Mohammad A Faghihi

Assistant Professor

  • 4213 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

  • 4213 Citations
  • 50 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

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

Erratum: Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia (The American Journal of Human Genetics (2019)104(4)(767–773), (S0002929719300977), (10.1016/j.ajhg.2019.03.001))

Farazi Fard, M. A., Rebelo, A. P., Buglo, E., Nemati, H., Dastsooz, H., Gehweiler, I., Reich, S., Reichbauer, J., Quintáns, B., Ordóñez-Ugalde, A., Cortese, A., Courel, S., Abreu, L., Powell, E., Danzi, M. C., Martuscelli, N. B., Bis-Brewer, D. M., Tao, F., Zarei, F., Habibzadeh, P. & 22 othersYavarian, M., Modarresi, F., Silawi, M., Tabatabaei, Z., Yousefi, M., Farpour, H. R., Kessler, C., Mangold, E., Kobeleva, X., Tournev, I., Chamova, T., Mueller, A. J., Haack, T. B., Tarnopolsky, M., Gan-Or, Z., Rouleau, G. A., Synofzik, M., Sobrido, M. J., Jordanova, A., Schüle, R., Zuchner, S. L. & Faghihi, M. A., Jan 1 2019, In : American journal of human genetics.

Research output: Contribution to journalComment/debate

Hereditary Spastic Paraplegia
Medical Genetics

HDAC Inhibitors Induce BDNF Expression and Promote Neurite Outgrowth in Human Neural Progenitor Cells-Derived Neurons

Bagheri, A., Habibzadeh, P., Razavipour, S. F., Volmar, C. H., Chee, N. T., Brothers, S. P., Wahlestedt, C. R., Mowla, S. J. & Faghihi, M. A., Mar 5 2019, In : International journal of molecular sciences. 20, 5

Research output: Contribution to journalArticle

Open Access
Histone Deacetylase Inhibitors
Brain-Derived Neurotrophic Factor

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