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Research in Developmental Disabilities
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June 12, 2013
Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome
Waverly Harrell, Shaun Eack, Stephen R Hooper, et al.
Biological Psychiatry
|
May 29, 2012
Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study
Vandana Shashi, Aravindhan Veerapandiyan, Matcheri S Keshavan, et al.
Journal of Genetic Counseling
|
April 3, 2023
Unraveling non-participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors
Allyn McConkie-Rosell, Rebecca C Spillmann, Kelly Schoch, et al.
Journal of Genetic Counseling
|
August 4, 2010
Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling
Vandana Shashi, Matcheri Keshavan, Jessica Kaczorowski, et al.
Psychiatry Research
|
May 22, 2010
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome
Vandana Shashi, Timothy D Howard, Matcheri S Keshavan, et al.
Journal of Medical Genetics
|
May 15, 2012
Clinical application of exome sequencing in undiagnosed genetic conditions
Anna C Need, Vandana Shashi, Yuki Hitomi, et al.
Journal of Genetic Counseling
|
January 26, 2019
Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era
Ellen F Macnamara, Kelly Schoch, Emily Glanton, et al.
Orphanet Journal of Rare Diseases
|
September 4, 2023
Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1
Kelly Schoch, Allyn McConkie-Rosell, Nicole Walley, et al.
European Journal of Human Genetics : EJHG
|
July 6, 2012
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms
Vandana Shashi, Alan Francis, Stephen R Hooper, et al.
Journal of Genetic Counseling
|
January 4, 2018
Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?
Allyn McConkie-Rosell, Stephen R Hooper, Loren D M Pena, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 69) with videos related to
Sort By:
Page
of 7
Research in Developmental Disabilities
|
June 12, 2013
Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome
Waverly Harrell, Shaun Eack, Stephen R Hooper, et al.
Biological Psychiatry
|
May 29, 2012
Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study
Vandana Shashi, Aravindhan Veerapandiyan, Matcheri S Keshavan, et al.
Journal of Genetic Counseling
|
April 3, 2023
Unraveling non-participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors
Allyn McConkie-Rosell, Rebecca C Spillmann, Kelly Schoch, et al.
Journal of Genetic Counseling
|
August 4, 2010
Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling
Vandana Shashi, Matcheri Keshavan, Jessica Kaczorowski, et al.
Psychiatry Research
|
May 22, 2010
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome
Vandana Shashi, Timothy D Howard, Matcheri S Keshavan, et al.
Journal of Medical Genetics
|
May 15, 2012
Clinical application of exome sequencing in undiagnosed genetic conditions
Anna C Need, Vandana Shashi, Yuki Hitomi, et al.
Journal of Genetic Counseling
|
January 26, 2019
Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era
Ellen F Macnamara, Kelly Schoch, Emily Glanton, et al.
Orphanet Journal of Rare Diseases
|
September 4, 2023
Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1
Kelly Schoch, Allyn McConkie-Rosell, Nicole Walley, et al.
European Journal of Human Genetics : EJHG
|
July 6, 2012
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms
Vandana Shashi, Alan Francis, Stephen R Hooper, et al.
Journal of Genetic Counseling
|
January 4, 2018
Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?
Allyn McConkie-Rosell, Stephen R Hooper, Loren D M Pena, et al.
Page
of 7