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Ellen Hanson

Showing results (31-40 of 43) with videos related to

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Translational Psychiatry|January 22, 2019
Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Plos One|December 11, 2012
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disordersSek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variantRaphael Bernier, Kyle J Steinman, Beau Reilly, et al.
Molecular Genetics and Metabolism|March 7, 2024
Consensus guidelines for the diagnosis and management of succinic semialdehyde dehydrogenase deficiencyItay Tokatly Latzer, Mariarita Bertoldi, Nenad Blau, et al.
Biological Psychiatry|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.
Biological Psychiatry|January 9, 2016
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and InhibitionLoyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, et al.
The Journal of Clinical Investigation|June 30, 2026
Astrocytes contribute to olanzapine-mediated reversal of Kleefstra Syndrome-associated neurodevelopmental regressionKarlijn Vermeulen-Kalk, Shan Wang, Joost Kummeling, et al.
Archives of General Psychiatry|November 9, 2011
A multisite study of the clinical diagnosis of different autism spectrum disordersCatherine Lord, Eva Petkova, Vanessa Hus, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Translational Psychiatry|January 22, 2019
Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Plos One|December 11, 2012
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disordersSek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variantRaphael Bernier, Kyle J Steinman, Beau Reilly, et al.
Molecular Genetics and Metabolism|March 7, 2024
Consensus guidelines for the diagnosis and management of succinic semialdehyde dehydrogenase deficiencyItay Tokatly Latzer, Mariarita Bertoldi, Nenad Blau, et al.
Biological Psychiatry|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.
Biological Psychiatry|January 9, 2016
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and InhibitionLoyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, et al.
The Journal of Clinical Investigation|June 30, 2026
Astrocytes contribute to olanzapine-mediated reversal of Kleefstra Syndrome-associated neurodevelopmental regressionKarlijn Vermeulen-Kalk, Shan Wang, Joost Kummeling, et al.
Archives of General Psychiatry|November 9, 2011
A multisite study of the clinical diagnosis of different autism spectrum disordersCatherine Lord, Eva Petkova, Vanessa Hus, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Pageof 5