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2. Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework

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3. Experiences in providing a community educational resource for the All of Us Researcher Workbench.

4. Response to Spurdle et al.

5. Developing a disease-specific annotation protocol for VHL gene curation using Hypothes.is.

6. CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.

7. Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).

8. Evolution of germline TP53 variant classification in children with cancer.

9. Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.

10. A community approach to the cancer-variant-interpretation bottleneck.

11. ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines.

13. Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures.

14. Response to Maya et al.

15. A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.

16. Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).

17. Standard operating procedure for curation and clinical interpretation of variants in cancer.

18. A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen).

19. Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework.

20. Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels.

21. Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.

22. The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.

23. Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.

24. Pathogenic Germline Variants in 10,389 Adult Cancers.

25. Somatic cancer variant curation and harmonization through consensus minimum variant level data.

26. Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease.

27. SV-STAT accurately detects structural variation via alignment to reference-based assemblies.

28. Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogs.

29. Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing.

30. Assessing structural variation in a personal genome-towards a human reference diploid genome.

31. Transcriptional enhancers in protein-coding exons of vertebrate developmental genes.

32. The importance of being cis: evolution of orthologous fish and mammalian enhancer activity.

33. cneViewer: a database of conserved non-coding elements for studies of tissue-specific gene regulation.