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Is your paper here?
2,657 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.
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Warren HR,
Evangelou E,
Cabrera CP,
Gao H,
Ren M,
Mifsud B,
Ntalla I,
Surendran P,
Liu C,
Cook JP,
Kraja AT,
Drenos F
and 47 more — show all
Loh M,
Verweij N,
Marten J,
Karaman I,
Lepe MP,
O'Reilly PF,
Knight J,
Snieder H,
Kato N,
He J,
Tai ES,
Said MA,
Porteous D,
Alver M,
Poulter N,
Farrall M,
Gansevoort RT,
Padmanabhan S,
Mägi R,
Stanton A,
Connell J,
Bakker SJ,
Metspalu A,
Shields DC,
Thom S,
Brown M,
Sever P,
Esko T,
Hayward C,
van der Harst P,
Saleheen D,
Chowdhury R,
Chambers JC,
Chasman DI,
Chakravarti A,
Newton-Cheh C,
Lindgren CM,
Levy D,
Kooner JS,
Keavney B,
Tomaszewski M,
Samani NJ,
Howson JM,
Tobin MD,
Munroe PB,
Ehret GB,
Wain LV
International Consortium of Blood Pressure (ICBP) 1000G Analyses · BIOS Consortium and 9 more consortia
Nature genetics · 2017 · PMID 28135244 · open access
12 pages+
Association analyses based on false discovery rate implicate new loci for coronary artery disease
Nelson CP,
Goel A,
Butterworth AS,
Kanoni S,
Webb TR,
Marouli E,
Zeng L,
Ntalla I,
Lai FY,
Hopewell JC,
Giannakopoulou O,
Jiang T
and 50 more — show all
Hamby SE,
Di Angelantonio E,
Assimes TL,
Bottinger EP,
Chambers JC,
Clarke R,
Palmer CNA,
Cubbon RM,
Ellinor P,
Ermel R,
Evangelou E,
Franks PW,
Grace C,
Gu D,
Hingorani AD,
Howson JMM,
Ingelsson E,
Kastrati A,
Kessler T,
Kyriakou T,
Lehtimäki T,
Lu X,
Lu Y,
März W,
McPherson R,
Metspalu A,
Pujades-Rodriguez M,
Ruusalepp A,
Schadt EE,
Schmidt AF,
Sweeting MJ,
Zalloua PA,
AlGhalayini K,
Keavney BD,
Kooner JS,
Loos RJF,
Patel RS,
Rutter MK,
Tomaszewski M,
Tzoulaki I,
Zeggini E,
Erdmann J,
Dedoussis G,
Björkegren JLM,
Schunkert H,
Farrall M,
Danesh J,
Samani NJ,
Watkins H,
Deloukas P
EPIC-CVD Consortium · CARDIoGRAMplusC4D and 1 more consortia
Nature genetics · 2017 · PMID 28714975
12 pages+
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Howard DM,
Adams MJ,
Shirali M,
Clarke TK,
Marioni RE,
Davies G,
Coleman JRI,
Alloza C,
Shen X,
Barbu MC,
Wigmore EM,
Gibson J
and 9 more — show all
23andMe Research Team
Nature communications · 2018 · PMID 29662059 · open access
12 pages+
Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Khawaja AP,
Cooke Bailey JN,
Wareham NJ,
Scott RA,
Simcoe M,
Igo RP Jr,
Song YE,
Wojciechowski R,
Cheng CY,
Khaw PT,
Pasquale LR,
Haines JL
and 4 more — show all
UK Biobank Eye and Vision Consortium · NEIGHBORHOOD Consortium
Nature genetics · 2018 · PMID 29785010 · open access
12 pages+
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
and 86 more — show all
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
Sim XL,
Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Jansen IE,
Savage JE,
Watanabe K,
