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Andrea L Rideout

Showing results (1-10 of 18) with videos related to

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Journal of Geriatric Psychiatry and Neurology|August 7, 2023
Atypical Neuropsychiatric Presentation of FTD-ALS Caused by a Pathogenic Repeat Expansion in <i>C9orf72</i>: A Case ReportMarissa A LeBlanc, Amy Gough, Andrea L Rideout, et al.
The Medical Clinics of North America|October 5, 2019
Genetics and Precision Medicine: Heritable Thoracic Aortic DiseaseErin Demo, Christina Rigelsky, Andrea L Rideout, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 15, 2019
A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrixStylianos Z Karoulias, Aude Beyens, Zerina Balic, et al.
Journal of Genetic Counseling|January 31, 2008
Interactive genetic counseling role-play: a novel educational strategy for family physiciansSean M Blaine, June C Carroll, Andrea L Rideout, et al.
Canadian Family Physician Medecin De Famille Canadien|December 17, 2009
Genetics: schizophreniaAndrea L Rideout, June C Carroll, Sean M Blaine, et al.
American Journal of Human Genetics|July 7, 2009
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2Duane L Guernsey, Haiyan Jiang, Susan C Evans, et al.
Plos Genetics|September 25, 2010
Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth diseaseDuane L Guernsey, Haiyan Jiang, Karen Bedard, et al.
European Journal of Psychotraumatology|May 23, 2024
The mental health and traumatic experiences of mothers of children with 22q11DSAlexandra Finless, Andrea L Rideout, Ting Xiong, et al.
Orphanet Journal of Rare Diseases|August 18, 2025
Evaluating the relationship between caregiver depression, social support, and children's internalizing and externalizing symptoms in families affected by 22q11.2 deletion syndromeHolly Carbyn, Abiaz Hossain, Raquel L Dias, et al.
American Journal of Medical Genetics. Part A|November 19, 2013
Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patientsShimul Chowdhury, Anne M Bandholz, Sandhya Parkash, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Geriatric Psychiatry and Neurology|August 7, 2023
Atypical Neuropsychiatric Presentation of FTD-ALS Caused by a Pathogenic Repeat Expansion in <i>C9orf72</i>: A Case ReportMarissa A LeBlanc, Amy Gough, Andrea L Rideout, et al.
The Medical Clinics of North America|October 5, 2019
Genetics and Precision Medicine: Heritable Thoracic Aortic DiseaseErin Demo, Christina Rigelsky, Andrea L Rideout, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 15, 2019
A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrixStylianos Z Karoulias, Aude Beyens, Zerina Balic, et al.
Journal of Genetic Counseling|January 31, 2008
Interactive genetic counseling role-play: a novel educational strategy for family physiciansSean M Blaine, June C Carroll, Andrea L Rideout, et al.
Canadian Family Physician Medecin De Famille Canadien|December 17, 2009
Genetics: schizophreniaAndrea L Rideout, June C Carroll, Sean M Blaine, et al.
American Journal of Human Genetics|July 7, 2009
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2Duane L Guernsey, Haiyan Jiang, Susan C Evans, et al.
Plos Genetics|September 25, 2010
Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth diseaseDuane L Guernsey, Haiyan Jiang, Karen Bedard, et al.
European Journal of Psychotraumatology|May 23, 2024
The mental health and traumatic experiences of mothers of children with 22q11DSAlexandra Finless, Andrea L Rideout, Ting Xiong, et al.
Orphanet Journal of Rare Diseases|August 18, 2025
Evaluating the relationship between caregiver depression, social support, and children's internalizing and externalizing symptoms in families affected by 22q11.2 deletion syndromeHolly Carbyn, Abiaz Hossain, Raquel L Dias, et al.
American Journal of Medical Genetics. Part A|November 19, 2013
Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patientsShimul Chowdhury, Anne M Bandholz, Sandhya Parkash, et al.
Pageof 2