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• von Stülpnagel C, Ensslen M, Møller RS, Pal DK, Masnada S, Veggiotti P, Piazza E, Dreesmann M, Hartlieb T, Herberhold T, Hughes E, Koch M, Kutzer C, Hoertnagel K, Nitanda J, Pohl M, Rostásy K, Haack TB, Stöhr K, Kluger G, Borggraefe I. Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs. European Journal of Paediatric Neurology. 2017 May;21(3):530-541. DOI: 10.1016/j.ejpn.2017.01.001.

• Addis L, Virdee JK, Vidler LR, Collier DA, Pal DK, Ursu D. Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency - molecular profiling and functional rescue. Scientific Reports. 2017 Feb 27;7(1):66. DOI: 10.1038/s41598-017-00115-w.

• Depienne C, Nava C, Keren B, Heide S, Rastetter A, Passemard S, Chantot-Bastaraud S, Moutard ML, Agrawal PB, VanNoy G, Stoler JM, Amor DJ, Billette de Villemeur T, Doummar D, Alby C, Cormier-Daire V, Garel C, Marzin P, Scheidecker S, de Saint-Martin A, Hirsch E, Korff C, Bottani A, Faivre L, Verloes A, Orzechowski C, Burglen L, Leheup B, Roume J, Andrieux J, Sheth F, Datar C, Parker MJ, Pasquier L, Odent S, Naudion S, Delrue MA, Le Caignec C, Vincent M, Isidor B, Renaldo F, Stewart F, Toutain A, Koehler U, Häckl B, von Stülpnagel C, Kluger G, Møller RS, Pal D, Jonson T, Soller M, Verbeek NE, van Haelst MM, de Kovel C, Koeleman B, Monroe G, van Haaften G; DDD Study, Attié-Bitach T, Boutaud L, Héron D, Mignot C. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU. Human Genetics. 2017 Apr;136(4):463-479. DOI: 10.1007/s00439-017-1772-0.

• Strug LJ, Pal DK. Reply to: Is a microRNA-328 binding site in PAX6 associated with Rolandic epilepsy? Annals of Clinical and Translational Neurology. 2017 Mar 23;4(4):278-280. DOI: 10.1002/acn3.403.

• Smith AB, Dawes P, Smith S, Pal DK. A specific deficit of auditory processing in children with Rolandic Epilepsy and their relatives. Epilepsy Behaviour. 2017 Jul;72:135-139. DOI: 10.1016/j.yebeh.2017.04.043.

• Tee AR, Sampson JR, Pal DK & Bateman JM (2016). The role of mTOR signalling in neurogenesis, insights from tuberous sclerosis complex. Seminars in cell & developmental biology ; (Vol. 52, pp. 12-20). Academic Press. DOI: 10.1016/j.semcdb.2016.01.040

• Mignot C, von Stülpnagel C, Nava C, Ville D, Sanlaville D, Lesca G, Rastetter A, Gachet B, Marie Y, Korenke GC, Borggraefe I, Hoffmann-Zacharska D, Szczepanik E, Rudzka-Dybała M, Yiş U, Çağlayan H, Isapof A, Marey I, Panagiotakaki E, Korff C, Rossier E, Riess A, Beck-Woedl S, Rauch A, Zweier C, Hoyer J, Reis A, Mironov M, Bobylova M, Mukhin K, Hernandez-Hernandez L, Maher B, Sisodiya S, Kuhn M, Glaeser D, Wechuysen S, Myers CT, Mefford HC, Hörtnagel K, Biskup S; EuroEPINOMICS-RES MAE working group, Lemke JR, Héron D, Kluger G, Depienne C (2016). Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy. Journal of medical genetics, jmedgenet-2015. DOI: 10.1136/jmedgenet-2015-103451

• Panjwani N, Addis L, Crosbie J, Wirrell E, Auvin S, Caraballo RH, Gomez K, Gupta R, Hughes E, Jackman J Kinali M, McCormick D, Oren C, Scott D, Taylor J, Stanek J, Trounce J, Clarke T, Akman CI, Kugler SL, Mandelbaum DE, McGoldrick P, Novotny EJ, Wolf ST, Arnold P, Schachar R, Pal DK, Strug LJ (2016). A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy. Annals of Clinical and Translational Neurology. DOI: 10.1002/acn3.320

