Personal Details

Name: Ali Mohammad
Surname: Ahadi
Nationality: Iranian
Date of Birth: 1973
Tel: 09122094047

Fax: 03814424419
Place of Birth: kashan, Iran
Email Addresses: Ahadi_al@yahoo.com

Educations

P.HD. in Molecular Genetics,Tarbiat Modarres University                       

M .Sc. in Genetics , Tarbiat Modarres University .

B.Sc. in Zoology , Isfahan University  .                              .

Work Experiences

Study of genetic alteration in some type of epileptic disorder in IRAN.

Study of Genetic diversity in Iranian ethnic groups by PCR-RFLP method . Design and production of Herpesviridae family detection kits.

Design of a multiplex nested consensus PCR for detection of Herpesviridae family in biological samples.

Design and production of DNA size marker.

Teaching

Molecular Genetic, medical genetic , cancer genetic, population genetics, developmental genetics.

Membership in Societies etc

Medical genetic society of Iran, Epilepsy Society of Iran , Neurogenetic society of Iran .

Publications in refreed journals

Tafreshi NK, Sadeghizadeh M, Amini-Bavil-Olyaee S, Ahadi AM, Jahanzad I, Roostaee MH.Development of a multiplex nested consensus PCR for detection and identification of major human herpesviruses in CNS infections. J Clin Virol. (2005)32(4):318-24.

Ali-Mohammad Ahadi, Majid Sadeghizadeh, Koorosh Gharagozli and Massoud Houshmand. Confirmation of R82Q Mutation in g2 Subunit of Gamma Amino Butyric Acid Receptor in an Iranian Family .Pakistan Journal of Biological Sciences 9 (14): 2704-2707, 2006.

Mohammad Khalaj-Kondori, Majid Sadeghizadeh , Khosro Khajeh, Hossein Naderi-Manesh, Ali Mohammad Ahadi and Abdorahman Emamzadeh, Cloning, Sequence Analysis and Three-dimensional Structure Prediction of DNA Pol I from Thermophilic Geobacillus sp. MKK Isolated from an Iranian Hot Spring.2007(142):200-208.

Books

Proceeding papers

Ahadi AM., Sadeghizadeh M., Gharagoozli K., Houshmand M. .An A8296G mutation in mito-chondrial tRNAlys gene: Many phenotypes caused by similar genotype. In press.

Ahadi AM., Sadeghizadeh M., Gharagoozli K., Houshmand M.Prevalence and incidence of epilepsy in Iranian families: A descriptive analysis. In press

Ahadi AM., Sadeghizadeh M., Gharagoozli K., Houshmand M..A short report. A new point mutation in SCN1A Subunit in a family with generalized epilepsy and febrile seizure plus(GEFS+).in press.

On–going research projects

[1] Preimplantation gender determination of sheep embryos by single cell PCR method.

[2] Study of genetic alteration of epileptic patient in Chahar Mahal province.

[3] construction of genome store of epileptic patient.