For researchers

Is your paper here?

2,676 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.

44 matches for Kim B, showing the first 20.

Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals
Scientific reports · 2020 · PMID 32514006 · open access
10 pages
rs138158275 rs117897057 rs72930155 rs55817236 rs142439069 rs150772085
Genome-wide association study identifies novel susceptibilities to adult moyamoya disease
Journal of human genetics · 2023 · PMID 37365321
8 pages
rs117343774 rs7211327 rs2887022 rs41301888 rs7525578 rs3869145
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
rs1116357 rs1575972 rs9309245 rs67156297 rs7107784 rs78627331
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)
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 pages
rs11667918 rs1046875 rs3755157 Type 2 Diabetes
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Human molecular genetics · 2014 · PMID 24861553
4 pages
rs2535633 rs11030104 rs574367 rs591166
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures
Nature communications · 2016 · PMID 26733130 · open access
3 pages
rs577721086 rs71382995 rs115242848
Genome-wide association study of occupational attainment as a proxy for cognitive reserve
Brain : a journal of neurology · 2022 · PMID 34613391
3 pages
rs448809 rs3741368 rs55769536
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
rs73079014 rs34427167 rs35800293
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
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
Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women
Australian Ovarian Cancer Study Group
Gynecologic oncology · 2019 · PMID 30898391
2 pages
rs1934363 rs7748275
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
rs17737404 rs11257600
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Human molecular genetics · 2022 · PMID 34850884
2 pages
rs145720245 rs7911501
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
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
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

Showing 20 of 44 · page 2 of 3

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.