Ries-Levavi L - Search Results

1

Female fragile X premutation carriers are at increased risk for metabolic syndrome from early adulthood.

Gruber N, Haham LM, Raanani H, Cohen Y, Gabis L, Berkenstadt M, Ries-Levavi L, Elizur S, Pinhas-Hamiel O. Gruber N, et al. Among authors: ries levavi l. Nutr Metab Cardiovasc Dis. 2022 Apr;32(4):1010-1018. doi: 10.1016/j.numecd.2021.11.018. Epub 2021 Dec 7. Nutr Metab Cardiovasc Dis. 2022. PMID: 35086765

2

Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests.

Berkenstadt M, Ries-Levavi L, Cuckle H, Peleg L, Barkai G. Berkenstadt M, et al. Prenat Diagn. 2007 Nov;27(11):991-4. doi: 10.1002/pd.1815. Prenat Diagn. 2007. PMID: 17705235

3

FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and the general population display distinct distribution patterns.

Laitman Y, Ries-Levavi L, Berkensdadt M, Korach J, Perri T, Pras E, Friedman E. Laitman Y, et al. Among authors: ries levavi l. Genet Res (Camb). 2014 Oct 8;96:e11. doi: 10.1017/S0016672314000147. Genet Res (Camb). 2014. PMID: 25579682 Free PMC article.

4

The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.

Laitman Y, Boker-Keinan L, Berkenstadt M, Liphsitz I, Weissglas-Volkov D, Ries-Levavi L, Sarouk I, Pras E, Friedman E. Laitman Y, et al. Among authors: ries levavi l. Cancer Genet. 2016 Mar;209(3):70-4. doi: 10.1016/j.cancergen.2015.12.006. Epub 2015 Dec 22. Cancer Genet. 2016. PMID: 26778106

5

[FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].

Elizur S, Berkenstadt M, Ries-Levavi L, Gruber N, Pinhas-Hamiel O, Hassin-Baer S, Raas-Rothschild A, Raanani H, Cukierman-Yaffe T, Orvieto R, Cohen Y, Gabis L. Elizur S, et al. Among authors: ries levavi l. Harefuah. 2018 Apr;157(4):241-244. Harefuah. 2018. PMID: 29688643 Review. Hebrew.

6

Preimplantation genetic diagnosis versus prenatal diagnosis-decision-making among pregnant FMR1 premutation carriers.

Haham LM, Avrahami I, Domniz N, Ries-Levavi L, Berkenstadt M, Orvieto R, Cohen Y, Elizur SE. Haham LM, et al. Among authors: ries levavi l. J Assist Reprod Genet. 2018 Nov;35(11):2071-2075. doi: 10.1007/s10815-018-1293-3. Epub 2018 Aug 22. J Assist Reprod Genet. 2018. PMID: 30136016 Free PMC article.

7

[FROM GENETICS OF FRAGILE X SYNDROME TO DEVELOPMENT OF TARGETED AND PERSONALIZED DRUG THERAPY].

Gabis LV, Shefer S, Gruber N, Raviv R, Cohen Y, Berkenstadt M, Ries-Levavi L, Pinhas-Hamiel O, Elizur S. Gabis LV, et al. Among authors: ries levavi l. Harefuah. 2018 Aug;157(8):529-533. Harefuah. 2018. PMID: 30175572 Review. Hebrew.

8

Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers.

Domniz N, Ries-Levavi L, Cohen Y, Marom-Haham L, Berkenstadt M, Pras E, Glicksman A, Tortora N, Latham GJ, Hadd AG, Nolin SL, Elizur SE. Domniz N, et al. Among authors: ries levavi l. Front Genet. 2018 Dec 13;9:606. doi: 10.3389/fgene.2018.00606. eCollection 2018. Front Genet. 2018. PMID: 30619448 Free PMC article.

9

Expanded targeted preconception screening panel in Israel: findings and insights.

Reches A, Ofen Glassner V, Goldstein N, Yeshaya J, Delmar G, Portugali E, Hallas T, Weinstein A, Kurolap A, Berkenstadt M, Mantsour T, Abu-Gutstein L, Ries-Levavi L, Reznik-Wolf H, Behar DM, Yaron Y, Pras E, Baris Feldman H. Reches A, et al. Among authors: ries levavi l. J Med Genet. 2024 May 6:jmg-2023-109629. doi: 10.1136/jmg-2023-109629. Online ahead of print. J Med Genet. 2024. PMID: 38719349

10

Colorectal and Endometrial Cancer Risk and Age at Diagnosis in BLMAsh Mutation Carriers.

Schayek H, Laitman Y, Katz LH, Pras E, Ries-Levavi L, Barak F, Friedman E. Schayek H, et al. Among authors: ries levavi l. Isr Med Assoc J. 2017 Jun;19(6):365-367. Isr Med Assoc J. 2017. PMID: 28647934 Free article.

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