Dopaminergic Dysregulation in Syndromic Autism Spectrum Disorders: Insights From Genetic Mouse Models

Generation of a DAT-P2A-Flpo mouse line for intersectional genetic targeting of dopamine neuron subpopulations

(2021) Daniel J. Kramer et al.   Cell Reports

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

(2020) F. Kyle Satterstrom et al.   CELL

Classification of Midbrain Dopamine Neurons Using Single-Cell Gene Expression Profiling Approaches

(2020) Jean-Francois Poulin et al.   TRENDS IN NEUROSCIENCES

Altered dopaminergic pathways and therapeutic effects of intranasal dopamine in two distinct mouse models of autism

(2020) Owen Y. Chao et al.   Molecular Brain

An expanded palette of dopamine sensors for multiplex imaging in vivo

(2020) Tommaso Patriarchi et al.   NATURE METHODS

Next-generation GRAB sensors for monitoring dopaminergic activity in vivo

(2020) Fangmiao Sun et al.   NATURE METHODS

Anatomically segregated basal ganglia pathways allow parallel behavioral modulation

(2020) Jaeeon Lee et al.   NATURE NEUROSCIENCE

Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

(2020) Gokul Ramaswami et al.   Nature Communications

Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND Network

(2019) Danielle A. Baribeau et al.   Translational Psychiatry

Single-cell RNA sequencing reveals midbrain dopamine neuron diversity emerging during mouse brain development

(2019) Katarína Tiklová et al.   Nature Communications

Dopamine and Cognitive Control in Prefrontal Cortex

(2019) Torben Ott et al.   TRENDS IN COGNITIVE SCIENCES

Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in SLC6A3

(2019) Nicholas G. Campbell et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Dissociable dopamine dynamics for learning and motivation

(2019) Ali Mohebi et al.   NATURE

Autism-linked dopamine transporter mutation alters striatal dopamine neurotransmission and dopamine-dependent behaviors

(2019) Gabriella E. DiCarlo et al.   JOURNAL OF CLINICAL INVESTIGATION

Three divisions of the mouse caudal striatum differ in the proportions of dopamine D1 and D2 receptor-expressing cells, distribution of dopaminergic axons, and composition of cholinergic and GABAergic interneurons

(2019) Yuta Miyamoto et al.   Brain Structure & Function

Rett Syndrome in Males: The Different Clinical Course in Two Brothers with the Same Microduplication MECP2 Xq28

(2019) Maria Bernarda Pitzianti et al.   International Journal of Environmental Research and Public Health

An open cortico-basal ganglia loop allows limbic control over motor output via the nigrothalamic pathway

(2019) Sho Aoki et al.   eLife

Loss of fragile X mental retardation protein precedes Lewy pathology in Parkinson’s disease

(2019) Yi Tan et al.   ACTA NEUROPATHOLOGICA

Depth-resolved fiber photometry with a single tapered optical fiber implant

(2019) Filippo Pisano et al.   NATURE METHODS

Tsc1-mTORC1 signaling controls striatal dopamine release and cognitive flexibility

(2019) Polina Kosillo et al.   Nature Communications

Single-Cell RNA-Seq of Mouse Dopaminergic Neurons Informs Candidate Gene Selection for Sporadic Parkinson Disease

(2018) Paul W. Hook et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies

(2018) Anwesha Banerjee et al.   BRAIN RESEARCH

Dopaminergic dysfunction in neurodevelopmental disorders: recent advances and synergistic technologies to aid basic research

(2018) J Elliott Robinson et al.   CURRENT OPINION IN NEUROBIOLOGY

Deciphering MECP2 -associated disorders: disrupted circuits and the hope for repair

(2018) Zilong Qiu   CURRENT OPINION IN NEUROBIOLOGY

Rett syndrome: insights into genetic, molecular and circuit mechanisms

(2018) Jacque P. K. Ip et al.   NATURE REVIEWS NEUROSCIENCE

Spectrally Resolved Fiber Photometry for Multi-component Analysis of Brain Circuits

(2018) Chengbo Meng et al.   NEURON

Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain

(2018) Arpiar Saunders et al.   CELL

Mapping projections of molecularly defined dopamine neuron subtypes using intersectional genetic approaches

(2018) Jean-Francois Poulin et al.   NATURE NEUROSCIENCE

Psychomotor Dysfunction in Rett Syndrome: Insights into the Neurochemical and Circuit Roots

