Shkedi-Rafid S - Search Results

1

BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening.

Shkedi-Rafid S, Gabai-Kapara E, Grinshpun-Cohen J, Levy-Lahad E. Shkedi-Rafid S, et al. Genet Med. 2012 Jul;14(7):688-94. doi: 10.1038/gim.2012.31. Genet Med. 2012. PMID: 22481128 Free article.

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

Common founder BRCA2 pathogenic variants and breast cancer characteristics in Ethiopian Jews.

Lieberman S, Chen-Shtoyerman R, Levi Z, Shkedi-Rafid S, Zuckerman S, Bernstein-Molho R, Levi GR, Shachar SS, Flugelman A, Libman V, Kedar I, Naftaly-Nathan S, Lagovsky I, Peretz T, Karminsky N, Carmi S, Levy-Lahad E, Goldberg Y. Lieberman S, et al. Among authors: shkedi rafid s. Breast Cancer Res Treat. 2022 May;193(1):217-224. doi: 10.1007/s10549-022-06557-9. Epub 2022 Mar 12. Breast Cancer Res Treat. 2022. PMID: 35278150

4

Genetic testing of children for adult-onset conditions: opinions of the British adult population and implications for clinical practice.

Shkedi-Rafid S, Fenwick A, Dheensa S, Lucassen AM. Shkedi-Rafid S, et al. Eur J Hum Genet. 2015 Oct;23(10):1281-5. doi: 10.1038/ejhg.2014.221. Epub 2014 Nov 5. Eur J Hum Genet. 2015. PMID: 25370041 Free PMC article.

5

Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research.

Dheensa S, Fenwick A, Shkedi-Rafid S, Crawford G, Lucassen A. Dheensa S, et al. Genet Med. 2016 Apr;18(4):290-301. doi: 10.1038/gim.2015.72. Epub 2015 Jun 25. Genet Med. 2016. PMID: 26110233 Free PMC article. Review.

6

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

7

Cancer patients' understandings of genetic variants of uncertain significance in clinical care.

Amano Y, Raz A, Timmermans S, Shkedi-Rafid S. Amano Y, et al. Among authors: shkedi rafid s. J Community Genet. 2022 Aug;13(4):381-388. doi: 10.1007/s12687-022-00594-z. Epub 2022 May 26. J Community Genet. 2022. PMID: 35616809 Free PMC article.

8

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

9

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.

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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