Items where Subject is "B Life Science > Genetics and Genomics"

A

Ashitha, S. N. and Avinash, M. V. and Ramachandra, N. B. (2017) Whole exome sequencing of discordant diseases in Monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and epileptic seizures. Meta Gene, 12. 134 - 137. ISSN 2214-5400

Ashitha, S. N. and Ramachandra, N. B. (2020) Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders. Neuroscience, 438. pp. 25-40. ISSN 1873-7544

Avinash, M. V. and Prakash, P. and Ramachandra, N. B. (2016) Copy number variation of UGT 2B genes in Indian families using whole genome scans. Journal of Nucleic Acids. ISSN 2090-021X

Avinash, M. V. and Saldanha, Marita and Prakash, P. and Ramachandra, N. B. (2014) Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165 (7). pp. 572-580. ISSN 1552-485X

C

Chaithra, S. and Agarwala, Swati and Ramachandra, N. B. (2022) High-risk genes involved in common septal defects of congenital heart disease. Gene, 840. ISSN 1879-0038

Chowdanayaka, Rajanikanth and Ramachandra, N. B. (2021) Rapid Divergence of Key Spermatogenesis Genes in nasuta-Subgroup of Drosophila. Journal of Molecular Evolution, 90. pp. 2-16.

D

Dhanesh, M. and Anitha, A. P. and Suresh, A. P. and Shyamala, K. C. and Chandrasekar, Adimoolam and Ashitha, S. N. M. and Srividhya, Dhurbagula and Sridevi, T. and Pardhanandana Reddy Pengaluru (2019) Association of AVPR1A gene microsatellites with autism spectrum disorder in south Indian population. International Journal of Scientific Research in Biological Sciences, 6 (1). pp. 203-207. ISSN 2347-7520

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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).

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 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

H

Hemavathi, C. and Shobha Jagannath (2004) Air pollution effects on pigment content of two avenue trees in Mysore City. Pollut. Res., 23. pp. 307-309.

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Jahromi, Sareh Raeiszadeh and Mahesh, P. A. and Jayaraj, B. S. and Madhunapantula, Subba Rao V. and Amrutha, D. Holla and Sangeetha, V. and Ramachandra, N. B. (2014) Serum levels of IL-10, IL-17F and IL-33 in patients with asthma: a case–control study. Journal of Asthma, 51 (10). pp. 1004-1013. ISSN 1532-4303

K

Keshava, M. and Shyamala, B. and Reichert, Heinrich and Rodrigues, Veronica (2010) Comparative Analysis of Olfactory System Organization in Flies and Social Hymenopterans. Journal of Neurogenetics, 24. p. 31. ISSN 0167-7063,

Koushik, P. and DSouza, S. M. and Ramachandra, N. B. (2021) De novo assembly, annotation and gene expression profiles of gonads of Cytorace-3, a hybrid lineage of Drosophila nasuta nasuta and D. n. albomicans. Genomics and Informatics, 19 (1). pp. 1-12. ISSN 2234-0742

Kundu, Satyajit and Rejwana, Najneen and Al Banna, Md. Hasan and Kawuki, Joseph and Ghosh, Susmita and Alshahrani, Najim Z. and Dukhi, Natisha and Kundu, Subarna and Dey, Rakhi and Hagan, John Elvis and Nsiah-Asamoah, Christiana Naa Atsreh and Malini, S. S. (2022) Linking Depressive and Anxiety Symptoms with Diet Quality of University Students: A Cross-Sectional Study during the COVID-19 Pandemic in India. Healthcare, 10 (10).

M

Maleki, A. and Naveen, J. A. and Ramachandra, N. B. (2020) The possible role of point mutations and activation of the CDC27 Gene in progression of multiple myeloma. Meta Gene, 26.

Manasa Prabhanjan and Suresh, Raviraj V. and Megha, N. Murthy and Ramachandra, N. B. (2016) Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations. Diabetes Research and Clinical Practice, 113. 160 - 170. ISSN 1872-8227

Megha Murthy, N. and Avinash, M. V. and Seshachalam, K. B. and Ramachandra, N. B. (2016) High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts. Neurological Research, 38 (9). pp. 775-785.

Megha Murthy, N. and Blauwendraat, Cornelis and Hardy, John and Sebastian, Guelfi and Lewis, Patrick A. and Trabzuni, Daniah (2017) Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3. Neurogenetics, 18 (3). pp. 121-133. ISSN 1364-6753

N

Nachappa, S. A. and Neelambike, S. M. and Amruthavalli, C. and Ramachandra, N. B. (2018) Detection of first-line drug resistance mutations and drug-protein interaction dynamics from tuberculosis patients in South India. Microbial drug resistance (Larchmont, N.Y.), 24 (4). pp. 377-385.

