Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Reut, Matar"'
Autor:
Naama Oresntein, Arie Koifman, Efrat Sofrin-Drucker, Adi Reches, Noa Rhurman-Shahar, Gal Zaks-Hoffer, Nurit Magal, Doron M. Behar, Yael Goldberg, Daphna Marom, Mordechai Shohat, Lina Basel-Salmon, Noa Shefer Averbuch, Lily Bazak, Reut Matar, Sagi Josefberg, Nesia Kropach-Gilad, Rachel Michaelson-Cohen, Rivka Sukenik-Halevy, Avi Fellner, Liat Salzer-Sheelo, Monika Weiss-Hubshmann, Idit Maya
Publikováno v:
Genetics in Medicine. 22:1703-1709
Increased implementation of complex genetic technologies in clinical practice emphasizes the urgency of genomic literacy and proficiency for medical professionals. We evaluated our genomic education model. We assessed the 5-day, extended format progr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a0d192c9c4ae452d21066ee1b9e6279
https://doi.org/10.1038/s41436-020-0868-4
https://doi.org/10.1038/s41436-020-0868-4
Autor:
Pola Smirin-Yosef, Mordechai Shohat, Shiri Yacobson, Elisheva Bitton, Reut Matar, Ifaat Agmon-Fishman, Mali Salmon-Divon, Lina Basel-Salmon, Sne Morag, Sarit Kahana, Idit Maya
Publikováno v:
Human Genetics. 140:553-563
The population of Israel is ethnically diverse, and individuals from different ethnic groups share specific genetic variations. These variations, which have been passed on from common ancestors, are usually reported in public databases as rare varian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4f9082484beeeac09f744001cbab24c
https://doi.org/10.1007/s00439-020-02225-4
https://doi.org/10.1007/s00439-020-02225-4
Autor:
Lena Sagi-Dain, Liat Salzer Sheelo, Dana Brabbing-Goldstein, Reut Matar, Sarit Kahana, Ifaat Agmon-Fishman, Cochava Klein, Merav Gurevitch, Lina Basel-Salmon, Idit Maya
Publikováno v:
Obstetrics and gynecology. 139(5)
To examine the effect of maternal age on the rate of clinically significant chromosomal microarray analysis results in pregnancies with abnormal maternal serum screening and to establish the residual risk for abnormal microarray findings after omitti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e49edebc8631e8a87aff0f7de7225c51
https://pubmed.ncbi.nlm.nih.gov/35576346
https://pubmed.ncbi.nlm.nih.gov/35576346
Autor:
Liat Salzer-Sheelo, Uri Polak, Ayelet Barg, Sarit Kahana, Shiri Yacobson, Ifaat Agmon-Fishman, Cochava Klein, Reut Matar, Noa Rurman-Shahar, Lena Sagi-Dain, Lina Basel-Salmon, Idit Maya, Rivka Sukenik-Halevy
Publikováno v:
Archives of gynecology and obstetrics. 306(4)
This study aimed to evaluate the prevalence of clinically significant (pathogenic and likely pathogenic) variants detected by chromosomal microarray (CMA) tests performed for prenatally and postnatally detected congenital heart defects.A retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34e648db8a2bff49b9244a7e02026b1b
https://pubmed.ncbi.nlm.nih.gov/35083553
https://pubmed.ncbi.nlm.nih.gov/35083553
Autor:
Guy Shapira, Reut Matar, Avital Polsky, David E. Golan, Chen Raff, Noam Shomron, Lina Basel-Salmon, Tom Rabinowitz, Artem Danilevsky
Publikováno v:
Genome Research. 29:428-438
In the last decade, noninvasive prenatal diagnosis (NIPD) has emerged as an effective procedure for early detection of inherited diseases during pregnancy. This technique is based on using cell-free DNA (cfDNA) and fetal cfDNA (cffDNA) in maternal bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72347c791710ef7fb4e03112952b36a0
https://doi.org/10.1101/gr.235796.118
https://doi.org/10.1101/gr.235796.118
Autor:
