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1. Genetic predictors of blood pressure traits are associated with preeclampsia

2. Variant level heritability estimates of type 2 diabetes in African Americans

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

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

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

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

7. Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach

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

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

10. 47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations

11. Genome-wide association study of susceptibility to hospitalised respiratory infections [version 2; peer review: 1 approved, 2 approved with reservations]

12. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

13. A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.

14. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

15. Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders

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

17. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions

18. Angiopoietin-Like4 Is a Novel Marker of COVID-19 Severity

19. The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene

20. Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

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

22. Medical records-based chronic kidney disease phenotype for clinical care and 'big data' observational and genetic studies

23. Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network.

24. Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort

25. ShareDNA: a smartphone app to facilitate family communication of genetic results

27. Childhood exposures to environmental chemicals and neurodevelopmental outcomes in congenital heart disease.

28. Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.

29. Enrichment sampling for a multi-site patient survey using electronic health records and census data.

30. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network

31. Differences in atheroma between Caucasian and Asian subjects with anterior stroke: A vessel wall MRI study

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

33. Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis

34. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.

35. A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

36. Genomic Medicine Year in Review: 2022

37. Multiancestral polygenic risk score for pediatric asthma

38. Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

39. Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network

40. Genomic considerations for FHIR®; eMERGE implementation lessons.

41. Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results

43. Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies.

44. Risk‐reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system

45. Centers for Mendelian Genomics: A decade of facilitating gene discovery

46. New insights into the genetic etiology of Alzheimer's disease and related dementias

47. Conducting a large, multi-site survey about patients’ views on broad consent: challenges and solutions

49. Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

50. Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia

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