Saul A. Mullen

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

Arvid Suls, Saul A. Mullen, Yvonne Weber et al. · Annals of Neurology · 2009 · 297 citations

Medicine, Genetics, Molecular Genetics +17

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 et al. · Human Molecular Genetics · 2009 · 264 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Mohamad A. Mikati, Yong‐hui Jiang, Michael P. Carboni et al. · Annals of Neurology · 2015 · 223 citations

Medicine, Pharmacology, Pharmacotherapy +17

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

Todor Arsov, Katherine R. Smith, John A. Damiano et al. · The American Journal of Human Genetics · 2011 · 162 citations · Full text

Medicine, Molecular Genetics, Neuroscience +4

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

Saul A. Mullen, Arvid Suls, Peter De Jonghe et al. · Neurology · 2010 · 159 citations

Life Sciences, Genetics, Molecular Genetics +17