For researchers

Is your paper here?

2,682 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.

661 matches for Er J, showing the first 20.

Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · open access
12 pages+
rs7923245 rs1193232 rs12914773 rs34096939 rs7144274 rs7545279
Mapping the proteo-genomic convergence of human diseases
Science (New York, N.Y.) · 2021 · PMID 34648354
12 pages+
rs8192884 rs10269741 rs149895214 rs2300433 rs933093 rs12461354
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+
rs7856817 rs11626768 rs180705493 rs2811468 rs532566544 rs5752963
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs6538539 rs708228 rs17571951 rs61828917 rs815609 rs16940992
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
rs4980383 rs10995187 rs10087804 rs9397436 rs3819405 rs34066050
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs79495865 rs1871045 rs80102379 rs7819706 rs1473781 rs6876198
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
rs61734651 rs11881070 rs11152089 rs143796236 rs222835 rs11643684
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
23andMe Research Team
Nature genetics · 2022 · PMID 35835914
12 pages+
rs7802268 rs78154941 rs782219 rs918606 rs11173201 rs114391861
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
12 pages+
rs76992529 rs2453544 rs74934947 rs754490766 rs77271279 rs10785996
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs7927901 rs2088627 rs7976280 rs4372816 rs7806537 rs3183099
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
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+
rs2096884 rs7948776 rs8006022 rs8088446 rs8101705 rs8177375
Rare and common genetic determinants of metabolic individuality and their effects on human health
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
rs117327331 rs112281307 rs13258200 rs2640465 rs662962 rs6710692
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs10065698 rs1028212 rs1079558 rs10863958 rs2357475 rs10918790
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs2527927 rs704417 rs117042741 rs35564340 rs1919364 rs11108175
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs61208973 rs568849616 rs76181804 rs9290877 rs9594366 rs16856530
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs1873164 rs2762049 rs55824920 rs72798148 rs8019721 rs1724411
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature medicine · 2023 · PMID 37464041
12 pages+
rs34269011 rs2964003 rs4776729 rs1825119 rs12517438 rs1931388
Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry
Nature communications · 2023 · PMID 37669986 · open access
12 pages+
rs74979471 rs810066 rs367848985 rs114213467 rs3730403 rs74030616

Showing 20 of 661 · page 6 of 34

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.