Evangeline Wassmer - Concepedia

Author

Evangeline Wassmer

Also Known As

Alasdair Parker, Deborah Whitehorn, E Wassmer, E. Wassmer, EVANGELINE WASSMER, Emma Wakeling, Evan Reid, Evangaline Wassmer, Evangeline Wassmer, John A. Todd

254

Publications

14K

Citations

H-Index

165

Concepts

All Affiliations

Birmingham Children's Hospital University College London Great Ormond Street Hospital Evelina London Children's Healthcare Guy's and St Thomas' NHS Foundation Trust

About

Evangeline Wassmer is an author at Birmingham Children's Hospital specializing in medicine, neurology, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	34	4.8K
2	Social Sciences	10	10	428
3	Public Health	6	6	1.1K
4	Health Sciences	4	4	291
5	Education	2	2	32

Evangeline Wassmer

Publications

11.9K

Citations

H-Index

Page 1

	Year	Citations
International Pediatric Multiple Sclerosis Study Group criteria for pediatric multiple sclerosis and immune-mediated central nervous system demyelinating disorders: revisions to the 2007 definitions Lauren Krupp, Marc Tardieu, Maria Pia Amato, Multiple Sclerosis Journal	2013	1.1K
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature Gillian Rice, Paul R. Kasher, Gabriella Forte, Nature Genetics Autoimmune DiseaseGenetic DisorderGeneticsPathogenesisImmunology	2012	916
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response Gillian Rice, Jacquelyn Bond, Aruna Asipu, Nature Genetics AllergyAutoimmune DiseasePathogenesisImmunologyInnate Immune Response	2009	680
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i> Yanick J. Crow, Diana Chase, Johanna L. Schmidt, American Journal of Medical Genetics Part A	2015	589
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease Keren Carss, Gavin Arno, Marie Erwood, The American Journal of Human Genetics Whole-genome SequencingAllelic VariantGenetic DisorderMedicineGenetics	2016	463
Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome Gillian Rice, Teresa Patrick, Rekha Parmar, The American Journal of Human Genetics CardiomyopathyHeart FailureCardiorenal SyndromesCardiovascular DiseaseMolecular Phenotype	2007	442
Disease Course and Treatment Responses in Children With Relapsing Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease Yael Hacohen, Yu Yi M. Wong, Christian Lechner, JAMA Neurology	2018	403
Childhood arterial ischaemic stroke incidence, presenting features, and risk factors: a prospective population-based study Andrew A. Mallick, Vijeya Ganesan, Fenella J. Kirkham, The Lancet Neurology HypertensionVascular DiseaseCerebrovascular DiseaseThrombosisStroke	2013	366
Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease Russell C. Dale, Fabienne Brilot, Lisa Duffy, Neurology	2014	336
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens Yael Hacohen, Sukhvir Wright, Patrick Waters, Journal of Neurology Neurosurgery & Psychiatry	2012	258

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