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.

39 matches for Kim YJ, showing the first 20.

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
rs6026748 rs11128722 rs6891344 rs6271 rs2493134 rs12940887
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human molecular genetics · 2017 · PMID 28334899
12 pages+
rs2188380 rs2144300 rs11984636 rs3786247 rs11208004 rs2244608
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Nature genetics · 2018 · PMID 30297969
12 pages+
rs7918400 rs1796330 rs17836088 rs1061810 rs4925109 rs11820019
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
rs11044991 rs8084192 rs3774427 rs751985 rs6590811 rs62501779
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs61342118 rs7656416 rs12907887 rs73085586 rs13086331 rs117737118
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+
rs146474788 rs17256082 rs12784552 rs142484519 rs118164457 rs7063597
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+
rs11207980 rs598253 rs57825321 rs12603290 rs186793936 rs9844432
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
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+
rs9344003 rs12974635 rs10519014 rs11691472 rs2679184 rs2854915
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+
rs12035737 rs61855849 rs4487569 rs35950463 rs12053049 rs7032795
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
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+
rs7973752 rs58539858 rs1983023 rs2008584 rs16982206 rs3826837
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
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs17791513 rs6813195 rs17106184 rs849135 rs2261181 rs9936385
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs17287293 rs11118555 rs13030174 rs826838 rs11578508 rs4140885
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs151113194 rs762517 rs12012576 rs139120857 rs5942972 rs7063103
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
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
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Nature communications · 2016 · PMID 26818947 · open access
6 pages
rs1116357 rs1575972 rs9309245 rs67156297 rs7107784 rs78627331

Showing 20 of 39 · 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.