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Genomic Center

The GENOMIC CENTER in Numbers

1

Gene Therapy

12 ONGOING RESEARCH PROJECTS

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2

Oncology

5 ONGOING RESEARCH PROJECTS

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3

Drug Discovery & Delivery

8 ONGOING RESEARCH PROJECTS

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Publications

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population

Rotem Greenberg, Ofer Isakov, Bella Davidov, Morad Khayat, Shirly Amar, Atalia Shtorch- Asor, Jumana Haddad Halloun, Sarit Farage Barhom, Daphne Chapman Shimshoni, Dana Brabbing-Goldstein, Maria Karter, Yael Avigdor, Isabelle Espanioly, Valerie Drasinover, Olga Krivoruk, Harel Zalts, Rivka Sukenik-Halevy, Shira Litz Philipsborn, Ran D Balicer, Shay Ben-Shachar

Journal of Medical Gentics

2026

Incorporation of clinical and molecular variant properties improves the performance of in silico pathogenicity prediction tools

Ofer Isakov, Reut Ashwal-Fluss, Dina Marek-Yagel, Shamil Sunyaev, Shay Ben-Shachar

Genetics in Medicine

2026

Evaluating the Impact of ClinGen Variant Curation Expert Panel Criteria Specifications on Variant Interpretation across Multiple Genes

Dina Marek-Yagel, Rotem Greenberg, Michal Naftali, Shay Ben Shachar, Ofer Isakov

The Journal of Molecular Diagnostics

2026

Psychologically informed reminder messages for promoting BRCA1/2 carrier screening: evidence from a large-scale population-based study

Tom Mushkat, Rotem Greenberg, Ofer Isakov, Samah Hayek, Hadassah Raskas, Shay Ben-Shachar, Adi Berliner-Senderey

European Journal of Public Health

2026

N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder

Asier Iturrate, Nurit Assia Batzir, Ranit Jaron, David Garcia-Valentin, Julian Nevado, Jair Tenorio-Castano, Pablo Lapunzina, Kamila Lee, Rotem Greenberg, Dvora Sassi, Sharon Aharoni, Alla Kuzminsky, Lina Basel-Salmon, Naama Orenstein, Yakov Fellig, Shay Ben-Shachar, Dina Marek-Yagel, Victor L Ruiz-Perez

European Journal of Human Genetics

2026

Genetics First Approach: Expanding the Utility of Genetic Testing by Non-Geneticist Physicians

Rotem Greenberg, Noa Shefer Averbuch, Lena Sagi-Dain, Idit Maya, Noa Ruhrman Shahar, Nesia Kropach-Gilad, Dina Mark-Yagel, Ran D Balicer, Shay Ben Shachar

Genetics in Medicine

2025

No association between FMR1 premutation and either ADHD or anxiety in 53,707 women undergoing genetic testing for family planning purposes

Liraz Klausner, Shai Carmi, Shay Ben-Shachar, Noa Lev-El Halabi, Lina Basel-Salmon, Dana Brabbing-Goldstein

Genetics in Medicine

2025

Community-oriented, hospital level genetics: a new approach to improve access for underserved communities

Yoel Gofin, Fadel Tibi, Eliana Fanous, Shay Ben-Shachar, Rivka Sukenik-Halevy

Pediatric Research

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, Ofer Isakov, Michal Naftali, Elena Friedman, Lily Bazak, Daniel Monakier, Alvit Veber, Nechama Shalva, Amitai Segev, Moti Haim, Lena Sagi-Dain, Lilach Benyamini, Adel Shalata, Sagi Josefsberg Ben Yehoshua, Lina Basel Salmon, Sara Hoss, Shay Ben-Shachar

Circulation: Genomic and Precision Medicine

2025

PANGEN: an online platform for the comparison and creation of diagnostic gene panels

Ofer Isakov, Dina Marek-Yagel, Rotem Greenberg, Michal Naftali, Shay Ben-Shachar

Database

2024

Characterization of the indications for performing gene panel sequencing tests in a genomic center

Rotem Greenberg, Ofer Isakov, S Ben Shahar, Lena Sagi-Dain

Harefuah

2023

Carrier screening program for BRCA1/BRCA2 pathogenic variants among Ashkenazi Jewish women in Israel: An observational study

Rotem Greenberg, Efrat Aharonov-Majar, Ofer Isakov, Samah Hayek, Naama Elefant, Ran D Balicer, Adi Berliner Senderey, Shay Ben-Shachar

Genetics in Medicine Open

2023

The Ivan and Francesca Berkowitz Family Living Laboratory
 

Untangling the precise factors that underlie medical mysteries can illuminate individualized treatments based on a person’s genetic predispositions, immune profile, health history, and lifestyle. Such insights can propel forward the science and practice of precision medicine and have a profound effect on human health.

In a decisive step forward on this quest, Harvard Medical School in Boston and Clalit Research Institute in Tel Aviv have launched a joint precision medicine effort, enabled by a donation from the Berkowitz family.  

We have established The Ivan and Francesca Berkowitz Family Living Laboratory Collaboration at Harvard Medical School and Clalit Research Institute. The program has two arms:

- The Ivan and Francesca Berkowitz Family Living Laboratory at HMS.

- The Ivan and Francesca Berkowitz Family Precision Medicine Clinic at Clalit. 

 

The two arms work together to conduct joint research. They also feature a clinical component that provides diagnosis and care for patients with rare, undiagnosed, and hard-to-treat conditions, in addition to research.

We Are Visionaries

Our vision of precision medicine is possible thanks to technological advances that enable rapid sequencing and decoding of the human genome. Along with this, the development of advanced computing capabilities enables the analysis  of various types of data in very large amounts (Big Data).

Clalit's new genomic center was established as a significant part of this innovative medical vision and gives our clients a much faster and more professional response due to the center's close interface with the clinical staff.

Pink Poppy Flowers
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We provide whole exome and whole genome sequencing, advanced bioinformatics and genomic variants’ analysis:

  • Sequencing and bioinformatics services

  • Genetic population studies/ specific disorders

  • Retrospective genomic control groups

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