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Alison McInnes

Showing results (21-30 of 34) with videos related to

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Journal of Neuroscience Research|October 9, 2007
Developmental expression profile of quaking, a candidate gene for schizophrenia, and its target genes in human prefrontal cortex and hippocampus shows regional specificityTara L Lauriat, Lily Shiue, Vahram Haroutunian, et al.
Autism Research : Official Journal of the International Society for Autism Research|February 18, 2011
Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactionsTakeshi Sakurai, Nathan P Dorr, Nagahide Takahashi, et al.
BMC Psychiatry|March 23, 2005
A genetic study of autism in Costa Rica: multiple variables affecting IQ scores observed in a preliminary sample of autistic casesL Alison McInnes, Patricia Jiménez González, Elina R Manghi, et al.
Psychotherapy and Psychosomatics|January 26, 2016
A Randomized Controlled Trial of Mindfulness-Based Cognitive Therapy for Treatment-Resistant DepressionStuart J Eisendrath, Erin Gillung, Kevin L Delucchi, et al.
Brain Research|October 3, 2006
Characterization of KIAA0513, a novel signaling molecule that interacts with modulators of neuroplasticity, apoptosis, and the cytoskeletonTara L Lauriat, Stella Dracheva, Joachim Kremerskothen, et al.
Journal of Affective Disorders|May 18, 2023
The effects of ketamine on symptoms of depression and anxiety in real-world care settings: A retrospective controlled analysisTuuli M Hietamies, L Alison McInnes, Andrew J Klise, et al.
Molecular Autism|August 4, 2010
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical regionL Alison McInnes, Alisa Nakamine, Marion Pilorge, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33Kyung Sue Hong, L Alison McInnes, Susan K Service, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
Duplication of 17(p11.2p11.2) in a male child with autism and severe language delayAlisa Nakamine, Leonid Ouchanov, Patricia Jiménez, et al.
Journal of Medical Genetics|September 15, 2006
An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autismLisa Edelmann, Aaron Prosnitz, Sherly Pardo, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Journal of Neuroscience Research|October 9, 2007
Developmental expression profile of quaking, a candidate gene for schizophrenia, and its target genes in human prefrontal cortex and hippocampus shows regional specificityTara L Lauriat, Lily Shiue, Vahram Haroutunian, et al.
Autism Research : Official Journal of the International Society for Autism Research|February 18, 2011
Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactionsTakeshi Sakurai, Nathan P Dorr, Nagahide Takahashi, et al.
BMC Psychiatry|March 23, 2005
A genetic study of autism in Costa Rica: multiple variables affecting IQ scores observed in a preliminary sample of autistic casesL Alison McInnes, Patricia Jiménez González, Elina R Manghi, et al.
Psychotherapy and Psychosomatics|January 26, 2016
A Randomized Controlled Trial of Mindfulness-Based Cognitive Therapy for Treatment-Resistant DepressionStuart J Eisendrath, Erin Gillung, Kevin L Delucchi, et al.
Brain Research|October 3, 2006
Characterization of KIAA0513, a novel signaling molecule that interacts with modulators of neuroplasticity, apoptosis, and the cytoskeletonTara L Lauriat, Stella Dracheva, Joachim Kremerskothen, et al.
Journal of Affective Disorders|May 18, 2023
The effects of ketamine on symptoms of depression and anxiety in real-world care settings: A retrospective controlled analysisTuuli M Hietamies, L Alison McInnes, Andrew J Klise, et al.
Molecular Autism|August 4, 2010
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical regionL Alison McInnes, Alisa Nakamine, Marion Pilorge, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33Kyung Sue Hong, L Alison McInnes, Susan K Service, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
Duplication of 17(p11.2p11.2) in a male child with autism and severe language delayAlisa Nakamine, Leonid Ouchanov, Patricia Jiménez, et al.
Journal of Medical Genetics|September 15, 2006
An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autismLisa Edelmann, Aaron Prosnitz, Sherly Pardo, et al.
Pageof 4