Search Results - "Meyers, Lindsay"

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    Survey of checkpoints along the pathway to diverse biomedical research faculty by Meyers, Lindsay C, Brown, Abigail M, Moneta-Koehler, Liane, Chalkley, Roger

    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 by Ruzante, Juliana M, Olin, Katherine, Munoz, Breda, Nawrocki, Jeff, Selvarangan, Rangaraj, Meyers, Lindsay

    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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    Turner Syndrome in Girls Presenting with Coarctation of the Aorta by Eckhauser, Aaron, MD, MSCI, South, Sarah T., PhD, Meyers, Lindsay, MS, LCGC, Bleyl, Steven B., MD, PhD, Botto, Lorenzo D., MD

    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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    Expanding the genetic and clinical spectrum of the NONO‐associated X‐linked intellectual disability syndrome by Carlston, Colleen M., Bleyl, Steven B., Andrews, Ashley, Meyers, Lindsay, Brown, Sara, Bayrak‐Toydemir, Pinar, Bale, James F., Botto, Lorenzo D.

    “…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 by Tannour-Louet, Mounia, Han, Shuo, Corbett, Sean T, Louet, Jean-Francois, Yatsenko, Svetlana, Meyers, Lindsay, Shaw, Chad A, Kang, Sung-Hae L, Cheung, Sau Wai, Lamb, Dolores J

    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 by Brown, Abigail M, Meyers, Lindsay C, Varadarajan, Janani, Ward, Nicholas J, Cartailler, Jean-Philippe, Chalkley, Roger G, Gould, Kathleen L, Petrie, Kimberly A

    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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    Expanding the phenotype of CACNA1C mutation disorders by Gakenheimer‐Smith, Lindsey, Meyers, Lindsay, Lundahl, Derek, Menon, Shaji C., Bunch, T. Jared, Sawyer, Briana L., Tristani‐Firouzi, Martin, Etheridge, Susan P.

    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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    Epidemiological dynamics of enterovirus D68 in the United States and implications for acute flaccid myelitis by Park, Sang Woo, Pons-Salort, Margarita, Messacar, Kevin, Cook, Camille, Meyers, Lindsay, Farrar, Jeremy, Grenfell, Bryan T

    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 by Knight, Linda M., Miller, Erin, Kovach, Joshua, Arscott, Patricia, von Alvensleben, Johannes C., Bradley, David, Valdes, Santiago O., Ware, Stephanie M., Meyers, Lindsay, Travers, Curtis D., Campbell, Robert M., Etheridge, Susan P.

    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 by Yetman, Anji T, Starr, Lois J, Bleyl, Steven B, Meyers, Lindsay, Delaney, Jeffrey W

    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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    A role for Apolipoprotein A-I in the pathogenesis of multiple sclerosis by Meyers, Lindsay, Groover, Chassidy J, Douglas, Joshua, Lee, Sangmin, Brand, David, Levin, Michael C, Gardner, Lidia A

    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 by Nawrocki, Jeff, Olin, Katherine, Holdrege, Martin C, Hartsell, Joel, Meyers, Lindsay, Cox, Charles, Powell, Michaela, Cook, Camille V, Jones, Jay, Robbins, Tom, Hemmert, Andrew, Ginocchio, Christine C

    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 by Berg, Alizabeth E., Meyers, Lindsay L., Dent, Karin M., Rothwell, Erin W., Everitt, Melanie D.

    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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