• Rosch RE, Farquhar M, Gringras P, & Pal DK (2016). Narcolepsy following yellow fever vaccination: A case report. Frontiers in Neurology; 7. DOI: 10.3389/fneur.2016.00130

• Møller RS, Larsen LHG, Johannesen KM, Talvik I, Talvik T, Vaher U, Miranda M, Farooq M, Nielsen JEK, Lavard L, Linnet K, Hao Q, Uldall P, Frangu M, Tommerup N, Baig SM, Born PA, Gellert P, Nikanorova M, Olofsson K, Jepsen B, Marjanovic D, Lana Al-Zehhawi, Peñalva SJ, Krag-Olsen B, Brusgaard K, Hjalgrim H, Rubboli G, Pal DK, Dahl HA (2016). Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. Molecular Syndromology; 7(4), 210-219. DOI: 10.1159/000448369

• Tang S, Hughes E, Lascelles K, Simpson MA, & Pal DK. (2016). New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy. American Journal of Medical Genetics Part A. DOI: 10.1002/ajmg.a.37935.

• de Kovel CG, Brilstra EH, van Kempen MJ, Van't Slot R, Nijman IJ, Afawi Z, De Jonghe P, Djémié T, Guerrini R, Hardies K, Helbig I, Hendrickx R, Kanaan M, Kramer U, Lehesjoki AE, Lemke JR, Marini C, Mei D, Møller RS, Pendziwiat M, Stamberger H, Suls A, Weckhuysen S; EuroEPINOMICS RES Consortium, Koeleman BP (2016). Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients. Molecular Genetics & Genomic Medicine 4(5), 568-580. DOI: 10.1002/mgg3.235.

• Pal DK, Ferrie C, Addis L, Akiyama T, Capovilla G, Caraballo R, de Saint-Martin A, Fejerman N, Guerrini R, Hamandi K, Helbig I, Ioannides AA, Kobayashi K, Lal D, Lesca G, Muhle H, Neubauer BA, Pisano T, Rudolf G, Seegmuller C, Shibata T, Smith A, Striano P, Strug LJ, Szepetowski P, Valeta T, Yoshinaga H, Koutroumanidis M (2016). Idiopathic focal epilepsies: the “lost tribe”. Epileptic Disorders; 18(3), 252-288. DOI: 10.1684/epd.2016.0839.

• de Lange IM, Helbig KL, Weckhuysen S, Møller RS, Velinov M, Dolzhanskaya N, Marsh E, Helbig I, Devinsky O, Tang S, Mefford HC, Myers CT, van Paesschen W, Striano P, van Gassen K, van Kempen M1, de Kovel CG, Piard J, Minassian BA, Nezarati MM, Pessoa A, Jacquette A, Maher B, Balestrini S, Sisodiya S, Warde MT, De St Martin A, Chelly J, EuroEPINOMICS-RES MAE working group, van 't Slot R, Van Maldergem L, Brilstra EH, Koeleman BP (2016). De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy. Journal of Medical Genetics pii: jmedgenet-2016-103909. DOI: 10.1136/jmedgenet-2016-103909.

• Addis L, Ahn JW, Dobson R, Dixit A, Ogilvie C. M, Pinto D, & Parr JR (2015). Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation. Human mutation; 36(9), 842-850.

• Addis L, Rosch RE, Valentin A, Makoff A, Robinson R, Everett KV, Pal DK (2016). Analysis of rare copy number variation in absence epilepsies. Neurology Genetics, 2(2), e56.

• Smith AB, Dawes P, Pal DK (2016). Defining auditory processing deficits in children with Rolandic Epilepsy and their relatives. Epilepsia; in review.

• Colonna A, Smith AB, Smith S, Gringras P, Pal DK (2016). Consolidation of facial emotion processing during sleep in typically developing children: a crossover trial. PLoS One; in review.

