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Andrologia|February 1, 2020
A male Down syndrome with two normal boys: Cytogenetic, paternity and andrological investigationsOmid Jazayeri, Nassim Gorjizadeh
Clinical Case Reports|October 3, 2022
49,XXXXY syndrome: A case study and a systematic review of clinical features among the Iranian populationMahboubeh Rajabzadeh, Nafiseh Taheri, Omid Jazayeri
Best Practice & Research. Clinical Gastroenterology|March 24, 2018
Lifestyle alters GUT-bacteria function: Linking immune response and hostOmid Jazayeri, S Mojtaba Daghighi, Farhad Rezaee
Journal of Genetics|October 18, 2023
AICRF: ancestry inference of admixed population with deep conditional random fieldFarhad Alizadeh, Hamid Jazayeriy, Omid Jazayeri, et al.
Laboratory Medicine|June 3, 2022
Pathogenic Homozygous Mutations in the DBT Gene (c.1174A>C) Result in Maple Syrup Urine Disease in a rs12021720 CarrierMorteza Alijanpour, Omid Jazayeri, Shima Soleimani Amiri, et al.
Biomedica : Revista Del Instituto Nacional De Salud|December 22, 2021
Up-regulation of Arl4a gene expression by broccoli aqueous extract is associated with improved spermatogenesis in mouse testesOmid Jazayeri, Setareh Farahmand Araghi, Tahereh A Aghajanzadeh, et al.
Drug Research|August 18, 2021
Astaxanthin Induces the Expression of CatSper1 Gene and Protects Sperms in Toxicity Induced by Cadmium in MiceEnsieh Saberi, Fereshteh Mir Mohammadrezaei, Omid Jazayeri, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|October 28, 2025
Whole-Exome Sequencing Revealed a Novel De Novo Pathogenic EFTUD2 Variant in Mandibulofacial Dysostosis, Guion-Almeida Type: Reinforcing Links to Choanal and Oesophageal AtresiaOmid Jazayeri, Nassim Gorjizadeh, Mohammad Reza Salehiomran, et al.
JBRA Assisted Reproduction|May 7, 2024
Paternal thrombophilia and recurrent implantation failure: an exploratory case-control studySedighe Esmaeilzadeh, Omid Jazayeri, Mir Mohammad Reza Aghajani, et al.
European Journal of Medical Genetics|November 10, 2015
A novel homozygous insertion and review of published mutations in the NNT gene causing familial glucocorticoid deficiency (FGD)Omid Jazayeri, Xuanzhu Liu, Cleo C van Diemen, et al.
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