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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
Liyanage UE,
Law MH,
Han X,
An J,
Ong JS,
Gharahkhani P,
Gordon S,
Neale RE,
Olsen CM,
MacGregor S,
Whiteman DC
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
12 pages+
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Han X,
Qassim A,
An J,
Marshall H,
Zhou T,
Ong JS,
Hassall MM,
Hysi PG,
Foster PJ,
Khaw PT,
Mackey DA,
Gharahkhani P
and 4 more — show all
Human molecular genetics · 2019 · PMID 31809533
12 pages+
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Craig JE,
Han X,
Qassim A,
Hassall M,
Cooke Bailey JN,
Kinzy TG,
Khawaja AP,
An J,
Marshall H,
Gharahkhani P,
Igo RP Jr,
Graham SL
and 47 more — show all
Healey PR,
Ong JS,
Zhou T,
Siggs O,
Law MH,
Souzeau E,
Ridge B,
Hysi PG,
Burdon KP,
Mills RA,
Landers J,
Ruddle JB,
Agar A,
Galanopoulos A,
White AJR,
Willoughby CE,
Andrew NH,
Best S,
Vincent AL,
Goldberg I,
Radford-Smith G,
Martin NG,
Montgomery GW,
Vitart V,
Hoehn R,
Wojciechowski R,
Jonas JB,
Aung T,
Pasquale LR,
Cree AJ,
Sivaprasad S,
Vallabh NA,
Viswanathan AC,
Pasutto F,
Haines JL,
Klaver CCW,
van Duijn CM,
Casson RJ,
Foster PJ,
Khaw PT,
Hammond CJ,
Mackey DA,
Mitchell P,
Lotery AJ,
Wiggs JL,
Hewitt AW,
MacGregor S
NEIGHBORHOOD consortium · UK Biobank Eye and Vision Consortium
Nature genetics · 2020 · PMID 31959993
12 pages+
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Gharahkhani P,
Jorgenson E,
Hysi P,
Khawaja AP,
Pendergrass S,
Han X,
Ong JS,
Hewitt AW,
Segrè AV,
Rouhana JM,
Hamel AR,
Igo RP Jr
and 67 more — show all
Choquet H,
Qassim A,
Josyula NS,
Cooke Bailey JN,
Bonnemaijer PWM,
Iglesias A,
Siggs OM,
Young TL,
Vitart V,
Thiadens AAHJ,
Karjalainen J,
Uebe S,
Melles RB,
Nair KS,
Luben R,
Simcoe M,
Amersinghe N,
Cree AJ,
Hohn R,
Poplawski A,
Chen LJ,
Rong SS,
Aung T,
Vithana EN,
Tamiya G,
Shiga Y,
Yamamoto M,
Nakazawa T,
Currant H,
Birney E,
Wang X,
Auton A,
Lupton MK,
Martin NG,
Ashaye A,
Olawoye O,
Williams SE,
Akafo S,
Ramsay M,
Hashimoto K,
Kamatani Y,
Akiyama M,
Momozawa Y,
Foster PJ,
Khaw PT,
Morgan JE,
Strouthidis NG,
Kraft P,
Kang JH,
Pang CP,
Pasutto F,
Mitchell P,
Lotery AJ,
Palotie A,
van Duijn C,
Haines JL,
Hammond C,
Pasquale LR,
Klaver CCW,
Hauser M,
Khor CC,
Mackey DA,
Kubo M,
Cheng CY,
Craig JE,
MacGregor S,
Wiggs JL
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
Thorp JG,
Campos AI,
Grotzinger AD,
Gerring ZF,
An J,
Ong JS,
Wang W,
Shringarpure S,
Byrne EM,
MacGregor S,
Martin NG,
Medland SE
and 2 more — show all
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
12 pages+
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Currant H,
Hysi P,
Fitzgerald TW,
Gharahkhani P,
Bonnemaijer PWM,
Senabouth A,
Hewitt AW,
Atan D,
Aung T,
Charng J,
Choquet H,
Craig J
and 22 more — show all
Khaw PT,
Klaver CCW,
Kubo M,
Ong JS,
Pasquale LR,
Reisman CA,
Daniszewski M,
Powell JE,
Pébay A,
Simcoe MJ,
Thiadens AAHJ,
van Duijn CM,
Yazar S,
Jorgenson E,
MacGregor S,
Hammond CJ,
Mackey DA,
Wiggs JL,
Foster PJ,
Patel PJ,
Birney E,
Khawaja AP
UK Biobank Eye and Vision Consortium · International Glaucoma Genetics Consortium
PLoS genetics · 2021 · PMID 33979322 · open access
12 pages+
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
Han X,
Gharahkhani P,
Hamel AR,
Ong JS,
Rentería ME,
Mehta P,
Dong X,
Pasutto F,
Hammond C,
Young TL,
Hysi P,
Lotery AJ
and 18 more — show all
Jorgenson E,
Choquet H,
Hauser M,
Cooke Bailey JN,
Nakazawa T,
Akiyama M,
Shiga Y,
Fuller ZL,
Wang X,
Wang X,
Hewitt AW,
Craig JE,
Pasquale LR,
Mackey DA,
Wiggs JL,
Khawaja AP,
Segrè AV,
MacGregor S
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
MacGregor S,
Ong JS,
An J,
Han X,
Zhou T,
Siggs OM,
Law MH,
Souzeau E,
Sharma S,
Lynn DJ,
Beesley J,
Sheldrick B
and 20 more — show all
