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Vitamin D status in children with a psychiatric diagnosis, autism spectrum disorders, or internalizing disorders

Frontiers in psychiatry, 2022-09, Vol.13, p.958556-958556

2022

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Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome

Translational psychiatry, 2022-03, Vol.12 (1), p.97-97, Article 97

2022

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Challenging behavior in children and adolescents with Dravet syndrome: Exploring the lived experiences of parents

Epilepsy & behavior, 2023-01, Vol.138, p.108978-108978, Article 108978

2023

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Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2024-03, Vol.195 (2), p.e32956-n/a

2024

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Neurobiological perspective of 22q11.2 deletion syndrome

The Lancet. Psychiatry, 2019-11, Vol.6 (11), p.951-960

2019

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Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes

Epilepsy & behavior, 2024-05, Vol.154, p.109726-109726, Article 109726

2024

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The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?

Psychiatric genetics, 2024-04

2024

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AMPT-induced monoamine depletion in humans: evaluation of two alternative [123I]IBZM SPECT procedures

European journal of nuclear medicine and molecular imaging, 2008-07, Vol.35 (7), p.1350-1356

2008

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A normative chart for cognitive development in a genetically selected population

Neuropsychopharmacology (New York, N.Y.), 2022-06, Vol.47 (7), p.1379-1386

2022

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Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings

Behavioral and brain functions, 2007-04, Vol.3 (1), p.19-19

2007

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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins

Human molecular genetics, 2019-11, Vol.28 (22), p.3724-3733

2019

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Intellectual and Behavioral Phenotypes of Smith–Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant

Genes, 2023-07, Vol.14 (8), p.1514

2023

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Quality of life in SCN1A-related seizure disorders across the lifespan

Brain communications, 2024, Vol.6 (5), p.fcae285

2024

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Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review

Movement disorders clinical practice (Hoboken, N.J.), 2023-01, Vol.10 (1), p.17-31

2023

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COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome

Synapse (New York, N.Y.), 2011-09, Vol.65 (9), p.967-970

2011

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The effect of Ecstasy on memory is moderated by a functional polymorphism in the cathechol-O-methyltransferase (COMT) gene

European neuropsychopharmacology, 2009-02, Vol.19 (2), p.116-124

2009

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Intellectual and Behavioral Phenotypes of Smith–Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic IRAI1/I Variant

Genes, 2023-07, Vol.14 (8)

2023

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Concerns about genetic risk testing for opioid use disorder

The Lancet. Psychiatry, 2024-10

2024

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COMT Val 158 met genotype and striatal D 2/3 receptor binding in adults with 22q11 deletion syndrome

Synapse (New York, N.Y.), 2011-09, Vol.65 (9), p.967-970

2011

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COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome

Synapse (New York, N.Y.), 2011-09, Vol.65 (9), p.967-970

2011

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Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

Current psychiatry reports, 2021-03, Vol.23 (3), p.13-13, Article 13

2021

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Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology

The American journal of psychiatry, 2022-03, Vol.179 (3), p.189-203

2022

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White Matter Brain Structure in Asperger’s Syndrome

Comprehensive Guide to Autism, p.1905-1927

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Vitamin D status in children with a psychiatric diagnosis, autism spectrum disorders, or internalizing disorders

Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome

Challenging behavior in children and adolescents with Dravet syndrome: Exploring the lived experiences of parents

Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review

Neurobiological perspective of 22q11.2 deletion syndrome

Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes

The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?

AMPT-induced monoamine depletion in humans: evaluation of two alternative [123I]IBZM SPECT procedures

A normative chart for cognitive development in a genetically selected population

Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings

Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins

Intellectual and Behavioral Phenotypes of Smith–Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant

Quality of life in SCN1A-related seizure disorders across the lifespan

Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review

COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome

The effect of Ecstasy on memory is moderated by a functional polymorphism in the cathechol-O-methyltransferase (COMT) gene

Intellectual and Behavioral Phenotypes of Smith–Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic IRAI1/I Variant

Concerns about genetic risk testing for opioid use disorder

COMT Val 158 met genotype and striatal D 2/3 receptor binding in adults with 22q11 deletion syndrome

COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology

White Matter Brain Structure in Asperger’s Syndrome

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