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Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel.
Invest Ophthalmol Vis Sci. 2014 Dec 16;56(1):420-30. doi: 10.1167/iovs.14-15647.
Invest Ophthalmol Vis Sci. 2014.
PMID: 25515582
Free PMC article.
Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF.
Lazar CH, Kimchi A, Namburi P, Mutsuddi M, Zelinger L, Beryozkin A, Ben-Simhon S, Obolensky A, Ben-Neriah Z, Argov Z, Pikarsky E, Fellig Y, Marks-Ohana D, Ratnapriya R, Banin E, Sharon D, Swaroop A.
Lazar CH, et al.
Hum Mutat. 2015 Sep;36(9):836-41. doi: 10.1002/humu.22822. Epub 2015 Jul 14.
Hum Mutat. 2015.
PMID: 26077327
Free PMC article.
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Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies.
Beryozkin A, Shevah E, Kimchi A, Mizrahi-Meissonnier L, Khateb S, Ratnapriya R, Lazar CH, Blumenfeld A, Ben-Yosef T, Hemo Y, Pe'er J, Averbuch E, Sagi M, Boleda A, Gieser L, Zlotogorski A, Falik-Zaccai T, Alimi-Kasem O, Jacobson SG, Chowers I, Swaroop A, Banin E, Sharon D.
Beryozkin A, et al. Among authors: lazar ch.
Sci Rep. 2015 Aug 26;5:13187. doi: 10.1038/srep13187.
Sci Rep. 2015.
PMID: 26306921
Free PMC article.
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Biology and therapy of inherited retinal degenerative disease: insights from mouse models.
Veleri S, Lazar CH, Chang B, Sieving PA, Banin E, Swaroop A.
Veleri S, et al. Among authors: lazar ch.
Dis Model Mech. 2015 Feb;8(2):109-29. doi: 10.1242/dmm.017913.
Dis Model Mech. 2015.
PMID: 25650393
Free PMC article.
Review.
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Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D.
Namburi P, et al. Among authors: lazar ch.
Am J Hum Genet. 2016 Sep 1;99(3):777-784. doi: 10.1016/j.ajhg.2016.07.010.
Am J Hum Genet. 2016.
PMID: 27588452
Free PMC article.
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Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D.
Namburi P, et al. Among authors: lazar ch.
Am J Hum Genet. 2016 Nov 3;99(5):1222-1223. doi: 10.1016/j.ajhg.2016.09.012.
Am J Hum Genet. 2016.
PMID: 27814526
Free PMC article.
No abstract available.
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Screening of mecI Gene in Staphylococcus Strains Isolated in Transylvania Region of Romania.
Jakab E, Colcieru M, Jakab RI, Gabri EE, Lázár CH, Török E, Kremmer B, Mészáros TJ, Katona Á, Fazakas E, Coldea L, Popescu O.
Jakab E, et al. Among authors: lazar ch.
Microb Drug Resist. 2019 Jun;25(5):639-643. doi: 10.1089/mdr.2018.0205. Epub 2019 Jan 3.
Microb Drug Resist. 2019.
PMID: 30614756
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