Hossein NajmabadiÂ
ProfessorÂ
Genetics Research
University of Social Welfare and Rehabilitation Sciences
Iran
Biography
Dr. Hossein Najmabadi is currently working as a Professor in the Department of Genetics Research, University of Social Welfare and Rehabilitation Sciences, Iran. His research interests includes prevent genetic disabilities and disorders by the establishment of a nationwide strategy for the early prenatal diagnosis of genetic disorders. He is serving as an editorial member and reviewer of several international reputed journals. Dr. Hossein Najmabadi is the member of many international affiliations. He has successfully completed his Administrative responsibilities. He has authored of many research articles/books related to prevent genetic disabilities and disorders by the establishment of a nationwide strategy for the early prenatal diagnosis of genetic disorders.
Research Interest
Prevent genetic disabilities and disorders by the establishment of a nationwide strategy for the early prenatal diagnosis of genetic disorders.
Publications
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Kahrizi K, Mohseni M, Nishimura C, Bazazzadegan N, Fischer SM, Dehghani A, Sayfati M, Taghdiri M, Jamali P, Smith RJ, Azizi F, Najmabadi H. Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment. Eur J Pediatr. 2009;168(6):651-3.
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A.W. Kuss, M. Garshasbi, K. Kahrizi, A. Tzschach, F. Behjati, H. Darvish, L. Abbasi Moheb, L. Puettmann, A. Zecha, R. QWeob,amm. H. Hu. M. Mohseni, S.S. Abedini, A. Rajab, Ch. Hertzberg, D. Weiczorek, R.Ullmann, S. Ghasemi-Firozabadi, S. Banihashemi, S. Arzhangi, v. Hadavi, Gh. Bahrami-Monajemi, M. Kasiri, M. Falah, P. Nekoei, A. Dehghan, M. Sobhani, P. Jamali, H.H. Ropers, H. Najmabadi. Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots. Human Genetics;[Epub ahead of print].
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Darvish H, Esmaeeli-Nieh S, Monajemi GB, Mohseni M, Ghasemi-Firouzabadi S, Abedini SS, Bahman I, Jamali P, Azimi S, Mojahedi F, Dehghan A, Shafeghati Y, Jankhah A, Falah M, Soltani Banavandi MJ, Ghani-Kakhi M, Garshasbi M, Rakhshani F, Naghavi A, Tzschach A, Neitzel H, Ropers HH, Kuss AW, Behjati F, Kahrizi K, Najmabadi H. A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. J Med Genet. 2010;47(12):823-8.
