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Saul A. Mullen | Researchclopedia

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Saul A. Mullen

Box Hill Hospital ORCID

70

Works

3,118

Citations

26

h-index

36

i10-index

Research Topics

Epilepsy research and treatment Genomics and Rare Diseases Genetics and Neurodevelopmental Disorders

Affiliations

Royal Children's Hospital2015–2025

Box Hill Hospital2013–2026

University of Antwerp2010–2010

University of Melbourne2009–2025

University of South Australia2015–2015

Top Works

Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1

Arvid Suls,Saul A. Mullen,et al.

2009296 citations

Diet and metabolism studies

Metabolism and Genetic Disorders

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Leanne M. Dibbens,Saul A. Mullen,et al.

2009263 citations

Quinidine in the treatment of<scp>KCNT</scp>1‐positive epilepsies

Mohamad A. Mikati,Yong‐hui Jiang,et al.

2015221 citations

Copy number variants are frequent in genetic generalized epilepsy with intellectual disability

Saul A. Mullen,Gemma L. Carvill,et al.

2013186 citations

Kufs Disease, the Major Adult Form of Neuronal Ceroid Lipofuscinosis, Caused by Mutations in CLN6

Todor Arsov,Katherine R. Smith,et al.

2011162 citations

Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency

Saul A. Mullen,Arvid Suls,et al.

2010159 citations

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Michael Steffens,Costin Leu,et al.

2012149 citations

Precision therapy for epilepsy due to <i>KCNT1</i> mutations

Saul A. Mullen,Patrick W. Carney,et al.

2017145 citations

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

Todor Arsov,Saul A. Mullen,et al.

2012142 citations