المؤلفون: Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi

المصدر: npj Genomic Medicine, Vol 9, Iss 1, Pp 1-11 (2024)

مصطلحات موضوعية: Medicine, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2056-7944

URL الوصول: https://doaj.org/article/d0de56f0485d43639ba3ed001723c22f

المؤلفون: Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi

المصدر: Genetics in Medicine Open, Vol 2, Iss , Pp 101510- (2024)

مصطلحات موضوعية: Genetics, QH426-470, Medicine

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2949774424006563; https://doaj.org/toc/2949-7744

URL الوصول: https://doaj.org/article/2b6cd8a2516d4c7dba834e7f5dd8bf1b

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

المصدر: Molecular Genetics & Genomic Medicine, Vol 11, Iss 5, Pp n/a-n/a (2023)

مصطلحات موضوعية: FGF3, Iran, LAMM syndrome, whole‐exome sequencing, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2324-9269

URL الوصول: https://doaj.org/article/39d97996c2e04ea79d5a364f6c386c99

المؤلفون: Kimia Najafi, Soheila Gholami, Azadeh Moshtagh, Masood Bazrgar, Neda Sadatian, Golemaryam Abbasi, Parvin Rostami, Soheila Khalili, Mojgan Babanejad, Bahareh Nourmohammadi, Negin Faramarzi Garous, Hossein Najmabadi, Roxana Kariminejad

المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)

مصطلحات موضوعية: array comparative genomic hybridization, chromosomal abnormality, consanguinity, miscarriage, recurrent abortion, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2324-9269

URL الوصول: https://doaj.org/article/ab057e8a446d4424b39cf48405a5896b

المؤلفون: Reyhaneh Kameli, Mandana Hasanzad, Zahra Tahmasebi Fard, Mojgan Babanejad, Mahdieh Imeni, Lotfollah Feizi Barnaji, Atoosa Madadkar, Seyed Hamid Jamaldini

المصدر: Research in Molecular Medicine, Vol 4, Iss 4, Pp 38-44 (2016)

مصطلحات موضوعية: CYP2C9*2, CYP2C9*3, VKORC1, Warfarin, RFLP, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://rmm.mazums.ac.ir/browse.php?a_code=A-10-26-31&slc_lang=en&sid=1; https://doaj.org/toc/2322-1348; https://doaj.org/toc/2322-133X

URL الوصول: https://doaj.org/article/1ee80feb357846efa2c120fa05277d4d

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

المصدر: Human Genetics. 141:623-631

مصطلحات موضوعية: Hearing Loss, Sensorineural, Mutation, Genetics, Humans, Deafness, Iran, Hearing Loss, Genetics (clinical), Pedigree

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b712c07ee5f8171709a72eaaa6a2ea3
https://doi.org/10.1007/s00439-021-02421-w

المؤلفون: Reihaneh Alikhani, Fatemeh Ostaresh, Mojgan Babanejad, Nilofar Bazazzadegan, Hossein Najmabadi, Kimia Kahrizi

المصدر: Iranian Rehabilitation Journal, Vol 13, Iss 3, Pp 64-68 (2015)

مصطلحات موضوعية: Autosomal recessive non-syndromic hearing loss, Homozygosity mapping, Linkage analysis, Iran, Medicine, Vocational rehabilitation. Employment of people with disabilities, HD7255-7256

وصف الملف: electronic resource

Relation: http://irj.uswr.ac.ir/browse.php?a_code=A-10-382-1&slc_lang=en&sid=1; https://doaj.org/toc/1735-3602; https://doaj.org/toc/1735-3610

URL الوصول: https://doaj.org/article/c8fd4f2cc54249be9eb9626121585a86

المؤلفون: Mahdieh Imeni, Mandana Hasanzad, Tahereh Naji, Behzad Poopak, Mojgan Babanejad, Hamid Reza Sanati, Reyhaneh Kameli, Atoosa Madadkar, Zahra Hosseini Khah, Seyed Hamid Jamaldini

المصدر: Research in Molecular Medicine, Vol 1, Iss 3, Pp 18-23 (2013)

مصطلحات موضوعية: Coronary artery disease (CAD), Lipoprotein lipase (LPL), Hind III Polymorphism, RFLP, dyslipidemia, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://rmm.mazums.ac.ir/browse.php?a_code=A-10-26-18&slc_lang=en&sid=1; https://doaj.org/toc/2322-1348; https://doaj.org/toc/2322-133X

URL الوصول: https://doaj.org/article/3dd783e7dccb49efb014ed852796be95

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0871f42e194feb0aeae554f7d0b00072
https://doi.org/10.1038/s10038-020-0740-z

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

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

URL الوصول: https://doaj.org/article/79fd04af3bb24427b0fb3bb4a1628908

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2652aadda21337130620b09922d67a
https://europepmc.org/articles/PMC8195868/

