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29 results on '"Sullivan, Kathleen"'

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

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

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

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

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

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

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

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

9. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome

10. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome

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

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

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

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

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

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

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

18. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

19. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

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

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

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

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

24. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

25. Variants in PRKAR1Bcause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

26. Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

27. An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

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

29. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

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