Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders
S Niranjana Murthy, Ashitha, V Suresh, Raviraj, Nallur B, Ramachandra
Published in Genomics (San Diego, Calif.) (01.01.2021)
Published in Genomics (San Diego, Calif.) (01.01.2021)
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Journal Article
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia
Veerappa, Avinash M., Saldanha, Marita, Padakannaya, Prakash, Ramachandra, Nallur B.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2013)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2013)
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Journal Article
Integrated in silico functional analysis predicts autism spectrum disorders to be burdened by deleterious variations within CHD8 core domains and its CHD7-binding motif
S. Niranjana Murthy, Ashitha, Thangalazhi Balakrishnan, Suryanarayanan, Nallur B., Ramachandra
Published in Network modeling and analysis in health informatics and bioinformatics (Wien) (01.12.2022)
Published in Network modeling and analysis in health informatics and bioinformatics (Wien) (01.12.2022)
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Journal Article
Simultaneous Detection of Drug-resistant Mutations in Mycobacterium tuberculosis and Determining their Role through In Silico Docking
Nachappa, Somanna Ajjamada, Neelambike, Sumana M, Sarikhani, Ahmad, Ramachandra, Nallur B
Published in Infectious disorders drug targets (2021)
Published in Infectious disorders drug targets (2021)
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Association between ADAM33 Single-Nucleotide Polymorphisms and Treatment Response to Inhaled Corticosteroids and a Long-Acting Beta-Agonist in Asthma
Vishweswaraiah, Sangeetha, Ramachandra, Nallur B, Joshi, Neha, Parthasarathi, Ashwaghosha, Kaleem Ullah, Mohammed, Siddaiah, Jayaraj Biligere, Holla, Amrutha D, Chakraborty, Samarpana, Agrawal, Anurag, Mahesh, Padukudru Anand
Published in Diagnostics (Basel) (22.01.2023)
Published in Diagnostics (Basel) (22.01.2023)
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Journal Article
Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma
Vishweswaraiah, Sangeetha, MSc, Veerappa, Avinash M., PhD, Mahesh, Padukudru A., MBBS, DTCD, DNB, Jayaraju, Biligere Siddaiah, MBBS, MD, DM, Krishnarao, Chaya Sindaghatta, MBBS, DTCD, DNB, Ramachandra, Nallur B., PhD
Published in Annals of allergy, asthma, & immunology (01.10.2014)
Published in Annals of allergy, asthma, & immunology (01.10.2014)
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Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects
Gholipoorfeshkecheh, Rahim, Agarwala, Swati, G, Kavya, Krishnappa, Santhosh, Savitha, Mysore R., Ramachandra, Nallur B.
Published in Egyptian Journal of Medical Human Genetics (30.10.2020)
Published in Egyptian Journal of Medical Human Genetics (30.10.2020)
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Journal Article
Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes
Veerappa, Avinash M, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, Megha, Suresh, Raviraj V, Manjegowda, Dinesh S, Ramachandra, Nallur B
Published in PloS one (24.04.2015)
Published in PloS one (24.04.2015)
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Journal Article
Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays
Veerappa, Avinash M, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, Megha, Manjegowda, Dinesh S, Nayaka, Radhika, Ramachandra, Nallur B
Published in PloS one (03.07.2013)
Published in PloS one (03.07.2013)
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Journal Article
Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression
Veerappa, Avinash M, Murthy, Megha N, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Suresh, Raviraj V, Nachappa, Somanna Ajjamada, Prashali, Nelchi, Yadav, Sangeetha Nuggehalli, Srikanta, Manjula Arsikere, Manjegowda, Dinesh S, Seshachalam, Keshava B, Ramachandra, Nallur B
Published in PloS one (28.02.2014)
Published in PloS one (28.02.2014)
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