Ramachandra NB - Search Results

1

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

Veerappa AM, Padakannaya P, Ramachandra NB. Veerappa AM, et al. Among authors: ramachandra nb. Funct Integr Genomics. 2013 Aug;13(3):285-93. doi: 10.1007/s10142-013-0323-6. Epub 2013 May 26. Funct Integr Genomics. 2013. PMID: 23708688

2

An examination of candidate gene SNPs for dyslexia in an Indian sample.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB. Venkatesh SK, et al. Among authors: ramachandra nb. Behav Genet. 2011 Jan;41(1):105-9. doi: 10.1007/s10519-010-9441-2. Epub 2011 Jan 4. Behav Genet. 2011. PMID: 21203818

3

Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB. Venkatesh SK, et al. Among authors: ramachandra nb. J Hum Genet. 2013 Aug;58(8):531-8. doi: 10.1038/jhg.2013.46. Epub 2013 May 16. J Hum Genet. 2013. PMID: 23677054

4

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

Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB. Veerappa AM, et al. Among authors: ramachandra nb. J Hum Genet. 2013 Aug;58(8):539-47. doi: 10.1038/jhg.2013.47. Epub 2013 May 16. J Hum Genet. 2013. PMID: 23677055

5

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

Veerappa AM, Vishweswaraiah S, Lingaiah K, Murthy M, Manjegowda DS, Nayaka R, Ramachandra NB. Veerappa AM, et al. Among authors: ramachandra nb. PLoS One. 2013 Jul 3;8(7):e66843. doi: 10.1371/journal.pone.0066843. Print 2013. PLoS One. 2013. PMID: 23843967 Free PMC article.

6

Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB. Venkatesh SK, et al. Among authors: ramachandra nb. Gene. 2013 Oct 25;529(2):215-9. doi: 10.1016/j.gene.2013.08.017. Epub 2013 Aug 14. Gene. 2013. PMID: 23954868

7

Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB. Venkatesh SK, et al. Among authors: ramachandra nb. Psychiatr Genet. 2014 Feb;24(1):10-20. doi: 10.1097/YPG.0000000000000009. Psychiatr Genet. 2014. PMID: 24362368

8

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

Veerappa AM, Murthy MN, Vishweswaraiah S, Lingaiah K, Suresh RV, Nachappa SA, Prashali N, Yadav SN, Srikanta MA, Manjegowda DS, Seshachalam KB, Ramachandra NB. Veerappa AM, et al. Among authors: ramachandra nb. PLoS One. 2014 Feb 28;9(2):e90391. doi: 10.1371/journal.pone.0090391. eCollection 2014. PLoS One. 2014. PMID: 24587348 Free PMC article.

9

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

Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB. Veerappa AM, et al. Among authors: ramachandra nb. Am J Med Genet B Neuropsychiatr Genet. 2013 Dec;162B(8):889-97. doi: 10.1002/ajmg.b.32199. Epub 2013 Sep 20. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 24591081

10

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

Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB. Veerappa AM, et al. Among authors: ramachandra nb. Am J Med Genet B Neuropsychiatr Genet. 2014 Oct;165B(7):572-80. doi: 10.1002/ajmg.b.32260. Epub 2014 Aug 19. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 25139666

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

88 results

Search Page