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Kahana, Sarit
29  results:
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1

Chromosomal microarray testing yield in 829 cases of microc..:

Sukenik-Halevy, Rivka ; Mevorach, Nir ; Basel-Salmon, Lina...
Archives of Gynecology and Obstetrics.  , 2024
Link: https://doi.org/10.1007/..
 
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2

Exploring inheritance, and clinical penetrance of distal Xq..:

Levy, Michal ; Elron, Eyal ; Shohat, Mordechai...
Journal of Human Genetics.  69 (2024)  7 - p. 337-343 , 2024
Link: https://doi.org/10.1038/..
 
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3

Proximal 1q21 duplication: A syndrome or a susceptibility l..:

Levy, Michal ; Shohat, Mordechai ; Kahana, Sarit...
American Journal of Medical Genetics Part A.  191 (2023)  10 - p. 2551-2557 , 2023
Link: https://doi.org/10.1002/..
 
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4

Prevalence of high-penetrant copy number variants in 7734 l..:

Sagi-Dain, Lena ; Salzer Sheelo, Liat ; Brabbing-Goldstein, Dana...
American Journal of Obstetrics & Gynecology MFM.  5 (2023)  12 - p. 101201 , 2023
Link: https://doi.org/10.1016/..
 
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5

Residual risk for clinically significant copy number varian..:

Maya, Idit ; Salzer Sheelo, Liat ; Brabbing-Goldstein, Dana...
American Journal of Obstetrics and Gynecology.  226 (2022)  4 - p. 562.e1-562.e8 , 2022
Link: https://doi.org/10.1016/..
 
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6

Chromosomal Microarray Analysis Compared With Noninvasive P..:

Sagi-Dain, Lena ; Salzer Sheelo, Liat ; Brabbing-Goldstein, Dana...
Obstetrics & Gynecology.  139 (2022)  5 - p. 877-887 , 2022
Link: https://doi.org/10.1097/..
 
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7

Prenatal and postnatal chromosomal microarray analysis in 8..:

Salzer-Sheelo, Liat ; Polak, Uri ; Barg, Ayelet...
Archives of Gynecology and Obstetrics.  306 (2022)  4 - p. 1007-1013 , 2022
Link: https://doi.org/10.1007/..
 
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8

The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions..:

Maya, Idit ; Kahana, Sarit ; Agmon‐Fishman, Ifaat...
American Journal of Medical Genetics Part A.  185 (2021)  5 - p. 1461-1467 , 2021
Link: https://doi.org/10.1002/..
 
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9

A study of normal copy number variations in Israeli populat..:

Maya, Idit ; Smirin-Yosef, Pola ; Kahana, Sarit...
Human Genetics.  140 (2020)  3 - p. 553-563 , 2020
Link: https://doi.org/10.1007/..
 
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10

Based on a cohort of 52,879 microarrays, recurrent intragen..:

Maya, Idit ; Kahana, Sarit ; Agmon-Fishman, Ifaat...
European Journal of Medical Genetics.  63 (2020)  10 - p. 104008 , 2020
Link: https://doi.org/10.1016/..
 
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11

Should We Report 15q11.2 BP1-BP2 Deletions and Duplications..:

Maya, Idit ; Perlman, Sharon ; Shohat, Mordechai...
Journal of Clinical Medicine.  9 (2020)  8 - p. 2602 , 2020
Link: https://doi.org/10.3390/..
 
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12

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk ..:

Sagi-Dain, Lena ; Cohen Vig, Lital ; Kahana, Sarit...
Genetics in Medicine.  21 (2019)  11 - p. 2462-2467 , 2019
Link: https://doi.org/10.1038/..
 
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13

When genotype is not predictive of phenotype: implications ..:

Maya, Idit ; Sharony, Reuven ; Yacobson, Shiri...
Genetics in Medicine.  20 (2018)  1 - p. 128-131 , 2018
Link: https://doi.org/10.1038/..
 
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14

A de-novo interstitial microduplication involving 2p16.1-p1..:

Mimouni-Bloch, Aviva ; Yeshaya, Josepha ; Kahana, Sarit..
European Journal of Paediatric Neurology.  19 (2015)  6 - p. 711-715 , 2015
Link: https://doi.org/10.1016/..
 
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15

Proteasome inhibitors sensitize glioma cells and glioma ste..:

Kahana, Sarit ; Finniss, Susan ; Cazacu, Simona...
Cellular Signalling.  23 (2011)  8 - p. 1348-1357 , 2011
Link: https://doi.org/10.1016/..
 
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