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Publications by Wray, Naomi R.

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Number of items: 4.

Journal article

Zeng, Yanni; Navarro, Pau; Shirali, Masoud; Howard, David M.; Adams, Mark J.; Hall, Lynsey S.; Clarke, Toni-Kim; Thomson, Pippa A.; Smith, Blair H.; Murray, Alison; Padmanabhan, Sandosh; Hayward, Caroline; Boutin, Thibaud; MacIntyre, Donald J.; Lewis, Cathryn M.; Wray, Naomi R.; Mehta, Divya; Penninx, Brenda W. J. H.; Milaneschi, Yuri; Baune, Bernhard T.; Air, Tracy; Hottenga, Jouke-Jan; Mbarek, Hamdi; Castelao, Enrique; Pistis, Giorgio; Schulze, Thomas G.; Streit, Fabian; Forstner, Andreas J.; Byrne, Enda M.; Martin, Nicholas G.; Breen, Gerome; Müller-Myhsok, Bertram; Lucae, Susanne; Kloiber, Stefan; Domenici, Enrico; Deary, Ian J.; Porteous, David J.; Haley, Chris S.; McIntosh, Andrew M. (2017): Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. In: Biological Psychiatry, Vol. 82, No. 5: pp. 312-321

Mace, Aurelien; Tuke, Marcus A.; Deelen, Patrick; Kristiansson, Kati; Mattsson, Hannele; Noukas, Margit; Sapkota, Yadav; Schick, Ursula; Porcu, Eleonora; Rüeger, Sina; McDaid, Aaron F.; Porteous, David; Winkler, Thomas W.; Salvi, Erika; Shrine, Nick; Liu, Xueping; Ang, Wei Q.; Zhang, Weihua; Feitosa, Mary F.; Venturini, Cristina; Most, Peter J. van der; Rosengren, Anders; Wood, Andrew R.; Beaumont, Robin N.; Jones, Samuel E.; Ruth, Katherine S.; Yaghootkar, Hanieh; Tyrrell, Jessica; Havulinna, Aki S.; Boers, Harmen; Mägi, Reedik; Kriebel, Jennifer; Müller-Nurasyid, Martina; Perola, Markus; Nieminen, Markku; Lokki, Marja-Liisa; Kahonen, Mika; Viikari, Jorma S.; Geller, Frank; Lahti, Jari; Palotie, Aarno; Koponen, Päivikki; Lundqvist, Annamari; Rissanen, Harri; Bottinger, Erwin P.; Afaq, Saima; Wojczynski, Mary K.; Lenzini, Petra; Nolte, Ilja M.; Sparso, Thomas; Schupf, Nicole; Christensen, Kaare; Perls, Thomas T.; Newman, Anne B.; Werge, Thomas; Snieder, Harold; Spector, Timothy D.; Chambers, John C.; Koskinen, Seppo; Melbye, Mads; Raitakari, Olli T.; Lehtimäki, Terho; Tobin, Martin D.; Wain, Louise V.; Sinisalo, Juha; Peters, Annette; Meitinger, Thomas; Martin, Nicholas G.; Wray, Naomi R.; Montgomery, Grant W.; Medland, Sarah E.; Swertz, Morris A.; Vartiainen, Erkki; Borodulin, Katja; Männistö, Satu; Murray, Anna; Bochud, Murielle; Jacquemont, Sebastien; Rivadeneira, Fernando; Hansen, Thomas F.; Oldehinkel, Albertine J.; Mangino, Massimo; Province, Michael A.; Deloukas, Panos; Kooner, Jaspal S.; Freathy, Rachel M.; Pennell, Craig; Feenstra, Bjarke; Strachan, David P.; Lettre, Guillaume; Hirschhorn, Joel; Cusi, Daniele; Heid, Iris M.; Hayward, Caroline; Männik, Katrin; Beckmann, Jacques S.; Loos, Ruth J. F.; Nyholt, Dale R.; Metspalu, Andres; Eriksson, Johan G.; Weedon, Michael N.; Salomaa, Veikko; Franke, Lude; Reymond, Alexandre; Frayling, Timothy M.; Kutalik, Zoltan (2017): CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. In: Nature Communications, Vol. 8, 744

