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Page 1
Spinal Muscular Atrophy and Common Therapeutic Advances.
Bozorg Qomi S, Asghari A, Salmaninejad A, Mojarrad M. Bozorg Qomi S, et al. Among authors: salmaninejad a. Fetal Pediatr Pathol. 2019 Jun;38(3):226-238. doi: 10.1080/15513815.2018.1520374. Epub 2019 May 7. Fetal Pediatr Pathol. 2019. PMID: 31060440 Review.
Molecular Genetics of Cleidocranial Dysplasia.
Motaei J, Salmaninejad A, Jamali E, Khorsand I, Ahmadvand M, Shabani S, Karimi F, Nazari MS, Ketabchi G, Naqipour F. Motaei J, et al. Among authors: salmaninejad a. Fetal Pediatr Pathol. 2021 Oct;40(5):442-454. doi: 10.1080/15513815.2019.1710792. Epub 2020 Jan 26. Fetal Pediatr Pathol. 2021. PMID: 31984822
Common therapeutic advances for Duchenne muscular dystrophy (DMD).
Salmaninejad A, Jafari Abarghan Y, Bozorg Qomi S, Bayat H, Yousefi M, Azhdari S, Talebi S, Mojarrad M. Salmaninejad A, et al. Int J Neurosci. 2021 Apr;131(4):370-389. doi: 10.1080/00207454.2020.1740218. Epub 2020 Apr 3. Int J Neurosci. 2021. PMID: 32241218 Review.
AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data.
Quinodoz M, Peter VG, Bedoni N, Royer Bertrand B, Cisarova K, Salmaninejad A, Sepahi N, Rodrigues R, Piran M, Mojarrad M, Pasdar A, Ghanbari Asad A, Sousa AB, Coutinho Santos L, Superti-Furga A, Rivolta C. Quinodoz M, et al. Among authors: salmaninejad a. Nat Commun. 2021 Jan 22;12(1):518. doi: 10.1038/s41467-020-20584-4. Nat Commun. 2021. PMID: 33483490 Free PMC article.
Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.
Rehman AU, Sepahi N, Bedoni N, Ravesh Z, Salmaninejad A, Cancellieri F, Peter VG, Quinodoz M, Mojarrad M, Pasdar A, Asad AG, Ghalamkari S, Piran M, Piran M, Superti-Furga A, Rivolta C. Rehman AU, et al. Among authors: salmaninejad a. Sci Rep. 2021 Sep 29;11(1):19332. doi: 10.1038/s41598-021-98677-3. Sci Rep. 2021. PMID: 34588515 Free PMC article.
68 results