Search Results - "Meyers, Lindsay"
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Survey of checkpoints along the pathway to diverse biomedical research faculty
Published in PloS one (16-01-2018)“…There is a persistent shortage of underrepresented minority (URM) faculty who are involved in basic biomedical research at medical schools. We examined the…”
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Real-time gastrointestinal infection surveillance through a cloud-based network of clinical laboratories
Published in PloS one (30-04-2021)“…Acute gastrointestinal infection (AGI) represents a significant public health concern. To control and treat AGI, it is critical to quickly and accurately…”
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FilmArray, an automated nested multiplex PCR system for multi-pathogen detection: development and application to respiratory tract infection
Published in PloS one (19-10-2011)“…The ideal clinical diagnostic system should deliver rapid, sensitive, specific and reproducible results while minimizing the requirements for specialized…”
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Turner Syndrome in Girls Presenting with Coarctation of the Aorta
Published in The Journal of pediatrics (01-11-2015)“…Objective To evaluate the frequency of Turner syndrome in a population-based, statewide cohort of girls with coarctation of the aorta. Study design The Utah…”
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The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele
Published in Nature communications (08-11-2021)“…The genetic architecture of atrial fibrillation (AF) encompasses low impact, common genetic variants and high impact, rare variants. Here, we characterize a…”
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Expanding the genetic and clinical spectrum of the NONO‐associated X‐linked intellectual disability syndrome
Published in American journal of medical genetics. Part A (01-05-2019)“…The NONO gene encodes a nuclear protein involved in RNA metabolism. Hemizygous loss‐of‐function NONO variants have been associated with syndromic intellectual…”
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Identification of de novo copy number variants associated with human disorders of sexual development
Published in PloS one (26-10-2010)“…Disorders of sexual development (DSD), ranging in severity from genital abnormalities to complete sex reversal, are among the most common human birth defects…”
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From goal to outcome: Analyzing the progression of biomedical sciences PhD careers in a longitudinal study using an expanded taxonomy
Published in FASEB bioAdvances (01-11-2023)“…Biomedical sciences PhDs pursue a wide range of careers inside and outside academia. However, there is little data regarding how career interests of PhD…”
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Clinical utility of a next generation sequencing panel assay for Marfan and Marfan-like syndromes featuring aortopathy
Published in American journal of medical genetics. Part A (01-08-2015)“…Aortopathy can be defined as aortic dilation, aneurysm, dissection, and tortuosity. Familial aortopathy may occur secondary to fibrillin‐1 (FBN1) mutations in…”
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Expanding the phenotype of CACNA1C mutation disorders
Published in Molecular genetics & genomic medicine (01-06-2021)“…Background Pathogenic variants in the L‐type Ca2+ channel gene CACNA1C cause a multi‐system disorder that includes severe long QT syndrome (LQTS), congenital…”
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Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus
Published in American journal of medical genetics. Part A (01-12-2015)“…Wolff–Parkinson–White (WPW) syndrome is a common cause of supraventricular tachycardia that carries a risk of sudden cardiac death. To date, mutations in only…”
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Automated Real-Time Collection of Pathogen-Specific Diagnostic Data: Syndromic Infectious Disease Epidemiology
Published in JMIR public health and surveillance (06-07-2018)“…Health care and public health professionals rely on accurate, real-time monitoring of infectious diseases for outbreak preparedness and response. Early…”
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Epidemiological dynamics of enterovirus D68 in the United States and implications for acute flaccid myelitis
Published in Science translational medicine (10-03-2021)“…Acute flaccid myelitis (AFM) recently emerged in the United States as a rare but serious neurological condition since 2012. Enterovirus D68 (EV-D68) is thought…”
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Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathy
Published in Heart rhythm (01-01-2020)“…The efficacy of cascade screening for the inherited heart conditions long QT syndrome (LQTS) and hypertrophic cardiomyopathy (HCM) is incompletely…”
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Progressive Aortic Dilation Associated With ACTA2 Mutations Presenting in Infancy
Published in Pediatrics (Evanston) (01-07-2015)“…Mutations in the gene ACTA2 are a recognized cause of aortic aneurysms with aortic dissection in adulthood. Recently, a specific mutation (Arg179His) in this…”
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Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors
Published in Journal of genetic counseling (01-02-2022)“…Congenital heart disease (CHD) is an indication which spans multiple specialties across various genetic counseling practices. This practice resource aims to…”
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A role for Apolipoprotein A-I in the pathogenesis of multiple sclerosis
Published in Journal of neuroimmunology (15-12-2014)“…Abstract Apolipoprotein A1 (Apo A-I), the most abundant component of high-density lipoprotein (HDL), is an anti-inflammatory molecule, yet its potential role…”
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The Effects of Social Distancing Policies on Non-SARS-CoV-2 Respiratory Pathogens
Published in Open forum infectious diseases (01-07-2021)“…Abstract Background The initial focus of the US public health response to coronavirus disease 2019 (COVID-19) was the implementation of numerous social…”
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Psychological impact of sports restriction in asymptomatic adolescents with hypertrophic cardiomyopathy, dilated cardiomyopathy, and long QT syndrome
Published in Progress in pediatric cardiology (01-06-2018)“…Adolescents with cardiomyopathy and arrhythmia syndromes are at increased risk for sudden death. As such, adolescents with these conditions are often…”
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Enterovirus D68 outbreak detection through a syndromic disease epidemiology network
Published in Journal of clinical virology (01-03-2020)“…[Display omitted] •An algorithm to predict the presence enterovirus D68 among a commercial respiratory disease diagnostic test was developed.•The algorithm was…”
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