Related references
Note: Only part of the references are listed.Cross-species considerations in models of neurodevelopmental disorders
Sally M. Till et al.
TRENDS IN NEUROSCIENCES (2022)
Controlling litter effects to enhance rigor and reproducibility with rodent models of neurodevelopmental disorders
Jessica A. Jimenez et al.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2021)
Defining and Intervening on Cumulative Environmental Neurodevelopmental Risks: Introducing a Complex Systems Approach
Devon C. Payne-Sturges et al.
ENVIRONMENTAL HEALTH PERSPECTIVES (2021)
Early Developmental EEG and Seizure Phenotypes in a Full Gene Deletion of Ubiquitin Protein Ligase E3A Rat Model of Angelman Syndrome
Heather A. Born et al.
ENEURO (2021)
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
Behrang Mahjani et al.
MOLECULAR AUTISM (2021)
Functional rescue in an Angelman syndrome model following treatment with lentivector transduced hematopoietic stem cells
Anna Adhikari et al.
HUMAN MOLECULAR GENETICS (2021)
Toward Standardized Guidelines for Investigating Neural Circuit Control of Behavior in Animal Research
Alan S. Lewis et al.
ENEURO (2021)
Use of mouse models to investigate the contributions of CNVs associated with schizophrenia and autism to disease mechanisms
Steven E. Hyman
CURRENT OPINION IN GENETICS & DEVELOPMENT (2021)
Drug development for Autism Spectrum Disorder (ASD): Progress, challenges, and future directions
James T. McCracken et al.
EUROPEAN NEUROPSYCHOPHARMACOLOGY (2021)
Excessive Laughter-like Vocalizations, Microcephaly, and Translational Outcomes in the Ube3a Deletion Rat Model of Angelman Syndrome
Elizabeth L. Berg et al.
JOURNAL OF NEUROSCIENCE (2021)
Recent ultra-rare inherited variants implicate new autism candidate risk genes
Amy B. Wilfert et al.
NATURE GENETICS (2021)
Insulin-like growth factor-2 does not improve behavioral deficits in mouse and rat models of Angelman Syndrome
Elizabeth L. Berg et al.
MOLECULAR AUTISM (2021)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom et al.
CELL (2020)
Beyond the looking glass: recent advances in understanding the impact of environmental exposures on neuropsychiatric disease
Jonathan A. Hollander et al.
NEUROPSYCHOPHARMACOLOGY (2020)
Insufficient Evidence for Autism-Specific Genes
Scott M. Myers et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2020)
Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome
E. L. Berg et al.
TRANSLATIONAL PSYCHIATRY (2020)
The ARRIVE guidelines 2.0: updated guidelines for reporting animal research
Nathalie Percie du Sert et al.
JOURNAL OF PHYSIOLOGY-LONDON (2020)
ARRIVE GUIDELINES 2.0
Wendy Sprague
VETERINARY CLINICAL PATHOLOGY (2020)
Arriving again: 10 years on, ARRIVE 2.0 offers a simplified set of reporting guidelines
Alla Katsnelson
LAB ANIMAL (2020)
Lost in translation: At the crossroads of face validity and translational utility of behavioral assays in animal models for the development of therapeutics
J. L. Silverman et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2020)
Outcome Measures for Core Symptoms of Intellectual Disability: State of the Field
Audrey Thurm et al.
AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES (2020)
Transcriptional subtyping explains phenotypic variability in genetic subtypes of autism spectrum disorder
Sandy Trinh et al.
DEVELOPMENT AND PSYCHOPATHOLOGY (2020)
Analyzing test batteries in animal models of psychopathology with multivariate analysis of variance (MANOVA): One possible approach to increase external validity
Yelena Stukalin et al.
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR (2019)
Rigor and reproducibility in rodent behavioral research
Maria Gulinello et al.
NEUROBIOLOGY OF LEARNING AND MEMORY (2019)
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove et al.
