| Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder P Szafranski, AV Dharmadhikari, E Brosens, P Gurha, KE Kołodziejska, ... Genome research 23 (1), 23-33, 2013 | 138 | 2013 |
| Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q 11.2, Specifically Breakpoints 1 to 2 P Chaste, SJ Sanders, KN Mohan, L Klei, Y Song, MT Murtha, V Hus, ... Autism research 7 (3), 355-362, 2014 | 61 | 2014 |
| A therapeutic trial of pro‐methylation dietary supplements in Angelman syndrome LM Bird, WH Tan, CA Bacino, SU Peters, SA Skinner, I Anselm, ... American Journal of Medical Genetics Part A 155 (12), 2956-2963, 2011 | 59 | 2011 |
| Identification of a region of the DNMT1 methyltransferase that regulates the maintenance of genomic imprints E Borowczyk, KN Mohan, L D'Aiuto, MC Cirio, JR Chaillet Proceedings of the National Academy of Sciences 106 (49), 20806-20811, 2009 | 55 | 2009 |
| Methyltransferases mediate cell memory of a genotoxic insult RE Rugo, JT Mutamba, KN Mohan, T Yee, JR Chaillet, JS Greenberger, ... Oncogene 30 (6), 751-756, 2011 | 49 | 2011 |
| Distinct roles of DMAP1 in mouse development KN Mohan, F Ding, JR Chaillet Molecular and Cellular Biology 31 (9), 1861-1869, 2011 | 47 | 2011 |
| Transient DNMT1 suppression reveals hidden heritable marks in the genome. TJM McGraw S, Zhang JX, Farag M, Chan D, Caron M, Konermann C, Oakes CC ... Nucleic Acids Research 43 ((3)), :1485-1497, 2015 | 45 | 2015 |
| Cell and molecular biology of DNA methyltransferase 1 KN Mohan, JR Chaillet International review of cell and molecular biology 306, 1-42, 2013 | 42 | 2013 |
| Characterization of TTAGG telomeric repeats, their interstitial occurrence and constitutively active telomerase in the mealybug Planococcus lilacinus (Homoptera; Coccoidea) KN Mohan, BS Rani, PS Kulashreshta, JS Kadandale Chromosoma 120 (2), 165-175, 2011 | 28 | 2011 |
| Mouse ES cells overexpressing DNMT1 produce abnormal neurons with upregulated NMDA/NR1 subunit L D'Aiuto, R Di Maio, KN Mohan, C Minervini, F Saporiti, I Soreca, ... Differentiation 82 (1), 9-17, 2011 | 22 | 2011 |
| DNMT1: catalytic and non-catalytic roles in different biological processes KN Mohan Epigenomics 14 (10), 629-643, 2022 | 21 | 2022 |
| Stem cell models to investigate the role of DNA methylation machinery in development of neuropsychiatric disorders KN Mohan Stem Cells International 2016, 2016 | 15 | 2016 |
| Reproducible differentiation and characterization of neurons from mouse embryonic stem cells S Saxena, S Choudhury, KN Mohan MethodsX 7, 101073, 2020 | 14 | 2020 |
| Analysis of transcript levels of a few schizophrenia candidate genes in neurons from a transgenic mouse embryonic stem cell model overexpressing DNMT1 S Saxena, PA Maroju, S Choudhury, A Anne, KN Mohan Gene 757, 144934, 2020 | 11 | 2020 |
| 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 KN Mohan, YE Cao, J Pham, SW Cheung, L Hoffner, ZZ Ou, U Surti, ... Journal of Human Genetics 64 (3), 253-255, 2019 | 11 | 2019 |
| Dysregulation of schizophrenia-associated genes and genome-wide hypomethylation in neurons overexpressing DNMT1 S Saxena, S Choudhury, PA Maroju, A Anne, L Kumar, KN Mohan Epigenomics 13 (19), 1539-1555, 2021 | 10 | 2021 |
| Mealybug as a model for studying responses to high doses of ionizing radiation KN Mohan, J Ge, JS Kadandale Current topics in ionizing radiation research, 2012 | 10 | 2012 |
| Isolation and analysis of sequences showing sex-specific cytosine methylation in the mealybug Planococcus lilacinus KN Mohan, HS Chandra Molecular Genetics and Genomics 274 (6), 557-568, 2005 | 10 | 2005 |
| CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders. NMK Addepalli A, Kalyani S, Singh M, Bandyopadhyay D PLoS One 15 (1), e0228156, 2020 | 9 | 2020 |
| Analysis of 15q11. 2 CNVs in an Indian population with schizophrenia S Saxena, P Kkani, C Ramasubramanian, SG Kumar, R Monisha, ... Annals of Human Genetics 83 (3), 187-191, 2019 | 9 | 2019 |
