For researchers

Is your paper here?

2,665 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.

214 matches for Ng K, showing the first 20.

Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25
COLUMBUS Consortium
Nature communications · 2014 · PMID 25327703 · open access
1 page
rs140068132
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
Inflammatory bowel diseases · 2015 · PMID 25489960
1 page
rs224143
A genome-wide association study of body mass index across early life and childhood
International journal of epidemiology · 2015 · PMID 25953783 · open access
1 page
rs11676272
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
Human genetics · 2015 · PMID 25963972 · open access
1 page
rs6059655
Genome-wide interaction study of gene-by-occupational exposure and effects on FEV1 levels
The Journal of allergy and clinical immunology · 2015 · PMID 25979521
1 page
rs159497
Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans
Inflammatory bowel diseases · 2016 · PMID 26398853
1 page
rs76418789
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
1 page
rs1333037
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility
American journal of human genetics · 2016 · PMID 27132594
1 page
rs17293443
Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans
Gastroenterology · 2016 · PMID 27569725
1 page
rs3766920
Genome-wide association of trajectories of systolic blood pressure change
BMC proceedings · 2016 · PMID 27980656 · open access
1 page
rs17112252
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Age at Menarche
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
iPSYCH-SSI-Broad Group
Nature communications · 2017 · PMID 28537267 · open access
1 page
rs12700667
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and 4 more consortia
Diabetes · 2018 · PMID 29703844
1 page
rs9942471
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Genetic analyses of diverse populations improves discovery for complex traits
Nature · 2019 · PMID 31217584
1 page
Obesity and Body Weight
Bilirubin and risk of ischemic heart disease in Korea: a two-sample Mendelian randomization study
Epidemiology and health · 2019 · PMID 31319653 · open access
1 page
rs2119503
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response
South Africa Zulu Type 2 Diabetes Case-Control Study
Nature communications · 2019 · PMID 31324766 · open access
1 page
rs1465146591
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
rs17097556

Showing 20 of 214 · page 10 of 11

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.