NATURE GENETICS (2019)
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants
F. Kyle Satterstrom et al.
NATURE NEUROSCIENCE (2019)
Genetic backgrounds have unique seizure response profiles and behavioral outcomes following convulsant administration
Nycole Ashley Copping et al.
EPILEPSY & BEHAVIOR (2019)
Apparent Genetic Rescue of Adult Shank3 Exon 21 Insertion Mutation Mice Tempered by Appropriate Control Experiments
Haley E. Speed et al.
ENEURO (2019)
Argus: An open-source and flexible software application for automated quantification of behavior during social interaction in adult zebrafish
Soaleha Shams et al.
BEHAVIOR RESEARCH METHODS (2019)
Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder
Elizabeth L. Berg et al.
AUTISM RESEARCH (2018)
Behavioral and neuroanatomical approaches in models of neurodevelopmental disorders: opportunities for translation
Jill L. Silverman et al.
CURRENT OPINION IN NEUROLOGY (2018)
Diagnosis of Autism Spectrum Disorder After Age 5 in Children Evaluated Longitudinally Since Infancy
Sally Ozonoff et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2018)
Different Behavioral Experiences Produce Distinctive Parallel Changes in, and Correlate With, Frontal Cortex and Hippocampal Global Post-translational Histone Levels
Marissa Sobolewski et al.
FRONTIERS IN INTEGRATIVE NEUROSCIENCE (2018)
Mouse Social Interaction Test (MoST): a quantitative computer automated analysis of behavior
Panayotis K. Thanos et al.
JOURNAL OF NEURAL TRANSMISSION (2017)
Does age matter? The impact of rodent age on study outcomes
Samuel J. Jackson et al.
LABORATORY ANIMALS (2017)
Autism genetics - an overview
Jiani Yin et al.
PRENATAL DIAGNOSIS (2017)
Animal models for autism in 2017 and the consequential implications to drug discovery
Kathryn K. Chadman
EXPERT OPINION ON DRUG DISCOVERY (2017)
A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility
Fabrizia C. Guarnieri et al.
HUMAN MOLECULAR GENETICS (2017)
Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome
Nycole A. Copping et al.
HUMAN MOLECULAR GENETICS (2017)
Early brain development in infants at high risk for autism spectrum disorder
Heather Cody Hazlett et al.
NATURE (2017)
Germline Chd8 haploinsufficiency alters brain development in mouse
Andrea L. Gompers et al.
NATURE NEUROSCIENCE (2017)
Autism genetics: opportunities and challenges for clinical translation
Jacob A. S. Vorstman et al.
NATURE REVIEWS GENETICS (2017)
TOUCHSCREEN LEARNING DEFICITS AND NORMAL SOCIAL APPROACH BEHAVIOR IN THE SHANK3B MODEL OF PHELAN McDERMID SYNDROME AND AUTISM
Nycole A. Copping et al.
NEUROSCIENCE (2017)
Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits
Randall J. Platt et al.
CELL REPORTS (2017)
Neural circuitry at age 6 months associated with later repetitive behavior and sensory responsiveness in autism
Jason J. Wolff et al.
MOLECULAR AUTISM (2017)
Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism
Sameer C. Dhamne et al.
MOLECULAR AUTISM (2017)
Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder
Robin P. Goin-Kochel et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2017)
Genetic control of social behavior: Lessons from mutant mice
Giovanni Provenzano et al.
BEHAVIOURAL BRAIN RESEARCH (2017)
Early Communication Deficits in the Shank1 Knockout Mouse Model for Autism Spectrum Disorder: Developmental Aspects and Effects of Social Context
A. Oezge Sungur et al.
AUTISM RESEARCH (2016)
Increased Surface Area, but not Cortical Thickness, in a Subset of Young Boys With Autism Spectrum Disorder
Haruhisa Ohta et al.
AUTISM RESEARCH (2016)
Cortical Thickness Change in Autism During Early Childhood
Elizabeth Smith et al.
HUMAN BRAIN MAPPING (2016)
Prevalence and Characteristics of Autism Spectrum Disorder Among 4-Year-Old Children in the Autism and Developmental Disabilities Monitoring Network
Deborah L. Christensen et al.
JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS (2016)
Men and mice: Relating their ages
Sulagna Dutta et al.
LIFE SCIENCES (2016)
CHD8 haploinsufficiency results in autistic-like phenotypes in mice
Yuta Katayama et al.
NATURE (2016)
Genetic Background Limits Generalizability of Genotype-Phenotype Relationships
Laura J. Sittig et al.
NEURON (2016)
The side-by-side exploratory test: a simple automated protocol for the evaluation of adult zebrafish behavior simultaneously with social interaction
Isabel C. Schaefer et al.
BEHAVIOURAL PHARMACOLOGY (2015)
Affective communication in rodents: serotonin and its modulating role in ultrasonic vocalizations
Markus Woehr et al.
BEHAVIOURAL PHARMACOLOGY (2015)
A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
Pauline Chaste et al.
BIOLOGICAL PSYCHIATRY (2015)
Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior
Matthieu Genestine et al.
HUMAN MOLECULAR GENETICS (2015)
Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model
Sara Silva-Santos et al.
JOURNAL OF CLINICAL INVESTIGATION (2015)
Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits
Haley E. Speed et al.
JOURNAL OF NEUROSCIENCE (2015)
GABA(B) Receptor Agonist R-Baclofen Reverses Social Deficits and Reduces Repetitive Behavior in Two Mouse Models of Autism
J. L. Silverman et al.
NEUROPSYCHOPHARMACOLOGY (2015)
Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism
Jacob Ellegood et al.
NEUROTHERAPEUTICS (2015)
In tribute to Bob Blanchard: Divergent behavioral phenotypes of 16p11.2 deletion mice reared in same-genotype versus mixed-genotype cages
Mu Yang et al.
PHYSIOLOGY & BEHAVIOR (2015)
Risk of Bias in Reports of In Vivo Research: A Focus for Improvement
Malcolm R. Macleod et al.
PLOS BIOLOGY (2015)
Experimenter effects on behavioral test scores of eight inbred mouse strains under the influence of ethanol
Martin Bohlen et al.
BEHAVIOURAL BRAIN RESEARCH (2014)
Improving and Accelerating Drug Development for Nervous System Disorders
Diana E. Pankevich et al.
NEURON (2014)
Improving basic and translational science by accounting for litter-to-litter variation in animal models
Stanley E. Lazic et al.
BMC NEUROSCIENCE (2013)
Early brain enlargement and elevated extra-axial fluid in infants who develop autism spectrum disorder
Mark D. Shen et al.
BRAIN (2013)
Affective communication in rodents: ultrasonic vocalizations as a tool for research on emotion and motivation
Markus Woehr et al.
CELL AND TISSUE RESEARCH (2013)
Loss of Predominant Shank3 Isoforms Results in Hippocampus-Dependent Impairments in Behavior and Synaptic Transmission
Mehreen Kouser et al.
JOURNAL OF NEUROSCIENCE (2013)
A novel X-linked disorder with developmental delay and autistic features
Namik Kaya et al.
ANNALS OF NEUROLOGY (2012)
PTEN signaling in autism spectrum disorders
Jing Zhou et al.
CURRENT OPINION IN NEUROBIOLOGY (2012)
Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4
E. Ey et al.
GENES BRAIN AND BEHAVIOR (2012)
Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in Adolescent Shank3 Null Mutant Mice
Mu Yang et al.
JOURNAL OF NEUROSCIENCE (2012)
Sex Differences in the Brain: The Not So Inconvenient Truth
Margaret M. McCarthy et al.
JOURNAL OF NEUROSCIENCE (2012)
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Patricia B. S. Celestino-Soper et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Negative Allosteric Modulation of the mGluR5 Receptor Reduces Repetitive Behaviors and Rescues Social Deficits in Mouse Models of Autism
Jill L. Silverman et al.
SCIENCE TRANSLATIONAL MEDICINE (2012)
Autism genetics: searching for specificity and convergence
Jamee M. Berg et al.
