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Mark Levin

6PUBLICATIONS
56CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Pacific Peoples and disabilityDevelopmental genetics (incl. sex determination)Major global burdens of diseaseCancer genetics
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Journal

Publications (6)

Sort by Publication Date:
|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

|Jul 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients.

Mark D Levin, Sulagna C Saitta, Karen W Gripp

Pageof 1

Frequent Collaborators

3 joint publications

Beth A Kozel

1 joint publications

Jennifer M Kalish

1 joint publications

Laryssa A Huryn

1 joint publications

Lev Prasov

1 joint publications

Wadih M Zein

1 joint publications

Catherine A Cukras

1 joint publications

Brian P Brooks

1 joint publications

Robert B Hufnagel

1 joint publications

Delong Liu

1 joint publications

Charles J Billington

Frequent Collaborators

3 joint publications

Beth A Kozel

1 joint publications

Jennifer M Kalish

1 joint publications

Laryssa A Huryn

1 joint publications

Lev Prasov

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