Hagar Mor-Shaked

11PUBLICATIONS
25CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Diagnostic radiographyGene mappingMolecular targets
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Publications (11)

|Feb 27, 2026
CUL3-Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype.

Yoel Gofin, Tania Dery, Tamar Tenne

|Sep 27, 2025
High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics.

Rivka Birnbaum, Maya Slovik, Shamir Zenvirt

|Sep 27, 2025
A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss-of-Function of DMRT2.

Jonathan Rips, Hagar Mor-Shaked, Oded Shamriz

|Aug 06, 2025
Exploring the unique characteristics of genes with dual autosomal dominant and recessive inheritance: mechanisms, phenotypes and candidate identification.

Shlomit Ezer, Tal Sido, Jonathan Rips

|May 30, 2025
Long-Read Whole-Genome Sequencing Uncovers a Deletion Upstream to HOXD13 Causing Synpolydactyly.

Jonathan Rips, Rivka Birnbaum, Chaim Jalas

|May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome.

Shiyu Luo, Valérie Gailus-Durner, Bobbi McGivern

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Frequent Collaborators

6 joint publications

Tamar Harel

2 joint publications

Hagit Daum

2 joint publications

Jonathan Rips

1 joint publications

Tzipora Falik-Zaccai