Search Results - "Veerappa, Avinash M." :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD)

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD)

by Radhakrishna, Uppala, Albayrak, Samet, Zafra, Rita, Baraa, Alosh, Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Mahishi, Deepthi, Saiyed, Nazia, Mishra, Nitish K, Guda, Chittibabu, Ali-Fehmi, Rouba, Bahado-Singh, Ray O
Published in PloS one (21.03.2019)

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Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis

Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis

by Kattimani, Yogita, Veerappa, Avinash M.
Published in Autoimmunity (Chur, Switzerland) (19.05.2018)

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Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF)

Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF)

by Radhakrishna, Uppala, Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Zafra, Rita, Albayrak, Samet, Sitharam, Prajna H, Saiyed, Nazia M, Mishra, Nitish K, Guda, Chittibabu, Bahado-Singh, Ray
Published in PloS one (13.09.2018)

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Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia

Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia

by Veerappa, Avinash M., Saldanha, Marita, Padakannaya, Prakash, Ramachandra, Nallur B.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2013)

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Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity

Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity

by Veerappa, Avinash M, Saldanha, Marita, Padakannaya, Prakash, Ramachandra, Nallur B
Published in Journal of human genetics (01.08.2013)

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Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism

Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism

by Agarwala, Swati, Veerappa, Avinash M., Ramachandra, Nallur B.
Published in Egyptian Journal of Medical Human Genetics (15.12.2020)

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Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma

Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma

by 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)

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Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes

Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes

by 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)

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Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays

Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays

by Veerappa, Avinash M, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, Megha, Manjegowda, Dinesh S, Nayaka, Radhika, Ramachandra, Nallur B
Published in PloS one (03.07.2013)

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Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression

Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression

by 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)

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Cascade of interactions between candidate genes reveals convergent mechanisms in keratoconus disease pathogenesis

Cascade of interactions between candidate genes reveals convergent mechanisms in keratoconus disease pathogenesis

by Veerappa, Avinash M.
Published in Ophthalmic genetics (04.03.2021)

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Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers

Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers

by Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Mahesh, Padukudru A, Jahromi, Sareh R, Ramachandra, Nallur B
Published in Allergy, asthma & immunology research (01.05.2015)

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Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans

Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans

by Veerappa, Avinash M., Ramachandra, Nallur B., Padakannaya, Prakash
Published in Journal of Nucleic Acids (01.01.2016)

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CloudATAC: a cloud-based framework for ATAC-Seq data analysis

CloudATAC: a cloud-based framework for ATAC-Seq data analysis

by Veerappa, Avinash M, Rowley, M Jordan, Maggio, Angela, Beaudry, Laura, Hawkins, Dale, Kim, Allen, Sethi, Sahil, Sorgen, Paul L, Guda, Chittibabu
Published in Briefings in bioinformatics (23.07.2024)

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Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis

Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis

by Kattimani, Yogita, Veerappa, Avinash M.
Published in Multiple sclerosis and related disorders (01.05.2018)

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Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics

Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics

by Veerappa, Avinash M., Saldanha, Marita, Padakannaya, Prakash, Ramachandra, Nallur B.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.10.2014)

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Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome

Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome

by Veerappa, Avinash M, Padakannaya, Prakash, Ramachandra, Nallur B
Published in Functional & integrative genomics (01.08.2013)

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Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature

Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature

by Kodaganur, Srinivas Gopinath, Kapoor, Saketh, Veerappa, Avinash M, Tontanahal, Sagar Jagannath, Sarda, Astha, Yathish, S, Prakash, D Ravi, Kumar, Arun
Published in Molecular vision (02.08.2013)

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High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts

High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts

by Murthy, Megha N, Veerappa, Avinash M, Seshachalam, Keshava B, Ramachandra, Nallur B
Published in Neurological research (New York) (01.09.2016)

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Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach

Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach

by Suresh, Raviraj V, Lingaiah, Kusuma, Veerappa, Avinash M, Ramachandra, Nallur B
Published in Indian journal of medical research (New Delhi, India : 1994) (01.01.2017)

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