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D St Clair

Showing results (101-110 of 114) with videos related to

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Molecular Psychiatry|January 23, 2002
A family-based and case-control association study of the NOTCH4 gene and schizophreniaJ B Fan, J X Tang, N F Gu, et al.
Oncogenesis|January 31, 2017
Inhibition of the integrin/FAK signaling axis and c-Myc synergistically disrupts ovarian cancer malignancyB Xu, J Lefringhouse, Z Liu, et al.
Molecular Psychiatry|January 25, 2014
DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to SullivanD J Porteous, P A Thomson, J K Millar, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 6, 2011
Polygenic dissection of the bipolar phenotypeM L Hamshere, M C O'Donovan, I R Jones, et al.
Molecular Psychiatry|March 5, 2008
DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorderW Hennah, P Thomson, A McQuillin, et al.
The British Journal of Psychiatry : the Journal of Mental Science|July 2, 2009
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic conceptM L Hamshere, E K Green, I R Jones, et al.
Molecular Psychiatry|December 17, 2008
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotypeN Craddock, L Jones, I R Jones, et al.
Neurology|July 10, 2002
Contribution of APOE promoter polymorphisms to Alzheimer's disease riskJ-C Lambert, L Araria-Goumidi, L Myllykangas, et al.
Molecular Psychiatry|November 6, 2013
Common genetic variants on 1p13.2 associate with risk of autismK Xia, H Guo, Z Hu, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Molecular Psychiatry|January 23, 2002
A family-based and case-control association study of the NOTCH4 gene and schizophreniaJ B Fan, J X Tang, N F Gu, et al.
Oncogenesis|January 31, 2017
Inhibition of the integrin/FAK signaling axis and c-Myc synergistically disrupts ovarian cancer malignancyB Xu, J Lefringhouse, Z Liu, et al.
Molecular Psychiatry|January 25, 2014
DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to SullivanD J Porteous, P A Thomson, J K Millar, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 6, 2011
Polygenic dissection of the bipolar phenotypeM L Hamshere, M C O'Donovan, I R Jones, et al.
Molecular Psychiatry|March 5, 2008
DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorderW Hennah, P Thomson, A McQuillin, et al.
The British Journal of Psychiatry : the Journal of Mental Science|July 2, 2009
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic conceptM L Hamshere, E K Green, I R Jones, et al.
Molecular Psychiatry|December 17, 2008
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotypeN Craddock, L Jones, I R Jones, et al.
Neurology|July 10, 2002
Contribution of APOE promoter polymorphisms to Alzheimer's disease riskJ-C Lambert, L Araria-Goumidi, L Myllykangas, et al.
Molecular Psychiatry|November 6, 2013
Common genetic variants on 1p13.2 associate with risk of autismK Xia, H Guo, Z Hu, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Pageof 12