Lina Basel-Salmon

4PUBLICATIONS
16CO-AUTHORS
Neurology and neuromuscular diseasesCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|Sep 30, 2025
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder.

Asier Iturrate, Nurit Assia Batzir, Ranit Jaron

|Jan 27, 2025
Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy.

Noa Ruhrman Shahar, Dina Marek-Yagel, Rotem Greenberg

|Apr 17, 2024
Exploring inheritance, and clinical penetrance of distal Xq28 duplication syndrome: insights from 47 new unpublished cases.

Michal Levy, Eyal Elron, Mordechai Shohat

|Feb 13, 2024
Phenotypic compatibility and specificity in genomic variant classification.

Lina Basel-Salmon

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Frequent Collaborators

2 joint publications

Rotem Greenberg

1 joint publications

Noa Ruhrman Shahar

1 joint publications

Ofer Isakov

1 joint publications

Lily Bazak