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.

30 matches for Aits I, showing the first 20.

Genome-wide association study of hematological and biochemical traits in a Japanese population
Nature genetics · 2010 · PMID 20139978
12 pages+
rs7775698 rs2236496 rs2858942 rs2279434 rs11966072 rs11204538
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence
Molecular psychiatry · 2019 · PMID 29326435 · open access
12 pages+
rs55692411 rs2878628 rs2647261 rs26949 rs2074613 rs116418977
A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans
Frontiers in genetics · 2021 · PMID 34054925 · open access
12 pages+
rs138997002 rs6913361 rs79658451 rs2780215 rs148899910 rs1211163
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
rs76676074 rs9659479 rs2768762 rs11240092 rs28873209 rs11264765
Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia
American journal of human genetics · 2021 · PMID 34469753
12 pages+
rs6020427 rs9526636 rs2834736 rs214053 rs2250127 rs34762068
The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians
Nature communications · 2022 · PMID 36333282 · open access
12 pages+
rs150183244 rs16923500 rs1799872 rs144394643 rs116403919 rs870992
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
rs1275923 rs371071053 rs74315329 rs6762719 rs115378818 rs3015326
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Nature genetics · 2026 · PMID 41565855
12 pages+
rs924150 rs8089099 rs4791806 rs41522747 rs340121 rs2609260
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117)
Molecular psychiatry · 2017 · PMID 28937693 · open access
11 pages
rs145452708 rs28712821 rs29001570 rs140089781 rs9841829 rs114026228
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
KidneyGen Consortium · CKDGen Consortium and 1 more consortia
Nature genetics · 2012 · PMID 22797727
6 pages
rs17730281 rs11868441 rs10767873 rs2074356 rs17730436 rs11864909
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children
Human molecular genetics · 2013 · PMID 23263863
4 pages
rs2340727 rs4657616 rs7203560 rs5987027
Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits
Nature genetics · 2017 · PMID 27992416
4 pages
rs73536079 rs142261172 rs5922858 Insomnia
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
PLoS genetics · 2017 · PMID 28453575 · open access
4 pages
rs145546625 rs1349471 rs148323035 rs113342804
Multivariate genome-wide analysis of aging-related traits identifies novel loci and new drug targets for healthy aging
Nature aging · 2023 · PMID 37550455 · open access
4 pages
rs16843603 rs12705966 rs13141210 rs28455998
A genome-wide association study of metabolic traits in human urine
Nature genetics · 2011 · PMID 21572414
3 pages
rs8101881 rs17279437 Urinary Metabolites
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
BioBank Japan Project · CHARGE Consortium
Human molecular genetics · 2013 · PMID 23446634
3 pages
rs762516 rs13008603 rs13339636
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
rs138534124 rs2238675 rs8102280
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Nature genetics · 2009 · PMID 19060910
2 pages
rs3764261 rs2650000
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
rs17428471 rs17080102
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788

Showing 20 of 30 · page 1 of 2

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.