Works by Tabatabaiefar, Mohammad Amin

Results: 83

A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.

Published in:

2020

By:

Koohiyan, Mahbobeh;
Hashemzadeh-Chaleshtori, Morteza;
Salehi, Mansoor;
Abtahi, Hamidreza;
Noori-Daloii, Mohammad Reza;
Tabatabaiefar, Mohammad Amin;
Noori-Daloii, Mohammad Reza;
Tabatabaiefar, Mohammad Amin

Publication type:

journal article

A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family.

Published in:

2019

By:

Koohiyan, Mahbobeh;
Noori-Daloii, Mohammad Reza;
Hashemzadeh-Chaleshtori, Morteza;
Salehi, Mansoor;
Abtahi, Hamidreza;
Tabatabaiefar, Mohammad Amin;
Noori-Daloii, Mohammad Reza;
Tabatabaiefar, Mohammad Amin

Publication type:

journal article

Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.

Published in:

2019

By:

Zarepour, Narges;
Koohiyan, Mahbobeh;
Taghipour-Sheshdeh, Afsaneh;
Nemati-Zargaran, Fatemeh;
Saki, Nader;
Mohammadi-Asl, Javad;
Tabatabaiefar, Mohammad Amin;
Hashemzadeh-Chaleshtori, Morteza;
Tabatabaiefar, Mohammad Amin

Publication type:

journal article

Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation.

Published in:

PLoS ONE, 2023, v. 18, n. 2, p. 1, doi. 10.1371/journal.pone.0282304

By:

Ataei, Zahra;
Nouri, Zahra;
Tavakoli, Farial;
Pourreza, Mohammad Reza;
Narrei, Sina;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Genetic linkage analysis of DFNB22 in families with autosomal recessive non-syndromic hearing loss in Khuzestan province.

Published in:

Journal of Shahrekord University of Medical Sciences, 2019, v. 21, n. 5, p. 200, doi. 10.34172/jsums.2019.35

By:

Sadeghian, Ladan;
Tabatabaiefar, Mohammad Amin;
Chaleshtori, Morteza Hashemzadeh

Publication type:

Article

WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family.

Published in:

Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.648649

By:

Norouzi, Mahnaz;
Shafiei, Mohammad;
Abdollahi, Zeinab;
Miar, Paniz;
Galehdari, Hamid;
Emami, Mohammad Hasan;
Zeinalian, Mehrdad;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and In Silico Analysis.

Published in:

Clinical Genetics, 2025, v. 107, n. 3, p. 366, doi. 10.1111/cge.14658

By:

Biglari, Sajjad;
Nikuei, Pooneh;
Mir, Atefeh;
Vahidnezhad, Hassan;
Youssefian, Leila;
Moghaddam, Atefeh Sohanforooshan;
Tabatabaiefar, Mohammad Amin;
Saeidian, Amir Hossein;
Khorram, Erfan;
Fard, Mohammad Ali Farazi;
Farbood, Zahra;
Shahrooei, Mohammad;
Khorshid, Hamid Reza Khorram;
Esmaeilzadeh, Emran

Publication type:

Article

A novel heterozygous truncating variant in the AGO1 gene in an Iranian family with schizophrenia as an unreported symptom.

Published in:

Annals of Human Genetics, 2023, v. 87, n. 6, p. 295, doi. 10.1111/ahg.12524

By:

Mir, Atefeh;
Khorram, Erfan;
Song, Yongjun;
Lee, Hane;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

DOCK2 Deficiency and GATA2 Haploinsufficiency Can Underlie Critical Coronavirus Disease 2019 (COVID-19) Pneumonia.

