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Sex-specific disease modifiers in juvenile myoclonic epilepsy.
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Shakeshaft A, et al. Among authors: pal dk. Sci Rep. 2022 Feb 21;12(1):2785. doi: 10.1038/s41598-022-06324-2. Sci Rep. 2022. PMID: 35190554 Free PMC article.
Attention impairment in rolandic epilepsy: systematic review.
Kavros PM, Clarke T, Strug LJ, Halperin JM, Dorta NJ, Pal DK. Kavros PM, et al. Among authors: pal dk. Epilepsia. 2008 Sep;49(9):1570-80. doi: 10.1111/j.1528-1167.2008.01610.x. Epub 2008 Apr 11. Epilepsia. 2008. PMID: 18410358 Free article. Review.
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).
Strug LJ, Clarke T, Chiang T, Chien M, Baskurt Z, Li W, Dorfman R, Bali B, Wirrell E, Kugler SL, Mandelbaum DE, Wolf SM, McGoldrick P, Hardison H, Novotny EJ, Ju J, Greenberg DA, Russo JJ, Pal DK. Strug LJ, et al. Among authors: pal dk. Eur J Hum Genet. 2009 Sep;17(9):1171-81. doi: 10.1038/ejhg.2008.267. Epub 2009 Jan 28. Eur J Hum Genet. 2009. PMID: 19172991 Free PMC article.
The genetics of common epilepsies: common or distinct?
Pal DK, Strug LJ. Pal DK, et al. Lancet Neurol. 2014 Sep;13(9):859-60. doi: 10.1016/S1474-4422(14)70124-3. Epub 2014 Jul 30. Lancet Neurol. 2014. PMID: 25087077 Free article. No abstract available.
Prioritizing rare variants with conditional likelihood ratios.
Li W, Dobbins S, Tomlinson I, Houlston R, Pal DK, Strug LJ. Li W, et al. Among authors: pal dk. Hum Hered. 2015;79(1):5-13. doi: 10.1159/000371579. Epub 2015 Feb 3. Hum Hered. 2015. PMID: 25659987 Free PMC article.
340 results