(2018) Wenlin Liao   Developmental Neurobiology

Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience

(2018) Claudia Ciaccio et al.   European Journal of Medical Genetics

A Neural Circuit Mechanism for Encoding Aversive Stimuli in the Mesolimbic Dopamine System

(2018) Johannes W. de Jong et al.   NEURON

GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia

(2017) Naveen Khanzada et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

A retrospective chart review of the features of PTEN hamartoma tumour syndrome in children

(2017) Emily Hansen-Kiss et al.   JOURNAL OF MEDICAL GENETICS

Autism spectrum disorder: Consensus guidelines on assessment, treatment and research from the British Association for Psychopharmacology

(2017) Oliver D Howes et al.   JOURNAL OF PSYCHOPHARMACOLOGY

Excessive D1 Dopamine Receptor Activation in the Dorsal Striatum Promotes Autistic-Like Behaviors

(2017) Yunjin Lee et al.   MOLECULAR NEUROBIOLOGY

Autism gene Ube3a and seizures impair sociability by repressing VTA Cbln1

(2017) Vaishnav Krishnan et al.   NATURE

Dynamic Nigrostriatal Dopamine Biases Action Selection

(2017) Christopher D. Howard et al.   NEURON

VTA mTOR Signaling Regulates Dopamine Dynamics, Cocaine-Induced Synaptic Alterations, and Reward

(2017) Xiaojie Liu et al.   NEUROPSYCHOPHARMACOLOGY

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment

(2017) Walter E. Kaufmann et al.   PEDIATRICS

Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation

(2017) Zhu Wen et al.   Molecular Autism

Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications

(2017) Louisa Kalsner et al.   Molecular Genetics & Genomic Medicine

Molecular Diversity of Midbrain Development in Mouse, Human, and Stem Cells

(2016) Gioele La Manno et al.   CELL

The neuroanatomy of autism - a developmental perspective

(2016) Alex P. A. Donovan et al.   JOURNAL OF ANATOMY

Cellular distribution of the fragile X mental retardation protein in the mouse brain

(2016) Diego A.R. Zorio et al.   JOURNAL OF COMPARATIVE NEUROLOGY

Advancing the understanding of autism disease mechanisms through genetics

(2016) Luis de la Torre-Ubieta et al.   NATURE MEDICINE

The mouse cortico-striatal projectome

(2016) Houri Hintiryan et al.   NATURE NEUROSCIENCE

Morphological Alterations in the Thalamus, Striatum and Pallidum in Autism Spectrum Disorder

(2016) Manuela Schuetze et al.   NEUROPSYCHOPHARMACOLOGY

De novo genic mutations among a Chinese autism spectrum disorder cohort

(2016) Tianyun Wang et al.   Nature Communications

Striatal Circuits as a Common Node for Autism Pathophysiology

(2016) Marc V. Fuccillo   Frontiers in Neuroscience

Tuberous sclerosis complex

(2016) Elizabeth P. Henske et al.   Nature Reviews Disease Primers

Hyperactivity and lack of social discrimination in the adolescent Fmr1 knockout mouse

(2015) Emilie M. Sørensen et al.   BEHAVIOURAL PHARMACOLOGY

DRD3 gene and striatum in autism spectrum disorder

(2015) Wouter G. Staal et al.   BRITISH JOURNAL OF PSYCHIATRY

Behavioral phenotypes of genetic mouse models of autism

(2015) T. M. Kazdoba et al.   GENES BRAIN AND BEHAVIOR

MeCP2 in the Rostral Striatum Maintains Local Dopamine Content Critical for Psychomotor Control

(2015) San-Hua Su et al.   JOURNAL OF NEUROSCIENCE

Neurological and neuropsychiatric aspects of tuberous sclerosis complex

(2015) Paolo Curatolo et al.   LANCET NEUROLOGY

Mesolimbic dopamine signals the value of work

(2015) Arif A Hamid et al.   NATURE NEUROSCIENCE

Balancing Proliferation and Connectivity in PTEN-associated Autism Spectrum Disorder

(2015) Amanda K. Tilot et al.   Neurotherapeutics

Tuberous Sclerosis Associated Neuropsychiatric Disorders (TAND) and the TAND Checklist

(2015) Petrus J. de Vries et al.   PEDIATRIC NEUROLOGY

Low load for disruptive mutations in autism genes and their biased transmission

(2015) Ivan Iossifov et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Cytoplasm-predominant Pten associates with increased region-specific brain tyrosine hydroxylase and dopamine D2 receptors in mouse model with autistic traits

