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Showing results 21 to 32 of 32 < previous

	Title	Author(s)	Issue Date
	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
	DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes Journal:The American Journal of Human Genetics	Choufani, S Gibson, WT Turinsky, AL Chung, BHY Wang, T Garg, K Vitriolo, A Cohen, ASA Cyrus, S Goodman, S Chater-Diehl, E Brzezinski, J Brudno, M Luk, HM White, SM Lynch, SA Clericuzio, C Temple, IK Flinter, F MdConnell, V Cushing, T Bird, LM Splitt, M Kerr, B Scherer, SW Machado, J Imagawa, E Okamoto, N Matsumoto, N Testa, G Iascone, M Tenconi, R Caluseriu, O Mendoza-Londono, R Chitayat, D Cytrynabum, C Tatton-Brown, K Weksberg, R	2020
	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
	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
	Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion Journal:American Journal of Medical Genetics, Part A	Aldinger, KA Kogan, J Kimonis, V Fernandez, B Horn, D Klopocki, E Chung, B Toutain, A Weksberg, R Millen, KJ Barkovich, AJ Dobyns, WB	2013
	Cell Lineage-specific Genome-wide DNA Methylation Analysis of Patients with Paediatric-onset Systemic Lupus Erythematosus Journal:Epigenetics	Yeung, KS Lee, TL Mok, MY Mak, CCY Yang, W Chong, PCY Lee, PPW Ho, MHK Choufani, S Lau, CS Lau, YL Weksberg, R Chung, BHY	2019
	Blood cell type-specific genome-wide DNA methylation analysis of Chinese patients with early-onset systemic lupus erythematosus identifies loss of DNA methylation in genes related to the Type I Interferon pathway Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017	Chung, BHY Yeung, KS Mok, TKG Choufani, S Lau, YL Weksberg, R	2017
	Beckwith-Wiedemann Syndrome Journal:UpToDate	Chung, BHY Shuman, C Choufani, S Weksberg, R	2017
	Beckwith-Wiedemann Syndrome Journal:UpToDate	Chung, BHY Shuman, C Choufani, S Weksberg, R	2013
	Autism spectrum disorders and epigenetics Journal:Journal of the American Academy of Child and Adolescent Psychiatry	Grafodatskaya, D Chung, B Szatmari, P Weksberg, R	2010
	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
	2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial features Journal:American Journal of Medical Genetics, Part A	Chung, BH Stavropoulos, J Marshall, CR Weksberg, R Scherer, SW Yoon, G	2011

Showing results 21 to 32 of 32 < previous