Dror Sharon spends much of his time researching Genetics, Retinal degeneration, Retinitis pigmentosa, Mutation and Exome sequencing. His Mutation and Sanger sequencing investigations are all subjects of Genetics research. His research in Retinal degeneration intersects with topics in Bardet–Biedl syndrome and Genetic heterogeneity.
In his study, Nonsense mutation, GTPase and Retinal pigment epithelium is strongly linked to Disease gene identification, which falls under the umbrella field of Retinitis pigmentosa. He focuses mostly in the field of Mutation, narrowing it down to matters related to Phenotype and, in some cases, Genotype and Retinal. His Exome sequencing research incorporates themes from Genetic marker, Genetic analysis, Founder effect and Human genome.
Dror Sharon spends much of his time researching Genetics, Retinitis pigmentosa, Exome sequencing, Retinal and Gene. His study in Genetics concentrates on Disease gene identification, Mutation, Retinal degeneration, Sanger sequencing and Mutation. His research integrates issues of Consanguinity and Cohort study in his study of Disease gene identification.
In Retinitis pigmentosa, Dror Sharon works on issues like Pediatrics, which are connected to Cohort. When carried out as part of a general Exome sequencing research project, his work on Exome is frequently linked to work in Identification, therefore connecting diverse disciplines of study. His work carried out in the field of Retinal brings together such families of science as Phenotype, Retina, Proband and Disease.
Genetics, Retinitis pigmentosa, Retinal, Exome sequencing and Genetic analysis are his primary areas of study. His Genetics study is mostly concerned with Gene, DNA sequencing, Allele, Exon and Proband. The concepts of his Retinitis pigmentosa study are interwoven with issues in Nonsense mutation, Electroretinography, Pediatrics and ABCA4.
His Retinal study combines topics in areas such as Phenotype and Retina. His biological study spans a wide range of topics, including Sanger sequencing, Frameshift mutation, Mutation and Macular dystrophy. Dror Sharon combines subjects such as Mutation and Disease gene identification with his study of Genetic analysis.
His primary areas of study are Genetics, Gene, Disease, Mutation and Retinitis pigmentosa. By researching both Genetics and Uniparental Isodisomy, he produces research that crosses academic boundaries. His Mutation research integrates issues from Disease-causing Mutation, Genotype, Sanger sequencing, Human genetics and Mendelian inheritance.
His Retinitis pigmentosa research is multidisciplinary, incorporating elements of Exome sequencing, Genetic analysis, Founder effect, Frameshift mutation and Intronic Mutation. His Genetic analysis course of study focuses on Stargardt disease and Genetic heterogeneity, Pediatrics, Cohort and Proband. His work deals with themes such as Achromatopsia, In silico and Locus, which intersect with Allele.
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Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns
Carlo Rivolta;Dror Sharon;Margaret M. DeAngelis;Thaddeus P. Dryja.
Human Molecular Genetics (2002)
The olfactory receptor gene superfamily: data mining, classification, and nomenclature.
Gustavo Glusman;Anita Bahar;Dror Sharon;Yitzhak Pilpel.
Mammalian Genome (2000)
RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa
Dror Sharon;Michael A. Sandberg;Vivian W. Rabe;Melissa Stillberger.
American Journal of Human Genetics (2003)
Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE).
Dror Sharon;Seth Blackshaw;Constance L. Cepko;Thaddeus P. Dryja.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Shared Mutations in NR2E3 in Enhanced S-cone Syndrome, Goldmann-Favre Syndrome, and Many Cases of Clumped Pigmentary Retinal Degeneration
Dror Sharon;Michael A. Sandberg;Rafael C. Caruso;Eliot L. Berson.
Archives of Ophthalmology (2003)
Primate Evolution of an Olfactory Receptor Cluster: Diversification by Gene Conversion and Recent Emergence of Pseudogenes ☆
Dror Sharon;Gustavo Glusman;Yitzhak Pilpel;Miriam Khen.
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
Isabelle Audo;Kinga Bujakowska;Kinga Bujakowska;Kinga Bujakowska;Elise Orhan;Elise Orhan;Elise Orhan;Charlotte M. Poloschek.
American Journal of Human Genetics (2012)
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene
Koji M. Nishiguchi;Richard G. Tearle;Yangfan P. Liu;Edwin C. Oh.
Proceedings of the National Academy of Sciences of the United States of America (2013)
A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews
Lina Zelinger;Eyal Banin;Alexey Obolensky;Liliana Mizrahi-Meissonnier.
American Journal of Human Genetics (2011)
An integrated genetic linkage map of avocado
D. Sharon;P. B. Cregan;S. Mhameed;M. Kusharska.
Theoretical and Applied Genetics (1997)
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