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Ann Swillen

Showing results (81-90 of 98) with videos related to

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American Journal of Human Genetics|April 21, 2015
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion SyndromeElisabeth E Mlynarski, Molly B Sheridan, Michael Xie, et al.
JAMA Psychiatry|February 26, 2015
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndromeJacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 30, 2021
A normative chart for cognitive development in a genetically selected populationAnia M Fiksinski, Carrie E Bearden, Anne S Bassett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
Molecular Psychiatry|July 24, 2024
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplicationsRuben C Gur, Carrie E Bearden, Sebastien Jacquemont, et al.
The American Journal of Psychiatry|March 1, 2014
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion SyndromeMaude Schneider, Martin Debbané, Anne S Bassett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndromeSólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjectsYingjie Zhao, Tingwei Guo, Ania Fiksinski, et al.
Nature Medicine|November 10, 2020
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndromeRobert W Davies, Ania M Fiksinski, Elemi J Breetvelt, et al.
The American Journal of Psychiatry|July 29, 2017
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeAnne S Bassett, Chelsea Lowther, Daniele Merico, et al.
Pageof 10

Showing results (81-90 of 98) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|April 21, 2015
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion SyndromeElisabeth E Mlynarski, Molly B Sheridan, Michael Xie, et al.
JAMA Psychiatry|February 26, 2015
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndromeJacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 30, 2021
A normative chart for cognitive development in a genetically selected populationAnia M Fiksinski, Carrie E Bearden, Anne S Bassett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
Molecular Psychiatry|July 24, 2024
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplicationsRuben C Gur, Carrie E Bearden, Sebastien Jacquemont, et al.
The American Journal of Psychiatry|March 1, 2014
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion SyndromeMaude Schneider, Martin Debbané, Anne S Bassett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndromeSólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjectsYingjie Zhao, Tingwei Guo, Ania Fiksinski, et al.
Nature Medicine|November 10, 2020
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndromeRobert W Davies, Ania M Fiksinski, Elemi J Breetvelt, et al.
The American Journal of Psychiatry|July 29, 2017
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeAnne S Bassett, Chelsea Lowther, Daniele Merico, et al.
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