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DNA Methylation and Susceptibility to Autism Spectrum Disorder

Annual review of medicine, 2019-01, Vol.70 (1), p.151-166

2019

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Potential of Epigenetic Therapy for Prader-Willi Syndrome

Trends in pharmacological sciences (Regular ed.), 2019-09, Vol.40 (9), p.605-608

2019

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Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone HIST1H1E and literature review

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2018-06, Vol.177 (4), p.426-433

2018

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TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice

Nature communications, 2021-06, Vol.12 (1), p.3359-3359, Article 3359

2021

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Epigenetic therapy of Prader–Willi syndrome

Translational research : the journal of laboratory and clinical medicine, 2019-06, Vol.208, p.105-118

2019

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When lungs and weights tell different stories

Pediatric pulmonology, 2024-04, Vol.59 (4), p.1047-1059

2024

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Maternal valproic acid exposure leads to neurogenesis defects and autism-like behaviors in non-human primates

Translational psychiatry, 2019-10, Vol.9 (1), p.267-13, Article 267

2019

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Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate

Cell research, 2017-10, Vol.27 (10), p.1293-1297

2017

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Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndrome

Nature medicine, 2017-02, Vol.23 (2), p.213-222

2017

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Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism

Nature communications, 2016-05, Vol.7 (1), p.11459-11459, Article 11459

2016

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Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility

Human mutation, 2012-12, Vol.33 (12), p.1635-1638

2012

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Alterations and correlations of the gut microbiome, metabolism and immunity in patients with primary biliary cirrhosis

Environmental microbiology, 2016-07, Vol.18 (7), p.2272-2286

2016

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Potassium channel dysfunction in human neuronal models of Angelman syndrome

Science (American Association for the Advancement of Science), 2019-12, Vol.366 (6472), p.1486-1492

2019

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A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network

Orphanet journal of rare diseases, 2017-04, Vol.12 (1), p.71-71, Article 71

2017

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Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses

Genetics in medicine, 2020-07, Vol.22 (7), p.1269-1275

2020

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A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay

Human mutation, 2022-12, Vol.43 (12), p.1816-1823

2022

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Exogenous genistein enhances soybean resistance to Xanthomonas axonopodis pv. glycines

Pest management science, 2022-08, Vol.78 (8), p.3664-3675

2022

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CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms

Human molecular genetics, 2019-02, Vol.28 (4), p.561-571

2019

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Brain region-specific disruption of Shank3 in mice reveals a dissociation for cortical and striatal circuits in autism-related behaviors

Translational psychiatry, 2018-04, Vol.8 (1), p.94-17, Article 94

2018

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Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3

PloS one, 2010-08, Vol.5 (8), p.e12278

2010

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CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors

Molecular autism, 2018-04, Vol.9 (1), p.23-23, Article 23

2018

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

Human molecular genetics, 2011-08, Vol.20 (15), p.3093-3108

2011

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Modeling autism in non‐human primates: Opportunities and challenges

Autism research, 2018-05, Vol.11 (5), p.686-694

2018

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Application of chitosan nanoparticles in quality and preservation of postharvest fruits and vegetables: A review

Comprehensive reviews in food science and food safety, 2023-05, Vol.22 (3), p.1722-1762

2023

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Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?

Journal of genetic counseling, 2018-08, Vol.27 (4), p.935-946

2018

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DNA Methylation and Susceptibility to Autism Spectrum Disorder

Potential of Epigenetic Therapy for Prader-Willi Syndrome

Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone HIST1H1E and literature review

TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice

Epigenetic therapy of Prader–Willi syndrome

When lungs and weights tell different stories

Maternal valproic acid exposure leads to neurogenesis defects and autism-like behaviors in non-human primates

Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate

Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndrome

Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility

Alterations and correlations of the gut microbiome, metabolism and immunity in patients with primary biliary cirrhosis

Potassium channel dysfunction in human neuronal models of Angelman syndrome

A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network

Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses

A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay

Exogenous genistein enhances soybean resistance to Xanthomonas axonopodis pv. glycines

CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms

Brain region-specific disruption of Shank3 in mice reveals a dissociation for cortical and striatal circuits in autism-related behaviors

Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3

CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors

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

Modeling autism in non‐human primates: Opportunities and challenges

Application of chitosan nanoparticles in quality and preservation of postharvest fruits and vegetables: A review

Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?

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