| Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B RH Wallace, DW Wang, R Singh, IE Scheffer, AL George, HA Phillips, ... Nature genetics 19 (4), 366-370, 1998 | 1446 | 1998 |
| Mutations in Kir2. 1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome NM Plaster, R Tawil, M Tristani-Firouzi, S Canún, S Bendahhou, ... Cell 105 (4), 511-519, 2001 | 1203 | 2001 |
| Molecular mechanism for an inherited cardiac arrhythmia PB Bennett, K Yazawa, N Makita, AL George Jr Nature 376 (6542), 683-685, 1995 | 1153 | 1995 |
| Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel. ME Gellens, AL George Jr, LQ Chen, M Chahine, R Horn, RL Barchi, ... Proceedings of the National Academy of Sciences 89 (2), 554-558, 1992 | 785 | 1992 |
| Molecular basis of charge movement in voltage-gated sodium channels N Yang, AL George, R Horn Neuron 16 (1), 113-122, 1996 | 763 | 1996 |
| Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes P Yang, H Kanki, B Drolet, T Yang, J Wei, PC Viswanathan, SH Hohnloser, ... Circulation 105 (16), 1943-1948, 2002 | 697 | 2002 |
| Prevalence of long-QT syndrome gene variants in sudden infant death syndrome M Arnestad, L Crotti, TO Rognum, R Insolia, M Pedrazzini, C Ferrandi, ... Circulation 115 (3), 361-367, 2007 | 672 | 2007 |
| A common polymorphism associated with antibiotic-induced cardiac arrhythmia F Sesti, GW Abbott, J Wei, KT Murray, S Saksena, PJ Schwartz, SG Priori, ... Proceedings of the National Academy of Sciences 97 (19), 10613-10618, 2000 | 638 | 2000 |
| PiggyBac transposon-mediated gene transfer in human cells MH Wilson, CJ Coates, AL George Molecular therapy 15 (1), 139-145, 2007 | 624 | 2007 |
| Identification of a mutation in the gene causing hyperkalemic periodic paralysis LJ Ptáček, AL George Jr, RC Griggs, R Tawil, RG Kallen, RL Barchi, ... Cell 67 (5), 1021-1027, 1991 | 475 | 1991 |
| Cardiac ion channels DM Roden, JR Balser, AL George Jr, ME Anderson Annual review of physiology 64 (1), 431-475, 2002 | 455 | 2002 |
| Molecular basis of an inherited epilepsy C Lossin, DW Wang, TH Rhodes, CG Vanoye, AL George Neuron 34 (6), 877-884, 2002 | 442 | 2002 |
| Calmodulin mutations associated with recurrent cardiac arrest in infants L Crotti, CN Johnson, E Graf, GM De Ferrari, BF Cuneo, M Ovadia, ... Circulation 127 (9), 1009-1017, 2013 | 439 | 2013 |
| Cardiac Sodium Channel (SCN5A) Variants Associated with Atrial Fibrillation D Darbar, PJ Kannankeril, BS Donahue, G Kucera, T Stubblefield, ... Circulation 117 (15), 1927-1935, 2008 | 426 | 2008 |
| Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+ AT) of rBAT L Feliubadaló, M Font, J Purroy, F Rousaud, X Estivill, V Nunes, E Golomb, ... nature genetics 23 (1), 52-57, 1999 | 384 | 1999 |
| Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation M Chahine, AL George Jr, M Zhou, S Ji, W Sun, RL Barchi, R Horn Neuron 12 (2), 281-294, 1994 | 380 | 1994 |
| Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family DB Mount, A Mercado, L Song, J Xu, AL George, E Delpire, G Gamba Journal of Biological Chemistry 274 (23), 16355-16362, 1999 | 362 | 1999 |
| Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome DW Wang, K Yazawa, AL George Jr, PB Bennett Proceedings of the National Academy of Sciences 93 (23), 13200-13205, 1996 | 342 | 1996 |
| Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita) AL George Jr, MA Crackower, JA Abdalla, AJ Hudson, GC Ebers Nature genetics 3 (4), 305-310, 1993 | 341 | 1993 |
| The genetic basis of variability in drug responses DM Roden, AL George Jr Nature reviews Drug discovery 1 (1), 37-44, 2002 | 339 | 2002 |
