Shirley Henderson - Concepedia

Author

Shirley Henderson

Also Known As

A. Giess, Anders Edsjö, Barbara De la Salle, R. Jackson, S Henderson, S. HENDERSON, S. Henderson, S.J. HENDERSON, S.J. Henderson, SHIRLEY HENDERSON

105

Publications

3.7K

Citations

H-Index

Concepts

All Affiliations

William Harvey Research Institute Queen Mary University of London University College London Genomics England University of Oxford

About

Shirley Henderson is an author at William Harvey Research Institute specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	567
2	Public Health	5	5	163
3	Engineering	1	1	66
4	Health Sciences	1	1	21
5	Natural Sciences	1	1	89

Shirley Henderson

Publications

Citations

H-Index

Page 1

	Year	Citations
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS Clare Turnbull, Richard H. Scott, Ellen Thomas, BMJ	2018	456
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns Anna Schuh, Jennifer Becq, Sean Humphray, Blood	2012	331
Mutations in Fibroblast Growth-Factor Receptor 3 in Sporadic Cases of Achondroplasia Occur Exclusively on the Paternally Derived Chromosome Douglas J. Wilkin, Jinny Szabo, Rhoda Cameron, The American Journal of Human Genetics	1998	225
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project Pauline Robbe, Niko Popitsch, Samantha J.L. Knight, Genetics in Medicine	2018	168
Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme Alona Sosinsky, John C. Ambrose, William Cross, Nature Medicine	2024	148
Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition Karen M. Lower, Jim R. Hughes, Marco De Gobbi, Proceedings of the National Academy of Sciences Nme4 ExpressionGeneticsGenomic MechanismMolecular BiologyGene Characterization	2009	89
A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias Noémi Roy, Edward A. Wilson, Shirley Henderson, British Journal of Haematology ImmunohematologyGenetic TestingGeneticsGenetic EpidemiologyDiagnosis	2016	88
Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults Alice E. Gallienne, Hélène Dreau, Anna Schuh, Haematologica	2011	81
Signatures of TOP1 transcription-associated mutagenesis in cancer and germline Martin A.M. Reijns, David Parry, Thomas Williams, Nature	2022	80
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis Ramita Dewan, Ruth Chia, Jinhui Ding, Neuron Amyotrophic Lateral SclerosisAlzheimer's DiseasePathologyDegenerative DiseaseFrontotemporal Dementia	2020	79

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