Victoria Parikh

33PUBLICATIONS
424CO-AUTHORS
Respiratory diseasesCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyMedical devices
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Publications (33)

|Jul 29, 2026
Damaging RBM20 E-rich domain variants are not rescued by gene replacement.

|Jul 12, 2026
Scaled Multidimensional Assays of Variant Effect Identify Sequence-Function Relationships in Hypertrophic Cardiomyopathy.

|Jul 08, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter Registry.

|Apr 30, 2026
Novel Truncating Variant c.1222DupC in RBM20 Causes Cardiomyopathy Consistent With Haploinsufficiency.

|Apr 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis.

|Mar 10, 2026
Truncating Variants in TTN are Associated With Primary Atrial Myopathy.

Daniel de Castro, Diane Fatkin, Enrique Rodriguez-Rubio

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Frequent Collaborators

20 joint publications

Euan Ashley

13 joint publications

Neal Lakdwala

11 joint publications

Jodie Ingles

11 joint publications

Matthew Wheeler