The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults von Mehrdad, Mahsa, Fardaei, Majid, Fararouei, Mohammad, Eftekhari, Mohammad Hassan

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The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients von Nguyen, Ngoc Minh Phuong, Khawajkie, Yassemine, Mechtouf, Nawel, Rezaei, Maryam, Breguet, Magali, Kurvinen, Elvira, Jagadeesh, Sujatha, Solmaz, Asli Ece, Aguinaga, Monica, Hemida, Reda, Harma, Mehmet Ibrahim, Rittore, Cécile, Rahimi, Kurosh, Arseneau, Jocelyne, Hovanes, Karine, Clisham, Ronald, Lenzi, Tiffanee, Scurry, Bonnie, Addor, Marie-Claude, Bagga, Rashmi, Nendaz, Genevieve Girardet, Finci, Vildana, Poke, Gemma, Grimes, Leslie, Gregersen, Nerine, York, Kayla, Bolze, Pierre-Adrien, Patel, Chirag, Mozdarani, Hossein, Puechberty, Jacques, Scotchie, Jessica, Fardaei, Majid, Harma, Muge, Gardner, R. J. McKinlay, Sahoo, Trilochan, Dudding-Byth, Tracy, Srinivasan, Radhika, Sauthier, Philippe, Slim, Rima

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Association of FTO rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults von Mehrdad, Mahsa, Doaei, Saeid, Gholamalizadeh, Maryam, Fardaei, Majid, Fararouei, Mohammad, Eftekhari, Mohammad Hassan

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The Effect of Short-Term Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Diet on Hunger Hormones, Anthropometric Parameters, and Brain Structures in Middle-Aged... von Arjmand, Golnaz, Abbas-Zadeh, Mojtaba

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Commentary: Profiling of UGT1A16, UGT1A160, UGT1A193, and UGT1A128 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing von Heydari, Mohammad Reza, Fardaei, Majid

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Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports von Dastsooz, Hassan, Nemati, Hamid, Fard, Mohammad Ali Farazi, Fardaei, Majid, Faghihi, Mohammad Ali

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Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature von Najmeh Moein-Vaziri, Jafar Fallahi, Bahia Namavar-Jahromi, Majid Fardaei, Mozhdeh Momtahan, Zahra Anvar

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Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles von Fallahi, Jafar, Anvar, Zahra, Razban, Vahid, Momtahan, Mozhdeh, Namavar-Jahromi, Bahia, Fardaei, Majid

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An immunocompetent patient with a nonsense mutation in NHEJ1 gene von Esmaeilzadeh, Hossein, Bordbar, Mohammad Reza, Hojaji, Zahra, Habibzadeh, Parham, Afshinfar, Dorna, Miryounesi, Mohammad, Fardaei, Majid, Faghihi, Mohammad Ali

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Expression Analysis of Multiple Genes May Involve in Antimony Resistance among Leishmania major Clinical Isolates from Fars Province, Central Iran von Ghobakhloo, Nafiseh, Motazedian, Mohammad Hossein, Fardaei, Majid

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Inferior Spear-like Lens Opacity as a Sign of Keratoconus von Salouti, Ramin, Khosravi, Amir, Fardaei, Majid, Zamani, Mohammad, Nejabat, Mahmoud, Ghoreyshi, Maryam, Yazdanpanah, Mahboobeh, Salouti, Kia, Nowroozzadeh, M Hossein

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient von Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana

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A Novel Missense Mutation in CLCN1 Gene in a Family with Autosomal Recessive Congenital Myotonia von Miryounesi, Md PhD, Mohammad, Ghafouri-Fard, Md PhD, Soudeh, Fardaei, PhD, Majid

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Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutations von Sadeghipour, Forough, Basiratnia, Mitra, Derakhshan, Ali, Fardaei, Majid

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VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran von Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid

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Segmental Duplications as a Complement Strategy to Short Tandem Repeats in the Prenatal Diagnosis of Down Syndrome von Miri, Mohammad Reza, Saberzadeh, Jamileh, Behzad Behbahani, Abbas, Tabei, Mohammad Bagher, Alipour, Mohsen, Fardaei, Majid

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Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA von Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Kamgarpour, Fatemeh, Dehghanian, Fatemeh, Fardaei, Majid

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Does the c.-273T>C variant in the upstream region of the HBB gene cause a thalassemia phenotype? von Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Dehghanian, Fatemeh, Kamgarpour, Fatemeh, Fardaei, Majid

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A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome von Taghdiri, Maryam, Dastsooz, Hassan, Fardaei, Majid, Mohammadi, Sanaz, Farazi Fard, Mohammad Ali, Faghihi, Mohammad Ali

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The First Case of a Small Supernumerary Marker Chromosome 18 in a Klinefelter Fetus: A Case Report von Saberzadeh, Jamileh, Miri, Mohammad Reza, Dianatpour, Mehdi, Behzad Behbahani, Abbas, Tabei, Mohammad Bagher, Alipour, Mohsen, Faghihi, Mohammad Ali, Fardaei, Majid

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