S. Saber

Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?

M. Houshmand, M. Sadeghizadeh, K. Banihashemi, 2010, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels

S. Saber, E. Zaklyazminskaya, A. Shestak, 2021, Frontiers in Genetics.

Complex genetic background in a large family with Brugada syndrome

A. V. Gavrilenko, M. Houshmand, S. Saber, 2015, Physiological reports.

Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics.

J. Svendsen, M. Houshmand, M. Olesen, 2012, The Canadian journal of cardiology.

Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene.

T. Mahmoudi, M. Houshmand, S. Saber, 2006, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Positive Brugada Challenge Test in V1R–V3R as a Predictor of Malignant Prognosis in Brugada Patients

S. Saber, Z. Emkanjoo, A. Aslani, 2013, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

Molecular Analysis of KCNQ1, KCNH2 and SCN5A Genes in Iranian Patients with Long QT Syndrome

S. Zeinali, S. Saber, A. Fazelifar, 2018 .

Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

S. Zeinali, S. Saber, A. Fazelifar, 2019, Iranian biomedical journal.

Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families.

S. Saber, M. Akbari, Zahra Zafari, 2017, Journal of electrocardiology.

Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange‐Nielsen syndrome in 2 Iranian families

S. Zeinali, S. Saber, A. Fazelifar, 2018, Journal of arrhythmia.

A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic Hearing Loss

S. Saber, Seyedeh Parisa Chavoshi Tarzjani, A. Ebrahimi, 2020, International medical case reports journal.

[Clinical polymorphisms and approaches of arrhythmias treatment in a family with δKPQ1505-1507 deletion in SCN5A gene].

A. V. Gavrilenko, M. Houshmand, S. Saber, 2014, Vestnik Rossiiskoi akademii meditsinskikh nauk.

Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas

M. Houshmand, S. Saber, Maryam Balali, 2016, Therapeutics and clinical risk management.