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1. Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical Practice

2. Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders

3. The Gene Curation Coalition: A global effort to harmonize gene–disease evidence resources

4. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

5. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.

6. Scaling national and international improvement in virtual gene panel curation via a collaborative approach to discordance resolution

7. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

8. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

9. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

10. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

11. Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

12. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

13. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

14. PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels

15. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

16. The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

17. A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

18. GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

19. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

20. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

21. The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources

22. Whole-genome sequencing of patients with rare diseases in a national health system

24. The InterPro protein families database: the classification resource after 15 years

25. Spectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma

26. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

28. InterPro in 2011: new developments in the family and domain prediction database

29. Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

30. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

32. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

33. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

34. Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension

35. InterPro: the integrative protein signature database

36. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

37. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

38. New developments in the InterPro database

39. De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

40. Gene family matters: expanding the HGNC resource

41. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018)

42. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

43. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

44. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

45. Erratum to: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (Scientific Reports, (2018), 8, 1, (1300), 10.1038/s41598-017-14403-y)

46. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

47. Characterization of Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension.

48. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

49. De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

50. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

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