Deb Pal

2022

Non‐Invasive Mobile EEG as a tool for seizure monitoring and management: a systematic review

Biondi, A., Santoro, V., Ruas Faro Viana, P., Laiou, P., Pal, D., Bruno, E. & Richardson, M., May 2022, In: Epilepsia. 63, 5, p. 1041-1063 23 p.

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30 Citations (Scopus)

512 Downloads (Pure)

2020

Epilepsy‐specific patient‐reported outcome measures of children's health‐related quality of life: A systematic review of measurement properties

Crudgington, H., Rogers, M., Morris, H., Gringras, P., Pal, D. K. & Morris, C., 1 Feb 2020, In: Epilepsia. 61, 2, p. 230-248 19 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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22 Citations (Scopus)

188 Downloads (Pure)

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

EuroEPINOMICS RES Consortium, 1 May 2020, In: Epilepsia. 61, 5, p. 995-1007 13 p.

Research output: Contribution to journal › Article › peer-review

Open Access

34 Citations (Scopus)

Trait Impulsivity in Juvenile Myoclonic Epilepsy

BIOJUME Consortium, 2 Dec 2020, In: Annals of Clinical and Translational Neurology. 8, 1, p. 138-152 15 p.

Research output: Contribution to journal › Article › peer-review

Open Access

26 Citations (Scopus)

2019

Psychosocial complications in juvenile myoclonic epilepsy

Syvertsen, M., Selmer, K., Enger, U., Nakken, K. O., Pal, D. K., Smith, A. & Koht, J., 22 Jan 2019, (E-pub ahead of print) In: Epilepsy and Behavior. 90, p. 122-128 7 p.

Research output: Contribution to journal › Article › peer-review

26 Citations (Scopus)

2018

Defining the phenotypic spectrum of SLC6A1 mutations

Johannesen, K. M., Gardella, E., Linnankivi, T., Courage, C., de Saint Martin, A., Lehesjoki, A. E., Mignot, C., Afenjar, A., Lesca, G., Abi-Warde, M. T., Chelly, J., Piton, A., Merritt, J. L., Rodan, L. H., Tan, W. H., Bird, L. M., Nespeca, M., Gleeson, J. G., Yoo, Y. & Choi, M. & 32 others, Chae, J. H., Czapansky-Beilman, D., Reichert, S. C., Pendziwiat, M., Verhoeven, J. S., Schelhaas, H. J., Devinsky, O., Christensen, J., Specchio, N., Trivisano, M., Weber, Y. G., Nava, C., Keren, B., Doummar, D., Schaefer, E., Hopkins, S., Dubbs, H., Shaw, J. E., Pisani, L., Myers, C. T., Tang, S., Tang, S., Pal, D. K., Millichap, J. J., Carvill, G. L., Helbig, K. L., Mecarelli, O., Striano, P., Helbig, I., Rubboli, G., Mefford, H. C. & Møller, R. S., 1 Feb 2018, In: Epilepsia. 59, 2, p. 389-402 14 p.

Research output: Contribution to journal › Article › peer-review

87 Citations (Scopus)

Incorporating epilepsy genetics into clinical practice: A 360° evaluation

Oates, S., Tang, S., Rosch, R., Lear, R., Hughes, E. F., Williams, R. E., Larsen, L. H. G., Hao, Q., Dahl, H. A., Møller, R. S. & Pal, D. K., 10 May 2018, In: NPJ Genomic medicine. 3, 1

Research output: Contribution to journal › Article › peer-review

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43 Citations (Scopus)

208 Downloads (Pure)

2016

De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy

de Lange, I. M., Helbig, K. L., Weckhuysen, S., Møller, R. S., Velinov, M., Dolzhanskaya, N., Marsh, E., Helbig, I., Devinsky, O., Tang, S., Mefford, H. C., Myers, C. T., van Paesschen, W., Striano, P., van Gassen, K., van Kempen, M., de Kovel, C. G. F., Piard, J., Minassian, B. A. & Nezarati, M. M. & 13 others, Pessoa, A., Jacquette, A., Maher, B., Balestrini, S., Sisodiya, S., Warde, M. T. A., De St Martin, A., Chelly, J., van 't Slot, R., Van Maldergem, L., Brilstra, E. H., Koeleman, B. P. C. & EuroEPINOMICS-RES MAE working group, Dec 2016, In: Journal of Medical Genetics. 53, 12, p. 850-858 9 p.

Research output: Contribution to journal › Article › peer-review

51 Citations (Scopus)

Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

Møller, R. S., Larsen, L. H. G., Johannesen, K. M., Talvik, I., Talvik, T., Vaher, U., Miranda, M. J., Farooq, M., Nielsen, J. E. K., Svendsen, L. L., Kjelgaard, D. B., Linnet, K. M., Hao, Q., Uldall, P., Frangu, M., Tommerup, N., Baig, S. M., Abdullah, U., Born, A. P. & Gellert, P. & 12 others, Nikanorova, M., Olofsson, K., Jepsen, B., Marjanovic, D., Al-Zehhawi, L. I. K., Peñalva, S. J., Krag-Olsen, B., Brusgaard, K., Hjalgrim, H., Rubboli, G., Pal, D. K. & Dahl, H. A., 1 Sept 2016, In: Molecular syndromology. 7, 4, p. 210-219 10 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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100 Citations (Scopus)

90 Downloads (Pure)

Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

Mignot, C., von Stülpnagel, C., Nava, C., Ville, D., Sanlaville, D., Lesca, G., Rastetter, A., Gachet, B., Marie, Y., Korenke, G. C., Borggraefe, I., Hoffmann-Zacharska, D., Szczepanik, E., Rudzka-Dybała, M., Yiş, U., Çağlayan, H., Isapof, A., Marey, I., Panagiotakaki, E. & Korff, C. & 26 others, 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, C. T., Mefford, H. C., Hörtnagel, K., Biskup, S., Lemke, J. R., Héron, D., Kluger, G., Depienne, C., EuroEPINOMICS-RES MAE working group & Pal, D. K., 17 Mar 2016, In: Journal of Medical Genetics.