• C. v. Stülpnagel, M. Ensslen, R. S Møller, DK Pal, S. Masnada, P. Veggiotti, E. Piazza, M. Dreesmann, T. Hartlieb, E. Hughes, M. Koch, Christina Kutzer, K. Hoertnagel, J. Nitanda, M. Pohl, K. Rostásy, K. Stöhr, G. Kluger, I. Borggraefe (2016). GRIN2A associated epilepsy: genetics, neurodevelopment, epileptic phenotype and the response to anticonvulsive drugs. European Journal of Paediatric Neurology; in review.

• Mellish LC, Dunkley C, Ferrie CD, & Pal DK (2015). Antiepileptic drug treatment of rolandic epilepsy and Panayiotopoulos syndrome: clinical practice survey and clinical trial feasibility. Archives of disease in childhood, 100(1), 62-67. DOI: 10.1136/archdischild-2013-304211

• Pal DK & Helbig I. (2015). Commentary: Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry. Epilepsia; 56(2):195-6. DOI: 10.1111/epi.12906

• Li W, Dobbins S, Tomlinson I, Houlston R, Pal DK, & Strug LJ. (2015). Prioritizing Rare Variants with Conditional Likelihood Ratios. Human heredity; 79(1), 5-13. DOI:10.1159/000371579

• Larsen J, Carvill GL, Gardella E, EuroEPINOMICS RES Consortium (2015). The phenotypic spectrum of SCN8A encephalopathy. Neurology; 84(5), 480-489. DOI: 10.1212/WNL.0000000000001211

• Syrbe S, Hedrich UB, Riesch E, EuroEPINOMICS RES (2015). De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy. Nature genetics; 47(4), 393-399. DOI: 10.1038/ng.3239

• Addis L, Joo A, Dobson R, Dixit A, Ogilvie C, Pinto D, Vaags A, Coon H, Chaste P, Ingason A, Wilson S, Parr J, Anfrieux J, Delobel B, Tumer A, Isidor B, Luuzzi V, Aubell K, Koilinen H, Curran S, Spector T, Marshall C, Scherer S, Strug L, Collier DA, Pal DK. (2015). Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation. Human mutation 36(9), 842-850. DOI: 10.1002/humu.22816

• Smith AB, Bajomo O, & Pal DK (2015). A meta‐analysis of literacy and language in children with rolandic epilepsy. Developmental Medicine & Child Neurology 57(11), 1019-1026. DOI:10.1111/dmcn.12856

• Colonna, A., Smith, A. B., Pal, D. K., & Gringras, P. (2015). Novel mechanisms, treatments, and outcome measures in childhood sleep. Frontiers in psychology; 6. DOI: 10.3389/fpsyg.2015.00602

• Larsen J, Johannesen K, Ek J, Tang S, Marini C, Blichfeldt S, Kibæk M, von Spiczak S, Weckhuysen S, Frangu M, Neubauer BA, Uldall P, Striano P, Zara F, MAE working group of the EuroEPINOMICS RES Consortium, Kleiss R, Simpson M, Muhle H, Nikanorova M, Jepsen B, Tommerup N, Stephani U, Gurrini R, Dunø M, Hjalgrim H,14, Pal DK, Helbig I, Møller RS. (2015). The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. Epilepsia; 56(12), e203-e208. DOI: 10.1111/epi.13222

• Yaiza Hernández Vega, Anna Smith, Hannah Cockerill, Shan Tang, Zaloa Agirre-Arrizubieta, Sushma Goyal, Marisa Pina, Cigdem I Akman, Nicola Jolleff, Colm McGinnity, Kumudini Gomez, Rajesh Gupta, Elaine Hughes, John Jackman, David McCormick, Caroline Oren, David Scott, Jacqueline Taylor, John Trounce, Tara Clarke, Huntley Hardison, Steven Kugler, David Mandelbaum, Edward Novotny, Patricia McGoldrick, Steven Wolf, Theodore Chiang, Lisa J Strug, Deb K Pal (2015). Risk factors for reading disability in families with rolandic epilepsy. Epilepsy & Behavior; 53, 174-179. DOI: 10.1016/j.yebeh.2015.10.016