Bryois J,
Williams DM,
Steinberg S,
Sealock J,
Karlsson IK,
Hägg S,
Athanasiu L,
Voyle N,
Proitsi P
and 41 more — show all
Witoelar A,
Stringer S,
Aarsland D,
Almdahl IS,
Andersen F,
Bergh S,
Bettella F,
Bjornsson S,
Brækhus A,
Bråthen G,
de Leeuw C,
Desikan RS,
Djurovic S,
Dumitrescu L,
Fladby T,
Hohman TJ,
Jonsson PV,
Kiddle SJ,
Rongve A,
Saltvedt I,
Sando SB,
Selbæk G,
Shoai M,
Skene NG,
Snaedal J,
Stordal E,
Ulstein ID,
Wang Y,
White LR,
Hardy J,
Hjerling-Leffler J,
Sullivan PF,
van der Flier WM,
Dobson R,
Davis LK,
Stefansson H,
Stefansson K,
Pedersen NL,
Ripke S,
Andreassen OA,
Posthuma D
Nature genetics · 2019 · PMID 30617256
12 pages+
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data
Tachmazidou I,
Hatzikotoulas K,
Southam L,
Esparza-Gordillo J,
Haberland V,
Zheng J,
Johnson T,
Koprulu M,
Zengini E,
Steinberg J,
Wilkinson JM,
Bhatnagar S
and 9 more — show all
arcOGEN Consortium
Nature genetics · 2019 · PMID 30664745 · open access
12 pages+
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters
Bonnemaijer PWM,
Leeuwen EMV,
Iglesias AI,
Gharahkhani P,
Vitart V,
Khawaja AP,
Simcoe M,
Höhn R,
Cree AJ,
Igo RP,
Gerhold-Ay A,
Nickels S
and 16 more — show all
Wilson JF,
Hayward C,
Boutin TS,
Polašek O,
Aung T,
Khor CC,
Amin N,
Lotery AJ,
Wiggs JL,
Cheng CY,
Hysi PG,
Hammond CJ,
Thiadens AAHJ,
MacGregor S,
Klaver CCW,
Duijn CMV
International Glaucoma Genetics Consortium · NEIGHBORHOOD consortium and 1 more consortia
Communications biology · 2019 · PMID 31798171 · open access
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 association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Fan Q,
Pozarickij A,
Tan NYQ,
Guo X,
Verhoeven VJM,
Vitart V,
Guggenheim JA,
Miyake M,
Tideman JWL,
Khawaja AP,
Zhang L,
MacGregor S
and 46 more — show all
Höhn R,
Chen P,
Biino G,
Wedenoja J,
Saffari SE,
Tedja MS,
Xie J,
Lanca C,
Wang YX,
Sahebjada S,
Mazur J,
Mirshahi A,
Martin NG,
Yazar S,
Pennell CE,
Yap M,
Haarman AEG,
Enthoven CA,
Polling J,
Hewitt AW,
Jaddoe VWV,
van Duijn CM,
Hayward C,
Polasek O,
Tai ES,
Yoshikatsu H,
Hysi PG,
Young TL,
Tsujikawa A,
Wang JJ,
Mitchell P,
Pfeiffer N,
Pärssinen O,
Foster PJ,
Fossarello M,
Yip SP,
Williams C,
Hammond CJ,
Jonas JB,
He M,
Mackey DA,
Wong TY,
Klaver CCW,
Saw SM,
Baird PN,
Cheng CY
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · open access
12 pages+
Genetics of 35 blood and urine biomarkers in the UK Biobank
Sinnott-Armstrong N,
Tanigawa Y,
Amar D,
Mars N,
Benner C,
Aguirre M,
Venkataraman GR,
Wainberg M,
Ollila HM,
Kiiskinen T,
Havulinna AS,
Pirruccello JP
and 11 more — show all
Qian J,
Shcherbina A,
Rodriguez F,
Assimes TL,
Agarwala V,
Tibshirani R,
Hastie T,
Ripatti S,
Pritchard JK,
Daly MJ,
Rivas MA
FinnGen
Nature genetics · 2021 · PMID 33462484 · open access
12 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.