Alison L. Clarke

<i>GABRA1</i> and <i>STXBP1</i> : Novel genetic causes of Dravet syndrome

Gemma L. Carvill, Sarah Weckhuysen, Jacinta M. McMahon et al. · Neurology · 2014 · 260 citations

Life Sciences, Genetics, Molecular Genetics +17

Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy

Heneu O. Tan, Christopher A. Reid, Frank N. Single et al. · Proceedings of the National Academy of Sciences · 2007 · 216 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

A Thr357 to Ser Polymorphism in Homozygous and Compound Heterozygous Subjects Causes Absent or Reduced P2X7 Function and Impairs ATP-induced Mycobacterial Killing by Macrophages

Anne N. Shemon, Ronald Sluyter, Suran L. Fernando et al. · Journal of Biological Chemistry · 2005 · 169 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

An Arg307 to Gln Polymorphism within the ATP-binding Site Causes Loss of Function of the Human P2X7 Receptor

Ben J. Gu, Ronald Sluyter, Kristen K. Skarratt et al. · Journal of Biological Chemistry · 2004 · 144 citations · Full text

Life Sciences, Molecular Genetics, Pharmacology +15

Augmented currents of an <i>HCN2</i> variant in patients with febrile seizure syndromes

Leanne M. Dibbens, Christopher A. Reid, Bree Hodgson et al. · Annals of Neurology · 2009 · 111 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17