Marta W Szulik

8PUBLICATIONS
19CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthCardiology (incl. cardiovascular diseases)Gene and molecular therapyMedical devices
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Publications (8)

|Aug 20, 2026
The SMYD1 p.Asn101Ser is a partial loss-of-function variant that impairs mitochondrial function and leads to early-onset cardiomyopathy.

|Apr 27, 2026
Perm1 Gene Therapy Mitigates PRDM16-Associated Cardiomyopathy.

|Nov 02, 2025
Expression profiles of histone H4K20 methylation and its associated enzymes in mouse cardiac disease and human heart failure.

Samuel Hickenlooper, Cameron Brady, Ryan Bia

|Dec 19, 2023
Nonsense Variant PRDM16-Q187X Causes Impaired Myocardial Development and TGF-β Signaling Resulting in Noncompaction Cardiomyopathy in Humans and Mice.

Bo Sun, Omid M T Rouzbehani, Ryan J Kramer

|May 22, 2023
SMYD1a protects the heart from ischemic injury by regulating OPA1-mediated cristae remodeling and supercomplex formation.

Marta W Szulik, Steven Valdez, Maureen Walsh

|Mar 29, 2023
Identification of Two Homozygous Variants in MYBPC3 and SMYD1 Genes Associated with Severe Infantile Cardiomyopathy.

Marta W Szulik, Miguel Reyes-Múgica, Daniel F Marker

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Frequent Collaborators

2 joint publications

Enrique Balderas

2 joint publications

Colin T Maguire

2 joint publications

Scott Cho

2 joint publications

Timothy M Locke