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.

18 matches for Han K.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs1983546 rs12930096 rs12444261 rs1052536 rs1396515 rs1805128
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs116353863 rs117079142 rs11884596 rs12708491 rs4901473 rs6469654
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
Lifestage Sex-Specific Genetic Effects on Metabolic Disorders in an Adult Population in Korea: The Korean Genome and Epidemiology Study
International journal of molecular sciences · 2022 · PMID 36233190 · open access
12 pages+
rs17410996 rs75326924 rs6467314 rs4821130 rs10422861 rs2494746
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+
rs2527927 rs704417 rs117042741 rs35564340 rs1919364 rs11108175
Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants
Nature communications · 2020 · PMID 32139696 · open access
10 pages
rs17268829 rs10760444 rs71559437 rs6964587 rs4496150 rs9833888
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Nature genetics · 2014 · PMID 25086665 · open access
5 pages
rs9581943 rs2736098 rs6971499 rs7190458 Pancreatic Cancer
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Nature communications · 2018 · PMID 29422604 · open access
4 pages
rs13303010 rs1517037 rs4795218 rs2941471
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1
DRIVE GAME-ON Consortium
Nature genetics · 2014 · PMID 25038754 · open access
3 pages
rs4951011 rs10474352 rs2290203
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
rs10094872 rs35226131 Pancreatic Cancer
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Human molecular genetics · 2010 · PMID 20460270
2 pages
rs17095355 Biliary Atresia
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
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval
Heart rhythm · 2012 · PMID 22342860
1 page
rs7219669
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer
PLoS genetics · 2012 · PMID 22383897 · open access
1 page
rs9485372
Genome-wide association study confirming association of HLA-DP with protection against chronic hepatitis B and viral clearance in Japanese and Korean
PloS one · 2012 · PMID 22737229 · open access
1 page
rs9277535
Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3
Nature genetics · 2012 · PMID 22863731
1 page
rs312691
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan · Korean Consortium of Hereditary Renal Diseases in Children and 2 more consortia
Kidney international · 2020 · PMID 32554042
1 page
rs2285450

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.