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2,660 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
Concannon P.
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+
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes
Robertson CC,
Inshaw JRJ,
Onengut-Gumuscu S,
Chen WM,
Santa Cruz DF,
Yang H,
Cutler AJ,
Crouch DJM,
Farber E,
Bridges SL Jr,
Edberg JC,
Kimberly RP
and 19 more — show all
Buckner JH,
Deloukas P,
Divers J,
Dabelea D,
Lawrence JM,
Marcovina S,
Shah AS,
Greenbaum CJ,
Atkinson MA,
Gregersen PK,
Oksenberg JR,
Pociot F,
Rewers MJ,
Steck AK,
Dunger DB,
Wicker LS,
Concannon P,
Todd JA,
Rich SS
Type 1 Diabetes Genetics Consortium
Nature genetics · 2021 · PMID 34127860 · open access
12 pages+
Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies
Crouch DJM,
Inshaw JRJ,
Robertson CC,
Ng E,
Zhang JY,
Chen WM,
Onengut-Gumuscu S,
Cutler AJ,
Sidore C,
Cucca F,
Pociot F,
Concannon P
and 2 more — show all
Genetic epidemiology · 2025 · PMID 39749473 · open access
7 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
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Eyre S,
Bowes J,
Diogo D,
Lee A,
Barton A,
Martin P,
Zhernakova A,
Stahl E,
Viatte S,
McAllister K,
Amos CI,
Padyukov L
and 32 more — show all
Toes RE,
Huizinga TW,
Wijmenga C,
Trynka G,
Franke L,
Westra HJ,
Alfredsson L,
Hu X,
Sandor C,
de Bakker PI,
Davila S,
Khor CC,
Heng KK,
Andrews R,
Edkins S,
Hunt SE,
Langford C,
Symmons D,
Concannon P,
Onengut-Gumuscu S,
Rich SS,
Deloukas P,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Ärlsetig L,
Martin J,
Rantapää-Dahlqvist S,
Plenge RM,
Raychaudhuri S,
Klareskog L,
Gregersen PK,
Worthington J
Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate · Wellcome Trust Case Control Consortium
Nature genetics · 2012 · PMID 23143596 · open access
4 pages
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker KB,
Ramus SJ,
Tyrer J,
Lee A,
Shen HC,
Beesley J,
Lawrenson K,
McGuffog L,
Healey S,
Lee JM,
Spindler TJ,
Lin YG
and 277 more — show all
Pejovic T,
Bean Y,
Li Q,
Coetzee S,
Hazelett D,
Miron A,
Southey M,
Terry MB,
Goldgar DE,
Buys SS,
Janavicius R,
Dorfling CM,
van Rensburg EJ,
Neuhausen SL,
Ding YC,
Hansen TV,
Jønson L,
Gerdes AM,
Ejlertsen B,
Barrowdale D,
Dennis J,
Benitez J,
Osorio A,
Garcia MJ,
Komenaka I,
Weitzel JN,
Ganschow P,
Peterlongo P,
Bernard L,
Viel A,
Bonanni B,
Peissel B,
Manoukian S,
Radice P,
Papi L,
Ottini L,
Fostira F,
Konstantopoulou I,
Garber J,
Frost D,
Perkins J,
Platte R,
Ellis S,
Godwin AK,
Schmutzler RK,
Meindl A,
Engel C,
Sutter C,
Sinilnikova OM,
Damiola F,
Mazoyer S,
Stoppa-Lyonnet D,
Claes K,
De Leeneer K,
Kirk J,
Rodriguez GC,
Piedmonte M,
O'Malley DM,
de la Hoya M,
Caldes T,
Aittomäki K,
Nevanlinna H,
Collée JM,
Rookus MA,
Oosterwijk JC,
Tihomirova L,
Tung N,
Hamann U,
Isaccs C,
Tischkowitz M,
Imyanitov EN,
Caligo MA,
Campbell IG,
Hogervorst FB,
Olah E,
Diez O,
Blanco I,
Brunet J,
Lazaro C,
Pujana MA,
Jakubowska A,
Gronwald J,
Lubinski J,
Sukiennicki G,
Barkardottir RB,
Plante M,
Simard J,
Soucy P,
Montagna M,
Tognazzo S,
Teixeira MR,
Pankratz VS,
Wang X,
Lindor N,
Szabo CI,
Kauff N,
Vijai J,
Aghajanian CA,
Pfeiler G,
Berger A,
Singer CF,
Tea MK,
Phelan CM,
Greene MH,
Mai PL,
Rennert G,
Mulligan AM,
Tchatchou S,