• Addis L, Rosch RE, Valentin A, Makoff A, Robinson R, Everett KV, Nashef L & Pal DK. (2016). Analysis of rare copy number variation in absence epilepsies. Neurology Genetics; 2(2), e56. DOI: 10.1212/NXG.0000000000000056

• Lim L, Chantiluke K, Cubillo AI, Smith AB, Simmons A, Mehta MA, & Rubia K (2015). Disorder-specific grey matter deficits in attention deficit hyperactivity disorder relative to autism spectrum disorder. Psychological medicine; 45(05), 965-976. DOI: 10.1017/S0033291714001974

• Addis L, Chiang T, Clarke T, Hardison H, Kugler S, Mandelbaum D, Novotny E, Wolf S, Strug LJ, Pal DK. (2014). Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Genes, Brain and Behavior; 13(3), 333-340. DOI: 10.1111/gbb.12110

• Euro Epinomics-RES Consortium, Epilepsy Phenome/Genome P, Epi KC. (2014). De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies. The American Journal of Human Genetics; 95(4), 360-370. DOI: 10.1016/j.ajhg.2014.08.013

• Lemke JR, Hendrickx R, Geider K, Laube, B, Schwake M, Harvey RJ, & Neidhardt J (2014). GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy. Annals of neurology; 75(1), 147-154. DOI: 10.1002/ana.24073

• Nava C, Dalle C, Rastetter A, Striano P, de Kovel CG, Nabbout R, & Raffo, E. (2014). De novo mutations in HCN1 cause early infantile epileptic encephalopathy. Nature genetics; 46(6), 640-645. DOI: 10.1038/ng.2952

• Schubert J, Siekierska A, Langlois M, May P, Huneau C, Becker F, & Thiele H (2014). Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. Nature genetics; 46(12), 1327-1332. DOI: 10.1038/ng.3130

• Suls A, Jaehn JA, Kecskés A, Weber Y, Weckhuysen S, Craiu DC, & Von Spiczak S (2013). De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome. The American Journal of Human Genetics; 93(5), 967-975. DOI: 10.1016/j.ajhg.2013.09.017

• O'Harney AD, Marquand A, Rubia K, Chantiluke K, Smith AB, Cubillo A, & Filippone M (2014). Pseudo-Marginal Bayesian Multiple-Class Multiple-Kernel Learning for Neuroimaging Data. In ICPR (pp. 3185-3190).

• Derkach A, Chiang T, Gong J, Addis L, Dobbins S, Tomlinson I, & Strug LJ (2014). Association analysis using next generation sequence data from publicly available control groups: The robust variance score statistic. Bioinformatics; btu196. DOI: 10.1093/bioinformatics/btu196

• Pal DK, & Strug LJ (2014). The genetics of common epilepsies: common or distinct?. The Lancet Neurology; 13(9), 859-860. DOI: 10.1016/S1474-4422(14)70124-3

• Rubia K, Cubillo AI, Chantiluke K, & Smith AB (2014). S. 06.02 Effects of psychotropic drugs in the ADHD brain. European Neuropsychopharmacology; 24, S117. DOI: 10.1016/S0924-977X(14)70139-7

• Hart H, Chantiluke K, Cubillo AI, Smith AB, Simmons A, Brammer MJ, Marquand AF & Rubia K (2014). Pattern classification of response inhibition in ADHD: Toward the development of neurobiological markers for ADHD. Human brain mapping; 35(7), 3083-3094. DOI: 10.1002/hbm.22386

• Murphy CM, Christakou A, Daly EM, Ecker C, Giampietro V, Brammer M, Smith A & Rubia K. (2014). Abnormal functional activation and maturation of fronto-striato-temporal and cerebellar regions during sustained attention in autism spectrum disorder. American Journal of Psychiatry; 171(10), 1107-1116. DOI: 10.1176/appi.ajp.2014.12030352