Published in:

Journal of Clinical Immunology, 2025, v. 45, n. 1, p. 1, doi. 10.1007/s10875-025-01877-z

By:

Biglari, Sajjad;
Youssefian, Leila;
Tabatabaiefar, Mohammad Amin;
Saeidian, Amir Hossein;
Abtahi‐Naeini, Bahareh;
Khorram, Erfan;
Sherkat, Roya;
Moghaddam, Atefeh Sohanforooshan;
Mohaghegh, Fatemeh;
Rahimi, Maziyar;
Rahimi, Hamid;
Babaei, Sharareh;
Shahrooei, Mohammad;
Mozafari, Nikoo;
Zaresharifi, Shirin;
Vahidnezhad, Fatemeh;
Homayouni, Vida;
Tsoi, Lam C.;
Gudjonsson, Johann E.;
Hakonarson, Hakon

Publication type:

Article

A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review.

Published in:

Archives of Dermatological Research, 2025, v. 317, n. 1, p. 1, doi. 10.1007/s00403-025-04206-x

By:

Norouzi-Barough, Leyla;
Olyaei, Nasrin Alipour;
Carapito, Raphael;
Molitor, Anne;
Biglari, Sajjad;
Poostiyan, Nazila;
Shahrooei, Mohammad;
Vahidnezhad, Hassan;
Tabatabaiefar, Mohammad Amin;
Bahram, Seiamak;
Sherkat, Roya

Publication type:

Article

New Insight into Pathogenic Variant p.L275P on the Structure and Function of Steroidogenic Acute Regulatory Protein (STAR) Through Molecular Dynamics Simulation.

Published in:

Advanced Biomedical Research, 2025, v. 14, n. 5, p. 1, doi. 10.4103/abr.abr_439_23

By:

Aghaei, Shahrzad;
Tabatabaiefar, Mohammad Amin;
Saffari-Chaleshtori, Javad;
Korram, Erfan;
Amini, Sara Sadeghi;
Aghaei, Maryam;
Koohiyan, Mahbobeh;
Ataie, Zahra;
Samei, Payam;
Farrokhi, Effat

Publication type:

Article

A Homozygous Nonsense Variant in UVSSA Causes UV-sensitive Syndrome from Very Large Kindred: The First Report from Iran.

Published in:

Advanced Biomedical Research, 2023, v. 12, p. 1, doi. 10.4103/abr.abr_45_22

By:

Shadmehri, Azam Ahmadi;
Akbarian, Fahimeh;
Rahimi, Azadeh;
Pourreza, Mohammad Reza;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

BAT25, ACVR2, and TGFBR2 Mononucleotide STR Markers: A Triplex Panel for Microsatellite Instability Testing in Colorectal Tumors.

Published in:

Advanced Biomedical Research, 2022, v. 11, n. 9, p. 1, doi. 10.4103/abr.abr_205_21

By:

Miar, Paniz;
Tabatabaiefar, Mohammad Amin;
Abdollahi, Zeinab;
Noruzi, Mahnaz;
Kazemi, Mohammad;
Naimi, Azar;
Emami, Mohammad Hasan;
Izadi, Shahrokh;
Zeinalian, Mehrdad

Publication type:

Article

Bisulfite Treatment of CG-Rich Track of Trinucleotide Repeat Expansion Disorder: Make the Sequence Less CG Rich.

Published in:

Advanced Biomedical Research, 2021, p. 1, doi. 10.4103/abr.abr_144_19

By:

Abbasalian, Zahra Joz;
Khanahmad, Hossein;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

The Importance of SNPs at miRNA Binding Sites as Biomarkers of Gastric and Colorectal Cancers: A Systematic Review.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 3, p. 456, doi. 10.3390/jpm12030456

By:

Hajibabaie, Fatemeh;
Abedpoor, Navid;
Assareh, Nazanin;
Tabatabaiefar, Mohammad Amin;
Shariati, Laleh;
Zarrabi, Ali

Publication type:

Article

FREQUENCY OF GJB2 MUTATIONS IN FAMILIES WITH AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS IN KHUZESTAN PROVINCE.

