19 results on '"Kattman, Brandi"'
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2. eP369: Increased automation reduces turnaround time for submissions to ClinVar
3. G6PD deficiency and pharmacogenetics: safer prescribing with Medical Genetics Summaries (MGS)
4. ClinVar supports automated submission by API
5. How the NIH Genetic Testing Registry and Medical Genetics Summaries can help oncologists adopt pharmacogenetics guidelines.
6. ClinVar: improvements to accessing data
7. SPDI: data model for variants and applications at NCBI
8. GRAF-pop: A Fast Distance-Based Method To Infer Subject Ancestry from Multiple Genotype Datasets Without Principal Components Analysis
9. Personalizing cancer treatment using gene activity scores with the NIH Medical Genetics Summaries.
10. ClinVar at five years: Delivering on the promise
11. ClinGen's GenomeConnect registry enables patient‐centered data sharing
12. FDA review, CMS coverage, and NIH information for next generation sequencing.
13. Points to consider for sharing variant-level information from clinical genetic testing with ClinVar
14. ClinVar: improving access to variant interpretations and supporting evidence
15. Landscape scanning of cancer gene panels: A report from the NIH Genetic Testing Registry (GTR).
16. The NIH Genetic Testing Registry and content tailored for oncologists.
17. The NIH genetic testing registry: Hereditary, pharmacogenetic, and somatic tests for oncology practice.
18. The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency
19. Prenatal Identification of a Novel R937P L1CAM Missense Mutation
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