Research output: Contribution to journal › Article › peer-review

126 Citations (Scopus)

2015

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Syrbe, S., Hedrich, U. B. S., Riesch, E., Djémié, T., Müller, S., Møller, R. S., Maher, B., Hernandez-Hernandez, L., Synofzik, M., Caglayan, H. S., Arslan, M., Serratosa, J. M., Nothnagel, M., May, P., Krause, R., Löffler, H., Detert, K., Dorn, T., Vogt, H. & Krämer, G. & 30 others, Schöls, L., Mullis, P. E., Linnankivi, T., Lehesjoki, A.-E., Sterbova, K., Craiu, D. C., Hoffman-Zacharska, D., Korff, C. M., Weber, Y. G., Steinlin, M., Gallati, S., Bertsche, A., Bernhard, M. K., Merkenschlager, A., Kiess, W., Gonzalez, M., Züchner, S., Palotie, A., Suls, A., De Jonghe, P., Helbig, I., Biskup, S., Wolff, M., Maljevic, S., Schüle, R., Sisodiya, S. M., Weckhuysen, S., Lerche, H., Lemke, J. R. & EuroEPINOMICS RES, Apr 2015, In: Nature Genetics. 47, 4, p. 393-399 7 p.

Research output: Contribution to journal › Article › peer-review

214 Citations (Scopus)

The phenotypic spectrum of SCN8A encephalopathy

Larsen, J., Carvill, G. L., Gardella, E., Kluger, G., Schmiedel, G., Barisic, N., Depienne, C., Brilstra, E., Mang, Y., Nielsen, J. E. K., Kirkpatrick, M., Goudie, D., Goldman, R., Jähn, J. A., Jepsen, B., Gill, D., Döcker, M., Biskup, S., McMahon, J. M. & Koeleman, B. & 18 others, Harris, M., Braun, K., de Kovel, C. G. F., Marini, C., Specchio, N., Djémié, T., Weckhuysen, S., Tommerup, N., Troncoso, M., Troncoso, L., Bevot, A., Wolff, M., Hjalgrim, H., Guerrini, R., Scheffer, I. E., Mefford, H. C., Møller, R. S. & EuroEPINOMICS RES Consortium CRP, 3 Feb 2015, In: Neurology. 84, 5, p. 480-489 10 p.

Research output: Contribution to journal › Article › peer-review

242 Citations (Scopus)

2014

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Nava, C., Dalle, C., Rastetter, A., Striano, P., de Kovel, C. G. F., Nabbout, R., Cancès, C., Ville, D., Brilstra, E. H., Gobbi, G., Raffo, E., Bouteiller, D., Marie, Y., Trouillard, O., Robbiano, A., Keren, B., Agher, D., Roze, E., Lesage, S. & Nicolas, A. & 19 others, Brice, A., Baulac, M., Vogt, C., El Hajj, N., Schneider, E., Suls, A., Weckhuysen, S., Gormley, P., Lehesjoki, A.-E., De Jonghe, P., Helbig, I., Baulac, S., Zara, F., Koeleman, B. P. C., Haaf, T., LeGuern, E., Depienne, C., EuroEPINOMICS RES Consortium & Pal, D., Jun 2014, In: Nature Genetics. 46, 6, p. 640-645 6 p.

Research output: Contribution to journal › Article › peer-review

178 Citations (Scopus)

2010

Polyspike and Waves Do Not Predict Generalized Tonic-Clonic Seizures in Childhood Absence Epilepsy

Vierck, E., Cauley, R., Kugler, S. L., Mandelbaum, D. E., Pal, D. K. & Durner, M., Apr 2010, In: Journal of Child Neurology. 25, 4, p. 475 - 481 7 p.

Research output: Contribution to journal › Article › peer-review

22 Citations (Scopus)

2009

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)

Strug, L. J., Clarke, T., Chiang, T., Chien, M., Baskurt, Z., Li, W., Dorfman, R., Bali, B., Wirrell, E., Kugler, S. L., Mandelbaum, D. E., Wolf, S. M., McGoldrick, P., Hardison, H., Novotny, E. J., Ju, J., Greenberg, D. A., Russo, J. J. & Pal, D., Sept 2009, In: European Journal of Human Genetics. 17, 9, p. 1171-1181 11 p.

Research output: Contribution to journal › Article › peer-review

173 Citations (Scopus)

1999

Validation of a Bengali adaptation of the Conners' Parent Rating Scale (CPRS-48)

Pal, D. K., Chaudhury, G., Das, T. & Sengupta, S., Dec 1999, In: British Journal of Medical Psychology. 72 ( Pt 4), p. 525-33 9 p.

Research output: Contribution to journal › Article › peer-review

12 Citations (Scopus)

Deb Pal

Research output

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