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1. The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities.

4. Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

5. Clinical associations with a polygenic predisposition to benign lower white blood cell counts

6. Genetic sex validation for sample tracking in next-generation sequencing clinical testing

7. LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry.

8. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

9. Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.

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

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

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

13. Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder

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

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

17. Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system

18. The All of Us Research Program: Data quality, utility, and diversity

19. Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network

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

21. Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

22. Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

23. Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations

25. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

30. Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations

31. Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model

32. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

33. Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing

34. Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

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

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

37. Genetics of varicose veins reveals polygenic architecture and genetic overlap with arterial and venous disease

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

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

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

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

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

44. Precision medicine for developmental and epileptic encephalopathies in Africa—strategies for a resource-limited setting

45. Returning integrated genomic risk and clinical recommendations: The eMERGE study

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

47. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

48. Genome-wide polygenic score to predict chronic kidney disease across ancestries

49. The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research

50. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

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