Allison Matthews (nee Cotton)
Allison Matthews (nee Cotton)
UBC, BCCH Research Institute
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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), 1-15, 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
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
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 (2), 187-201, 2011
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 (11), 1-17, 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
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), 1-11, 2015
Family‐based transmission disequilibrium test (TDT) and case–control association studies reveal surfactant protein A (SP‐A) susceptibility alleles for respiratory distress …
J Floros, R Fan, A Matthews, S DiAngelo, J Luo, H Nielsen, M Dunn, ...
Clinical genetics 60 (3), 178-187, 2001
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
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
X-chromosome inactivation: molecular mechanisms from the human perspective
C Yang, AG Chapman, AD Kelsey, J Minks, AM Cotton, CJ Brown
Human genetics 130 (2), 175-185, 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
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
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
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
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), 1-10, 2013
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), 1-11, 2014
X chromosome inactivation: heterogeneity of heterochromatin
SK Sidhu, J Minks, SC Chang, AM Cotton, CJ Brown
Biochemistry and Cell Biology 86 (5), 370-379, 2008
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 (3), 435-445, 2018
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, 37324, 2016
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Artikelen 1–20