Search

Your search keyword '"Gail P, Jarvik"' showing total 440 results

Search Constraints

Start Over You searched for: Author "Gail P, Jarvik" Remove constraint Author: "Gail P, Jarvik" Search Limiters Available in Library Collection Remove constraint Search Limiters: Available in Library Collection
440 results on '"Gail P, Jarvik"'

Search Results

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31. Genomic Medicine Year in Review: 2022

32. Multiancestral polygenic risk score for pediatric asthma

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

34. 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

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

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

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

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

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

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

42. Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity

43. Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.

44. Harmonizing variant classification for return of results in the All of Us Research Program

45. Genomic medicine year in review: 2021

46. Neptune: an environment for the delivery of genomic medicine

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

48. PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity1[S]

49. Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index

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

Catalog

Books, media, physical & digital resources