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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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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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Sodium channels SCN1A, SCN2A and SCN3A in familial autism

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

2003

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Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline

JAMA : the journal of the American Medical Association, 2000-03, Vol.283 (12), p.1571

2000

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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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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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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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Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test

American journal of human genetics, 1996-09, Vol.59 (3), p.644-652

1996

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Evidence for a Susceptibility Gene for Autism on Chromosome 2 and for Genetic Heterogeneity

American journal of human genetics, 2001-06, Vol.68 (6), p.1514-1520

2001

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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

Volltextzugriff (PDF)

Molecular and cellular evidence for an oligodendrocyte abnormality in schizophrenia

Neurochemical research, 2002-10, Vol.27 (10), p.1193-1200

2002

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Novel neuritic clusters with accumulations of amyloid precursor protein and amyloid precursor-like protein 2 immunoreactivity in brain regions damaged by thiamine deficiency

The American journal of pathology, 1996-09, Vol.149 (3), p.1063-1071

1996

Volltextzugriff (PDF)

Increased expression of receptor phosphotyrosine phosphatase-β ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes

Translational psychiatry, 2011-05, Vol.1 (5), p.e8-e8

2011

Volltextzugriff (PDF)

Neuronal cyclooxygenase 2 expression in the hippocampal formation as a function of the clinical progression of Alzheimer disease

Archives of neurology (Chicago), 2001-03, Vol.58 (3), p.487

2001

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Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort

JAMA psychiatry (Chicago, Ill.), 2019-10, Vol.76 (10), p.1035

2019

Volltextzugriff (PDF)

Gene expression elucidates functional impact of polygenic risk for schizophrenia

Nature neuroscience, 2016-11, Vol.19 (11), p.1442

2016

Volltextzugriff (PDF)

Treatment with controlled-release lovastatin decreases serum concentrations of human β-amyloid (Aβ) peptide

The international journal of neuropsychopharmacology, 2001-06, Vol.4 (2), p.127-130

2001

Volltextzugriff (PDF)

Expression of APP in Brains of Transgenic Mice Containing the Entire Human APP Gene

Biochemical and biophysical research communications, 1993-12, Vol.197 (2), p.639-645

1993

Volltextzugriff (PDF)

The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison

European child & adolescent psychiatry, 2015-02, Vol.24 (2), p.173-183

2015

Volltextzugriff (PDF)

Maternal rheumatoid arthritis and risk of autism in the offspring

Psychological medicine, 2023-11, Vol.53 (15), p.7300-7308

2023

Volltextzugriff (PDF)

Recurrence Risk of Autism in Siblings and Cousins: A Multinational, Population-Based Study

Journal of the American Academy of Child and Adolescent Psychiatry, 2019-09, Vol.58 (9), p.866-875

2019

Volltextzugriff (PDF)

Association of Autism Spectrum Disorder With Prenatal Exposure to Medication Affecting Neurotransmitter Systems

JAMA psychiatry (Chicago, Ill.), 2018-12, Vol.75 (12), p.1217

2018

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Familial symptom domains in monozygotic siblings with autism

American journal of medical genetics, 2004-08, Vol.129B (1), p.76-81

2004

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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

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

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline

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

Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes

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

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

Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test

Evidence for a Susceptibility Gene for Autism on Chromosome 2 and for Genetic Heterogeneity

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

Molecular and cellular evidence for an oligodendrocyte abnormality in schizophrenia

Novel neuritic clusters with accumulations of amyloid precursor protein and amyloid precursor-like protein 2 immunoreactivity in brain regions damaged by thiamine deficiency

Increased expression of receptor phosphotyrosine phosphatase-β ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes

Neuronal cyclooxygenase 2 expression in the hippocampal formation as a function of the clinical progression of Alzheimer disease

Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort

Gene expression elucidates functional impact of polygenic risk for schizophrenia

Treatment with controlled-release lovastatin decreases serum concentrations of human β-amyloid (Aβ) peptide

Expression of APP in Brains of Transgenic Mice Containing the Entire Human APP Gene

The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison

Maternal rheumatoid arthritis and risk of autism in the offspring

Recurrence Risk of Autism in Siblings and Cousins: A Multinational, Population-Based Study

Association of Autism Spectrum Disorder With Prenatal Exposure to Medication Affecting Neurotransmitter Systems

Familial symptom domains in monozygotic siblings with autism

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