Published in:

Genetika (0534-0012), 2018, v. 50, n. 3, p. 837, doi. 10.2298/GENSR1803837T

By:

TAHMASEBI, Parisa;
CHALESHTORI, Morteza Hashemzadeh;
ABDOLLAHNEJAD, Fatemeh;
ALAVI, Zahra;
SADEGHIAN, Ladan;
TALEBI, Farah;
MOHAMMADI-ASL, Javad;
SAKI, Nader;
NEZHAD, Seyed Reza Kazemi;
TABATABAIEFAR, Mohammad Amin

Publication type:

Article

THE LACK OF CORRELATION BETWEEN TP53 MUTATIONS AND GASTRIC CANCER: A REPORT FROM A PROVINCE OF IRAN.

Published in:

Genetika (0534-0012), 2017, v. 49, n. 1, p. 235, doi. 10.2298/GENSR1701235S

By:

SAFFARI-CHALESHTORI, Javad;
TABATABAIEFAR, Mohammad-Amin;
GHASEMI-DEHKORDI, Payam;
FAROKHI, Effat;
MORADI, Mohammad-Taghi;
HASHEMZADEH-CHALESHTORI, Morteza

Publication type:

Article

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent.

Published in:

Cell Journal (Yakhteh), 2014, v. 16, n. 2, p. 225

By:

Mortezaee, Fatemeh Taghizade;
Tabatabaiefar, Mohammad Amin;
Chaleshtori, Morteza Hashemzadeh;
Miraj, Sepideh

Publication type:

Article

Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.

Published in:

BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01680-y

By:

Mir, Atefeh;
Song, Yongjun;
Lee, Hane;
Khanahmad, Hossein;
Khorram, Erfan;
Nasiri, Jafar;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss.

Published in:

2018

By:

Tabatabaiefar, Mohammad Amin;
Pourreza, Mohammad Reza;
Tahmasebi, Parisa;
Saki, Nader;
Hashemzadeh Chaleshtori, Morteza;
Salehi, Rasoul;
Mohammadi-asl, Javad

Publication type:

journal article

A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review.

Published in:

Journal of Genetics, 2023, v. 102, n. 2, p. 1, doi. 10.1007/s12041-023-01441-x

By:

Shakarami, Fatemeh;
Nouri, Zahra;
Khanahmad, Hossein;
Ghazavi, Mohamadreza;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.

Published in:

Endocrine (1355008X), 2019, v. 66, n. 2, p. 185, doi. 10.1007/s12020-019-02004-w

By:

Sobhani, Maryam;
Amin Tabatabaiefar, Mohammad;
Ghafouri-Fard, Soudeh;
Rajab, Asadollah;
Mozafarpour, Sarah;
Nasrniya, Samaneh;
Kajbafzadeh, Abdol-Mohammad;
Noori-Daloii, Mohammad Reza

Publication type:

Article

Study of VSX1 Mutations in Patients with Keratoconus in Southwest Iran Using PCR-Single-Strand Conformation Polymorphism/Heteroduplex Analysis and Sequencing Method.

Published in:

Acta Cytologica, 2013, v. 57, n. 6, p. 646, doi. 10.1159/000353297

By:

Dehkordi, Fatemeh azadegan;
Rashki, ahmad;
Bagheri, Nader;
Chaleshtori, Minoo Hashemzadeh;
Memarzadeh, Ezzatollah;
Salehi, ali;
Ghatreh, Homan;
Zandi, Farid;
Yazdanpanahi, Nasrin;
Tabatabaiefar, Mohammad amin;
Chaleshtori, Morteza Hashemzadeh

Publication type:

Article

Comparison of Real-Time PCR with Disk Diffusion, Agar Screen and E-test Methods for Detection of Methicillin-Resistant Staphylococcus aureus.

Published in:

Current Microbiology, 2010, v. 61, n. 6, p. 520, doi. 10.1007/s00284-010-9647-9

By:

Shariati, Laleh;
Validi, Majid;
Tabatabaiefar, Mohammad Amin;
Karimi, Ali;
Nafisi, Mohammad Reza

Publication type:

Article

Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family.

