For researchers

Is your paper here?

2,649 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.

20 matches for Ong JS.

Combined analysis of keratinocyte cancers identifies novel genome-wide loci
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
12 pages+
rs638907 rs2776348 rs144984465 rs11707807 rs138501911 rs6714430
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Human molecular genetics · 2019 · PMID 31809533
12 pages+
rs2092524 rs6999835 rs10862708 rs77587000 rs4839470 rs73173591
Using Mendelian randomization to evaluate the causal relationship between serum C-reactive protein levels and age-related macular degeneration
European journal of epidemiology · 2020 · PMID 31900758
12 pages+
rs28399607 rs146342974 rs9366639 rs77120325 rs16835819 rs56189574
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
NEIGHBORHOOD consortium · UK Biobank Eye and Vision Consortium
Nature genetics · 2020 · PMID 31959993
12 pages+
rs756481 rs984586 rs2188836 rs62172701 rs73153655 rs62038917
Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study
JAMA ophthalmology · 2020 · PMID 32352494
12 pages+
rs4145443 rs9911460 rs35638197 rs1367023 rs3007364 rs1896539
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs1412829 rs61870251 rs34175429 rs938604 rs1893261 rs62521288
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
12 pages+
rs10164055 rs9317758 rs609958 rs17708090 rs10821130 rs1554269
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
UK Biobank Eye and Vision Consortium · International Glaucoma Genetics Consortium
PLoS genetics · 2021 · PMID 33979322 · open access
12 pages+
rs62252355 rs2008905 rs73348111 rs13215351 rs79833181 rs2787394
Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging
International Glaucoma Genetics Consortium
JAMA ophthalmology · 2022 · PMID 35446358
12 pages+
rs2645775 rs7327928 rs10780724 rs11786528 rs4656745 rs80215053
A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma
23andMe Research Team
Nature communications · 2022 · PMID 36496446 · open access
12 pages+
rs9878566 rs251465 rs10830255 rs6989943 rs502803 rs2849695
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
rs1658436 rs4414666 rs17254069 rs280875 rs2218471 rs13090630
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Nature genetics · 2018 · PMID 30054594
10 pages
rs12699251 rs10505100 rs61861119 rs73174345 rs11710139 rs9284802
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
7 pages
rs10982622 rs2145318 rs2597301 rs1431196 rs2106353 rs9372625
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
23andMe Research Team
The Journal of investigative dermatology · 2022 · PMID 34813871
5 pages
rs7943603 rs1888621 rs112761681 rs9322309 rs6737159
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
rs7282609 rs10940767 rs4676893 Gastroesophageal Reflux Disease
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking
Lifelines Cohort Study
Nature communications · 2025 · PMID 40849414 · open access
4 pages
rs3778977 rs4908704 rs8070929 Exotropia
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level
Wellcome Trust Case Control Consortium 2 (WTCCC2) · Esophageal Adenocarcinoma Genetics Consortium (EAGLE) and 1 more consortia
Gut · 2023 · PMID 35882562
2 pages
rs72760500 rs2687197
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia
23andMe Research Team · Substance Use Disorders Working Group of the Psychiatric Genomics Consortium and 1 more consortia
Nature neuroscience · 2018 · PMID 30150663
1 page
rs17761723
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9
Psychological medicine · 2020 · PMID 31530331
1 page
rs62158169
Exploring the Germline Genetics of In Situ and Invasive Cutaneous Melanoma: A Genome-Wide Association Study Meta-Analysis
JAMA dermatology · 2024 · PMID 39141363
1 page
rs958219

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.