Lata Vadlamudi

Array-Based Gene Discovery with Three Unrelated Subjects Shows SCARB2/LIMP-2 Deficiency Causes Myoclonus Epilepsy and Glomerulosclerosis

Samuel F. Berkovic, Leanne M. Dibbens, Alicia Oshlack et al. · The American Journal of Human Genetics · 2008 · 255 citations · Full text

Rare Diseases, Systems Biology, Three Unrelated Subjects +10

Mutations in mammalian target of rapamycin regulator <i>DEPDC5</i> cause focal epilepsy with brain malformations

Ingrid E. Scheffer, Sarah E. Heron, Brigid M. Regan et al. · Annals of Neurology · 2014 · 218 citations · Full text

Genetics, Depdc5 Mutations, Disease Gene Identification +20

Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults

Floor E. Jansen, Lynette G. Sadleir, Louise A. Harkin et al. · Neurology · 2006 · 159 citations

Genetic epilepsy with febrile seizures plus

Yuehua Zhang, Rosemary Burgess, Jodie P. Malone et al. · Neurology · 2017 · 131 citations

Timing of De Novo Mutagenesis — A Twin Study of Sodium-Channel Mutations

Lata Vadlamudi, Leanne M. Dibbens, Kate Lawrence et al. · New England Journal of Medicine · 2010 · 104 citations · Full text

Brain Development, Genetics, Molecular Biology +22