Shank3 Transgenic and Prenatal Zinc-Deficient Autism Mouse Models Show Convergent and Individual Alterations of Brain Structures in MRI

Brain Lateralization in Mice Is Associated with Zinc Signaling and Altered in Prenatal Zinc Deficient Mice That Display Features of Autism Spectrum Disorder

(2018) Stefanie Grabrucker et al.   Frontiers in Molecular Neuroscience

Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3

(2017) Stefanie Pfaender et al.   Scientific Reports

SHANK3 Deficiency Impairs Heat Hyperalgesia and TRPV1 Signaling in Primary Sensory Neurons

(2016) Qingjian Han et al.   NEURON

Gender Dependent Evaluation of Autism like Behavior in Mice Exposed to Prenatal Zinc Deficiency

(2016) Stefanie Grabrucker et al.   Frontiers in Behavioral Neuroscience

Neuroanatomical Phenotypes Are Consistent With Autism-Like Behavioral Phenotypes in the 15q11-13 Duplication Mouse Model

(2015) Jacob Ellegood et al.   Autism Research

Case report: an unexpected link between partial deletion of the SHANK3 gene and Heller’s dementia infantilis, a rare subtype of autism spectrum disorder

(2015) Anne Philippe et al.   BMC Psychiatry

Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism

(2015) Jacob Ellegood et al.   Neurotherapeutics

Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration

(2015) Diana Wiesner et al.   HUMAN MOLECULAR GENETICS

Longitudinal changes in cortical thickness in autism and typical development

(2014) Brandon A. Zielinski et al.   BRAIN

Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity

(2014) J Ellegood et al.   MOLECULAR PSYCHIATRY

High Resolution Magnetic Resonance Imaging for Characterization of the Neuroligin-3 Knock-in Mouse Model Associated with Autism Spectrum Disorder

(2014) Manoj Kumar et al.   PLoS One

Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases

(2014) Maria Grazia Figura et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Genetic Effects on Cerebellar Structure Across Mouse Models of Autism Using a Magnetic Resonance Imaging Atlas

(2013) Patrick E. Steadman et al.   Autism Research

Zinc deficiency dysregulates the synaptic ProSAP/Shank scaffold and might contribute to autism spectrum disorders

(2013) Stefanie Grabrucker et al.   BRAIN

A role for synaptic zinc in ProSAP/Shank PSD scaffold malformation in autism spectrum disorders

(2013) Andreas M. Grabrucker   Developmental Neurobiology

Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay

(2013) Ozlem Bozdagi et al.   Molecular Autism

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

(2013) Latha Soorya et al.   Molecular Autism

Environmental Factors in Autism

(2013) Andreas M. Grabrucker   Frontiers in Psychiatry

Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion

(2012) Kimberly A. Aldinger et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in Adolescent Shank3 Null Mutant Mice

(2012) M. Yang et al.   JOURNAL OF NEUROSCIENCE

Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2

(2012) Michael J. Schmeisser et al.   NATURE

Neuroanatomical analysis of the BTBR mouse model of autism using magnetic resonance imaging and diffusion tensor imaging

(2012) Jacob Ellegood et al.   NEUROIMAGE

Neuroanatomical Assessment of the Integrin β3 Mouse Model Related to Autism and the Serotonin System Using High Resolution MRI

(2012) Jacob Ellegood et al.   Frontiers in Psychiatry

Brain abnormalities in a Neuroligin3 R451C knockin mouse model associated with autism

(2011) Jacob Ellegood et al.   Autism Research

Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation

(2011) Andreas M Grabrucker et al.   EMBO JOURNAL

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

(2011) Xiaoming Wang et al.   HUMAN MOLECULAR GENETICS

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

(2011) João Peça et al.   NATURE

Structural MRI in Autism Spectrum Disorder

(2011) RONG CHEN et al.   PEDIATRIC RESEARCH

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism

(2011) G. Horev et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies

(2011) Andreas M. Grabrucker et al.   TRENDS IN CELL BIOLOGY

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

(2011) Ozlem Bozdagi et al.   Molecular Autism

Synaptopathy: dysfunction of synaptic function?

(2010) Nils Brose et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Structural and functional magnetic resonance imaging of autism spectrum disorders

(2010) Kimberly A. Stigler et al.   BRAIN RESEARCH

A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

(2010) Kerstin E. Braunstein et al.   HUMAN MOLECULAR GENETICS

Can Magnetic Resonance Imaging Aid Diagnosis of the Autism Spectrum?

(2010) J. L. Stevenson et al.   JOURNAL OF NEUROSCIENCE

Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging

(2010) Jacob Ellegood et al.   NEUROIMAGE

Autism

(2009) Susan E Levy et al.   LANCET

Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp21lox mice

(2008) Nupur Nag et al.   BEHAVIOURAL BRAIN RESEARCH