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179 results on '"Ruzhnikov, Maura"'

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

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

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

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

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

6. Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy

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

11. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

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

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

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

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

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

19. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.

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

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

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

23. Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing

24. Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy

25. Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review

26. Infantile Spasms of Unknown Cause: Predictors of Outcome and Genotype-Phenotype Correlation

27. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

31. De novo FRMD5 Missense Variants in Patients with Childhood‐Onset Ataxia, Prominent Nystagmus, and Seizures.

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

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

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

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

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

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

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

40. Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome.

42. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

44. Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock

45. Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy

47. Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting

48. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

49. Biochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the ABCD1 Gene

50. Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

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