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Michael Gill

Showing results (151-160 of 329) with videos related to

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Journal of Attention Disorders|August 11, 2016
Childhood-Diagnosed ADHD, Symptom Progression, and Reversal Learning in AdulthoodHazel McCarthy, Jessica Stanley, Richard Piech, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|May 16, 2015
Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorderJanette Tong, Leigh-Anne McKinley, Tarrant D R Cummins, et al.
British Journal of Cancer|May 25, 2016
Are there biological differences between screen-detected and interval colorectal cancers in the English Bowel Cancer Screening Programme?Elizabeth Walsh, Colin J Rees, Michael Gill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2008
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studiesRichard J L Anney, Elaine Kenny, Colm T O'Dushlaine, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2009
Association of the alpha4 integrin subunit gene (ITGA4) with autismCatarina Correia, Ana M Coutinho, Joana Almeida, et al.
Plos One|December 2, 2011
Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathologyAnnette E Rünker, Colm O'Tuathaigh, Mark Dunleavy, et al.
Neurobiology of Aging|January 14, 2014
Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sampleCiara Fahey, Susan Byrne, Russell McLaughlin, et al.
Neuroscience Letters|March 23, 2010
Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studiesKatherine E Tansey, Keeley J Brookes, Matthew J Hill, et al.
Schizophrenia Research|June 14, 2005
Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPsKevin A McGhee, Derek W Morris, Siobhan Schwaiger, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 30, 2012
No evidence that common genetic risk variation is shared between schizophrenia and autismJacob A S Vorstman, Richard J L Anney, Eske M Derks, et al.
Pageof 33

Showing results (151-160 of 329) with videos related to

Sort By:
Pageof 33
Journal of Attention Disorders|August 11, 2016
Childhood-Diagnosed ADHD, Symptom Progression, and Reversal Learning in AdulthoodHazel McCarthy, Jessica Stanley, Richard Piech, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|May 16, 2015
Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorderJanette Tong, Leigh-Anne McKinley, Tarrant D R Cummins, et al.
British Journal of Cancer|May 25, 2016
Are there biological differences between screen-detected and interval colorectal cancers in the English Bowel Cancer Screening Programme?Elizabeth Walsh, Colin J Rees, Michael Gill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2008
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studiesRichard J L Anney, Elaine Kenny, Colm T O'Dushlaine, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2009
Association of the alpha4 integrin subunit gene (ITGA4) with autismCatarina Correia, Ana M Coutinho, Joana Almeida, et al.
Plos One|December 2, 2011
Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathologyAnnette E Rünker, Colm O'Tuathaigh, Mark Dunleavy, et al.
Neurobiology of Aging|January 14, 2014
Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sampleCiara Fahey, Susan Byrne, Russell McLaughlin, et al.
Neuroscience Letters|March 23, 2010
Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studiesKatherine E Tansey, Keeley J Brookes, Matthew J Hill, et al.
Schizophrenia Research|June 14, 2005
Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPsKevin A McGhee, Derek W Morris, Siobhan Schwaiger, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 30, 2012
No evidence that common genetic risk variation is shared between schizophrenia and autismJacob A S Vorstman, Richard J L Anney, Eske M Derks, et al.
Pageof 33