Publications by authors named "Reilly M"

Objective: Neurofilaments are the major scaffolding proteins for the neuronal cytoskeleton, and variants in have recently been described to cause axonal Charcot-Marie-Tooth disease type 2CC (CMT2CC).

Methods: In this large observational study, we present phenotype-genotype correlations on 30 affected and 3 asymptomatic mutation carriers from eight families.

Results: The majority of patients presented in adulthood with motor-predominant and lower limb-predominant symptoms and the average age of onset was 31.

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Dominant mutations in ubiquitously expressed transfer RNA (tRNA) synthetase genes cause axonal peripheral neuropathy, accounting for at least six forms of Charcot-Marie-Tooth (CMT) disease. Genetic evidence in mouse and models suggests a gain-of-function mechanism. In this study, we used in vivo, cell type–specific transcriptional and translational profiling to show that mutant tRNA synthetases activate the integrated stress response (ISR) through the sensor kinase GCN2 (general control nonderepressible 2).

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Article Synopsis
  • Genetic testing is important for understanding family screening, diagnosis, and prognosis in patients with hypertrophic cardiomyopathy (HCM), but it also has socio-economic and psychological impacts.
  • Conventional methods for predicting positive genotypes in HCM patients have limited accuracy, which led researchers to explore using deep learning techniques, specifically deep convolutional neural networks (DCNN), to analyze echocardiographic images for better predictions.
  • The study found that combining the Mayo and Toronto HCM Genotype scores with DCNN-derived probabilities significantly improved predictive accuracy for identifying positive genotypes in HCM patients, demonstrating better performance than traditional models alone.
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  • The study explored the link between body mass index (BMI) and disability in children with Charcot-Marie-Tooth disease (CMT), comparing them to a group of healthy children.
  • It found a higher percentage of CMT children categorized as severely underweight, underweight, and obese, while fewer were considered healthy weight compared to the healthy group.
  • The research indicated that children with CMT who were either severely underweight or obese experienced greater disability than those with a healthy weight, highlighting the impact of BMI on their well-being.
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Introduction: Anti-D alloimmunization is the most common cause of severe hemolytic disease of the fetus and newborn (HDFN). The management of pregnancies affected by less frequent red blood cell (RBC) antibodies poses a challenge to clinicians, and perinatal outcomes are less well described. This study aimed to describe the frequency of clinically significant RBC antibodies in our pregnant population and analyze the risk of prenatal and postnatal treatment for HDFN in relation to our national risk classification system and management guidelines.

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Background: Obesity is an established risk factor for severe COVID-19 outcomes. The mechanistic underpinnings of this association are not well-understood.

Objective: To evaluate the mediating role of systemic inflammation in obesity-associated COVID-19 outcomes.

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Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) typically presents in middle life with a combination of neuropathy, ataxia and vestibular disease, with patients reporting progressive imbalance, oscillopsia, sensory disturbance and a dry cough. Examination identifies a sensory neuropathy or neuronopathy and bilaterally impaired vestibulo-ocular reflex. The underlying genetic basis is of biallelic AAGGG expansions in the second intron of replication factor complex subunit 1 (RFC1).

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Hundreds of interventional clinical trials have been launched in the United States to identify effective treatment strategies for combating the coronavirus disease 2019 (COVID-19) pandemic. However, to date, only a small fraction of these trials have completed enrollment, delaying the scientific investigation of COVID-19 and its treatment options. This study presents novel metrics to examine the geographic alignment between COVID-19 hotspots and interventional clinical trial sites and evaluate trial access over time during the evolving pandemic.

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Inflammation increases the risk of cardiometabolic disease. Delineating specific inflammatory pathways and biomarkers of their activity could identify the mechanistic underpinnings of the increased risk. Plasma levels of kynurenine, a metabolite involved in inflammation, associates with cardiometabolic disease risk.

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Implementation of wildfire- and climate-adaptation strategies in seasonally dry forests of western North America is impeded by numerous constraints and uncertainties. After more than a century of resource and land use change, some question the need for proactive management, particularly given novel social, ecological, and climatic conditions. To address this question, we first provide a framework for assessing changes in landscape conditions and fire regimes.