• Hart H, Marquand AF, Smith A, Cubillo A, Simmons A, Brammer M, & Rubia K (2014). Predictive neurofunctional markers of attention-deficit/hyperactivity disorder based on pattern classification of temporal processing. Journal of the American Academy of Child & Adolescent Psychiatry; 53(5), 569-578. DOI: 10.1016/j.jaac.2013.12.024

• Rubia K, Alegria AA, Cubillo AI, Smith AB, Brammer MJ, & Radua J (2014). Effects of stimulants on brain function in attention-deficit/hyperactivity disorder: a systematic review and meta-analysis. Biological psychiatry 76(8), 616-628. DOI: 10.1016/j.biopsych.2013.10.016

• Cubillo A, Smith AB, Barrett N, Giampietro V, Brammer MJ, Simmons A, & Rubia K (2014). Shared and drug-specific effects of atomoxetine and methylphenidate on inhibitory brain dysfunction in medication-naive ADHD boys. Cerebral Cortex; 24(1), 174-185. DOI: 10.1093/cercor/bhs296

• Addis L, Lin JJ, Pal DK, Hermann B, & Caplan R (2013). Imaging and genetics of language and cognition in pediatric epilepsy. Epilepsy & Behavior; 26(3), 303-312. DOI: 10.1016/j.yebeh.2012.09.014

• Tropeano M, Ahn JW, Dobson RJB, Breen G, Rucker J, Dixit A, Pal DK, McGuffin P, Farmer A, White PS, Andrieux J, Vassos E, Ogilvie CM, Curran S & Collier DA(2013). Male-biased autosomal effect of 16p13. 11 copy number variation in neurodevelopmental disorders. PLoS One; 8(4), e61365. DOI: 10.1371/journal.pone.0061365

• Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K, Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn JA, Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E,Pal DK, Veri K, Vaher U, Talvik T, Dimova P, Guerrero López R, Serratosa JM, Linnankivi T, Lehesjoki AE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, Kurlemann G, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Sperner J, Becker F, Weber YG, Feucht M, Steinböck H, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J, Harvey RJ, Hoffmann P, Herms S, Altmüller J, Toliat MR, Thiele H, Nürnberg P, Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, von Spiczak S. (2013). Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nature genetics; 45(9), 1067-1072. DOI: 10.1038/ng.2728

• Lesca G, Rudolf G, Bruneau N, Lozovaya N, Labalme A, Boutry-Kryza N, Salmi M, Tsintsadze T, Addis L, Motte J, Wright S, Tsintsadze V, Michel A, Doummar D, Lascelles K, Strug L, Waters P, de Bellescize J, Vrielynck P, de Saint Martin A, Ville D, Ryvlin P, Arzimanoglou A, Hirsch E, Vincent A, Pal DK, Burnashev N, Sanlaville D, Szepetowski P. (2013). GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nature Genetics; 45(9), 1061-1066. DOI: 10.1038/ng.2726

• Rubia K, Lim L, Ecker C, Halari R, Giampietro V, Simmons A, & Smith A (2013). Effects of age and gender on neural networks of motor response inhibition: from adolescence to mid-adulthood. Neuroimage; 83, 690-703. DOI :10.1016/j.neuroimage.2013.06.078

• Smith A, Cubillo A, Barrett N, Giampietro V, Simmons A, Brammer M, & Rubia K (2013). Neurofunctional effects of methylphenidate and atomoxetine in boys with attention-deficit/hyperactivity disorder during time discrimination. Biological psychiatry; 74(8), 615-622. DOI: 10.1016/j.biopsych.2013.03.030

• Lim L, Marquand A, Cubillo AA, Smith AB, Chantiluke K, Simmons A, & Rubia K (2013). Disorder-specific predictive classification of adolescents with attention deficit hyperactivity disorder (ADHD) relative to autism using structural magnetic resonance imaging. PloS one; 8(5), e63660. DOI: 10.1371/journal.pone.0063660

• Cubillo A, Smith AB, Barrett N, Giampietro V, Brammer M, Simmons A, & Rubia K (2014). Drug-specific laterality effects on frontal lobe activation of atomoxetine and methylphenidate in attention deficit hyperactivity disorder boys during working memory. Psychological medicine; 44(03), 633-646. DOI: 10.1017/S0033291713000676

