Simone C. Yendle - Concepedia

Concepedia

Author

Simone C. Yendle

The University of Melbourne ORCID

Also Known As

S. C. Yendle, S. Yendle, S.C. Yendle, Simone C Yendle, Simone C. Yendle, Simone Yendle

14

Publications

2.7K

Citations

13

H-Index

16

Concepts

All Affiliations

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

SC

About

Simone C. Yendle is an author at The University of Melbourne specializing in neurogenetics, medicine, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	1.2K
2	Neuroscience	5	5	1.2K
3	Neurology	4	4	510
4	Social Sciences	2	2	125
5	Molecular Medicine	1	1	54

Simone C. Yendle

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13

Publications

2.7K

Citations

13

H-Index

	Year	Citations
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1 Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle, Nature Genetics GeneticsNovo MutationsNeurotransmissionNeuroscienceEpileptic Encephalopathies Identifies	2013	683
<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Annals of Neurology	2011	494
GRIN2A mutations cause epilepsy-aphasia spectrum disorders Gemma L. Carvill, Brigid M. Regan, Simone C. Yendle, Nature Genetics Genetic DisorderGrin2a MutationsNeurologyNeuroscienceNeuropathology	2013	372
Rare copy number variants are an important cause of epileptic encephalopathies Heather C. Mefford, Simone C. Yendle, Cynthia L. Hsu, Annals of Neurology	2011	243
Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology Claudia B. Catarino, Joan Liu, Ioannis Liagkouras, Brain	2011	218
Clinical spectrum of early-onset epileptic encephalopathies associated with <i>STXBP1</i> mutations Liesbet Deprez, Sarah Weckhuysen, Philip Holmgren, Neurology	2010	167
Mutations in <i><scp>KCNT</scp>1</i> cause a spectrum of focal epilepsies Rikke S. Møller, Sarah E. Heron, Line H.G. Larsen, Epilepsia	2015	147
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome Bronwyn E. Grinton, Sarah E. Heron, James T. Pelekanos, Epilepsia	2015	125
De novo <i>SCN1A</i> mutations in migrating partial seizures of infancy Daniel Carranza Rojo, L Hamiwka, Jacinta M. McMahon, Neurology	2011	105
Reduction of seizure frequency after epilepsy surgery in a patient with <scp><i>STXBP1</i></scp> encephalopathy and clinical description of six novel mutation carriers Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx, Epilepsia Neurological DisorderGeneticsWest SyndromeGenetic EpidemiologyClinical Neurology	2013	71

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