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Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date	Views
	2q23.1 microdeletion involving the MBD5 gene - large deletion associated with a relatively mild phenotype Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009	Chung, BHY Stavropoulos, DJ Weksberg, R Yoon, G	2009	38
	Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2010	Chung, BHY Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Weksberg, R	2010
	Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Chung, B Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Weksberg, R	2010
	Dysmorphology assessment on a population basesd cohort of 150 newfoundland children with autism spectrum disorder Proceeding/Conference:30th Annual David W. Smith Workshop	Fernandez, BA Turner, L MacKay, S Weksberg, R Chung, BHY Roberts, W Vardy, C Whitten, K Marshal, C Scherer, SW	2009	39
	Genome-wide DNA methylation analysis of Hong Kong Chinese systemic lupus erythematosus patients identified hypomethylated genes related to type I interferon Proceeding/Conference:Epigenomics of Common Diseases Conference	Yeung, KS Choufani, S Chen, YA Grafodatskaya, D Lee, PPW Yang, W Weksberg, R Lau, YL Chung, BHY	2013
	NSD1+/- DNA methylation (DNAm) signature: A novel functional diagnostic tool for Sotos syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014	Chonufani, S Cytrynbaum, C Chung, BHY Turinsky, AL Grafodatskaya, D Chen, YA Luk, HM Lo, IFM Lam, STS Stavropoulos, DJ Gibson, B Reardon, M Brudno, M Mendoza-Londono, R Chitayat, D Weksberg, R	2014
	Overgrowth with increased proliferation of fibroblast and matrix metalloproteinse activity related to reduced T1MP1: a new syndrome Proceeding/Conference:32nd Annual David W. Smith Workshop	Chung, BHY Hinek, A Shannon, P Keating, S Weksberg, R Shah, V Blaser, S Hawkins, C Chitayat, D	2011	126
	Role of epigenetic dysregulation in neurodevelopmental syndromes: lessons from KDM5C mutations Proceeding/Conference:ICHG-ASHG 2011 Joint Meeting	Grafodatskaya, D Chung, BHY Butcher, DT Goodman, S Choufan, S Lou, Y Zhao, C Rajendram, R Abidi, FE Skinner, C Hamilton, J Scherer, SW Schwartz, CE Weksberg, R	2011	119
	Sex specific methylation differences within the promoter of the non-coding RNA on the chromosome Xp11.4 suggest the maternal imprinted pattern Proceeding/Conference:Annual Meeting of the Organization for the study of Sex Differences, OSDD 2009	Grafodatskay, D Roberts, LJ Zha, CO Lo, Y Chung, BHY Scherer, SW Weksberg, R	2009	96
	Social skills impairments in girls with Turner syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Inbar-Feigenberg, M Grafodatskaya, D Choufani, S Chung, BHY Roberts, LJ Russell, C Roberts, W Hamilton, J Weksberg, R	2013	134
	A specific DNA methylation signature associated with NSD1+/- mutations in Sotos syndrome reveals a significant genome-wide loss of DNA methylation (DNAm) targeting CGs in regulatory regions of key developmental genes Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Choufani, S Cytrynbaum, C Turinsky, AL Chen, YA Grafodatskaya, D Xiang, J Feigenberg, M Chung, BHY Stavropoulos, DJ Mendoza-Londono, R Chitayat, D Gibson, WT Reardon, M Brudno, M Weksberg, R	2013

Showing results 1 to 11 of 11