Article

(2021) A Novel Mutation in Aicardi-Goutières' Syndrome: A Case Report. Journal of Pediatric Neurology. pp. 50-53. ISSN 13042580 (ISSN)

(2020) Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations. Clinical Case Reports. pp. 2975-2984. ISSN 2050-0904

(2019) Genetic analysis of 320 Iranian patients affected by deafness using Sanger sequencing and Next Generation Sequencing (NGS) methods. European Journal of Human Genetics. p. 1222. ISSN 1018-4813

(2019) Hereditary Ataxia with a novel Mutation in the Senataxin Gene: A case Report. Iranian Journal of Medical Sciences. pp. 262-264. ISSN 0253-0716

(2019) A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia. Cellular & Molecular Biology Letters. p. 8. ISSN 1425-8153

(2018) Investigating the Association Between miR-608 rs4919510 and miR-149 rs2292832 with Colorectal Cancer in Iranian Population. Microrna. pp. 100-106. ISSN 2211-5374 (Electronic)

(2018) Mutation analysis of ECM1 gene in two related iranian patients affected by lipoid proteinosis. Acta Med Iran. pp. 474-477. ISSN 00446025 (ISSN)

(2018) A novel mutation associated with dentinogenesis imperfecta in a patient with hearing loss: A case report. Journal of Mazandaran University of Medical Sciences. pp. 183-188. ISSN 17359279 (ISSN)

(2017) Evaluating the association of VSX1 mutation with keratoconus and the granular corneal dystrophy in an Iranian family. International Eye Science. pp. 1023-1027. ISSN 16725123 (ISSN)

(2016) No association between ITGAV rs3738919 and rs3768777 polymorphisms and rheumatoid arthritis susceptibility in Iranian population. Laboratoriumsmedizin-Journal of Laboratory Medicine. pp. 413-417. ISSN 0342-3026

(2015) Association of 1082g/a estrogen receptor genes polymorphisms with recurrent abortions using as-pcr. Scientific Journal of Kurdistan University of Medical Sciences. pp. 93-101. ISSN 1560652X (ISSN)

(2014) Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family. Cell Journal. pp. 91-94. ISSN 2228-5806

(2012) Osteopetrosis; a report of two Iranian patients with autosomal recessive inheritance pattern. Int J Mol Cell Med. pp. 173-7. ISSN 2251-9637 (Print) 2251-9637

(2012) A Study of ribotype patterns of salmonella enterica serovar enteritidis strains Isolated in Tehran, Iran. Journal of Isfahan Medical School. ISSN 10277595 (ISSN)

(2011) DETECTION OF THE GJB2 MUTATION IN IRANIAN CHILDREN WITH HEARING LOSS TREATED WITH COCHLEAR IMPLANTATION. Balkan Journal of Medical Genetics. pp. 19-23. ISSN 1311-0160

(2011) Detecting Rare Triple Heteroplasmic Substitutions in the Mitochondrial DNA Control Region: A Potential Concern for Forensic DNA Studies. Cell Journal. pp. 103-106. ISSN 2228-5806

(2008) Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan. Archives of Medical Research. pp. 131-133. ISSN 0188-4409

(2007) Isolation of clinical strains of Pseudomonas aeruginosa harboring different plasmids. Pak J Biol Sci. pp. 3020-2. ISSN 1028-8880 (Print) 1028-8880

(2007) Sequence analysis of mitochondrial DNA hypervariable regions: An approach to personal identification. Archives of Medical Research. pp. 345-349. ISSN 0188-4409

(2007) An outbreak of gastroenteritis of unknown origin in Tehran, July 2003. Pak J Biol Sci. pp. 1138-40. ISSN 1028-8880 (Print) 1028-8880

(2006) Linear and circular plasmids in skin and cerebrospinal fluid isolates of Borrelia burgdorferi agent of lyme disease. Pakistan Journal of Biological Sciences. pp. 2787-2793. ISSN 10288880 (ISSN)

(2006) OspA sequence comparison and protection against Borrelia burgdorferi infection in gerbils by recombinant OspA protein. Iranian Journal of Public Health. pp. 16-24. ISSN 2251-6085

(2004) Isolated congenital anosmia locus maps to 18p11.23-q12.2. Journal of Medical Genetics. pp. 299-303. ISSN 0022-2593

(2004) Isolated congenital anosmia with morphologically normal olfactory bulb in two Iranian families: A new clinical entity? American Journal of Medical Genetics Part A. pp. 307-309. ISSN 1552-4825