Dagan E - Search Results

1

A nonsense mutation in the human homolog of Drosophila rogdi causes Kohlschutter-Tonz syndrome.

Mory A, Dagan E, Illi B, Duquesnoy P, Mordechai S, Shahor I, Romani S, Hawash-Moustafa N, Mandel H, Valente EM, Amselem S, Gershoni-Baruch R. Mory A, et al. Among authors: dagan e. Am J Hum Genet. 2012 Apr 6;90(4):708-14. doi: 10.1016/j.ajhg.2012.03.005. Am J Hum Genet. 2012. PMID: 22482807 Free PMC article.

2

A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred.

Mory A, Ruiz FX, Dagan E, Yakovtseva EA, Kurolap A, Parés X, Farrés J, Gershoni-Baruch R. Mory A, et al. Among authors: dagan e. Eur J Hum Genet. 2014 Mar;22(3):419-22. doi: 10.1038/ejhg.2013.157. Epub 2013 Jul 24. Eur J Hum Genet. 2014. PMID: 23881059 Free PMC article.

3

Kohlschutter-Tonz syndrome: clinical and genetic insights gained from 16 cases deriving from a close-knit village in Northern Israel.

Mory A, Dagan E, Shahor I, Mandel H, Illi B, Zolotushko J, Kurolap A, Chechik E, Valente EM, Amselem S, Gershoni-Baruch R. Mory A, et al. Among authors: dagan e. Pediatr Neurol. 2014 Apr;50(4):421-6. doi: 10.1016/j.pediatrneurol.2014.01.006. Epub 2014 Jan 7. Pediatr Neurol. 2014. PMID: 24630287

4

BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study.

Dagan E, Cohen Y, Mory A, Adir V, Borochowitz Z, Raanani H, Kurolap A, Melikhan-Revzin S, Meirow D, Gershoni-Baruch R. Dagan E, et al. Eur J Hum Genet. 2014 Feb;22(2):277-9. doi: 10.1038/ejhg.2013.281. Epub 2013 Nov 27. Eur J Hum Genet. 2014. PMID: 24281364 Free PMC article.

5

A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema.

Melikhan-Revzin S, Kurolap A, Dagan E, Mory A, Gershoni-Baruch R. Melikhan-Revzin S, et al. Among authors: dagan e. Lymphat Res Biol. 2015 Jun;13(2):107-11. doi: 10.1089/lrb.2014.0044. Epub 2015 Jun 2. Lymphat Res Biol. 2015. PMID: 26091405

6

Hereditary breast/ovarian cancer--pitfalls in genetic counseling.

Dagan E, Gershoni-Baruch R. Dagan E, et al. Clin Genet. 2001 Oct;60(4):310-3. doi: 10.1034/j.1399-0004.2001.600410.x. Clin Genet. 2001. PMID: 11683778

7

Anticipation in hereditary breast cancer.

Dagan E, Gershoni-Baruch R. Dagan E, et al. Clin Genet. 2002 Aug;62(2):147-50. doi: 10.1034/j.1399-0004.2002.620207.x. Clin Genet. 2002. PMID: 12220452

8

Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype.

Dagan E, Friedman E, Paperna T, Carmi N, Gershoni-Baruch R. Dagan E, et al. Eur J Hum Genet. 2002 Nov;10(11):724-8. doi: 10.1038/sj.ejhg.5200880. Eur J Hum Genet. 2002. PMID: 12404104

9

Henoch-Schonlein purpura: polymorphisms in thrombophilia genes.

Dagan E, Brik R, Broza Y, Gershoni-Baruch R. Dagan E, et al. Pediatr Nephrol. 2006 Aug;21(8):1117-21. doi: 10.1007/s00467-006-0155-x. Epub 2006 Jun 22. Pediatr Nephrol. 2006. PMID: 16791607

10

"I do not want my baby to suffer as I did"; prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: a case report and genetic counseling considerations.

Dagan E, Gershoni-Baruch R, Kurolap A, Goldberg Y, Fried G. Dagan E, et al. Genet Test Mol Biomarkers. 2014 Jul;18(7):461-6. doi: 10.1089/gtmb.2013.0513. Epub 2014 Jun 10. Genet Test Mol Biomarkers. 2014. PMID: 24915046 Review.

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