Publications
The latest tweets from .Dr Ghaffari are shown in this feed
PostsPage
Presentations
Seminars in Clinical Genetics
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 […]
Uncategorized
Master Projects
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
2013-2014: Mutation Analysis of RP2 Gene in X-Linked Retinitis Pigmentosa patients
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
2011-2012: Mutation Analysis of RHO Gene in Autosomal Dominant Retinitis Pigmentosa patients
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, […]
2017
2017-Present: “Genetic Profiling of Common Hereditary Disorders to Identify the Distribution of Mutations in Iran Provinces: Hope Project”
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 […]
2010
Comprehensive Genomic Approach to Inherited Retinal Dystrophies using Next Generation 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 […]
2007
2007-2011: Determining the Distribution of Different Modes of Inheritance among Iranian Patients with Retinitis Pigmentosa by Pedigree Analysis of ~14000 Iranian RP patients from >4000 Families registered in Iran RP Society
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 […]
1998
Comparative Genomic Hybridisation in the investigation of haematological malignancies
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
1998
A case of follicular lymphoma with double minutes and 3p26 amplification
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