Nachappa, Somanna Ajjamada and Neelambike, Sumana M. and Ramachandra, N. B. (2022) Differential expression of the Mycobacterium tuberculosis heat shock protein genes in response to drug-induced stress. Tuberculosis, 134. ISSN 1472-9792

Naik, Srilata Puru and Mahesh, P. A. and Jayaraj, B. S. and Madhunapantula, M. V. and Jahromi, Sarah Raeiszadeh and Yadav, Manish Kumar (2017) Evaluation of inflammatory markers interleukin-6 (IL-6) and matrix metalloproteinase-9 (MMP-9) in asthma. Journal of Asthma, 54 (6). pp. 584-593. ISSN 1532-4303

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Prakash, T. and Ramachandra, N.B. (2020) Integrated network and gene ontology analysis identifies key genes and pathways for coronary artery diseases. Avicenna Journal of Medical Biotechnology, 13 (1). pp. 12-23.

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Radhika, P. N. and Ramachandra, N. B. (2014) Divergence of the gene aly in experimentally evolved cytoraces, the members of the nasuta-albomicans complex of Drosophila. Insect Molecular Biology, 23 (4). pp. 435-443. ISSN 1365-2583

Raeiszadeh Jahromi, Sareh and Bijanzadeh, Mahdi and Mahesh, P. A. and Sangeetha, V. and Ramachandra, N. B. (2014) Single nucleotide polymorphism and Asthma: from conformational variations to structural alternations. Molecular and Biochemical Diagnosis Journal, 1 (2). pp. 63-75.

Ramachandra, N. B. and Ranganath, H. A. (1996) Evolution of the nasuta-albomicans complex of Drosophila. Current Science, 71 (7). pp. 515-517.

Rao, P. M. and Ranganath, H. A. (1990) An Allozyme Phylogeny of some members of the immigrans species group of drosophila. Genetica, 82 (3). pp. 177-181.

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Somanna, A. N. and Neelambike, S. M. and Sarikhani, A. and Ramachandra, N. B. (2021) Simultaneous detection of drug-resistant mutations in mycobacterium tuberculosis and determining their role through in silico docking. Infectious Disorders: Drug Targets, 21 (1). pp. 134-141.

Somanna, A. N. and Sumana, M. N. and Chokkanna, A. and Ramachandra, N. B. (2018) Detection of first-line drug resistance mutations and drug–protein interaction dynamics from tuberculosis patients in South India. Microbial Drug Resistance, 24 (4). pp. 377-385. ISSN 1931-8448

Suresh, R. V. and Narayannapa and Savitha and Ambika S. Udupa and Kusuma, L. and Sunil Kumar, P. and Ramachandra, N. B. (2017) Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome. Current Medicine Research and Practice, 7 (1). 6 - 10. ISSN 2352-0817

Suresh, Raviraj V. and Kusuma, L. and Avinash, M. V. and Ramachandra, N. B. (2017) Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: a copy number variation approach. Indian Journal of Medical Research, 145 (1). pp. 39-50. ISSN 0975-9174

Swati, A. and Ramachandra Nallur, B. (2021) Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse. Egyptian Journal of Medical Human Genetics, 22 (1). pp. 1-13.

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Tejaswini, Prakash and Avinash, V. and Ramachandra, N. B. (2017) Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn’s disease in monozygotic twins. Autoimmunity, 50 (5). pp. 275-276. ISSN 1607-842X

Tejaswini, Prakash and Ramachandra, N. B. (2022) Prioritizing Candidate Genes for Type 2 Diabetes Mellitus using Integrated Network and Pathway Analysis. Avicenna Journal of Medical Biotechnology, 14 (3). pp. 239-246.

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Veerappa, A. M. and Suresh, R. V. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Manjegowda, D. S. and Padakannaya, P. and Ramachandra, N. B. (2015) Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization. GENETICS RESEARCH, 97. ISSN 1469-5073

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Yogita Kattimani and Avinash, M. V. (2018) Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis. Autoimmunity, 51 (4). pp. 147-151. ISSN 1607-842X

Yogita Kattimani and Avinash, M. V. (2018) Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis. Multiple Sclerosis and Related Disorders, 22. 153 - 156. ISSN 2211-0356

Yoirentomba Meetei, Sinam and Chatterjee, Arunita and Ranjini, M. S. and Poojari, Adarsh and Aarthi Nagarajan and Ramachandra, N. B. and Upendra, N. (2016) A newly evolved drosophila cytorace-9 shows trade-off between longevity and immune response. Infection, Genetics and Evolution, 44. 1 - 7. ISSN 1567-7257