Mills RA,
Landers J,
Ruddle JB,
Graham SL,
Healey PR,
White AJR,
Casson RJ,
Best S,
Grigg JR,
Goldberg I,
Powell JE,
Whiteman DC,
Radford-Smith GL,
Martin NG,
Montgomery GW,
Burdon KP,
Mackey DA,
Gharahkhani P,
Craig JE,
Hewitt AW
Nature genetics · 2018 · PMID 30054594
10 pages
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
Ong JS,
An J,
Han X,
Law MH,
Nandakumar P,
Schumacher J,
Gockel I,
Bohmer A,
Jankowski J,
Palles C,
Olsen CM,
Neale RE
and 8 more — show all
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
7 pages
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
Liyanage UE,
MacGregor S,
Bishop DT,
Shi J,
An J,
Ong JS,
Han X,
Scolyer RA,
Martin NG,
Medland SE,
Byrne EM,
Green AC
and 14 more — show all
Saw RPM,
Thompson JF,
Stretch J,
Spillane A,
Jiang Y,
Tian C,
Gordon SG,
Duffy DL,
Olsen CM,
Whiteman DC,
Long GV,
Iles MM,
Landi MT,
Law MH
23andMe Research Team
The Journal of investigative dermatology · 2022 · PMID 34813871
5 pages
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
An J,
Gharahkhani P,
Law MH,
Ong JS,
Han X,
Olsen CM,
Neale RE,
Lai J,
Vaughan TL,
Gockel I,
Thieme R,
Böhmer AC
and 6 more — show all
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking
He W,
van der Most PJ,
Ong JS,
Hwang LD,
Wu Y,
Magnø MS,
Vehof J,
Krebs K,
Mauring L,
Õunap K,
Abner E,
Martin NG
and 12 more — show all
Plotnikov D,
Jiang C,
Melles RB,
Gharahkhani P,
Snieder H,
Palumaa T,
Kaljurand K,
Guggenheim JA,
Mackey DA,
Engle EC,
Choquet H,
MacGregor S
Lifelines Cohort Study
Nature communications · 2025 · PMID 40849414 · open access
4 pages
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
Schröder J,
Chegwidden L,
Maj C,
Gehlen J,
Speller J,
Böhmer AC,
Borisov O,
Hess T,
Kreuser N,
Venerito M,
Alakus H,
May A
and 56 more — show all
Gerges C,
Schmidt T,
Thieme R,
Heider D,
Hillmer AM,
Reingruber J,
Lyros O,
Dietrich A,
Hoffmeister A,
Mehdorn M,
Lordick F,
Stocker G,
Hohaus M,
Reim D,
Kandler J,
Müller M,
Ebigbo A,
Fuchs C,
Bruns CJ,
Hölscher AH,
Lang H,
Grimminger PP,
Dakkak D,
Vashist Y,
May S,
Görg S,
Franke A,
Ellinghaus D,
Galavotti S,
Veits L,
Weismüller J,
Dommermuth J,
Benner U,
Rösch T,
Messmann H,
Schumacher B,
Neuhaus H,
Schmidt C,
Wissinowski TT,
Nöthen MM,
Dong J,
Ong JS,
Buas MF,
Thrift AP,
Vaughan TL,
Tomlinson I,
Whiteman DC,
Fitzgerald RC,
Jankowski J,
Vieth M,
Mayr A,
Gharahkhani P,
MacGregor S,
Gockel I,
Palles C,
Schumacher J
Wellcome Trust Case Control Consortium 2 (WTCCC2) · Esophageal Adenocarcinoma Genetics Consortium (EAGLE) and 1 more consortia
Gut · 2023 · PMID 35882562
2 pages
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia
Pasman JA,
Verweij KJH,
Gerring Z,
Stringer S,
Sanchez-Roige S,
Treur JL,
Abdellaoui A,
Nivard MG,
Baselmans BML,
Ong JS,
Ip HF,
van der Zee MD
and 36 more — show all
Bartels M,
Day FR,
Fontanillas P,
Elson SL,
de Wit H,
Davis LK,
MacKillop J,
Derringer JL,
Branje SJT,
Hartman CA,
Heath AC,
van Lier PAC,
Madden PAF,
Mägi R,
Meeus W,
Montgomery GW,
Oldehinkel AJ,
Pausova Z,
Ramos-Quiroga JA,
Paus T,
Ribases M,
Kaprio J,
Boks MPM,
Bell JT,
Spector TD,
Gelernter J,
Boomsma DI,
Martin NG,
MacGregor S,
Perry JRB,
Palmer AA,
Posthuma D,
Munafò MR,
Gillespie NA,
Derks EM,
Vink JM
23andMe Research Team · Substance Use Disorders Working Group of the Psychiatric Genomics Consortium and 1 more consortia
Nature neuroscience · 2018 · PMID 30150663
1 page
Exploring the Germline Genetics of In Situ and Invasive Cutaneous Melanoma: A Genome-Wide Association Study Meta-Analysis
Ingold N,
Seviiri M,
Ong JS,
Neale RE,
Pandeya N,
Whiteman DC,
Olsen CM,
Martin NG,
Duffy DL,
Khosrotehrani K,
Hayward N,
Montgomery GW
and 2 more — show all
JAMA dermatology · 2024 · PMID 39141363
1 page
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.