Suranjith L. Seneviratne

Author

Also Known As

Aine O’Dwyer, Alba Sanchis-Juan, Alex Richter, El-Owaidy, Rasha, Kenneth Smith, R S H Pumphrey, Ravishankar Sargur, S L Seneviratne, S Seneviratne, S. L. Seneviratne

211

Publications

10.1K

Citations

H-Index

101

Concepts

All Affiliations

University College London The Royal Free Hospital University of Manchester University of Freiburg University Medical Center Utrecht

About

Suranjith L. Seneviratne is an author at University College London specializing in medicine, immunology, and autoimmunity.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	27	3.8K
2	Allergy	9	9	808
3	Public Health	5	5	290
4	Allergy Medicine	3	3	192
5	Natural Sciences	1	1	285

Suranjith L. Seneviratne

Publications

6.1K

Citations

H-Index

Page 1

	Year	Citations
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations Desirée Schubert, Claudia Bode, Rupert Kenefeck, Nature Medicine ImmunogeneticsAutoimmune DiseaseImmunodeficienciesGeneticsImmunology	2014	805
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
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects Charlotte Schwab, Annemarie Gabrysch, Peter Olbrich, Journal of Allergy and Clinical Immunology Clinical ImmunologyAllergyLymphocyte DevelopmentMedicineImmunodeficiencies	2018	423
Longitudinal Analysis of CD8<sup>+</sup>T Cells Specific for Structural and Nonstructural Hepatitis B Virus Proteins in Patients with Chronic Hepatitis B: Implications for Immunotherapy George Webster, Stephanie Reignat, David J. Brown, Journal of Virology	2004	383
The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency Laura Gámez‐Díaz, Dietrich August, Polina Stepensky, Journal of Allergy and Clinical Immunology Protein FunctionProtein ExpressionGenetic DisorderNatural SciencesGenetics	2016	285
COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience Adrian Shields, Siobhan O. Burns, Sinisa Savic, Journal of Allergy and Clinical Immunology Primary ImmunodeficiencySecondary ImmunodeficiencyUnited Kingdom ExperienceCovid-19 PandemicCovid-19 Epidemiology	2020	234
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans Paul Tuijnenburg, Hana Lango Allen, Siobhan O. Burns, Journal of Allergy and Clinical Immunology Primary ImmunodeficiencyDisease SusceptibilityImmune Cell DevelopmentGeneticsImmunodeficiencies	2018	227
Escaping High Viral Load Exhaustion Stephanie Reignat, George Webster, David J. Brown, The Journal of Experimental Medicine	2002	216
Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency Claudia Wehr, Andrew R. Gennery, Caroline A. Lindemans, Journal of Allergy and Clinical Immunology Primary ImmunodeficiencyTransplantationMarrow TransplantationStem Cell TransplantationImmunology	2015	138
The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1 Mark Depner, Sebastian Fuchs, Jan Raabe, Journal of Clinical Immunology	2015	137

Page 1