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2,662 papers hold this site up. Every variant and condition page names
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16 matches for
Barrett JC.
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+
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Onengut-Gumuscu S,
Chen WM,
Burren O,
Cooper NJ,
Quinlan AR,
Mychaleckyj JC,
Farber E,
Bonnie JK,
Szpak M,
Schofield E,
Achuthan P,
Guo H
and 14 more — show all
Fortune MD,
Stevens H,
Walker NM,
Ward LD,
Kundaje A,
Kellis M,
Daly MJ,
Barrett JC,
Cooper JD,
Deloukas P,
Todd JA,
Wallace C,
Concannon P,
Rich SS
Type 1 Diabetes Genetics Consortium
Nature genetics · 2015 · PMID 25751624 · open access
12 pages+
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Liu JZ,
van Sommeren S,
Huang H,
Ng SC,
Alberts R,
Takahashi A,
Ripke S,
Lee JC,
Jostins L,
Shah T,
Abedian S,
Cheon JH
and 28 more — show all
Cho J,
Dayani NE,
Franke L,
Fuyuno Y,
Hart A,
Juyal RC,
Juyal G,
Kim WH,
Morris AP,
Poustchi H,
Newman WG,
Midha V,
Orchard TR,
Vahedi H,
Sood A,
Sung JY,
Malekzadeh R,
Westra HJ,
Yamazaki K,
Yang SK,
Barrett JC,
Alizadeh BZ,
Parkes M,
Bk T,
Daly MJ,
Kubo M,
Anderson CA,
Weersma RK
International Multiple Sclerosis Genetics Consortium · International IBD Genetics Consortium
Nature genetics · 2015 · PMID 26192919
12 pages+
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
de Lange KM,
Moutsianas L,
Lee JC,
Lamb CA,
Luo Y,
Kennedy NA,
Jostins L,
Rice DL,
Gutierrez-Achury J,
Ji SG,
Heap G,
Nimmo ER
and 20 more — show all
Edwards C,
Henderson P,
Mowat C,
Sanderson J,
Satsangi J,
Simmons A,
Wilson DC,
Tremelling M,
Hart A,
Mathew CG,
Newman WG,
Parkes M,
Lees CW,
Uhlig H,
Hawkey C,
Prescott NJ,
Ahmad T,
Mansfield JC,
Anderson CA,
Barrett JC
Nature genetics · 2017 · PMID 28067908 · open access
12 pages+
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Barrett JC,
Hansoul S,
Nicolae DL,
Cho JH,
Duerr RH,
Rioux JD,
Brant SR,
Silverberg MS,
Taylor KD,
Barmada MM,
Bitton A,
Dassopoulos T
and 49 more — show all
Datta LW,
Green T,
Griffiths AM,
Kistner EO,
Murtha MT,
Regueiro MD,
Rotter JI,
Schumm LP,
Steinhart AH,
Targan SR,
Xavier RJ,
Libioulle C,
Sandor C,
Lathrop M,
Belaiche J,
Dewit O,
Gut I,
Heath S,
Laukens D,
Mni M,
Rutgeerts P,
Van Gossum A,
Zelenika D,
Franchimont D,
Hugot JP,
de Vos M,
Vermeire S,
Louis E,
Cardon LR,
Anderson CA,
Drummond H,
Nimmo E,
Ahmad T,
Prescott NJ,
Onnie CM,
Fisher SA,
Marchini J,
Ghori J,
Bumpstead S,
Gwilliam R,
Tremelling M,
Deloukas P,
Mansfield J,
Jewell D,
Satsangi J,
Mathew CG,
Parkes M,
Georges M,
Daly MJ
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Trynka G,
Hunt KA,
Bockett NA,
Romanos J,
Mistry V,
Szperl A,
Bakker SF,
Bardella MT,
Bhaw-Rosun L,
Castillejo G,
de la Concha EG,
de Almeida RC
and 52 more — show all
Dias KR,
van Diemen CC,
Dubois PC,
Duerr RH,
Edkins S,
Franke L,
Fransen K,
Gutierrez J,
Heap GA,
Hrdlickova B,
Hunt S,
Plaza Izurieta L,
Izzo V,
Joosten LA,
Langford C,
Mazzilli MC,
Mein CA,
Midah V,
Mitrovic M,
Mora B,
Morelli M,
Nutland S,
Núñez C,
Onengut-Gumuscu S,
Pearce K,
Platteel M,
Polanco I,
Potter S,
Ribes-Koninckx C,
Ricaño-Ponce I,
Rich SS,
Rybak A,
Santiago JL,
Senapati S,
Sood A,
Szajewska H,
Troncone R,
Varadé J,
Wallace C,
Wolters VM,
Zhernakova A,
Thelma BK,
Cukrowska B,
Urcelay E,
Bilbao JR,
Mearin ML,
Barisani D,
Barrett JC,
Plagnol V,
Deloukas P,
Wijmenga C,
van Heel DA
Spanish Consortium on the Genetics of Coeliac Disease (CEGEC) · PreventCD Study Group and 1 more consortia
Nature genetics · 2011 · PMID 22057235 · open access
7 pages
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis
Liu JZ,
Almarri MA,
Gaffney DJ,
Mells GF,
Jostins L,
Cordell HJ,
Ducker SJ,
Day DB,
Heneghan MA,
Neuberger JM,
Donaldson PT,
Bathgate AJ
and 7 more — show all
UK Primary Biliary Cirrhosis (PBC) Consortium · Wellcome Trust Case Control Consortium 3
