Search

Your search keyword '"Eason J."' showing total 509 results

Search Constraints

Start Over You searched for: Author "Eason J." Remove constraint Author: "Eason J."
509 results on '"Eason J."'

Search Results

2. Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

6. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

9. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

10. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

11. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

15. Large-scale discovery of novel genetic causes of developmental disorders

23. Skeletal Muscle Grids for Assessing Current Distributions from Defibrillation Shocks

24. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

25. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

26. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

27. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores.

29. Re: Germline BRCA Mutations are Associated with Higher Risk of Nodal Involvement, Distant Metastasis, and Poor Survival Outcomes in Prostate Cancer

37. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

40. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

45. Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders

47. Neonatology and neonatal drug dosage guidelines

49. De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

50. Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

Catalog

Books, media, physical & digital resources