Published in:

Acta Diabetologica, 2020, v. 57, n. 1, p. 81, doi. 10.1007/s00592-019-01381-y

By:

Pourreza, Mohammad Reza;
Sobhani, Maryam;
Rahimi, Azadeh;
Aramideh, Mehdi;
Kajbafzadeh, Abdol-Mohammad;
Noori-Daloii, Mohammad Reza;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

The Role of Epigenetics in the Induction of Fetal Hemoglobin: A Combination Therapy Approach.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2014, v. 8, n. 1, p. 9

By:

Ahmadvand, Mohammad;
Noruzinia, Mehrdad;
Fard, Ali Dehghani;
Zohour, Mostafa Montazer;
Tabatabaiefar, Mohammad Amin;
Soleimani, Masoud;
Kaviani, Saeid;
Abroun, Saeid;
Beiranvand, Sahar;
Saki, Najmaldin

Publication type:

Article

The silencing effect of miR-30a on ITGA4 gene expression in vitro: an approach for gene therapy.

Published in:

Research in Pharmaceutical Sciences, 2017, v. 12, n. 6, p. 456, doi. 10.4103/1735-5362.217426

By:

Darzi, Leila;
Boshtam, Maryam;
Shariati, Laleh;
Kouhpayeh, Shirin;
Gheibi, Azam;
Mirian, Mina;
Rahimmanesh, Ilnaz;
Khanahmad, Hossein;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Selection of Optimal Bioinformatic Tools and Proper Reference for Reducing the Alignment Error in Targeted Sequencing Data.

Published in:

Journal of Medical Signals & Sensors, 2021, v. 11, n. 1, p. 37, doi. 10.4103/jmss.JMSS_7_20

By:

Nodehi, Hannane Mohammadi;
Tabatabaiefar, Mohammad Amin;
Sehhati, Mohammadreza

Publication type:

Article

Correction: Decellularized skin pretreatment by monophosphoryl lipid A and lactobacillus casei supernatant accelerate skin recellularization.

Published in:

2025

By:

Jalili, Ali;
Shojaei-Ghahrizjani, Fereshteh;
Tabatabaiefar, Mohammad Amin;
Rahmati, Shima

Publication type:

Correction Notice

Engineered zinc‐finger nuclease to generate site‐directed modification in the KLF1 gene for fetal hemoglobin induction.

Published in:

Journal of Cellular Biochemistry, 2019, v. 120, n. 5, p. 8438, doi. 10.1002/jcb.28130

By:

Shariati, Laleh;
Modarressi, Mohammad Hossein;
Tabatabaiefar, Mohammad Amin;
Kouhpayeh, Shirin;
Hejazi, Zahra;
Shahbazi, Mansoureh;
Sabzehei, Faezeh;
Salehi, Mansoor;
Khanahmad, Hossein

Publication type:

Article

Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation.

Published in:

Journal of Cellular Biochemistry, 2019, v. 120, n. 3, p. 3367, doi. 10.1002/jcb.27607

By:

Shadmehri, Azam Ahmadi;
Fattahi, Najmeh;
Pourreza, Mohammad Reza;
Koohiyan, Mahboobeh;
Zarifi, Shahnaz;
Darbouy, Mojtaba;
Sharifi, Reza;
Tavakkoly Bazzaz, Javad;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Inducing indel mutation in the <italic>SOX6</italic> gene by zinc finger nuclease for gamma reactivation: An approach towards gene therapy of beta thalassemia.

Published in:

Journal of Cellular Biochemistry, 2018, v. 119, n. 3, p. 2512, doi. 10.1002/jcb.26412

By:

Modares Sadeghi, Mehran;
Shariati, Laleh;
Hejazi, Zahra;
Shahbazi, Mansoureh;
Tabatabaiefar, Mohammad Amin;
Khanahmad, Hossein

Publication type:

Article

Genetic disruption of the KLF1 gene to overexpress the γ-globin gene using the CRISPR/ Cas9 system.

