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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.
8 matches for
Radford-Smith G.
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Franke A,
McGovern DP,
Barrett JC,
Wang K,
Radford-Smith GL,
Ahmad T,
Lees CW,
Balschun T,
Lee J,
Roberts R,
Anderson CA,
Bis JC
and 84 more — show all
Bumpstead S,
Ellinghaus D,
Festen EM,
Georges M,
Green T,
Haritunians T,
Jostins L,
Latiano A,
Mathew CG,
Montgomery GW,
Prescott NJ,
Raychaudhuri S,
Rotter JI,
Schumm P,
Sharma Y,
Simms LA,
Taylor KD,
Whiteman D,
Wijmenga C,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Cohen A,
Colombel JF,
Cottone M,
Stronati L,
Denson T,
De Vos M,
D'Inca R,
Dubinsky M,
Edwards C,
Florin T,
Franchimont D,
Gearry R,
Glas J,
Van Gossum A,
Guthery SL,
Halfvarson J,
Verspaget HW,
Hugot JP,
Karban A,
Laukens D,
Lawrance I,
Lemann M,
Levine A,
Libioulle C,
Louis E,
Mowat C,
Newman W,
Panés J,
Phillips A,
Proctor DD,
Regueiro M,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Seibold F,
Steinhart AH,
Stokkers PC,
Torkvist L,
Kullak-Ublick G,
Wilson D,
Walters T,
Targan SR,
Brant SR,
Rioux JD,
D'Amato M,
Weersma RK,
Kugathasan S,
Griffiths AM,
Mansfield JC,
Vermeire S,
Duerr RH,
Silverberg MS,
Satsangi J,
Schreiber S,
Cho JH,
Annese V,
Hakonarson H,
Daly MJ,
Parkes M
Nature genetics · 2010 · PMID 21102463
12 pages+
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Anderson CA,
Boucher G,
Lees CW,
Franke A,
D'Amato M,
Taylor KD,
Lee JC,
Goyette P,
Imielinski M,
Latiano A,
Lagacé C,
Scott R
and 101 more — show all
Amininejad L,
Bumpstead S,
Baidoo L,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Colombel JF,
Denson LA,
De Vos M,
Dubinsky M,
Edwards C,
Ellinghaus D,
Fehrmann RS,
Floyd JA,
Florin T,
Franchimont D,
Franke L,
Georges M,
Glas J,
Glazer NL,
Guthery SL,
Haritunians T,
Hayward NK,
Hugot JP,
Jobin G,
Laukens D,
Lawrance I,
Lémann M,
Levine A,
Libioulle C,
Louis E,
McGovern DP,
Milla M,
Montgomery GW,
Morley KI,
Mowat C,
Ng A,
Newman W,
Ophoff RA,
Papi L,
Palmieri O,
Peyrin-Biroulet L,
Panés J,
Phillips A,
Prescott NJ,
Proctor DD,
Roberts R,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Schumm P,
Seibold F,
Sharma Y,
Simms LA,
Seielstad M,
Steinhart AH,
Targan SR,
van den Berg LH,
Vatn M,
Verspaget H,
Walters T,
Wijmenga C,
Wilson DC,
Westra HJ,
Xavier RJ,
Zhao ZZ,
Ponsioen CY,
Andersen V,
Torkvist L,
Gazouli M,
Anagnou NP,
Karlsen TH,
Kupcinskas L,
Sventoraityte J,
Mansfield JC,
Kugathasan S,
Silverberg MS,
Halfvarson J,
Rotter JI,
Mathew CG,
Griffiths AM,
Gearry R,
Ahmad T,
Brant SR,
Chamaillard M,
Satsangi J,
Cho JH,
Schreiber S,
Daly MJ,
Barrett JC,
Parkes M,
Annese V,
