The new genomic editing system (CRISPR)

by Mehrdad Talebi, Mohammad Yahya Vahidi Mehrjardi
Published 2019-10-01

A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)

by Masoud Dehghan Tezerjani, Mohammad Yahya Vahidi Mehrjardi, Mohammad Yahya Vahidi Mehrjardi, Hossein Hozhabri, Masoud Rahmanian
Published 2020-06-01

Is there any relationship between mutation in CPS1 Gene and pregnancy loss?

by Mehrdad Talebi, Mohammad Yahya Vahidi Mehrjardi, Kambiz Kalhor, Mohammadreza Dehghani
Published 2019-05-01

Genetic Susceptibility to Transient and Permanent Neonatal Diabetes Mellitus

by Masoud Dehghan Tezerjani, Mohammad Yahya Vahidi Mehrjardi, Seyed Mehdi Kalantar, Mohammadreza Dehghani
Published 2015-11-01

A novel mutation in CYP17A1 gene leads to congenital adrenal hyperplasia: A case report

by Majid Nazari, Mohammad Yahya Vahidi Mehrjardi, Nosrat Neghab, Mahdi Aghabagheri, Nasrin Ghasemi
Published 2019-06-01

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
Published 2016-03-01

Testicular expression of TDRD1, TDRD5, TDRD9 and TDRD12 in azoospermia

by Emad Babakhanzadeh, Ali Khodadadian, Saadi Rostami, Iraj Alipourfard, Mohsen Aghaei, Majid Nazari, Mehdi Hosseinnia, Mohammad Yahya Vahidi Mehrjardi, Yalda Jamshidi, Nasrin Ghasemi
Published 2020-02-01

Circulating microRNA-122, microRNA-126-3p and microRNA-146a are associated with inflammation in patients with pre-diabetes and type 2 diabetes mellitus: A case control study.

by Fahime Zeinali, Seyed Mohsen Aghaei Zarch, Alireza Jahan-Mihan, Seyed Mehdi Kalantar, Mohammad Yahya Vahidi Mehrjardi, Hossein Fallahzadeh, Mahdieh Hosseinzadeh, Masoud Rahmanian, Hassan Mozaffari-Khosravi
Published 2021-01-01

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
Published 2016-10-01

Effects of synbiotic supplementation on gut microbiome, serum level of TNF-α, and expression of microRNA-126 and microRNA-146a in patients with type 2 diabetes mellitus: study prot...

by Fahime Zeinali, Seyed Mohsen Aghaei Zarch, Mohammad Yahya Vahidi Mehrjardi, Seyed Mehdi Kalantar, Alireza Jahan-mihan, Elham Karimi-Nazari, Hossein Fallahzadeh, Mahdieh Hosseinzadeh-Shamsi-Anar, Masoud Rahmanian, Mohammad Reza Fazeli, Hassan Mozaffari-Khosravi
Published 2020-04-01

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycan...

by Reza Maroofian, Moniek Riemersma, Lucas T. Jae, Narges Zhianabed, Marjolein H. Willemsen, Willemijn M. Wissink-Lindhout, Michèl A. Willemsen, Arjan P. M. de Brouwer, Mohammad Yahya Vahidi Mehrjardi, Mahmoud Reza Ashrafi, Benno Kusters, Tjitske Kleefstra, Yalda Jamshidi, Mojila Nasseri, Rolph Pfundt, Thijn R. Brummelkamp, Mohammad Reza Abbaszadegan, Dirk J. Lefeber, Hans van Bokhoven
Published 2017-12-01

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

by Hugh J. McMillan, Aida Telegrafi, Amanda Singleton, Megan T. Cho, Daniel Lelli, Francis C. Lynn, Julie Griffin, Alexander Asamoah, Tuula Rinne, Corrie E. Erasmus, David A. Koolen, Charlotte A. Haaxma, Boris Keren, Diane Doummar, Cyril Mignot, Islay Thompson, Lea Velsher, Mohammadreza Dehghani, Mohammad Yahya Vahidi Mehrjardi, Reza Maroofian, Michel Tchan, Cas Simons, John Christodoulou, Elena Martín-Hernández, Maria J. Guillen Sacoto, Lindsay B. Henderson, Heather McLaughlin, Laurie L. Molday, Robert S. Molday, Grace Yoon
Published 2018-05-01