Sagi-Dain L - Search Results

1

Genetic counseling of high-risk isolated populations: A worldwide challenge.

Sagi-Dain L, Weissman I, Cohen-Kfir N, Kalfon L, Edri N, Shasha Lavski H, Peleg A, Falik-Zaccai TC. Sagi-Dain L, et al. Birth Defects Res. 2020 Mar 1;112(4):316-320. doi: 10.1002/bdr2.1633. Birth Defects Res. 2020. PMID: 32115902

2

Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review.

Sagi-Dain L, Peleg A, Sagi S. Sagi-Dain L, et al. Prenat Diagn. 2017 Nov;37(11):1061-1066. doi: 10.1002/pd.5160. Epub 2017 Oct 15. Prenat Diagn. 2017. PMID: 28944967 Review.

3

First-Trimester Crown-Rump Length and Risk of Chromosomal Aberrations-A Systematic Review and Meta-analysis.

Sagi-Dain L, Peleg A, Sagi S. Sagi-Dain L, et al. Obstet Gynecol Surv. 2017 Oct;72(10):603-609. doi: 10.1097/OGX.0000000000000490. Obstet Gynecol Surv. 2017. PMID: 29059452 Review.

4

Microarray analysis in pregnancies with isolated unilateral kidney agenesis.

Sagi-Dain L, Maya I, Peleg A, Reches A, Banne E, Baris HN, Tenne T, Singer A, Ben-Shachar S. Sagi-Dain L, et al. Pediatr Res. 2018 Apr;83(4):825-828. doi: 10.1038/pr.2018.3. Epub 2018 Feb 7. Pediatr Res. 2018. PMID: 29320483

5

Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results.

Sagi-Dain L, Maya I, Falik-Zaccai T, Feingold-Zadok M, Lev D, Yonath H, Kaliner E, Frumkin A, Ben Shachar S, Singer A. Sagi-Dain L, et al. Eur J Obstet Gynecol Reprod Biol. 2018 Mar;222:80-83. doi: 10.1016/j.ejogrb.2018.01.015. Epub 2018 Jan 23. Eur J Obstet Gynecol Reprod Biol. 2018. PMID: 29367169

6

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants.

Johnston JJ, van der Smagt JJ, Rosenfeld JA, Pagnamenta AT, Alswaid A, Baker EH, Blair E, Borck G, Brinkmann J, Craigen W, Dung VC, Emrick L, Everman DB, van Gassen KL, Gulsuner S, Harr MH, Jain M, Kuechler A, Leppig KA, McDonald-McGinn DM, Can NTB, Peleg A, Roeder ER, Rogers RC, Sagi-Dain L, Sapp JC, Schäffer AA, Schanze D, Stewart H, Taylor JC, Verbeek NE, Walkiewicz MA, Zackai EH, Zweier C; Members of the Undiagnosed Diseases Network; Zenker M, Lee B, Biesecker LG. Johnston JJ, et al. Genet Med. 2018 Oct;20(10):1175-1185. doi: 10.1038/gim.2017.249. Epub 2018 Feb 22. Genet Med. 2018. PMID: 29469822 Free PMC article.

7

Microarray analysis in pregnancies with isolated echogenic bowel.

Singer A, Maya I, Koifman A, Nasser Samra N, Baris HN, Falik-Zaccai T, Ben Shachar S, Sagi-Dain L. Singer A, et al. Early Hum Dev. 2018 Apr;119:25-28. doi: 10.1016/j.earlhumdev.2018.02.014. Epub 2018 Mar 6. Early Hum Dev. 2018. PMID: 29522884

8

Whole-exome sequencing reveals a novel missense mutation in the MARS gene related to a rare Charcot-Marie-Tooth neuropathy type 2U.

Sagi-Dain L, Shemer L, Zelnik N, Zoabi Y, Orit S, Adir V, Schif A, Peleg A. Sagi-Dain L, et al. J Peripher Nerv Syst. 2018 Jun;23(2):138-142. doi: 10.1111/jns.12264. Epub 2018 May 9. J Peripher Nerv Syst. 2018. PMID: 29582526

9

Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review.

Sagi-Dain L, Singer A, Josefsberg S, Peleg A, Lev D, Samra NN, Bar-Shira A, Zeligson S, Maya I, Ben-Shachar S. Sagi-Dain L, et al. Ultrasound Obstet Gynecol. 2019 Jun;53(6):810-815. doi: 10.1002/uog.20208. Ultrasound Obstet Gynecol. 2019. PMID: 30584678 Free article.

10

Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy.

Motta M, Sagi-Dain L, Krumbach OHF, Hahn A, Peleg A, German A, Lissewski C, Coppola S, Pantaleoni F, Kocherscheid L, Altmüller F, Schanze D, Logeswaran T, Chahrokh-Zadeh S, Munzig A, Nakhaei-Rad S, Cavé H, Ahmadian MR, Tartaglia M, Zenker M. Motta M, et al. Hum Mol Genet. 2020 Jul 21;29(11):1772-1783. doi: 10.1093/hmg/ddz108. Hum Mol Genet. 2020. PMID: 31108500

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