Identification of a Missense Mutation in GJA8 Gene in an Iranian Family with Autosomal Dominant Congenital Cataract

por Asghari, Mahla, Abedini, Soheila, Farshidianfar, Melika, Tajbakhsh, Amir, Derakhshan, Akbar, Pasdar, Alireza
Publicado 2023

Green tea improves rat sperm quality and reduced cadmium chloride damage effect in spermatogenesis cycle

por Mahmoudi, Reza, Azizi, Arsalan, Abedini, Soheila, Hemayatkhah Jahromi, Vahid, Abidi, Hassan, Jafari Barmak, Mehrzad
Publicado 2018

Association of rs4784227-CASC16 (LOC643714 locus) and rs4782447-ACSF3 polymorphisms and their association with breast cancer risk among Iranian population

por Tajbakhsh, Amir, Farjami, Zahra, Darroudi, Susan, Ayati, Seyed Hasan, Vakili, Fatemeh, Asghari, Mahla, Alimardani, Maliheh, Abedini, Soheila, Kushyar, Mohammad Mahdi, Pasdar, Alireza
Publicado 2019

Association of PICK1 and BDNF variations with increased risk of methamphetamine dependence among Iranian population: a case–control study

por Tajbakhsh, Amir, Alimardani, Maliheh, Asghari, Mahla, Abedini, Soheila, Saghafi Khadem, Sohrab, Nesaei Bajestani, Abolfazl, Alipoor, Forough, Alidoust, Maryam, Savardashtaki, Amir, Hashemian, Peyman, Pasdar, Alireza
Publicado 2021

Evaluating the Association between CCR5delta32 Polymorphism (rs333) and the Risk of Breast Cancer in a Cohort of Iranian Population

por TAJBAKHSH, Amir, FARJAMI, Zahra, NESAEI-BAJESTANI, Abolfazl, AFZALJAVAN, Fahimeh, RIVANDI, Mahdi, MOEZZI, Atefeh, ABEDINI, Soheila, ASGHARI, Mahla, KOOSHYAR, Mohammad Mahdi, HOMAEI SHANDIZ, Fatemeh, PASDAR, Alireza
Publicado 2021

Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome

por Rad, Aboulfazl, Najafi, Maryam, Suri, Fatemeh, Abedini, Soheila, Loum, Stephen, Karimiani, Ehsan Ghayoor, Daftarian, Narsis, Murphy, David, Doosti, Mohammad, Moghaddasi, Afrooz, Ahmadieh, Hamid, Sabbaghi, Hamideh, Rajati, Mohsen, Hashemi, Narges, Vona, Barbara, Schmidts, Miriam
Publicado 2022

The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders

por Saffari, Afshin, Lau, Tracy, Tajsharghi, Homa, Karimiani, Ehsan Ghayoor, Kariminejad, Ariana, Efthymiou, Stephanie, Zifarelli, Giovanni, Sultan, Tipu, Toosi, Mehran Beiraghi, Sedighzadeh, Sahar, Siu, Victoria Mok, Ortigoza-Escobar, Juan Darío, AlShamsi, Aisha M, Ibrahim, Shahnaz, Al-Sannaa, Nouriya Abbas, Al-Hertani, Walla, Sandra, Whalen, Tarnopolsky, Mark, Alavi, Shahryar, Li, Chumei, Day-Salvatore, Debra-Lynn, Martínez-González, Maria Jesús, Levandoski, Kristin M, Bedoukian, Emma, Madan-Khetarpal, Suneeta, Idleburg, Michaela J, Menezes, Minal Juliet, Siddharth, Aishwarya, Platzer, Konrad, Oppermann, Henry, Smitka, Martin, Collins, Felicity, Lek, Monkol, Shahrooei, Mohmmad, Ghavideldarestani, Maryam, Herman, Isabella, Rendu, John, Faure, Julien, Baker, Janice, Bhambhani, Vikas, Calderwood, Laurel, Akhondian, Javad, Imannezhad, Shima, Mirzadeh, Hanieh Sadat, Hashemi, Narges, Doosti, Mohammad, Safi, Mojtaba, Ahangari, Najmeh, Torbati, Paria Najarzadeh, Abedini, Soheila, Salpietro, Vincenzo, Gulec, Elif Yilmaz, Eshaghian, Safieh, Ghazavi, Mohammadreza, Pascher, Michael T, Vogel, Marina, Abicht, Angela, Moutton, Sébastien, Bruel, Ange-Line, Rieubland, Claudine, Gallati, Sabina, Strom, Tim M, Lochmüller, Hanns, Mohammadi, Mohammad Hasan, Alvi, Javeria Raza, Zackai, Elaine H, Keena, Beth A, Skraban, Cara M, Berger, Seth I, Andrew, Erin H, Rahimian, Elham, Morrow, Michelle M, Wentzensen, Ingrid M, Millan, Francisca, Henderson, Lindsay B, Dafsari, Hormos Salimi, Jungbluth, Heinz, Gomez-Ospina, Natalia, McRae, Anne, Peter, Merlene, Veltra, Danai, Marinakis, Nikolaos M, Sofocleous, Christalena, Ashrafzadeh, Farah, Pehlivan, Davut, Lemke, Johannes R, Melki, Judith, Benezit, Audrey, Bauer, Peter, Weis, Denisa, Lupski, James R, Senderek, Jan, Christodoulou, John, Chung, Wendy K, Goodchild, Rose, Offiah, Amaka C, Moreno-De-Luca, Andres, Suri, Mohnish, Ebrahimi-Fakhari, Darius, Houlden, Henry, Maroofian, Reza
Publicado 2023