Mohammad Reza Pourreza
机构: Isfahan University of Medical Sciences
每年引用次数
引用次数
引用: 121
H-指数: 6
I10-指数 : 3
出版物: 19
A Report of a Novel Mutation in Human Prostacyclin Receptor Gene in Patients Affected with Migraine.
Fariborz Khorvash , Majid Kheirollahi , Mohammad Kazemi , Gilda Amini
Iranian Journal of Psychiatry 12 ( 3) 219 -222
2
2017
Genetic Linkage Analysis of the DFNB21 Locus in Autosomal Recessive Hearing Loss in large families from Khuzestan Province.
Reza Ghasemikhah , Nader Saki , Morteza Hashemzadeh Chaleshtori , Samira Asgharzadeh
Arak Medical University Journal 20 ( 3) 31 -38
2017
A pathogenic variant in the transforming growth factor beta I (TGFBI) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review
Gholamhossein Yaghoobi , Aliasgar Mohammadi , Mohammad Reza Pourreza , Mohammad Amin Tabatabaiefar
Iranian Journal of Basic Medical Sciences 23 ( 8) 1020 -1027
2020
A Novel Stop-Gain Mutation in MSH2 Gene Among a Persian Family Fulfilling Classic Amsterdam Criteria for Lynch Syndrome
Morteza Hashemzadeh-Chaleshtori , Mohammad Hassan Emami , Mehrdad Zeinalian , Mohammad Reza Pourreza
2021
Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family
Mohammad Reza Pourreza , Maryam Sobhani , Azadeh Rahimi , Mehdi Aramideh
Acta Diabetologica 57 ( 1) 81 -87
3
2020
A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred
Javad Mohammadi-asl , Mohammad Reza Pourreza , Aliasgar Mohammadi , Ameneh Eskandari
Journal of Dermatological Science 88 ( 1) 134 -138
1
2017
Genetic study of the BRAF gene reveals new variants and high frequency of the V600E mutation among Iranian ameloblastoma patients.
Maryam Soltani , Mohammad Amin Tabatabaiefar , Zhaleh Mohsenifar , Mohammad Reza Pourreza
Journal of Oral Pathology & Medicine 47 ( 1) 86 -90
13
2018
GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants
Mahbobeh Koohiyan , Morteza Hashemzadeh-Chaleshtori , Mansoor Salehi , Hamidreza Abtahi
International Journal of Pediatric Otorhinolaryngology 107 121 -126
17
2018
Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.
Ladan Sadeghian , Mohammad Amin Tabatabaiefar , Najmeh Fattahi , Mohammad Reza Pourreza
International Journal of Pediatric Otorhinolaryngology 124 99 -105
2
2019
A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss.
Mohammad Amin Tabatabaiefar , Mohammad Reza Pourreza , Parisa Tahmasebi , Nader Saki
Otolaryngology-Head and Neck Surgery 158 ( 6) 1084 -1092
2
2018
Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation.
Azam Ahmadi Shadmehri , Najmeh Fattahi , Mohammad Reza Pourreza , Mahboobeh Koohiyan
Journal of Cellular Biochemistry 120 ( 3) 3367 -3372
1
2019
A novel pathogenic variant in the FZD6 gene causes
Javad Mohammadi-asl , Mohammad Reza Pourreza
The British journal of dermatology 173 886 -886
2015
Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation
Zahra Ataei , Zahra Nouri , Farial Tavakoli , Mohammad Reza Pourreza
PLoS One 18 ( 2) e0282304 -e0282304
5
2023
Somatic BRAF V600E Mutation in Familial Colorectal Cancer Type X: A New Study in Central Iran
Mehrdad Zeinalian , Mohammad Hassan Emami , Mohammad Reza Pourreza , Mohammad Amin Tabatabaiefar
Jentashapir Journal of Cellular and Molecular Biology 12 ( 2)
1
2021
A Homozygous Nonsense Variant in UVSSA Causes UV-sensitive Syndrome from Very Large Kindred: The First Report from Iran
Azam Ahmadi Shadmehri , Fahimeh Akbarian , Azadeh Rahimi , Mohammad Reza Pourreza
Advanced Biomedical Research 12 264 -264
2023
BRAF gene mutation in Iranian familial colorectal cancer patients at risk for Lynch syndrome.
Mehrdad Zeinalian , Mohammad Hassan Emami , Mohammad Reza Pourreza , Mohammad Amin Tabatabaiefar
Iranian Journal of Gastroenterology & Hepatology (GOVARESH) 22 ( 3)
2017
Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family
Aliasgar Mohammadi , Marziyeh Hoseinzadeh , Sina Narrei , Mohammad Reza Pourreza
Egyptian Journal of Medical Human Genetics 25 ( 1) 102 -102
2024
Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper.
MohammadAmin Tabatabaiefar , MohammadReza Pourreza , Hannane Mohammadi , Ladan Sadeghian
Advanced Biomedical Research 7 ( 1) 141
2
2018
Wave functions of anharmonic oscillators
Mohammad Pourreza , Davood Afshar
a a 2 ( 2) 1 -1