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Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism.
Arch Iran Med. 2020 Dec 1;23(12):842-847. doi: 10.34172/aim.2020.112.
Arch Iran Med. 2020.
PMID: 33356342
Free article.
Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability Patients.
InanlooRahatloo K, Peymani F, Kahrizi K, Najmabadi H.
InanlooRahatloo K, et al. Among authors: peymani f.
Neuroscience. 2019 Apr 15;404:423-444. doi: 10.1016/j.neuroscience.2019.01.029. Epub 2019 Feb 10.
Neuroscience. 2019.
PMID: 30742961
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Guidelines for clinical interpretation of variant pathogenicity using RNA phenotypes.
Smirnov D, Schlieben LD, Peymani F, Berutti R, Prokisch H.
Smirnov D, et al. Among authors: peymani f.
Hum Mutat. 2022 Aug;43(8):1056-1070. doi: 10.1002/humu.24416. Epub 2022 Jun 29.
Hum Mutat. 2022.
PMID: 35645004
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RNA sequencing role and application in clinical diagnostic.
Peymani F, Farzeen A, Prokisch H.
Peymani F, et al.
Pediatr Investig. 2022 Mar 5;6(1):29-35. doi: 10.1002/ped4.12314. eCollection 2022 Mar.
Pediatr Investig. 2022.
PMID: 35382420
Free PMC article.
Review.
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Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H.
Abolhassani A, et al. Among authors: peymani f.
NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0.
NPJ Genom Med. 2024.
PMID: 38374194
Free PMC article.
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