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1. The Human Phenotype Ontology in 2024: phenotypes around the world

2. Minimum information and guidelines for reporting a Multiplexed Assay of Variant Effect

5. Loss of transient receptor potential channel 5 causes obesity and postpartum depression

6. Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation

8. Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships—allelic requirement, inheritance modes, and disease mechanisms

9. GA4GH: International policies and standards for data sharing across genomic research and healthcare

10. A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes

14. PSMC5 insufficiency and P320R mutation impair proteasome function

15. Registered access: authorizing data access

16. De novo mutations in regulatory elements in neurodevelopmental disorders.

17. Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions

20. The Human Phenotype Ontology in 2017

21. Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

22. The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant

23. Population screening requires robust evidence—genomics is no exception

24. The Human Phenotype Ontology in 2024: phenotypes around the world

25. Quantifying the contribution of recessive coding variation to developmental disorders

26. A framework for an evidence-based gene list relevant to autism spectrum disorder

27. The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery

29. Large-scale evaluation of outcomes following a genetic diagnosis in children with severe developmental disorders

31. A cellular census of human lungs identifies novel cell states in health and in asthma

32. Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populations

36. Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

37. Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms

38. Optimizing the Diagnosis of Rare Genomic Disease in the UK and Ireland

39. Challenges of whole genome sequencing in population newborn screening.

40. Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations

41. Contribution of retrotransposition to developmental disorders

44. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data

46. Whole genome sequencing of ‘mutation-negative’ individuals with Cornelia de Lange Syndrome

47. De novo putative loss‐of‐function variants in TAF4 are associated with a neuro‐developmental disorder

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

50. Databases in Human and Medical Genetics

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