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A Consistent Theory of Tachyons with Interesting Physics for Neutrinos

Symmetry (Basel), 2022-06, Vol.14 (6), p.1172

Schwartz, Charles

2022

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Tachyon Interactions

Symmetry (Basel), 2023-01, Vol.15 (1), p.209

Schwartz, Charles

2023

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Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms

Neuroscience and biobehavioral reviews, 2014-10, Vol.46 Pt 2, p.161-174

2014

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Theoretical Search for Gravitational Bound States of Tachyons

Particles, 2022-09, Vol.5 (3), p.331-345

Schwartz, Charles

2022

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Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery

American journal of human genetics, 2012-04, Vol.90 (4), p.579-590

2012

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Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes

PloS one, 2015-02, Vol.10 (2), p.e0116454-e0116454

2015

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Pitolisant versus placebo or modafinil in patients with narcolepsy: a double-blind, randomised trial

Lancet neurology, 2013-11, Vol.12 (11), p.1068-1075

2013

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EXPERIMENT AND THEORY IN COMPUTATIONS OF THE He ATOM GROUND STATE

International journal of modern physics. E, Nuclear physics, 2006-06, Vol.15 (4), p.877-888

SCHWARTZ, CHARLES

2006

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Spermine synthase and MYC cooperate to maintain colorectal cancer cell survival by repressing Bim expression

Nature communications, 2020-06, Vol.11 (1), p.3243-16, Article 3243

2020

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Impact of high intensity interval exercise on executive function and brain derived neurotrophic factor in healthy college aged males

Physiology & behavior, 2018-07, Vol.191, p.116-122

2018

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Safety and efficacy of pitolisant on cataplexy in patients with narcolepsy: a randomised, double-blind, placebo-controlled trial

Lancet neurology, 2017-03, Vol.16 (3), p.200-207

2017

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Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions

American journal of human genetics, 2019-04, Vol.104 (4), p.685-700

2019

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eIF2γ Mutation that Disrupts eIF2 Complex Integrity Links Intellectual Disability to Impaired Translation Initiation

Molecular cell, 2012-11, Vol.48 (4), p.641-646

2012

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Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome

Nature communications, 2017-11, Vol.8 (1), p.1257-15, Article 1257

2017

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A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation

Human molecular genetics, 2014-01, Vol.23 (2), p.418-433

2014

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Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes

American journal of human genetics, 2018-01, Vol.102 (1), p.156-174

2018

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Coding exons function as tissue-specific enhancers of nearby genes

Genome research, 2012-06, Vol.22 (6), p.1059-1068

2012

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Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders

Genetics in medicine, 2021-06, Vol.23 (6), p.1065-1074

2021

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Evolution of operative techniques and perfusion strategies for minimally invasive mitral valve repair

The Journal of thoracic and cardiovascular surgery, 2012-04, Vol.143 (4), p.S68-S70

2012

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Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly

American journal of human genetics, 2010-02, Vol.86 (2), p.185-195

2010

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Effects of exercise training on ANGPTL3/8 and ANGPTL4/8 and their associations with cardiometabolic traits

Journal of lipid research, 2024-02, Vol.65 (2), p.100495-100495, Article 100495

2024

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Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity

Human molecular genetics, 2015-05, Vol.24 (10), p.2861-2872

2015

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The MCT8 thyroid hormone transporter and Allan–Herndon–Dudley syndrome

Baillière's best practice & research. Clinical endocrinology & metabolism, 2007-06, Vol.21 (2), p.307-321

2007

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Defining the 3′Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome

International journal of molecular sciences, 2023-07, Vol.24 (13), p.10712

2023

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The Future of Clinical Diagnosis: Moving Functional Genomics Approaches to the Bedside

Clinics in laboratory medicine, 2020-06, Vol.40 (2), p.221-230

2020

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A Consistent Theory of Tachyons with Interesting Physics for Neutrinos

Tachyon Interactions

Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms

Theoretical Search for Gravitational Bound States of Tachyons

Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery

Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes

Pitolisant versus placebo or modafinil in patients with narcolepsy: a double-blind, randomised trial

EXPERIMENT AND THEORY IN COMPUTATIONS OF THE He ATOM GROUND STATE

Spermine synthase and MYC cooperate to maintain colorectal cancer cell survival by repressing Bim expression

Impact of high intensity interval exercise on executive function and brain derived neurotrophic factor in healthy college aged males

Safety and efficacy of pitolisant on cataplexy in patients with narcolepsy: a randomised, double-blind, placebo-controlled trial

Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions

eIF2γ Mutation that Disrupts eIF2 Complex Integrity Links Intellectual Disability to Impaired Translation Initiation

Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome

A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation

Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes

Coding exons function as tissue-specific enhancers of nearby genes

Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders

Evolution of operative techniques and perfusion strategies for minimally invasive mitral valve repair

Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly

Effects of exercise training on ANGPTL3/8 and ANGPTL4/8 and their associations with cardiometabolic traits

Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity

The MCT8 thyroid hormone transporter and Allan–Herndon–Dudley syndrome

Defining the 3′Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome

The Future of Clinical Diagnosis: Moving Functional Genomics Approaches to the Bedside

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