المؤلفون: Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi, Michael Nothnagel

المصدر: PLoS Genetics, Vol 15, Iss 9, p e1008385 (2019)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/4315684f000740c9942734ccd2e1d473Test

المؤلفون: Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi

المصدر: Journal of Rehabilitation, Vol 8, Iss 3, Pp 35-41 (2007)

مصطلحات موضوعية: GJB2 mutations, 35delG, Iran, Hereditary hearing loss, Autosomal inheritance, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

العلاقة: http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-188&slc_lang=en&sid=1Test; https://doaj.org/toc/1607-2960Test

الوصول الحر: https://doaj.org/article/e891523139e44bb594ba117ed736daccTest

المؤلفون: Seyed Hamid Jamaldini, Mojgan Babanejad, Reza Mozaffari, Nooshin Nikzat, Khadijeh Jalalvand, Azadeh Badiei, Hamidreza Sanati, Farshad Shakerian, Mahdi Afshari, Kimia Kahrizi, Hossein Najmabadi

المصدر: Acta Medica Iranica, Vol 52, Iss 5 (2014)

مصطلحات موضوعية: Coronary artery disease, LDLR locus, Single nucleotide polymorphism, SMARCA4 gene, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: https://acta.tums.ac.ir/index.php/acta/article/view/4618Test; https://doaj.org/toc/0044-6025Test; https://doaj.org/toc/1735-9694Test

الوصول الحر: https://doaj.org/article/79fd04af3bb24427b0fb3bb4a1628908Test

المؤلفون: Ramak Badr, Bahareh Shoja-Saffar, Niloofar Bazzaz-Zadegan, Khadijeh Jalalvand, Kimia Kahrizi, Hossein Najm-Abadi

المصدر: Journal of Rehabilitation, Vol 10, Iss 4, Pp 0-0 (2010)

مصطلحات موضوعية: Non-syndromeic hearing loss, Recessive autosomal heredity, Haplotype analysis, Iran, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

العلاقة: http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-44-41&slc_lang=en&sid=1Test; https://doaj.org/toc/1607-2960Test

الوصول الحر: https://doaj.org/article/c8d216d795394ef8bc27827ecbeab8c8Test

المؤلفون: Hanieh Behravan, Ahmad Piroozmand, Azam Ghaziasadi, Khadijeh Jalalvand, Mahdieh Koshki, Fatemeh Tavangar, Angila Ataei-Pirkooh, Farid Yousefi, Masoumeh Bayani, Zohreh Fattahi, Hamed Fakhim, Mojtaba Varshochi, Mohammad Khazeni, Zakiye Mokhames, Fariba Shahraki-Sanavi, Reza Malekzadeh, Maryam Beheshtian, Yousef Yahyapour, Seyed Jalal Kiani, Fariba Keramat, Shokouh Ghafari, Behrooz Ataei, Alireza Abdollahi, Afagh Moattari, Fatemeh Keshavarzi, Mohammad Reza Haghshenas, Alireza AnsariMoghaddam, Maryam Azad, Mohammad Hassan Pouriayevali, Mohsen Moghadami, Azarakhsh Azaran, Zohreh Elahi, Farhang Babamahmoodi, Mohamad Soveyzi, Kimia Kahrizi, Hamid Reza Khorram Khorshid, Vahdat Poortahmasebi, Reza Najafipour, Farzane Zare Ashrafi, Akram Ezani, Farid Azizi Jalilian, Mostafa Salehi-Vaziri, Seyed Mohammad Jazayeri, Seyed Mohammad Hashemi-Shahri, Abdolvahab Moradi, Ali Mojtahedi, Fatemeh Ghodratpour, Marzieh Mohseni, Davod Javanmard, Mahsa Tavakoli, Ali Jafarpour, Hossein Najmabadi, Alijan Tabarraei, Alireza Soleimani, Tahmineh Jalali, Elahe Nasri, Mahmood Yaghoubi, Marzieh Kalhor, Farah Bokharaei-Salim, Iman Rezaeiazhar, Masood Ziaee

المصدر: Archives of Iranian Medicine. 25:508-522

مصطلحات موضوعية: Genetics, Whole genome sequencing, education.field_of_study, Mutation, Genetic diversity, Lineage (genetic), Population, Outbreak, General Medicine, Biology, medicine.disease_cause, Genome, medicine, education, Clade

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234661a7c997f97453fa3ecb1054d7e1Test
https://doi.org/10.34172/aim.2022.83Test

المؤلفون: Gholam Abbas Kaydani, Seyedeh Elham Mortazavi, Seyed Amir Momeni, Talat Mokhtari-Azad, Fatemeh Aghakhani Moghadam, Hanieh Behravan, Mohammad Khazeni, Azarakhsh Azaran, Zakiye Mokhames, Farhad Jeddi, Ebrahim Kord, Seyed Mohammad Hashemi-Shahri, Azam Ghaziasadi, Alijan Tabarraei, Fatemeh Ghodratpour, Masood Ziaee, Ali Jafarpour, Jila Yavarian, Abdolvahab Moradi, Azar Hadadi, Zohreh Fattahi, Hossein Najmabadi, Shokouh Ghafari, Issa Jahanzad, Reza Malekzadeh, Marzieh Mohseni, Farid Yousefi, Shahram Habibzadeh, Seyed Mohammad Jazayeri, Khadijeh Jalalvand, Saber Soltani, Kimia Kahrizi, Alireza Soleimani, Sadegh Ali Azimi, Reza Najafipour, Alireza Abdollahi, Fatemeh Keshavarzi

