The effect of the energy head and the inlet and outlet key width on discharge coefficient of Piano key weir od Shima Komeili, Mohammad Mehdi Heidari

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Molecular Mechanisms and Genes involved in Infertile Men with Varicocele: A Systematic Review od Seyede Nafiseh Tabatabaei, Mohammad Mehdi Heidari

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Analysis of Missense Mutations of CX3CR1 Gene in Patients with Recurrent Pregnancy Loss Using Bioinformatics Tools od Bahareh Mazrouei, Mohammad Mehdi Heidari, Mehri Khatami

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A numerical model for calculating velocity distribution in cross-section of an open channel od Hanieh Kakavandi, Mohammad Mehdi Heidari, Rasool Ghobadian

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Improvement of the performance of NSGA-II and MOPSO algorithms in multi-objective optimization of urban water distribution networks based on modification of decision space od Negin Zarei, Arash Azari, Mohammad Mehdi Heidari

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Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis od Mohammad Mehdi Heidari, Mehri Khatami, Yaser Tahamtan

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Review of Genetic Changes and Factors Causing Cardiac Arrhythmias od Mehri Khatami, Mohammad Mehdi Heidari, Bahareh Mazrouei, Rojin Aflaki

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Molecular Mechanisms of Recurrent Pregnancy Loss od Bahareh Mazrouei, , Mohammad Mehdi Heidari, Mehri Khatami, Maryam Tahmasebi

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Accuracy Evaluation of Methods for Determining Jet Trajectory Characteristics in Flip Bucket od Eghbal Khorami, Mohammad Mehdi Heidari‬‏, Rasoul Ghobadian

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A nonsense mutation in MME gene associates with autosomal recessive late‐onset Charcot–Marie–Tooth disease od Zeinab Jamiri, Rana Khosravi, Mohammad Mehdi Heidari, Ebrahim Kiani, Javad Gharechahi

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Studying the Pathogenic Effect of New Nucleotide Changes in the Promoter Region of the TERT Gene in Patients with Glioblastoma Brain Tumor od Farzaneh Owlia, Mohammad Mehdi Heidari, Mehri Khatami, Ehsan Ziaei, Mohammad Ali Broomand

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Genomic and bioinformatics analysis of nucleotide changes in the coding regions of the CCDC103 gene in patients with Tetralogy of Fallot (TOF): A type of Congenital Heart Defects od Zahra Moghadambarati, Mehri Khatami, Mohammad Mehdi Heidari, Mehdi HadadZadeh, Reihane Ghorbanian

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Genetic Causes of Familial Adenomatous Polyposis (FAP), Risk Factors and Clinical Outcomes od Mohammad Mehdi Heidari, Elham Afkhami aqhda, Maryam Tahmasebi, Mehri Khatami, Zahra Shaker Ardakani

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Molecular Study of Nucleotide Changes of ATPase6 and MT-CYB Genes in the Mitochondrial Genome of Patients with Familial Adenomatous Polyposis (FAP) od Mohammad Mehdi Heidari, Fatemeh Ebrahimi, Zahra Shaker Ardakani, Mahsa Mirzaei, Shima Mirhosseini, Mehri Khatami

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Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease od Mohammad Mehdi Heidari, Mehri Khatami, Akram Kamalipour, Mustafa Kalantari, Mahsa Movahed, Mohammad Hayet Emmamy, Mehdi Hadadzadeh, José Bragança, Mohsen Namnabat, Bahareh Mazrouei

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