Zuckerman S - Search Results

1

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection.

Aran A, Rosenfeld N, Jaron R, Renbaum P, Zuckerman S, Fridman H, Zeligson S, Segel R, Kohn Y, Kamal L, Kanaan M, Segev Y, Mazaki E, Rabinowitz R, Shen O, Lee M, Walsh T, King MC, Gulsuner S, Levy-Lahad E. Aran A, et al. Among authors: zuckerman s. Neurology. 2016 May 24;86(21):2016-24. doi: 10.1212/WNL.0000000000002704. Epub 2016 Apr 29. Neurology. 2016. PMID: 27164683 Free PMC article.

2

Prenatal sonographic diagnosis of retinal nonattachment.

Shen O, Zuckerman S, Cohen P, Rabinowitz R. Shen O, et al. Among authors: zuckerman s. J Ultrasound Med. 2014 Jun;33(6):1095-7. doi: 10.7863/ultra.33.6.1095. J Ultrasound Med. 2014. PMID: 24866619 No abstract available.

3

A new prenatal sonographic sign of epidermolysis bullosa.

Chen D, Zuckerman S, Akerman Y, Shen O. Chen D, et al. Among authors: zuckerman s. J Clin Ultrasound. 2021 Jan;49(1):59-61. doi: 10.1002/jcu.22922. Epub 2020 Sep 16. J Clin Ultrasound. 2021. PMID: 32935879

4

Conflicts regarding genetic counseling for fragile X syndrome screening: a survey of clinical geneticists and genetic counselors in Israel.

Lieberman S, Zuckerman S, Levy-Lahad E, Altarescu G. Lieberman S, et al. Among authors: zuckerman s. Am J Med Genet A. 2011 Sep;155A(9):2154-60. doi: 10.1002/ajmg.a.34155. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834046

5

Carrier screening for Krabbe disease in an isolated inbred community.

Ezer S, Zuckerman S, Segel R, Zlotogora J. Ezer S, et al. Among authors: zuckerman s. Am J Med Genet A. 2022 Sep;188(9):2555-2559. doi: 10.1002/ajmg.a.62882. Epub 2022 Jul 1. Am J Med Genet A. 2022. PMID: 35775617

6

Attitudes of couples identified through screening as carriers of Gaucher disease type 1.

Zuckerman S, Lahad A, Zimran A, Levy-Lahad E, Sagi M. Zuckerman S, et al. Clin Genet. 2008 Dec;74(6):566-70. doi: 10.1111/j.1399-0004.2008.01063.x. Epub 2008 Jul 21. Clin Genet. 2008. PMID: 18651845

7

Carrier screening for Gaucher disease: lessons for low-penetrance, treatable diseases.

Zuckerman S, Lahad A, Shmueli A, Zimran A, Peleg L, Orr-Urtreger A, Levy-Lahad E, Sagi M. Zuckerman S, et al. JAMA. 2007 Sep 19;298(11):1281-90. doi: 10.1001/jama.298.11.1281. JAMA. 2007. PMID: 17878420

8

Expanding the phenotypic spectrum of COLEC10-Related 3MC syndrome: A glimpse into COLEC10-Related 3MC syndrome in the Ashkenazi Jewish population.

Rabin R, Hirsch Y, Chung WK, Ekstein J, Levy-Lahad E, Zuckerman S, Mor-Shaked H, Meiner V, Booth KT, Pappas J. Rabin R, et al. Among authors: zuckerman s. Am J Med Genet A. 2022 Oct;188(10):3110-3117. doi: 10.1002/ajmg.a.62943. Epub 2022 Aug 9. Am J Med Genet A. 2022. PMID: 35943032

9

Response to ACMG guideline: carrier screening in individuals of Ashkenazi Jewish decent.

Levy-Lahad E, Zuckerman S, Sagi M. Levy-Lahad E, et al. Among authors: zuckerman s. Genet Med. 2008 Jun;10(6):462; author reply 463. doi: 10.1097/gim.0b013e3181776230. Genet Med. 2008. PMID: 18496217 No abstract available.

10

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: zuckerman 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

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