Analysis of IFN-γ (+874 A/T) and IL-10 (-1082 G/A) genes polymorphisms with risk of schizophrenia. by Dor Mohammad kordi Tamandani, Azizoallah Mojahed, Maryam Najafi

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Analysis of methylation and expression profile of MOB1A in blood, saliva, and tissue of patients with oral squamous cell carcinoma (OSCC) and precancerous patients by Hanieh Soleimani, Mohammad Rigi Ladez, Dor Mohammad Kordi-Tamandani

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Association of miR-132 and miR-185 Genes Methylation and their Expression Profile with Risk of Congenital Factor XIII Deficiency by Dor Mohammad Kordi-Tamandani, Zohreh Rezaei, Akbar Dorgalaleh-Mail

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Analysis of Expression Profiles of GLI3A, LATS2 and MOB1A genes in Patients with Congenital hypothyroidism by Sepideh Eisazaei, Maryam Nakhaee-Moghadam, Dor-Mohammad Kordi Tamandani

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Strategies for whole-exome sequencing analysis in a case series study of familial male infertility by Masomeh Askari, Dor Mohammad Kordi Tamandani, Navid Almadani, Mehdi Totonch

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Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia by Tahereh Dianat, Dor Mohammad Kordi Tamandani, Maryam Najafi, Ali Khajeh

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Correlation between resistance to trastuzumab and miR-141 relative expression in the BT-474 human breast cancer cell line by Zohreh Rezaei, Dor Mohammad Kordi-Tamandani, Ahmadreza Sebzari, Kazem Dastjerdi

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Composition and Diversity Differences between Colon Microbiome of Colorectal Cancer Patients and Healthy Individuals by Age by Hosseinali Abdi, Dor Mohammad Kordi-Tamandani, Milad Lagzian, Alireza Bakhshipour

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Analysis of DRD1 gene expression pattern in patients with glaucoma by Mojtaba Reyhani, Mohammad Arish, Alireza Maleki, Shahram Banaie, Dor Mohammad Kordi-Tamandani

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The relationship between FXIII Val34Leu and PAI-1 4G/5G gene polymorphisms and recurrent miscarriage in women from Golestan province by Nazanin Ghaderi Nejad, Fojan saboori, Nader Mansour Samaei, Dor Mohammad Kordi-Tamandani

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Identification of a <i>TPP1</i> Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update by Tayebeh Baranzehi, Dor Mohammad Kordi-Tamandani, Maryam Najafi, Ali Khajeh, Miriam Schmidts

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Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer by Seyed Mohsen Miresmaeili, Dor Mohammad Kordi Tamandani, Seyed Mehdi Kalantar, Seyed Mohammad Moshtaghioun

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Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients by Sajad Rafiee Komachali, Zakieh Siahpoosh, Sara Rafiee Komachali, Dor Mohammad Kordi Tamandani, Mansoor Salehi

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Evaluation of Promoter Hypermethylation, Expression and, Oxytocin Receptor Gene (OXTR) Polymorphism with the Risk of Oral Squamous Cell Carcinoma by Behnaz Hassanpour, Mohammad Ayoub Rigi-Ladiz, Tayebeh Baranzehi, Mohammad Javad Ashraf, DorMohammad Kordi-Tamandani

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Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis by Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts

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