Leora Lee

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8

M. Marra, F. Zahir, S. Langlois, 2019, Journal of Human Genetics.

Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

Steven J. M. Jones, M. Marra, K. Mungall, 2017, BMC Genomics.

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8

M. Marra, F. Zahir, S. Langlois, 2019, Journal of Human Genetics.

The Sclerotinia sclerotiorum Slt2 mitogen-activated protein kinase ortholog, SMK3, is required for infection initiation but not lesion expansion.

D. Hegedus, Jenny Poon, S. Gyawali, 2016, Canadian journal of microbiology.

Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

M. Marra, K. Mungall, Hye-Jung E. Chun, 2017, BMC Genomics.