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

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

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

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

6. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

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

9. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

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

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

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

15. Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

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

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

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

20. De novo variants in DENND5B cause a neurodevelopmental disorder

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

22. Transcriptomics and chromatin accessibility in multiple African population samples

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

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

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

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

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

41. Reducing loneliness and improving well-being among older adults with animatronic pets.

42. Loss-of-function in RBBP5results in a syndromic neurodevelopmental disorder associated with microcephaly

43. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

44. Dominant missense variants in SREBF2are associated with complex dermatological, neurological, and skeletal abnormalities

47. De novo variants in MRTFBhave gain-of-function activity in Drosophilaand are associated with a novel neurodevelopmental phenotype with dysmorphic features

48. Older Adult Caregivers’ Experiences in an Online, Interactive Mindfulness Intervention

49. Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease.

50. Impact of genome build on RNA-seq interpretation and diagnostics.

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