Steven Petrou - Concepedia

Author

Steven Petrou

Also Known As

Cromer, Brett A., Giuliano Avanzini, Petrou, Steven, S P Petrou, S Petrou, S. Petrou, STEVEN P. PETROU, Stephanie Schorge, Steve Petrou, Steven P Petrou

362

Publications

15.8K

Citations

H-Index

171

Concepts

All Affiliations

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

About

Steven Petrou is an author at The University of Melbourne specializing in medicine, neuroscience, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	68	5.5K
2	Engineering	7	7	387
3	Natural Sciences	6	6	393
4	Health Sciences	3	3	101
5	Education	1	1	58

Steven Petrou

171

Publications

12.3K

Citations

H-Index

Page 1

	Year	Citations
Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures Robyn H. Wallace, Carla Marini, Steven Petrou, Nature Genetics Neurobiology Of DiseaseFebrile SeizuresNeuropharmacologyNeuroscienceNeurology	2001	781
Truncation of the GABAA-Receptor γ2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures Plus Louise A. Harkin, David N. Bowser, Leanne M. Dibbens, The American Journal of Human Genetics Generalized EpilepsyNeurobiology Of DiseaseNeurophysiologyNeuropharmacologyFebrile Seizures Plus	2002	439
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy Sarah E. Heron, Katherine R. Smith, Melanie Bahlo, Nature Genetics ChannelopathiesMissense MutationsHyperpolarization (Biology)NeurophysiologyGenetics	2012	405
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens, Nature Genetics GeneticsNeuroscienceCentral Nervous SystemMedicinePotassium Homeostasis	2014	311
A Glu-496 to Ala Polymorphism Leads to Loss of Function of the Human P2X7 Receptor Ben J. Gu, Weiyi Zhang, Rebecca A. Worthington, Journal of Biological Chemistry	2001	310
<i>KCNT1</i>gain of function in 2 epilepsy phenotypes is reversed by quinidine Carol J. Milligan, Melody Li, Elena V. Gazina, Annals of Neurology	2014	293
<i>GABRA1</i> and <i>STXBP1</i> : Novel genetic causes of Dravet syndrome Gemma L. Carvill, Sarah Weckhuysen, Jacinta M. McMahon, Neurology	2014	254
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
Critical Care Decisions in Fetal and Neonatal Medicine: Ethical Issues Margaret Brazier, Andrew Whitelaw, David Archard, NursingNeonatal ResuscitationCritical Care MedicineNeonatologyMedical Ethics	2007	223
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures Gemma L. Carvill, Jacinta M. McMahon, Amy Schneider, The American Journal of Human Genetics Neurobiology Of DiseaseMolecular NeuroscienceNeurophysiologyGeneticsExperimental Neuropathology	2015	221

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