Shomron N - Search Results

1

Machine learning-enhanced noninvasive prenatal testing of monogenic disorders.

Liscovitch-Brauer N, Mesika R, Rabinowitz T, Volkov H, Grad M, Matar RT, Basel-Salmon L, Tadmor O, Beker A, Shomron N. Liscovitch-Brauer N, et al. Among authors: shomron n. Prenat Diagn. 2024 Aug;44(9):1024-1032. doi: 10.1002/pd.6570. Epub 2024 Apr 30. Prenat Diagn. 2024. PMID: 38687007

2

Genome-wide noninvasive prenatal diagnosis of monogenic disorders: Current and future trends.

Rabinowitz T, Shomron N. Rabinowitz T, et al. Among authors: shomron n. Comput Struct Biotechnol J. 2020 Sep 14;18:2463-2470. doi: 10.1016/j.csbj.2020.09.003. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 33005308 Free PMC article. Review.

3

Bayesian-based noninvasive prenatal diagnosis of single-gene disorders.

Rabinowitz T, Polsky A, Golan D, Danilevsky A, Shapira G, Raff C, Basel-Salmon L, Matar RT, Shomron N. Rabinowitz T, et al. Among authors: shomron n. Genome Res. 2019 Mar;29(3):428-438. doi: 10.1101/gr.235796.118. Epub 2019 Feb 20. Genome Res. 2019. PMID: 30787035 Free PMC article.

4

Improved noninvasive fetal variant calling using standardized benchmarking approaches.

Rabinowitz T, Deri-Rozov S, Shomron N. Rabinowitz T, et al. Among authors: shomron n. Comput Struct Biotechnol J. 2020 Dec 31;19:509-517. doi: 10.1016/j.csbj.2020.12.032. eCollection 2021. Comput Struct Biotechnol J. 2020. PMID: 33510858 Free PMC article.

5

Genome-Wide Noninvasive Prenatal Diagnosis of SNPs and Indels.

Rabinowitz T, Shomron N. Rabinowitz T, et al. Among authors: shomron n. Methods Mol Biol. 2021;2243:227-248. doi: 10.1007/978-1-0716-1103-6_11. Methods Mol Biol. 2021. PMID: 33606260

6

Genome-Wide Noninvasive Prenatal Diagnosis of De Novo Mutations.

Peretz-Machluf R, Rabinowitz T, Shomron N. Peretz-Machluf R, et al. Among authors: shomron n. Methods Mol Biol. 2021;2243:249-269. doi: 10.1007/978-1-0716-1103-6_12. Methods Mol Biol. 2021. PMID: 33606261

7

Two intronic cis-acting variants in both alleles of the POLR3A gene cause progressive spastic ataxia with hypodontia.

Fellner A, Lossos A, Kogan E, Argov Z, Gonzaga-Jauregui C, Shuldiner AR, Darawshe M, Bazak L, Lidzbarsky G, Shomron N, Basel-Salmon L, Goldberg Y. Fellner A, et al. Among authors: shomron n. Clin Genet. 2021 May;99(5):713-718. doi: 10.1111/cge.13929. Epub 2021 Feb 15. Clin Genet. 2021. PMID: 33491183

8

Hippocampal differential expression underlying the neuroprotective effect of delta-9-tetrahydrocannabinol microdose on old mice.

Shapira G, Israel-Elgali I, Grad M, Avnat E, Rachmany L, Sarne Y, Shomron N. Shapira G, et al. Among authors: shomron n. Front Neurosci. 2023 Jul 18;17:1182932. doi: 10.3389/fnins.2023.1182932. eCollection 2023. Front Neurosci. 2023. PMID: 37534036 Free PMC article.

9

Genomic Markers Associated with Cytomegalovirus DNAemia in Kidney Transplant Recipients.

Shapira G, Volkov H, Fabian I, Mohr DW, Bettinotti M, Shomron N, Avery RK, Arav-Boger R. Shapira G, et al. Among authors: shomron n. Viruses. 2023 Nov 8;15(11):2227. doi: 10.3390/v15112227. Viruses. 2023. PMID: 38005904 Free PMC article.

10

Altered White Matter and microRNA Expression in a Murine Model Related to Williams Syndrome Suggests That miR-34b/c Affects Brain Development via Ptpru and Dcx Modulation.

Grad M, Nir A, Levy G, Trangle SS, Shapira G, Shomron N, Assaf Y, Barak B. Grad M, et al. Among authors: shomron n. Cells. 2022 Jan 4;11(1):158. doi: 10.3390/cells11010158. Cells. 2022. PMID: 35011720 Free PMC article.

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