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.
7 matches for
Stevens H.
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+
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
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Wang TJ,
Zhang F,
Richards JB,
Kestenbaum B,
van Meurs JB,
Berry D,
Kiel DP,
Streeten EA,
Ohlsson C,
Koller DL,
Peltonen L,
Cooper JD
and 64 more — show all
O'Reilly PF,
Houston DK,
Glazer NL,
Vandenput L,
Peacock M,
Shi J,
Rivadeneira F,
McCarthy MI,
Anneli P,
de Boer IH,
Mangino M,
Kato B,
Smyth DJ,
Booth SL,
Jacques PF,
Burke GL,
Goodarzi M,
Cheung CL,
Wolf M,
Rice K,
Goltzman D,
Hidiroglou N,
Ladouceur M,
Wareham NJ,
Hocking LJ,
Hart D,
Arden NK,
Cooper C,
Malik S,
Fraser WD,
Hartikainen AL,
Zhai G,
Macdonald HM,
Forouhi NG,
Loos RJ,
Reid DM,
Hakim A,
Dennison E,
Liu Y,
Power C,
Stevens HE,
Jaana L,
Vasan RS,
Soranzo N,
Bojunga J,
Psaty BM,
Lorentzon M,
Foroud T,
Harris TB,
Hofman A,
Jansson JO,
Cauley JA,
Uitterlinden AG,
Gibson Q,
Järvelin MR,
Karasik D,
Siscovick DS,
Econs MJ,
Kritchevsky SB,
Florez JC,
Todd JA,
Dupuis J,
Hyppönen E,
Spector TD
Lancet (London, England) · 2010 · PMID 20541252
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
Seven newly identified loci for autoimmune thyroid disease
Cooper JD,
Simmonds MJ,
Walker NM,
Burren O,
Brand OJ,
Guo H,
Wallace C,
Stevens H,
Coleman G,
Franklyn JA,
Todd JA,
Gough SC
Wellcome Trust Case Control Consortium
Human molecular genetics · 2012 · PMID 22922229 · 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.