Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

57 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.
Silberstein M, Weissbrod O, Otten L, Tzemach A, Anisenia A, Shtark O, Tuberg D, Galfrin E, Gannon I, Shalata A, Borochowitz ZU, Dechter R, Thompson E, Geiger D. Silberstein M, et al. Among authors: shalata a. Bioinformatics. 2013 Jan 15;29(2):197-205. doi: 10.1093/bioinformatics/bts658. Epub 2012 Nov 18. Bioinformatics. 2013. PMID: 23162081 Free PMC article.
Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia.
Samra N, Jansen NS, Morani I, Kakun RR, Zaid R, Paperna T, Garcia-Dominguez M, Viner Y, Frankenthal H, Shinwell ES, Portnov I, Bakry D, Shalata A, Shapira Rootman M, Kidron D, Claessens LA, Wevers RA, Mandel H, Vertegaal ACO, Weiss K. Samra N, et al. Among authors: shalata a. J Med Genet. 2023 Nov;60(11):1133-1141. doi: 10.1136/jmg-2023-109267. Epub 2023 Jul 17. J Med Genet. 2023. PMID: 37460201
Medical genetics in Israel's diverse population.
Shalev SA, Zlotogora J, Shalata A, Levy-Lahad E. Shalev SA, et al. Among authors: shalata a. Lancet. 2017 Jun 24;389(10088):2453-2455. doi: 10.1016/S0140-6736(17)30875-9. Epub 2017 May 8. Lancet. 2017. PMID: 28495108 No abstract available.
Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype.
Shalata A, Mahroom M, Milewicz DM, Limin G, Kassum F, Badarna K, Tarabeih N, Assy N, Fell R, Cohen H, Nashashibi M, Livoff A, Azab M, Habib G, Geiger D, Weissbrod O, Nseir W. Shalata A, et al. Orphanet J Rare Dis. 2018 Mar 15;13(1):41. doi: 10.1186/s13023-018-0769-7. Orphanet J Rare Dis. 2018. PMID: 29544503 Free PMC article.
57 results