Aravind Kumar Bandari, PhD

Title(s)Postdoctoral Scholar, Dermatology
SchoolSchool of Medicine
Address2340 Sutter Street
San Francisco CA 94115
Phone--
ORCID ORCID Icon0000-0001-6786-520X Additional info
vCardDownload vCard

    Collapse Biography 
    Collapse Education and Training
    Institute of Bioinformatics, Bangalore, IndiaPh.D.10/2020Biomedical Sciences
    Osmania University, Hyderabad, IndiaM.Sc06/2012Genetics
    Osmania University, Hyderabad, IndiaB.Sc06/2010Biomedical Sciences
    Collapse Awards and Honors
    Manipal Academy of Higher educationPh.D  - 10/2Aravind Kumar Bandari

    Collapse Overview 
    Collapse Overview
    Dr. Aravind Kumar Bandari completed his Ph.D. studies at the Institute of Bioinformatics in Bangalore and obtained his Ph.D. Degree from Manipal Academy of Higher Education in Manipal. His thesis was focussed on the genomics of inherited immune disorders using next generation sequencing. Post Ph.D., he was involved in exploring genomic and proteomics approaches to improve diagnostic and therapeutic options for infectious disease -Tuberculosis. At UCSF, He is currently involved in studying molecular and genetic alterations in skin cancer.

    Collapse Featured Content 
    Collapse Twitter

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    Altmetrics Details 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. A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability. Front Psychiatry. 2020; 11:354. Muthusamy B, Bellad A, Prasad P, Bandari AK, Bhuvanalakshmi G, Kiragasur RM, Girimaj SC, Pandey A. PMID: 32499722; PMCID: PMC7247441.
      View in: PubMed   Mentions: 2  
    2. A Novel Missense Variant in PHF6 Gene Causing Börjeson-Forssman-Lehman Syndrome. J Mol Neurosci. 2020 Sep; 70(9):1403-1409. Bellad A, Bandari AK, Pandey A, Girimaji SC, Muthusamy B. PMID: 32399860.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    3. A Novel Splice Site Mutation in IFNGR2 in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases. Front Immunol. 2019; 10:1964. Bandari AK, Muthusamy B, Bhat S, Govindaraj P, Rajagopalan P, Dalvi A, Shankar S, Raja R, Reddy KS, Madkaikar M, Pandey A. PMID: 31497017; PMCID: PMC6712061.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    4. Family-Based Next-Generation Sequencing Study Identifies an IL2RG Variant in an Infant with Primary Immunodeficiency. OMICS. 2019 May; 23(5):285-290. Bandari AK, Bhat S, Archana MV, Yadavalli S, Patel K, Rajagopalan P, Madugundu AK, Madkaikar M, Reddy K, Muthusamy B, Pandey A. PMID: 31100039; PMCID: PMC6534087.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. Exome sequencing reveals a novel splice site variant in HUWE1 gene in patients with suspected Say-Meyer syndrome. Eur J Med Genet. 2020 Jan; 63(1):103635. Muthusamy B, Nguyen TT, Bandari AK, Basheer S, Selvan LDN, Chandel D, Manoj J, Gayen S, Seshagiri S, Chandra Girimaji S, Pandey A. PMID: 30797980; PMCID: PMC6974397.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells