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Molecular Genetics & Genomic Medicine|October 1, 2019
ALU transposition induces familial hypertrophic cardiomyopathyLandry Nfonsam, Lijia Huang, Nancy Carson, et al.
JIMD Reports|June 17, 2016
Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) DeficiencyAmanda Smith, Skye McBride, Julien L Marcadier, et al.
Neuropathology and Applied Neurobiology|April 7, 2021
Advanced molecular pathology for rare tumours: A national feasibility study and model for centralised medulloblastoma diagnosticsStephen Crosier, Debbie Hicks, Edward C Schwalbe, et al.
International Journal of Molecular Sciences|December 11, 2022
An Exploratory Study Provides Insights into MMP9 and Aβ Levels in the Vitreous and Blood across Different Ages and in a Subset of AMD PatientsSavannah A Lynn, Flavie Soubigou, Jennifer M Dewing, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 14, 2022
Remote ECG monitoring to reduce complications following transcatheter aortic valve implantations: the Redirect TAVI studyMadhu Kailash Natarajan, Tej Narendra Sheth, Harindra Channa Wijeysundera, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|June 30, 2020
HIV Prevalence Among Women Who Exchange Sex for Money or Drugs-4 U.S. CitiesLina M Nerlander, Senad Handanagic, Kristen L Hess, et al.
Geroscience|May 22, 2023
Unique trans-kingdom microbiome structural and functional signatures predict cognitive decline in older adultsDiptaraj S Chaudhari, Shalini Jain, Vinod K Yata, et al.
JMIR Research Protocols|January 6, 2023
Engaging Black or African American and Hispanic or Latino Men Who Have Sex With Men for HIV Testing and Prevention Services Through Technology: Protocol for the iSTAMP Comparative Effectiveness TrialRuth Dana, Stephen Sullivan, Robin J MacGowan, et al.
Human Mutation|October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxiaSarah L Sawyer, Jeremy Schwartzentruber, Chandree L Beaulieu, et al.
The Journal of Molecular Diagnostics : JMD|February 8, 2019
Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care SettingHussein Daoud, Mahdi Ghani, Landry Nfonsam, et al.
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