Kandarp Joshi

ORCID: 0000-0002-2153-0110
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About
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Research Areas
  • RNA modifications and cancer
  • Cancer-related molecular mechanisms research
  • Genomics and Phylogenetic Studies
  • Eating Disorders and Behaviors
  • Circular RNAs in diseases
  • Genomics and Rare Diseases
  • MicroRNA in disease regulation
  • RNA Research and Splicing
  • Pregnancy and preeclampsia studies
  • Child Nutrition and Feeding Issues
  • Mycobacterium research and diagnosis
  • interferon and immune responses
  • Berberine and alkaloids research
  • Cancer-related gene regulation
  • Adolescent and Pediatric Healthcare
  • Tuberculosis Research and Epidemiology
  • Molecular Biology Techniques and Applications
  • Epigenetics and DNA Methylation
  • RNA and protein synthesis mechanisms
  • Biomedical Text Mining and Ontologies
  • Ferroptosis and cancer prognosis
  • Genetic Associations and Epidemiology
  • Inflammasome and immune disorders
  • Sodium Intake and Health
  • Genomics, phytochemicals, and oxidative stress

Johns Hopkins University
2023-2025

Johns Hopkins All Children's Hospital
2023-2025

Sidney Kimmel Comprehensive Cancer Center
2023-2025

Kyoto University
2021-2024

Johns Hopkins Medicine
2023

RIKEN Center for Biosystems Dynamics Research
2022

NHS Grampian
2019-2021

University of Aberdeen
2019-2021

City Hospital
2021

Institute of Genomics and Integrative Biology
2013-2021

With the advent of next-generation sequencing, large-scale initiatives for mining whole genomes and exomes have been employed to better understand global or population-level genetic architecture. India encompasses more than 17% world population with extensive diversity, but is under-represented in sequencing datasets. This gave us impetus perform analyze genome 1029 healthy Indian individuals under pilot phase 'IndiGen' program. We generated a compendium 55,898,122 single allelic variants...

10.1093/nar/gkaa923 article EN cc-by-nc Nucleic Acids Research 2020-10-22

Recent studies suggest that long non-coding RNAs (lncRNAs) contribute to medulloblastoma (MB) formation and progression. We have identified an lncRNA, lnc-HLX-2-7, as a potential therapeutic target in group 3 (G3) MBs. lnc-HLX-2-7 RNA specifically accumulates the promoter region of HLX, sense-overlapping gene which activates HLX expression by recruiting multiple factors, including enhancer elements. sequencing chromatin immunoprecipitation reveal binds promoters several oncogenes, TBX2,...

10.1016/j.celrep.2024.113938 article EN cc-by-nc Cell Reports 2024-03-01

31 Background: Prostate Cancer (PCa) is one of the leading causes cancer deaths among men worldwide. Although Prostate-Specific Antigen (PSA) test widely used for screening, several advisory groups recommend against PSA because its non-specific and suboptimal performance. Hence, there an urgent unmet need novel more accurate biomarker panels PCa detection. Methods: To develop alternate assay, we collected voided urine (50 ml) from 236 pre- 198 matched post-prostatectomy with PCa, 76 benign...

10.1200/jco.2025.43.5_suppl.31 article EN Journal of Clinical Oncology 2025-02-10

The field of epitranscriptomics is undergoing a technology-driven revolution. During past decades, RNA modifications like N6-methyladenosine (m6A), pseudouridine (ψ), and 5-methylcytosine (m5C) became acknowledged for playing critical roles in cellular processes. Direct sequencing by Oxford Nanopore Technologies (ONT) enabled the detection native RNA, detecting noncanonical nucleosides properties raw data. Consequently, field's cutting edge has heavy component computer science, opening new...

10.1038/s42004-025-01507-0 article EN cc-by Communications Chemistry 2025-04-12

With a higher throughput and lower cost in sequencing, second generation sequencing technology has immense potential for translation into clinical practice the realization of pharmacogenomics based patient care. The systematic analysis whole genome sequences to assess variability pharmacokinetics pharmacodynamics responses towards drugs would be next step future medicine line with vision personalizing medicine.

