For researchers

Is your paper here?

3,082 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.

209 matches for Rotter J, showing the first 20.

Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Nature genetics · 2022 · PMID 35697868
4 pages
rs501740 rs55834511 rs78529941 rs9856926
Genome-wide association study of blood pressure and hypertension
Nature genetics · 2009 · PMID 19430479
3 pages
rs2681472 rs2384550 Blood Pressure
Genome-wide association of lipid-lowering response to statins in combined study populations
PloS one · 2010 · PMID 20339536 · open access
3 pages
rs10091038 rs8014194 Cholesterol (LDL, HDL and Total)
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Nature genetics · 2012 · PMID 22544366
3 pages
rs10821415 rs10824026 rs7164883
Discovery and fine mapping of serum protein loci through transethnic meta-analysis
LifeLines Cohort Study
American journal of human genetics · 2012 · PMID 23022100
3 pages
rs204999 rs11078597 rs4561508
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia
CARDIoGRAM Consortium
Human molecular genetics · 2013 · PMID 23620142
3 pages
rs6503905 rs12940923 rs800292
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
rs1230666 rs10944479 Thyroid Autoimmunity (TPO Antibodies)
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
3 pages
rs12416687 rs16833934 rs4842666
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
rs12599112 rs11940694 Alcohol Consumption
Genetic Variants Associated with Circulating Parathyroid Hormone
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
rs4443100 rs35194449 rs4074995
Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at <i>ID2</i>
Heart (British Cardiac Society) · 2018 · PMID 29127183
3 pages
rs45567533 rs13105921 rs146974314
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
3 pages
rs11196033 rs2912063 rs844396
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
3 pages
rs492571 rs17788930 rs12310367
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
3 pages
rs17737404 rs2236033 rs11257600
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis
American journal of respiratory and critical care medicine · 2019 · PMID 31339356
3 pages
rs73199442 rs7739124 rs7744971
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
Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose
Diabetologia · 2021 · PMID 33842983
3 pages
rs17085593 rs12684488 rs72470563
Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project
Trans-Omics for Precision Medicine (TOPMed) Stroke Working Group, the NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Stroke · 2022 · PMID 34727735
3 pages
rs60380775 rs141857337 rs150022429
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
3 pages
rs830463 rs111490516 rs62033408
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

Showing 20 of 209 · page 7 of 11

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.