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.

195 matches for Rotter JI, showing the first 20.

Multi-ethnic genome-wide association study for atrial fibrillation
Nature genetics · 2018 · PMID 29892015
12 pages+
rs10027347 rs10165883 rs1044258 rs10479177 rs10760361 rs10842383
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
Nature communications · 2018 · PMID 30046033 · open access
12 pages+
rs12678719 rs4430933 rs6599250 rs343849 rs255292 rs7538988
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Nature communications · 2018 · PMID 30061609 · open access
12 pages+
rs252746 rs143246821 rs916888 rs963406 rs79294353 rs111898810
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
rs2400509 rs7555285 rs76719272 rs72683923 rs34413141 rs1585453
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Nature genetics · 2018 · PMID 30297969
12 pages+
rs2431115 rs6780171 rs2642588 rs7918400 rs1796330 rs17836088
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
rs4445669 rs9298749 rs10957494 rs77819282 rs1045476 rs28502438
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+
rs12083537 rs67129560 rs4752829 rs12749227 rs4845623 rs9271608
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
rs10066990 rs10851885 rs11039221 rs111449836 rs12722725 rs13417750
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs114846969 rs6029549 rs556107 rs117753190 rs6489786 rs217358
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs75267082 rs62432759 rs1051447 rs948493 rs9397738 rs13157326
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs12790943 rs74375025 rs6998967 rs73065147 rs147215801 rs35692677
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs79321945 rs94111 rs1037100 rs179146 rs287606 rs3825751
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs60573766 rs186568031 rs117267808 rs4711389 rs75536691 rs7787720
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs5762879 rs62100531 rs62250976 rs62308111 rs6546232 rs7081113
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs576668364 rs59521405 rs6058638 rs6072078 rs6912255 rs6922558
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs767105335 rs77357563 rs2306899 rs2273171 rs4846567 rs117874826
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs17205972 rs7596872 rs55940034 rs2303655 rs55897749 rs72934583
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
rs1200108 rs6669560 rs116792882 rs12515400 rs840464 rs35523808

Showing 20 of 195 · page 2 of 10

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.