Mohan KN - Search Results

1

CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders.

Addepalli A, Kalyani S, Singh M, Bandyopadhyay D, Mohan KN. Addepalli A, et al. Among authors: mohan kn. PLoS One. 2020 Jan 29;15(1):e0228156. doi: 10.1371/journal.pone.0228156. eCollection 2020. PLoS One. 2020. PMID: 31995602 Free PMC article.

2

Analysis of 15q11.2 CNVs in an Indian population with schizophrenia.

Saxena S, Kkani P, Ramasubramanian C, Kumar SG, Monisha R, Prasad Rao G, Mohan KN. Saxena S, et al. Among authors: mohan kn. Ann Hum Genet. 2019 May;83(3):187-191. doi: 10.1111/ahg.12300. Epub 2019 Feb 19. Ann Hum Genet. 2019. PMID: 30779116

3

Improved Multiplex Ligation-dependent Probe Amplification (i-MLPA) for rapid copy number variant (CNV) detection.

Saxena S, Gowdhaman K, Kkani P, Vennapusa B, Rama Subramanian C, Ganesh Kumar S, Mohan KN. Saxena S, et al. Among authors: mohan kn. Clin Chim Acta. 2015 Oct 23;450:19-24. doi: 10.1016/j.cca.2015.07.028. Epub 2015 Jul 31. Clin Chim Acta. 2015. PMID: 26234520

4

Functional Analysis of DNMT1 SNPs (rs2228611 and rs2114724) Associated with Schizophrenia.

Saxena S, Maroju PA, Choudhury S, Voina VC, Naik P, Gowdhaman K, Kkani P, Chennoju K, Ganesh Kumar S, Ramasubramanian C, Prasad Rao G, Jamma T, Narayan KP, Mohan KN. Saxena S, et al. Among authors: mohan kn. Genet Res (Camb). 2021 Mar 31;2021:6698979. doi: 10.1155/2021/6698979. eCollection 2021. Genet Res (Camb). 2021. PMID: 33854407 Free PMC article.

5

Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.

Mohan KN, Cao Y, Pham J, Cheung SW, Hoffner L, Ou ZZ, Surti U, Cook EH, Beaudet AL. Mohan KN, et al. J Hum Genet. 2019 Mar;64(3):253-255. doi: 10.1038/s10038-018-0543-7. Epub 2018 Dec 12. J Hum Genet. 2019. PMID: 30542208

6

Dysregulation of schizophrenia-associated genes and genome-wide hypomethylation in neurons overexpressing DNMT1.

Saxena S, Choudhury S, Maroju PA, Anne A, Kumar L, Mohan KN. Saxena S, et al. Among authors: mohan kn. Epigenomics. 2021 Oct;13(19):1539-1555. doi: 10.2217/epi-2021-0133. Epub 2021 Oct 14. Epigenomics. 2021. PMID: 34647491

7

DNMT1: catalytic and non-catalytic roles in different biological processes.

Mohan KN. Mohan KN. Epigenomics. 2022 May;14(10):629-643. doi: 10.2217/epi-2022-0035. Epub 2022 Apr 12. Epigenomics. 2022. PMID: 35410490 Review.

8

Genome-wide methylation analysis of post-mortem cerebellum samples supports the role of peroxisomes in autism spectrum disorder.

Anne A, Saxena S, Mohan KN. Anne A, et al. Among authors: mohan kn. Epigenomics. 2022 Sep;14(17):1015-1027. doi: 10.2217/epi-2022-0184. Epub 2022 Sep 26. Epigenomics. 2022. PMID: 36154275

9

Reproducible differentiation and characterization of neurons from mouse embryonic stem cells.

Saxena S, Choudhury S, Mohan KN. Saxena S, et al. Among authors: mohan kn. MethodsX. 2020 Sep 22;7:101073. doi: 10.1016/j.mex.2020.101073. eCollection 2020. MethodsX. 2020. PMID: 33083240 Free PMC article.

10

Stem Cell Models to Investigate the Role of DNA Methylation Machinery in Development of Neuropsychiatric Disorders.

Mohan KN. Mohan KN. Stem Cells Int. 2016;2016:4379425. doi: 10.1155/2016/4379425. Epub 2015 Dec 20. Stem Cells Int. 2016. PMID: 26798355 Free PMC article. Review.

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