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1. Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

3. Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders

4. Synaptic processes and immune-related pathways implicated in Tourette syndrome.

6. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

9. Paroxysmal Dyskinesias

10. Motor Stereotypies

14. Ataxia

15. Myoclonus

16. Motor Assessments

22. Dystonia

26. Parkinsonism

28. Cerebral Palsy

30. Tremor

32. Sex Differences in People with Tourette Syndrome and Persistent Motor or Vocal Tic Disorder in the Tourette Association of America International Consortium for Genetics Database

35. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.

37. Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene

38. Copy Number Variation in Obsessive-Compulsive Disorder and Tourette Syndrome: A Cross-Disorder Study

39. Genetic association signal near NTN4 in Tourette syndrome

40. Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

41. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.

43. Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2.

44. Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome

47. Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

48. The Challenge of Examining Social Determinants of Health in People Living with Tourette Syndrome

49. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

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