Hakonarson H,
Radford-Smith G,
Duerr RH,
Vermeire S,
Weersma RK,
Rioux JD
Nature genetics · 2011 · PMID 21297633 · open access
12 pages+
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Jostins L,
Ripke S,
Weersma RK,
Duerr RH,
McGovern DP,
Hui KY,
Lee JC,
Schumm LP,
Sharma Y,
Anderson CA,
Essers J,
Mitrovic M
and 94 more — show all
Ning K,
Cleynen I,
Theatre E,
Spain SL,
Raychaudhuri S,
Goyette P,
Wei Z,
Abraham C,
Achkar JP,
Ahmad T,
Amininejad L,
Ananthakrishnan AN,
Andersen V,
Andrews JM,
Baidoo L,
Balschun T,
Bampton PA,
Bitton A,
Boucher G,
Brand S,
Büning C,
Cohain A,
Cichon S,
D'Amato M,
De Jong D,
Devaney KL,
Dubinsky M,
Edwards C,
Ellinghaus D,
Ferguson LR,
Franchimont D,
Fransen K,
Gearry R,
Georges M,
Gieger C,
Glas J,
Haritunians T,
Hart A,
Hawkey C,
Hedl M,
Hu X,
Karlsen TH,
Kupcinskas L,
Kugathasan S,
Latiano A,
Laukens D,
Lawrance IC,
Lees CW,
Louis E,
Mahy G,
Mansfield J,
Morgan AR,
Mowat C,
Newman W,
Palmieri O,
Ponsioen CY,
Potocnik U,
Prescott NJ,
Regueiro M,
Rotter JI,
Russell RK,
Sanderson JD,
Sans M,
Satsangi J,
Schreiber S,
Simms LA,
Sventoraityte J,
Targan SR,
Taylor KD,
Tremelling M,
Verspaget HW,
De Vos M,
Wijmenga C,
Wilson DC,
Winkelmann J,
Xavier RJ,
Zeissig S,
Zhang B,
Zhang CK,
Zhao H,
Silverberg MS,
Annese V,
Hakonarson H,
Brant SR,
Radford-Smith G,
Mathew CG,
Rioux JD,
Schadt EE,
Daly MJ,
Franke A,
Parkes M,
Vermeire S,
Barrett JC,
Cho JH
International IBD Genetics Consortium (IIBDGC)
Nature · 2012 · PMID 23128233 · 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-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Landi MT,
Bishop DT,
MacGregor S,
Machiela MJ,
Stratigos AJ,
Ghiorzo P,
Brossard M,
Calista D,
Choi J,
Fargnoli MC,
Zhang T,
Rodolfo M
and 140 more — show all
Trower AJ,
Menin C,
Martinez J,
Hadjisavvas A,
Song L,
Stefanaki I,
Scolyer R,
Yang R,
Goldstein AM,
Potrony M,
Kypreou KP,
Pastorino L,
Queirolo P,
Pellegrini C,
Cattaneo L,
Zawistowski M,
Gimenez-Xavier P,
Rodriguez A,
Elefanti L,
Manoukian S,
Rivoltini L,
Smith BH,
Loizidou MA,
Del Regno L,
Massi D,
Mandala M,
Khosrotehrani K,
Akslen LA,
Amos CI,
Andresen PA,
Avril MF,
Azizi E,
Soyer HP,
Bataille V,
Dalmasso B,
Bowdler LM,
Burdon KP,
Chen WV,
Codd V,
Craig JE,
Dębniak T,
Falchi M,
Fang S,
Friedman E,
Simi S,
Galan P,
Garcia-Casado Z,
Gillanders EM,
Gordon S,
Green A,
Gruis NA,
Hansson J,
Harland M,
Harris J,
Helsing P,
Henders A,
Hočevar M,
Höiom V,
Hunter D,
Ingvar C,
Kumar R,
Lang J,
Lathrop GM,
Lee JE,
Li X,
Lubiński J,
Mackie RM,
Malt M,
Malvehy J,
McAloney K,
Mohamdi H,
Molven A,
Moses EK,
Neale RE,
Novaković S,
Nyholt DR,
Olsson H,
Orr N,
Fritsche LG,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
