Mohammad A Faghihi

Assistant Professor

  • 4091 Citations
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  • 7 Similar Profiles
Long Noncoding RNA Medicine & Life Sciences
Untranslated RNA Medicine & Life Sciences
Genes Medicine & Life Sciences
Antisense RNA Medicine & Life Sciences
Alzheimer Disease Medicine & Life Sciences
RNA Medicine & Life Sciences
MicroRNAs Medicine & Life Sciences
Mutation Medicine & Life Sciences

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Projects 2013 2017

Antisense RNA
Brain-Derived Neurotrophic Factor
Untranslated RNA
Rett Syndrome

Research Output 2004 2019

  • 4091 Citations
  • 46 Article
  • 1 Chapter

A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: A Case report

Ziyaee, F., Shorafa, E., Dastsooz, H., Habibzadeh, P., Nemati, H., Saeed, A., Silawi, M., Farazi Fard, M. A., Faghihi, M. A. & Dastgheib, S. A., Jan 14 2019, In : BMC Medical Genetics. 20, 1, 13.

Research output: Contribution to journalArticle

Muscular Dystrophies
Computational Biology

The first case of a small supernumerary marker chromosome 18 in a klinefelter fetus: A case report

Saberzadeh, J., Miri, M. R., Dianatpour, M., Behbahani, A. B., Tabei, M. B., Alipour, M., Faghihi, M. A. & Fardaei, M., Jan 1 2019, In : Iranian Journal of Medical Sciences. 44, 1, p. 65-69 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 18
Genetic Markers
Fluorescence In Situ Hybridization
Microsatellite Repeats

A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: A case report

Esmaeilzadeh, H., Bordbar, M. R., Dastsooz, H., Silawi, M., Fard, M. A. F., Adib, A., Kafashan, A., Tabatabaei, Z., Sadeghipour, F. & Faghihi, M. A., Jul 20 2018, In : BMC Medical Genetics. 19, 1, 123.

Research output: Contribution to journalArticle

Wiskott-Aldrich Syndrome
Inflammatory Bowel Diseases

Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: A case report

Maghami, F., Tabei, S. M. B., Moravej, H., Dastsooz, H., Modarresi, F., Silawi, M. & Faghihi, M. A., May 25 2018, In : BMC Medical Genetics. 19, 1, 86.

Research output: Contribution to journalArticle

Osteogenesis Imperfecta
Inheritance Patterns

A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis

Bordbar, M. R., Modarresi, F., Farazi Fard, M. A., Dastsooz, H., Shakib Azad, N. & Faghihi, M. A., May 3 2017, In : BMC Medical Genetics. 18, 1, 49.

Research output: Contribution to journalArticle

Hemophagocytic Lymphohistiocytosis
Missense Mutation