Search

Your search keyword '"Scott, Daryl A."' showing total 657 results

Search Constraints

Start Over You searched for: Author "Scott, Daryl A." Remove constraint Author: "Scott, Daryl A."
657 results on '"Scott, Daryl A."'

Search Results

1. Monoallelic de novo AJAP1 loss-of-function variants disrupt trans-synaptic control of neurotransmitter release.

2. PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.

3. Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation

4. Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

5. Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus.

6. Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data.

7. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

8. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

9. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

10. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

11. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

12. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

14. De novo variants in DENND5B cause a neurodevelopmental disorder

15. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

16. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

17. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

19. NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum.

20. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

21. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

22. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

23. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

24. Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum

25. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

26. Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

27. Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

28. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

29. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

30. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

31. Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation

32. Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.

33. Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.

34. ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model

36. Videographic criticism and the art of creative thinking.

37. Genotype–phenotype correlations in individuals with pathogenic RERE variants

38. Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension

39. High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and Coloboma

40. De novo variants in DENND5B cause a neurodevelopmental disorder

41. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

42. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

45. A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay

46. Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variants

47. Abstract 9544: PRDM16 Loss in 1p36 Deletion Syndrome is Associated With Worse Cardiovascular Outcomes: A Multi-Institutional Registry Study

48. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

49. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

50. Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder

Catalog

Books, media, physical & digital resources