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Rebecca McClellan

Observed name: R. McClellan
ORCID: 0000-0002-7020-7758
Observed ORCID: 0000-0002-7020-7758
OpenAlex ID: A5023655761
Clinical whole exome sequencing in child neurology practice
2014 · Siddharth Srivastava, Julie S. Cohen, et al. · Annals of Neurology · 277
DNM1 encephalopathy
2017 · Sarah von Spiczak, Katherine L. Helbig, et al. · Neurology · 112
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Natural history and genotype‐phenotype correlations in 72 individuals with SATB2 ‐associated syndrome
2018 · Yuri A. Zarate, Constance L. Smith‐Hicks, et al. · American Journal of Medical Genetics Part A · 71
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly
2015 · Yizhou Ye, Megan T. Cho, et al. · Molecular Case Studies · 65
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Clinical laboratory studies in Barth Syndrome
2014 · Hilary J. Vernon, Yana Sandlers, et al. · Molecular Genetics and Metabolism · 45
New targets for monitoring and therapy in Barth syndrome
2016 · W. Reid Thompson, Brittany DeCroes, et al. · Genetics in Medicine · 43
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Mutations in FARS2 and non‐fatal mitochondrial dysfunction in two siblings
2015 · Hilary J Vernon, Rebecca McClellan, et al. · American Journal of Medical Genetics Part A · 37
Functional exercise capacity, strength, balance and motion reaction time in Barth syndrome
2019 · Brittany Hornby, Rebecca McClellan, et al. · Orphanet Journal of Rare Diseases · 28
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Variants in the transcriptional corepressor BCORL1 are associated with an X‐linked disorder of intellectual disability, dysmorphic features, and behavioral abnormalities
2019 · Anju Shukla, Katta M. Girisha, et al. · American Journal of Medical Genetics Part A · 21
Anxiety and depression in inherited channelopathy patients with implantable cardioverter-defibrillators
2021 · Sajya M. Singh, Brittney Murray, et al. · Heart Rhythm O2 · 18
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Intellectual developmental disorder with cardiac arrhythmia syndrome in a child with compound heterozygous GNB5 variants
2018 · H. Vernon, J. Cohen, et al. · Clinical Genetics · 17
C-reactive Protein Elevation Is Associated With QTc Interval Prolongation in Patients Hospitalized With COVID-19
2022 · Nino Isakadze, Marc C. Engels, et al. · Frontiers in Cardiovascular Medicine · 12
Unraveling Complexities in Genetically Elusive Long QT Syndrome
2024 · Babken Asatryan, Brittney Murray, et al. · Circulation Arrhythmia and Electrophysiology · 10
Incorporation of genetic testing significantly increases the number of individuals diagnosed with familial hypercholesterolemia
2020 · Emily E. Brown, Kathleen H. Byrne, et al. · Journal of clinical lipidology · 7
Tuberous Sclerosis Complex
2017 · Tanjala T. Gipson, Andrea Poretti, et al. · Oxford University Press eBooks · 6
Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association
2025 · Jessica L. Fetterman, Patrick F. Chinnery, et al. · Circulation · 5
Acquired Long QT and Ventricular Arrhythmias in the Setting of Acute Inflammation
2021 · Dominik Beer, Nino Isakadze, et al. · JACC Case Reports · 4
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Cardiovascular Genetic Counseling Is Associated With Improved Patient-Reported Outcomes Across Clinical Indications and Settings
2026 · Brittney Murray, Catherine Gordon, et al. · Circulation Genomic and Precision Medicine · 2
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The emerging role of metabolomics analysis in genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)
2025 · Marcus J. Miller, Maria Laura Duque Lasio, et al. · Genetics in Medicine · 2
Cover Image, Volume 179A, Number 5, May 2019
2019 · Anju Shukla, Katta M. Girisha, et al. · American Journal of Medical Genetics Part A · 2
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Abstract 14500: Physical Activity in Individuals With the Long Qt Syndrome: Baseline Data From the Lifestyle and Exercise in Long Qt Study (live Lqts)
2020 · Rachel J Lampert, Sharlene Day, et al. · Circulation · 1
Genetic Counseling Educational Videos Significantly Improve Access to Genetic Testing and Counseling for Inpatients with Cardiovascular Disease
2026 · Emily E. Brown, Bryana Rivers, et al. · medRxiv
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Is it time for a paradigm shift? Tailored online video education instead of pretest genetic counseling facilitates high genetic test uptake and informed choice for adults seeking cardiovascular genetic testing
2026 · Bryana J. Rivers, Brittney Murray, et al. · medRxiv
Ap-534523-002 Accelerating Access to Guideline-directed Genetic Test Results While Maintaining the Patient-reported Benefits of Cardiovascular Genetic Counseling: Results of Resequence-gc (nct05422573)
2026 · Brittney A. Murray, Bryana J. Rivers, et al. · Heart Rhythm
Reproductive decision‐making for Barth syndrome carriers: Unexplored complexities
2025 · Julia Castro, Cynthia A. James, et al. · Journal of Genetic Counseling
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Works count: 32
Citation count: 785
H-index: 12
I10-index: 13
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