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Shuba Krishna

Observed name: Shuba krishna
OpenAlex ID: A5112428968
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
2014 · Catherine A Brownstein, Alan H Beggs, et al. · Genome biology · 435
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Transcriptional regulation of osteopontin and the metastatic phenotype: Evidence for a Ras-activated enhancer in the human OPN promoter
2003 · David T. Denhardt, Devra Mistretta, et al. · Clinical & Experimental Metastasis · 102
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Recurrent and novel GLB1 mutations in India
2015 · Abdul Mueed Bidchol, Ashwin Dalal, et al. · Gene · 25
Identification of Novel Mutations inABCA4Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease
2015 · Rajani Battu, Anshuman Verma, et al. · BioMed Research International · 25
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Identification of a novel glucokinase mutation in an Indian woman with GCK-MODY
2016 · Sujeet Jha, Samreen Siddiqui, et al. · The Lancet Diabetes & Endocrinology · 9
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Assessment of a Highly Curated Somatic Oncology Database to Aid in the Interpretation of Clinically Important Variants in Next-Generation Sequencing Results
2020 · Stephanie J. Yaung, Shuba Krishna, et al. · Journal of Molecular Diagnostics · 8
Abstract 5456: Clinical validation of NAVIFY® Mutation Profiler for solid tumor NGS variant interpretation
2020 · Sidney Alexander Scudder, Anoop Grewal, et al. · Cancer Research · 8
Clinical and genetic analysis of Indian patients with NDP-related retinopathies
2017 · Dhandayuthapani Sudha, Aparna Ganapathy, et al. · International Ophthalmology · 8
Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss
2016 · Dhandayuthapani Sudha, Irene Rosita Pia Patric, et al. · Ophthalmic Genetics · 5
Comparing Classifications from Multiple Variant Annotation Software Solutions Using Real-World Next Generation Sequencing Data from Oncology Testing
2024 · Roy Khalife, Tara M. Love, et al. · Journal of Molecular Pathology · 3
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Abstract 249: Comparison of variant classification between molecular diagnostics experts and decision support software
2021 · Stephanie J. Yaung, Shuba Krishna, et al. · Cancer Research · 1
Abstract 169: Ephesus - A curated content knowledgebase for the clinical interpretation of genomic variants
2021 · Jian Li, Lili Niu, et al. · Cancer Research · 1
Evaluation of Navify Mutation Profiler Tertiary Analysis Software Assessing for Hematologic Malignancies
2025 · Ruby Singhrao, Michael J. Clark, et al. · Journal of Molecular Pathology
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Abstract 2351: Genomics annotation and interpretation in somatic oncology using structured data from a clinical knowledgebase
2024 · Jian Li, Lili Niu, et al. · Cancer Research
Abstract 5236: Clinical evaluation of somatic genomic alteration annotation for hematological malignancies using tertiary analysis software
2022 · Ruby Singhrao, Lisha Capucion, et al. · Cancer Research
Ephesus: A curation workflow tool for the clinical interpretation of genomic variants.
2020 · Jian Li, Lili Niu, et al. · Journal of Clinical Oncology
Works count: 17
Citation count: 630
H-index: 8
I10-index: 4
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