21. Guideline‐based and bioinformatic reassessment of lesion‐associated gene and variant pathogenicity in focal human epilepsies. (20th October 2018) Authors: Niestroj, Lisa‐Marie; Du, Juanjiangmeng; Nothnagel, Michael; May, Patrick; Palotie, Aarno; Daly, Mark J.; Nürnberg, Peter; Blümcke, Ingmar; Lal, Dennis Journal: Epilepsia Issue: Volume 59:issue 11(2018) Page Start: 2145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
22. Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. Issue 9 (29th July 2017) Authors: Pérez-Palma, Eduardo; Helbig, Ingo; Klein, Karl Martin; Anttila, Verneri; Horn, Heiko; Reinthaler, Eva Maria; Gormley, Padhraig; Ganna, Andrea; Byrnes, Andrea; Pernhorst, Katharina; Toliat, Mohammad R; Saarentaus, Elmo; Howrigan, Daniel P; Hoffman, Per; Miquel, Juan Francisco; De Ferrari, Giancar... Journal: Journal of medical genetics Issue: Volume 54:Issue 9(2017) Page Start: 598 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
23. Idiopathic focal epilepsies: the "lost tribe"th. Issue 3 (9th September 2016) Authors: Pal, Deb K.; Ferrie, Colin; Addis, Laura; Akiyama, Tomoyuki; Capovilla, Giuseppe; Caraballo, Roberto; de Saint‐Martin, Anne; Fejerman, Natalio; Guerrini, Renzo; Hamandi, Khalid; Helbig, Ingo; Ioannides, Andreas A.; Kobayashi, Katsuhiro; Lal, Dennis; Lesca, Gaetan; Muhle, Hiltrud; Neubauer, Bernd ... Journal: Epileptic disorders Issue: Volume 18:Issue 3(2016:Sep.) Page Start: 252 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
24. Lessons learned from 40 novel PIGA patients and a review of the literature. (26th May 2020) Authors: Bayat, Allan; Knaus, Alexej; Pendziwiat, Manuela; Afenjar, Alexandra; Barakat, Tahsin Stefan; Bosch, Friedrich; Callewaert, Bert; Calvas, Patrick; Ceulemans, Berten; Chassaing, Nicolas; Depienne, Christel; Endziniene, Milda; Ferreira, Carlos R.; Moura de Souza, Carolina Fischinger; Freihuber, Céc... Journal: Epilepsia Issue: Volume 61:issue 6(2020) Page Start: 1142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
25. MISCAST: MIssense variant to protein StruCture Analysis web SuiTe. Issue Volume 48:Issue W1(2020) (13th May 2020) Authors: Iqbal, Sumaiya; Hoksza, David; Pérez-Palma, Eduardo; May, Patrick; Jespersen, Jakob B; Ahmed, Shehab S; Rifat, Zaara T; Heyne, Henrike O; Rahman, M Sohel; Cottrell, Jeffrey R; Wagner, Florence F; Daly, Mark J; Campbell, Arthur J; Lal, Dennis Journal: Nucleic acids research Issue: Volume 48:Issue W1(2020) Page Start: W132 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
26. Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumours. Issue 11 (November 2021) Authors: Blumcke, Ingmar; Budday, Silvia; Poduri, Annapurna; Lal, Dennis; Kobow, Katja; Baulac, Stephanie Journal: Lancet neurology Issue: Volume 20:Issue 11(2021) Page Start: 943 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
27. Polygenic risk heterogeneity among focal epilepsies. (14th October 2020) Authors: Gramm, Marie; Leu, Costin; Pérez‐Palma, Eduardo; Ferguson, Lisa; Jehi, Lara; Daly, Mark J.; Najm, Imad M.; Busch, Robyn M.; Lal, Dennis Journal: Epilepsia Issue: Volume 61:issue 11(2020) Page Start: e179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
28. Progress in Understanding and Treating SCN2A-Mediated Disorders. Issue 7 (July 2018) Authors: Sanders, Stephan J.; Campbell, Arthur J.; Cottrell, Jeffrey R.; Moller, Rikke S.; Wagner, Florence F.; Auldridge, Angie L.; Bernier, Raphael A.; Catterall, William A.; Chung, Wendy K.; Empfield, James R.; George, Alfred L.; Hipp, Joerg F.; Khwaja, Omar; Kiskinis, Evangelos; Lal, Dennis; Malhotra,... Journal: Trends in neurosciences Issue: Volume 41:Issue 7(2018) Page Start: 442 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
29. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study. Issue 8 (August 2018) Authors: May, Patrick; Girard, Simon; Harrer, Merle; Bobbili, Dheeraj R; Schubert, Julian; Wolking, Stefan; Becker, Felicitas; Lachance-Touchette, Pamela; Meloche, Caroline; Gravel, Micheline; Niturad, Cristina E; Knaus, Julia; De Kovel, Carolien; Toliat, Mohamad; Polvi, Anne; Iacomino, Michele; Guerrero-... Journal: Lancet neurology Issue: Volume 17:Issue 8(2018) Page Start: 699 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
30. Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. (25th January 2013) Authors: Lal, Dennis; Trucks, Holger; Møller, Rikke S.; Hjalgrim, Helle; Koeleman, Bobby P. C.; de Kovel, Carolien G. F.; Visscher, Frank; Weber, Yvonne G.; Lerche, Holger; Becker, Felicitas; Schankin, Christoph J.; Neubauer, Bernd A.; Surges, Rainer; Kunz, Wolfram S.; Zimprich, Fritz; Franke, Andre; Illi... Journal: Epilepsia Issue: Volume 54:issue 2(2013:Feb.) Page Start: 265 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