The candidate is fully trained in pediatrics, medical genetics, and child neurology, and this K08 will allow protected time for the consolidation of skills and establishment of his career as an independent researcher in neurogenetics. The candidate's immediate career goals are to integrate phenotyping, molecular genetics, and computer science skills, and establish a research lab the bridges between next-generation genomic sequencing technologies and bioinformatics. Long term career goals are to further the understanding of the key neurodevelopmental disorders affecting large numbers of children in the United States -- epilepsy, autism, and intellectual disability. Inclusive in these goals are th identification of targets for new disease therapies. Environment The proposed work will be performed at the Seattle Children's Research Institute (SCRI), and whole genome sequencing will be completed at the University Of Washington (UW). UW has a longstanding commitment to excellence in medical research, including world-class resources in the Department of Genome Sciences. Research The proposed project addresses infantile spasms - a significant cause of neurologic morbidity in the pediatric population, and for which new therapies are much needed. We believe the best new therapies will arise when underlying mechanisms of pathogenesis are understood. In this proposal we expand on evidence from our group and others that abnormalities of ventral forebrain development and synapse function account for ISS pathogenesis, by designing experiments that integrate cutting-edge genomics with novel bioinformatics approaches. We expect to improve the clinical classification of the disorders presenting with infantile spasms with a new technique of quantitative phenotyping. We expect to identify several new genetic causes of infantile spasms, and to connect those genes to pathways of pathogenesis that can be acted upon in the future development of disease-specific therapies. Finally, we will deploy a publicly available web-based tool that will help in the diagnosis, counseling, and future therapy selection for these disorders.

Public Health Relevance

Infantile spasms are a severe epilepsy disorder affecting 1 in every 2000-4000 live births, and can be associated with neurologic sequelae such as intractable epilepsy and autism that are a significant burden on public health. Understanding the biological causes of infantile spasms should identify new treatment targets.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08NS078054-03
Application #
8795761
Study Section
NST-2 Subcommittee (NST)
Program Officer
Fureman, Brandy E
Project Start
2013-02-15
Project End
2016-01-31
Budget Start
2015-02-01
Budget End
2016-01-31
Support Year
3
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Rochester
Department
Neurology
Type
School of Medicine & Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Silveira-Moriyama, Laura; Paciorkowski, Alex R (2018) Genetic Diagnostics for Neurologists. Continuum (Minneap Minn) 24:18-36
Lee, Bo Hoon; Reijnders, Margot R F; Abubakare, Oluwatobi et al. (2018) Expanding the neurodevelopmental phenotype of PURA syndrome. Am J Med Genet A 176:56-67
Park, Kaylee; Seltzer, Laurie E; Tuttle, Emily et al. (2017) PLXNA1 developmental encephalopathy with syndromic features: A case report and review of the literature. Am J Med Genet A :
Zhang, Jimmy F; James, Francis; Shukla, Anju et al. (2017) India Allele Finder: a web-based annotation tool for identifying common alleles in next-generation sequencing data of Indian origin. BMC Res Notes 10:233
Olson, Heather E; Kelly, McKenna; LaCoursiere, Christopher M et al. (2017) Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression. Ann Neurol 81:419-429
Pröschel, Christoph; Hansen, Jeanne N; Ali, Adil et al. (2017) Epilepsy-causing sequence variations in SIK1 disrupt synaptic activity response gene expression and affect neuronal morphology. Eur J Hum Genet 25:216-221
Garavelli, Livia; Ivanovski, Ivan; Caraffi, Stefano Giuseppe et al. (2017) Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients. Genet Med 19:691-700
Papandreou, Apostolos; Schneider, Ruth B; Augustine, Erika F et al. (2016) Delineation of the movement disorders associated with FOXG1 mutations. Neurology 86:1794-800
Ma, Mandy; Adams, Heather R; Seltzer, Laurie E et al. (2016) Phenotype Differentiation of FOXG1 and MECP2 Disorders: A New Method for Characterization of Developmental Encephalopathies. J Pediatr 178:233-240.e10
Lee, Bo Hoon; Smith, Tristram; Paciorkowski, Alex R (2015) Autism spectrum disorder and epilepsy: Disorders with a shared biology. Epilepsy Behav 47:191-201

Showing the most recent 10 out of 23 publications