Zenvirt S - Search Results

1

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. Among authors: zenvirt s. 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.

2

Single-nucleotide polymorphism-based chromosomal microarray analysis provides clues and insights into disease mechanisms.

Daum H, Meiner V, Hacohen N, Zvi N, Eilat A, Drai-Hasid R, Yagel S, Zenvirt S, Frumkin A. Daum H, et al. Among authors: zenvirt s. Ultrasound Obstet Gynecol. 2019 Nov;54(5):655-660. doi: 10.1002/uog.20230. Ultrasound Obstet Gynecol. 2019. PMID: 30693591 Free article.

3

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. Among authors: zenvirt s. 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.

4

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: zenvirt 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

5

A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD).

Ben-Neriah Z, Michaelson-Cohen R, Inbar-Feigenberg M, Nadjari M, Zeligson S, Shaag A, Zenvirt S, Elpeleg O, Levy-Lahad E. Ben-Neriah Z, et al. Among authors: zenvirt s. Am J Med Genet A. 2011 Nov;155A(11):2801-6. doi: 10.1002/ajmg.a.34240. Epub 2011 Oct 11. Am J Med Genet A. 2011. PMID: 21990102

6

Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencing.

Berger I, Ben-Neriah Z, Dor-Wolman T, Shaag A, Saada A, Zenvirt S, Raas-Rothschild A, Nadjari M, Kaestner KH, Elpeleg O. Berger I, et al. Among authors: zenvirt s. Mol Genet Metab. 2011 Dec;104(4):517-20. doi: 10.1016/j.ymgme.2011.09.020. Epub 2011 Sep 24. Mol Genet Metab. 2011. PMID: 22019070

7

Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.

Maor-Sagie E, Cinnamon Y, Yaacov B, Shaag A, Goldsmidt H, Zenvirt S, Laufer N, Richler C, Frumkin A. Maor-Sagie E, et al. Among authors: zenvirt s. J Assist Reprod Genet. 2015 Jun;32(6):887-91. doi: 10.1007/s10815-015-0445-y. Epub 2015 Apr 22. J Assist Reprod Genet. 2015. PMID: 25899990 Free PMC article.

8

Isolated truncus arteriosus associated with a mutation in the plexin-D1 gene.

Ta-Shma A, Pierri CL, Stepensky P, Shaag A, Zenvirt S, Elpeleg O, Rein AJ. Ta-Shma A, et al. Among authors: zenvirt s. Am J Med Genet A. 2013 Dec;161A(12):3115-20. doi: 10.1002/ajmg.a.36194. Epub 2013 Oct 29. Am J Med Genet A. 2013. PMID: 24254849

9

A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews.

Edvardson S, Jalas C, Shaag A, Zenvirt S, Landau C, Lerer I, Elpeleg O. Edvardson S, et al. Among authors: zenvirt s. Am J Med Genet A. 2011 May;155A(5):1170-2. doi: 10.1002/ajmg.a.33972. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465660

10

An SNX10 mutation causes malignant osteopetrosis of infancy.

Aker M, Rouvinski A, Hashavia S, Ta-Shma A, Shaag A, Zenvirt S, Israel S, Weintraub M, Taraboulos A, Bar-Shavit Z, Elpeleg O. Aker M, et al. Among authors: zenvirt s. J Med Genet. 2012 Apr;49(4):221-6. doi: 10.1136/jmedgenet-2011-100520. J Med Genet. 2012. PMID: 22499339

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

21 results

Search Page