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6 matches for
Preisig M.
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
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
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 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
Meta-analysis of genome-wide association studies of anxiety disorders
Otowa T,
Hek K,
Lee M,
Byrne EM,
Mirza SS,
Nivard MG,
Bigdeli T,
Aggen SH,
Adkins D,
Wolen A,
Fanous A,
Keller MC
and 35 more — show all
Castelao E,
Kutalik Z,
Van der Auwera S,
Homuth G,
Nauck M,
Teumer A,
Milaneschi Y,
Hottenga JJ,
Direk N,
Hofman A,
Uitterlinden A,
Mulder CL,
Henders AK,
Medland SE,
Gordon S,
Heath AC,
Madden PA,
Pergadia ML,
van der Most PJ,
Nolte IM,
van Oort FV,
Hartman CA,
Oldehinkel AJ,
Preisig M,
Grabe HJ,
Middeldorp CM,
Penninx BW,
Boomsma D,
Martin NG,
Montgomery G,
Maher BS,
van den Oord EJ,
Wray NR,
Tiemeier H,
Hettema JM
Molecular psychiatry · 2016 · PMID 26754954 · open access
2 pages
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Power RA,
Tansey KE,
Buttenschøn HN,
Cohen-Woods S,
Bigdeli T,
Hall LS,
Kutalik Z,
Lee SH,
Ripke S,
Steinberg S,
Teumer A,
Viktorin A
and 64 more — show all
Wray NR,
Arolt V,
Baune BT,
Boomsma DI,
Børglum AD,
Byrne EM,
Castelao E,
Craddock N,
Craig IW,
Dannlowski U,
Deary IJ,
Degenhardt F,
Forstner AJ,
Gordon SD,
Grabe HJ,
Grove J,
Hamilton SP,
Hayward C,
Heath AC,
Hocking LJ,
Homuth G,
Hottenga JJ,
Kloiber S,
Krogh J,
Landén M,
Lang M,
Levinson DF,
Lichtenstein P,
Lucae S,
MacIntyre DJ,
Madden P,
Magnusson PKE,
Martin NG,
McIntosh AM,
Middeldorp CM,
Milaneschi Y,
Montgomery GW,
Mors O,
Müller-Myhsok B,
Nyholt DR,
Oskarsson H,
Owen MJ,
Padmanabhan S,
Penninx BWJH,
Pergadia ML,
Porteous DJ,
Potash JB,
Preisig M,
Rivera M,
Shi J,
Shyn SI,
Sigurdsson E,
Smit JH,
Smith BH,
Stefansson H,
Stefansson K,
Strohmaier J,
Sullivan PF,
Thomson P,
Thorgeirsson TE,
Van der Auwera S,
Weissman MM,
Breen G,
Lewis CM
CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium
Biological psychiatry · 2017 · PMID 27519822 · open access
1 page
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Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
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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
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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?
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