Nature genetics · 2012 · PMID 22961000 · open access
6 pages
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Barrett JC,
Clayton DG,
Concannon P,
Akolkar B,
Cooper JD,
Erlich HA,
Julier C,
Morahan G,
Nerup J,
Nierras C,
Plagnol V,
Pociot F
and 6 more — show all
Type 1 Diabetes Genetics Consortium
Nature genetics · 2009 · PMID 19430480 · open access
4 pages
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Zeggini E,
Weedon MN,
Lindgren CM,
Frayling TM,
Elliott KS,
Lango H,
Timpson NJ,
Perry JR,
Rayner NW,
Freathy RM,
Barrett JC,
Shields B
and 14 more — show all
Morris AP,
Ellard S,
Groves CJ,
Harries LW,
Marchini JL,
Owen KR,
Knight B,
Cardon LR,
Walker M,
Hitman GA,
Morris AD,
Doney AS,
McCarthy MI,
Hattersley AT
Wellcome Trust Case Control Consortium (WTCCC)
Science (New York, N.Y.) · 2007 · PMID 17463249
3 pages
Multiple common variants for celiac disease influencing immune gene expression
Dubois PC,
Trynka G,
Franke L,
Hunt KA,
Romanos J,
Curtotti A,
Zhernakova A,
Heap GA,
Adány R,
Aromaa A,
Bardella MT,
van den Berg LH
and 55 more — show all
Bockett NA,
de la Concha EG,
Dema B,
Fehrmann RS,
Fernández-Arquero M,
Fiatal S,
Grandone E,
Green PM,
Groen HJ,
Gwilliam R,
Houwen RH,
Hunt SE,
Kaukinen K,
Kelleher D,
Korponay-Szabo I,
Kurppa K,
MacMathuna P,
Mäki M,
Mazzilli MC,
McCann OT,
Mearin ML,
Mein CA,
Mirza MM,
Mistry V,
Mora B,
Morley KI,
Mulder CJ,
Murray JA,
Núñez C,
Oosterom E,
Ophoff RA,
Polanco I,
Peltonen L,
Platteel M,
Rybak A,
Salomaa V,
Schweizer JJ,
Sperandeo MP,
Tack GJ,
Turner G,
Veldink JH,
Verbeek WH,
Weersma RK,
Wolters VM,
Urcelay E,
Cukrowska B,
Greco L,
Neuhausen SL,
McManus R,
Barisani D,
Deloukas P,
Barrett JC,
Saavalainen P,
Wijmenga C,
van Heel DA
Nature genetics · 2010 · PMID 20190752 · open access
3 pages
Imputation-based meta-analysis of severe malaria in three African populations
Band G,
Le QS,
Jostins L,
Pirinen M,
Kivinen K,
Jallow M,
Sisay-Joof F,
Bojang K,
Pinder M,
Sirugo G,
Conway DJ,
Nyirongo V
and 22 more — show all
Kachala D,
Molyneux M,
Taylor T,
Ndila C,
Peshu N,
Marsh K,
Williams TN,
Alcock D,
Andrews R,
Edkins S,
Gray E,
Hubbart C,
Jeffreys A,
Rowlands K,
Schuldt K,
Clark TG,
Small KS,
Teo YY,
Kwiatkowski DP,
Rockett KA,
Barrett JC,
Spencer CC
Malaria Genomic Epidemiology Network · Malaria Genomic Epidemiological Network
PLoS genetics · 2013 · PMID 23717212 · open access
3 pages
Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
Cooper JD,
Smyth DJ,
Smiles AM,
Plagnol V,
Walker NM,
Allen JE,
Downes K,
Barrett JC,
Healy BC,
Mychaleckyj JC,
Warram JH,
Todd JA
Nature genetics · 2008 · PMID 18978792
2 pages
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration
Curtis J,
Luo Y,
Zenner HL,
Cuchet-Lourenço D,
Wu C,
Lo K,
Maes M,
Alisaac A,
Stebbings E,
Liu JZ,
Kopanitsa L,
Ignatyeva O
and 11 more — show all
Balabanova Y,
Nikolayevskyy V,
Baessmann I,
Thye T,
Meyer CG,
Nürnberg P,
Horstmann RD,
Drobniewski F,
Plagnol V,
Barrett JC,
Nejentsev S
Nature genetics · 2015 · PMID 25774636 · open access
2 pages
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Frayling TM,
Timpson NJ,
Weedon MN,
Zeggini E,
Freathy RM,
Lindgren CM,
Perry JR,
Elliott KS,
Lango H,
Rayner NW,
Shields B,
Harries LW
and 29 more — show all
Barrett JC,
Ellard S,
Groves CJ,
Knight B,
Patch AM,
Ness AR,
Ebrahim S,
Lawlor DA,
Ring SM,
Ben-Shlomo Y,
Jarvelin MR,
Sovio U,
Bennett AJ,
Melzer D,
Ferrucci L,
Loos RJ,
Barroso I,
Wareham NJ,
Karpe F,
Owen KR,
Cardon LR,
Walker M,
Hitman GA,
Palmer CN,
Doney AS,
Morris AD,
Smith GD,
Hattersley AT,
McCarthy MI
Science (New York, N.Y.) · 2007 · PMID 17434869
1 page
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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
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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?
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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.