Levy-Lahad E - Search Results

1

Collaborative genomics for human health and cooperation in the Mediterranean region.

Ozçelik T, Kanaan M, Avraham KB, Yannoukakos D, Mégarbané A, Tadmouri GO, Middleton L, Romeo G, King MC, Levy-Lahad E. Ozçelik T, et al. Nat Genet. 2010 Aug;42(8):641-5. doi: 10.1038/ng0810-641. Nat Genet. 2010. PMID: 20664644

2

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.

Shaag A, Walsh T, Renbaum P, Kirchhoff T, Nafa K, Shiovitz S, Mandell JB, Welcsh P, Lee MK, Ellis N, Offit K, Levy-Lahad E, King MC. Shaag A, et al. Hum Mol Genet. 2005 Feb 15;14(4):555-63. doi: 10.1093/hmg/ddi052. Epub 2005 Jan 13. Hum Mol Genet. 2005. PMID: 15649950

3

Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.

Pierce SB, Walsh T, Chisholm KM, Lee MK, Thornton AM, Fiumara A, Opitz JM, Levy-Lahad E, Klevit RE, King MC. Pierce SB, et al. Am J Hum Genet. 2010 Aug 13;87(2):282-8. doi: 10.1016/j.ajhg.2010.07.007. Epub 2010 Jul 30. Am J Hum Genet. 2010. PMID: 20673864 Free PMC article.

4

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.

Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Abu Rayyan A, Parzefall T, Lev D, Shalev S, Frydman M, Davidov B, Shohat M, Rahile M, Lieberman S, Levy-Lahad E, Lee MK, Shomron N, King MC, Walsh T, Kanaan M, Avraham KB. Brownstein Z, et al. Genome Biol. 2011 Sep 14;12(9):R89. doi: 10.1186/gb-2011-12-9-r89. Genome Biol. 2011. PMID: 21917145 Free PMC article.

5

Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.

Pierce SB, Gersak K, Michaelson-Cohen R, Walsh T, Lee MK, Malach D, Klevit RE, King MC, Levy-Lahad E. Pierce SB, et al. Am J Hum Genet. 2013 Apr 4;92(4):614-20. doi: 10.1016/j.ajhg.2013.03.007. Epub 2013 Mar 28. Am J Hum Genet. 2013. PMID: 23541342 Free PMC article.

6

Mutant ADA2 in vasculopathies.

Segel R, King MC, Levy-Lahad E. Segel R, et al. N Engl J Med. 2014 Jul 31;371(5):481. doi: 10.1056/NEJMc1405506. N Engl J Med. 2014. PMID: 25083540 No abstract available.

7

Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award.

King MC, Levy-Lahad E, Lahad A. King MC, et al. JAMA. 2014 Sep 17;312(11):1091-2. doi: 10.1001/jama.2014.12483. JAMA. 2014. PMID: 25198398 No abstract available.

8

Precision medicine meets public health: population screening for BRCA1 and BRCA2.

Levy-Lahad E, Lahad A, King MC. Levy-Lahad E, et al. J Natl Cancer Inst. 2014 Dec 30;107(1):420. doi: 10.1093/jnci/dju420. Print 2015 Jan. J Natl Cancer Inst. 2014. PMID: 25550384 No abstract available.

9

Proposed shift in screening for breast cancer--reply.

King MC, Lahad A, Levy-Lahad E. King MC, et al. JAMA. 2015 Feb 3;313(5):525-6. doi: 10.1001/jama.2014.17442. JAMA. 2015. PMID: 25647216 No abstract available.

10

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.

Tenenbaum-Rakover Y, Weinberg-Shukron A, Renbaum P, Lobel O, Eideh H, Gulsuner S, Dahary D, Abu-Rayyan A, Kanaan M, Levy-Lahad E, Bercovich D, Zangen D. Tenenbaum-Rakover Y, et al. J Med Genet. 2015 Jun;52(6):391-9. doi: 10.1136/jmedgenet-2014-102921. Epub 2015 Apr 14. J Med Genet. 2015. PMID: 25873734

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