Lena Sagi-Dain, Idit Maya, Sarit Kahana, Dana Brabbing-Goldstein, Merav Gurevitch, Reut Matar, Lina Basel-Salmon, Ifaat Agmon-Fishman, Liat Salzer Sheelo, Cochava Klein
Publikováno v:
American Journal of Obstetrics and Gynecology. 226:562.e1-562.e8
BACKGROUND Chromosomal microarray analysis detects a clinically significant amount of copy number variants in approximately 1% of low-risk pregnancies. As the constantly growing use of noninvasive prenatal screening has facilitated the detection of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7886658914b22ae6ef6321ca7e0a328
https://doi.org/10.1016/j.ajog.2021.11.016
https://doi.org/10.1016/j.ajog.2021.11.016
Autor:
Tamar Tenne, Reut Matar, Ifaat Agmon-Fishman, Rivka Sukenik-Halevy, Shiri Yacobson, Lina Basel-Salmon, Sarit Kahana, Mordechai Shohat, Sharon Perlman, Idit Maya
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 8
Journal of Clinical Medicine, Vol 9, Iss 2602, p 2602 (2020)
Volume 9
Issue 8
Journal of Clinical Medicine, Vol 9, Iss 2602, p 2602 (2020)
Copy number variations of the 15q11.2 region at breakpoints 1-2 (BP1-BP2) have been associated with variable phenotypes and low penetrance. Detection of such variations in the prenatal setting can result in significant parental anxiety. The clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b94b62f4bf42b773000ed7b30c589e
Autor:
Idit, Maya, Pola, Smirin-Yosef, Sarit, Kahana, Sne, Morag, Shiri, Yacobson, Ifaat, Agmon-Fishman, Reut, Matar, Elisheva, Bitton, Mordechai, Shohat, Lina, Basel-Salmon, Mali, Salmon-Divon
Publikováno v:
Human genetics. 140(3)
The population of Israel is ethnically diverse, and individuals from different ethnic groups share specific genetic variations. These variations, which have been passed on from common ancestors, are usually reported in public databases as rare varian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b1c9b1544f8fe83f974482f1ed81d11
https://pubmed.ncbi.nlm.nih.gov/32980975
https://pubmed.ncbi.nlm.nih.gov/32980975
Autor:
Rachel, Michaelson-Cohen, Liat, Salzer-Sheelo, Rivka, Sukenik-Halevy, Arie, Koifman, Avi, Fellner, Adi, Reches, Daphna, Marom, Doron M, Behar, Efrat, Sofrin-Drucker, Gal, Zaks-Hoffer, Monika, Weiss-Hubshmann, Naama, Oresntein, Nesia, Kropach-Gilad, Noa, Rhurman-Shahar, Noa Shefer, Averbuch, Nurit, Magal, Lily, Bazak, Sagi, Josefberg, Reut, Matar, Yael, Goldberg, Mordechai, Shohat, Lina, Basel-Salmon, Idit, Maya
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 22(10)
Increased implementation of complex genetic technologies in clinical practice emphasizes the urgency of genomic literacy and proficiency for medical professionals. We evaluated our genomic education model.We assessed the 5-day, extended format progra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0cb7c00588d29e5e4d0d525d40f452dc
https://pubmed.ncbi.nlm.nih.gov/32616942
https://pubmed.ncbi.nlm.nih.gov/32616942
Autor:
Cochava Klein, Reuven Sharony, Mordechai Shohat, Lena Sagi-Dain, Sarit Kahana, Racheli Berger, Idit Maya, Lina Basel-Salmon, Reut Matar, Ifaat Agmon-Fishman
Publikováno v:
European journal of medical genetics. 63(10)
Introduction Congenital contractural arachnodactyly (CCA) is a rare connective tissue disorder, associated with heterozygous mutations in the FBN2 gene. The objective of this study was to evaluate the prevalence of an intragenic deletion encompassing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4d461326d8ed2d8ad51939468bc58d7
https://pubmed.ncbi.nlm.nih.gov/32702406
https://pubmed.ncbi.nlm.nih.gov/32702406