Peter B. Kang

University of Vermont — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

45h-index9.0kcitations289works2.12yr avg
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Research Topics

Muscle Physiology and Disorders(95), Neurogenetic and Muscular Disorders Research(66), Genetic Neurodegenerative Diseases(35), RNA Research and Splicing(29), Cardiomyopathy and Myosin Studies(29)

Publications284 total

Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patients.
Scientific Reports·2025· 1 citedOpen Access
An integrative description of a new species of marine water bear (Heterotardigrada: Echiniscoididae) from the tidal zone of the east coast of Korea
The European Zoological Journal·2025Open Access
Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular Dystrophy
Neurology·2025· 2 citedOpen Access
Accelerating Medical Record Data Abstraction and Analysis in Muscular Dystrophy
Neurology Clinical Practice·2025Open Access
The impact of <i>Hnrnpl</i> deficiency on transcriptional patterns of developing muscle cells
FEBS Open Bio·2025Open Access
<scp>ACSS2</scp> involved in acetyl‐ <scp>CoA</scp> synthesis regulates skeletal muscle function
FEBS Letters·2025Open Access
Limb-Girdle Muscular Dystrophy Scientific Workshop
Neurology Clinical Practice·2025
<i>JAG2</i> -related muscular dystrophy and Notch signaling dysfunction in muscle stem cells
2025Open Access
Reduction of Preexisting AAV9 Antibody Titers Before Onasemnogene Abeparvovec Administration in Twins With Spinal Muscular Atrophy
Neurology·2025· 2 cited
Preclinical quality, safety, and efficacy of a CGMP iPSC-derived myogenic progenitor product for the treatment of muscular dystrophies
Molecular Therapy·2025· 7 citedOpen Access
Author response for "ACSS2 involved in acetyl-CoA synthesis regulates skeletal muscle function"
2025
Missense variants in <i>TUBA4A</i> cause myo-tubulinopathies
2025· 1 citedOpen Access
Clinical Trial Readiness in Limb Girdle Muscular Dystrophy R1 (LGMDR1): A GRASP Consortium Study
Annals of Clinical and Translational Neurology·2025· 1 citedOpen Access
Message From the Editors to Our Reviewers
Neurology Genetics·2025Open Access
Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria
Genetics in Medicine·2025· 30 citedOpen Access
The Second Decade of <i>Neurology® Genetics</i> Beckons
Neurology Genetics·2025Open Access
Effects of <scp>HMG CoA</scp> reductase ( <scp>HMGCR</scp> ) deficiency on skeletal muscle development
FEBS Journal·2025· 3 citedOpen Access
Predicting the phenotype of Pompe Disease from features of GAA variants
European Journal of Human Genetics·2025· 1 cited
1 Politics in Republic of China (Taiwan): Historical Observation
Nomos Verlagsgesellschaft mbH & Co. KG eBooks·2025
Benchmarking of germline copy number variant callers from whole genome sequencing data for clinical applications
Bioinformatics Advances·2024· 1 citedOpen Access
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Frequent Co-authors

Basil T. Darras(14), Louis M. Kunkel(9), Elicia Estrella(8), Alan H. Beggs(8), A. Reghan Foley(5), Anne O’Donnell‐Luria(5), Kathryn N. North(5), Carsten G. Bönnemann(5), Kevin M. Flanigan(5), Satomi Mitsuhashi(5), Monkol Lek(4), Hemakumar M. Reddy(4), Richard S. Finkel(4), Michael McDermott(4), Iris Eisenberg(4), Hart G.W. Lidov(4), Steven M. Harrison(4), Jennifer A. Myers(4), Genri Kawahara(4), Jamie L. Marshall(3)