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

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

3. Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

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

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

6. 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)

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

8. Pathogenic Germline Variants in 10,389 Adult Cancers

10. 16. ClinGen Cancer Variant Interpretation (CVI) Committee: Pilot guidance for somatic cancer variant curation expert panels

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

13. Macrocephaly and developmental delay caused by missense variants in RAB5C

14. Response to Spurdle et al

16. P103: Operationalizing structured curated scientific literature (CIViC and Hypothesis) in developing gene-specific recommendations of the ClinGen VHL Variant Curation Expert Panel

18. Macrocephaly and developmental delay caused by missense variants in RAB5C

19. Response to Maya et al.

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

22. P061: ATM and PALB2 variant curation guidelines progress update: ClinGen Hereditary Breast, Ovarian, and Pancreatic Cancer Variant Curation Expert Panel

25. P673: Batch ClinVar submission support in ClinGen’s Variant Curation Interface (VCI)

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

27. 112. ClinGen Somatic Cancer Variant Interpretation (CVI) committee and the Somatic Cancer expert panel process

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

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

30. Specifications of the ACMG/AMP Variant Classification Guidelines for Germline DICER1 Variant Curation.

31. eP055: The Clinical Genome Resource (ClinGen) Somatic Cancer Clinical Domain Working Group

32. eP063: Genetic variants associated with childhood cancers: Curation initiatives of the ClinGen Somatic Cancer Pediatric Taskforce

33. 45. Community curation for Von Hippel Lindau disease

34. 15. Standard procedure for the curation and maintenance of cancer-specific gene lists

35. 17. Multi-consortia initiative to standardize the representation and curation of oncogenic fusions

36. Correction: 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)

37. Abstract 449: A standard operating procedure for the curation of gene fusions

38. Abstract 210: Advancing knowledgebase representation of pediatric cancer variants through ClinGen/CIViC collaboration

39. Evolution of the open-access CIViC knowledgebase is driven by the needs of the cancer variant interpretation community

40. A systematic approach to identify functional motifs within vertebrate developmental enhancers

41. A web-based educational program to support the updated ACMG/ ClinGen technical standards for constitutional copy number variant classification

42. ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

43. 68. ClinGen Cancer Variant Interpretation (CVI): Updates and recommendations on the ClinGen/CGC/VICC Oncogenicity SOP.

44. Abstract 3215: ClinGen somatic cancer working group: Disseminating standardized cancer molecular diagnostic data and evidence through global collaboration and expert curation

45. Abstract 3211: Evolution of the CIViC knowledgebase for community driven curation of clinical variants in cancer

46. Abstract 1096: Harmonization standards from the Variant Interpretation for Cancer Consortium

47. Abstract A58: Curation of pediatric cancer variants within the Clinical Genome Resource (ClinGen)

48. 46. ClinGen somatic cancer working group: Enhancing standardized interpretation of cancer genetic data for clinical use

49. 30. Curation of genetic variants in childhood cancers within the Clinical Genome Resource (ClinGen)

50. Clinical genetics lacks standard definitions and protocols for the collection and use of diversity measures

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