Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Y. Takarae

Catechol-O-Methyltransferase Polymorphism Modulates Cognitive Control in Children With Chromosome 22q11.2 Deletion Syndrome

Cognitive, Affective and Behavioral Neuroscience

Behavioral Neuroscience

Cognitive Neuroscience

English

Related publications

Cognitive Correlates of a Functional COMT Polymorphism in Children With 22q11.2 Deletion Syndrome

Clinical Genetics

English

A Multilevel Analysis of Cognitive Dysfunction and Psychopathology Associated With Chromosome 22q11.2 Deletion Syndrome in Children

Development and Psychopathology

Educational Psychology

English

COMT and Anxiety and Cognition in Children With Chromosome 22q11.2 Deletion Syndrome

Psychiatry Research

Biological Psychiatry

English

Sclerocornea Associated With the Chromosome 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A

English

Atypical Development of the Executive Attention Network in Children With Chromosome 22q11.2 Deletion Syndrome

Journal of Neurodevelopmental Disorders

Cognitive Neuroscience

Forensic Medicine

English

Catechol-O-Methyltransferase Polymorphism in Women With Uterine Leiomyoma and Adenomyosis

Vestnik of Saint Petersburg University. Medicine

English

Effects of a Functional COMT Polymorphism on Prefrontal Cognitive Function in Patients With 22q11.2 Deletion Syndrome

American Journal of Psychiatry

English

Language Skills in Children With Velocardiofacial Syndrome (Deletion 22q11.2)

Journal of Pediatrics

English

How Might Stress Contribute to Increased Risk for Schizophrenia in Children With Chromosome 22q11.2 Deletion Syndrome?

Journal of Neurodevelopmental Disorders

Cognitive Neuroscience

Forensic Medicine

English