Works by Ashrafi, Farzane Zare

Results: 10

A Frameshift Variant in ANKRD24 Implicates Its Role in Human Non‐Syndromic Hearing Loss.

Published in:

Clinical Genetics, 2025, v. 107, n. 2, p. 214, doi. 10.1111/cge.14635

By:

Kazemi, Negar;
Rezvani Rezvandeh, Raziye;
Zare Ashrafi, Farzane;
Shokouhian, Ebrahim;
Edizadeh, Masoud;
Booth, Kevin T. A.;
Kahrizi, Kimia;
Najmabadi, Hossein;
Mohseni, Marzieh

Publication type:

Article

Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.

Published in:

Clinical Genetics, 2024, v. 105, n. 6, p. 611, doi. 10.1111/cge.14491

By:

Mehvari, Sepideh;
Karimian Fathi, Nahid;
Saki, Sara;
Asadnezhad, Maryam;
Arzhangi, Sanaz;
Ghodratpour, Fatemeh;
Mohseni, Marzieh;
Zare Ashrafi, Farzane;
Sadeghian, Saeed;
Boroumand, Mohammadali;
Shokohizadeh, Fatemeh;
Rostami, Elham;
Boroumand, Rahnama;
Najafipour, Reza;
Malekzadeh, Reza;
Riazalhosseini, Yasser;
Akbari, Mohammadreza;
Lathrop, Mark;
Najmabadi, Hossein;
Hosseini, Kaveh

Publication type:

Article

A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4.

Published in:

Archives of Iranian Medicine (AIM), 2024, v. 27, n. 9, p. 522, doi. 10.34172/aim.28745

By:

Ashrafi, Farzane Zare;
Dorgaleleh, Saeed;
Rezvandeh, Raziye Rezvani;
Kazemi, Negar;
Azizi, Nasrin;
Edizadeh, Masoud;
Azizi, Mohammad Hossein;
Kahrizi, Kimia;
Najmabadi, Hossein;
Najafipour, Reza;
Mohseni, Marzieh

Publication type:

Article

Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups.

Published in:

Archives of Iranian Medicine (AIM), 2024, v. 27, n. 2, p. 79, doi. 10.34172/aim.2024.13

By:

Alinaghi, Somayeh;
Mohseni, Marzieh;
Fattahi, Zohreh;
Beheshtian, Maryam;
Ghodratpour, Fatemeh;
Zare Ashrafi, Farzane;
Arzhangi, Sanaz;
Jalalvand, Khadijeh;
Najafipour, Reza;
Khorram Khorshid, Hamid Reza;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort.

Published in:

Archives of Iranian Medicine (AIM), 2023, v. 26, n. 4, p. 186, doi. 10.34172/aim.2023.29

By:

Ashrafi, Farzane Zare;
Akhtarkhavari, Tara;
Fattahi, Zohreh;
Asadnezhad, Maryam;
Beheshtian, Maryam;
Arzhangi, Sanaz;
Najmabadi, Hossein;
Kahrizi, Kimia

Publication type:

Article

An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene.

Published in:

Archives of Iranian Medicine (AIM), 2023, v. 26, n. 3, p. 176, doi. 10.34172/aim.2023.27

By:

Mohseni, Marzieh;
Mohammadi, Yusuf;
Ashrafi, Farzane Zare;
Ghodratpour, Fatemeh;
Jalalvand, Khadijeh;
Arzhangi, Sanaz;
Babanejad, Mojgan;
Azizi, Mohammad Hossein;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations.

Published in:

Archives of Iranian Medicine (AIM), 2023, v. 26, n. 2, p. 69, doi. 10.34172/aim.2023.12

By:

Ashrafi, Farzane Zare;
Mohseni, Marzieh;
Beheshtian, Maryam;
Fattahi, Zohreh;
Ghodratpour, Fatemeh;
Keshavarzi, Fatemeh;
Behravan, Hanieh;
Kalhor, Marzieh;
Jalalvand, Khadijeh;
Azad, Maryam;
Koshki, Mahdieh;
Jafarpour, Ali;
Ghaziasadi, Azam;
Abdollahi, Alireza;
Kiani, Seyed Jalal;
Ataei-Pirkooh, Angila;
Azhar, Iman Rezaei;
Bokharaei-Salim, Farah;
Haghshenas, Mohammad Reza;
Babamahmoodi, Farhang

Publication type:

Article

Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends.

Published in:

Archives of Iranian Medicine (AIM), 2022, v. 25, n. 8, p. 508, doi. 10.34172/aim.2022.83

By:

Fattahi, Zohreh;
Mohseni, Marzieh;
Beheshtian, Maryam;
Jafarpour, Ali;
Jalalvand, Khadijeh;
Keshavarzi, Fatemeh;
Behravan, Hanieh;
Ghodratpour, Fatemeh;
Ashrafi, Farzane Zare;
Kalhor, Marzieh;
Azad, Maryam;
Koshki, Mahdieh;
Ghaziasadi, Azam;
Soveyzi, Mohamad;
Abdollahi, Alireza;
Kiani, Seyed Jalal;
Ataei-Pirkooh, Angila;
Rezaeiazhar, Iman;
Bokharaei-Salim, Farah;
Haghshenas, Mohammad Reza

Publication type:

Article

Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism.

Published in:

Archives of Iranian Medicine (AIM), 2020, v. 23, n. 12, p. 842, doi. 10.34172/aim.2020.112

By:

Kazemi, Goli;
Peymani, Fatemeh;
Mohseni, Marzieh;
Ashrafi, Farzane Zare;
Arzhangi, Sanaz;
Ardalani, Fariba;
Moghaddam, Fatemeh Aghakhani;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran.

Published in:

Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 2, p. 1, doi. 10.1002/mgg3.70080

By:

Mohseni, Marzieh;
Ashrafi, Farzane Zare;
Abbaspour Rodbaneh, Ehsan;
Mokabber, Haleh;
Vafaei, Maryam;
Nobakht, Ramiz;
Keshavarzi, Fatemeh;
Arzhangi, Sanaz;
Arish, Sara;
Azar, Zahra Nematollahi;
Kahrizi, Kimia;
Najmabadi, Hossein;
Davarnia, Behzad

Publication type:

Article