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1. Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder

2. Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation

3. Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex

4. Full-Spectrum Neuronal Diversity and Stereotypy through Whole Brain Morphometry

5. Altered striatal actin dynamics drives behavioral inflexibility in a mouse model of fragile X syndrome

6. The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder

7. Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes

9. Skewed X-chromosome Inactivation in Unsolved Neurodevelopmental Disease Cases Can Guide Re-evaluation for X-linked Genes

13. Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

14. CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD

15. Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

18. Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome

19. How rare and common risk variation jointly affect liability for autism spectrum disorder

20. Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder

21. KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity

22. Prospective and detailed behavioral phenotyping in DDX3X syndrome

23. Expanding the clinical phenotype of the ultra‐rare Skraban‐Deardorff syndrome: Two novel individuals with WDR26 loss‐of‐function variants and a literature review

24. Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis

25. Prospective and detailed behavioral phenotyping in DDX3X syndrome

28. Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis

30. How rare and common risk variation jointly affect liability for autism spectrum disorder

31. Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

33. Translational derepression of Elavl4 isoforms at their alternative 5′ UTRs determines neuronal development

34. Episignatures stratifying ADNP syndrome show modest correlation with phenotype

35. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

36. Cohort profile: Epidemiology and Genetics of Obsessive–compulsive disorder and chronic tic disorders in Sweden (EGOS)

38. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

40. Deletion of the KH1 Domain ofFmr1Leads to Transcriptional Alterations and Attentional Deficits in Rats

41. 31DISCOVERY AND CHARACTERIZATION OF 102 GENES ASSOCIATED WITH AUTISM FROM EXOME SEQUENCING OF 37,269 INDIVIDUALS

42. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

43. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

44. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

46. Identification of rare de novo epigenetic variations in congenital disorders

47. Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations

49. De Novo Sequence and Copy Number Variants are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

50. Prospective investigation of FOXP1 syndrome

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