المصدر: Transboundary and Emerging Diseases

مصطلحات موضوعية: Most recent common ancestor, 040301 veterinary sciences, viruses, Lineage (evolution), Zoology, Genome, Viral, Iran, Biology, SARS‐CoV‐2, Virus, Disease Outbreaks, law.invention, 0403 veterinary science, phylogenetic study, 03 medical and health sciences, COVID‐19, law, Pandemic, Animals, Phylogeny, 030304 developmental biology, whole genome sequencing, 0303 health sciences, Genetic diversity, General Veterinary, General Immunology and Microbiology, SARS-CoV-2, COVID-19, Outbreak, Original Articles, 04 agricultural and veterinary sciences, General Medicine, Transmission (mechanics), Mutation (genetic algorithm), Original Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c82245f4fea38cae05cc1b94f251910Test
https://doi.org/10.1111/tbed.14104Test

المؤلفون: Kimia Kahrizi, Fariba Ardalani, Mojdeh Akbari, Mojgan Babanejad, Kevin T. Booth, Hossein Najmabadi, Haleh Habibi, Khadijeh Jalalvand, Nooshin Nikzat, Fatemeh Ghodratpour, Omid Ali Adeli, Marzieh Mohseni, Payman Jamali, Hela Azaiez, Sanaz Arzhangi

المصدر: J Hum Genet

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Proband, Adolescent, Genotype, Hearing loss, Hearing Loss, Sensorineural, Iran, 030105 genetics & heredity, Biology, Article, Frameshift mutation, Male infertility, Diagnosis, Differential, Young Adult, 03 medical and health sciences, Exon, Genetics, medicine, Humans, Genetic Predisposition to Disease, Frameshift Mutation, Hearing Loss, Gene, Genetic Association Studies, Infertility, Male, Genetics (clinical), Loss function, High-Throughput Nucleotide Sequencing, Exons, medicine.disease, Pedigree, 030104 developmental biology, Mutation (genetic algorithm), Female, Protein Tyrosine Phosphatases, medicine.symptom

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0871f42e194feb0aeae554f7d0b00072Test
https://doi.org/10.1038/s10038-020-0740-zTest

المؤلفون: Marzieh Mohseni, Kevin T. Booth, Atefeh Khoshaeen, Fatemeh Bahrami, Payman Jamali, Hossein Najmabadi, Niloofar Bazazzadegan, Kimia Kahrizi, Nooshin Nikzat, Farkhonde Habibi, Richard J.H. Smith, Fariba Ardalani, Mojgan Babanejad, Hanieh Behravan, Fatemeh Keshavarzi, Michael Nothnagel, Faezeh Jahanshad, Seyed Morteza Seifati, Fatemeh Ghodratpour, Sanaz Arzhangi, Behzad Davarnia, Zohreh Mehrjoo, Holger Thiele, Khadijeh Jalalvand, Maryam Beheshtian, Hela Azaiez, Sepide Mirzaei, Hasan Otukesh

المصدر: Clin Genet

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Candidate gene, Adolescent, Hearing loss, Consanguinity, 030105 genetics & heredity, Biology, Iran, DNA sequencing, Article, Cohort Studies, 03 medical and health sciences, Young Adult, Locus heterogeneity, Exome Sequencing, Genetics, medicine, Humans, Exome, Genetic Predisposition to Disease, Child, Hearing Loss, Gene, Genetics (clinical), Exome sequencing, Genetic heterogeneity, High-Throughput Nucleotide Sequencing, Middle Aged, medicine.disease, Pedigree, 030104 developmental biology, Child, Preschool, Mutation, Female, medicine.symptom

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2652aadda21337130620b09922d67aTest
https://europepmc.org/articles/PMC8195868Test/

المؤلفون: Seyed Morteza Seifati, Maryam Beheshtian, Kevin T. Booth, Behzad Davarnia, Faezeh Jahanshad, Farkhonde Habibi, Michael Nothnagel, Atefeh Khoshaeen, Hanieh Behravan, K. Kahrizi, Fatemeh Ghodratpour, Sanaz Arzhangi, Fatemeh Bahrami, Hossein Najmabadi, Payman Jamali, Marzieh Mohseni, Fariba Ardalani, Mojgan Babanejad, Khadijeh Jalalvand, Hela Azaiez, Sepide Mirzaei, Holger Thiele, Zohreh Mehrjoo, Hasan Otukesh, Nooshin Nikzat, Richard J.H. Smith, Fatemeh Keshavarzi, Niloofar Bazazzadegan

مصطلحات موضوعية: Novel gene, Hearing loss, medicine, Computational biology, Biology, medicine.symptom, Exome sequencing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c907ed7b80c8ef2500764b3b5e3a683fTest
https://doi.org/10.1111/cge.13956/v4/response1Test

المؤلفون: Hoda Mehregan, Nooshin Nikzat, Marzieh Mohseni, Kimia Kahrizi, Sussan Banihashemi, Khadijeh Jalalvand, Hossein Najmabadi, Sanaz Arzhangi

المصدر: International Journal of Pediatric Otorhinolaryngology. 117:115-126

مصطلحات موضوعية: Male, Proband, MYO15A, Hearing loss, Hearing Loss, Sensorineural, Consanguinity, Deafness, Iran, Myosins, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Ezrin, 030225 pediatrics, Exome Sequencing, otorhinolaryngologic diseases, Humans, Medicine, 030223 otorhinolaryngology, Exome sequencing, Genetics, Sanger sequencing, business.industry, General Medicine, medicine.disease, Otorhinolaryngology, Mutation, Pediatrics, Perinatology and Child Health, symbols, FERM Domains, Female, Sensorineural hearing loss, medicine.symptom, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab4d6c7ba59003be868f155916fc522Test
https://doi.org/10.1016/j.ijporl.2018.11.025Test