Bigdeli, Tim B.; Ripke, Stephan; Bacanu, Silviu-Alin; Lee, Sang Hong; Wray, Naomi R.; Gejman, Pablo V.; Rietschel, Marcella; Cichon, Sven; St. Clair, David; Corvin, Aiden; Kirov, George; McQuillin, Andrew; Gurling, Hugh; Rujescu, Dan; Andreassen, Ole A.; Werge, Thomas; Blackwood, Douglas H. R.; Pato, Carlos N.; Pato, Michele T.; Malhotra, Anil K.; O'Donovan, Michael C.; Kendler, Kenneth S.; Fanous, Ayman H. (2016): Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, Vol. 171, No. 2: pp. 276-289

Hou, Liping; Heilbronner, Urs; Degenhardt, Franziska; Adli, Mazda; Akiyama, Kazufumi; Akula, Nirmala; Ardau, Raffaella; Arias, Barbara; Backlund, Lena; Banzato, Claudio E. M.; Benabarre, Antoni; Bengesser, Susanne; Bhattacharjee, Abesh Kumar; Biernacka, Joanna M.; Birner, Armin; Brichant-Petitjean, Clara; Bui, Elise T.; Cervantes, Pablo; Chen, Guo-Bo; Chen, Hsi-Chung; Chillotti, Caterina; Cichon, Sven; Clark, Scott R.; Colom, Francesc; Cousins, David A.; Cruceanu, Cristiana; Czerski, Piotr M.; Dantas, Clarissa R.; Dayer, Alexandre; Etain, Bruno; Falkai, Peter; Forstner, Andreas J.; Frisen, Louise; Fullerton, Janice M.; Gard, Sebastien; Garnham, Julie S.; Goes, Fernando S.; Grof, Paul; Gruber, Oliver; Hashimoto, Ryota; Hauser, Joanna; Herms, Stefan; Hoffmann, Per; Hofmann, Andrea; Jamain, Stephane; Jimenez, Esther; Kahn, Jean-Pierre; Kassem, Layla; Kittel-Schneider, Sarah; Kliwicki, Sebastian; König, Barbara; Kusumi, Ichiro; Lackner, Nina; Laje, Gonzalo; Landen, Mikael; Lavebratt, Catharina; Leboyer, Marion; Leckband, Susan G.; Lopez Jaramillo, Carlos A.; MacQueen, Glenda; Manchia, Mirko; Martinsson, Lina; Mattheisen, Manuel; McCarthy, Michael J.; McElroy, Susan L.; Mitjans, Marina; Mondimore, Francis M.; Monteleone, Palmiero; Nievergelt, Caroline M.; Noethen, Markus M.; Oesby, Urban; Ozaki, Norio; Perlis, Roy H.; Pfennig, Andrea; Reich-Erkelenz, Daniela; Rouleau, Guy A.; Schofield, Peter R.; Schubert, K. Oliver; Schweizer, Barbara W.; Seemueller, Florian; Severino, Giovanni; Shekhtman, Tatyana; Shilling, Paul D.; Shimoda, Kazutaka; Simhandl, Christian; Slaney, Claire M.; Smoller, Jordan W.; Squassina, Alessio; Stamm, Thomas; Stopkova, Pavla; Tighe, Sarah K.; Tortorella, Alfonso; Turecki, Gustavo; Volkert, Julia; Witt, Stephanie; Wright, Adam; Young, L. Trevor; Zandi, Peter P.; Potash, James B.; DePaulo, J. Raymond; Bauer, Michael; Reininghaus, Eva Z.; Novak, Tomas; Aubry, Jean-Michel; Maj, Mario; Baune, Bernhard T.; Mitchell, Philip B.; Vieta, Eduard; Frye, Mark A.; Rybakowski, Janusz K.; Kuo, Po-Hsiu; Kato, Tadafumi; Grigoroiu-Serbanescu, Maria; Reif, Andreas; Del Zompo, Maria; Bellivier, Frank; Schalling, Martin; Wray, Naomi R.; Kelsoe, John R.; Alda, Martin; Rietschel, Marcella; McMahon, Francis J.; Schulze, Thomas G. (2016): Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. In: Lancet, Vol. 387, No. 10023: pp. 1085-1093

This list was generated on Sun Jun 16 03:03:50 2019 CEST.