For researchers

Is your paper here?

2,685 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.

216 matches for Ng K, showing the first 20.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs4140885 rs180242 rs17796783 rs17287293 rs11118555 rs13030174
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
8 pages
rs12012576 rs6527977 rs139120857 rs5942972 rs7063103 rs62603531
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
rs1864163 rs920915 rs8135665 rs8017304 rs9542236 rs13081855
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
The Lancet. Respiratory medicine · 2019 · PMID 30552067 · open access
7 pages
rs144829310 rs11603634 rs1986009 rs10519068 rs7305461 rs703816
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
rs9411377 rs6083037 rs10747514 rs7051718 rs16867574 rs57328376
Genetic predictors of participation in optional components of UK Biobank
Nature communications · 2021 · PMID 33563987 · open access
7 pages
rs12189679 rs2622102 rs11134465 rs1565440 rs1261078 rs2049604
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Stroke · 2018 · PMID 29273593
6 pages
rs9614159 rs74388387 rs9907978 rs10782008 rs117353193 Moyamoya Disease
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Nature communications · 2018 · PMID 29374233 · open access
6 pages
rs2736099 rs143093668 rs6915893 rs78781855 rs1005277 Telomere Length and Epigenetic Age Acceleration
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
Gastroenterology · 2019 · PMID 30529582
6 pages
rs7542665 rs201395236 rs113569514 rs3830041 rs77969132 rs1886450
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
rs10808546 rs35254673 rs4401144 rs118039278 rs73149487 Abdominal Aortic Aneurysm
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
rs1799884 rs1046896 rs6474359 rs7998202 Type 2 Diabetes
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
American journal of human genetics · 2013 · PMID 23273568
5 pages
rs6705628 rs4852324 rs6804441 rs34330 rs729302
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Novel genetic loci affecting facial shape variation in humans
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
rs8077906 rs12504954 rs79732694 rs56049331 rs34032897
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
KORA-Study Group · Nantes Referral Center for inherited cardiac arrhythmia
Nature genetics · 2022 · PMID 35210625
5 pages
rs11645463 rs7433206 rs34760424 rs41310232 Brugada Syndrome
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
VA Million Veteran Program
PLoS genetics · 2022 · PMID 35653334 · open access
5 pages
rs3812813 rs12143563 rs139405583 rs2197973 rs1840086
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs76110445 rs12415501 rs60401382 rs72934589 Cardioembolic Stroke
Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease
NIDDK Inflammatory Bowel Disease Genetics Consortium · International Inflammatory Bowel Disease Genetics Consortium
Inflammatory bowel diseases · 2023 · PMID 37262302
5 pages
rs1265061 rs2395158 rs361525 rs7171171 rs11754821

Showing 20 of 216 · page 5 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.