For researchers

Is your paper here?

2,663 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 Kim D, showing the first 20.

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
SpiroMeta Consortium · International COPD Genetics Consortium
Nature genetics · 2019 · PMID 30804561 · open access
12 pages+
rs62191105 rs10760580 rs629619 rs72626215 rs35584079 rs12466981
Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits
Scientific reports · 2022 · PMID 35121771 · open access
12 pages+
rs61754482 rs10420069 rs2991378 rs2221198 rs73185547 rs563964
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+
rs12669223 rs3768301 rs72830009 rs7100404 rs7076754 rs835576
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+
rs1919364 rs11108175 rs78341008 rs9983528 rs280097 rs7810512
Genome-wide association study and fine-mapping on Korean biobank to discover renal trait-associated variants
Kidney research and clinical practice · 2024 · PMID 37919891 · open access
12 pages+
rs6556316 rs4075959 rs12987055 rs11762900 rs11853157 rs1558259
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1475655 rs67269808 rs7304270 rs2658746 rs75417759 rs12746673
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Nature communications · 2024 · PMID 38658550 · open access
12 pages+
rs7897298 rs3131101 rs188819358 rs7864436 rs11681642 rs3850986
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
rs4418214 rs2523590 rs2255221 rs2395029 rs9262632 HIV-1 Viral Control
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
Gastroenterology · 2019 · PMID 30529582
6 pages
rs7542665 rs201395236 rs113569514 rs3830041 rs77969132 rs1886450
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
Nature genetics · 2013 · PMID 23583980 · open access
5 pages
rs1278769 rs2609255 rs11191865 rs1981997 Interstitial Lung Disease
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Nature genetics · 2009 · PMID 19396169
3 pages
rs6918981 rs13273123 Height
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits
MAGIC consortium
Nature genetics · 2011 · PMID 21909109
3 pages
rs2286276 rs7232775 rs11216126
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colorectal Transdisciplinary (CORECT) Study and 1 more consortia
Gastroenterology · 2016 · PMID 26965516
3 pages
rs2450115 rs4919687 rs6061231
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
Human molecular genetics · 2016 · PMID 27702942
3 pages
rs80227144 rs7005606 Hirschsprung Disease
Genome-wide association study of occupational attainment as a proxy for cognitive reserve
Brain : a journal of neurology · 2022 · PMID 34613391
3 pages
rs55769536 rs448809 rs3741368
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
HGG advances · 2022 · PMID 35399580 · open access
3 pages
rs3751813 rs6817771 rs9922708
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Nature genetics · 2023 · PMID 37337107
3 pages
rs2075836 rs57917667 rs75413466
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Psychiatry research · 2024 · PMID 38335777
3 pages
rs34427167 rs35800293 rs73079014
Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color
Nature communications · 2024 · PMID 38849341 · open access
3 pages
rs77310623 rs800884 rs33932559
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colorectal Transdisciplinary (CORECT) Study and 1 more consortia
Nature genetics · 2014 · PMID 24836286 · open access
2 pages
rs704017 rs1800469

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.