Dennis Lal
Dennis Lal
Assistant Professor and Assistant Staff at Cleveland Clinic; Visiting Scientist at Broad Institute
Bestätigte E-Mail-Adresse bei broadinstitute.org - Startseite
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Zitiert von
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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
3752013
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
1402018
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
1152011
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
1112018
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
1072016
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
1062014
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
912019
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
882013
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
862015
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
TILAE Consortium
Nature communications 9, 2018
792018
16p11. 2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy
EM Reinthaler, D Lal, S Lebon, MS Hildebrand, HHM Dahl, BM Regan, ...
Human molecular genetics 23 (22), 6069-6080, 2014
652014
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
602016
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
D Lal, H Trucks, RS Møller, H Hjalgrim, BPC Koeleman, CGF de Kovel, ...
Epilepsia 54 (2), 265-271, 2013
582013
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
552015
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy
EM Reinthaler, D Lal, W Jurkowski, M Feucht, H Steinböck, ...
Epilepsia 55 (8), e89-e93, 2014
542014
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
532019
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
482018
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
P May, S Girard, M Harrer, DR Bobbili, J Schubert, S Wolking, F Becker, ...
The Lancet Neurology 17 (8), 699-708, 2018
452018
Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes
EM Reinthaler, B Dejanovic, D Lal, M Semtner, Y Merkler, A Reinhold, ...
Annals of neurology 77 (6), 972-986, 2015
452015
Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes
EM Reinthaler, B Dejanovic, D Lal, M Semtner, Y Merkler, A Reinhold, ...
Annals of neurology 77 (6), 972-986, 2015
452015
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