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Avinash M Veerappa

Showing results (1-10 of 23) with videos related to

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Ophthalmic Genetics|February 8, 2021
Cascade of interactions between candidate genes reveals convergent mechanisms in keratoconus disease pathogenesisAvinash M Veerappa
Multiple Sclerosis and Related Disorders|May 6, 2018
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosisYogita Kattimani, Avinash M Veerappa
Autoimmunity|July 13, 2018
Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosisYogita Kattimani, Avinash M Veerappa
Functional & Integrative Genomics|May 28, 2013
Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosomeAvinash M Veerappa, Prakash Padakannaya, Nallur B Ramachandra
Journal of Nucleic Acids|April 20, 2016
Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome ScansAvinash M Veerappa, Prakash Padakannaya, Nallur B Ramachandra
Journal of Human Genetics|May 17, 2013
Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticityAvinash M Veerappa, Marita Saldanha, Prakash Padakannaya, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2014
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexiaAvinash M Veerappa, Marita Saldanha, Prakash Padakannaya, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2014
Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexicsAvinash M Veerappa, Marita Saldanha, Prakash Padakannaya, et al.
The Indian Journal of Medical Research|June 3, 2017
Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approachRaviraj V Suresh, Kusuma Lingaiah, Avinash M Veerappa, et al.
Genetics Research|January 13, 2015
Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian familyDinesh S Manjegowda, Manu Prasad, Avinash M Veerappa, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Ophthalmic Genetics|February 8, 2021
Cascade of interactions between candidate genes reveals convergent mechanisms in keratoconus disease pathogenesisAvinash M Veerappa
Multiple Sclerosis and Related Disorders|May 6, 2018
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosisYogita Kattimani, Avinash M Veerappa
Autoimmunity|July 13, 2018
Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosisYogita Kattimani, Avinash M Veerappa
Functional & Integrative Genomics|May 28, 2013
Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosomeAvinash M Veerappa, Prakash Padakannaya, Nallur B Ramachandra
Journal of Nucleic Acids|April 20, 2016
Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome ScansAvinash M Veerappa, Prakash Padakannaya, Nallur B Ramachandra
Journal of Human Genetics|May 17, 2013
Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticityAvinash M Veerappa, Marita Saldanha, Prakash Padakannaya, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2014
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexiaAvinash M Veerappa, Marita Saldanha, Prakash Padakannaya, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2014
Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexicsAvinash M Veerappa, Marita Saldanha, Prakash Padakannaya, et al.
The Indian Journal of Medical Research|June 3, 2017
Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approachRaviraj V Suresh, Kusuma Lingaiah, Avinash M Veerappa, et al.
Genetics Research|January 13, 2015
Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian familyDinesh S Manjegowda, Manu Prasad, Avinash M Veerappa, et al.
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