Aravind Kumar Bandari, PhD
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| Title(s) | Postdoctoral Scholar, Dermatology |
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| School | School of Medicine |
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| Address | 2340 Sutter Street
San Francisco CA 94115
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| Phone | -- |
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ORCID
.gif) | 0000-0001-6786-520X  |
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| vCard | Download vCard |
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Biography
| Institute of Bioinformatics, Bangalore, India | Ph.D. | 10/2020 | Biomedical Sciences |
| Osmania University, Hyderabad, India | M.Sc | 06/2012 | Genetics |
| Osmania University, Hyderabad, India | B.Sc | 06/2010 | Biomedical Sciences |
| Manipal Academy of Higher education | Ph.D
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| 10/2 | Aravind Kumar Bandari |
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.
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Bibliographic
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.
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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.
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PubMed Mentions:
3
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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.
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PubMed Mentions:
5 Fields:
Translation:
HumansCells
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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.
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PubMed Mentions:
9 Fields:
Translation:
HumansCells
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Family-Based Next-Generation Sequencing Study Identifies an IL2RG Variant in an Infant with Primary Immunodeficiency. OMICS. 2019 05; 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.
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PubMed Mentions: Fields:
Translation:
Humans
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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.
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PubMed Mentions:
9 Fields:
Translation:
HumansCells
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| Year | Publications |
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| 2019 | 3 |
| 2020 | 2 |
This graph shows the number and percent of publications by field.
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This graph shows the number and percent of publications by field.
Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications.
Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written.
To see the data as text,
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