Mohammad A Faghihi

Assistant Professor

  • 4542 Citations
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  • 8 Similar Profiles
Long Noncoding RNA Medicine & Life Sciences
Untranslated RNA Medicine & Life Sciences
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Antisense RNA Medicine & Life Sciences
Alzheimer Disease Medicine & Life Sciences
RNA Medicine & Life Sciences
MicroRNAs Medicine & Life Sciences

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Projects 2013 2017

Antisense RNA
Brain-Derived Neurotrophic Factor
Untranslated RNA
Rett Syndrome

Research Output 2004 2019

  • 4542 Citations
  • 54 Article
  • 1 Chapter
  • 1 Comment/debate

An immunocompetent patient with a nonsense mutation in NHEJ1 gene

Esmaeilzadeh, H., Bordbar, M. R., Hojaji, Z., Habibzadeh, P., Afshinfar, D., Miryounesi, M., Fardaei, M. & Faghihi, M. A., Mar 21 2019, In : BMC medical genetics. 20, 1, 45.

Research output: Contribution to journalArticle

Open Access
Nonsense Codon
V(D)J Recombination
Autoimmune Hemolytic Anemia
1 Citation (Scopus)

A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: A case report

Zareifar, S., Dastsooz, H., Shahriari, M., Faghihi, M. A., Shekarkhar, G., Bordbar, M., Zekavat, O. R. & Shakibazad, N., Jul 9 2019, In : BMC medical genetics. 20, 1, 122.

Research output: Contribution to journalArticle

Open Access
Fanconi Anemia
Inborn Genetic Diseases

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
1 Citation (Scopus)

A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment

Habibzadeh, P., Inaloo, S., Silawi, M., Dastsooz, H., Farazi Fard, M. A., Sadeghipour, F., Faghihi, Z., Rezaeian, M., Yavarian, M., Böhm, J. & Faghihi, M. A., Sep 4 2019, In : Frontiers in Neurology. 10, 944.

Research output: Contribution to journalArticle

Open Access
Spastic Paraparesis

Association between rs2303861 polymorphism in CD82 gene and non-alcoholic fatty liver disease: a preliminary case-control study

Habibzadeh, P., Honarvar, B., Silawi, M., Bahramjahan, S., Kazemi, A., Faghihi, M. A. & Lankarani, K., Aug 31 2019, In : Croatian medical journal. 60, 4, p. 361-368 8 p.

Research output: Contribution to journalArticle

Case-Control Studies
Quality Control
Non-alcoholic Fatty Liver Disease
Body Mass Index