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Publications by Deepak Gill
Targeted Resequencing in Epileptic Encephalopathies Identifies De Novo Mutations in CHD2 and SYNGAP1
Nature Genetics
Genetics
Rare Copy Number Variants Are an Important Cause of Epileptic Encephalopathies
Annals of Neurology
Neurology
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Epileptic Encephalopathies – Next Generation Diagnostics
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De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy
American Journal of Human Genetics
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Early-Onset Epileptic Encephalopathy and Severe Developmental Delay in an Association With De Novo Double Mutations in NF1 and MAGEL2
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OC48 Re-Interrogation of Whole Exome Sequencing Data in Developmental Epileptic Encephalopathies
A Case-Control Collapsing Analysis Identifies Epilepsy Genes Implicated in Trio Sequencing Studies Focused on De Novo Mutations
PLoS Genetics
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A Pedigree-Based Prediction Model Identifies Carriers of Deleterious De Novo Mutations in Families With Li-Fraumeni Syndrome
Toward Understanding De Novo Germline Mutations in Mammals
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Molecular Biology