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1. Familial co-segregation and the emerging role of long-read sequencing to re-classify variants of uncertain significance in inherited retinal diseases

2. Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

3. Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

4. Adults with lysosomal storage diseases in the undiagnosed diseases network

5. Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation

6. Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men

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

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

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

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

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

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

15. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

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

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

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

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

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

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

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

26. Rare loss of function variants in candidate genes and risk of colorectal cancer

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

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

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

35. Actionable exomic incidental findings in 6503 participants: challenges of variant classification

37. Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition

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

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

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

42. List of contributors

44. Schizencephaly

45. Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

47. Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders

48. The Current State of Genetic Testing Platforms for Inherited Retinal Diseases

50. List of Contributors

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