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Gholipoorfeshkecheh, R. and Swati Agarwala and Santhosh, K. and Savitha, M. R. and Narayanappa, D. and Ramachandra, N. B. (2020) Nuclear Co-repressor 1: A Potential Candidate Gene in the Manifestation of Congenital Heart Diseases. International Journal of Human Genetics, 20 (2). pp. 55-65. ISSN 2456-6330
Gholipoorfeshkecheh, R. and Agarwala, S. and Krishnappa, S. and Savitha, M. R. and Narayanappa, D. and Ramachandra, N. B. (2020) Variants in HEY genes manifest in ventricular septal defects of congenital heart disease. Gene Reports, 19.
Gholipoorfeshkecheh, R. and Agarwala, S. and Kavya, G. and Krishnappa, S. and Savitha, M. R. and Ramachandra, N. B. (2020) Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects. Egyptian Journal of Medical Human Genetics, 21 (1).
Dinesh, S. M. and Lingaiah, K. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (10). pp. 715-720.
Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (7-8). pp. 483-487.
Mahdi, Bijanzadeh and Mahesh, P. A. and Savitha, M. R. and Pradeep Kumar, B. S. and Jayaraj and Ramachandra, N. B. (2010) Inheritance patterns, consanguinity & risk for asthma. Indian Journal of Heterocyclic Chemistry, 132 (1). pp. 48-55. ISSN 0971-1627
Dinesh, S. M. and Kusuma, L. and Smitha, R. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2010) Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India. Genetic Testing and Molecular Biomarkers, 14 (6). pp. 873-879. ISSN 1945-0257
Bijanzadeh, Mahdi and Ramachandra, N. B. and Mahesh, P. A. and Savitha, M. R. and Manjunath, B. S. and Jayaraj, B. S. (2009) Lack of association between asthma and ABO blood group. LUNG, 187 (6). pp. 389-392. ISSN 1432-1750
Bijanzadeh, Mahdi and Ramachandra, N. B. and Mahesh, P. A. and Savitha, M. R. and Vijayakumar, G. S. and Pradeep Kumar and Manjunath, B. S. and Jayaraj, B. S. (2009) Soluble intercellular adhesion molecule-1 and e-selectin in patients with asthma exacerbation. LUNG, 187 (5). pp. 315-320. ISSN 1432-1750
Smitha, R. and Savitha, M. R. and Krishnamurthy, Balasundaram and Doddaiah, Narayanappa and Prasanth, S. N. and Ramachandra, N. B. (2007) Association between pericentric inversion in chromosome 9 and congenital heart defects. International Journal of Human Genetics, 7 (3). pp. 241-248. ISSN 0972-3757
Savitha, M. R. and Krishnamurthy, B. and Ashok, D. A. and Ramachandra, N. B. (2007) Self abortion of attacks in patients with hot water epilepsy. Indian Pediatrics, 44 (4). p. 298. ISSN 0974-7559
Smitha, R. and Harshavardhan Gawde, M. and Hyderi, Abbas and Savitha, M. R. and Patel, Zareen M. and Krishnamurthy, Balasundaram and Ramachandra, N. B. (2006) De novo isochromosome 18p in a female dysmorphic child. Journal of Applied Genetics, 47 (4). pp. 397-401. ISSN 2190-3883
