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2,651 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.
9 matches for
Jones A.
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci
Jones AV,
Tilley M,
Gutteridge A,
Hyde C,
Nagle M,
Ziemek D,
Gorman D,
Fauman EB,
Chen X,
Miller MR,
Tian C,
Hu Y
and 3 more — show all
Human molecular genetics · 2017 · PMID 28199695 · open access
12 pages+
Identification of nine new susceptibility loci for endometrial cancer
O'Mara TA,
Glubb DM,
Amant F,
Annibali D,
Ashton K,
Attia J,
Auer PL,
Beckmann MW,
Black A,
Bolla MK,
Brauch H,
Brenner H
and 114 more — show all
Brinton L,
Buchanan DD,
Burwinkel B,
Chang-Claude J,
Chanock SJ,
Chen C,
Chen MM,
Cheng THT,
Clarke CL,
Clendenning M,
Cook LS,
Couch FJ,
Cox A,
Crous-Bous M,
Czene K,
Day F,
Dennis J,
Depreeuw J,
Doherty JA,
Dörk T,
Dowdy SC,
Dürst M,
Ekici AB,
Fasching PA,
Fridley BL,
Friedenreich CM,
Fritschi L,
Fung J,
García-Closas M,
Gaudet MM,
Giles GG,
Goode EL,
Gorman M,
Haiman CA,
Hall P,
Hankison SE,
Healey CS,
Hein A,
Hillemanns P,
Hodgson S,
Hoivik EA,
Holliday EG,
Hopper JL,
Hunter DJ,
Jones A,
Krakstad C,
Kristensen VN,
Lambrechts D,
Marchand LL,
Liang X,
Lindblom A,
Lissowska J,
Long J,
Lu L,
Magliocco AM,
Martin L,
McEvoy M,
Meindl A,
Michailidou K,
Milne RL,
Mints M,
Montgomery GW,
Nassir R,
Olsson H,
Orlow I,
Otton G,
Palles C,
Perry JRB,
Peto J,
Pooler L,
Prescott J,
Proietto T,
Rebbeck TR,
Risch HA,
Rogers PAW,
Rübner M,
Runnebaum I,
Sacerdote C,
Sarto GE,
Schumacher F,
Scott RJ,
Setiawan VW,
Shah M,
Sheng X,
Shu XO,
Southey MC,
Swerdlow AJ,
Tham E,
Trovik J,
Turman C,
Tyrer JP,
Vachon C,
VanDen Berg D,
Vanderstichele A,
Wang Z,
Webb PM,
Wentzensen N,
Werner HMJ,
Winham SJ,
Wolk A,
Xia L,
Xiang YB,
Yang HP,
Yu H,
Zheng W,
Zheng W,
Pharoah PDP,
Dunning AM,
Kraft P,
De Vivo I,
Tomlinson I,
Easton DF,
Spurdle AB,
Thompson DJ
Nature communications · 2018 · PMID 30093612 · open access
6 pages
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Hughes O,
Bentley AR,
Breeze CE,
Aguet F,
Xu X,
Nadkarni G,
Sun Q,
Lin BM,
Gilliland T,
Meyer MC,
Du J,
Raffield LM
and 62 more — show all
Kramer H,
Morton RW,
Gouveia MH,
Atkinson EG,
Valladares-Salgado A,
Wacher-Rodarte N,
Dueker ND,
Guo X,
Hai Y,
Adeyemo A,
Best LG,
Cai J,
Chen G,
Chong M,
Doumatey A,
Eales J,
Goodarzi MO,
Ipp E,
Irvin MR,
Jiang M,
Jones AC,
Kooperberg C,
Krieger JE,
Lange EM,
Lanktree MB,
Lash JP,
Lotufo PA,
Loos RJF,
Ha My VT,
Peralta-Romero J,
Qi L,
Raffel LJ,
Rich SS,
Rodriquez EJ,
Tarazona-Santos E,
Taylor KD,
Umans JG,
Wen J,
Young BA,
Yu Z,
Zhang Y,
Ida Chen YD,
Rundek T,
Rotter JI,
Cruz M,
Fornage M,
Lima-Costa MF,
Pereira AC,
Paré G,
Natarajan P,
Cole SA,
Carson AP,
Lange LA,
Li Y,
Perez-Stable EJ,
Do R,
Charchar FJ,
Tomaszewski M,
Mychaleckyj JC,
Rotimi C,
Morris AP,
Franceschini N
Cell genomics · 2024 · PMID 38190104 · open access
5 pages
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Houlston RS,
Cheadle J,
Dobbins SE,
Tenesa A,
Jones AM,
Howarth K,
Spain SL,
Broderick P,
Domingo E,
Farrington S,
Prendergast JG,
Pittman AM
and 33 more — show all
Theodoratou E,
Smith CG,
Olver B,
Walther A,
Barnetson RA,
Churchman M,
Jaeger EE,
Penegar S,
Barclay E,
Martin L,
Gorman M,
Mager R,
Johnstone E,
Midgley R,
Niittymäki I,
Tuupanen S,
Colley J,
Idziaszczyk S,
Thomas HJ,
Lucassen AM,
Evans DG,
Maher ER,
Maughan T,
Dimas A,
Dermitzakis E,
Cazier JB,
Aaltonen LA,
Pharoah P,
Kerr DJ,
Carvajal-Carmona LG,
Campbell H,
