| Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array EM Price, AM Cotton, LL Lam, P Farré, E Emberly, CJ Brown, ... Epigenetics & chromatin 6, 1-15, 2013 | 543 | 2013 |
| Translating dosage compensation to trisomy 21 J Jiang, Y Jing, GJ Cost, JC Chiang, HJ Kolpa, AM Cotton, DM Carone, ... Nature 500 (7462), 296-300, 2013 | 434 | 2013 |
| Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation AM Cotton, EM Price, MJ Jones, BP Balaton, MS Kobor, CJ Brown Human molecular genetics 24 (6), 1528-1539, 2015 | 293 | 2015 |
| Derivation of consensus inactivation status for X-linked genes from genome-wide studies BP Balaton, AM Cotton, CJ Brown Biology of sex differences 6, 1-11, 2015 | 217 | 2015 |
| Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome AM Cotton, B Ge, N Light, V Adoue, T Pastinen, CJ Brown Genome biology 14, 1-17, 2013 | 188 | 2013 |
| DNA methylation is globally disrupted and associated with expression changes in chronic obstructive pulmonary disease small airways EA Vucic, R Chari, KL Thu, IM Wilson, AM Cotton, JY Kennett, M Zhang, ... American journal of respiratory cell and molecular biology 50 (5), 912-922, 2014 | 164 | 2014 |
| Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation AM Cotton, L Lam, JG Affleck, IM Wilson, MS Penaherrera, DE McFadden, ... Human genetics 130, 187-201, 2011 | 163 | 2011 |
| Variable escape from X‐chromosome inactivation: Identifying factors that tip the scales towards expression SB Peeters, AM Cotton, CJ Brown Bioessays 36 (8), 746-756, 2014 | 119 | 2014 |
| Inactive X chromosome-specific reduction in placental DNA methylation AM Cotton, L Avila, MS Penaherrera, JG Affleck, WP Robinson, CJ Brown Human molecular genetics 18 (19), 3544-3552, 2009 | 96 | 2009 |
| Different measures of “genome-wide” DNA methylation exhibit unique properties in placental and somatic tissues EM Price, AM Cotton, MS Peñaherrera, DE McFadden, MS Kobor, ... Epigenetics 7 (6), 652-663, 2012 | 94 | 2012 |
| Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease M Sharma, D Leung, M Momenilandi, LCW Jones, L Pacillo, AE James, ... Journal of Experimental Medicine 220 (5), 2023 | 83 | 2023 |
| X-chromosome inactivation: molecular mechanisms from the human perspective C Yang, AG Chapman, AD Kelsey, J Minks, AM Cotton, CJ Brown Human genetics 130, 175-185, 2011 | 80 | 2011 |
| Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders M Tarailo-Graovac, JYA Zhu, A Matthews, CDM Van Karnebeek, ... Genetics in medicine 19 (12), 1300-1308, 2017 | 78 | 2017 |
| Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains AM Cotton, CY Chen, LL Lam, WW Wasserman, MS Kobor, CJ Brown Human molecular genetics 23 (5), 1211-1223, 2014 | 73 | 2014 |
| Atypical cerebral palsy: genomics analysis enables precision medicine AM Matthews, I Blydt-Hansen, B Al-Jabri, J Andersen, M Tarailo-Graovac, ... Genetics in Medicine 21 (7), 1621-1628, 2019 | 55 | 2019 |
| XIST-induced silencing of flanking genes is achieved by additive action of repeat a monomers in human somatic cells J Minks, SEL Baldry, C Yang, AM Cotton, CJ Brown Epigenetics & chromatin 6, 1-10, 2013 | 51 | 2013 |
| Integration of genomics and metabolomics for prioritization of rare disease variants: a 2018 literature review E Graham, J Lee, M Price, M Tarailo-Graovac, A Matthews, U Engelke, ... Journal of Inherited Metabolic Disease 41, 435-445, 2018 | 50 | 2018 |
| Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: a potential treatment target? GA Horvath, M Demos, C Shyr, A Matthews, L Zhang, S Race, ... Molecular genetics and metabolism 117 (1), 42-48, 2016 | 48 | 2016 |
| Differentially methylated CpG island within human XIST mediates alternative P2 transcription and YY1 binding AG Chapman, AM Cotton, AD Kelsey, CJ Brown BMC genetics 15, 1-11, 2014 | 44 | 2014 |
| YY1 binding association with sex-biased transcription revealed through X-linked transcript levels and allelic binding analyses C Chen, W Shi, BP Balaton, AM Matthews, Y Li, DJ Arenillas, A Mathelier, ... Scientific reports 6 (1), 37324, 2016 | 43 | 2016 |
Carolyn J. BrownProfessor, Medical Genetics, Life Sciences Institute, University of British ColumbiaVerified email at ubc.ca