Works matching AU Beheshtian, Maryam

Results: 35

COVID‐19 knowledge, attitudes, and practices among Iranian pregnant and postpartum women: A national study.

Published in:

Journal of Obstetrics & Gynaecology Research, 2023, v. 49, n. 9, p. 2295, doi. 10.1111/jog.15724

By:

Changizi, Nasrin;
Eshraghi, Nooshin;
Ghafoori, Faezeh;
Hejazi, Saiedeh;
Hadipour Jahromy, Leila;
Farahani, Zahra;
Sharifi, Hamid;
Beheshtian, Maryam

Publication type:

Article

Role of ATP-Binding Cassette Transporters in the Chemoresistance of Anaplastic Thyroid Cancer: A Systematic Review.

Published in:

Endocrinology, 2019, v. 160, n. 8, p. 2015, doi. 10.1210/en.2019-00241

By:

Abbasifarid, Elnaz;
Sajjadi-Jazi, Sayed Mahmoud;
Beheshtian, Maryam;
Samimi, Hilda;
Larijani, Bagher;
Haghpanah, Vahid

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

Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-76815-x

By:

Khanbazi, Ali;
Beheshtian, Maryam;
Azad, Maryam;
Akbari Kelishomi, Masoumeh;
Afroozan, Fariba;
Fatehi, Fatemeh;
Noudehi, Khadijeh;
Zamanian Najafabadi, Shima;
Omrani, Mohammadamin;
Habibi, Haleh;
Taghdiri, Maryam;
Abdi Rad, Isa;
Nafissi, Shahriar;
Jankhah, Aria;
Yazdan, Hilda;
Daneshmand, Parvaneh;
Saberi, Seyed Hosseinali;
Kahrizi, Kimia;
Kariminejad, Ariana;
Najmabadi, Hossein

Publication type:

Article

Iran's Multiple Indicator Demographic and Health Survey - 2010: Study Protocol.

Published in:

International Journal of Preventive Medicine, 2014, v. 5, n. 5, p. 632

By:

Rashidian, Arash;
Shahanjarini, Akram Karimi;
Khosravi, Ardeshir;
Elahi, Elham;
Beheshtian, Maryam;
Shakibazadeh, Elham;
Khabiri, Roghayeh;
Arab, Mohammad;
Zakeri, Mohammad-Reza

Publication type:

Article

Improved Diagnostic Yield in Recessive Intellectual Disability Utilizing Systematic Whole Exome Sequencing Data Reanalysis.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 612, doi. 10.1111/cge.14692

By:

Fattahi, Zohreh;
Shokouhian, Ebrahim;
Peymani, Fatemeh;
Babanejad, Mojgan;
Beheshtian, Maryam;
Edizadeh, Masoud;
Molaei, Negar;
Alagha, Parnian;
Ghodratpour, Fatemeh;
Keshavarzi, Fatemeh;
Moghadam, Masoumeh Goleyjani;
Arzhangi, Sanaz;
Kahrizi, Kimia;
Najmabadi, Hossein

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

Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families.

Published in:

Clinical Genetics, 2019, v. 95, n. 6, p. 718, doi. 10.1111/cge.13549

By:

Beheshtian, Maryam;
Fattahi, Zohreh;
Fadaee, Mahsa;
Vazehan, Raheleh;
Jamali, Payman;
Parsimehr, Elham;
Kamgar, Mahboubeh;
Zonooz, Mehrshid Faraji;
Mahdavi, Shokouh Sadat;
Kalhor, Zahra;
Arzhangi, Sanaz;
Abedini, Seyedeh Sedigheh;
Kermani, Farahnaz Sabbagh;
Mojahedi, Faezeh;
Kalscheuer, Vera M.;
Ropers, Hans‐Hilger.;
Kariminejad, Ariana;
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

Developing a household survey tool for health equity: A practical guide in Islamic Republic of Iran.

Published in:

Medical Journal of the Islamic Republic of Iran, 2015, v. 29, p. 1

By:

Beheshtian, Maryam;
Khosravi, Ardeshir;
Olyaeemanesh, Alireza;
Malekafzali, Hossein;
Esfahani, Shirin Bonakdar;
Ghavamabad, Leila Hosseiny;
Sagha, Fatemeh;
Aghamohammadi, Saeideh;
Nouri, Mahnaz;
Kazemi, Elaheh;
Zakeri, Mohammadreza

Publication type:

Article

Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations.

Published in:

Journal of Genetics, 2016, v. 95, n. 3, p. 667, doi. 10.1007/s12041-016-0682-6

By:

BEHESHTIAN, MARYAM;
IZADI, NASIM;
KRIEGSHAUSER, GERNOT;
KAHRIZI, KIMIA;
MEHR, ELHAM;
ROSTAMI, MARYAM;
HOSSEINI, MASOUMEH;
AZAD, MARYAM;
MONTAJABINIAT, MONA;
KARIMINEJAD, ARIANA;
NEMETH, STEFAN;
OBERKANINS, CHRISTIAN;
NAJMABADI, HOSSEIN

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

Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.

Published in:

NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00393-0

By:

Abolhassani, Ayda;
Fattahi, Zohreh;
Beheshtian, Maryam;
Fadaee, Mahsa;
Vazehan, Raheleh;
Ahangari, Fatemeh;
Dehdahsi, Shima;
Faraji Zonooz, Mehrshid;
Parsimehr, Elham;
Kalhor, Zahra;
Peymani, Fatemeh;
Mozaffarpour Nouri, Maryam;
Babanejad, Mojgan;
Noudehi, Khadijeh;
Fatehi, Fatemeh;
Zamanian Najafabadi, Shima;
Afroozan, Fariba;
Yazdan, Hilda;
Bozorgmehr, Bita;
Azarkeivan, Azita

Publication type:

Article

Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.

