Publications by authors named "Reut Matar"

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Don't lose sight: rare extramedullary involvement of myeloid/lymphoid neoplasm with translocation in blast phase.
Neta Sternbach, Omer Y Bialer, Alon Rozental, Adi Shacham-Abulafia, Shiri Yacobson, Reut T Matar

Haematologica· December 2025

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The Value of ROH Metrics for Predicting Morbidity: Insights From a Large Cohort Analysis of Chromosomal Microarray.
Lena Sagi-Dain, Michal Levy, Reut Matar, Sarit Kahana, Ifaat Agmon-Fishman

Clin Genet· May 2025

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Is There an Alternative "Advanced Maternal Age" Threshold for Recommendation of Invasive Prenatal Testing?
Idit Maya, Liat Salzer Sheelo, Dana Brabbing-Goldstein, Reut Matar, Sarit Kahana

J Obstet Gynaecol Can· May 2025

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2q13 Distal Microdeletion: Considering Evidence for an Emerging Syndrome Versus Susceptibility Locus: Twenty-Five New Cases and Review of the Literature.
Eyal Elron, Mordechai Shohat, Lina Basel-Salmon, Sarit Kahana, Reut Matar

Am J Med Genet A· April 2025

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The Diagnostic Yield of Chromosomal Microarray Analysis in Third-Trimester Fetal Abnormalities.
Eyal Elron, Idit Maya, Noa Shefer-Averbuch, Sarit Kahana, Reut Matar

Am J Perinatol· December 2024

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Regions of Homozygocity size patterns among diverse ethnic groups in Israel: Toward tailored diagnostic reporting thresholds.
Idit Maya, Michal Levy, Reut Matar, Sarit Kahana, Ifaat Agmon-Fishman

Am J Med Genet A· December 2024

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Exploring the human genomic landscape: patterns of common homozygosity regions in a large middle eastern cohort.
Lena Sagi-Dain, Michal Levy, Reut Matar, Sarit Kahana, Ifaat Agmon-Fishman

Hum Mol Genet· November 2024

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Chromosomal microarray testing yield in 829 cases of microcephaly: a clinical characteristics-based analysis for prenatal and postnatal cases.
Rivka Sukenik-Halevy, Nir Mevorach, Lina Basel-Salmon, Reut Tomashov Matar, Sarit Kahana

Arch Gynecol Obstet· September 2024

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Machine learning-enhanced noninvasive prenatal testing of monogenic disorders.
Noa Liscovitch-Brauer, Ravit Mesika, Tom Rabinowitz, Hadas Volkov, Meitar Grad, Reut Tomashov Matar

Prenat Diagn· August 2024

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The new face of cystic fibrosis in the era of population genetic carrier screening.
Miri Dotan, Hannah Blau, Amihood Singer, Patrick Stafler, Dario Prais, Reut Matar

J Cyst Fibros· July 2024

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A Founder Variant Associated with Early Onset Recurrent Melanoma and Various Solid Malignancies.
Aasem Abu Shtaya, Inbal Kedar, Lily Bazak, Lina Basel-Salmon, Sarit Farage Barhom, Reut Matar

Genes (Basel)· March 2024

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Prevalence of high-penetrant copy number variants in 7734 low-risk pregnancies.
Lena Sagi-Dain, Liat Salzer Sheelo, Dana Brabbing-Goldstein, Reut Matar, Sarit Kahana

Am J Obstet Gynecol MFM· December 2023

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Proximal 1q21 duplication: A syndrome or a susceptibility locus?
Michal Levy, Mordechai Shohat, Sarit Kahana, Reut Matar, Kochav Klein

Am J Med Genet A· October 2023

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Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects.
Liat Salzer-Sheelo, Uri Polak, Ayelet Barg, Sarit Kahana, Shiri Yacobson, Reut Matar

Arch Gynecol Obstet· October 2022

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Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening.
Lena Sagi-Dain, Liat Salzer Sheelo, Dana Brabbing-Goldstein, Reut Matar, Sarit Kahana

Obstet Gynecol· May 2022

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Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings.
Idit Maya, Liat Salzer Sheelo, Dana Brabbing-Goldstein, Reut Matar, Sarit Kahana

Am J Obstet Gynecol· April 2022

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The phenotype of 15 cases with rare 8q24.13-q24.3 deletions-A new syndrome or still an enigma?
Idit Maya, Sarit Kahana, Ifaat Agmon-Fishman, Cochava Klein, Reut Matar

Am J Med Genet A· May 2021

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A study of normal copy number variations in Israeli population.
Idit Maya, Pola Smirin-Yosef, Sarit Kahana, Sne Morag, Shiri Yacobson, Reut Matar

Hum Genet· March 2021

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Teaching clinicians practical genomic medicine: 7 years' experience in a tertiary care center.
Rachel Michaelson-Cohen, Liat Salzer-Sheelo, Rivka Sukenik-Halevy, Arie Koifman, Avi Fellner, Reut Matar

Genet Med· October 2020

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Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.
Idit Maya, Sarit Kahana, Ifaat Agmon-Fishman, Cochava Klein, Reut Matar

Eur J Med Genet· October 2020

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Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Reut Matar

Genet Med· November 2019

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Bayesian-based noninvasive prenatal diagnosis of single-gene disorders.
Tom Rabinowitz, Avital Polsky, David Golan, Artem Danilevsky, Guy Shapira, Reut Tomashov Matar

Genome Res· March 2019

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