Dalia Kasperavičiūtė

Author

Also Known As

A. Kousathanas, Bigdeli, Tim B., Cecilie B. Hartberg, D Kasperaviciute, D. Kasperaviciute, D. Kasperavičiūtė, Dalia Kasperaviciute, Dalia Kasperaviciūte, Dalia Kasperavičiūte, Dalia Kasperavičiūte˙

134

Publications

11.8K

Citations

H-Index

122

Concepts

All Affiliations

University College London Genomics England Queen Mary University of London William Harvey Research Institute National Hospital for Neurology and Neurosurgery

About

Dalia Kasperavičiūtė is an author at University College London specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	30	4K
2	Public Health	7	7	898
3	Engineering	3	3	657
4	Natural Sciences	3	3	711
5	Health Sciences	1	1	272

Dalia Kasperavičiūtė

Publications

7.3K

Citations

H-Index

Page 1

	Year	Citations
HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans Mark McCormack, Ana Alfirevic, Stéphane Bourgeois, New England Journal of Medicine	2011	899
PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels Antonio Rueda Martin, Eleanor Williams, Rebecca E. Foulger, Nature Genetics Panelapp CrowdsourcesFunctional GenomicsEngineeringData ScienceBiological Database	2019	554
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek, Nature Communications Epilepsy TherapiesGeneticsGenetic EpidemiologyMolecular GeneticsMonogenic Epilepsy Genes	2018	493
A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia Anna C. Need, Dongliang Ge, Michael E. Weale, PLoS Genetics Genome-wide Association StudyPsychiatryRisk PredictionPsychotic DisorderGenetics	2009	445
Genetic architecture of subcortical brain structures in 38,851 individuals Claudia L. Satizábal, Hieab H.H. Adams, Derrek P. Hibar, Nature Genetics Brain StructureDevelopmental Cognitive NeuroscienceNeuroanatomyGeneticsNeuroscience	2019	282
Substitution mutational signatures in whole-genome–sequenced cancers in the UK population Andrea Degasperi, Xueqing Zou, Tauanne Dias Amarante, Science BioinformaticsWhole-genome SequencingFunctional GenomicsSomatic VariantTumor Heterogeneity	2022	272
Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes Erin L. Heinzen, Rodney A. Radtke, Thomas Urban, The American Journal of Human Genetics	2010	258
Novel genetic loci underlying human intracranial volume identified through genome-wide association Hieab H.H. Adams, Derrek P. Hibar, Vincent Chouraki, Nature Neuroscience Genome-wide Association StudyGenome-wide AssociationGeneticsHuman Intracranial VolumeGenetic Epidemiology	2016	255
The genetic basis of DOORS syndrome: an exome-sequencing study Philippe M. Campeau, Dalia Kasperavičiūtė, James T. Lu, The Lancet Neurology	2013	227
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Jennifer C. Schymick, Sonja W. Scholz, Hon‐Chung Fung, The Lancet Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisFirst Stage AnalysisGeneticsMedicine	2007	221

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