Avinash M. Veerappa

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

Avinash M. Veerappa, Prakash Padakannaya, Nallur B. Ramachandra · Functional & Integrative Genomics · 2013 · 56 citations

Human X-chromosome-transposed Region, Developmental Biology, Genetics +9

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

Uppala Radhakrishna, Samet Albayrak, Rita Zafra et al. · PLoS ONE · 2019 · 51 citations · Full text

Placental Epigenetics, Epigenetic Change, Genetics +23

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

Avinash M. Veerappa, Marita Saldanha, Prakash Padakannaya et al. · Journal of Human Genetics · 2013 · 47 citations · Full text

New Genes, Molecular Neuroscience, Genetic Disorder +9

Genome‐wide copy number scan identifies disruption of <i>PCDH11X</i> in developmental dyslexia

Avinash M. Veerappa, Marita Saldanha, Prakash Padakannaya et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2013 · 39 citations

Neurodevelopmental Disorders, Genetic Disorder, Genetics +13

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

Uppala Radhakrishna, Sangeetha Vishweswaraiah, Avinash M. Veerappa et al. · PLoS ONE · 2018 · 26 citations · Full text

Tof Cases, Epigenetic Change, Genetics +25