Unraveling the dark matter, long non-coding RNAs, in male reproductive diseases: A narrative review by Masoud Dehghan Tezerjani, Seyed Mehdi Kalantar

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Investigating the association between polymorphism of follicle-stimulating hormone receptor gene and ovarian response in controlled ovarian hyperstimulation by Mohammad Hasan Sheikhha, Maryam Eftekhar, Seyed Mehdi Kalantar

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Effects of gamma radiation on fetal development in mice by Tahere Dehghan, Hossein Mozdarani, Arezoo Khoradmehr, Seyed Mehdi Kalantar

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CAG repeat polymorphism in androgen receptor and infertility: A case-control study by Shiva Sharestani, Seyed Mehdi Kalantar, Nasrin Ghasemi, Ehsan Farashahi Yazd

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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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Mutation analysis of exon1 of bone morphogenetic protein-15 gene in Iranian patients with polycystic ovarian syndrome by Anahita Mehdizadeh, Mohammad Hasan Sheikhha, Seyed Mehdi Kalantar, Bibi Shahnaz Aali, Azam Ghanei

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Association of SNP rs.2414096 CYP19 gene with polycystic ovarian syndrome in Iranian women by Anahita Mehdizadeh, Seyed Mehdi Kalantar, Mohammad Hassan Sheikhha, Bibi Shahnaz Aali, Azam Ghanei

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Effects of phosalone plant pesticide on sperm parameters and sexual hormone levels in Wistar rats: An experimental study by Fahime Mazaheri, Kazem Kamali Aliabad, Seyed Mehdi Kalantar, Noosha Ziya, Arezoo Khoradmehr, Morteza Anvari

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The frequency of TP53 R72P and MDM2 309T>G polymorphisms in Iranian infertile men with spermatogenetic failure: A case-control study by Zeinab Ebrahim Abadi, Maryam Khademi Bami, Maryam Golzadeh, Seyed Mehdi Kalantar, Mohammad Hasan Sheikhha

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Frequency of chromosomal aneuploidy in high quality embryos from young couples using preimplantation genetic screening by Farzaneh Fesahat, Fatemeh Montazeri, Mohammad Hasan Sheikhha, Hojjatollah Saeedi, Razieh Dehghani Firouzabadi, Seyed Mehdi Kalantar

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Aberrant expression of microRNAs 16 and 21 and gene targets in women with unexplained recurrent miscarriage: A case-control study by Noorodin Karami, Seyed Hamidreza Mirabutalebi, Fatemeh Montazeri, Seyed Mehdi Kalantar, Mohammad Hasan Sheikhha, Maryam Eftekhar

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Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report by Mohammad Yahya VAHIDI MEHRJARDI, Masoud DEHGHAN TEZERJANI, Mahmoud NORI-SHADKAM, Seyed Mehdi KALANTAR, Mohammadreza DEHGHANI

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The association of RBX1 and BAMBI gene expression with oocyte maturation in PCOS women by Kimia Monshizadeh, Masoud Tajamolian, Fatemeh Anbari, Mohammad Yahya Vahidi Mehrjardi, Seyed Mehdi Kalantar, Mohammadreza Dehghani

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Investigating the expressions of miRNA-125b and TP53 in endometriosis. Does it underlie cancer-like features of endometriosis? A case-control study by Elnaz Hajimaqsoudi, Farzaneh Darbeheshti, Seyed Mehdi Kalantar, Atiyeh Javaheri, Seyed Hamidreza Mirabutalebi, Mohammad Hasan Sheikhha

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Transforming Growth Factor Beta Leucine10 Proline Variation and Breast Cancer Risk in Iranian Women by Masoud Dehghan Tezerjani, Mahdi Beik, Seyed Milad Kalantar, Azam Rasti, Seyed Mehdi Kalantar, Seyed Mostafa Shiryazdi

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SULF 1 gene polymorphism, rs6990375 is in significant association with fetus failure in IVF technique by Eskandar Taghizadeh, Seyed Mehdi Kalantar, Reza Mahdian, Mohammad Hasan Sheikhha, Ehsan Farashahi-Yazd, Saeed Ghasemi, Zahra Shahbazi

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Comparing the advantages, disadvantages and diagnostic power of different non-invasive pre-implantation genetic testing: A literature review by Noorodin Karami, Farzaneh Iravani, Sareh Bakhshandeh Bavarsad, Samira Asadollahi, Seyed Mehdi Hoseini, Fateme Montazeri, Seyed Mehdi Kalantar

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Comparison of chromosomal instability of human amniocytes in primary and long-term cultures in AmnioMAX II and DMEM media: A cross-sectional study by Seyed Mehdi Hoseini, Fateme Montazeri, Maryam Moghaddam-Matin, Ahmad Reza Bahrami, Hassan Heidarian Meimandi, Saeed Ghasemi-Esmailabad, Seyed Mehdi Kalantar

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The relationship between the expression levels of miR-135a and HOXA10 gene in the eutopic and ectopic endometrium by Seyed Hamidreza Mirabutalebi, Noorodin Karami, Fatemeh Montazeri, Farzaneh Fesahat, Mohammad Hasan Sheikhha, Elnaz Hajimaqsoodi, Mojgan Karimi Zarchi, Seyed Mehdi Kalantar

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A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report by Masoud DEHGHAN TEZERJANI, Reza MAROOFIAN, Mohammad Yahya VAHIDI MEHRJARDI, Barry A. CHIOZA, Shiva ZAMANINEJAD, Seyed Mehdi KALANTAR, Mahmoud NORI-SHADKAM, Hamidreza GHADIMI, Emma L. BAPLE, Andrew H. CROSBY, Mohammadreza DEHGHANI

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