Works matching AU Mohseni, Marzieh

Results: 33

Iranome: A catalog of genomic variations in the Iranian population.

Published in:

Human Mutation, 2019, v. 40, n. 11, p. 1968, doi. 10.1002/humu.23880

By:

Fattahi, Zohreh;
Beheshtian, Maryam;
Mohseni, Marzieh;
Poustchi, Hossein;
Sellars, Erin;
Nezhadi, Sayyed Hossein;
Amini, Amir;
Arzhangi, Sanaz;
Jalalvand, Khadijeh;
Jamali, Peyman;
Mohammadi, Zahra;
Davarnia, Behzad;
Nikuei, Pooneh;
Oladnabi, Morteza;
Mohammadzadeh, Akbar;
Zohrehvand, Elham;
Nejatizadeh, Azim;
Shekari, Mohammad;
Bagherzadeh, Maryam;
Shamsi‐Gooshki, Ehsan

Publication type:

Article

Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease.

Published in:

Medical Principles & Practice, 2015, v. 24, n. 4, p. 351, doi. 10.1159/000430842

By:

Mehrjoo, Zohreh;
Najmabadi, amin;
abedini, Seyedeh Sedigheh;
Mohseni, Marzieh;
Kamali, Koorosh;
Najmabadi, Hossein;
Khorram Khorshid, Hamid Reza

Publication type:

Article

Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment.

Published in:

2009

By:

Kahrizi, Kimia;
Mohseni, Marzieh;
Nishimura, Carla;
Bazazzadegan, Niloofar;
Fischer, Stephanie M.;
Dehghani, Atefeh;
Sayfati, Morteza;
Taghdiri, Maryam;
Jamali, Payman;
Smith, Richard J. H.;
Azizi, Fereydoun;
Najmanabi, Hossein;
Najmabadi, Hossein

Publication type:

journal article

Investigation of the Relationship Between a Genetic Polymorphism in ACTN3 and Elite Sport Performance Among Iranian Soccer Players.

Published in:

Iranian Rehabilitation Journal, 2017, v. 15, n. 2, p. 149, doi. 10.18869/NRIP.IRJ.15.2.149

By:

Honarpour, Asal;
Mohseni, Marzieh;
Hajiagha, Siamak Ghavidel;
Irani, Shiva;
Najmabadi, Hossein

Publication type:

Article

Mutation profile of BBS genes in Iranian patients with Bardet-Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genes.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 7, p. 368, doi. 10.1038/jhg.2014.28

By:

Fattahi, Zohreh;
Rostami, Parvin;
Najmabadi, Amin;
Mohseni, Marzieh;
Kahrizi, Kimia;
Akbari, Mohammad Reza;
Kariminejad, Ariana;
Najmabadi, Hossein

Publication type:

Article

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

Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran.

Published in:

Clinical Genetics, 2021, v. 100, n. 1, p. 59, doi. 10.1111/cge.13956

By:

Mohseni, Marzieh;
Babanejad, Mojgan;
Booth, Kevin T.;
Jamali, Payman;
Jalalvand, Khadijeh;
Davarnia, Behzad;
Ardalani, Fariba;
Khoshaeen, Atefeh;
Arzhangi, Sanaz;
Ghodratpour, Fatemeh;
Beheshtian, Maryam;
Jahanshad, Faezeh;
Otukesh, Hasan;
Bahrami, Fatemeh;
Seifati, Seyed Morteza;
Bazazzadegan, Niloofar;
Habibi, Farkhonde;
Behravan, Hanieh;
Mirzaei, Sepide;
Keshavarzi, Fatemeh

Publication type:

Article

Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients.

Published in:

Clinical Genetics, 2021, v. 99, n. 1, p. 187, doi. 10.1111/cge.13845

By:

Beheshtian, Maryam;
Akhtarkhavari, Tara;
Mehvari, Sepideh;
Mohseni, Marzieh;
Fattahi, Zohreh;
Abedini, Seyedeh Sedigheh;
Arzhangi, Sanaz;
Fadaee, Mahsa;
Jamali, Payman;
Najafipour, Reza;
Kalscheuer, Vera M.;
Hu, Hao;
Ropers, Hans‐Hilger;
Najmabadi, Hossein;
Kahrizi, Kimia

Publication type:

Article

Effect of inbreeding on intellectual disability revisited by trio sequencing.

Published in:

Clinical Genetics, 2019, v. 95, n. 1, p. 151, doi. 10.1111/cge.13463

By:

Kahrizi, Kimia;
Hosseini, Masoumeh;
Fattahi, Zohreh;
Beheshtian, Maryam;
Mohseni, Marzieh;
Mehvari, Sepideh;
Mehrjoo, Zohreh;
Akhtarkhavari, Tara;
Ghaderi, Zhila;
Rahimi, Maryam;
Arzhangi, Sanaz;
Falahat Chian, Milad;
Sadeghinia, Farnaz;
Najmabadi, Hossein;
Pourfatemi, Fatemeh;
Mojahedi, Faezeh;
Khodaie‐Ardakani, Mohammad‐Reza;
Najafipour, Reza;
Hu, Hao;
Kalscheuer, Vera M.