10.1371/journal.pone.0071554 article EN cc-by PLoS ONE 2013-08-23

The human mitochondrial genome has been reported to have a very high mutation rate as compared with the nuclear genome. A large number of mutations show significant phenotypic association and are involved in broad spectrum diseases. In recent years, there remarkable progress understanding genetics. availability next-generation sequencing (NGS) technologies not only reduced cost by orders magnitude but also provided us good quality sequences coverage, thereby enabling decoding this study, we...

10.1002/humu.22767 article EN Human Mutation 2015-02-13

Mycobacterium tuberculosis, along with closely related species, commonly known as M. tuberculosis complex (MTBC), causes in humans and other organisms. Tuberculosis is a disease high morbidity mortality, especially the third world. The genetic variability between clinical isolates of MTBC has been poorly understood, although recent years have seen re-sequencing large number from around availability genomic data multiple public domain would potentially offer unique opportunity toward...

10.1093/database/bat083 article EN cc-by Database 2014-01-01

Abstract Long noncoding RNA s (lnc s) are a recently discovered class of functional encoded by metazoan genomes. Recent studies suggest larger regulatory role for lnc in critical biological and disease processes. Mounting evidence on the regulating key processes immune system prompted us to hypothesize as regulators pathophysiology Sjögren's syndrome ( SS ). We used two similar approaches based reanalysis microarray expression datasets curation ‐protein coding gene interactions from...

10.1111/1756-185x.12752 article EN International Journal of Rheumatic Diseases 2015-09-30

One of the most common RNA modifications found in mammalian brain is N6-methyladenosine (m6A) and this modification has been implicated fine-tuning neuronal gene expression by regulating metabolism with consequent impact on function behaviour. The presence, absence, overall influence m6A any given transcript governed so-called machinery genes include 'writers', 'erasers' 'readers.' Changes functional pathophysiology major depression (MD) its consequence mediated regulation not explored. To...

10.1016/j.psycom.2022.100089 article EN cc-by-nc-nd Psychiatry Research Communications 2022-11-25

Abstract Recent technological advances in sequencing DNA and RNA modifications using high-throughput platforms have generated vast epigenomic epitranscriptomic datasets whose power transforming life science is yet fully unleashed. Currently available silico methods facilitated the identification, positioning quantitative comparisons of individual modification sites. However, essential challenge to link specific ‘epi-marks’ gene expression particular context cellular biological processes...

10.1093/bib/bbad521 article EN public-domain Briefings in Bioinformatics 2024-01-22

Pregnancy is a special condition where many metabolic changes may occur because of increased requirement essential micronutrients such as iron and iodine. Foetal thyroid starts producing its own hormones after 12 weeks gestation. Therefore, the first trimester very crucial for meeting hormone requirements mother foetus. Iodine deficiency affect mental physical growth Hence, it important to establish programme on screening pregnant women dysfunction tests along with established status...

10.1017/s2040174413000470 article EN Journal of Developmental Origins of Health and Disease 2013-11-27

Background Evidence suggests that investing in specialist eating disorders services for young people with anorexia nervosa could have important implications the NHS, potential to improve health outcomes and reduce costs through reductions number length of hospital admissions. Objectives The primary objectives were evaluate cost-effectiveness alternative community-based models service provision model impact changes services. Design Observational surveillance study using Child Adolescent...

10.3310/hsdr07370 article EN publisher-specific-oa Health Services and Delivery Research 2019-10-01

We describe here the draft genome sequence of Sporosarcina pasteurii, a urease-producing bacterium with potential applications in biocement production.

10.1128/genomea.01256-13 article EN Genome Announcements 2014-01-31

Abstract The prognosis of childhood medulloblastoma (MB) is often poor, and it usually requires aggressive therapy that adversely affects quality life. microRNA-211 (miR-211) was previously identified as an important regulator cells descend from neural cells. Since medulloblastomas primarily affect with similar ontogeny, we investigated the role mechanism miR-211 in MB. Here showed expression highly downregulated cell lines, PDXs, clinical samples different MB subgroups (SHH, Group 3, 4)...

