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S LEBLOND

Showing results (41-50 of 94) with videos related to

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American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Scientific Reports|December 20, 2017
Heritability of the melatonin synthesis variability in autism spectrum disordersMarion Benabou, Thomas Rolland, Claire S Leblond, et al.
Neurogenetics|May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALSJay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Genes, Brain, and Behavior|September 20, 2012
Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4E Ey, M Yang, A M Katz, et al.
Gene|April 28, 2015
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patientsPaloma Gonzalez-Perez, Ute Woehlbier, Ru-Ju Chian, et al.
Journal of Applied Genetics|October 5, 2018
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiologySaida Lahbib, Claire S Leblond, Mariem Hamza, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structuresAnna Maruani, Guillaume Huguet, Anita Beggiato, et al.
European Journal of Medical Genetics|February 23, 2023
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndromeAline Vitrac, Claire S Leblond, Thomas Rolland, et al.
Annual Review of Genetics|November 25, 2024
A Genetic Bridge Between Medicine and Neurodiversity for AutismClaire S Leblond, Thomas Rolland, Eli Barthome, et al.
Acta Neuropathologica Communications|February 27, 2016
Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTDMichael Niblock, Bradley N Smith, Youn-Bok Lee, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Scientific Reports|December 20, 2017
Heritability of the melatonin synthesis variability in autism spectrum disordersMarion Benabou, Thomas Rolland, Claire S Leblond, et al.
Neurogenetics|May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALSJay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Genes, Brain, and Behavior|September 20, 2012
Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4E Ey, M Yang, A M Katz, et al.
Gene|April 28, 2015
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patientsPaloma Gonzalez-Perez, Ute Woehlbier, Ru-Ju Chian, et al.
Journal of Applied Genetics|October 5, 2018
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiologySaida Lahbib, Claire S Leblond, Mariem Hamza, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structuresAnna Maruani, Guillaume Huguet, Anita Beggiato, et al.
European Journal of Medical Genetics|February 23, 2023
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndromeAline Vitrac, Claire S Leblond, Thomas Rolland, et al.
Annual Review of Genetics|November 25, 2024
A Genetic Bridge Between Medicine and Neurodiversity for AutismClaire S Leblond, Thomas Rolland, Eli Barthome, et al.
Acta Neuropathologica Communications|February 27, 2016
Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTDMichael Niblock, Bradley N Smith, Youn-Bok Lee, et al.
Pageof 10