Shirley Henderson
Maastricht University(NL)
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Cancer Genomics and Diagnostics, Genomics and Rare Diseases, Prenatal Screening and Diagnostics
Most-Cited Works
- → The 100 000 Genomes Project: bringing whole genome sequencing to the NHS(2018)466 cited
- → Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns(2012)331 cited
- → Mutations in Fibroblast Growth-Factor Receptor 3 in Sporadic Cases of Achondroplasia Occur Exclusively on the Paternally Derived Chromosome(1998)227 cited
- → Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project(2018)186 cited
- → Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme(2024)157 cited
- → EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies(2014)108 cited
- → Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBL(2016)105 cited
- → Fibrinolysis: strategies to enhance the treatment of acute ischemic stroke(2018)99 cited
- → Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition(2009)90 cited
- → A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias(2016)89 cited