Albee Messing

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

Michael Brenner, Odile Boespflug‐Tanguy, Diana Rodriguez et al. · Nature Genetics · 2001 · 681 citations

Mendelian Disorder, Disease Mechanism, Genetic Disorder +9

hGFAP‐cre transgenic mice for manipulation of glial and neuronal function in vivo

Lang Zhuo, Martin Theis, Ikuri Álvarez-Maya et al. · genesis · 2001 · 662 citations

Deletion of the KV1.1 Potassium Channel Causes Epilepsy in Mice

Sharon L. Smart, Valeri Lopantsev, Chuan-Li Zhang et al. · Neuron · 1998 · 600 citations · Full text

Molecular Neuroscience, Hyperpolarization (Biology), Neurophysiology +10

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy

Steven A. Moore, Fumiaki Saito, Jianguo Chen et al. · Nature · 2002 · 570 citations

Rare Diseases, Medicine, Degenerative Disease +7

Early inactivation of p53 tumor suppressor gene cooperating with NF1 loss induces malignant astrocytoma

Yuan Zhu, Frantz Guignard, Dawen Zhao et al. · Cancer Cell · 2005 · 536 citations · Full text

Neuro-oncology, Glioma, Medicine +10