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.

75 matches for Rich SS, showing the first 20.

Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
rs8102280 rs138534124 rs2238675
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
rs11863726 rs2562181 rs35837297
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
The European respiratory journal · 2024 · PMID 38097206 · open access
3 pages
rs1233604 rs11623779 rs9649071
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
rs150607032 rs190975828 rs192018195
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
PLoS genetics · 2011 · PMID 21829377 · open access
2 pages
rs2236212 rs174468
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
rs7764819 rs11654749
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium
Circulation. Cardiovascular genetics · 2013 · PMID 23362303
2 pages
rs860873 rs6675668
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis
Boston Children's JIA Registry · British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group and 7 more consortia
Nature genetics · 2013 · PMID 23603761 · open access
2 pages
rs10174238 rs72698115
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study
American journal of respiratory and critical care medicine · 2014 · PMID 24383474
2 pages
rs7698250 rs10411619
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans
COMPASS and METASTROKE Consortia
Stroke · 2015 · PMID 26089329
2 pages
rs4471613 rs9899375
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
2 pages
rs116843064 rs60839105
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Journal of medical genetics · 2016 · PMID 27587472
2 pages
rs247616 Cholesterol (LDL, HDL and Total)
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
COPDGene Investigators · ECLIPSE Investigators and 5 more consortia
Nature genetics · 2017 · PMID 28166215
2 pages
rs17035917 rs11727735
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Nature communications · 2018 · PMID 29343764 · open access
2 pages
rs10745742 Vitamin D Deficiency and the GC Gene
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
rs11257600 rs17737404
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
2 pages
rs73345162 rs73517714
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
Diabetologia · 2022 · PMID 34951656
2 pages
rs10887773 rs6975024
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
Communications biology · 2023 · PMID 37587153 · open access
2 pages
rs717894 rs57112407
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
PLoS genetics · 2011 · PMID 21347282 · open access
1 page
rs7801190
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
American journal of respiratory and critical care medicine · 2012 · PMID 22837378
1 page
rs8031948

Showing 20 of 75 · page 3 of 4

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.