For researchers

Is your paper here?

2,665 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.

82 matches for M Y, showing the first 20.

Genetic association study identifies genetic variants for non-alcoholic fatty liver without comorbidities in the Korean population
Genes & genomics · 2023 · PMID 37133724
2 pages
rs7996045 Nonalcoholic Fatty Liver Disease (NAFLD)
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes
Nature communications · 2023 · PMID 37696869 · open access
2 pages
rs4769312 rs6121609
Identification of new genetic risk variants for type 2 diabetes
PLoS genetics · 2010 · PMID 20862305 · open access
1 page
rs10906115
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
rs9470794
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
Breast cancer research : BCR · 2012 · PMID 22452962 · open access
1 page
rs13393577
Genome-wide meta-analyses of smoking behaviors in African Americans
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
rs2036527
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
Nature genetics · 2012 · PMID 23160099
1 page
rs10262453
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Proceedings of the National Academy of Sciences of the United States of America · 2013 · PMID 23267103
1 page
rs8176704
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population
Journal of human genetics · 2013 · PMID 23575436
1 page
rs11066453
Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations
Genomics & informatics · 2013 · PMID 24124408 · open access
1 page
rs6736587
Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions
BMC medical genetics · 2014 · PMID 24903457 · open access
1 page
rs13390641
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
Inflammatory bowel diseases · 2015 · PMID 25489960
1 page
rs224143
Association of common variants in the calcium-sensing receptor gene with serum calcium levels in East Asians
Journal of human genetics · 2015 · PMID 25972035
1 page
rs13068893
Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population
Bone · 2016 · PMID 26686025
1 page
rs2446422
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans
Gastroenterology · 2016 · PMID 27569725
1 page
rs3766920
Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians
Scientific reports · 2018 · PMID 29572449 · open access
1 page
rs75444904
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
1 page
rs492571
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
1 page
rs9821797

Showing 20 of 82 · page 4 of 5

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.