GENOME BIOLOGY (2012)
Shank3 mutant mice display autistic-like behaviours and striatal dysfunction
Joao Peca et al.
NATURE (2011)
Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses
Sarah R. Gilman et al.
NEURON (2011)
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
Mark Etherton et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
The clinical implications of mouse models of enhanced anxiety
Simone B. Sartori et al.
FUTURE NEUROLOGY (2011)
Animal models of neuropsychiatric disorders
Eric J. Nestler et al.
NATURE NEUROSCIENCE (2010)
Behavioural phenotyping assays for mouse models of autism
Jill L. Silverman et al.
NATURE REVIEWS NEUROSCIENCE (2010)
Positive Results Increase Down the Hierarchy of the Sciences
Daniele Fanelli
PLOS ONE (2010)
Do Pressures to Publish Increase Scientists' Bias? An Empirical Support from US States Data
Daniele Fanelli
PLOS ONE (2010)
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
Ozlem Bozdagi et al.
MOLECULAR AUTISM (2010)
Novel De Novo SHANK3 Mutation in Autistic Patients
Julie Gauthier et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)
Increased anxiety-like behavior in mice lacking the inhibitory synapse cell adhesion molecule neuroligin 2
J. Blundell et al.
GENES BRAIN AND BEHAVIOR (2009)
Standards for the publication of mouse mutant studies
W. E. Crusio et al.
GENES BRAIN AND BEHAVIOR (2009)
Pharmacological Inhibition of mTORC1 Suppresses Anatomical, Cellular, and Behavioral Abnormalities in Neural-Specific Pten Knock-Out Mice
Jing Zhou et al.
JOURNAL OF NEUROSCIENCE (2009)
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
Mark R. Etherton et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Behavioral Differences among C57BL/6 Substrains: Implications for Transgenic and Knockout Studies
Camron D. Bryant et al.
JOURNAL OF NEUROGENETICS (2008)
Behavioral phenotyping strategies for mutant mice
Jacqueline N. Crawley
NEURON (2008)
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
Stephane Jamain et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Advances in behavioral genetics: mouse models of autism
S. S. Moy et al.
MOLECULAR PSYCHIATRY (2008)
Contribution of SHANK3 mutations to autism spectrum disorder
Rainald Moessner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Cortical folding abnormalities in autism revealed by surface-based morphometry
Christine Wu Nordahl et al.
JOURNAL OF NEUROSCIENCE (2007)
Neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice
Katsuhiko Tabuchi et al.
SCIENCE (2007)
Mouse behavioral assays relevant to the symptoms of autism
Jacqueline N. Crawley
BRAIN PATHOLOGY (2007)
A seizure-prone phenotype is associated with altered free-running rhythm in Pten mutant mice
Shiori Ogawa et al.
BRAIN RESEARCH (2007)
Situational factors, conditions and individual variables which can determine ultrasonic vocalizations in male adult Wistar rats
Rainer K. W. Schwarting et al.
BEHAVIOURAL BRAIN RESEARCH (2007)
Mouse behavioral tasks relevant to autism: Phenotypes of 10 inbred strains
Sheryl S. Moy et al.
BEHAVIOURAL BRAIN RESEARCH (2007)
Pten regulates neuronal arborization and social interaction in mice
Chang-Hyuk Kwon et al.
NEURON (2006)
X-Linked creatine transporter deficiency in two patients with severe mental retardation and autism
P Póo-Argüelles et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2006)
The use of behavioral test batteries, II: Effect of test interval
R Paylor et al.
PHYSIOLOGY & BEHAVIOR (2006)
Negative results and impact factor - A lesson from neonatology
Y Littner et al.
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE (2005)
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
F Laumonnier et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Comparison of the genomes of human and mouse lays the foundation of genome zoology
RD Emes et al.
HUMAN MOLECULAR GENETICS (2003)
Initial sequencing and comparative analysis of the mouse genome
RH Waterston et al.
NATURE (2002)
The use of behavioral test batteries: Effects of training history
KL McIlwain et al.
PHYSIOLOGY & BEHAVIOR (2001)
Share Paper