Dunlop MG,
Tomlinson IP
COGENT Consortium · CORGI Consortium and 2 more consortia
Nature genetics · 2010 · PMID 20972440 · open access
4 pages
Multiple newly identified loci associated with prostate cancer susceptibility
Eeles RA,
Kote-Jarai Z,
Giles GG,
Olama AA,
Guy M,
Jugurnauth SK,
Mulholland S,
Leongamornlert DA,
Edwards SM,
Morrison J,
Field HI,
Southey MC
and 34 more — show all
Severi G,
Donovan JL,
Hamdy FC,
Dearnaley DP,
Muir KR,
Smith C,
Bagnato M,
Ardern-Jones AT,
Hall AL,
O'Brien LT,
Gehr-Swain BN,
Wilkinson RA,
Cox A,
Lewis S,
Brown PM,
Jhavar SG,
Tymrakiewicz M,
Lophatananon A,
Bryant SL,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Woodhouse CJ,
Thompson A,
Christmas T,
Ogden C,
Fisher C,
Jamieson C,
Cooper CS,
English DR,
Hopper JL,
Neal DE,
Easton DF
UK Genetic Prostate Cancer Study Collaborators · British Association of Urological Surgeons' Section of Oncology and 1 more consortia
Nature genetics · 2008 · PMID 18264097
3 pages
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Painter JN,
O'Mara TA,
Morris AP,
Cheng THT,
Gorman M,
Martin L,
Hodson S,
Jones A,
Martin NG,
Gordon S,
Henders AK,
Attia J
and 65 more — show all
McEvoy M,
Holliday EG,
Scott RJ,
Webb PM,
Fasching PA,
Beckmann MW,
Ekici AB,
Hein A,
Rübner M,
Hall P,
Czene K,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Lambrechts D,
Lambrechts D,
Amant F,
Annibali D,
Depreeuw J,
Vanderstichele A,
Goode EL,
Cunningham JM,
Dowdy SC,
Winham SJ,
Trovik J,
Hoivik E,
Werner HMJ,
Krakstad C,
Ashton K,
Otton G,
Proietto T,
Tham E,
Mints M,
Ahmed S,
Healey CS,
Shah M,
Pharoah PDP,
Dunning AM,
Dennis J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Zondervan KT,
Nyholt DR,
MacGregor S,
Montgomery GW,
Tomlinson I,
Easton DF,
Thompson DJ,
Spurdle AB
Cancer medicine · 2018 · PMID 29608257 · open access
3 pages
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
Fogh I,
Ratti A,
Gellera C,
Lin K,
Tiloca C,
Moskvina V,
Corrado L,
Sorarù G,
Cereda C,
Corti S,
Gentilini D,
Calini D
and 53 more — show all
Castellotti B,
Mazzini L,
Querin G,
Gagliardi S,
Del Bo R,
Conforti FL,
Siciliano G,
Inghilleri M,
Saccà F,
Bongioanni P,
Penco S,
Corbo M,
Sorbi S,
Filosto M,
Ferlini A,
Di Blasio AM,
Signorini S,
Shatunov A,
Jones A,
Shaw PJ,
Morrison KE,
Farmer AE,
Van Damme P,
Robberecht W,
Chiò A,
Traynor BJ,
Sendtner M,
Melki J,
Meininger V,
Hardiman O,
Andersen PM,
Leigh NP,
Glass JD,
Overste D,
Diekstra FP,
Veldink JH,
van Es MA,
Shaw CE,
Weale ME,
Lewis CM,
Williams J,
Brown RH,
Landers JE,
Ticozzi N,
Ceroni M,
Pegoraro E,
Comi GP,
D'Alfonso S,
van den Berg LH,
Taroni F,
Al-Chalabi A,
Powell J,
Silani V
SLAGEN Consortium and Collaborators
Human molecular genetics · 2014 · PMID 24256812
2 pages
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms
Tapper W,
Jones AV,
Kralovics R,
Harutyunyan AS,
Zoi K,
Leung W,
Godfrey AL,
Guglielmelli P,
Callaway A,
Ward D,
Aranaz P,
White HE
and 38 more — show all
Waghorn K,
Lin F,
Chase A,
Baxter EJ,
Maclean C,
Nangalia J,
Chen E,
Evans P,
Short M,
Jack A,
Wallis L,
Oscier D,
Duncombe AS,
Schuh A,
Mead AJ,
Griffiths M,
Ewing J,
Gale RE,
Schnittger S,
Haferlach T,
Stegelmann F,
Döhner K,
Grallert H,
Strauch K,
Tanaka T,
Bandinelli S,
Giannopoulos A,
Pieri L,
Mannarelli C,
Gisslinger H,
Barosi G,
Cazzola M,
Reiter A,
Harrison C,
Campbell P,
Green AR,
Vannucchi A,
Cross NC
Nature communications · 2015 · PMID 25849990 · open access
2 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.