• Christakou A, Murphy CM, Chantiluke K, Cubillo AI, Smith AB, Giampietro V, & Rubia K. (2013). Disorder-specific functional abnormalities during sustained attention in youth with attention deficit hyperactivity disorder (ADHD) and with autism. Molecular psychiatry; 18(2), 236-244. DOI: 10.1038/mp.2012.41

• Christakou A, Murphy CM, Chantiluke K, Cubillo AI, Smith AB, Giampietro V, & Rubia K (2013). Disorder-specific functional abnormalities during sustained attention in youth with attention deficit hyperactivity disorder (ADHD) and with autism. Molecular psychiatry; 18(2), 236-244. DOI: 10.1038/mp.2011.185

• Smith AB, Kavros PM, Clarke T, Dorta NJ, Tremont G, & Pal DK (2012). A neurocognitive endophenotype associated with rolandic epilepsy. Epilepsia; 53(4), 705-711. DOI: 10.1111/j.1528-1167.2011.03371.x

• Tang S and Pal DK, (2012). Dissecting the genetic basis of myoclonic‐astatic epilepsy. Epilepsia; 53(8), pp.1303-1313. DOI: 10.1111/j.1528-1167.2012.03581.x

• Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Wolf SM, Greenberg DA, Hardison HH, Kugler SL, Mandelbaum DE, Novotny EJ, Pal DK (2012). The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in rolandic epilepsy. PloS one; 7(7), e40696. DOI: 10.1371/journal.pone.0040696

• Cubillo A, Halari R, Smith A, Taylor E, & Rubia K (2012). A review of fronto-striatal and fronto-cortical brain abnormalities in children and adults with Attention Deficit Hyperactivity Disorder (ADHD) and new evidence for dysfunction in adults with ADHD during motivation and attention. Cortex; 48(2), 194-215. DOI: 10.1016/j.cortex.2011.04.007

• Heng HS, Tang SS, Goyal S, Wraige EA, & Lim MJ (2012). Beneficial use of steroids in hereditary neuropathy with liability to pressure palsy. Developmental Medicine & Child Neurology; 54(2), 183-186. DOI: 10.1111/j.1469-8749.2011.04131.x

• Tang SS, Fernandez D, Lazarou LP, Singh R, & Fallon P (2012). MECP2 triplication in 3 brothers–A rarely described cause of familial neurological regression in boys. European Journal of Paediatric Neurology; 16(2), 209-212. DOI: 10.1016/j.ejpn.2011.07.011

• Tang SS, Clarke T, Owens J, & Pal DK (2011). Sleep Behavior Disturbances in Rolandic Epilepsy. Journal of Child Neurology; 26(2), 239 - 243. DOI: 10.1177/0883073810381925

• Pal DK. (2011). Commentary on: Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies. Epilepsia; 52(1), 1-9. DOI: 10.1111/j.1528-1167.2010.02734.x

• Pal, DK (2011). Epilepsy and neurodevelopmental disorders of language. Current opinion in neurology; 24(2), 126-131. DOI: 10.1097/WCO.0b013e328344634a

• Pong AW, Pal DK, & Chung WK (2011). Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist. Pediatric neurology; 44(5), 317-327. DOI: 10.1016/j.pediatrneurol.2011.01.017

• Smith A, Giampietro V, Brammer M, Halari R, Simmons A, & Rubia K (2011). Functional development of fronto-striato-parietal networks associated with time perception. Frontiers in human neuroscience; 5, 136. DOI: 10.3389/fnhum.2011.00136

• Rubia K, Cubillo A, Woolley J, Brammer MJ, & Smith A (2011). Disorder‐specific dysfunctions in patients with attention‐deficit/hyperactivity disorder compared to patients with obsessive‐compulsive disorder during interference inhibition and attention allocation. Human brain mapping; 32(4), 601-611. DOI: 10.1002/hbm.21048

