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Aparna Prasad

Showing results (41-50 of 51) with videos related to

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Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
The Journal of Investigative Dermatology|April 4, 2016
Identification of Gene Mutations and Fusion Genes in Patients with Sézary SyndromeAparna Prasad, Raquel Rabionet, Blanca Espinet, et al.
Journal of Neurodevelopmental Disorders|February 9, 2019
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disordersGregory Costain, Susan Walker, Bob Argiropoulos, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
BMC Genomics|November 8, 2006
A second generation radiation hybrid map to aid the assembly of the bovine genome sequenceOliver C Jann, Jan Aerts, Michelle Jones, et al.
American Journal of Human Genetics|January 3, 2012
Rare deletions at the neurexin 3 locus in autism spectrum disorderAndrea K Vaags, Anath C Lionel, Daisuke Sato, et al.
American Journal of Human Genetics|April 17, 2012
SHANK1 Deletions in Males with Autism Spectrum DisorderDaisuke Sato, Anath C Lionel, Claire S Leblond, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
BMC Genomics|December 26, 2008
A first generation whole genome RH map of the river buffalo with comparison to domestic cattleM Elisabete J Amaral, Jason R Grant, Penny K Riggs, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Neurology. Genetics|February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disordersE Robert Wassman, Karen S Ho, Diana Bertrand, et al.
The Journal of Investigative Dermatology|April 4, 2016
Identification of Gene Mutations and Fusion Genes in Patients with Sézary SyndromeAparna Prasad, Raquel Rabionet, Blanca Espinet, et al.
Journal of Neurodevelopmental Disorders|February 9, 2019
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disordersGregory Costain, Susan Walker, Bob Argiropoulos, et al.
Nature Biotechnology|May 10, 2011
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsDalila Pinto, Katayoon Darvishi, Xinghua Shi, et al.
BMC Genomics|November 8, 2006
A second generation radiation hybrid map to aid the assembly of the bovine genome sequenceOliver C Jann, Jan Aerts, Michelle Jones, et al.
American Journal of Human Genetics|January 3, 2012
Rare deletions at the neurexin 3 locus in autism spectrum disorderAndrea K Vaags, Anath C Lionel, Daisuke Sato, et al.
American Journal of Human Genetics|April 17, 2012
SHANK1 Deletions in Males with Autism Spectrum DisorderDaisuke Sato, Anath C Lionel, Claire S Leblond, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
BMC Genomics|December 26, 2008
A first generation whole genome RH map of the river buffalo with comparison to domestic cattleM Elisabete J Amaral, Jason R Grant, Penny K Riggs, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Pageof 6