(2015) Xin He et al.   Molecular Autism

Autism spectrum disorders and neuropathology of the cerebellum

(2015) David R. Hampson et al.   Frontiers in Neuroscience

Natural Neural Projection Dynamics Underlying Social Behavior

(2014) Lisa A. Gunaydin et al.   CELL

Pten haploinsufficient mice show broad brain overgrowth but selective impairments in autism-relevant behavioral tests

(2014) Amy E. Clipperton-Allen et al.   HUMAN MOLECULAR GENETICS

Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

Decoding the contribution of dopaminergic genes and pathways to autism spectrum disorder (ASD)

(2014) Michael Nguyen et al.   NEUROCHEMISTRY INTERNATIONAL

Fragile X Mental Retardation Protein Regulates Synaptic and Behavioral Plasticity to Repeated Cocaine Administration

(2014) Laura N. Smith et al.   NEURON

Improvement of the Rett Syndrome Phenotype in a Mecp2 Mouse Model Upon Treatment with Levodopa and a Dopa-Decarboxylase Inhibitor

(2014) Karolina Szczesna et al.   NEUROPSYCHOPHARMACOLOGY

The rare DAT coding variant Val559 perturbs DA neuron function, changes behavior, and alters in vivo responses to psychostimulants

(2014) M. A. Mergy et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Defining Midbrain Dopaminergic Neuron Diversity by Single-Cell Gene Expression Profiling

(2014) Jean-Francois Poulin et al.   Cell Reports

Autism spectrum disorder associated with low serotonin in CSF and mutations in the SLC29A4 plasma membrane monoamine transporter (PMAT) gene

(2014) Dea Adamsen et al.   Molecular Autism

SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking

(2014) E Bowton et al.   Translational Psychiatry

Changes in the Development of Striatum Are Involved in Repetitive Behavior in Autism

(2013) Marieke Langen et al.   BIOLOGICAL PSYCHIATRY

MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome

(2013) Fang-Chi Kao et al.   Brain Structure & Function

The amygdala and the relevance detection theory of autism: an evolutionary perspective

(2013) Tiziana Zalla et al.   Frontiers in Human Neuroscience

Association of the Catechol-o-Methyltransferase Gene Polymorphisms with Korean Autism Spectrum Disorders

(2013) Hee Jeong Yoo et al.   JOURNAL OF KOREAN MEDICAL SCIENCE

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

(2013) P J Hamilton et al.   MOLECULAR PSYCHIATRY

The translation of translational control by FMRP: therapeutic targets for FXS

(2013) Jennifer C Darnell et al.   NATURE NEUROSCIENCE

Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference

(2013) Darcy A. Krueger et al.   PEDIATRIC NEUROLOGY

Changes in Sensitivity of Reward and Motor Behavior to Dopaminergic, Glutamatergic, and Cholinergic Drugs in a Mouse Model of Fragile X Syndrome

(2013) Eric W. Fish et al.   PLoS One

Dysregulation of synaptic plasticity precedes appearance of morphological defects in a Pten conditional knockout mouse model of autism

(2013) K. Takeuchi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder

(2013) Deepak Verma et al.   PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY

Coordinate Regulation of Mature Dopaminergic Axon Morphology by Macroautophagy and the PTEN Signaling Pathway

(2013) Keiichi Inoue et al.   PLoS Genetics

DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families

(2012) Joe A Hettinger et al.   Behavioral and Brain Functions

PTEN deletion enhances survival, neurite outgrowth and function of dopamine neuron grafts to MitoPark mice

(2012) Y. Zhang et al.   BRAIN

Consensus Paper: Pathological Role of the Cerebellum in Autism

(2012) S. Hossein Fatemi et al.   CEREBELLUM

PTEN signaling in autism spectrum disorders

(2012) Jing Zhou et al.   CURRENT OPINION IN NEUROBIOLOGY

Selective preservation of MeCP2 in catecholaminergic cells is sufficient to improve the behavioral phenotype of male and female Mecp2-deficient mice

(2012) M. Lang et al.   HUMAN MOLECULAR GENETICS

Ca2+/Calmodulin-dependent Protein Kinase IIα (αCaMKII) Controls the Activity of the Dopamine Transporter

(2012) Thomas Steinkellner et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Pathway-specific dopaminergic deficits in a mouse model of Angelman syndrome