• Cubillo A, Smith AB, Barrett N, Giampietro V, Simmons A, & Rubia K (2011). S. 07.06 Differential effects of methylphenidate and atomoxetine on brain activation in medication-naïve children with ADHD. European Neuropsychopharmacology; 21, S197. DOI: 10.1016/S0924-977X(11)70267-X

• Rubia K, Halari R, Cubillo A, Smith AB, Mohammad AM, Brammer M, & Taylor E (2011). Methylphenidate normalizes fronto-striatal underactivation during interference inhibition in medication-naive boys with attention-deficit hyperactivity disorder. Neuropsychopharmacology; 36(8), 1575-1586. DOI: 10.1038/npp.2011.30

• Smith AB, Halari R, Giampetro V, Brammer M, & Rubia K (2011). Developmental effects of reward on sustained attention networks. Neuroimage; 56(3), 1693-1704. DOI: 10.1016/j.neuroimage.2011.01.072

• Surana P, Tang S, McDougall M, Tong CYW, Menson E, & Lim M (2011). Neurological complications of pandemic influenza A H1N1 2009 infection: European case series and review. European journal of pediatrics; 170(8), 1007-1015. DOI: 10.1007/s00431-010-1392-3

• Tang S, Lin JP, Hughes E, Lim M, & Lascelles K (2011). P01. 5 Encephalopathic course with neurological deterioration and neuroimaging abnormalities in children with SCN1A mutation associated epilepsy. European Journal of Paediatric Neurology; 15, S33.

• Tang S, Lin JP, Hughes E, Siddiqui A, Lim M, & Lascelles K (2011). Encephalopathy and SCN1A mutations. Epilepsia; 52(4), e26-e30. DOI: 10.1111/j.1528-1167.2011.03019.x

• Tang SS, Siddiqui A, Andronikou S, McDougall M, Martinez-Alier N, & Lundy CT (2011). Acute encephalopathy in childhood associated with novel influenza a h1n1 virus infection: clinical and neuroimaging findings. The Ulster medical journal; 80(1), 49.

• Strug LJ, Hodge SE, Chiang T, Pal DK, Corey P, and Rohde C. (2010). A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and Frequentist analysis, European Journal of Human Genetics; 18(8):933-41. DOI: 10.1038/ejhg.2010.47

• Pal DK, Strug LJ, Veliskova, J, Chachua T, Velisek L & Greenberg DA (2010). Major susceptibility genes for common idiopathic epilepsies: ELP4 in rolandic epilepsy and BRD2 in juvenile myoclonic epilepsy. Epilepsia; 51(5):73.

• Pal DK, Pong AW, Chung WK. (2010). Genetic evaluation and genetic counseling in the epilepsies, Nature Reviews Neurology; 6(8):445-53. DOI: 10.1038/nrneurol.2010.92

• Vierck E, Cauley R, Kugler SL, Shah N, Mandelbaum DE, Pal DK, Durner M. (2010). Polyspike and wave does not predict GTCS in childhood absence epilepsy, Journal of Child Neurology; 25(4):475-81.

• Ferraro TN, Dlugos DJ, Hakonarson H, & Buono RJ (2010). Strategies for studying the epilepsy genome. Epilepsia; 51(5):58.

• Pal D K, Li W, Clarke T, Lieberman P, & Strug LJ (2010). Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves. Genes, Brain and Behavior; 9(8), 1004-1012. DOI: 10.1111/j.1601-183X.2010.00648.x

• Campbell LE, Azuma R, Ambery F, Stevens A, Smith A, Morris RG, & Murphy KC (2010). Executive functions and memory abilities in children with 22q11. 2 deletion syndrome. Australian and New Zealand Journal of Psychiatry; 44(4), 364-371. DOI: 10.3109/00048670903489882

• Rubia K, Hyde Z, Halari R, Giampietro V, & Smith A (2010). Effects of age and sex on developmental neural networks of visual–spatial attention allocation. Neuroimage; 51(2), 817-827. DOI: 10.1016/j.neuroimage.2010.02.058

Register for Symposium on Idiopathic Focal Epilepsies

Please complete the form below to register your interest in the upcoming symposium. For questions and further details please contact amber.collingwood@kcl.ac.uk.

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