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235 results on '"Lebo, Matthew S."'

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1. Preparing to Integrate Generative Pretrained Transformer Series 4 models into Genetic Variant Assessment Workflows: Assessing Performance, Drift, and Nondeterminism Characteristics Relative to Classifying Functional Evidence in Literature

2. Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

3. The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change

4. The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care

6. Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

8. Development of a clinical polygenic risk score assay and reporting workflow

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

11. Twenty-Five Years of Germline Genetic Testing and What May Lie Ahead

12. Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease

13. Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

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

15. Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test

16. Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

17. Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol

19. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

21. Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study

23. Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

24. Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers

25. Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

26. The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change

28. The Evolution of a Large Biobank at Mass General Brigham

30. Additional file 1 of Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

31. Additional file 1 of Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization

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

33. Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

34. Validation of a Trans-Ancestry Polygenic Risk Score for Type 2 Diabetes in Diverse Populations

35. Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations

37. Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project

39. Additional file of Dynamic, mating-induced gene expression changes in female head and brain tissues of Drosophila melanogaster

40. Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository

41. A Framework for Automated Gene Selection in Genomic Screening

42. Airmen and health-care providers’ attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project

43. Prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test

44. An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

47. Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry

49. Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study

50. Automated Typing of Red Blood Cell and Platelet Antigens from Whole Genome Sequencing

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