For researchers

Is your paper here?

2,677 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.

215 matches for Ng K, showing the first 20.

A genome-wide association study of early menopause and the combined impact of identified variants
ReproGen Consortium
Human molecular genetics · 2013 · PMID 23307926 · open access
2 pages
rs1046089 Age at Menopause
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
PLoS genetics · 2013 · PMID 24204295 · open access
2 pages
rs17212223 rs7744020
A central role for GRB10 in regulation of islet function in man
PLoS genetics · 2014 · PMID 24699409 · open access
2 pages
rs12549902 rs11187144
Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians
Human molecular genetics · 2014 · PMID 25035420
2 pages
rs2483280 rs7433306
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
Nature communications · 2015 · PMID 26416764 · open access
2 pages
rs1351592 rs11031006
HLA-B*57:01 Confers Susceptibility to Pazopanib-Associated Liver Injury in Patients with Cancer
Clinical cancer research : an official journal of the American Association for Cancer Research · 2016 · PMID 26546620
2 pages
rs1800625 Pazopanib-Associated Liver Injury
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers
Alzheimer’s Disease Neuroimaging Initiative (ADNI) · Alzheimer Disease Genetic Consortium (ADGC)
Acta neuropathologica · 2017 · PMID 28247064
2 pages
rs769449 rs9527039
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Nature communications · 2017 · PMID 28425483 · open access
2 pages
rs9501251 Primary Biliary Cholangitis
Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry
PRACTICAL/ELLIPSE Consortium
Journal of the National Cancer Institute · 2017 · PMID 29117387 · open access
2 pages
rs75823044 rs78554043
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
rs11218708 Pemphigus Vulgaris
Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans
PLoS genetics · 2018 · PMID 30248107 · open access
2 pages
rs1866188 rs12651896
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
American journal of human genetics · 2019 · PMID 31178129
2 pages
rs11646213 rs145119400
Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants
Scientific reports · 2019 · PMID 31235810 · open access
2 pages
rs1006923 rs7331212
Genetic Landscape of the ACE2 Coronavirus Receptor
GenOMICC Consortium† · IMI-DIRECT Consortium†
Circulation · 2022 · PMID 35387486 · open access
2 pages
rs5992134 rs3094087
Identification of shared loci associated with both Crohn's disease and leprosy in East Asians
Human molecular genetics · 2022 · PMID 35512355
2 pages
rs10817678 rs9271011
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population
China pUlmonary Thromboembolism REgistry Study (CURES) investigators
BMC medicine · 2023 · PMID 37076872 · open access
2 pages
rs35801946 rs4843804
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature genetics · 2023 · PMID 37770635
2 pages
rs10899970 rs62555371
Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study
Investigative ophthalmology & visual science · 2024 · PMID 38767907 · open access
2 pages
rs2300163 rs3743680

Showing 20 of 215 · page 8 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.