(2012) Thorfinn T. Riday et al.   JOURNAL OF CLINICAL INVESTIGATION

Dampened dopamine-mediated neuromodulation in prefrontal cortex of fragile X mice

(2012) Kush Paul et al.   JOURNAL OF PHYSIOLOGY-LONDON

FMRP targets distinct mRNA sequence elements to regulate protein expression

(2012) Manuel Ascano et al.   NATURE

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

(2012) Brian J. O’Roak et al.   NATURE

Regulation of Presynaptic Neurotransmission by Macroautophagy

(2012) Daniela Hernandez et al.   NEURON

High-Throughput Sequencing of mGluR Signaling Pathway Genes Reveals Enrichment of Rare Variants in Autism

(2012) Raymond J. Kelleher III et al.   PLoS One

Altered Serotonin, Dopamine and Norepinepherine Levels in 15q Duplication and Angelman Syndrome Mouse Models

(2012) M. Febin Farook et al.   PLoS One

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

(2012) B. J. O'Roak et al.   SCIENCE

Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC

(2012) Claudio Toma et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

Basal ganglia morphometry and repetitive behavior in young children with autism spectrum disorder

(2011) Annette Estes et al.   Autism Research

Inverted-U–Shaped Dopamine Actions on Human Working Memory and Cognitive Control

(2011) Roshan Cools et al.   BIOLOGICAL PSYCHIATRY

Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain

(2011) Nicolas Panayotis et al.   BMC NEUROSCIENCE

FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

(2011) Jennifer C. Darnell et al.   CELL

Pten ablation in adult dopaminergic neurons is neuroprotective in Parkinson's disease models

(2011) Andrii Domanskyi et al.   FASEB JOURNAL

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders

(2011) C. P. Schaaf et al.   HUMAN MOLECULAR GENETICS

Safety and Tolerability of Aripiprazole for Irritability in Pediatric Patients With Autistic Disorder

(2011) Ronald N. Marcus et al.   JOURNAL OF CLINICAL PSYCHIATRY

Loss of Mecp2 in Substantia Nigra Dopamine Neurons Compromises the Nigrostriatal Pathway

(2011) S. C. Gantz et al.   JOURNAL OF NEUROSCIENCE

Efficacy of Risperidone in Managing Maladaptive Behaviors for Children With Autistic Spectrum Disorder: A Meta-Analysis

(2011) Akanksha Sharma et al.   Journal of Pediatric Health Care

Phosphatase and tensin homologue (PTEN) regulates synaptic plasticity independently of its effect on neuronal morphology and migration

(2011) Margaret Sperow et al.   JOURNAL OF PHYSIOLOGY-LONDON

AAV Transduction of Dopamine Neurons With Constitutively Active Rheb Protects From Neurodegeneration and Mediates Axon Regrowth

(2011) Sang Ryong Kim et al.   MOLECULAR THERAPY

Identification of risk factors for autism spectrum disorders in tuberous sclerosis complex

(2011) A. L. Numis et al.   NEUROLOGY

Current Perspectives on Motor Functioning in Infants, Children, and Adults With Autism Spectrum Disorders

(2011) Anjana N. Bhat et al.   PHYSICAL THERAPY

Dopamine Release and Uptake Impairments and Behavioral Alterations Observed in Mice that Model Fragile X Mental Retardation Syndrome

(2010) Jenny L. Fulks et al.   ACS Chemical Neuroscience

TheMECP2duplication syndrome

(2010) Melissa B. Ramocki et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Rett syndrome: Revised diagnostic criteria and nomenclature

(2010) Jeffrey L. Neul et al.   ANNALS OF NEUROLOGY

Brain Serotonin and Dopamine Transporter Bindings in Adults With High-Functioning Autism

(2010) Kazuhiko Nakamura et al.   ARCHIVES OF GENERAL PSYCHIATRY

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly

(2010) Kim L. McBride et al.   Autism Research

Analysis of unsupported gait in toddlers with autism

(2010) Gianluca Esposito et al.   BRAIN & DEVELOPMENT

Autism severity is associated with child and maternal MAOA genotypes

(2010) IL Cohen et al.   CLINICAL GENETICS

PTEN is recruited to the postsynaptic terminal for NMDA receptor-dependent long-term depression

(2010) Sandra Jurado et al.   EMBO JOURNAL

Roles of Fragile X Mental Retardation Protein in Dopaminergic Stimulation-induced Synapse-associated Protein Synthesis and Subsequent α-Amino-3-hydroxyl-5-methyl-4-isoxazole-4-propionate (AMPA) Receptor Internalization

