OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss
Akram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
Molecular Biology Reports (2020) Vol. 47, Iss. 7, pp. 5355-5364
Closed Access | Times Cited: 12
Akram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
Molecular Biology Reports (2020) Vol. 47, Iss. 7, pp. 5355-5364
Closed Access | Times Cited: 12
Showing 12 citing articles:
A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family
Akram Sarmadi, Samaneh Adelian, Zahra Nouri, et al.
Egyptian Journal of Medical Human Genetics (2025) Vol. 26, Iss. 1
Open Access
Akram Sarmadi, Samaneh Adelian, Zahra Nouri, et al.
Egyptian Journal of Medical Human Genetics (2025) Vol. 26, Iss. 1
Open Access
A novel method for detecting nine hotspot mutations of deafness genes in one tube
Yang Yu, Jun Zhang, Yuxia Zhan, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Yang Yu, Jun Zhang, Yuxia Zhan, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 1
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 1
Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study
Shahrzad Aghaei, Sepideh Parvizpour, Effat Farrokhi, et al.
Journal of Biomolecular Structure and Dynamics (2022) Vol. 41, Iss. 19, pp. 9850-9864
Closed Access | Times Cited: 5
Shahrzad Aghaei, Sepideh Parvizpour, Effat Farrokhi, et al.
Journal of Biomolecular Structure and Dynamics (2022) Vol. 41, Iss. 19, pp. 9850-9864
Closed Access | Times Cited: 5
Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients
Ying Fu, Shasha Huang, Xue Gao, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Ying Fu, Shasha Huang, Xue Gao, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Hearing Features and Cochlear Implantation Outcomes in Patients With PathogenicMYO15AVariants: a Multicenter Observational Study
Pey‐Yu Chen, Cheng‐Yu Tsai, Jiunn‐Liang Wu, et al.
Ear and Hearing (2021) Vol. 43, Iss. 4, pp. 1198-1207
Closed Access | Times Cited: 5
Pey‐Yu Chen, Cheng‐Yu Tsai, Jiunn‐Liang Wu, et al.
Ear and Hearing (2021) Vol. 43, Iss. 4, pp. 1198-1207
Closed Access | Times Cited: 5
Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Neuromuscular Disorders (2022) Vol. 32, Iss. 9, pp. 776-784
Closed Access | Times Cited: 3
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Neuromuscular Disorders (2022) Vol. 32, Iss. 9, pp. 776-784
Closed Access | Times Cited: 3
Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non‐syndromic hearing loss
Luming Wang, Yue Zhang, Qiuxia Xue, et al.
Journal of Clinical Laboratory Analysis (2022) Vol. 36, Iss. 10
Open Access | Times Cited: 3
Luming Wang, Yue Zhang, Qiuxia Xue, et al.
Journal of Clinical Laboratory Analysis (2022) Vol. 36, Iss. 10
Open Access | Times Cited: 3
Clinical and molecular analysis of a novel variant responsive to salbutamol monotherapy during COVID-19 outbreak related to congenital and late-onset of myasthenic syndrome in large kindred
Zahra Nouri, Javad Saffari-Chaleshtori, Akram Sarmadi, et al.
Research Square (Research Square) (2024)
Open Access
Zahra Nouri, Javad Saffari-Chaleshtori, Akram Sarmadi, et al.
Research Square (Research Square) (2024)
Open Access
Genetic analysis of TRIOBP and MYO15A variants in Iranian families with autosomal recessive non-syndromic hearing loss
Nasrin Azizi, Hamid Reza Khorram Khorshid, Kimia Kahrizi, et al.
Human Gene (2024) Vol. 42, pp. 201331-201331
Closed Access
Nasrin Azizi, Hamid Reza Khorram Khorshid, Kimia Kahrizi, et al.
Human Gene (2024) Vol. 42, pp. 201331-201331
Closed Access
Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees
Samane Nasrniya, Paniz Miar, Sina Narrei, et al.
Laboratory Medicine (2021) Vol. 53, Iss. 2, pp. 111-122
Closed Access | Times Cited: 2
Samane Nasrniya, Paniz Miar, Sina Narrei, et al.
Laboratory Medicine (2021) Vol. 53, Iss. 2, pp. 111-122
Closed Access | Times Cited: 2
Analysis of Genetic Variations in Connexin 26 (GJB2) Gene among Nonsyndromic Hearing Impairment: Familial Study
Smita Hegde, Rajat Hegde, Suyamindra S. Kulkarni, et al.
Global Medical Genetics (2022) Vol. 09, Iss. 02, pp. 152-158
Open Access | Times Cited: 1
Smita Hegde, Rajat Hegde, Suyamindra S. Kulkarni, et al.
Global Medical Genetics (2022) Vol. 09, Iss. 02, pp. 152-158
Open Access | Times Cited: 1
