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Publications by Ruth Ottman
Ultra-Rare Genetic Variation in Common Epilepsies: A Case-Control Sequencing Study
The Lancet Neurology
Neurology
Genetic Causal Attribution of Epilepsy and Its Implications for Felt Stigma
Epilepsia
Neurology
Depression and Genetic Causal Attribution of Epilepsy in Multiplex Epilepsy Families
Epilepsia
Neurology
Prevalence and Features of Unreported Dystonia in a Family Study of “Pure” Essential Tremor
Parkinsonism and Related Disorders
Gerontology
Geriatrics
Neurology
Transient, Isolated Head Tremor in “Unaffected” Individuals: Is Essential Tremor an Even More Prevalent Disease Than We Suppose?
Frontiers in Neurology
Neurology
Whole Genome Sequencing and Rare Variant Analysis in Essential Tremor Families
PLoS ONE
Multidisciplinary
Psychiatrists’ Views of the Genetic Bases of Mental Disorders and Behavioral Traits and Their Use of Genetic Tests
Journal of Nervous and Mental Disease
Psychiatry
Mental Health
Causal Models for Investigating Complex Genetic Disease: II. What Causal Models Can Tell Us About Penetrance for Additive, Heterogeneity, and Multiplicative Two-Locus Models
Human Heredity
Genetics
Frequency of Known Mutations in Early-Onset Parkinson Disease
Archives of Neurology
Identification of Epilepsy Genes in Human and Mouse
Annual Review of Genetics
Genetics
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