For researchers

Is your paper here?

2,661 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.

32 matches for Kim BJ, showing the first 20.

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Human molecular genetics · 2015 · PMID 25429064
12 pages+
rs7184046 rs13072744 rs3755206 rs3771381 rs1865760 rs11970475
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
rs1544935 rs1870634 rs2891168 rs56131196 rs72689147 rs2487928
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
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+
rs58244401 rs6590816 rs6712094 rs2270860 rs1004467 rs4684242
Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population
Journal of clinical medicine · 2019 · PMID 30823506 · open access
12 pages+
rs78458145 rs116969723 rs118107419 rs6741819 rs727333 rs59626274
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs28599782 rs111246699 rs11205766 rs3735567 rs12403994 rs60054445
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
rs116785379 rs12120358 rs76107698 rs2039982 rs4143303 rs218174
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
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+
rs759831202 rs952170 rs11167778 rs1338668 rs749804194 rs9976784
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
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+
rs227756 rs2277886 rs2524074 rs2609334 rs3743369 rs507903
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+
rs742761 rs10165093 rs2926700 rs11216916 rs3858910 rs4992759
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs77813615 rs7022365 rs12655753 rs62137415 rs76485553 rs140400323
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Nature communications · 2024 · PMID 38658550 · open access
12 pages+
rs12364994 rs2236270 rs76227013 rs36163299 rs2770807 rs62585352
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 association study identifies novel susceptibilities to adult moyamoya disease
Journal of human genetics · 2023 · PMID 37365321
8 pages
rs3869145 rs79994440 rs74790219 rs117343774 rs7211327 rs2887022
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
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
rs78627331 rs1116357 rs1575972 rs9309245 rs67156297 rs7107784
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits
Scientific reports · 2019 · PMID 30718733 · open access
6 pages
rs77768175 rs2303790 rs66626994 rs151193009 rs2980888 Cholesterol (LDL, HDL and Total)

Showing 20 of 32 · 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.