Publication type:

Article

GJB2 mutations in Baluchi population.

Published in:

Journal of Genetics, 2008, v. 87, n. 2, p. 195, doi. 10.1007/s12041-008-0031-5

By:

NAGHAVI, ANOOSH;
NISHIMURA, CARLA;
KAHRIZI, KIMIA;
RIAZALHOSSEINI, YASSER;
BAZAZZADEGAN, NILOOFAR;
MOHSENI, MARZIEH;
SMITH, RICHARD J. H.;
NAJMABADI, HOSSEIN

Publication type:

Article

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.

Published in:

Human Genetics, 2011, v. 129, n. 2, p. 141, doi. 10.1007/s00439-010-0907-3

By:

Kuss, Andreas Walter;
Garshasbi, Masoud;
Kahrizi, Kimia;
Tzschach, Andreas;
Behjati, Farkhondeh;
Darvish, Hossein;
Abbasi-Moheb, Lia;
Puettmann, Lucia;
Zecha, Agnes;
Weißmann, Robert;
Hu, Hao;
Mohseni, Marzieh;
Abedini, Seyedeh;
Rajab, Anna;
Hertzberg, Christoph;
Wieczorek, Dagmar;
Ullmann, Reinhard;
Ghasemi-Firouzabadi, Saghar;
Banihashemi, Susan;
Arzhangi, Sanaz

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

Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 5, p. 1, doi. 10.1002/mgg3.2168

By:

Jamshidi, Fereshteh;
Shokouhian, Ebrahim;
Mohseni, Marzieh;
Kahrizi, Kimia;
Najmabadi, Hossein;
Babanejad, Mojgan

Publication type:

Article

Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.

Published in:

Iranian Biomedical Journal, 2016, v. 20, n. 4, p. 201, doi. 10.7508/ibj.2016.04.003

By:

Mohseni, Marzieh;
Razzaghmanesh, Mohammad;
Mehr, Elham Parsi;
Zare, Hanieh;
Beheshtian, Maryam;
Najmabadi, Hossein

Publication type:

Article

SARS-CoV-2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions.

Published in:

Transboundary & Emerging Diseases, 2022, v. 69, n. 3, p. 1375, doi. 10.1111/tbed.14104

By:

Fattahi, Zohreh;
Mohseni, Marzieh;
Jalalvand, Khadijeh;
Moghadam, Fatemeh Aghakhani;
Ghaziasadi, Azam;
Keshavarzi, Fatemeh;
Yavarian, Jila;
Jafarpour, Ali;
Mortazavi, Seyedeh Elham;
Ghodratpour, Fatemeh;
Behravan, Hanieh;
Khazeni, Mohammad;
Momeni, Seyed Amir;
Jahanzad, Issa;
Moradi, Abdolvahab;
Tabarraei, Alijan;
Azimi, Sadegh Ali;
Kord, Ebrahim;
Hashemi-Shahri, Seyed Mohammad;
Azaran, Azarakhsh

Publication type:

Article

Haplogroup Structure and Genetic Variation Analyses of Mitochondrial Genome SNPs in the Iranian Population.

Published in:

Archives of Iranian Medicine (AIM), 2025, v. 28, n. 3, p. 140, doi. 10.34172/aim.33639

By:

Ghasemi, Masoumeh;
Mohseni, Marzieh;
Fattahi, Zohreh;
Edizadeh, Masoud;
Beheshtian, Maryam;
Keshavarzi, Fatemeh;
Jalalvand, Khadijeh;
Omrani, Mohammadamin;
Khanbazi, Ali;
Riazalhosseini, Yasser;
Akbari, Mohammad Reza;
Kahrizi, Kimia;
Najmabadi, Hossein

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

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

Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease.

Published in:

Archives of Iranian Medicine (AIM), 2022, v. 25, n. 9, p. 600, doi. 10.34172/aim.2022.95

By:

Hosseinpour, Maryam;
Ardalani, Fariba;
Mohseni, Marzieh;
Beheshtian, Maryam;
Arzhangi, Sanaz;
Ossareh, Shahrzad;
Najmabadi, Hossein;
Nobakht, Ali;
Kahrizi, Kimia;
Broumand, Behrooz

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

Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum.

Published in:

Archives of Iranian Medicine (AIM), 2020, v. 23, n. 7, p. 426, doi. 10.34172/aim.2020.39

By:

Taghizadeh, Sara;
Vazehan, Raheleh;
Beheshtian, Maryam;
Sadeghinia, Farnaz;
Fattahi, Zohreh;
Mohseni, Marzieh;
Arzhangi, Sanaz;
Nafissi, Shahriar;
Kariminejad, Ariana;
Najmabadi, Hossein;
Kahrizi, Kimia

Publication type:

Article

Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.

