For researchers

Is your paper here?

2,657 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.

16 matches for Hwang MY.

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+
rs6590816 rs6712094 rs2270860 rs1004467 rs4684242 rs4980389
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs60573766 rs186568031 rs117267808 rs4711389 rs75536691 rs7787720
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+
rs7856817 rs11626768 rs180705493 rs2811468 rs532566544 rs5752963
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+
rs79495865 rs7819706 rs1473781 rs6876198 rs3743140 rs3806155
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+
rs6139332 rs2014307 rs630839 rs6514424 rs6677770 rs505317
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+
rs150183244 rs16923500 rs1799872 rs144394643 rs116403919 rs870992
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs62015803 rs6766511 rs74847755 rs12140915 rs11063029 rs321234
Large-scale cross-ancestry genome-wide meta-analysis of serum urate
Nature communications · 2024 · PMID 38658550 · open access
12 pages+
rs62450856 rs7175469 rs35368205 rs2834321 rs2855818 rs288762
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs139120857 rs5942972 rs7063103 rs62603531 rs151113194 rs762517
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)
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
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
Shared genetic architectures of subjective well-being in East Asian and European ancestry populations
Nature human behaviour · 2022 · PMID 35589828
1 page
rs7189864

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.