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D W Morris

Showing results (51-60 of 73) with videos related to

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Psychological Medicine|January 10, 2018
Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activationG Donohoe, J Holland, D Mothersill, et al.
Allergy|May 24, 2018
Esophageal IgG4 levels correlate with histopathologic and transcriptomic features in eosinophilic esophagitisC E Rosenberg, M K Mingler, J M Caldwell, et al.
Translational Psychiatry|January 16, 2014
Effects of ZNF804A on auditory P300 response in schizophreniaT O'Donoghue, D W Morris, C Fahey, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|May 1, 2010
BDNF Val66Met polymorphism is associated with aggressive behavior in schizophreniaG Spalletta, D W Morris, F Angelucci, et al.
Molecular Psychiatry|October 16, 2013
Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disordersE M Kenny, P Cormican, S Furlong, et al.
Neuroscience Letters|September 18, 2012
Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137E Cummings, G Donohoe, A Hargreaves, et al.
Translational Psychiatry|January 25, 2017
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controlsD Cosgrove, D Harold, O Mothersill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 12, 2007
Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sampleA Corvin, K A McGhee, K Murphy, et al.
Human Molecular Genetics|April 6, 2000
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15qD W Morris, L Robinson, D Turic, et al.
Molecular Psychiatry|April 30, 2014
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disabilityS E McCarthy, J Gillis, M Kramer, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Psychological Medicine|January 10, 2018
Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activationG Donohoe, J Holland, D Mothersill, et al.
Allergy|May 24, 2018
Esophageal IgG4 levels correlate with histopathologic and transcriptomic features in eosinophilic esophagitisC E Rosenberg, M K Mingler, J M Caldwell, et al.
Translational Psychiatry|January 16, 2014
Effects of ZNF804A on auditory P300 response in schizophreniaT O'Donoghue, D W Morris, C Fahey, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|May 1, 2010
BDNF Val66Met polymorphism is associated with aggressive behavior in schizophreniaG Spalletta, D W Morris, F Angelucci, et al.
Molecular Psychiatry|October 16, 2013
Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disordersE M Kenny, P Cormican, S Furlong, et al.
Neuroscience Letters|September 18, 2012
Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137E Cummings, G Donohoe, A Hargreaves, et al.
Translational Psychiatry|January 25, 2017
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controlsD Cosgrove, D Harold, O Mothersill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 12, 2007
Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sampleA Corvin, K A McGhee, K Murphy, et al.
Human Molecular Genetics|April 6, 2000
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15qD W Morris, L Robinson, D Turic, et al.
Molecular Psychiatry|April 30, 2014
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disabilityS E McCarthy, J Gillis, M Kramer, et al.
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