Published in:

Archives of Iranian Medicine (AIM), 2020, v. 23, n. 5, p. 319, doi. 10.34172/aim.2020.21

By:

Mehrjoo, Zohreh;
Kahrizi, Kimia;
Mohseni, Marzieh;
Akbari, Mojdeh;
Arzhangi, Sanaz;
Jalalvand, Khadijeh;
Najmabadi, Hossein;
Farhadi, Mohammad;
Mohseni, Mohammad;
Asghari, Alimohamad;
Mohebbi, Saleh;
Daneshi, Ahmad

Publication type:

Article

Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment.

Published in:

Archives of Iranian Medicine (AIM), 2019, v. 22, n. 4, p. 189

By:

Mehregan, Hoda;
Mohseni, Marzieh;
Akbari, Mojdeh;
Jalalvand, Khadijeh;
Arzhangi, Sanaz;
Nikzat, Nooshin;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

Published in:

Archives of Iranian Medicine (AIM), 2016, v. 19, n. 10, p. 724

By:

Beheshtian, Maryam;
Babanejad, Mojgan;
Azaiez, Hela;
Bazazzadegan, Niloofar;
Kolbe, Diana;
Sloan-Heggen, Christina;
Arzhangi, Sanaz;
Booth, Kevin;
Mohseni, Marzieh;
Frees, Kathy;
Azizi, Mohammad Hossein;
Daneshi, Ahmad;
Farhadi, Mohammad;
Kahrizi, Kimia;
Smith, Richard J. H.;
Najmabadi, Hossein

Publication type:

Article

Impact of Whole Exorne Sequencing among Iranian Patients with Autosomal Recessive Retinitis Pigmentosa.

Published in:

Archives of Iranian Medicine (AIM), 2015, v. 18, n. 11, p. 776

By:

Beheshtian, Maryam;
Rad, Samira Saee;
Babanejad, Mojgan;
Mohseni, Marzieh;
Hashemi, Hassan;
Eshghabadi, Arash;
Hajizadeh, Fedra;
Akbari, Mohammad Reza;
Kahrizi, Kimia;
Esfahani, Mohammad Riazi;
Najmabadi, Hossein

Publication type:

Article

Distinct genetic variation and heterogeneity of the Iranian population.

Published in:

PLoS Genetics, 2019, v. 15, n. 9, p. 1, doi. 10.1371/journal.pgen.1008385

By:

Mehrjoo, Zohreh;
Fattahi, Zohreh;
Beheshtian, Maryam;
Mohseni, Marzieh;
Poustchi, Hossein;
Ardalani, Fariba;
Jalalvand, Khadijeh;
Arzhangi, Sanaz;
Mohammadi, Zahra;
Khoshbakht, Shahrouz;
Najafi, Farid;
Nikuei, Pooneh;
Haddadi, Mohammad;
Zohrehvand, Elham;
Oladnabi, Morteza;
Mohammadzadeh, Akbar;
Jafari, Mandana Hadi;
Akhtarkhavari, Tara;
Gooshki, Ehsan Shamsi;
Haghdoost, Aliakbar

Publication type:

Article

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

Published in:

Nature, 2011, v. 478, n. 7367, p. 57, doi. 10.1038/nature10423

By:

Najmabadi, Hossein;
Hu, Hao;
Garshasbi, Masoud;
Zemojtel, Tomasz;
Abedini, Seyedeh Sedigheh;
Chen, Wei;
Hosseini, Masoumeh;
Behjati, Farkhondeh;
Haas, Stefan;
Jamali, Payman;
Zecha, Agnes;
Mohseni, Marzieh;
Püttmann, Lucia;
Vahid, Leyla Nouri;
Jensen, Corinna;
Moheb, Lia Abbasi;
Bienek, Melanie;
Larti, Farzaneh;
Mueller, Ines;
Weissmann, Robert

Publication type:

Article

Genetic etiology of hearing loss in Iran.

Published in:

Human Genetics, 2022, v. 141, n. 3/4, p. 623, doi. 10.1007/s00439-021-02421-w

By:

Babanejad, Mojgan;
Beheshtian, Maryam;
Jamshidi, Fereshteh;
Mohseni, Marzieh;
Booth, Kevin T.;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

Identification of Three Novel Frameshift Mutations in the PKD1 Gene in Iranian Families with Autosomal Dominant Polycystic Kidney Disease Using Efficient Targeted Next-Generation Sequencing.

Published in:

Kidney & Blood Pressure Research, 2018, v. 43, n. 2, p. 471, doi. 10.1159/000488471

By:

Ranjzad, Fariba;
Aghdami, Nasser;
Tara, Ahmad;
Mohseni, Marzieh;
Moghadasali, Reza;
Basiri, Abbas

Publication type:

Article