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Folate-mediated transgenerational inheritance of sperm DNA methylation patterns correlate with spinal axon regeneration

Epigenetics, 2024-12, Vol.19 (1), p.2380930

2024

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Early-life stress links 5-hydroxymethylcytosine to anxiety-related behaviors

Epigenetics, 2017-04, Vol.12 (4), p.264-276

2017

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Epigenetic impact of a 1-week intensive multimodal group program for adolescents with multiple adverse childhood experiences

Scientific reports, 2022-10, Vol.12 (1), p.17177-17177, Article 17177

2022

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Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility

Neurobiology of disease, 2013-01, Vol.49, p.211-220

2013

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DNA methylation and hydroxymethylation have distinct genome-wide profiles related to axonal regeneration

Epigenetics, 2021-01, Vol.16 (1), p.64-78

2021

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Genome-wide alterations in hippocampal 5-hydroxymethylcytosine links plasticity genes to acute stress

Neurobiology of disease, 2016-02, Vol.86, p.99-108

2016

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Perinatal protein malnutrition results in genome-wide disruptions of 5-hydroxymethylcytosine at regions that can be restored to control levels by an enriched environment

Epigenetics, 2021-10, Vol.16 (10), p.1085-1101

2021

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Sex-specific hippocampal 5-hydroxymethylcytosine is disrupted in response to acute stress

Neurobiology of disease, 2016-12, Vol.96, p.54-66

2016

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Cord blood DNA methylation modifications in infants are associated with white matter microstructure in the context of prenatal maternal depression and anxiety

Scientific reports, 2021-06, Vol.11 (1), p.12181-12181, Article 12181

2021

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New hope: the emerging role of 5-hydroxymethylcytosine in mental health and disease

Epigenomics, 2016-07, Vol.8 (7), p.981-991

2016

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Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and mice

BMC genomics, 2014-02, Vol.15 (1), p.131-131, Article 131

2014

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Glyoxalase 1 and its substrate methylglyoxal are novel regulators of seizure susceptibility

Epilepsia (Copenhagen), 2013-04, Vol.54 (4), p.649-657

2013

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Purified regenerating retinal neurons reveal regulatory role of DNA methylation-mediated Na+/K+-ATPase in murine axon regeneration

Communications biology, 2023-01, Vol.6 (1), p.120-120, Article 120

2023

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Hippocampal and peripheral blood DNA methylation signatures correlate at the gene and pathway level in a mouse model of autism

Human molecular genetics, 2023-12, Vol.32 (24), p.3312-3322

2023

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Effects of an epilepsy-causing mutation in the SCN1A sodium channel gene on cocaine-induced seizure susceptibility in mice

Psychopharmacology, 2013-07, Vol.228 (2), p.263-270

2013

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Gene by environment interaction mouse model reveals a functional role for 5-hydroxymethylcytosine in neurodevelopmental disorders

Genome research, 2022-02, Vol.32 (2), p.266-279

2022

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Early-life febrile seizures worsen adult phenotypes in Scn1a mutants

Experimental neurology, 2017-07, Vol.293, p.159-171

2017

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Differentially Methylated Genes in Saliva are linked to Childhood Stress

Scientific reports, 2018-07, Vol.8 (1), p.10785-8, Article 10785

2018

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PAX8/PAX8-AS1 DNA methylation levels are associated with objective sleep duration in persons with unexplained hypersomnolence using a deep phenotyping approach

Sleep (New York, N.Y.), 2021-10, Vol.44 (10), p.1

2021

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Genome-wide disruption of 5-hydroxymethylcytosine in a mouse model of autism

Human molecular genetics, 2015-12, Vol.24 (24), p.7121-7131

2015

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DNA Hypomethylation in Blood Links B3GALT4 and ZADH2 to Alzheimer's Disease

Journal of Alzheimer's disease, 2018-01, Vol.66 (3), p.927-934

2018

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Altered Function of the SCN1A Voltage-gated Sodium Channel Leads to γ-Aminobutyric Acid-ergic (GABAergic) Interneuron Abnormalities

The Journal of biological chemistry, 2010-03, Vol.285 (13), p.9823-9834

2010

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Disruption of DNA methylation-mediated cranial neural crest proliferation and differentiation causes orofacial clefts in mice

Proceedings of the National Academy of Sciences - PNAS, 2024-01, Vol.121 (3), p.e2317668121-e2317668121

2024

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Whole genome methylation sequencing in blood identifies extensive differential DNA methylation in late‐onset dementia due to Alzheimer's disease

Alzheimer's & dementia, 2024-02, Vol.20 (2), p.1050-1062

2024

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The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

Human molecular genetics, 2007-12, Vol.16 (23), p.2892-2899

2007

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Folate-mediated transgenerational inheritance of sperm DNA methylation patterns correlate with spinal axon regeneration

Early-life stress links 5-hydroxymethylcytosine to anxiety-related behaviors

Epigenetic impact of a 1-week intensive multimodal group program for adolescents with multiple adverse childhood experiences

Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility

DNA methylation and hydroxymethylation have distinct genome-wide profiles related to axonal regeneration

Genome-wide alterations in hippocampal 5-hydroxymethylcytosine links plasticity genes to acute stress

Perinatal protein malnutrition results in genome-wide disruptions of 5-hydroxymethylcytosine at regions that can be restored to control levels by an enriched environment

Sex-specific hippocampal 5-hydroxymethylcytosine is disrupted in response to acute stress

Cord blood DNA methylation modifications in infants are associated with white matter microstructure in the context of prenatal maternal depression and anxiety

New hope: the emerging role of 5-hydroxymethylcytosine in mental health and disease

Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and mice

Glyoxalase 1 and its substrate methylglyoxal are novel regulators of seizure susceptibility

Purified regenerating retinal neurons reveal regulatory role of DNA methylation-mediated Na+/K+-ATPase in murine axon regeneration

Hippocampal and peripheral blood DNA methylation signatures correlate at the gene and pathway level in a mouse model of autism

Effects of an epilepsy-causing mutation in the SCN1A sodium channel gene on cocaine-induced seizure susceptibility in mice

Gene by environment interaction mouse model reveals a functional role for 5-hydroxymethylcytosine in neurodevelopmental disorders

Early-life febrile seizures worsen adult phenotypes in Scn1a mutants

Differentially Methylated Genes in Saliva are linked to Childhood Stress

PAX8/PAX8-AS1 DNA methylation levels are associated with objective sleep duration in persons with unexplained hypersomnolence using a deep phenotyping approach

Genome-wide disruption of 5-hydroxymethylcytosine in a mouse model of autism

DNA Hypomethylation in Blood Links B3GALT4 and ZADH2 to Alzheimer's Disease

Altered Function of the SCN1A Voltage-gated Sodium Channel Leads to γ-Aminobutyric Acid-ergic (GABAergic) Interneuron Abnormalities

Disruption of DNA methylation-mediated cranial neural crest proliferation and differentiation causes orofacial clefts in mice

Whole genome methylation sequencing in blood identifies extensive differential DNA methylation in late‐onset dementia due to Alzheimer's disease

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

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