Cohen Y - Search Results

1

Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review.

Fink DA, Nelson LM, Pyeritz R, Johnson J, Sherman SL, Cohen Y, Elizur SE. Fink DA, et al. Among authors: cohen y. Front Genet. 2018 Nov 27;9:529. doi: 10.3389/fgene.2018.00529. eCollection 2018. Front Genet. 2018. PMID: 30542367 Free PMC article. Review.

2

FMR6 may play a role in the pathogenesis of fragile X-associated premature ovarian insufficiency.

Elizur SE, Dratviman-Storobinsky O, Derech-Haim S, Lebovitz O, Dor J, Orvieto R, Cohen Y. Elizur SE, et al. Among authors: cohen y. Gynecol Endocrinol. 2016;32(4):334-7. doi: 10.3109/09513590.2015.1116508. Epub 2015 Dec 11. Gynecol Endocrinol. 2016. PMID: 26652047

3

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: cohen y. Front Genet. 2018 Dec 13;9:606. doi: 10.3389/fgene.2018.00606. eCollection 2018. Front Genet. 2018. PMID: 30619448 Free PMC article.

4

Pathophysiology Mechanisms in Fragile-X Primary Ovarian Insufficiency.

Elizur SE, Friedman Gohas M, Dratviman-Storobinsky O, Cohen Y. Elizur SE, et al. Among authors: cohen y. Methods Mol Biol. 2019;1942:165-171. doi: 10.1007/978-1-4939-9080-1_14. Methods Mol Biol. 2019. PMID: 30900184

5

Elevated levels of FMR1 mRNA in granulosa cells are associated with low ovarian reserve in FMR1 premutation carriers.

Elizur SE, Lebovitz O, Derech-Haim S, Dratviman-Storobinsky O, Feldman B, Dor J, Orvieto R, Cohen Y. Elizur SE, et al. Among authors: cohen y. PLoS One. 2014 Aug 25;9(8):e105121. doi: 10.1371/journal.pone.0105121. eCollection 2014. PLoS One. 2014. PMID: 25153074 Free PMC article.

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: cohen y. 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

Fragile X Premutation Carrier Epidemiology and Symptomatology in Israel-Results from a Tertiary Child Developmental Center.

Gabis LV, Gruber N, Berkenstadt M, Shefer S, Attia OL, Mula D, Cohen Y, Elizur SE. Gabis LV, et al. Among authors: cohen y. Cerebellum. 2016 Oct;15(5):595-8. doi: 10.1007/s12311-016-0804-y. Cerebellum. 2016. PMID: 27312842

8

[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: cohen y. Harefuah. 2018 Aug;157(8):529-533. Harefuah. 2018. PMID: 30175572 Review. Hebrew.

9

Does the presence of AGG interruptions within the CGG repeat tract have a protective effect on the fertility phenotype of female FMR1 premutation carriers?

Friedman-Gohas M, Kirshenbaum M, Michaeli A, Domniz N, Elizur S, Raanani H, Orvieto R, Cohen Y. Friedman-Gohas M, et al. Among authors: cohen y. J Assist Reprod Genet. 2020 Apr;37(4):849-854. doi: 10.1007/s10815-020-01701-0. Epub 2020 Feb 24. J Assist Reprod Genet. 2020. PMID: 32096109 Free PMC article.

10

FMRpolyG accumulates in FMR1 premutation granulosa cells.

Friedman-Gohas M, Elizur SE, Dratviman-Storobinsky O, Aizer A, Haas J, Raanani H, Orvieto R, Cohen Y. Friedman-Gohas M, et al. Among authors: cohen y. J Ovarian Res. 2020 Feb 26;13(1):22. doi: 10.1186/s13048-020-00623-w. J Ovarian Res. 2020. PMID: 32101156 Free PMC article.

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

1,894 results

Search Page