Mohammad A Faghihi

Assistant Professor

  • 4009 Citations
20042018
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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
Epigenomics
Untranslated RNA
Rett Syndrome

Research Output 2004 2018

  • 4009 Citations
  • 44 Article
  • 1 Chapter

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
Colitis
Mutation
Genes
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
Mutation
Genes
Inheritance Patterns
Exome

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
Mutation
Genes
Missense Mutation
Parents

A novel mutation in ERCC8 gene causing cockayne syndrome

Taghdiri, M., Dastsooz, H., Fardaei, M., Mohammadi, S., Fard, M. A. F. & Faghihi, M. A., Aug 9 2017, In : Frontiers in Pediatrics. 5, 169.

Research output: Contribution to journalArticle

Cockayne Syndrome
Mutation
Genes
Microcephaly
Parents

Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene

Karimzadeh, P., Naderi, S., Modarresi, F., Dastsooz, H., Nemati, H., Farokhashtiani, T., Shamsian, B. S., Inaloo, S. & Faghihi, M. A., Jul 17 2017, In : BMC Medical Genetics. 18, 1, 73.

Research output: Contribution to journalArticle

GM1 Gangliosidosis
Age of Onset
Mutation
Genes
Missense Mutation