Ruti Parvari

10PUBLICATIONS
13CO-AUTHORS
Gene and molecular therapyCancer geneticsCardiology (incl. cardiovascular diseases)Neurology and neuromuscular diseasesCellular interactions (incl. adhesion, matrix, cell wall)
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Publications (10)

|May 27, 2023
A Novel Mutation in the ADAMTS10 Associated with Weil-Marchesani Syndrome with a Unique Presentation of Developed Membranes Causing Severe Stenosis of the Supra Pulmonic, Supramitral, and Subaortic Areas in the Heart.

Aviva Levitas, Liam Aspit, Neta Lowenthal

|May 13, 2023
Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred.

Pierre Majdalani, Uri Yoel, Tayseer Nasasra

|Jan 21, 2023
A Missense Variation in PHACTR2 Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans.

Pierre Majdalani, Aviva Levitas, Hanna Krymko

|Oct 21, 2022
Duchenne Muscular Dystrophy and Early Onset Hypertrophic Cardiomyopathy associated with Mutations in Dystrophin and Hypertrophic Cardiomyopathy-Associated Genes.

Liam Aspit, Noga Arwas, Hanna Krymko

|Sep 16, 2022
Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes.

Baker Elsana, Ahed Imtirat, Ronit Yagev

|Sep 09, 2022
Dock10 Regulates Cardiac Function under Neurohormonal Stress.

Liad Segal, Sharon Etzion, Sigal Elyagon

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Frequent Collaborators

2 joint publications

Yoram Etzion

2 joint publications

Aviva Levitas

2 joint publications

Pierre Majdalani

2 joint publications

Raz Zarivach