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1. Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel

2. A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early Check implementation

5. Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel

9. Supplementary Materials, Figure S1-S4, Table S1-S9 from Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C

10. Data from Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C

13. O35: Feasibility of expanded newborn screening using genome sequencing for early actionable conditions in a diverse city

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

17. Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C

23. Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional Assay

25. Phenotypic continuum between POLE‐related recessive disorders: A case report and literature review.

35. Additional file 2: of Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls

37. Additional file 4: of Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls

38. Additional file 6: of Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls

39. Additional file 3: of Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls

40. Additional file 5: of Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls

41. Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA repor

43. Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report

44. Chimerism involving a RB1 pathogenic variant in monochorionic dizygotic twins with twin–twin transfusion syndrome.

46. Gene‐specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel

47. MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer

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