Randerson-Moor J,
Requena C,
Rowe C,
Samani NJ,
Sanna M,
Schadendorf D,
Schulze HJ,
Simms LA,
Smithers M,
Song F,
Swerdlow AJ,
van der Stoep N,
Kukutsch NA,
Visconti A,
Wallace L,
Ward SV,
Wheeler L,
Sturm RA,
Hutchinson A,
Jones K,
Malasky M,
Vogt A,
Zhou W,
Pooley KA,
Elder DE,
Han J,
Hicks B,
Hayward NK,
Kanetsky PA,
Brummett C,
Montgomery GW,
Olsen CM,
Hayward C,
Dunning AM,
Martin NG,
Evangelou E,
Mann GJ,
Long G,
Pharoah PDP,
Easton DF,
Barrett JH,
Cust AE,
Abecasis G,
Duffy DL,
Whiteman DC,
Gogas H,
De Nicolo A,
Tucker MA,
Newton-Bishop JA,
Peris K,
Chanock SJ,
Demenais F,
Brown KM,
Puig S,
Nagore E,
Shi J,
Iles MM,
Law MH
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · 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
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Law MH,
Bishop DT,
Lee JE,
Brossard M,
Martin NG,
Moses EK,
Song F,
Barrett JH,
Kumar R,
Easton DF,
Pharoah PDP,
Swerdlow AJ
and 63 more — show all
Kypreou KP,
Taylor JC,
Harland M,
Randerson-Moor J,
Akslen LA,
Andresen PA,
Avril MF,
Azizi E,
Scarrà GB,
Brown KM,
Dębniak T,
Duffy DL,
Elder DE,
Fang S,
Friedman E,
Galan P,
Ghiorzo P,
Gillanders EM,
Goldstein AM,
Gruis NA,
Hansson J,
Helsing P,
Hočevar M,
Höiom V,
Ingvar C,
Kanetsky PA,
Chen WV,
Landi MT,
Lang J,
Lathrop GM,
Lubiński J,
Mackie RM,
Mann GJ,
Molven A,
Montgomery GW,
Novaković S,
Olsson H,
Puig S,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
van der Stoep N,
van Doorn R,
Whiteman DC,
Craig JE,
Schadendorf D,
Simms LA,
Burdon KP,
Nyholt DR,
Pooley KA,
Orr N,
Stratigos AJ,
Cust AE,
Ward SV,
Hayward NK,
Han J,
Schulze HJ,
Dunning AM,
Bishop JAN,
Demenais F,
Amos CI,
MacGregor S,
Iles MM
GenoMEL Consortium · Essen-Heidelberg Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26237428 · open access
2 pages
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Heap GA,
Weedon MN,
Bewshea CM,
Singh A,
Chen M,
Satchwell JB,
Vivian JP,
So K,
Dubois PC,
Andrews JM,
Annese V,
Bampton P
and 44 more — show all
Barnardo M,
Bell S,
Cole A,
Connor SJ,
Creed T,
Cummings FR,
D'Amato M,
Daneshmend TK,
Fedorak RN,
Florin TH,
Gaya DR,
Greig E,
Halfvarson J,
Hart A,
Irving PM,
Jones G,
Karban A,
Lawrance IC,
Lee JC,
Lees C,
Lev-Tzion R,
Lindsay JO,
Mansfield J,
Mawdsley J,
Mazhar Z,
Parkes M,
Parnell K,
Orchard TR,
Radford-Smith G,
Russell RK,
Reffitt D,
Satsangi J,
Silverberg MS,
Sturniolo GC,
Tremelling M,
Tsianos EV,
van Heel DA,
Walsh A,
Watermeyer G,
Weersma RK,
Zeissig S,
Rossjohn J,
Holden AL,
Ahmad T
International Serious Adverse Events Consortium · IBD Pharmacogenetics Study Group
Nature genetics · 2014 · PMID 25217962
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.