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1. LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder.

2. Identification of a DNA methylation episignature for recurrent constellations of embryonic malformations

5. Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

7. Blepharophimosis with intellectual disability and Helsmoortel‐Van Der Aa Syndrome share episignature and phenotype.

8. Autistic Disorder: A 20 Year Chronicle

9. Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711

12. SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X‐Linked Intellectual Disability.

13. Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis.

14. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

15. Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports

18. Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability

19. Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy

20. Characterization of a Clinically and Biologically Defined Subgroup of Patients with Autism Spectrum Disorder and Identification of a Tailored Combination Treatment.

22. Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

23. PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.

24. Sleep disturbances in Phelan‐McDermid syndrome: Clinical and metabolic profiling of 56 individuals

25. Elucidating the clinical and molecular spectrum ofSMARCC2-associated NDD in a cohort of 65 affected individuals

26. PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation

27. Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability

28. Multisite Study of Optical Genome Mapping of Retrospective and Prospective Constitutional Disorder Cohorts

32. Functional assessment of homozygous ALDH18A1 variants reveals alterations in amino acid and antioxidant metabolism

33. Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

35. Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders

36. 6. Optical genome mapping as a potential Tier1 test for Postnatal Chromosomal Disorders – results of multi-institutional validation study of 331 retrospective clinical samples

43. Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly

44. Fine-Scale Survey of X Chromosome Copy Number Variants and Indels Underlying Intellectual Disability

45. Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow

46. Multi-site Technical Performance and Concordance of Optical Genome Mapping: Constitutional Postnatal Study for SV, CNV, and Repeat Array Analysis

48. Increased p53 signaling impairs neural differentiation in HUWE1-promoted intellectual disabilities

49. ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons

50. Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders.

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