Laura Jansen
Laura Jansen
Associate Professor of Neurology, Washington University
Verified email at
Cited by
Cited by
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
LA Jansen, GM Mirzaa, GE Ishak, BJ O'Roak, JB Hiatt, WH Roden, ...
Brain 138 (6), 1613-1628, 2015
Impaired glial glutamate transport in a mouse tuberous sclerosis epilepsy model
M Wong, KC Ess, EJ Uhlmann, LA Jansen, W Li, PB Crino, S Mennerick, ...
Annals of neurology 54 (2), 251-256, 2003
Association of MTOR mutations with developmental brain disorders, including megalencephaly, focal cortical dysplasia, and pigmentary mosaicism
GM Mirzaa, CD Campbell, N Solovieff, CP Goold, LA Jansen, S Menon, ...
JAMA neurology 73 (7), 836-845, 2016
Response to treatment in a prospective national infantile spasms cohort.
KG Knupp
Ann Neurol 79 (3), 475-484, 2016
Abnormal glutamate homeostasis and impaired synaptic plasticity and learning in a mouse model of tuberous sclerosis complex
LH Zeng, Y Ouyang, V Gazit, JR Cirrito, LA Jansen, KC Ess, KA Yamada, ...
Neurobiology of disease 28 (2), 184-196, 2007
Epileptogenesis and Reduced Inward Rectifier Potassium Current in Tuberous Sclerosis Complex‐1–Deficient Astrocytes
LA Jansen, EJ Uhlmann, PB Crino, DH Gutmann, M Wong
Epilepsia 46 (12), 1871-1880, 2005
How should children with West syndrome be efficiently and accurately investigated? Results from the National Infantile Spasms Consortium.
EC Wirrell
Epilepsia 56 (4), 617-625, 2015
Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly
AR Paciorkowski, SS McDaniel, LA Jansen, H Tully, E Tuttle, ...
Epilepsia 56 (3), 422-430, 2015
Impaired maturation of cortical GABAA receptor expression in pediatric epilepsy
LA Jansen, LD Peugh, WH Roden, JG Ojemann
Epilepsia 51 (8), 1456-1467, 2010
Review of commercially available epilepsy genetic panels
C Chambers, LA Jansen, R Dhamija
Journal of genetic counseling 25 (2), 213-217, 2016
Glial localization of antiquitin: implications for pyridoxine‐dependent epilepsy
LA Jansen, RF Hevner, WH Roden, SH Hahn, S Jung, SM Gospe Jr
Annals of neurology 75 (1), 22-32, 2014
Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome
CS Cheah, RE Westenbroek, WH Roden, F Kalume, JC Oakley, ...
Channels 7 (6), 468-472, 2013
Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort.
KG Knupp
Epilepsia 57 (11), 1834-1842, 2016
De novo mutations in SIK1 cause a spectrum of developmental epilepsies
J Hansen, C Snow, E Tuttle, DH Ghoneim, CS Yang, A Spencer, ...
The American Journal of Human Genetics 96 (4), 682-690, 2015
Somatic mosaicism in Menkes disease suggests choroid plexus‐mediated copper transport to the developing brain
A Donsante, P Johnson, LA Jansen, SG Kaler
American journal of medical genetics Part A 152 (10), 2529-2534, 2010
Mechanism of catecholamine synthesis inhibition by neuropeptide Y: role of Ca2+ channels and protein kinases
LA McCullough
J Neurochem 67, 1090-1099, 1996
Altered GABAA receptor subunit expression and pharmacology in human Angelman syndrome cortex
WH Roden, LD Peugh, LA Jansen
Neuroscience letters 483 (3), 167-172, 2010
Neuropeptide Y inhibition of calcium channels in PC-12 pheochromocytoma cells.
LA McCullough
Am J Physiol-Cell Ph 274, C1290-C1297, 1998
Neuropeptide Y inhibits depolarization-stimulated catecholamine synthesis in rat pheochromocytoma cells.
LA McCullough
Eur J Pharmacol 287, 271-277, 1995
The epilepsy genetics initiative: systematic reanalysis of diagnostic exomes increases yield
Epilepsy Genetics Initiative, SF Berkovic, DB Goldstein, EL Heinzen, ...
Epilepsia 60 (5), 797-806, 2019
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