Saul A. Mullen - Concepedia

Author

Saul A. Mullen

Also Known As

Paul Lightfoot, S Mullen, S. A. Mullen, S. Mullen, S.A. Mullen, Saul A Mullen, Saul A. Mullen, Saul Alator Mullen, Saul Mullen

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

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

About

Saul A. Mullen is an author at The University of Melbourne specializing in medicine, neurology, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	765
2	Social Sciences	3	3	488
3	Public Health	1	1	10
4	Cell Biology	1	1	162
5	Diabetes	1	1	296

Saul A. Mullen

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1 Arvid Suls, Saul A. Mullen, Yvonne Weber, Annals of Neurology Absence EpilepsiesEarly-onset Absence EpilepsyEarly‐onset Absence EpilepsyGeneticsGenetic Epidemiology	2009	296
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance Leanne M. Dibbens, Saul A. Mullen, Heather C. Mefford, Human Molecular Genetics	2009	263
Quinidine in the treatment of<scp>KCNT</scp>1‐positive epilepsies Mohamad A. Mikati, Yong‐hui Jiang, Michael P. Carboni, Annals of Neurology	2015	220
Kufs Disease, the Major Adult Form of Neuronal Ceroid Lipofuscinosis, Caused by Mutations in CLN6 Todor Arsov, Katherine R. Smith, John A. Damiano, The American Journal of Human Genetics Neuro-oncologyKufs DiseasePathologyMajor Adult FormNeurology	2011	162
Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency Saul A. Mullen, Arvid Suls, Peter De Jonghe, Neurology	2010	159
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert, Human Molecular Genetics	2012	149
Precision therapy for epilepsy due to <i>KCNT1</i> mutations Saul A. Mullen, Patrick W. Carney, Annie Roten, Neurology	2017	144
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies Todor Arsov, Saul A. Mullen, Sue Rogers, Annals of Neurology	2012	142
<i>CHD2</i>variants are a risk factor for photosensitivity in epilepsy Elizabeth Galizia, Candace T. Myers, Costin Leu, Brain GeneticsGenetic EpidemiologyUnique Chd2 VariantsDisease Gene IdentificationSynaptic Signaling	2015	135
Glucose Transporter 1 Deficiency as a Treatable Cause of Myoclonic Astatic Epilepsy Saul A. Mullen, Carla Marini, Arvid Suls, Archives of Neurology	2011	134

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