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Journal of Genetics|September 6, 2014
Roles of the troponin isoforms during indirect flight muscle development in DrosophilaSalam Herojeet Singh, Prabodh Kumar, Nallur B Ramachandra, et al.Psychiatric Genetics|December 24, 2013
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian populationShyamala K Venkatesh, Anand Siddaiah, Prakash Padakannaya, et al.Gene|October 9, 2020
Allopatric sibling species pair Drosophila nasuta nasuta and Drosophila nasuta albomicans exhibit expression divergence in ovarian transcriptomesKoushik Ponnanna, Stafny M DSouza, C Amruthavalli, et al.Behavior Genetics|January 5, 2011
An examination of candidate gene SNPs for dyslexia in an Indian sampleShyamala K Venkatesh, Anand Siddaiah, Prakash Padakannaya, et al.Novartis Foundation Symposium|June 26, 2008
Unusual cellular disposition of the mitochondrial molecular chaperones Hsp60, Hsp70 and Hsp10Radhey S Gupta, Nallur B Ramachandra, Timothy Bowes, et al.Gene|August 20, 2013
Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexiaShyamala K Venkatesh, Anand Siddaiah, Prakash Padakannaya, et al.Journal of Human Genetics|May 17, 2013
Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian populationShyamala K Venkatesh, Anand Siddaiah, 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.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 7