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c907ed7b80c8ef2500764b3b5e3a683f
https://doi.org/10.1111/cge.13956/v4/response1

المؤلفون: Hakimeh Azarafra, Marzieh Mohseni, Omid Ali Adeli, Kimia Kahrizi, Maryam Beheshtian, Farnaz Sadeghnia, Nooshin Nikzat, Mojgan Babanejad, Hossein Najmabadi

المصدر: International Journal of Pediatric Otorhinolaryngology. 104:195-199

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Ataxia, Adolescent, Mutation, Missense, Iran, 030105 genetics & heredity, Receptors, G-Protein-Coupled, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Atrophy, Exome Sequencing, medicine, Humans, Spinocerebellar Ataxias, Missense mutation, Young adult, Child, Hearing Loss, Gene, Genetic Association Studies, Exome sequencing, Genetics, business.industry, General Medicine, medicine.disease, Phenotype, Pedigree, Otorhinolaryngology, Pediatrics, Perinatology and Child Health, Spinocerebellar ataxia, Female, medicine.symptom, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255fa93c196282648250c9bced7a289b
https://doi.org/10.1016/j.ijporl.2017.11.014

المؤلفون: Hossein Najmabadi, Marzieh Mohseni, Niloofar Bazazzadegan, Kimia Kahrizi, Sanaz Arzhangi, Mojgan Babanejad, Masoud Motasaddi Zarandy, Nooshin Nikzat

المصدر: International journal of pediatric otorhinolaryngology. 126

مصطلحات موضوعية: Male, medicine.medical_specialty, Heterozygote, Adolescent, Hearing loss, Hearing Loss, Sensorineural, Iran, Connexins, 03 medical and health sciences, Gjb2 gene, Consanguinity, 0302 clinical medicine, Keratoderma, Palmoplantar, 030225 pediatrics, otorhinolaryngologic diseases, medicine, Humans, 030223 otorhinolaryngology, business.industry, De novo mutation, General Medicine, Sequence Analysis, DNA, medicine.disease, Dermatology, Pedigree, Connexin 26, Palmoplantar keratoderma, Otorhinolaryngology, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Mutation, Sensorineural hearing loss, Female, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7238427478cb31802cbd5364291a144d
https://pubmed.ncbi.nlm.nih.gov/31785923

المؤلفون: Zahra Tahmasebi Fard, Reyhaneh Kameli, Mandana Hasanzad, Seyed Hamid Jamaldini, Mojgan Babanejad, Lotfollah Feizi Barnaji, Atoosa Madadkar, Mahdieh Imeni

المصدر: Research in Molecular Medicine, Vol 4, Iss 4, Pp 38-44 (2016)

مصطلحات موضوعية: lcsh:R5-920, biology, Chemistry, Warfarin dose, Vitamin K Epoxide Reductase Complex Subunit 1, Cytochrome P450, General Medicine, Pharmacology, CYP2C9*3, CYP2C9*2, VKORC1, biology.protein, RFLP, cardiovascular diseases, Warfarin, lcsh:Medicine (General)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34c7ac4e311cfb603f262bb6f1884945
https://doi.org/10.18869/acadpub.rmm.4.4.38

المؤلفون: Mojgan Babanejad, Alireza Ramezani, Mohammad Hossein Jabbarpour Bonyadi, Roham Soheilian, Masoud Soheilian, Hamid-Reza Moein, Mehdi Yaseri

المصدر: International Ophthalmology. 37:1161-1168

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, genetic structures, Single-nucleotide polymorphism, Polymerase Chain Reaction, Gastroenterology, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Humans, Allele, Gene, Aged, Retrospective Studies, Aged, 80 and over, Polymorphism, Genetic, biology, business.industry, C-reactive protein, Elevated crp, DNA, Macular degeneration, medicine.disease, Exudative age-related macular degeneration, eye diseases, Ophthalmology, C-Reactive Protein, 030104 developmental biology, Complement Factor H, Factor H, Wet Macular Degeneration, 030221 ophthalmology & optometry, biology.protein, Female, sense organs, business, Biomarkers, Tomography, Optical Coherence, Follow-Up Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f213450058e762ebd5c5eb5e9b22e3a8
https://doi.org/10.1007/s10792-016-0373-6

المؤلفون: Nooshin Nikzat, Kevin T. Booth, Richard J.H. Smith, Allen C. Simpson, Kimia Kahrizi, Maryam Beheshtian, Reza Mozafari, Fariba Ardalani, Mojgan Babanejad, Farahnaz Sabbagh, Kathy L. Frees, Nicole C. Meyer, Leila Jamali, Zohreh Mehrjoo, Niloofar Bazazzadegan, Sanaz Arzhangi, Hossein Khodaei, Christina M. Sloan-Heggen, Tara Akhtarkhavari, Maryam Taghdiri, Hela Azaiez, Mohammad Farhadi, Marzieh Mohseni, Hasan Otukesh, Seyed Morteza Seifati, Hossein Najmabadi, Saeideh Vaziri, Ahmad Daneshi

