101 Title: NGS in infertility: A new window for diagnosis and treatment Date: Thursday Bahman 5, 1396 January 25, 2018 Organizer: Dr. Saeed Reza Ghaffari Scientific Secretary Dr. Saeed Reza Ghaffari 100 Title: Clinical Application […]
RP Hope Project Developmental Delay CP Neonatal Screening for inherited metabolic disorders Inherited Metabolic Disorders First Trimester Screening of aneuploidies Application of Next Generation Sequencing in Routine Clinical Practice Genetic counseling Network Glanzman Recurrent Abortion […]
2013-2014: Mutation Analysis of RP2 Gene in X-Linked Retinitis Pigmentosa patients Mutation analysis of RP2 gene using Sanger sequencing technique in 11 families with apparent X-Linked inheritance. Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati Other Investigators: R Tabatabaee, A […]
2011-2012: Mutation Analysis of RHO Gene in Autosomal Dominant Retinitis Pigmentosa patients Mutation analysis of RHO gene using Sanger sequencing technique in 108 patients with autosomal dominant RP. Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati Other Investigators: D Roshandel, […]
Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati The first phase of this project which attracted >700,000$ has focused on genetic profiling of 1000 patients (in the first phase) with inborn errors of metabolism, neurogenetic disorders or inherited retinal dystrophies by targeted capture sequencing […]
Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati Phase 1 (2010-2012): Targeted capture sequencing of selected families with high score of autosomal recessive RP Among analyzed pedigrees, 9 families were selected in the first phase […]
Principal Investigator: SR Ghaffari Principal associate Investigator: M Rafati Other Investigators: N Novin, S Khorrami, Following starting collaboration with Iran RP Society, the database of RP patients was redesigned to add new data about genetic aspects of […]
Comparative Genomic Hybridisation in the investigation of haematological malignancies S.R. Ghaffari; E. Boyd; J. Stewart; J.M. Connor Journal of Medical Genetics. 34(9S):37S, SEP 1997 Full Text
A case of follicular lymphoma with double minutes and 3p26 amplification Saeed R Ghaffari, E Boyd, L Patterson, Jm Connor Journal of Medical Genetics. 35(1S):40S, SEP 1998 Full Text
CGH for constitutional chromosome abnormalities and prospects for CGH to Dna microarray targets SR Ghaffari Journal of Medical Genetics, 1998, 35, Full Text
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