Published in:

NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00393-0

By:

Abolhassani, Ayda;
Fattahi, Zohreh;
Beheshtian, Maryam;
Fadaee, Mahsa;
Vazehan, Raheleh;
Ahangari, Fatemeh;
Dehdahsi, Shima;
Faraji Zonooz, Mehrshid;
Parsimehr, Elham;
Kalhor, Zahra;
Peymani, Fatemeh;
Mozaffarpour Nouri, Maryam;
Babanejad, Mojgan;
Noudehi, Khadijeh;
Fatehi, Fatemeh;
Zamanian Najafabadi, Shima;
Afroozan, Fariba;
Yazdan, Hilda;
Bozorgmehr, Bita;
Azarkeivan, Azita

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

Vaccination effects on reducing COVID‐19 complications in pregnancy: A large‐scale report from Iran.

Published in:

International Journal of Gynecology & Obstetrics, 2023, v. 163, n. 3, p. 1012, doi. 10.1002/ijgo.15077

By:

Changizi, Nasrin;
Eshrati, Babak;
Salehi, Mohammadreza;
Beheshtian, Maryam;
Hadipour Jahromy, Leila;
Emami Afshar, Nehzat;
Hejazi, Saeideh;
Hantoushzadeh, Sedigheh;
Eslamian, Laleh;
Savaie, Mohsen;
Raeisi, Alireza;
Pooransari, Parichehr

Publication type:

Article

First Iranian Family with a Novel Missense Variant in MYO9B Gene Causing Charcot--Marie--Tooth Disease.

Published in:

Archives of Iranian Medicine (AIM), 2025, v. 28, n. 4, p. 236, doi. 10.34172/aim.33244

By:

Beheshtian, Maryam;
Nouri, Maryam Mozaffarpour;
Ahangari, Fatemeh;
Makvand, Mina;
Salmani, Banafsheh;
Kariminejad, Ariana;
Najmabadi, Hossein;
Nafissi, Shahriar

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

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

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

Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.

Published in:

Archives of Iranian Medicine (AIM), 2022, v. 25, n. 12, p. 788, doi. 10.34172/aim.2022.124

By:

Ehtesham, Naeim;
Mosallaei, Meysam;
Beheshtian, Maryam;
Khoshbakht, Shahrouz;
Fadaee, Mahsa;
Vazehan, Raheleh;
Zonooz, Mehrshid Faraji;
Karimzadeh, Parvaneh;
Kahrizi, Kimia;
Najmabadi, Hossein

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

CEP104 and CEP290; Genes with Ciliary Functions Cause Intellectual Disability in Multiple Families.

Published in:

Archives of Iranian Medicine (AIM), 2021, v. 24, n. 5, p. 364, doi. 10.34172/aim.2021.53

By:

Khoshbakht, Shahrouz;
Beheshtian, Maryam;
Fattahi, Zohreh;
Bazazzadegan, Niloofar;
Parsimehr, Elham;
Fadaee, Mahsa;
Vazehan, Raheleh;
Zonooz, Mehrshid Faraji;
Abolhassani, Ayda;
Makvand, Mina;
Kariminejad, Ariana;
Celik, Arzu;
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

Contribution of Iran in Elucidating the Genetic Causes of Autosomal Recessive Intellectual Disability.

Published in:

Archives of Iranian Medicine (AIM), 2019, v. 22, n. 8, p. 461

By:

Ataei, Reza;
Khoshbakht, Shahrouz;
Beheshtian, Maryam;
Abedini, Seyedeh Sedigheh;
Behravan, Hanieh;
Dizghandi, Saeed Esmaeili;
Ghodratpour, Fatemeh;
Mirzaei, Sepide;
Bahrami, Fatemeh;
Akbari, Mojdeh;
Keshavarzi, Fatemeh;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy.

Published in:

Archives of Iranian Medicine (AIM), 2017, v. 20, n. 9, p. 617

By:

Edizadeh, Masoud;
Vazehan, Raheleh;
Javadi, Fatemeh;
Dehdahsi, Shima;
Fadaee, Mahsa;
Zonooz, Mehrshid Faraji;
Parsimehr, Elham;
Ahangari, Fatemeh;
Abolhassani, Ayda;
Kalhor, Zahra;
Fattahi, Zohreh;
Beheshtian, Maryam;
Kariminejad, Ariana;
Akbari, Mohammad Reza;
Najmabadi, Hossein;
Nafissi, Shariar

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

Evaluating the application and clinical practice of adapted national preeclampsia and eclampsia guideline; a cross-sectional study from Iran.

Published in:

BMC Pregnancy & Childbirth, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12884-025-07228-5

By:

Beheshtian, Maryam;
Khorrami, Zahra;
Shariat, Mamak;
Farahani, Zahra;
Changizi, Nasrin

Publication type:

Article

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

Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 4, p. 1, doi. 10.1002/mgg3.1894

By:

Mosallaei, Meysam;
Ehtesham, Naeim;
Beheshtian, Maryam;
Khoshbakht, Shahrouz;
Davarnia, Behzad;
Kahrizi, Kimia;
Najmabadi, Hossein

Publication type:

Article

Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1418

By:

Mehvari, Sepideh;
Larti, Farzaneh;
Hu, Hao;
Fattahi, Zohreh;
Beheshtian, Maryam;
Abedini, Seyedeh Sedigheh;
Arzhangi, Sanaz;
Ropers, Hans‐Hilger;
Kalscheuer, Vera M.;
Auld, Daniel;
Kahrizi, Kimia;
Riazalhosseini, Yasser;
Najmabadi, Hossein

Publication type:

Article