المصدر: Journal of Medical Genetics. 52:823-829

مصطلحات موضوعية: MYO15A, medicine.medical_specialty, Hearing loss, Genes, Recessive, Consanguinity, Iran, Biology, Connexins, Article, Gene Frequency, Molecular genetics, otorhinolaryngologic diseases, Genetics, medicine, Humans, Genetic Predisposition to Disease, Hearing Loss, Genetic Association Studies, Genetics (clinical), Massive parallel sequencing, Genetic heterogeneity, Founder Effect, Connexin 26, Medical genetics, medicine.symptom, Founder effect

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73e2cc709ef1b865779bf39e22505b6b
https://doi.org/10.1136/jmedgenet-2015-103389

المؤلفون: Fariba Ardalani, Mojgan Babanejad, Kimia Kahrizi, Kevin T. Booth, Christina M. Sloan, Michael J. Schnieders, Nicole C. Meyer, Sanaz Arzhangi, Hela Azaiez, William T.A. Tollefson, Richard J.H. Smith, Allen C. Simpson, Hossein Najmabadi

المصدر: American Journal of Medical Genetics Part A. 167:2957-2965

مصطلحات موضوعية: Male, Models, Molecular, Heterozygote, Genetic Linkage, Nonsense mutation, Genes, Recessive, Locus (genetics), Deafness, Biology, Compound heterozygosity, Article, Genetic Heterogeneity, symbols.namesake, otorhinolaryngologic diseases, Genetics, Humans, Missense mutation, Hearing Loss, Genetics (clinical), Sanger sequencing, Massive parallel sequencing, Chromosomes, Human, Pair 10, Genetic heterogeneity, Homozygote, Disease gene identification, Pedigree, Haplotypes, Mutation, symbols, Female, Carrier Proteins

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde772d27d5591c410272a5ef00a0659
https://doi.org/10.1002/ajmg.a.37274

المؤلفون: Hossein Najmabadi, Guney Bademci, Aziz El-Amraoui, Kevin T. Booth, Kimia Kahrizi, Mojgan Babanejad, Richard J.H. Smith, Hela Azaiez, Mustafa Tekin, Davood Zare-Abdollahi, Sanaz Arzhangi, Hossein Daghagh, Duygu Duman

المساهمون: University of Iowa [Iowa City], University of Social Welfare and Rehabilitation Sciences [Tehran], University of Miami Leonard M. Miller School of Medicine (UMMSM), Ankara University School of Medicine [Turkey], Génétique et Physiologie de l'Audition, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), This research was supported in part by Iran National Science Foundation. Grant number: 95S47307 to K.K., NIDCD RO1s DC009645 to M.T., DC003544, DC002842 and DC012049 to R.J.S.

المصدر: Clinical Genetics
Clinical Genetics, 2018, 93 (4), pp.812-821. ⟨10.1111/cge.13170⟩

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Hearing loss, Genetic Linkage, Usher syndrome, [SDV]Life Sciences [q-bio], Hearing Loss, Sensorineural, Locus (genetics), Biology, Article, Frameshift mutation, 03 medical and health sciences, 0302 clinical medicine, Loss of Function Mutation, deafness, Genetics, medicine, otorhinolaryngologic diseases, Missense mutation, Humans, Genetic Predisposition to Disease, DFNB48, Frameshift Mutation, Gene, Genetics (clinical), Loss function, Calcium-Binding Proteins, non-syndromic hearing loss, Middle Aged, medicine.disease, Phenotype, CIB2, Pedigree, 030104 developmental biology, USH1J, Female, medicine.symptom, Usher Syndromes, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f56b273bba2ed65eae1cc3b24b69424f
https://europepmc.org/articles/PMC5851821/

المؤلفون: Hamid-Reza Moein, Masoud Soheilian, Mojgan Babanejad, Hossein Najmabadi, Mohammad R. Akbari, Azadeh Badiei, Mehdi Yaseri

المصدر: Ophthalmic Genetics. 37:144-149

مصطلحات موضوعية: Male, 0301 basic medicine, dbSNP, Genotyping Techniques, genetic structures, Single-nucleotide polymorphism, Iran, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Asian People, Gene Frequency, Risk Factors, Geographic Atrophy, Genotype, Humans, Genetic Predisposition to Disease, Allele, Allele frequency, Genetics (clinical), Aged, Aged, 80 and over, Genetics, Middle Aged, eye diseases, Genotype frequency, Ophthalmology, 030104 developmental biology, Case-Control Studies, Complement Factor H, Pediatrics, Perinatology and Child Health, Wet Macular Degeneration, 030221 ophthalmology & optometry, Female, Restriction fragment length polymorphism, Polymorphism, Restriction Fragment Length

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::138d2622aec4696ebf9a9d3a13d5ed56
https://doi.org/10.3109/13816810.2014.955585