For researchers
Is your paper here?
2,665 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.
80 matches for
UK Biobank,
showing the first 20.
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti HS,
Daghlas I,
Lane JM,
Huang Y,
Udler MS,
Wang H,
Ollila HM,
Jones SE,
Kim J,
Wood AR,
Weedon MN,
Aslibekyan S
and 2 more — show all
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
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+
Genetically Determined Serum Calcium Levels and Markers of Ventricular Repolarization: A Mendelian Randomization Study in the UK Biobank
Young WJ,
Warren HR,
Mook-Kanamori DO,
Ramírez J,
van Duijvenboden S,
Orini M,
Tinker A,
van Heemst D,
Lambiase PD,
Jukema JW,
Munroe PB,
Noordam R
Circulation. Genomic and precision medicine · 2021 · PMID 33887147
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+
Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank
Xue Z,
Yuan J,
Chen F,
Yao Y,
Xing S,
Yu X,
Li K,
Wang C,
Bao J,
Qu J,
Su J,
Chen H
EBioMedicine · 2022 · PMID 35841873 · open access
12 pages+
GWAS on retinal vasculometry phenotypes
Jiang X,
Hysi PG,
Khawaja AP,
Mahroo OA,
Xu Z,
Hammond CJ,
Foster PJ,
Welikala RA,
Barman SA,
Whincup PH,
Rudnicka AR,
Owen CG
and 1 more — show all
UK Biobank Eye and Vision Consortium
PLoS genetics · 2023 · PMID 36757925 · open access
12 pages+
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Zhou W,
Kanai M,
Wu KH,
Rasheed H,
Tsuo K,
Hirbo JB,
Wang Y,
Bhattacharya A,
Zhao H,
Namba S,
Surakka I,
Wolford BN
and 140 more — show all
Lo Faro V,
Lopera-Maya EA,
Läll K,
Favé MJ,
Partanen JJ,
Chapman SB,
Karjalainen J,
Kurki M,
Maasha M,
Brumpton BM,
Chavan S,
Chen TT,
Daya M,
Ding Y,
Feng YA,
Guare LA,
Gignoux CR,
Graham SE,
Hornsby WE,
Ingold N,
Ismail SI,
Johnson R,
Laisk T,
Lin K,
Lv J,
Millwood IY,
Moreno-Grau S,
Nam K,
Palta P,
Pandit A,
Preuss MH,
Saad C,
Setia-Verma S,
Thorsteinsdottir U,
Uzunovic J,
Verma A,
Zawistowski M,
Zhong X,
Afifi N,
Al-Dabhani KM,
Al Thani A,
Bradford Y,
Campbell A,
Crooks K,
de Bock GH,
Damrauer SM,
Douville NJ,
Finer S,
Fritsche LG,
Fthenou E,
Gonzalez-Arroyo G,
Griffiths CJ,
Guo Y,
Hunt KA,
Ioannidis A,
Jansonius NM,
Konuma T,
Lee MTM,
Lopez-Pineda A,
Matsuda Y,
Marioni RE,
Moatamed B,
Nava-Aguilar MA,
Numakura K,
Patil S,
Rafaels N,
Richmond A,
Rojas-Muñoz A,
Shortt JA,
Straub P,
Tao R,
Vanderwerff B,
Vernekar M,
Veturi Y,
Barnes KC,
Boezen M,
Chen Z,
Chen CY,
Cho J,
Smith GD,
Finucane HK,
Franke L,
Gamazon ER,
Ganna A,
Gaunt TR,
Ge T,
Huang H,
Huffman J,
Katsanis N,
Koskela JT,
Lajonchere C,
Law MH,
Li L,
Lindgren CM,
Loos RJF,
MacGregor S,
Matsuda K,
Olsen CM,
Porteous DJ,
Shavit JA,
Snieder H,
Takano T,
Trembath RC,
Vonk JM,
Whiteman DC,
Wicks SJ,
Wijmenga C,
Wright J,
Zheng J,
Zhou X,
Awadalla P,
Boehnke M,
Bustamante CD,
Cox NJ,
Fatumo S,
Geschwind DH,
Hayward C,
Hveem K,
Kenny EE,
Lee S,
Lin YF,
Mbarek H,
Mägi R,
Martin HC,
Medland SE,
Okada Y,
Palotie AV,
Pasaniuc B,
Rader DJ,
Ritchie MD,
Sanna S,
Smoller JW,
Stefansson K,
van Heel DA,
Walters RG,
Zöllner S,
Martin AR,
Willer CJ,
Daly MJ,
Neale BM
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
Comprehensive genetic study of the insulin resistance marker TG:HDL-C in the UK Biobank
Oliveri A,
Rebernick RJ,
Kuppa A,
Pant A,
Chen Y,
Du X,
Cushing KC,
Bell HN,
Raut C,
Prabhu P,
Chen VL,
Halligan BD
and 1 more — show all
Nature genetics · 2024 · PMID 38200128
12 pages+
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences
Burren OS,
Dhindsa RS,
Deevi SVV,
Wen S,
Nag A,
Mitchell J,
Hu F,
Loesch DP,
Smith KR,
Razdan N,
Olsson H,
Platt A
and 12 more — show all
Vitsios D,
Wu Q,
Codd V,
Nelson CP,
Samani NJ,
March RE,
Wasilewski S,
Carss K,
Fabre M,
Wang Q,
Pangalos MN,
Petrovski S
AstraZeneca Genomics Initiative
Nature genetics · 2024 · PMID 39192095 · open access
12 pages+
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117)
Clarke TK,
Adams MJ,
Davies G,
Howard DM,
Hall LS,
Padmanabhan S,
Murray AD,
Smith BH,
Campbell A,
Hayward C,
Porteous DJ,
Deary IJ
and 1 more — show all
Molecular psychiatry · 2017 · PMID 28937693 · open access
11 pages
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.