For researchers
Is your paper here?
2,662 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.
6 matches for
Dobbins SE.
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Houlston RS,
Cheadle J,
Dobbins SE,
Tenesa A,
Jones AM,
Howarth K,
Spain SL,
Broderick P,
Domingo E,
Farrington S,
Prendergast JG,
Pittman AM
and 33 more — show all
Theodoratou E,
Smith CG,
Olver B,
Walther A,
Barnetson RA,
Churchman M,
Jaeger EE,
Penegar S,
Barclay E,
Martin L,
Gorman M,
Mager R,
Johnstone E,
Midgley R,
Niittymäki I,
Tuupanen S,
Colley J,
Idziaszczyk S,
Thomas HJ,
Lucassen AM,
Evans DG,
Maher ER,
Maughan T,
Dimas A,
Dermitzakis E,
Cazier JB,
Aaltonen LA,
Pharoah P,
Kerr DJ,
Carvajal-Carmona LG,
Campbell H,
Dunlop MG,
Tomlinson IP
COGENT Consortium · CORGI Consortium and 2 more consortia
Nature genetics · 2010 · PMID 20972440 · open access
4 pages
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis
Whiffin N,
Hosking FJ,
Farrington SM,
Palles C,
Dobbins SE,
Zgaga L,
Lloyd A,
Kinnersley B,
Gorman M,
Tenesa A,
Broderick P,
Wang Y
and 19 more — show all
Barclay E,
Hayward C,
Martin L,
Buchanan DD,
Win AK,
Hopper J,
Jenkins M,
Lindor NM,
Newcomb PA,
Gallinger S,
Conti D,
Schumacher F,
Casey G,
Liu T,
Campbell H,
Lindblom A,
Houlston RS,
Tomlinson IP,
Dunlop MG
Swedish Low-Risk Colorectal Cancer Study Group
Human molecular genetics · 2014 · PMID 24737748
3 pages
Genome-wide association study identifies five susceptibility loci for glioma
Shete S,
Hosking FJ,
Robertson LB,
Dobbins SE,
Sanson M,
Malmer B,
Simon M,
Marie Y,
Boisselier B,
Delattre JY,
Hoang-Xuan K,
El Hallani S
and 25 more — show all
Idbaih A,
Zelenika D,
Andersson U,
Henriksson R,
Bergenheim AT,
Feychting M,
Lönn S,
Ahlbom A,
Schramm J,
Linnebank M,
Hemminki K,
Kumar R,
Hepworth SJ,
Price A,
Armstrong G,
Liu Y,
Gu X,
Yu R,
Lau C,
Schoemaker M,
Muir K,
Swerdlow A,
Lathrop M,
Bondy M,
Houlston RS
Nature genetics · 2009 · PMID 19578367
2 pages
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
Chubb D,
Weinhold N,
Broderick P,
Chen B,
Johnson DC,
Försti A,
Vijayakrishnan J,
Migliorini G,
Dobbins SE,
Holroyd A,
Hose D,
Walker BA
and 23 more — show all
Davies FE,
Gregory WA,
Jackson GH,
Irving JA,
Pratt G,
Fegan C,
Fenton JA,
Neben K,
Hoffmann P,
Nöthen MM,
Mühleisen TW,
Eisele L,
Ross FM,
Straka C,
Einsele H,
Langer C,
Dörner E,
Allan JM,
Jauch A,
Morgan GJ,
Hemminki K,
Houlston RS,
Goldschmidt H
Nature genetics · 2013 · PMID 23955597 · open access
2 pages
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer
Al-Tassan NA,
Whiffin N,
Hosking FJ,
Palles C,
Farrington SM,
Dobbins SE,
Harris R,
Gorman M,
Tenesa A,
Meyer BF,
Wakil SM,
Kinnersley B
and 23 more — show all
Campbell H,
Martin L,
Smith CG,
Idziaszczyk S,
Barclay E,
Maughan TS,
Kaplan R,
Kerr R,
Kerr D,
Buchanan DD,
Win AK,
Hopper J,
Jenkins M,
Lindor NM,
Newcomb PA,
Gallinger S,
Conti D,
Schumacher F,
Casey G,
Dunlop MG,
Tomlinson IP,
Cheadle JP,
Houlston RS
Scientific reports · 2015 · PMID 25990418 · open access
2 pages
Common variation at 10p12.31 near MLLT10 influences meningioma risk
Dobbins SE,
Broderick P,
Melin B,
Feychting M,
Johansen C,
Andersson U,
Brännström T,
Schramm J,
Olver B,
Lloyd A,
Ma YP,
Hosking FJ
and 15 more — show all
Lönn S,
Ahlbom A,
Henriksson R,
Schoemaker MJ,
Hepworth SJ,
Hoffmann P,
Mühleisen TW,
Nöthen MM,
Moebus S,
Eisele L,
Kosteljanetz M,
Muir K,
Swerdlow A,
Simon M,
Houlston RS
Nature genetics · 2011 · PMID 21804547 · open access
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.