For researchers
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.
8 matches for
Plagnol V.
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
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Plagnol V,
Hernandez DG,
Sharma M,
Sheerin UM,
Saad M,
Simón-Sánchez J,
Schulte C,
Lesage S,
Sveinbjörnsdóttir S,
Stefánsson K,
Martinez M
and 6 more — show all
International Parkinson Disease Genomics Consortium
Lancet (London, England) · 2011 · PMID 21292315
5 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
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
Todd JA,
Walker NM,
Cooper JD,
Smyth DJ,
Downes K,
Plagnol V,
Bailey R,
Nejentsev S,
Field SF,
Payne F,
Lowe CE,
Szeszko JS
and 28 more — show all
Hafler JP,
Zeitels L,
Yang JH,
Vella A,
Nutland S,
Stevens HE,
Schuilenburg H,
Coleman G,
Maisuria M,
Meadows W,
Smink LJ,
Healy B,
Burren OS,
Lam AA,
Ovington NR,
Allen J,
Adlem E,
Leung HT,
Wallace C,
Howson JM,
Guja C,
Ionescu-Tîrgovişte C,
Simmonds MJ,
Heward JM,
Gough SC,
Dunger DB,
Wicker LS,
Clayton DG
Genetics of Type 1 Diabetes in Finland · Wellcome Trust Case Control Consortium
Nature genetics · 2007 · PMID 17554260
3 pages
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases
Plagnol V,
Howson JM,
Smyth DJ,
Walker N,
Hafler JP,
Wallace C,
Stevens H,
Jackson L,
Simmonds MJ,
Bingley PJ,
Gough SC,
Todd JA
Type 1 Diabetes Genetics Consortium
PLoS genetics · 2011 · PMID 21829393 · open access
3 pages
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Franceschini N,
Giambartolomei C,
de Vries PS,
Finan C,
Bis JC,
Huntley RP,
Lovering RC,
Tajuddin SM,
Winkler TW,
Graff M,
Kavousi M,
Dale C
and 146 more — show all
Smith AV,
Hofer E,
van Leeuwen EM,
Nolte IM,
Lu L,
Scholz M,
Sargurupremraj M,
Pitkänen N,
Franzén O,
Joshi PK,
Noordam R,
Marioni RE,
Hwang SJ,
Musani SK,
Schminke U,
Palmas W,
Isaacs A,
Correa A,
Zonderman AB,
Hofman A,
Teumer A,
Cox AJ,
Uitterlinden AG,
Wong A,
Smit AJ,
Newman AB,
Britton A,
Ruusalepp A,
Sennblad B,
Hedblad B,
Pasaniuc B,
Penninx BW,
Langefeld CD,
Wassel CL,
Tzourio C,
Fava C,
Baldassarre D,
O'Leary DH,
Teupser D,
Kuh D,
Tremoli E,
Mannarino E,
Grossi E,
Boerwinkle E,
Schadt EE,
Ingelsson E,
Veglia F,
Rivadeneira F,
Beutner F,
Chauhan G,
Heiss G,
Snieder H,
Campbell H,
Völzke H,
Markus HS,
Deary IJ,
Jukema JW,
de Graaf J,
Price J,
Pott J,
Hopewell JC,
Liang J,
Thiery J,
Engmann J,
Gertow K,
Rice K,
Taylor KD,
Dhana K,
Kiemeney LALM,
Lind L,
Raffield LM,
Launer LJ,
Holdt LM,
Dörr M,
Dichgans M,
Traylor M,
Sitzer M,
Kumari M,
Kivimaki M,
Nalls MA,
Melander O,
Raitakari O,
Franco OH,
Rueda-Ochoa OL,
Roussos P,
Whincup PH,
Amouyel P,
Giral P,
Anugu P,
Wong Q,
Malik R,
Rauramaa R,
Burkhardt R,
Hardy R,
Schmidt R,
de Mutsert R,
Morris RW,
Strawbridge RJ,
Wannamethee SG,
Hägg S,
Shah S,
McLachlan S,
Trompet S,
Seshadri S,
Kurl S,
Heckbert SR,
Ring S,
Harris TB,
Lehtimäki T,
Galesloot TE,
Shah T,
de Faire U,
Plagnol V,
Rosamond WD,
Post W,
Zhu X,
Zhang X,
Guo X,
Saba Y,
Dehghan A,
Seldenrijk A,
Morrison AC,
Hamsten A,
Psaty BM,
van Duijn CM,
Lawlor DA,
Mook-Kanamori DO,
Bowden DW,
Schmidt H,
Wilson JF,
Wilson JG,
Rotter JI,
Wardlaw JM,
Deanfield J,
Halcox J,
Lyytikäinen LP,
Loeffler M,
Evans MK,
Debette S,
Humphries SE,
Völker U,
Gudnason V,
Hingorani AD,
Björkegren JLM,
Casas JP,
O'Donnell CJ
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · 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
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.