Andrulis IL,
Glendon G,
Toland AE,
Jensen UB,
Kruse TA,
Thomassen M,
Bojesen A,
Zidan J,
Friedman E,
Laitman Y,
Soller M,
Liljegren A,
Arver B,
Einbeigi Z,
Stenmark-Askmalm M,
Olopade OI,
Nussbaum RL,
Rebbeck TR,
Nathanson KL,
Domchek SM,
Lu KH,
Karlan BY,
Walsh C,
Lester J,
Hein A,
Ekici AB,
Beckmann MW,
Fasching PA,
Lambrechts D,
Van Nieuwenhuysen E,
Vergote I,
Lambrechts S,
Dicks E,
Doherty JA,
Wicklund KG,
Rossing MA,
Rudolph A,
Chang-Claude J,
Wang-Gohrke S,
Eilber U,
Moysich KB,
Odunsi K,
Sucheston L,
Lele S,
Wilkens LR,
Goodman MT,
Thompson PJ,
Shvetsov YB,
Runnebaum IB,
Dürst M,
Hillemanns P,
Dörk T,
Antonenkova N,
Bogdanova N,
Leminen A,
Pelttari LM,
Butzow R,
Modugno F,
Kelley JL,
Edwards RP,
Ness RB,
du Bois A,
Heitz F,
Schwaab I,
Harter P,
Matsuo K,
Hosono S,
Orsulic S,
Jensen A,
Kjaer SK,
Hogdall E,
Hasmad HN,
Azmi MA,
Teo SH,
Woo YL,
Fridley BL,
Goode EL,
Cunningham JM,
Vierkant RA,
Bruinsma F,
Giles GG,
Liang D,
Hildebrandt MA,
Wu X,
Levine DA,
Bisogna M,
Berchuck A,
Iversen ES,
Schildkraut JM,
Concannon P,
Weber RP,
Cramer DW,
Terry KL,
Poole EM,
Tworoger SS,
Bandera EV,
Orlow I,
Olson SH,
Krakstad C,
Salvesen HB,
Tangen IL,
Bjorge L,
van Altena AM,
Aben KK,
Kiemeney LA,
Massuger LF,
Kellar M,
Brooks-Wilson A,
Kelemen LE,
Cook LS,
Le ND,
Cybulski C,
Yang H,
Lissowska J,
Brinton LA,
Wentzensen N,
Hogdall C,
Lundvall L,
Nedergaard L,
Baker H,
Song H,
Eccles D,
McNeish I,
Paul J,
Carty K,
Siddiqui N,
Glasspool R,
Whittemore AS,
Rothstein JH,
McGuire V,
Sieh W,
Ji BT,
Zheng W,
Shu XO,
Gao YT,
Rosen B,
Risch HA,
McLaughlin JR,
Narod SA,
Monteiro AN,
Chen A,
Lin HY,
Permuth-Wey J,
Sellers TA,
Tsai YY,
Chen Z,
Ziogas A,
Anton-Culver H,
Gentry-Maharaj A,
Menon U,
Harrington P,
Lee AW,
Wu AH,
Pearce CL,
Coetzee G,
Pike MC,
Dansonka-Mieszkowska A,
Timorek A,
Rzepecka IK,
Kupryjanczyk J,
Freedman M,
Noushmehr H,
Easton DF,
Offit K,
Couch FJ,
Gayther S,
Pharoah PP,
Antoniou AC,
Chenevix-Trench G
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis
Hinks A,
Cobb J,
Marion MC,
Prahalad S,
Sudman M,
Bowes J,
Martin P,
Comeau ME,
Sajuthi S,
Andrews R,
Brown M,
Chen WM
and 27 more — show all
Concannon P,
Deloukas P,
Edkins S,
Eyre S,
Gaffney PM,
Guthery SL,
Guthridge JM,
Hunt SE,
James JA,
Keddache M,
Moser KL,
Nigrovic PA,
Onengut-Gumuscu S,
Onslow ML,
Rosé CD,
Rich SS,
Steel KJ,
Wakeland EK,
Wallace CA,
Wedderburn LR,
Woo P,
Bohnsack JF,
Haas JP,
Glass DN,
Langefeld CD,
Thomson W,
Thompson SD
Boston Children's JIA Registry · British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group and 7 more consortia
Nature genetics · 2013 · PMID 23603761 · open access
2 pages
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Sun X,
Verma SP,
Jia G,
Wang X,
Ping J,
Guo X,
Shu XO,
Chen J,
Derkach A,
Cai Q,
Liang X,
Long J
and 34 more — show all
Offit K,
Oh JH,
Reiner AS,
Watt GP,
Woods M,
Yang Y,
Ambrosone CB,
Ambs S,
Chen Y,
Concannon P,
Garcia-Closas M,
Gu J,
Haiman CA,
Hu JJ,
Huo D,
John EM,
Knight JA,
Li CI,
Lynch CF,
Mellemkjær L,
Nathanson KL,
Nemesure B,
Olopade OI,
Olshan AF,
Pal T,
Palmer JR,
Press MF,
Sanderson M,
Sandler DP,
Troester MA,
Zheng W,
Bernstein JL,
Buas MF,
Shu X
Cancer research · 2024 · PMID 38832928
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.