Published in:

Journal of Gene Medicine, 2016, v. 18, n. 10, p. 294, doi. 10.1002/jgm.2928

By:

Shariati, Laleh;
Khanahmad, Hossein;
Salehi, Mansoor;
Hejazi, Zahra;
Rahimmanesh, Ilnaz;
Tabatabaiefar, Mohammad Amin;
Modarressi, Mohammad Hossein

Publication type:

Article

New molecular insights into the A218V variant impact on the steroidogenic acute regulatory protein (STAR) associated with 46, XY disorders of sexual development.

Published in:

Molecular Genetics & Genomics, 2023, v. 298, n. 3, p. 693, doi. 10.1007/s00438-023-02006-4

By:

Aghaei, Shahrzad;
Farrokhi, Effat;
saffari-chaleshtori, Javad;
Hoseinzadeh, Marziyeh;
Molavi, Newsha;
Hashemipour, Mahin;
Rostampour, Noushin;
Asgharzadeh, Samira;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Griscelli syndrome type 1: a novel pathogenic variant, and review of literature.

Published in:

Molecular Genetics & Genomics, 2023, v. 298, n. 2, p. 485, doi. 10.1007/s00438-022-01971-6

By:

Khorram, Erfan;
Tabatabaiefar, Mohammad Amin;
Yaghini, Omid;
Khorrami, Mehdi;
Yazdani, Vida;
Fakhr, Fatemeh;
Amini, Masoomeh;
Kheirollahi, Majid

Publication type:

Article

Characterization of Oxacillinase and Metallo-β-Lactamas Genes and Molecular Typing of Clinical Isolates of Acinetobacter baumannii in Ahvaz, South-West of Iran.

Published in:

Jundishapur Journal of Microbiology, 2016, v. 9, n. 5, p. 1, doi. 10.5812/jjm.32388

By:

Shoja, Saeed;
Moosavian, Mojtaba;
Rostami, Soodabeh;
Abbasi, Fariba;
Tabatabaiefar, Mohammad Amin;
Peymani, Amir

Publication type:

Article

Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis.

Published in:

Jundishapur Journal of Microbiology, 2015, v. 8, n. 8, p. 1, doi. 10.5812/jjm.21701

By:

Azadegan-Dehkordi, Fatemeh;
Bagheri, Nader;
Shirzad, Mahsa;
Sanei, Mohammad Hossein;
Hashemzadeh-Chaleshtori, Morteza;
Rafieian-Kopaei, Mahmoud;
Tabatabaiefar, Mohammad Amin;
Shirzad, Hedayatollah

Publication type:

Article

Detection of Metallo-Beta Lactamases Among Carbapenem-Resistant Pseudomonas aeruginosa.

Published in:

Jundishapur Journal of Microbiology, 2014, v. 7, n. 11, p. 1, doi. 10.5812/jjm.12289

By:

Sheikh, Ahmad Farajzadeh;
Rostami, Soodabeh;
Jolodar, Abbas;
Tabatabaiefar, Mohammad Amin;
Khorvash, Farzin;
Saki, Azadeh;
Shoja, Saeed;
Sheikhi, Raheleh

Publication type:

Article

Post Neurosurgical Meningitis due to Colistin Heteroresistant Acinetobacter baumannii.

Published in:

Jundishapur Journal of Microbiology, 2014, v. 7, n. 10, p. 1, doi. 10.5812/jjm.12287

By:

Moosavian, Mojtaba;
Shoja, Saeed;
Nashibi, Roohangiz;
Ebrahimi, Nasim;
Tabatabaiefar, Mohammad Amin;
Rostami, Soodabeh;
Peymani, Amir

Publication type:

Article

A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family.

