Laura L. Klitten

Mutations in<i>SYNGAP1</i>Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency

Martin H. Berryer, Fadi F. Hamdan, Laura L. Klitten et al. · Human Mutation · 2012 · 280 citations

Life Sciences, Genetics, Molecular Genetics +17

Mutations in<i>NRXN1</i>in a family multiply affected with brain disorders:<i>NRXN1</i>mutations and brain disorders

Linh T. Duong, Laura L. Klitten, Rikke S. Møller et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2012 · 82 citations

Life Sciences, Genetics, Molecular Genetics +17

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 et al. · Epilepsia · 2013 · 71 citations

Medicine, Genetics, Epileptology +16

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

Eva M. Reinthaler, Dennis Lal, Sébastien Lebon et al. · Human Molecular Genetics · 2014 · 70 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Exon‐disrupting deletions of <scp><i>NRXN1</i></scp> in idiopathic generalized epilepsy

Rikke S. Møller, Yvonne Weber, Laura L. Klitten et al. · Epilepsia · 2013 · 67 citations · Full text

Life Sciences, Genetics, Neuroscience +15