Dennis Lal
Dennis Lal
Director of the Center for Neurogenetics at UTHealth; Visiting Scientist at Broad Institute
Verified email at - Homepage
Cited by
Cited by
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ...
Nature genetics 45 (9), 1067-1072, 2013
De novo variants in neurodevelopmental disorders with epilepsy
HO Heyne, T Singh, H Stamberger, R Abou Jamra, H Caglayan, D Craiu, ...
Nature genetics 50 (7), 1048-1053, 2018
Progress in understanding and treating SCN2A-mediated disorders
SJ Sanders, AJ Campbell, JR Cottrell, RS Moller, FF Wagner, ...
Trends in neurosciences 41 (7), 442-456, 2018
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Nature communications 9 (1), 5269, 2018
Delineating the GRIN1 phenotypic spectrum: a distinct genetic NMDA receptor encephalopathy
JR Lemke, K Geider, KL Helbig, HO Heyne, H Schütz, J Hentschel, ...
Neurology 86 (23), 2171-2178, 2016
Cyclin-dependent kinase-like 5 deficiency disorder: clinical review
HE Olson, ST Demarest, EM Pestana-Knight, LC Swanson, S Iqbal, D Lal, ...
Pediatric neurology 97, 18-25, 2019
ATP11C is critical for the internalization of phosphatidylserine and differentiation of B lymphocytes
M Yabas, CE Teh, S Frankenreiter, D Lal, CM Roots, B Whittle, ...
Nature immunology 12 (5), 441-449, 2011
A cross-disorder dosage sensitivity map of the human genome
RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ...
Cell 185 (16), 3041-3055. e25, 2022
DEPDC5 mutations in genetic focal epilepsies of childhood
D Lal, EM Reinthaler, J Schubert, H Muhle, E Riesch, G Kluger, K Jabbari, ...
Annals of neurology 75 (5), 788-792, 2014
RBFOX1 and RBFOX3 mutations in rolandic epilepsy
D Lal, EM Reinthaler, J Altmüller, MR Toliat, H Thiele, P Nürnberg, ...
PloS one 8 (9), e73323, 2013
Polygenic burden in focal and generalized epilepsies
C Leu, R Stevelink, AW Smith, SB Goleva, M Kanai, L Ferguson, ...
Brain 142 (11), 3473-3481, 2019
Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies
D Lal, AK Ruppert, H Trucks, H Schulz, CG de Kovel, ...
PLoS genetics 11 (5), e1005226, 2015
The ILAE consensus classification of focal cortical dysplasia: an update proposed by an ad hoc task force of the ILAE diagnostic methods commission
I Najm, D Lal, M Alonso Vanegas, F Cendes, I Lopes‐Cendes, A Palmini, ...
Epilepsia 63 (8), 1899-1919, 2022
Idiopathic focal epilepsies: the “lost tribe”
DK Pal, C Ferrie, L Addis, T Akiyama, G Capovilla, R Caraballo, ...
Epileptic Disorders 18 (3), 252-288, 2016
CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development
ST Demarest, HE Olson, A Moss, E Pestana‐Knight, X Zhang, S Parikh, ...
Epilepsia 60 (8), 1733-1742, 2019
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia
K Hardies, CGF De Kovel, S Weckhuysen, B Asselbergh, T Geuens, ...
Brain 138 (11), 3238-3250, 2015
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels
HO Heyne, D Baez-Nieto, S Iqbal, DS Palmer, A Brunklaus, P May, ...
Science translational medicine 12 (556), eaay6848, 2020
Common variant burden contributes to the familial aggregation of migraine in 1,589 families
P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ...
Neuron 98 (4), 743-753. e4, 2018
Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta‐analysis
A Stefanski, Y Calle‐López, C Leu, E Pérez‐Palma, E Pestana‐Knight, ...
Epilepsia 62 (1), 143-151, 2021
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