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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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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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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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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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Bioavailability and cardiovascular effects of adrenaline administered by Anapen 500 μg auto‐injector in healthy volunteers

British journal of clinical pharmacology, 2023-03, Vol.89 (3), p.1012-1019

2023

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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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A Decade of Minimally Invasive Mitral Repair: Long-Term Outcomes

The Annals of thoracic surgery, 2009-10, Vol.88 (4), p.1180-1184

2009

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XLMR genes: update 2007

European journal of human genetics : EJHG, 2008-04, Vol.16 (4), p.422-434

2008

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High-Risk Aortic Valve Replacement: Are the Outcomes as Bad as Predicted?

The Annals of thoracic surgery, 2008, Vol.85 (1), p.102-107

2008

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Outcomes of the RESTOR-MV Trial (Randomized Evaluation of a Surgical Treatment for Off-Pump Repair of the Mitral Valve)

Journal of the American College of Cardiology, 2010-12, Vol.56 (24), p.1984-1993

2010

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Decreased tryptophan metabolism in patients with autism spectrum disorders

Molecular autism, 2013-06, Vol.4 (1), p.16-16, Article 16

2013

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Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome

Clinical epigenetics, 2019-04, Vol.11 (1), p.64-17, Article 64

2019

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The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance

Epigenetics, 2017-11, Vol.12 (11), p.923-933

2017

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An inverse agonist of the histamine H3 receptor improves wakefulness in narcolepsy: Studies in orexin−/− mice and patients

Neurobiology of disease, 2008-04, Vol.30 (1), p.74-83

2008

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In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase

PloS one, 2011-05, Vol.6 (5), p.e20373

2011

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Zebrafish knockout of Down syndrome gene, DYRK1A , shows social impairments relevant to autism

Molecular autism, 2017-09, Vol.8 (1), p.50-14, Article 50

2017

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Protein sector analysis for the clustering of disease-associated mutations

BMC genomics, 2014-12, Vol.15 Suppl 11 (S11), p.S4-S4, Article S4

2014

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Administration of oxathridine, a first‐in‐class histamine‐3 receptor partial agonist in healthy male volunteers: Central nervous system depression and pseudo‐hallucinations

British journal of clinical pharmacology, 2024-01, Vol.90 (1), p.321-335

2024

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Revealing the Effects of Missense Mutations Causing Snyder-Robinson Syndrome on the Stability and Dimerization of Spermine Synthase

International journal of molecular sciences, 2016-01, Vol.17 (1), p.77-77

2016

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Body and diet composition of sympatric black and grizzly bears in the Greater Yellowstone Ecosystem

The Journal of wildlife management, 2014-01, Vol.78 (1), p.68-78

2014

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PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation

Disease models & mechanisms, 2023-04, Vol.16 (4)

2023

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Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

Nature genetics, 2010-06, Vol.42 (6), p.486-488

2010

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A Consistent Theory of Tachyons with Interesting Physics for Neutrinos

Tachyon Interactions

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

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

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

Bioavailability and cardiovascular effects of adrenaline administered by Anapen 500 μg auto‐injector in healthy volunteers

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

A Decade of Minimally Invasive Mitral Repair: Long-Term Outcomes

XLMR genes: update 2007

High-Risk Aortic Valve Replacement: Are the Outcomes as Bad as Predicted?

Outcomes of the RESTOR-MV Trial (Randomized Evaluation of a Surgical Treatment for Off-Pump Repair of the Mitral Valve)

Decreased tryptophan metabolism in patients with autism spectrum disorders

Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome

The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance

An inverse agonist of the histamine H3 receptor improves wakefulness in narcolepsy: Studies in orexin−/− mice and patients

In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase

Zebrafish knockout of Down syndrome gene, DYRK1A , shows social impairments relevant to autism

Protein sector analysis for the clustering of disease-associated mutations

Administration of oxathridine, a first‐in‐class histamine‐3 receptor partial agonist in healthy male volunteers: Central nervous system depression and pseudo‐hallucinations

Revealing the Effects of Missense Mutations Causing Snyder-Robinson Syndrome on the Stability and Dimerization of Spermine Synthase

Body and diet composition of sympatric black and grizzly bears in the Greater Yellowstone Ecosystem

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation

Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

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