Mark Levin

7PUBLICATIONS
60CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Pacific Peoples and disabilityDevelopmental genetics (incl. sex determination)Major global burdens of disease
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Publications (7)

|Sep 16, 2026
Feasibility of Functional Near-Infrared Spectroscopy in Assessing Prefrontal Cortical Activation During Behaviour Inhibition in Williams Syndrome.

|Jun 21, 2024
Increased heart rate fragmentation in those with Williams-Beuren syndrome suggests nonautonomic mechanistic contributors to sudden death risk.

Brianna M Cathey, Anna Bellach, James Troendle

|Feb 21, 2024
Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome.

Brian Walitt, Komudi Singh, Samuel R LaMunion

|Jan 31, 2024
Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome.

Delong Liu, Charles J Billington, Neelam Raja

|Jun 27, 2022
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome.

Laryssa A Huryn, Taylor Flaherty, Rosalie Nolen

|May 29, 2021
X-linked creatine transporter deficiency results in prolonged QTc and increased sudden death risk in humans and disease model.

Mark D Levin, Simona Bianconi, Andrew Smith

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Frequent Collaborators

4 joint publications

Beth A Kozel

1 joint publications

Jennifer M Kalish

1 joint publications

Laryssa A Huryn

1 joint publications

Lev Prasov