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Showing results (661-670 of 915) with videos related to

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Translational Psychiatry|February 6, 2019
Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND NetworkDanielle A Baribeau, Annie Dupuis, Tara A Paton, et al.
Journal of Autism and Developmental Disorders|January 4, 2021
DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental DisordersMichelle T Siu, Sarah J Goodman, Isaac Yellan, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.
Nature Genetics|June 30, 2001
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemiaZ Ma, S W Morris, V Valentine, et al.
Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.
G3 (Bethesda, Md.)|September 19, 2015
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion SyndromeDaniele Merico, Mehdi Zarrei, Gregory Costain, et al.
Brain : a Journal of Neurology|September 11, 2012
Early-onset Lafora body diseaseJulie Turnbull, Jean-Marie Girard, Hannes Lohi, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|May 29, 2020
Neurobiologic Rationale for Treatment of Apathy in Alzheimer's Disease With MethylphenidateChristopher H van Dyck, Amy F T Arnsten, Prasad R Padala, et al.
Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.
Pageof 92

Showing results (661-670 of 915) with videos related to

Sort By:
Pageof 92
Translational Psychiatry|February 6, 2019
Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND NetworkDanielle A Baribeau, Annie Dupuis, Tara A Paton, et al.
Journal of Autism and Developmental Disorders|January 4, 2021
DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental DisordersMichelle T Siu, Sarah J Goodman, Isaac Yellan, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.
Nature Genetics|June 30, 2001
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemiaZ Ma, S W Morris, V Valentine, et al.
Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.
G3 (Bethesda, Md.)|September 19, 2015
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion SyndromeDaniele Merico, Mehdi Zarrei, Gregory Costain, et al.
Brain : a Journal of Neurology|September 11, 2012
Early-onset Lafora body diseaseJulie Turnbull, Jean-Marie Girard, Hannes Lohi, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|May 29, 2020
Neurobiologic Rationale for Treatment of Apathy in Alzheimer's Disease With MethylphenidateChristopher H van Dyck, Amy F T Arnsten, Prasad R Padala, et al.
Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.
Pageof 92