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Gilliam, T. Conrad

One or more keywords matched the following properties of Gilliam, T. Conrad

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overview	Marjorie I. and Bernard A. Mitchell Distinguished Service Professor of Human Genetics Dean for Basic Science, Biological Sciences Division My research focuses on the identification and characterization of heritable mutations that affect the nervous system. Research projects vary from genetic mapping of rare (Mendelian) disease mutations and characterization of their downstream consequences to the study of common heritable disorders using mouse models as well as genomic and bioinformatic approaches. I am collaborating with experts in data-mining and network topology, systems biology, large-scale computing, and statistical genetics to develop new approaches to map the multi-gene determinants of common neuropsychiatric disorders. By reducing possible gene-gene combinations to those documented in the literature or whole genome databases, we avoid the penalties of multiple-testing. We are also collaborating to build software solutions for large-scale data mining and data integration.

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overview

Marjorie I. and Bernard A. Mitchell Distinguished Service Professor of Human Genetics Dean for Basic Science, Biological Sciences Division My research focuses on the identification and characterization of heritable mutations that affect the nervous system. Research projects vary from genetic mapping of rare (Mendelian) disease mutations and characterization of their downstream consequences to the study of common heritable disorders using mouse models as well as genomic and bioinformatic approaches. I am collaborating with experts in data-mining and network topology, systems biology, large-scale computing, and statistical genetics to develop new approaches to map the multi-gene determinants of common neuropsychiatric disorders. By reducing possible gene-gene combinations to those documented in the literature or whole genome databases, we avoid the penalties of multiple-testing. We are also collaborating to build software solutions for large-scale data mining and data integration.

One or more keywords matched the following items that are connected to Gilliam, T. Conrad

Item Type	Name
Concept	Epilepsy
Concept	Epilepsies, Partial
Concept	Genetics, Population
Concept	Epilepsy, Partial, Sensory
Academic Article	Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.
Academic Article	High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.
Academic Article	LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
Academic Article	Population-based study of SR-BI genetic variation and lipid profile.
Academic Article	The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.
Academic Article	Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation.
Academic Article	Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
Academic Article	Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.
Academic Article	Molecular genetics of human chromosome 4.
Academic Article	Molecular genetics of Huntington's disease.
Academic Article	Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder.
Academic Article	The Wilson disease gene is a copper transporting ATPase with homology to the Menkes Disease gene
Academic Article	Physical mapping, cloning, and genetic characterization of the Wilson disease locus

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Epilepsy
genetics