(2010) Hansen Wang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Line-Item Analysis of the Aberrant Behavior Checklist: Results from Two Studies of Aripiprazole in the Treatment of Irritability Associated with Autistic Disorder

(2010) Michael G. Aman et al.   JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY

Parkinsonism and cognitive decline in a fragile X mosaic male

(2010) Deborah Hall et al.   MOVEMENT DISORDERS

Loss of dopaminergic neurons and resulting behavioural deficits in mouse model of Angelman syndrome

(2010) Shalaka A. Mulherkar et al.   NEUROBIOLOGY OF DISEASE

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome

(2010) Richard M. Gustin et al.   NEUROBIOLOGY OF DISEASE

Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse

(2010) Nicolas Panayotis et al.   NEUROBIOLOGY OF DISEASE

Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome

(2010) M. Santos et al.   NEUROSCIENCE

Biogenic Amines in Rett Syndrome: The Usual Suspects

(2009) Jean-Christophe Roux et al.   BEHAVIOR GENETICS

Changes in the Developmental Trajectories of Striatum in Autism

(2009) Marieke Langen et al.   BIOLOGICAL PSYCHIATRY

Abnormal Behavior in a Chromosome- Engineered Mouse Model for Human 15q11-13 Duplication Seen in Autism

(2009) Jin Nakatani et al.   CELL

Serotonin and dopamine transporter binding in children with autism determined by SPECT

(2009) Ismo Makkonen et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly

(2009) Elizabeth A Varga et al.   GENETICS IN MEDICINE

PTEN hamartoma tumor syndrome: An overview

(2009) Judith A Hobert et al.   GENETICS IN MEDICINE

Examination of FMR1 transcript and protein levels among 74 premutation carriers

(2009) Emmanuel Peprah et al.   JOURNAL OF HUMAN GENETICS

Single Nigrostriatal Dopaminergic Neurons Form Widely Spread and Highly Dense Axonal Arborizations in the Neostriatum

(2009) W. Matsuda et al.   JOURNAL OF NEUROSCIENCE

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

(2009) Joseph T. Glessner et al.   NATURE

Aripiprazole in the Treatment of Irritability in Children and Adolescents With Autistic Disorder

(2009) R. Owen et al.   PEDIATRICS

Selective Deletion of PTEN in Dopamine Neurons Leads to Trophic Effects and Adaptation of Striatal Medium Spiny Projecting Neurons

(2009) Oscar Diaz-Ruiz et al.   PLoS One

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

(2009) R. C. Samaco et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Co-occurring conditions associated withFMR1gene variations: Findings from a national parent survey

(2008) Donald B. Bailey et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A DRD1 haplotype is associated with risk for autism spectrum disorders in male‐only affected sib‐pair families

(2008) Joe A. Hettinger et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

The TSC1–TSC2 complex: a molecular switchboard controlling cell growth

(2008) Jingxiang Huang et al.   BIOCHEMICAL JOURNAL

A Common Variant in DRD3 Receptor Is Associated with Autism Spectrum Disorder

(2008) Mariken de Krom et al.   BIOLOGICAL PSYCHIATRY

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism

(2008) C. S. Loat et al.   GENES BRAIN AND BEHAVIOR

Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

(2008) Teresa Temudo et al.   MOVEMENT DISORDERS

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

(2008) Amber Hogart et al.   NEUROBIOLOGY OF DISEASE

Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

(2008) J. L. Neul et al.   NEUROLOGY

Investigating genotype-phenotype relationships in Rett syndrome using an international data set

(2008) A. Bebbington et al.   NEUROLOGY

FMRP Acts as a Key Messenger for Dopamine Modulation in the Forebrain

(2008) Hansen Wang et al.   NEURON

Unique Properties of Mesoprefrontal Neurons within a Dual Mesocorticolimbic Dopamine System

(2008) Stephan Lammel et al.   NEURON

Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean

(2008) Hee Jeong Yoo et al.   NEUROSCIENCE RESEARCH

Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease

(2008) Deborah A. Hall et al.   PARKINSONISM & RELATED DISORDERS

MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

(2008) M. Chahrour et al.   SCIENCE

Phosphatase and tensin homolog, deleted on chromosome 10 deficiency in brain causes defects in synaptic structure, transmission and plasticity, and myelination abnormalities

(2007) M.M. Fraser et al.   NEUROSCIENCE