Grafodatskaya, Daria

Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

Cheung, A. Y. L., Horvath, L. M., Grafodatskaya, D., Pasceri, P., Weksberg, R., Hotta, A., Carrel, L., & Ellis, J. (2011) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersPluripotent Stem Cells Research

Cited by 271

Autism Spectrum Disorders and Epigenetics

Grafodatskaya, D., Chung, B., Szatmari, P., & Weksberg, R. (2010) · Journal of the American Academy of Child & Adolescent Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 235

CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions

Butcher, D. T., Cytrynbaum, C., Turinsky, A. L., Siu, M. T., Inbar-Feigenberg, M., Mendoza-Londono, R., Chitayat, D., Walker, S., Machado, J., Caluseriu, O., et al. (2017) · The American Journal of Human Genetics

Congenital Ear and Nasal AnomaliesEpigenetics and DNA Methylation

Cited by 200

Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray

Chen, Y.-A., Choufani, S., Ferreira, J. C., Grafodatskaya, D., Butcher, D. T., & Weksberg, R. (2011) · Genomics

Epigenetics and DNA MethylationGene expression and cancer classification

Cited by 90