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Fatemeh Peymani

Showing results (1-10 of 9) with videos related to

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Pediatric Investigation|April 6, 2022
RNA sequencing role and application in clinical diagnosticFatemeh Peymani, Aiman Farzeen, Holger Prokisch
Neuroscience|February 12, 2019
Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability PatientsKolsoum InanlooRahatloo, Fatemeh Peymani, Kimia Kahrizi, et al.
Human Mutation|June 1, 2022
Guidelines for clinical interpretation of variant pathogenicity using RNA phenotypesDmitrii Smirnov, Lea D Schlieben, Fatemeh Peymani, et al.
Archives of Iranian Medicine|December 28, 2020
Novel Mutation in <i>LARP7</i> in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial DysmorphismGoli Kazemi, Fatemeh Peymani, Marzieh Mohseni, et al.
Clinical Genetics|January 3, 2025
Improved Diagnostic Yield in Recessive Intellectual Disability Utilizing Systematic Whole Exome Sequencing Data ReanalysisZohreh Fattahi, Ebrahim Shokouhian, Fatemeh Peymani, et al.
Nature Communications|December 18, 2025
Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteriesJessica Pauli, Daniel Garger, Fatemeh Peymani, et al.
Annals of Clinical and Translational Neurology|April 25, 2026
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial DiseaseZhimei Liu, Xin Duan, Fatemeh Peymani, et al.
NPJ Genomic Medicine|February 19, 2024
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian populationAyda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, et al.
Brain : a Journal of Neurology|April 30, 2025
Pleiotropic effects of MORC2 derive from its epigenetic signatureFatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Pediatric Investigation|April 6, 2022
RNA sequencing role and application in clinical diagnosticFatemeh Peymani, Aiman Farzeen, Holger Prokisch
Neuroscience|February 12, 2019
Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability PatientsKolsoum InanlooRahatloo, Fatemeh Peymani, Kimia Kahrizi, et al.
Human Mutation|June 1, 2022
Guidelines for clinical interpretation of variant pathogenicity using RNA phenotypesDmitrii Smirnov, Lea D Schlieben, Fatemeh Peymani, et al.
Archives of Iranian Medicine|December 28, 2020
Novel Mutation in <i>LARP7</i> in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial DysmorphismGoli Kazemi, Fatemeh Peymani, Marzieh Mohseni, et al.
Clinical Genetics|January 3, 2025
Improved Diagnostic Yield in Recessive Intellectual Disability Utilizing Systematic Whole Exome Sequencing Data ReanalysisZohreh Fattahi, Ebrahim Shokouhian, Fatemeh Peymani, et al.
Nature Communications|December 18, 2025
Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteriesJessica Pauli, Daniel Garger, Fatemeh Peymani, et al.
Annals of Clinical and Translational Neurology|April 25, 2026
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial DiseaseZhimei Liu, Xin Duan, Fatemeh Peymani, et al.
NPJ Genomic Medicine|February 19, 2024
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian populationAyda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, et al.
Brain : a Journal of Neurology|April 30, 2025
Pleiotropic effects of MORC2 derive from its epigenetic signatureFatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, et al.
Pageof 1