For researchers
Is your paper here?
2,673 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.
11 matches for
Howard DM.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
Nagy R,
Boutin TS,
Marten J,
Huffman JE,
Kerr SM,
Campbell A,
Evenden L,
Gibson J,
Amador C,
Howard DM,
Navarro P,
Morris A
and 13 more — show all
Deary IJ,
Hocking LJ,
Padmanabhan S,
Smith BH,
Joshi P,
Wilson JF,
Hastie ND,
Wright AF,
McIntosh AM,
Porteous DJ,
Haley CS,
Vitart V,
Hayward C
Genome medicine · 2017 · PMID 28270201 · open access
12 pages+
Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism
Luciano M,
Hagenaars SP,
Davies G,
Hill WD,
Clarke TK,
Shirali M,
Harris SE,
Marioni RE,
Liewald DC,
Fawns-Ritchie C,
Adams MJ,
Howard DM
and 4 more — show all
Nature genetics · 2018 · PMID 29255261
12 pages+
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 association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117)
Clarke TK,
Adams MJ,
Davies G,
Howard DM,
Hall LS,
Padmanabhan S,
Murray AD,
Smith BH,
Campbell A,
Hayward C,
Porteous DJ,
Deary IJ
and 1 more — show all
Molecular psychiatry · 2017 · PMID 28937693 · open access
11 pages
Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression
Amare AT,
Vaez A,
Hsu YH,
Direk N,
Kamali Z,
Howard DM,
McIntosh AM,
McIntosh AM,
Tiemeier H,
Bültmann U,
Snieder H,
Hartman CA
Molecular psychiatry · 2020 · PMID 30626913 · open access
9 pages
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts
Sanchez-Roige S,
Palmer AA,
Fontanillas P,
Elson SL,
Adams MJ,
Howard DM,
Edenberg HJ,
Davies G,
Crist RC,
Deary IJ,
McIntosh AM,
Clarke TK
23andMe Research Team, the Substance Use Disorder Working Group of the Psychiatric Genomics Consortium
The American journal of psychiatry · 2019 · PMID 30336701
6 pages
A meta-analysis of genome-wide association studies of epigenetic age acceleration
Gibson J,
Russ TC,
Clarke TK,
Howard DM,
Hillary RF,
Evans KL,
Walker RM,
Bermingham ML,
Morris SW,
Campbell A,
Hayward C,
Murray AD
and 6 more — show all
PLoS genetics · 2019 · PMID 31738745 · open access
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 meta-analyses of stratified depression in Generation Scotland and UK Biobank
Hall LS,
Adams MJ,
Arnau-Soler A,
Clarke TK,
Howard DM,
Zeng Y,
Davies G,
Hagenaars SP,
Maria Fernandez-Pujals A,
Gibson J,
Wigmore EM,
Boutin TS
and 7 more — show all
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Translational psychiatry · 2018 · PMID 29317602 · open access
1 page
Factors associated with sharing e-mail information and mental health survey participation in large population cohorts
Adams MJ,
Hill WD,
Howard DM,
Dashti HS,
Davis KAS,
Campbell A,
Clarke TK,
Deary IJ,
Hayward C,
Porteous D,
Hotopf M,
McIntosh AM
International journal of epidemiology · 2020 · PMID 31263887 · 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.