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
Ward J.
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Howard DM,
Adams MJ,
Shirali M,
Clarke TK,
Marioni RE,
Davies G,
Coleman JRI,
Alloza C,
Shen X,
Barbu MC,
Wigmore EM,
Gibson J
and 9 more — show all
23andMe Research Team
Nature communications · 2018 · PMID 29662059 · open access
12 pages+
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
and 26 more — show all
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci
Smith DJ,
Escott-Price V,
Davies G,
Bailey ME,
Colodro-Conde L,
Ward J,
Vedernikov A,
Marioni R,
Cullen B,
Lyall D,
Hagenaars SP,
Liewald DC
and 20 more — show all
Luciano M,
Gale CR,
Ritchie SJ,
Hayward C,
Nicholl B,
Bulik-Sullivan B,
Adams M,
Couvy-Duchesne B,
Graham N,
Mackay D,
Evans J,
Smith BH,
Porteous DJ,
Medland SE,
Martin NG,
Holmans P,
McIntosh AM,
Pell JP,
Deary IJ,
O'Donovan MC
Molecular psychiatry · 2016 · PMID 27067015 · 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
Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression
Strawbridge RJ,
Ward J,
Lyall LM,
Tunbridge EM,
Cullen B,
Graham N,
Ferguson A,
Johnston KJA,
Lyall DM,
Mackay D,
Cavanagh J,
Howard DM
and 9 more — show all
Translational psychiatry · 2018 · PMID 30181555 · open access
2 pages
Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort
Strawbridge RJ,
Ward J,
Cullen B,
Tunbridge EM,
Hartz S,
Bierut L,
Horton A,
Bailey MES,
Graham N,
Ferguson A,
Lyall DM,
Mackay D
and 7 more — show all
Translational psychiatry · 2018 · PMID 29391395 · 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.