Brigid M. Regan - Concepedia

Author

Brigid M. Regan

The University of Melbourne ORCID

Also Known As

Alison M. Muir, Brigid M Regan, Brigid M. Regan, Brigid Regan, Costin Leu, Kevin McKenna, Mark I. Rees, Paula Pyzik

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

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

About

Brigid M. Regan is an author at The University of Melbourne specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	1.9K
2	Social Sciences	2	2	282
3	Cell Biology	2	2	280
4	Public Health	1	1	58
5	Immunology	1	1	62

Brigid M. Regan

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
GRIN2A mutations cause epilepsy-aphasia spectrum disorders Gemma L. Carvill, Brigid M. Regan, Simone C. Yendle, Nature Genetics Genetic DisorderGrin2a MutationsNeurologyNeuroscienceNeuropathology	2013	372
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
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, The American Journal of Human Genetics Allelic VariantUltra-rare Genetic VariationWhole-exome Sequencing StudyGeneticsGenetic Disorder	2019	298
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
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study Andrew S. Allen, Susannah T. Bellows, Samuel F. Berkovic, The Lancet Neurology Allelic VariantUltra-rare Genetic VariationMedicineGeneticsGenetic Disorder	2017	232
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
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
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies Gemma L. Carvill, Krysta L. Engel, Aishwarya Ramamurthy, The American Journal of Human Genetics Scn1a-associated Genetic EpilepsiesGenetic DisorderGeneticsPathologyMolecular Genetics	2018	120
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsy Piero Perucca, Ingrid E. Scheffer, A. Simon Harvey, Epilepsy Research BioinformaticsFunctional GenomicsNext-generation SequencingGeneticsWhole Exome	2017	102
Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability Felippe Borlot, Brigid M. Regan, Anne S. Bassett, JAMA Neurology	2017	94

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