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Examining the Efficacy of a Family Peer Advocate Model for Black and Hispanic Caregivers of Children with Autism Spectrum Disorder

Journal of autism and developmental disorders, 2017-05, Vol.47 (5), p.1314-1322

2017

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Rare structural variation of synapse and neurotransmission genes in autism

Molecular psychiatry, 2012-04, Vol.17 (4), p.402-411

2012

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A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome

Molecular autism, 2021-09, Vol.12 (1), p.62-62, Article 62

2021

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A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome

Molecular autism, 2022-01, Vol.13 (1), p.6-6, Article 6

2022

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Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome

Molecular autism, 2022-04, Vol.13 (1), p.17-17, Article 17

2022

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Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model

Molecular psychiatry, 2013-08, Vol.18 (8), p.889-897

2013

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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

Molecular psychiatry, 2010-09, Vol.15 (9), p.954-968

2010

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Association between a GABRB3 polymorphism and autism

Molecular psychiatry, 2002-01, Vol.7 (3), p.311-316

2002

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Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Molecular psychiatry, 2003-02, Vol.8 (2), p.186-194

2003

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Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene

Molecular psychiatry, 2008-02, Vol.13 (2), p.162-172

2008

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Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19

Molecular psychiatry, 2004-02, Vol.9 (2), p.144-150

2004

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Tau protein abnormalities associated with the progression of alzheimer disease type dementia

Neurobiology of aging, 2007-01, Vol.28 (1), p.1-7

2007

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SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects

Molecular psychiatry, 2008-04, Vol.13 (4), p.385-397

2008

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De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

Molecular psychiatry, 2013-12, Vol.18 (12), p.1315-1323

2013

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BACE (β-secretase) modulates the processing of APLP2 in vivo

Molecular and cellular neuroscience, 2004-04, Vol.25 (4), p.642-649

2004

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Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease

Molecular psychiatry, 2013-06, Vol.18 (6), p.635-636

2013

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Calsenilin Enhances Apoptosis by Altering Endoplasmic Reticulum Calcium Signaling

Molecular and cellular neuroscience, 2002-04, Vol.19 (4), p.552-559

2002

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Generation and Regulation of β‐Amyloid Peptide Variants by Neurons

Journal of neurochemistry, 1998-11, Vol.71 (5), p.1920-1925

1998

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Regulation of Secretion of Alzheimer Amyloid Precursor Protein by the Mitogen‐Activated Protein Kinase Cascade

Journal of neurochemistry, 1998-02, Vol.70 (2), p.524-530

1998

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Biochemical and immunocytochemical characterization of calsenilin in mouse brain

Neuroscience, 2002-01, Vol.114 (1), p.247-263

2002

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A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimerʼs disease and leads to death as early as the age of 28 years

Neuroreport, 1998-01, Vol.9 (2), p.217-221

1998

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The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

Trends in neurosciences (Regular ed.), 2009-07, Vol.32 (7), p.402-412

2009

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The Amyloid Precursor Protein and Its Regulatory Protein, FE65, in Growth Cones and Synapses In Vitro and In Vivo

The Journal of neuroscience, 2003-07, Vol.23 (13), p.5407-5415

2003

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Increased Secretion of the Amino‐Terminal Fragment of Amyloid Precursor Protein in Brains of Rats with a Constitutive Up‐Regulation of Protein Kinase C

Journal of neurochemistry, 1997-06, Vol.68 (6), p.2523-2529

1997

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The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders

Neuron, 2012-12, Vol.76 (6), p.1052-1056

2012

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Examining the Efficacy of a Family Peer Advocate Model for Black and Hispanic Caregivers of Children with Autism Spectrum Disorder

Rare structural variation of synapse and neurotransmission genes in autism

A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome

A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome

Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome

Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

Association between a GABRB3 polymorphism and autism

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19

Tau protein abnormalities associated with the progression of alzheimer disease type dementia

SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects

De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

BACE (β-secretase) modulates the processing of APLP2 in vivo

Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease

Calsenilin Enhances Apoptosis by Altering Endoplasmic Reticulum Calcium Signaling

Generation and Regulation of β‐Amyloid Peptide Variants by Neurons

Regulation of Secretion of Alzheimer Amyloid Precursor Protein by the Mitogen‐Activated Protein Kinase Cascade

Biochemical and immunocytochemical characterization of calsenilin in mouse brain

A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimerʼs disease and leads to death as early as the age of 28 years

The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

The Amyloid Precursor Protein and Its Regulatory Protein, FE65, in Growth Cones and Synapses In Vitro and In Vivo

Increased Secretion of the Amino‐Terminal Fragment of Amyloid Precursor Protein in Brains of Rats with a Constitutive Up‐Regulation of Protein Kinase C

The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders

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