Sureni V. Mullegama

Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder

Michael E. Talkowski, Sureni V. Mullegama, Jill A. Rosenfeld et al. · The American Journal of Human Genetics · 2011 · 246 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Smith-Magenis Syndrome Results in Disruption of CLOCK Gene Transcription and Reveals an Integral Role for RAI1 in the Maintenance of Circadian Rhythmicity

Stephen R. Williams, Deborah Zies, Sureni V. Mullegama et al. · The American Journal of Human Genetics · 2012 · 119 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Haploinsufficiency of SF3B2 causes craniofacial microsomia

Andrew T. Timberlake, Casey Griffin, Carrie L. Heike et al. · Nature Communications · 2021 · 88 citations · Full text

Dentistry, Genetics, Molecular Genetics +16

Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder

Sureni V. Mullegama, Jill A. Rosenfeld, Carmen Orellana et al. · European Journal of Human Genetics · 2013 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures

Stephen R. Williams, Sureni V. Mullegama, Jill A. Rosenfeld et al. · European Journal of Human Genetics · 2009 · 84 citations · Full text

Life Sciences, Neurology, Neuroscience +14