474 rs28721484
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs56288844 rs149520992 rs6987444 rs2852151 rs9385532 rs12083537
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy
Nature genetics · 2020 · PMID 32929287
12 pages+
rs1836798 rs12206866 rs55871547 rs6509428 rs12199079 rs78358948
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs759831202 rs952170 rs11167778 rs1338668 rs749804194 rs9976784
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+
rs227756 rs2277886 rs2524074 rs2609334 rs3743369 rs507903
Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies
Genetic epidemiology · 2025 · PMID 39749473 · open access
7 pages
rs60888743 rs8013873 rs1048055 rs4804000 rs12130424 rs7545300
Genome-wide search for genes affecting the age at diagnosis of type 1 diabetes
FinnDiane Study Group
Journal of internal medicine · 2021 · PMID 33179336 · open access
5 pages
rs34941730 rs116763857 rs9501130 rs35122968 rs3997848
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels
Nature genetics · 2015 · PMID 26366553 · open access
2 pages
rs570013781 rs5030868
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
Nature genetics · 2010 · PMID 20453840
1 page
rs2040406
FTO genotype is associated with phenotypic variability of body mass index
Nature · 2012 · PMID 22982992
1 page
rs7202116
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course
GIANT Consortium
Human molecular genetics · 2013 · PMID 23669352
1 page
rs1561288
Overexpression of the Cytokine BAFF and Autoimmunity Risk
The New England journal of medicine · 2017 · PMID 28445677
1 page
rs12253981
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Nature communications · 2020 · PMID 32231244 · open access
1 page
rs17831251
Genetic risk factors for COVID-19 and influenza are largely distinct
Colorado Center for Precision Medicine · Mayo Clinic Project Generation and 2 more consortia
Nature genetics · 2024 · PMID 39103650 · open access
1 page
rs2837112

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.