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Andrea Shugar

Showing results (1-10 of 22) with videos related to

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Journal of Genetic Counseling|November 29, 2016
Teaching Genetic Counseling Skills: Incorporating a Genetic Counseling Adaptation Continuum Model to Address Psychosocial ComplexityAndrea Shugar
The Clinical Teacher|February 8, 2022
Genetic simulation for high-stakes conversationsMaha Saleh, Andrea Shugar, Alison Dodds, et al.
Pediatric Dermatology|June 30, 2020
A novel ENPP1 mutation identified in a multigenerational family affected by Cole diseaseNiña Gabaton, Peter Kannu, Elena Pope, et al.
Journal of Genetic Counseling|May 10, 2026
To refer or not to refer? Exploring the cognitive process of genetic counselors' decision to refer a patient to another professionalR Beth Dugan, Kestutis Micke, Andrea Shugar, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotypeGregory Costain, Andrea Shugar, Pradeep Krishnan, et al.
Journal of Genetic Counseling|June 25, 2011
Personality traits associated with genetic counselor compassion fatigue: the roles of dispositional optimism and locus of controlMarie C Injeyan, Cheryl Shuman, Andrea Shugar, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|February 26, 2016
Internet Safety Issues for Adolescents and Adults with Intellectual DisabilitiesPetra C M Buijs, Erik Boot, Andrea Shugar, et al.
PEC Innovation|May 22, 2023
Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model conditionSimina Bogatan, Andrea Shugar, Syed Wasim, et al.
Journal of Cutaneous Medicine and Surgery|April 28, 2017
Mosaic Neurofibromatosis Type 1 in Children: A Single-Institution ExperienceIrene Lara-Corrales, Mitra Moazzami, Maria Teresa García-Romero, et al.
Pediatric Dermatology|May 13, 2026
Bridging the Diagnostic Gap in Neurofibromatosis Type 1: When to Consider NF1 cDNA SequencingBrent J Doolan, Minu J Chiramel, Mitch Hendry, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Genetic Counseling|November 29, 2016
Teaching Genetic Counseling Skills: Incorporating a Genetic Counseling Adaptation Continuum Model to Address Psychosocial ComplexityAndrea Shugar
The Clinical Teacher|February 8, 2022
Genetic simulation for high-stakes conversationsMaha Saleh, Andrea Shugar, Alison Dodds, et al.
Pediatric Dermatology|June 30, 2020
A novel ENPP1 mutation identified in a multigenerational family affected by Cole diseaseNiña Gabaton, Peter Kannu, Elena Pope, et al.
Journal of Genetic Counseling|May 10, 2026
To refer or not to refer? Exploring the cognitive process of genetic counselors' decision to refer a patient to another professionalR Beth Dugan, Kestutis Micke, Andrea Shugar, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotypeGregory Costain, Andrea Shugar, Pradeep Krishnan, et al.
Journal of Genetic Counseling|June 25, 2011
Personality traits associated with genetic counselor compassion fatigue: the roles of dispositional optimism and locus of controlMarie C Injeyan, Cheryl Shuman, Andrea Shugar, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|February 26, 2016
Internet Safety Issues for Adolescents and Adults with Intellectual DisabilitiesPetra C M Buijs, Erik Boot, Andrea Shugar, et al.
PEC Innovation|May 22, 2023
Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model conditionSimina Bogatan, Andrea Shugar, Syed Wasim, et al.
Journal of Cutaneous Medicine and Surgery|April 28, 2017
Mosaic Neurofibromatosis Type 1 in Children: A Single-Institution ExperienceIrene Lara-Corrales, Mitra Moazzami, Maria Teresa García-Romero, et al.
Pediatric Dermatology|May 13, 2026
Bridging the Diagnostic Gap in Neurofibromatosis Type 1: When to Consider NF1 cDNA SequencingBrent J Doolan, Minu J Chiramel, Mitch Hendry, et al.
Pageof 3