Published in:

International Journal of Audiology, 2019, v. 58, n. 10, p. 628, doi. 10.1080/14992027.2019.1619945

By:

Pourahmadiyan, Azam;
Alipour, Paria;
Fattahi, Najmeh;
Kasiri, Mahbubeh;
Rezaeian, Fateme;
Taghipour-Sheshdeh, Afsaneh;
Mohammadi-Asl, Javad;
Tabatabaiefar, Mohammad Amin;
Hashemzadeh Chaleshtori, Morteza

Publication type:

Article

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness.

Published in:

International Journal of Audiology, 2015, v. 54, n. 2, p. 124, doi. 10.3109/14992027.2014.944276

By:

Yazdanpanahi, Nasrin;
Tabatabaiefar, Mohammad Amin;
Bagheri, Nader;
Azadegan Dehkordi, Fatemeh;
Farrokhi, Effat;
Hashemzadeh Chaleshtori, Morteza

Publication type:

Article

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.

Published in:

Iranian Journal of Basic Medical Sciences, 2020, v. 23, n. 8, p. 1020, doi. 10.22038/ijbms.2020.36763.8757

By:

Mohammadi, Aliasgar;
Shadmehri, Azam Ahmadi;
Taghavi, Mahnaz;
Yaghoobi, Gholamhossein;
Pourreza, Mohammad Reza;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.

Published in:

Iranian Journal of Basic Medical Sciences, 2016, v. 19, n. 7, p. 772

By:

Reiisi, Somayeh;
Tabatabaiefar, Mohammad Amin;
Sanati, Mohammad Hosein;
Chaleshtori, Morteza Hashemzadeh

Publication type:

Article

A novel missense pathogenic variant c.9455T > G (p.L3152R) in CDH23 underlies autosomal recessive non-syndromic hearing loss.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00730-7

By:

Sadeghian, Ladan;
Hoseinzadeh, Marziyeh;
Pourreza, Mohammad reza;
Khalili, Saeed;
Fattahi, Najmeh;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00719-2

By:

Sarmadi, Akram;
Adelian, Samaneh;
Nouri, Zahra;
Javanmard, Shaghayegh Haghjooy;
Omidzadeh, Rasoul;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Evaluation of pathogenic variant in WFS1 in a patient with Wolfram syndrome.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00657-z

By:

Hoseinzadeh, Marziyeh;
Jahani, Mohammad Mehdi;
Nasrniya, Samane;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family.

Published in:

Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00578-3

By:

Mohammadi, Aliasgar;
Hoseinzadeh, Marziyeh;
Narrei, Sina;
Pourreza, Mohammad Reza;
Mohammadi, Yousof;
Norouzi, Mahnaz;
Sadeghian, Ladan;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Sero-molecular prevalence of toxoplasmosis in hemodialysis and peritoneal dialysis patients in Markazi Province, Iran.

Published in:

Tropical Medicine & Health, 2025, v. 53, n. 1, p. 1, doi. 10.1186/s41182-024-00676-3

By:

Sarmadian, Hossein;
Shojapour, Mana;
chegeni, Fereshteh;
Tabatabaiefar, Mohammad Amin;
Haghverdi, Farshid;
Sarmadian, Roham;
Ghasemikhah, Reza

Publication type:

Article

Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells.

Published in:

Iranian Biomedical Journal, 2015, v. 19, n. 3, p. 160

By:

Farrokhi, Effat;
Samani, Keihan Ghatreh;
Chaleshtori, Morteza Hashemzadeh;
Tabatabaiefar, Mohammad Amin

Publication type:

Article

Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.

Published in:

2025

By:

Mir, Atefeh;
Song, Yongjun;
Lee, Hane;
Khanahmad, Hossein;
Khorram, Erfan;
Nasiri, Jafar;
Tabatabaiefar, Mohammad Amin

Publication type:

Correction Notice