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Ali Hosseini Bereshneh

TitlePostdoc Fellows and Associates
InstitutionBaylor College of Medicine
DepartmentPostDoc
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Hosseini Bereshneh A, Rezaei Z, Jafarinia E, Rajabi F, Ashrafi MR, Tavasoli AR, Garshasbi M. Crystallographic modeling of the PNPT1:c.1453A>G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical features. Mitochondrion. 2021 07; 59:1-7. PMID: 33812062.
      Citations:    Fields:    Translation:HumansCells
    2. Zamani G, Hosseini Bereshneh A, Azizi Malamiri R, Bagheri S, Moradi K, Ashrafi MR, Tavasoli AR, Mohammadi M, Badv RS, Ghahvechi Akbari M, Heidari M. The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations. J Mol Neurosci. 2020 Oct; 70(10):1565-1573. PMID: 32436198.
      Citations: 1     Fields:    Translation:Humans
    3. Hosseini Bereshneh A, Hosseipour S, Rasoulinezhad MS, Pak N, Garshasbi M, Tavasoli AR. Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8. Eur J Med Genet. 2020 May; 63(5):103868. PMID: 32004679.
      Citations:    Fields:    Translation:Humans
    4. Hosseini Bereshneh A, Garshasbi M. Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report. J Med Case Rep. 2018 Sep 25; 12(1):281. PMID: 30249282; PMCID: PMC6154911.
      Citations: 2     Fields:    Translation:Humans
    5. Hosseini Bereshneh A, Morshedi F, Hematyar M, Kaki A, Garshasbi M. Pharmacogenetics and Personalized Medicine in Pancreatic Cancer. Acta Med Iran. 2017 Mar; 55(3):194-199. PMID: 28282719.
      Citations: 1     Fields:    Translation:Humans
    6. Salmaninejad A, Zamani MR, Pourvahedi M, Golchehre Z, Hosseini Bereshneh A, Rezaei N. Cancer/Testis Antigens: Expression, Regulation, Tumor Invasion, and Use in Immunotherapy of Cancers. Immunol Invest. 2016 Oct; 45(7):619-40. PMID: 27603913.
      Citations: 65     Fields:    Translation:HumansAnimalsCells
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