Articles with public access mandates - Dennis LalLearn more
Not available anywhere: 4
Review
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
Mandates: US National Institutes of Health, German Research Foundation
Review
Spectrum of GABAA receptor variants in epilepsy
S Maljevic, RS Møller, CA Reid, E Pérez-Palma, D Lal, P May, H Lerche
Current opinion in neurology 32 (2), 183-190, 2019
Mandates: National Health and Medical Research Council, Australia, German Research …
Review
Investigation of GRIN2A in common epilepsy phenotypes
D Lal, S Steinbrücker, J Schubert, T Sander, F Becker, Y Weber, H Lerche, ...
Epilepsy research 115, 95-99, 2015
Mandates: Austrian Science Fund, German Research Foundation
Review
Copy Number Variation Analysis from SNP Genotyping Microarrays in Large Cohorts of Neurological Disorders
E Perez-Palma, LM Niestroj, M Inca-Martínez, C Villaman, EI Sarihan, ...
Genomic Structural Variants in Nervous System Disorders, 173-195, 2022
Mandates: US National Institutes of Health, Michael J Fox Foundation, Parkinson's …
Available somewhere: 116
Review
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
Mandates: US National Institutes of Health, Austrian Science Fund, Research Foundation …
Review
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
Mandates: Research Foundation (Flanders), German Research Foundation, UK Medical …
Review
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
Mandates: US National Institutes of Health
Review
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Nature communications 9 (1), 5269, 2018
Mandates: US National Institutes of Health, National Health and Medical Research …
Review
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
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Review
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
Mandates: US National Institutes of Health, National Health and Medical Research …
Review
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
Mandates: Research Foundation (Flanders), German Research Foundation
Review
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
Mandates: US National Science Foundation, Swiss National Science Foundation, US …
Review
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies
RJL Anney, A Avbersek, D Balding, L Baum, F Becker, SF Berkovic, ...
The Lancet Neurology, 2014
Mandates: US National Institutes of Health, National Health and Medical Research …
Review
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
Mandates: US National Institutes of Health, National Institute for Health Research, UK
Review
CHD2 variants are a risk factor for photosensitivity in epilepsy
EC Galizia, CT Myers, C Leu, CGF De Kovel, T Afrikanova, ...
Brain 138 (5), 1198-1208, 2015
Mandates: US National Institutes of Health, National Health and Medical Research …
Review
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
Mandates: US National Institutes of Health, Austrian Science Fund, German Research …
Review
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
Mandates: US National Institutes of Health, Austrian Science Fund
Review
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
Mandates: US National Institutes of Health
Review
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
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Review
A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants
JA López-Rivera, E Pérez-Palma, J Symonds, AS Lindy, DA McKnight, ...
Brain 143 (4), 1099-1105, 2020
Mandates: US National Institutes of Health
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