Jillian M. Felie

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

Timothy W. Yu, Maria H. Chahrour, Michael E. Coulter et al. · Neuron · 2013 · 456 citations · Full text

Whole-exome Sequencing, Genetics, Syndromic Autism +1

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

Timothy W. Yu, Ganeshwaran H. Mochida, David J. Tischfield et al. · Nature Genetics · 2010 · 282 citations · Full text

Centrosome-associated Protein, Developmental Biology, Brain Structure +11

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Fowzan S. Alkuraya, Xuyu Cai, Carina Emery et al. · The American Journal of Human Genetics · 2011 · 219 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +5

A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts

Ganeshwaran H. Mochida, Vijay Ganesh, Jillian M. Felie et al. · The American Journal of Human Genetics · 2010 · 104 citations · Full text

Ophthalmology, Genetic Disorder, Medicine +7

CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development

Ganeshwaran H. Mochida, Vijay Ganesh, María I. de Michelena et al. · Nature Genetics · 2012 · 103 citations · Full text

Signal Transduction, Developmental Biology, Synaptic Signaling +8