10.1186/s40478-023-01684-w article EN cc-by Acta Neuropathologica Communications 2023-12-19

Medulloblastoma, the most common malignant pediatric brain tumor, is classified into four main molecular subgroups, but group 3 and 4 tumors are difficult to subclassify have a poor prognosis. Rapid point-of-care diagnostic prognostic assays needed improve medulloblastoma risk stratification management. N6-methyladenosine (m6A) RNA modification long non-coding RNAs (lncRNAs) play central role in tumor progression, their impact on gene expression associated clinical outcomes unknown. Here we...

10.1186/s40478-024-01848-2 article EN cc-by Acta Neuropathologica Communications 2024-08-28

A large repertoire of gene-centric data has been generated in the field zebrafish biology. Although bulk these are available public domain, most them not readily accessible or nonstandard formats. One major challenge is to unify and integrate widely scattered sources. We tested hypothesis that active community participation could be a viable option address this challenge. present here our approach create standards for assimilation sharing information system open database intercommunication....

10.1093/database/bau011 article EN Database 2014-02-26

Aim: Numerous drugs are being widely prescribed for COVID-19 treatment without any direct evidence the drug safety/efficacy in patients across diverse ethnic populations. Materials & methods: We analyzed whole genomes of 1029 Indian individuals (IndiGen) to understand extent drug–gene (pharmacogenetic), drug–drugand drug–drug–gene interactions ;associated with therapy population. Results: identified 30 clinically significant pharmacogenetic variants and 73 predicted deleterious variants....

10.2217/pgs-2021-0028 article EN Pharmacogenomics 2021-06-18

Evidence suggests specialist eating disorders services for children and adolescents with anorexia nervosa have the potential to improve outcomes reduce costs through reduced hospital admissions. This study aimed evaluate cost-effectiveness of assessment diagnosis in community-based child adolescent mental health (CAMHS) compared generic CAMHS nervosa. Observational, surveillance aged 8 17, contact UK or Republic Ireland a first episode Data were reported by clinicians at baseline, 6...

10.1186/s40337-021-00433-5 article EN cc-by Journal of Eating Disorders 2021-06-26

Abstract BACKGROUND Medulloblastoma (MB) is the predominant pediatric brain tumor, subdivided into four molecular subgroups, with group 3 and 4 tumors posing significant clinical challenges due to poor prognosis classification. This study investigates roles of N6-methyladenosine (m6A) long non-coding RNAs (lncRNAs) in MB, aiming develop diagnostic prognostic tools. METHODS We analyzed transcriptome from 1236 samples identify m6A-associated lncRNA signature (M6LSig). A multivariate-cox...

10.1093/neuonc/noae064.519 article EN cc-by-nc Neuro-Oncology 2024-06-18

Abstract Recent studies suggest that long non-coding RNAs (lncRNAs) contribute to medulloblastoma formation and progression. We have identified a lncRNA, lnc-HLX-2-7, as potential therapeutic target in group 3 (G3) medulloblastomas. lnc-HLX-2-7 RNA specifically accumulates the promoter region of HLX, its host gene, which activates HLX expression by recruiting multiple factors, including enhancer elements. sequencing chromatin immunoprecipitation reveal binds promoters several oncogenes,...

10.1093/neuonc/noae064.450 article EN cc-by-nc Neuro-Oncology 2024-06-18

<title>Abstract</title> Medulloblastoma, the most common malignant pediatric brain tumor, is classified into four main molecular subgroups, but group 3 and 4 tumors are difficult to subclassify have a poor prognosis. Rapid point-of-care diagnostic prognostic assays needed improve medulloblastoma risk stratification management. N6-methyladenosine (m6A) RNA modification long non-coding RNAs (lncRNAs) play central role in tumor progression, their impact on gene expression associated clinical...

10.21203/rs.3.rs-4810070/v1 preprint EN cc-by Research Square (Research Square) 2024-09-02
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