Search

Your search keyword '"Stuart A. Scott"' showing total 517 results

Search Constraints

Start Over You searched for: Author "Stuart A. Scott" Remove constraint Author: "Stuart A. Scott"
517 results on '"Stuart A. Scott"'

Search Results

1. Knowledge and attitudes on implementing cardiovascular pharmacogenomic testing

2. Enhanced Visible Light-Driven Photocatalytic Water-Splitting Reaction of Titanate Nanotubes Sensitised with Ru(II) Bipyridyl Complex

3. Pharmacogenomic polygenic risk score for clopidogrel responsiveness among Caribbean Hispanics: A candidate gene approach

4. Multi‐site Investigation of Genetic Determinants of Warfarin Dose Variability in Latinos

5. Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection

6. Standardizing CYP2D6 Genotype to Phenotype Translation: Consensus Recommendations from the Clinical Pharmacogenetics Implementation Consortium and Dutch Pharmacogenetics Working Group

7. Machine Learning for Prediction of Stable Warfarin Dose in US Latinos and Latin Americans

8. Familial inheritance of the 3q29 microdeletion syndrome: case report and review

9. Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints

10. Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study

11. 2042 CYP2C19*2 and PON1 Q192R polymorphisms are associated with platelet reactivity to clopidogrel in Puerto Rican Hispanics with cardiovascular disease

12. Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion

13. Revealing the Nature of Extreme Coronal-line Emitter SDSS J095209.56+214313.3

14. Exploring the Variable Sky with LINEAR. III. Classification of Periodic Light Curves

15. Exploring the Variable Sky with LINEAR. II. Halo Structure and Substructure Traced by RR Lyrae Stars to 30 kpc

17. Characterizing the Optical Variability of Bright Blazars: Variability-Based Selection of Fermi AGN

18. Exploring the Variable Sky with LINEAR. I. Photometric Recalibration with SDSS

21. An efficient genotyper and star-allele caller for pharmacogenomics

23. Characterization of Reference Materials for TPMT and NUDT15

24. Long‐read HiFi sequencing of NUDT15 : Phased full‐gene haplotyping and pharmacogenomic allele discovery

26. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2D6, CYP2C19, CYP2B6, SLC6A4, and HTR2A Genotypes and Serotonin Reuptake Inhibitor Antidepressants

30. Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update

31. Re-envisioning community genetics: community empowerment in preventive genomics

32. The exploration of NiO/Ca2Fe2O5/CaO in chemical looping methane conversion for syngas and H2 production

34. Solvability and nilpotency of expanded groups relative to the nearring of zero and congruence preserving functions

35. Recommendations for Clinical CYP2D6 Genotyping Allele Selection

36. TPMT and NUDT15 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase

39. Pharmacogenomic polygenic risk score for clopidogrel responsiveness among Caribbean Hispanics: A candidate gene approach

40. Aldy 4: An efficient genotyper and star-allele caller for pharmacogenomics

41. Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program

42. Attitudes on pharmacogenomic results as secondary findings among medical geneticists

43. Human Mutation special issue on innovations in genomic diagnostics

44. Limits of performance of chemical looping air separation in packed bed coupled with electricity production

45. Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial

46. Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection

47. Recommendations for Clinical Warfarin Genotyping Allele Selection

48. Haploinsufficiency of the basic helix–loop–helix transcription factor HAND2 causes congenital heart defects

49. VarCover

50. From Binary Groups to Terminal Rings

Catalog

Books, media, physical & digital resources