Dorothy Halliday - Concepedia

Author

Dorothy Halliday

Oxford University Hospitals NHS Trust ORCID

Also Known As

D Halliday, D J Halliday, D. Halliday, D.J.X. HALLIDAY, DOROTHY HALLIDAY, Dorothy Halliday, Dorothy J. Halliday, Halliday, D., Justin T. Jordan, Rebecca Collier

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

Oxford University Hospitals NHS Trust University of Manchester University of Oxford Manchester Academic Health Science Centre Cambridge University Hospitals NHS Foundation Trust

About

Dorothy Halliday is an author at Oxford University Hospitals NHS Trust specializing in medicine, pathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	1.1K
2	Engineering	3	3	97
3	Public Health	2	2	766
4	Health Sciences	1	1	41
5	Anesthesia	1	1	11

Dorothy Halliday

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Eric Legius, Ludwine Messiaen, P. Wolkenstein, Genetics in Medicine	2021	687
Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study Laurence Faivre, Gwenaëlle Collod‐Béroud, Bart Loeys, The American Journal of Human Genetics Marfan SyndromeMendelian DisorderGenetic DisorderMedicineGenetics	2007	593
Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers Elizabeth Page, Elizabeth Bancroft, Mark N. Brook, European Urology	2019	231
Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic <i>FBN1</i> Mutations Laurence Faivre, Alice Masurel‐Paulet, Gwenaëlle Collod‐Béroud, PEDIATRICS GeneticsGenetic EpidemiologyPathologyMolecular GeneticsRelated Type	2008	173
Cardiovascular manifestations in men and women carrying a FBN1 mutation Delphine Détaint, Laurence Faivre, Gwenaëlle Collod‐Béroud, European Heart Journal	2010	159
Schwannomatosis: a genetic and epidemiological study D. Gareth Evans, Naomi L. Bowers, Simon Tobi, Journal of Neurology Neurosurgery & Psychiatry	2018	158
Genetic Severity Score predicts clinical phenotype in NF2 Dorothy Halliday, Beatrice Emmanouil, Pieter Pretorius, Journal of Medical Genetics	2017	137
Mutations in <i>LZTR1</i> add to the complex heterogeneity of schwannomatosis Miriam J. Smith, B. Isidor, Christian Beetz, Neurology	2014	121
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset Miriam J. Smith, Jenny Higgs, Naomi L. Bowers, Journal of Medical Genetics	2011	119
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients Adam T. Hexter, Adrian L. Jones, Harry Joe, Journal of Medical Genetics	2015	104

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