Shkedi-Rafid S - Search Results

1

Clinicians' attitudes towards parental choice in the era of advanced genomic tests in pregnancy.

Macarov M, Meiner V, Chalk M, Hochner H, Shkedi-Rafid S. Macarov M, et al. Prenat Diagn. 2021 Aug;41(9):1066-1073. doi: 10.1002/pd.6010. Epub 2021 Jul 19. Prenat Diagn. 2021. PMID: 34259341

2

Clinicians' attitudes toward general screening of the Ashkenazi-Jewish population for prevalent founder BRCA1/2 and LRRK2 mutations.

Shkedi-Rafid S, Ofer-Bialer G, Meiner V, Calderon-Margalit R. Shkedi-Rafid S, et al. Public Health Genomics. 2013;16(4):174-83. doi: 10.1159/000351592. Epub 2013 Jun 28. Public Health Genomics. 2013. PMID: 23816973

3

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.

Shkedi-Rafid S, Fenwick A, Dheensa S, Wellesley D, Lucassen AM. Shkedi-Rafid S, et al. Prenat Diagn. 2016 Mar;36(3):252-9. doi: 10.1002/pd.4772. Epub 2016 Feb 17. Prenat Diagn. 2016. PMID: 26743561 Free PMC article.

4

Pregnant Genetic Counselors in an Era of Advanced Genomic Tests: What Do the Experts Test Prenatally?

Shkedi-Rafid S, Hashiloni-Dolev Y. Shkedi-Rafid S, et al. J Genet Couns. 2018 Sep;27(5):1167-1174. doi: 10.1007/s10897-018-0234-8. Epub 2018 Mar 3. J Genet Couns. 2018. PMID: 29502146

5

Role of late amniocentesis in the era of modern genomic technologies.

Daum H, Ben David A, Nadjari M, Zenvirt S, Helman S, Yanai N, Meiner V, Yagel S, Frumkin A, Shkedi Rafid S; collaborating authors. Daum H, et al. Ultrasound Obstet Gynecol. 2019 May;53(5):676-685. doi: 10.1002/uog.20113. Epub 2019 Apr 12. Ultrasound Obstet Gynecol. 2019. PMID: 30155922 Free article.

6

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.

Hochner H, Daum H, Douiev L, Zvi N, Frumkin A, Macarov M, Kimchi-Shaal A, Hacohen N, Eilat A, Faham D, Shkedi-Rafid S. Hochner H, et al. Obstet Gynecol. 2020 Jan;135(1):149-157. doi: 10.1097/AOG.0000000000003610. Obstet Gynecol. 2020. PMID: 31809435

7

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.

Stern S, Hacohen N, Meiner V, Yagel S, Zenvirt S, Shkedi-Rafid S, Macarov M, Valsky DV, Porat S, Yanai N, Frumkin A, Daum H. Stern S, et al. Ultrasound Obstet Gynecol. 2021 May;57(5):813-820. doi: 10.1002/uog.22026. Epub 2021 Apr 5. Ultrasound Obstet Gynecol. 2021. PMID: 32202684 Free article.

8

What is the meaning of a 'genomic result' in the context of pregnancy?

Shkedi-Rafid S, Horton R, Lucassen A. Shkedi-Rafid S, et al. Eur J Hum Genet. 2021 Feb;29(2):225-230. doi: 10.1038/s41431-020-00722-8. Epub 2020 Sep 14. Eur J Hum Genet. 2021. PMID: 32929236 Free PMC article.

9

Personalized prenatal genomic testing: Couples' experience with choice regarding uncertain and adult-onset findings from chromosomal-microarray-analysis.

Millo T, Douiev L, Popper D, Shkedi-Rafid S. Millo T, et al. Prenat Diagn. 2021 Feb;41(3):376-383. doi: 10.1002/pd.5856. Epub 2020 Nov 12. Prenat Diagn. 2021. PMID: 33128404

10

Detection of copy number variants associated with late-onset conditions in ~16 200 pregnancies: parameters for disclosure and pregnancy outcome.

Daum H, Segel R, Meiner V, Goldberg Y, Zeligson S, Weiss O, Stern S, Frumkin A, Zenvirt S, Ganz G, Shkedi-Rafid S. Daum H, et al. Among authors: shkedi rafid s. J Med Genet. 2023 Jan;60(1):99-105. doi: 10.1136/jmedgenet-2021-107890. Epub 2022 Mar 9. J Med Genet. 2023. PMID: 35264407

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