Emil K. Gustavsson - Concepedia

Author

Emil K. Gustavsson

Also Known As

Cornelis Blauwendraat, E Gustavsson, E K Gustavsson, E. K. Gustavsson, Elsa Gustavsson, Emil K. Gustavsson, Emil Gustavsson, Emil K Gustavsson, Emil K. Gustavsson, Emil Karl Gustavsson

Publications

Citations

H-Index

Concepts

All Affiliations

University of British Columbia University College London National Hospital for Neurology and Neurosurgery Great Ormond Street Hospital St Olav's University Hospital

About

Emil K. Gustavsson is an author at University of British Columbia specializing in medicine, genetics, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	898
2	Engineering	1	1	12
3	Public Health	1	1	30
4	Social Sciences	1	1	82
5	Biology	1	1	30

Emil K. Gustavsson

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
<i>ggtranscript</i> : an R package for the visualization and interpretation of transcript isoforms using <i>ggplot2</i> Emil K. Gustavsson, David Zhang, Regina H. Reynolds, Bioinformatics	2022	602
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A Anna‐Leigh Brown, Oscar G. Wilkins, Matthew J. Keuss, Nature	2022	471
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, Nature Genetics Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsDementiaGenetic Architecture	2021	448
DNAJC13 mutations in Parkinson disease Carles Vilariño‐Güell, Alex Rajput, Austen J. Milnerwood, Human Molecular Genetics	2013	307
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses Emil K. Gustavsson, Jordan Follett, Joanne Trinh, The Lancet Neurology	2024	96
A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism Joanne Trinh, Rim Amouri, John E. Duda, Neurobiology of Aging MedicineParkinson DiseaseDegenerative DiseaseDegenerative PathologyNeurology	2013	91
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study Joanne Trinh, Emil K. Gustavsson, Carles Vilariño‐Güell, The Lancet Neurology Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2016	84
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects Lynne Krohn, Karl Heilbron, Cornelis Blauwendraat, Nature Communications Sleep DisordersGeneticsGenetic EpidemiologyDisease Gene IdentificationSocial Sciences	2022	82
Altered dopamine release and monoamine transporters in Vps35 p.D620N knock-in mice Stefano Cataldi, Jordan Follett, Jesse D. Fox, npj Parkinson s Disease	2018	78
Normal and pathogenic variation of <i>RFC1</i> repeat expansions: implications for clinical diagnosis Natalia Dominik, Stefania Magri, Riccardo Curró, Brain Disease ProgressionImmunodeficienciesGeneticsDiagnosisPathology	2023	66

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