• CTLA‐4 Gene Polymorphism in Pediatric Type 1 Diabetes Mellitus: A Case–Control Study 

  Thammineni Aniketh, Raghavendra Gobbur, Gurushantappa S. Kadakol (BLDE ( DEEMED TO BE UNIVERSITY), 2026-05)

  Objective: To analyze the relationship between CTLA‐4 (+49A/G) polymorphism and pediatric type 1 diabetes mellitus (T1DM). Materials and Methods: The observational case–control study was done for 18 months in 44 children ...
• Mutation Analysis of Hemoglobin Subunit Beta (HBB) Gene in Beta-Thalassemia Patients in North Karnataka Population 

  Shweta Mathapati, Darshana Shah, S V Patil, Prachi Parvatikar, Gurushantappa Kadakol (BLDE ( DEEMED TO BE UNIVERSITY), 2026-07)

  Introduction: Beta-thalassemia is among the most frequent monogenic disorders around the globe. Over 100,000 children worldwide require regular transfusion due to beta-thalassemia, with India accounting for about 10% of ...
• Sustainable Fabrication of Onion-Peel Biogenic Silica Nanoparticles for Multimodal Characterization and In Vitro Bioactivity Profiling 

  Sphoorty Hungund, Raghunandan Deshpande, Arun K. Shettar, Gurushantappa Kadakol (BLDE ( DEEMED TO BE UNIVERSITY), 2026-04)

  Abstract: Introduction: This study aims to develop a sustainable method for synthesizing Biogenic Silica Nanoparticles (bSNPs) from onion peel waste and evaluate their physicochemical properties and in vitro bioactivit ...
• Consumption of hyperlipidemic diet and water intake in albino rats treated with eclipta alba. 

  Satheesh Naik K, Ramanath B, Bheemshetty S Patil, Sadhu Lokanadham. (2023)
• Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson’s Disease in the North Karnataka Population. 

  Rudragouda Bulagouda, Smita Hegde, Rajat Hegde, Ashwini Hiremath, G M Wali, Gurushantappa S Kadakol. (2023)
• Play dough as a teaching tool in the development of cardiovascular system for small group teaching. 

  Ashwini Balasaheb Nuchhi, Sandhya Vikas Yatagiri, Veena Srinivas Harwalkar, Rudragouda S Bulagouda. (2023)
• Comparison of the efficacy of dexmedetomidine and fentanyl as adjuvants to bupivacaine in arthroscopic knee surgeries. 

  Anusha Suntan, Basavaraj Patil, Deepa S D, Nirmala Devi Kagalkar, Vidya Patil, Sridevi Mulimani. (2023)
• Variations in the branching pattern of coeliac trunk: A cadaveric case series. 

  Sandhya Vikas Yatagiri, Ashwini Balasaheb Nuchhi, Veena Srinivas Harwalkar, Ravi Siddanagouda Bulagouda. (2023)
• Multiple Tortuous Arteries in Thoracic and Abdominal Walls: A Cadaveric Case Report. 

  Sandhya Vikas Yatagiri, Ashwini Balasaheb Nuchhi, Veena Srinivas Harwalkar, Ravi Siddanagouda Bulagouda. (2022)
• Anthropometry of Transfusion-Dependent Thalassemia Major Children and its Correlation with Pretransfusion Hemoglobin and Serum Ferritin: An Observational Study. 

  Veena S Harwalkar, T P Kulkarni, M M Patil, S S Kalyanshettar, Siddu Charki, R S Bulagouda. (2023)
• Early Triggers of a High-fat Diet on Glomerular Integrity. Acta Scientific Anatomy. 1(8): 1-3, 2022. 

  Bheemshetty S Patil, Pallavi S Kanthe. (2022)
• Writing Publishable Qualitative Scientific Research. 

  Ishwar Bagoji. (2018)
• Morphological Study on Fissures of Lungs in North Karnataka Population. 

  Qureshi MK, Bulagouda R S, Bagoji I B. (2021)
• Authors’ reply: Feedback to the Commentary on “Anatomical Variations of the Suprascapular Notch and its Importance in Suprascapular Entrapment Neuropathy” 

  Ishwar Bagoji, G A Hadimani, Ambadasu Bharatha. (2021)
• Comparative Study of Foramen Magnum in Dry Cadaveric Skulls and Computerized Tomography Images in North Interior Part of Karnataka Region. 

  Mohammad Tahir K Qureshi, Ishwar B Bagoji, R S Bulagouda, Gavishiddappa A Hadimani, M Lakshmi Narayan, Anand V Nimbal. (2022)
• Analysis of Genetic Variations in Connexin 26 (GJB2) Gene among Nonsyndromic Hearing Impairment: Familial Study. 

  Smita Hegde, Rajat Hegde, Suyamindra S Kulkarni, Kusal K Das, Pramod B Gai, Rudragouda S Bulagouda. (2022)
• Human homeostatic iron regulator gene polymorphism in autistic population of India; a case-control study 

  Hegde, Rajat; Hegde, Smita; Kulkarni, Suyamindra S.; Pandurangi, Aditya; Das, Kusal K. (BLDE(DU), 2022)

  Background: Autism is a heterogeneous neurodevelopmental disorder. Human homeostatic iron regulator (HFE) codes for HFE protein. HFE protein is very essential for inhibitory regulation of the endocytosis of iron. ...
• Clinical & Cytological Study on Klinefelter Syndrome 

  Biradar, Siddanagouda M; Bulagouda, Rudragouda S; Kadakol, Gurushantappa (BLDE( Deemed to be University), 2022)

  Klinefelter Syndrome is a chromosomal disorder with addition of X sex chromosome (47XXY) in males. A patient attended to our hospital with loss of secondary sexual characteristics and male infertility. Physical examination ...
• Molecular Cytogenetic Analysis of Congenital Heart Defects Children with Down syndrome. 

  Bheemshetty Patil, Rudragouda S Bulagouda, Gurushantappa S Kadakol. (2021)
• Molecular Analysis of HPV 16 and 18 in Saliva of the Patients with Oral Squamous Cell Carcinoma & Carcinoma of Cervix. 

  Gurushantappa S Kadakol, Rudragouda Bulagouda, Bheemshetty Patil. (2021)

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