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  • Hereditary sensory neuropathy type 1 (HSN1) is linked to mutations in an enzyme involved in lipid metabolism that lead to the production of neurotoxic compounds known as 1-deoxysphingolipid bases (DSBs).
  • Research using patient-derived induced pluripotent stem cells (iPSCs) showed that these DSBs contribute to neurotoxicity by disrupting critical cell signaling and reducing the growth of sensory neuron extensions (neurites).
  • The study also found that l-serine supplementation can mitigate these adverse effects, suggesting a potential therapeutic approach for HSN1.
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  • Pathogenic variants in mitochondrial DNA (mtDNA) lead to diverse clinical symptoms, especially in neuromuscular disorders, making diagnosis challenging.
  • A case study of an adult with progressive ataxia and neuropathy, who remained undiagnosed despite various genetic tests, revealed significant mitochondrial pathology through muscle biopsy.
  • Further investigation into the mitochondrial genome identified two variants linked to the disease, emphasizing the importance of muscle biopsy for accurate diagnosis and understanding the pathogenicity of new mtDNA variants.
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Amyotrophic lateral sclerosis (ALS) is a fatal neuromuscular disease in which patients gradually become paralyzed due to loss of motor function. Many genetically inheritable mutations have been linked to ALS; however, the majority of ALS patients are considered sporadic. Therefore, there is a need for a common therapy that is effective for all ALS patients.

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Purpose: Ocular brachytherapy is a standard-of-care surgical procedure for globe salvage in the treatment of uveal melanoma. The procedure involves the placement and subsequent removal of a radioactive plaque several days later. At many locations, patients are admitted on an inpatient basis until plaque removal due to radiation safety concerns.

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Reduction plating is a concept used to provisionally maintain reduction in the treatment of various fractures throughout the body. It is often used in challenging fracture patterns where the use of reduction clamps hinders placement of the definitive fixation construct. In this article, we present a technique for fixation of ankle fractures, in which a mini-fragment plate is used to keep provision reduction of the fracture, while the definitive plate is applied.

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Young adults have the highest rates of substance use of any age group. Although men historically have higher rates of substance use disorders (SUDs) than women, research shows this gender gap is narrowing. Young adults with comorbid psychiatric disorders are at increased risk for developing a SUD.

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Bisphenol A (BPA) is a high-production volume chemical used to manufacture consumer and medical-grade plastic products. Due to its ubiquity, the general population can incur daily environmental exposure to BPA, whereas heightened exposure has been reported in intensive care patients and industrial workers. Due to health concerns, structural analogs are being explored as replacements for BPA.

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We have produced gene expression profiles of all 302 neurons of the C. elegans nervous system that match the single-cell resolution of its anatomy and wiring diagram. Our results suggest that individual neuron classes can be solely identified by combinatorial expression of specific gene families.

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Human pluripotent stem cells (PSCs) such as embryonic stem cells (ESCs) or induced pluripotent stem cells (iPSCs) are of great value for studying developmental processes, disease modeling, and drug testing. One area in which the use of human PSCs has become of great interest in recent years is for in vitro models of the neuromuscular junction (NMJ). The NMJ is a synapse at which a motor neuron releases acetylcholine to bind to skeletal muscle and stimulate contraction.

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Background: Hypertrophic cardiomyopathy (HCM) is caused by mutations in the genes coding for proteins essential in normal myocardial contraction. However, it remains unclear through which molecular pathways gene mutations mediate the development of HCM. The objectives were to determine plasma protein biomarkers of HCM and to reveal molecular pathways differentially regulated in HCM.

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A precise sequence of axon guidance events is required for the development of the ocular motor system. Three cranial nerves grow toward, and connect with, six extraocular muscles in a stereotyped pattern, to control eye movements. The signaling protein alpha2-chimaerin (α2-CHN) plays a pivotal role in the formation of the ocular motor system; mutations in , encoding α2-CHN, cause the human eye movement disorder Duane Retraction Syndrome (DRS).

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The generation of the enormous diversity of neuronal cell types in a differentiating nervous system entails the activation of neuron type-specific gene batteries. To examine the regulatory logic that controls the expression of neuron type-specific gene batteries, we interrogate single cell expression profiles of all 118 neuron classes of the nervous system for the presence of DNA binding motifs of 136 neuronally expressed transcription factors. Using a phylogenetic footprinting pipeline, we identify regulatory motif enrichments among neuron class-specific gene batteries and we identify cognate transcription factors for 117 of the 118 neuron classes.

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Article Synopsis
  • Age-related mosaic chromosomal alterations (mCAs) are linked to increased risk of various infections and indicate clonal hematopoiesis.
  • A study involving over 768,000 individuals found that expanded mCAs were significantly associated with higher rates of infections like sepsis, pneumonia, and digestive system infections.
  • The research also identified 63 genetic loci related to mCAs, which are important for immune cell function, suggesting that mCAs could signal weakened immunity and a higher likelihood of infection.
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Background: The Lapidus procedure and scarf osteotomy are indicated for the operative treatment of hallux valgus; however, no prior studies have compared outcomes between the procedures. The aim of this study was to compare clinical and radiographic outcomes between patients with symptomatic hallux valgus treated with the modified Lapidus procedure versus scarf osteotomy.

Methods: This retrospective cohort study included patients treated by 1 of 7 fellowship-trained foot and ankle surgeons.

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