Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome

The impact of oxytocin on neurite outgrowth and synaptic proteins in Magel2 ‐deficient mice

(2021) Alexandra Reichova et al.   Developmental Neurobiology

Oxytocin administration in neonates shapes hippocampal circuitry and restores social behavior in a mouse model of autism

(2021) Alessandra Bertoni et al.   MOLECULAR PSYCHIATRY

How to study anxiety and depression in rodent models of chronic pain?

(2020) Mélanie Kremer et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome

(2020) E. L. Berg et al.   Translational Psychiatry

Phenotypic spectrum and genetic analysis in the fatal cases of Schaaf-Yang syndrome

(2020) Xuefei Chen et al.   MEDICINE

The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research

(2020) Nathalie Percie du Sert et al.   PLOS BIOLOGY

Cas9 gene therapy for Angelman syndrome traps Ube3a-ATS long non-coding RNA

(2020) Justin M. Wolter et al.   NATURE

The adult phenotype of Schaaf-Yang syndrome

(2020) Felix Marbach et al.   Orphanet Journal of Rare Diseases

Polysomnographic characteristics and sleep‐disordered breathing in Schaaf‐Yang syndrome

(2020) Weston T. Powell et al.   PEDIATRIC PULMONOLOGY

Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production

(2020) Helen Chen et al.   JCI Insight

MAGEL2 ‐related disorders: A study and case series

(2019) Jameson Patak et al.   CLINICAL GENETICS

Targeted protein degradation: expanding the toolbox

(2019) Matthieu Schapira et al.   NATURE REVIEWS DRUG DISCOVERY

The Year of the Rat: The Rat Genome Database at 20: a multi-species knowledgebase and analysis platform

(2019) Jennifer R Smith et al.   NUCLEIC ACIDS RESEARCH

DNA methylation dynamics of genomic imprinting in mouse development†

(2018) Jennifer M SanMiguel et al.   BIOLOGY OF REPRODUCTION

Schaaf-Yang syndrome overview: Report of 78 individuals

(2018) John McCarthy et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Inactivation of Magel2 suppresses oxytocin neurons through synaptic excitation-inhibition imbalance

(2018) Tayfun Ates et al.   NEUROBIOLOGY OF DISEASE

Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty

(2017) M. D. Fountain et al.   GENES BRAIN AND BEHAVIOR

From engineering to editing the rat genome

(2017) Stephen Meek et al.   MAMMALIAN GENOME

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

(2016) Surabi Veeraragavan et al.   HUMAN MOLECULAR GENETICS

Sleeve gastrectomy leads to weight loss in the Magel2 knockout mouse

(2016) Deanna M. Arble et al.   Surgery for Obesity and Related Diseases

BORIS: a free, versatile open-source event-logging software for video/audio coding and live observations

(2016) Olivier Friard et al.   Methods in Ecology and Evolution

Behavioral Phenotyping of Juvenile Long-Evans and Sprague-Dawley Rats: Implications for Preclinical Models of Autism Spectrum Disorders

(2016) Katherine M. Ku et al.   PLoS One

An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism

(2015) Hamid Meziane et al.   BIOLOGICAL PSYCHIATRY

USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder

(2015) Yi-Heng Hao et al.   MOLECULAR CELL

Fmr1 and Nlgn3 knockout rats: Novel tools for investigating autism spectrum disorders.

(2014) Shannon M. Hamilton et al.   BEHAVIORAL NEUROSCIENCE

Towards a therapy for Angelman syndrome by targeting a long non-coding RNA

(2014) Linyan Meng et al.   NATURE

Behavioural methods used in rodent models of autism spectrum disorders: Current standards and new developments

(2013) Markus Wöhr et al.   BEHAVIOURAL BRAIN RESEARCH

Regulation of WASH-Dependent Actin Polymerization and Protein Trafficking by Ubiquitination

(2013) Yi-Heng Hao et al.   CELL

Mouse models of Prader–Willi Syndrome: A systematic review

(2013) Sandrina Bervini et al.   FRONTIERS IN NEUROENDOCRINOLOGY

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

(2013) Christian P Schaaf et al.   NATURE GENETICS

Brain development in rodents and humans: Identifying benchmarks of maturation and vulnerability to injury across species

(2013) Bridgette D. Semple et al.   PROGRESS IN NEUROBIOLOGY

Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences

(2013) Anne Rieusset et al.   PLoS Genetics

A call for transparent reporting to optimize the predictive value of preclinical research

(2012) Story C. Landis et al.   NATURE

Research Domain Criteria (RDoC): Toward a New Classification Framework for Research on Mental Disorders

(2010) Thomas Insel et al.   AMERICAN JOURNAL OF PSYCHIATRY

A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene

(2010) Fabienne Schaller et al.   HUMAN MOLECULAR GENETICS

Comparison of the elevated plus and elevated zero mazes in treated and untreated male Sprague–Dawley rats: Effects of anxiolytic and anxiogenic agents

(2010) Amanda A. Braun et al.   PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR

Context representations, context functions, and the parahippocampal-hippocampal system

(2009) J. W. Rudy   LEARNING & MEMORY

Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

(2009) Alexia Thomas et al.   PSYCHOPHARMACOLOGY