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1. Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ familiesResearch in context

2. Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology

3. Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

4. Genetic Testing Preferences of Individuals in Families with Essential Tremor

5. Whole genome sequencing and rare variant analysis in essential tremor families.

6. Transient, Isolated Head Tremor in 'Unaffected' Individuals: Is Essential Tremor an Even More Prevalent Disease Than We Suppose?

7. Knowledge about Essential Tremor: A Study of Essential Tremor Families

8. Familial Aggregation of the Cerebellar Signs in Familial Essential Tremor

9. Essential Tremor in aCharcot-Marie-Tooth Type 2C Kindred Does Not Segregate with the TRPV4 R269H Mutation

10. How Many People in the United States Have Essential Tremor? Deriving a Population Estimate Based on Epidemiological Data

11. Clinical Classification of Borderline Cases in the Family Study of Essential Tremor: An Analysis of Phenotypic Features

12. The characterization of twenty sequenced human genomes.

13. Identification of patients with drug‐resistant epilepsy in electronic medical record data using the Observational Medical Outcomes Partnership Common Data Model

14. Reproduction and genetic causal attribution of epilepsy

15. Reproductive decision‐making in families containing multiple individuals with epilepsy

16. Epilepsy risk in offspring of affected parents; a cohort study of the 'maternal effect' in epilepsy

17. Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors

18. Quantitative analysis of phenotypic elements augments traditional electroclinical classification of common familial epilepsies

19. Concordance for Parkinson's disease in twins: A 20‐year update

20. Essential Tremor Families With Heterogeneous Motor Phenomenology: 'Mixed Motor Disorder'

21. Pygmalion in the genes? On the potentially negative impacts of polygenic scores for educational attainment

22. Patient characteristics and antiseizure medication pathways in newly diagnosed epilepsy: Feasibility and pilot results using the common data model in a single-center electronic medical record database

24. Impact of patient education videos on genetic counseling outcomes after exome sequencing

25. Validity of probands' reports and self-reports of essential tremor: Data from a large family study in North America

26. Familial aggregation of major depressive disorder in an African-American community

27. Gene tests in adults with epilepsy and intellectual disability

28. The 'maternal effect' on epilepsy risk: Analysis of familial epilepsies and reassessment of prior evidence

29. Epilepsy in families: Age at onset is a familial trait, independent of syndrome

30. Genetic attribution and perceived impact of epilepsy in multiplex epilepsy families

31. Parents’ interest in genetic testing of their offspring in multiplex epilepsy families

32. Return of individual results in epilepsy genomic research: A view from the field

33. Whole Genome Sequencing and Rare Variant Analysis in Essential Tremor Families

34. Identification of candidate genes for familial early-onset essential tremor

35. Attention-deficit/hyperactivity disorder symptoms in adults with self-reported epilepsy: Results from a national epidemiologic survey of epilepsy

36. Mood disorders in familial epilepsy: A test of shared etiology

37. Knowledge about Essential Tremor: A Study of Essential Tremor Families

38. Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact

39. Utility of EEG Activation Procedures in Epilepsy: A Population-Based Study

40. Action Tremor Asymmetry Profile Does Not Aggregate in Families with Essential Tremor

41. Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

42. De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies

43. Phenotypic analysis of 303 multiplex families with common epilepsies

44. Genetic testing preferences in families containing multiple individuals with epilepsy

45. Familial risk of epilepsy: a population-based study

46. Essential Tremor in aCharcot-Marie-Tooth Type 2C Kindred Does Not Segregate with the TRPV4 R269H Mutation

47. Whole genome sequencing and rare variant analysis in essential tremor families

48. Racial and ethnic differences in epilepsy classification among probands in the Epilepsy Phenome/Genome Project (EPGP)

49. Prevalence and features of unreported dystonia in a family study of 'pure' essential tremor

50. Evidence for a shared genetic susceptibility to migraine and epilepsy

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