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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.
15 matches for
Adams MJ.
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+
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Meng X,
Navoly G,
Giannakopoulou O,
Levey DF,
Koller D,
Pathak GA,
Koen N,
Lin K,
Adams MJ,
Rentería ME,
Feng Y,
Gaziano JM
and 66 more — show all
Stein DJ,
Zar HJ,
Campbell ML,
van Heel DA,
Trivedi B,
Finer S,
McQuillin A,
Bass N,
Chundru VK,
Martin HC,
Huang QQ,
Valkovskaya M,
Chu CY,
Kanjira S,
Kuo PH,
Chen HC,
Tsai SJ,
Liu YL,
Kendler KS,
Peterson RE,
Cai N,
Fang Y,
Sen S,
Scott LJ,
Burmeister M,
Loos RJF,
Preuss MH,
Actkins KV,
Davis LK,
Uddin M,
Wani AH,
Wildman DE,
Aiello AE,
Ursano RJ,
Kessler RC,
Kanai M,
Okada Y,
Sakaue S,
Rabinowitz JA,
Maher BS,
Uhl G,
Eaton W,
Cruz-Fuentes CS,
Martinez-Levy GA,
Campos AI,
Millwood IY,
Chen Z,
Li L,
Wassertheil-Smoller S,
Jiang Y,
Tian C,
Martin NG,
Mitchell BL,
Byrne EM,
Awasthi S,
Coleman JRI,
Ripke S,
Sofer T,
Walters RG,
McIntosh AM,
Polimanti R,
Dunn EC,
Stein MB,
Gelernter J,
Lewis CM,
Kuchenbaecker K
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
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
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
and 205 more — show all
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe and 1 more consortia
Nature genetics · 2018 · PMID 29700475 · open access
10 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
Minimal phenotyping yields genome-wide association signals of low specificity for major depression
Cai N,
Revez JA,
Adams MJ,
Andlauer TFM,
Breen G,
Byrne EM,
Clarke TK,
Forstner AJ,
Grabe HJ,
Hamilton SP,
Levinson DF,
Lewis CM
and 21 more — show all
Lewis G,
Martin NG,
Milaneschi Y,
Mors O,
Müller-Myhsok B,
Penninx BWJH,
Perlis RH,
Pistis G,
Potash JB,
Potash JB,
Preisig M,
Shi J,
Smoller JW,
Streit F,
Tiemeier H,
Uher R,
Van der Auwera S,
Viktorin A,
Weissman MM,
Kendler KS,
Flint J
MDD Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2020 · PMID 32231276
6 pages
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Blokland GAM,
Grove J,
Chen CY,
Cotsapas C,
Tobet S,
Handa R,
St Clair D,
Lencz T,
Mowry BJ,
Periyasamy S,
Cairns MJ,
Tooney PA
and 118 more — show all
Wu JQ,
Kelly B,
Kirov G,
Sullivan PF,
Corvin A,
Riley BP,
Esko T,
Milani L,
Jönsson EG,
Palotie A,
Ehrenreich H,
Begemann M,
Steixner-Kumar A,
Sham PC,
Iwata N,
Weinberger DR,
Gejman PV,
Sanders AR,
Buxbaum JD,
Rujescu D,
Giegling I,
Konte B,
Hartmann AM,
Bramon E,
Murray RM,
Pato MT,
Lee J,
Melle I,
Molden E,
Ophoff RA,
McQuillin A,
Bass NJ,
Adolfsson R,
Malhotra AK,
Martin NG,
Fullerton JM,
Mitchell PB,
Schofield PR,
Forstner AJ,
Degenhardt F,
Schaupp S,
Comes AL,
Kogevinas M,
Guzman-Parra J,
Reif A,
Streit F,
Sirignano L,
Cichon S,
Grigoroiu-Serbanescu M,
Hauser J,
Lissowska J,
Mayoral F,
Müller-Myhsok B,
Świątkowska B,
Schulze TG,
Nöthen MM,
Rietschel M,
Kelsoe J,
Leboyer M,
Jamain S,
Etain B,
Bellivier F,
Vincent JB,
Alda M,
O'Donovan C,
Cervantes P,
Biernacka JM,
Frye M,
McElroy SL,
Scott LJ,
Stahl EA,
Landén M,
Hamshere ML,
Smeland OB,
Djurovic S,
Vaaler AE,
Andreassen OA,
Baune BT,
Air T,
Preisig M,
Uher R,
Levinson DF,
Weissman MM,
Potash JB,
Shi J,
Knowles JA,
Perlis RH,
Lucae S,
Boomsma DI,
Penninx BWJH,
Hottenga JJ,
de Geus EJC,
Willemsen G,
Milaneschi Y,
Tiemeier H,
Grabe HJ,
Teumer A,
Van der Auwera S,
Völker U,
Hamilton SP,
Magnusson PKE,
Viktorin A,
Mehta D,
Mullins N,
Adams MJ,
Breen G,
McIntosh AM,
Lewis CM,
Hougaard DM,
Nordentoft M,
Mors O,
Mortensen PB,
Werge T,
Als TD,
Børglum AD,
Petryshen TL,
Smoller JW,
Goldstein JM
Schizophrenia Working Group of the Psychiatric Genomics Consortium · Bipolar Disorder Working Group of the Psychiatric Genomics Consortium and 3 more consortia
Biological psychiatry · 2022 · PMID 34099189
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 gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Coleman JRI,
Peyrot WJ,
Purves KL,
Davis KAS,
Rayner C,
Choi SW,
Hübel C,
Gaspar HA,
Kan C,
Van der Auwera S,
Adams MJ,
Lyall DM
and 14 more — show all
Choi KW,
Dunn EC,
Vassos E,
Danese A,
Maughan B,
Grabe HJ,
Lewis CM,
O'Reilly PF,
McIntosh AM,
Smith DJ,
Wray NR,
Hotopf M,
Eley TC,
Breen G
on the behalf of Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Molecular psychiatry · 2020 · PMID 31969693 · 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
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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.
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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.
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Tell us and it is fixed. Names come from the public record and initials are
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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
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keep in step, because the citation lives on the page that makes the claim.