Samane Nasrniya

Affiliations

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

Publications (4)

Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.

Laboratory medicine

Avec: Samane Nasrniya , Paniz Miar , Sina Narrei , Mahsa Sepehrnejad , Mohammad Hussein Nilforoush , Hamidreza Abtahi , Mohammad Amin Tabatabaiefar

A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.

BMC medical genetics

Avec: Akram Sarmadi , Samane Nasrniya , Maryam Soleimani Farsani , Sina Narrei , Zahra Nouri , Mahsa Sepehrnejad , Mohammad Hussein Nilforoush , Hamidreza Abtahi , Mohammad Amin Tabatabaiefar

Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.

Molecular biology reports

Avec: Akram Sarmadi , Samane Nasrniya , Sina Narrei , Zahra Nouri , Hamidreza Abtahi , Mohammad Amin Tabatabaiefar

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

Endocrine

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

Réseau de co-auteurs

Mohammad Amin Tabatabaiefar 4 collaborations

Sina Narrei 3 collaborations

Hamidreza Abtahi 3 collaborations

Mahsa Sepehrnejad 2 collaborations

Mohammad Hussein Nilforoush 2 collaborations

Akram Sarmadi 2 collaborations

Zahra Nouri 2 collaborations

Paniz Miar 1 collaboration

Maryam Soleimani Farsani 1 collaboration

Maryam Sobhani 1 collaboration

Soudeh Ghafouri-Fard 1 collaboration

Asadollah Rajab 1 collaboration

Sarah Mozafarpour 1 collaboration

Samaneh Nasrniya 1 collaboration

Abdol-Mohammad Kajbafzadeh 1 collaboration

Mohammad Reza Noori-Daloii 1 collaboration