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Sirenomelia: two case reports

Journal of medical case reports, 2021-04, Vol.15 (1), p.217-4, Article 217

2021

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A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract

Journal of human genetics, 2016-02, Vol.61 (2), p.177-179

2016

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

Audiology & neurotology, 2019, Vol.24 (5), p.258-263

2019

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A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel

Familial cancer, 2022-04, Vol.21 (2), p.137-142

2022

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A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features

Journal of human genetics, 2018-04, Vol.63 (4), p.487-491

2018

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Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran

International journal of pediatric otorhinolaryngology, 2015-11, Vol.79 (11), p.1892-1895

2015

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Livin, a novel marker in lymphoma type distinction

Annals of diagnostic pathology, 2014-06, Vol.18 (3), p.157-162

2014

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Production, purification, and in vivo evaluation of a novel multiepitope peptide vaccine consisted of immunodominant epitopes of SYCP1 and ACRBP antigens as a prophylactic melanoma vaccine

International immunopharmacology, 2019-11, Vol.76, p.105872-105872, Article 105872

2019

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Incidence rate of mycosis fungoides in Isfahan (Iran)

Journal of dermatology, 2010-08, Vol.37 (8), p.703-707

2010

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Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy

Epilepsy research, 2021-11, Vol.177, p.106782-106782, Article 106782

2021

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miR-326 and miR-26a, two potential markers for diagnosis of relapse and remission phases in patient with relapsing–remitting multiple sclerosis

Gene, 2014-07, Vol.544 (2), p.128-133

2014

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A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain

Life sciences (1973), 2021-03, Vol.269, p.118759, Article 118759

2021

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Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients

Gene, 2014-10, Vol.549 (1), p.1-6

2014

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Effect of single nucleotide polymorphisms in SEPS1 and SEPP1 on expression in the protein level in metabolic syndrome in subjects with cardiovascular disease

Molecular biology reports, 2019-12, Vol.46 (6), p.5685-5693

2019

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Evaluation of the utility of peripheral blood vs bone marrow in karyotype and fluorescence in situ hybridization for myelodysplastic syndrome diagnosis

Journal of clinical laboratory analysis, 2018-11, Vol.32 (9), p.e22586-n/a

2018

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A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

Journal of human genetics, 2018-04, Vol.63 (4), p.425-430

2018

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Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation

Gene, 2015-10, Vol.570 (1), p.150-152

2015

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Association of AHSG with alopecia and mental retardation (APMR) syndrome

Human genetics, 2017-03, Vol.136 (3), p.287-296

2017

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The Effect of Plasma Exchange on the Expression of FOXP3 and RORC2 in Relapsed Multiple Sclerosis Patients

Iranian journal of immunology, 2015-12, Vol.12 (4), p.311-318

2015

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A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family

International journal of pediatric otorhinolaryngology, 2015-04, Vol.79 (4), p.553-556

2015

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Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1

Journal of child neurology, 2015-04, Vol.30 (5), p.558-562

2015

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α-Globin Gene Mutations in Isfahan Province, Iran

Hemoglobin, 2014-06, Vol.38 (3), p.161-164

2014

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Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents

Cytogenetic and genome research, 2016-01, Vol.148 (1), p.1-5

2016

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Introducing a frameshift mutation to the POL sequence of HIV-1 provirus and evaluation of the immunogenic characteristics of the mutated virions (RINNL4-3)

Molekuliarnaia biologiia, 2012-05, Vol.46 (3), p.519

2012

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Sirenomelia: two case reports

A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract

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

A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel

A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features

Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran

Livin, a novel marker in lymphoma type distinction

Production, purification, and in vivo evaluation of a novel multiepitope peptide vaccine consisted of immunodominant epitopes of SYCP1 and ACRBP antigens as a prophylactic melanoma vaccine

Incidence rate of mycosis fungoides in Isfahan (Iran)

Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy

miR-326 and miR-26a, two potential markers for diagnosis of relapse and remission phases in patient with relapsing–remitting multiple sclerosis

A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain

Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients

Effect of single nucleotide polymorphisms in SEPS1 and SEPP1 on expression in the protein level in metabolic syndrome in subjects with cardiovascular disease

Evaluation of the utility of peripheral blood vs bone marrow in karyotype and fluorescence in situ hybridization for myelodysplastic syndrome diagnosis

A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation

Association of AHSG with alopecia and mental retardation (APMR) syndrome

The Effect of Plasma Exchange on the Expression of FOXP3 and RORC2 in Relapsed Multiple Sclerosis Patients

A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family

Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1

α-Globin Gene Mutations in Isfahan Province, Iran

Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents

Introducing a frameshift mutation to the POL sequence of HIV-1 provirus and evaluation of the immunogenic characteristics of the mutated virions (RINNL4-3)

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