Hagar Mor-Shaked

12PUBLICATIONS
26CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Diagnostic radiographyGene mapping
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Publications (12)

|Aug 16, 2026
When Fetal Anomalies Lead to Prognostic Clarification: An Underrecognized Application of Exome Sequencing.

|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

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Frequent Collaborators

6 joint publications

Tamar Harel

3 joint publications

Hagit Daum

3 joint publications

Jonathan Rips

1 joint publications

Tzipora Falik-Zaccai