Now showing items 1-3 of 3

    • Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression 

      Schosser, Alexandra; Butler, Amy W; Ising, Marcus; Perroud, Nader; Uher, Rudolf; Ng, Mandy Y; Cohen-Woods, Sarah; Craddock, Nick; Owen, Michael J; Korszun, Ania; Jones, Lisa; Jones, Ian; Gill, Michael; Rice, John P; Maier, Wolfgang; Mors, Ole; Rietschel, Marcella; Lucae, Susanne; Binder, Elisabeth B; Preisig, Martin; Perry, Julia; Tozzi, Federica; Muglia, Pierandrea; Aitchison, Katherine J; Breen, Gerome; Craig, Ian W; Farmer, Anne E; Müller-Myhsok, Bertram; McGuffin, Peter W; Lewis, Cathryn M (2011-07-05)
      Background: Suicidal behaviour can be conceptualised as a continuum from suicidal ideation, to suicidal attempts to completed suicide. In this study we identify genes contributing to suicidal behaviour in the depression ...
    • Modulatory effects of brain-derived neurotrophic factor Val66Met polymorphism on prefrontal regions in major depressive disorder 

      Legge, Rebecca MacGregor; Sendi, Shahbaz; Cole, James H; Cohen-Woods, Sarah; Costafreda, Sergi G; Simmons, Andrew; Farmer, Anne E; Aitchison, Katherine J; McGuffin, Peter W; Fu, Cynthia H Y (Royal College of Psychiatrists, 2015-05)
      Background Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism contributes to the development of depression (major depressive disorder, MDD), but it is unclear whether neural effects observed in healthy individuals ...
    • Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder 

      Rucker, James J H; Tansey, Katherine E; Rivera, Margarita; Pinto, Dalila; Cohen-Woods, Sarah; Uher, Rudolf; Aitchison, Katherine J; Craddock, Nick; Owen, Michael J; Jones, Lisa; Jones, Ian; Korszun, Ania; Barnes, Michael R; Preisig, Martin; Mors, Ole; Maier, Wolfgang; Rice, John P; Rietschel, Marcella; Holsboer, Florian; Farmer, Anne E; Craig, Ian W; Scherer, Stephen W; Scherer, Peter; Breen, Gerome (Elsevier, 15-02-20)
      Background Defining the molecular genomic basis of the likelihood of developing depressive disorder is a considerable challenge. We previously associated rare, exonic deletion copy number variants (CNV) with recurrent ...