For researchers

Is your paper here?

2,662 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.

174 matches for An K, showing the first 20.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs57737646 rs7315236 rs699465 rs10414501 rs77951490 rs78863347
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
rs11246003 rs7412010 rs149934734 rs35417544 rs62323682 rs4821939
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs2137897 rs2070464 rs112019128 rs6900627 rs4585546 rs3768419
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10180829 rs672769 rs10071837 rs4899520 rs75823898 rs112226333
Variants in urate transporters, ADH1B, GCKR and MEPE genes associate with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank
Annals of the rheumatic diseases · 2021 · PMID 33832965
12 pages+
rs28508560 rs28548845 rs72929103 rs75341455 rs114791459 rs114580333
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
rs9926128 rs535808923 rs61047863 rs189305788 rs781930992 rs968218067
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs2336147 rs10866641 rs67712855 rs748455 rs78308718 rs6875495
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
An Amish founder population reveals rare-population genetic determinants of the human lipidome
Communications biology · 2022 · PMID 35393526 · open access
12 pages+
rs190844068 rs533456288 rs181234756 rs184061227 rs59922153 rs184351458
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+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs12511815 rs4410938 rs8106249 rs1796765 rs113830231 rs112204156
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs4483592 rs1947066 rs144839021 rs1625595 rs197439 rs68049022
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+
rs12566345 rs1921907 rs210280 rs4696931 rs6727028 rs7070947
Lifestage Sex-Specific Genetic Effects on Metabolic Disorders in an Adult Population in Korea: The Korean Genome and Epidemiology Study
International journal of molecular sciences · 2022 · PMID 36233190 · open access
12 pages+
rs17410996 rs75326924 rs6467314 rs4821130 rs10422861 rs2494746
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+
rs7859362 rs4675253 rs6434979 rs4236382 rs10751097 rs10978941
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
rs8080583 rs35463555 rs11712309 rs186910 rs2478868 rs1123573
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs131246 rs4872527 rs10853047 rs1685635 rs2283368 rs572016
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups
GigaScience · 2024 · PMID 38626723 · open access
12 pages+
rs6692921 rs907054441 rs12554580 rs72618332 rs9818190 rs4446279
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs10865093 rs7431106 rs61946067 rs28986300 rs16948230 rs6801151
Variants in tubule epithelial regulatory elements mediate most heritable differences in human kidney function
Nature genetics · 2024 · PMID 39256582
12 pages+
rs6894631 rs34269854 rs3220814 rs236321 rs2471604 rs10512987

Showing 20 of 174 · page 2 of 9

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.