Douglas E. Crompton - Concepedia

Author

Douglas E. Crompton

Also Known As

D. Crompton, D. E. Crompton, D.E. Crompton, Douglas Crompton, Douglas E Crompton, Douglas E. Crompton, Douglas Ewan Crompton

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

The University of Melbourne Northern Health Florey Institute of Neuroscience and Mental Health Austin Health Royal Children's Hospital

About

Douglas E. Crompton is an author at The University of Melbourne specializing in medicine, neuropathology, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.3K
2	Social Sciences	4	4	355
3	Biology	1	1	52
4	Cell Biology	1	1	218
5	Molecular Genetics	1	1	52

Douglas E. Crompton

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in DEPDC5 cause familial focal epilepsy with variable foci Leanne M. Dibbens, Boukje de Vries, Simona Donatello, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsNeurogeneticsVariable Foci	2013	358
Mortality in Dravet syndrome Monica S. Cooper, Anne M. McIntosh, Douglas E. Crompton, Epilepsy Research MedicineDravet SyndromeDegenerative Disease	2016	302
Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy Richard D. Bagnall, Douglas E. Crompton, Slavé Petrovski, Annals of Neurology	2015	274
Mutations in mammalian target of rapamycin regulator <i>DEPDC5</i> cause focal epilepsy with brain malformations Ingrid E. Scheffer, Sarah E. Heron, Brigid M. Regan, Annals of Neurology GeneticsDepdc5 MutationsDisease Gene IdentificationSynaptic SignalingDepdc5-associated Malformations	2014	218
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation Patrick F. Chinnery, Douglas E. Crompton, D. Birchall, Brain	2006	200
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 Mark Corbett, Thessa Kroes, Liana Veneziano, Nature Communications	2019	154
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency Todor Arsov, Saul A. Mullen, John A. Damiano, Epilepsia Clinical DisordersGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2012	115
Deconstruction of Interhospital Transfer Workflow in Large Vessel Occlusion Felix Ng, Essie Low, Emily Andrew, Stroke	2017	91
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance Douglas E. Crompton, Ingrid E. Scheffer, I Taylor, Brain Clinical DisordersNeuropsychologyNeurobiology Of DiseaseBrain DevelopmentNeurological Disorder	2010	89
Melbourne Mobile Stroke Unit and Reperfusion Therapy Henry Zhao, Skye Coote, Damien Easton, Stroke	2020	87

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