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.

273 matches for Ng M, showing the first 20.

Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations
Gut · 2014 · PMID 23850713
3 pages
rs11235667 rs10947261 rs6856616
GWAS identifies four novel eosinophilic esophagitis loci
Nature communications · 2014 · PMID 25407941 · open access
3 pages
rs149864795 rs3815700 Eosinophilic Esophagitis
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate
Nature communications · 2015 · PMID 25775280
3 pages
rs2235371 rs13041247 Cleft Lip and Palate
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Gut · 2017 · PMID 26701879 · open access
3 pages
rs80142782 rs13361707 Non-Cardia Gastric Cancer
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Nature communications · 2016 · PMID 27005778 · open access
3 pages
rs74249229 rs73066442 rs2921604
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
Genetic signatures of high-altitude adaptation in Tibetans
Proceedings of the National Academy of Sciences of the United States of America · 2017 · PMID 28373541
3 pages
rs71673426 rs78720557 rs2584462
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
Nature genetics · 2017 · PMID 28892059
3 pages
rs4653767 rs143918452 rs9468199
Genetic variants of calcium and vitamin D metabolism in kidney stone disease
Nature communications · 2019 · PMID 31729369 · open access
3 pages
rs10917002 rs1170174 rs77648599
A prospective study of the associations among fine particulate matter, genetic variants, and the risk of colorectal cancer
Environment international · 2021 · PMID 33338681
3 pages
rs4971775 rs9313579 rs6950598
Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration-Brief Report
Arteriosclerosis, thrombosis, and vascular biology · 2021 · PMID 33730874
3 pages
rs1110572 rs77601270 rs141117870
Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants
BMC medicine · 2022 · PMID 35692035 · open access
3 pages
rs58983615 rs11239569 rs2269928
Expanded Clinical Pharmacogenetics Implementation Consortium Guideline for Medication Use in the Context of G6PD Genotype
Clinical pharmacology and therapeutics · 2023 · PMID 36049896
3 pages
rs1050828 rs1050829 G6PD Deficiency
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
rs2905432 rs2532363 rs7447717
The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay
Cell discovery · 2023 · PMID 37479695 · open access
3 pages
rs12718465 rs12081480 rs866262287
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Psychiatry research · 2024 · PMID 38335777
3 pages
rs35800293 rs73079014 rs34427167
Genome-wide association studies and Mendelian randomization analyses provide insights into the causes of early-onset colorectal cancer
Colorectal Transdisciplinary (CORECT) Study, the Colon Cancer Family Registry (CCFR), Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO)
Annals of oncology : official journal of the European Society for Medical Oncology · 2024 · PMID 38408508 · open access
3 pages
rs10808556 rs12427378 rs2427291
Genome-wide and phenome-wide studies provided insights into brain glymphatic system function and its clinical associations
Science advances · 2025 · PMID 39823331 · open access
3 pages
rs9961058 rs1845561 rs2435204

Showing 20 of 273 · page 8 of 14

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.