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.
5 matches for
Radstake TR.
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Miller FW,
Chen W,
O'Hanlon TP,
Cooper RG,
Vencovsky J,
Rider LG,
Danko K,
Wedderburn LR,
Lundberg IE,
Pachman LM,
Reed AM,
Ytterberg SR
and 13 more — show all
Padyukov L,
Selva-O'Callaghan A,
Radstake TR,
Isenberg DA,
Chinoy H,
Ollier WE,
Scheet P,
Peng B,
Lee A,
Byun J,
Lamb JA,
Gregersen PK,
Amos CI
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
9 pages
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci
Zhernakova A,
Stahl EA,
Trynka G,
Raychaudhuri S,
Festen EA,
Franke L,
Westra HJ,
Fehrmann RS,
Kurreeman FA,
Thomson B,
Gupta N,
Romanos J
and 24 more — show all
McManus R,
Ryan AW,
Turner G,
Brouwer E,
Posthumus MD,
Remmers EF,
Tucci F,
Toes R,
Grandone E,
Mazzilli MC,
Rybak A,
Cukrowska B,
Coenen MJ,
Radstake TR,
van Riel PL,
Li Y,
de Bakker PI,
Gregersen PK,
Worthington J,
Siminovitch KA,
Klareskog L,
Huizinga TW,
Wijmenga C,
Plenge RM
PLoS genetics · 2011 · PMID 21383967 · open access
4 pages
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
Radstake TR,
Gorlova O,
Rueda B,
Martin JE,
Alizadeh BZ,
Palomino-Morales R,
Coenen MJ,
Vonk MC,
Voskuyl AE,
Schuerwegh AJ,
Broen JC,
van Riel PL
and 51 more — show all
van 't Slot R,
Italiaander A,
Ophoff RA,
Riemekasten G,
Hunzelmann N,
Simeon CP,
Ortego-Centeno N,
González-Gay MA,
González-Escribano MF,
Airo P,
van Laar J,
Herrick A,
Worthington J,
Hesselstrand R,
Smith V,
de Keyser F,
Houssiau F,
Chee MM,
Madhok R,
Shiels P,
Westhovens R,
Kreuter A,
Kiener H,
de Baere E,
Witte T,
Padykov L,
Klareskog L,
Beretta L,
Scorza R,
Lie BA,
Hoffmann-Vold AM,
Carreira P,
Varga J,
Hinchcliff M,
Gregersen PK,
Lee AT,
Ying J,
Han Y,
Weng SF,
Amos CI,
Wigley FM,
Hummers L,
Nelson JL,
Agarwal SK,
Assassi S,
Gourh P,
Tan FK,
Koeleman BP,
Arnett FC,
Martin J,
Mayes MD
Spanish Scleroderma Group
Nature genetics · 2010 · PMID 20383147
3 pages
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
López-Isac E,
Acosta-Herrera M,
Kerick M,
Assassi S,
Satpathy AT,
Granja J,
Mumbach MR,
Beretta L,
Simeón CP,
Carreira P,
Ortego-Centeno N,
Castellvi I
and 30 more — show all
Bossini-Castillo L,
Carmona FD,
Orozco G,
Hunzelmann N,
Distler JHW,
Franke A,
Lunardi C,
Moroncini G,
Gabrielli A,
de Vries-Bouwstra J,
Wijmenga C,
Koeleman BPC,
Nordin A,
Padyukov L,
Hoffmann-Vold AM,
Lie B,
Proudman S,
Stevens W,
Nikpour M,
Vyse T,
Herrick AL,
Worthington J,
Denton CP,
Allanore Y,
Brown MA,
Radstake TRDJ,
Fonseca C,
Chang HY,
Mayes MD,
Martin J
European Scleroderma Group† · Australian Scleroderma Interest Group (ASIG)
Nature communications · 2019 · PMID 31672989 · open access
3 pages
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
Stahl EA,
Raychaudhuri S,
Remmers EF,
Xie G,
Eyre S,
Thomson BP,
Li Y,
Kurreeman FA,
Zhernakova A,
Hinks A,
Guiducci C,
Chen R
and 56 more — show all
Alfredsson L,
Amos CI,
Ardlie KG,
Barton A,
Bowes J,
Brouwer E,
Burtt NP,
Catanese JJ,
Coblyn J,
Coenen MJ,
Costenbader KH,
Criswell LA,
Crusius JB,
Cui J,
de Bakker PI,
De Jager PL,
Ding B,
Emery P,
Flynn E,
Harrison P,
Hocking LJ,
Huizinga TW,
Kastner DL,
Ke X,
Lee AT,
Liu X,
Martin P,
Morgan AW,
Padyukov L,
Posthumus MD,
Radstake TR,
Reid DM,
Seielstad M,
Seldin MF,
Shadick NA,
Steer S,
Tak PP,
Thomson W,
van der Helm-van Mil AH,
van der Horst-Bruinsma IE,
van der Schoot CE,
van Riel PL,
Weinblatt ME,
Wilson AG,
Wolbink GJ,
Wordsworth BP,
Wijmenga C,
Karlson EW,
Toes RE,
de Vries N,
Begovich AB,
Worthington J,
Siminovitch KA,
Gregersen PK,
Klareskog L,
Plenge RM
BIRAC Consortium · YEAR Consortium
Nature genetics · 2010 · PMID 20453842
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.