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BMC biology, 2023-07, Vol.21 (1), p.156-156, Article 156
2023
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Neurology, 2010-09, Vol.75 (13), p.1159
2010
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European journal of paediatric neurology, 2015-05, Vol.19, p.S104-S104
2015
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Journal of neurology, neurosurgery and psychiatry, 2014-04, Vol.85 (4), p.462-465
- Djémié, Tania
- Weckhuysen, Sarah
- Holmgren, Philip
- Hardies, Katia
- Van Dyck, Tine
- Hendrickx, Rik
- Schoonjans, An-Sofie
- Van Paesschen, Wim
- Jansen, Anna C
- De Meirleir, Linda
- Selim, Laila Abdel Moteleb
- Girgis, Marian Y
- Buyse, Gunnar
- Lagae, Lieven
- Smets, Katrien
- Smouts, Iris
- Claeys, Kristl G
- Van den Bergh, Vic
- Grisar, Thierry
- Blatt, Ilan
- Shorer, Zamir
- Roelens, Filip
- Afawi, Zaid
- Helbig, Ingo
- Ceulemans, Berten
- De Jonghe, Peter
- Suls, Arvid
2014
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Journal of neurology, neurosurgery and psychiatry, 2010, Vol.81 (1), p.90-93
2010
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Neurogenetics, 2013-02, Vol.14 (1), p.23-34
- van Harssel, J. J. T.
- Weckhuysen, S.
- van Kempen, M. J. A.
- Hardies, K.
- Verbeek, N. E.
- de Kovel, C. G. F.
- Gunning, W. B.
- van Daalen, E.
- de Jonge, M. V.
- Jansen, A. C.
- Vermeulen, R. J.
- Arts, W. F. M.
- Verhelst, H.
- Fogarasi, A.
- de Rijk-van Andel, J. F.
- Kelemen, A.
- Lindhout, D.
- De Jonghe, P.
- Koeleman, B. P. C.
- Suls, A.
- Brilstra, E. H.
2013
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Clinical neurophysiology, 2015-08, Vol.126 (8), p.e80-e80
2015
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Epilepsia (Copenhagen), 2017-07, Vol.58 (7), p.1119-1120
2017
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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
- Chatron, Nicolas
- Becker, Felicitas
- Morsy, Heba
- Schmidts, Miriam
- Hardies, Katia
- Tuysuz, Beyhan
- Roselli, Sandra
- Najafi, Maryam
- Alkaya, Dilek Uludag
- Ashrafzadeh, Farah
- Nabil, Amira
- Omar, Tarek
- Maroofian, Reza
- Karimiani, Ehsan Ghayoor
- Hussien, Haytham
- Kok, Fernando
- Ramos, Luiza
- Gunes, Nilay
- Bilguvar, Kaya
- Labalme, Audrey
- Alix, Eudeline
- Sanlaville, Damien
- de Bellescize, Julitta
- Poulat, Anne-Lise
- Moslemi, Ali-Reza
- Lerche, Holger
- May, Patrick
- Lesca, Gaetan
- Weckhuysen, Sarah
- Tajsharghi, Homa
2020
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Epilepsy research, 2019-10, Vol.156, p.106181-106181, Article 106181
2019
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Orphanet journal of rare diseases, 2015-09, Vol.10 (1), p.123-123, Article 123
- Panagiotakaki, Eleni
- De Grandis, Elisa
- Stagnaro, Michela
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- Sisodiya, Sanjay
- de Vries, Boukje
- Goubau, Christophe
- Weckhuysen, Sarah
- Kemlink, David
- Scheffer, Ingrid
- Lesca, Gaëtan
- Rabilloud, Muriel
- Klich, Amna
- Ramirez-Camacho, Alia
- Ulate-Campos, Adriana
- Campistol, Jaume
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- Moutard, Marie-Laure
- Doummar, Diane
- Hubsch-Bonneaud, Cecile
- Jaffer, Fatima
- Cross, Helen
- Gurrieri, Fiorella
- Tiziano, Danilo
- Nevsimalova, Sona
- Nicole, Sophie
- Neville, Brian
- van den Maagdenberg, Arn M J M
- Mikati, Mohamad
- Goldstein, David B
- Vavassori, Rosaria
- Arzimanoglou, Alexis
2015
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American journal of human genetics, 2018-12, Vol.103 (6), p.1022-1029
- Carvill, Gemma L.
- Engel, Krysta L.
- Ramamurthy, Aishwarya
- Cochran, J. Nicholas
- Roovers, Jolien
- Stamberger, Hannah
- Lim, Nicholas
- Schneider, Amy L.
- Hollingsworth, Georgie
- Holder, Dylan H.
- Regan, Brigid M.
- Lawlor, James
- Lagae, Lieven
- Ceulemans, Berten
- Bebin, E. Martina
- Nguyen, John
- Striano, Pasquale
- Zara, Federico
- Helbig, Ingo
- Møller, Rikke S.
- von Spiczak, Sarah
- Muhle, Hiltrud
- Caglayan, Hande
- Sterbova, Katalin
- Craiu, Dana
- Hoffman, Dorota
- Lehesjoki, Anna-Elina
- Selmer, Kaja
- Depienne, Christel
- Lemke, Johannes
- Marini, Carla
- Guerrini, Renzo
- Neubauer, Bernd
- Talvik, Tiina
- Leguern, Eric
- de Jonghe, Peter
- Weckhuysen, Sarah
- Barsh, Gregory S.
- Meisler, Miriam
- Berkovic, Samuel F.
- De Jonghe, Peter
- Scheffer, Ingrid E.
- Myers, Richard M.
- Cooper, Gregory M.
- Mefford, Heather C.
2018
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Nature genetics, 2014-06, Vol.46 (6), p.640-645
- Nava, Caroline
- Dalle, Carine
- Rastetter, Agnès
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- Schneider, Eberhard
- Suls, Arvid
- Weckhuysen, Sarah
- Gormley, Padhraig
- Lehesjoki, Anna-Elina
- De Jonghe, Peter
- Helbig, Ingo
- Baulac, Stéphanie
- Zara, Federico
- Koeleman, Bobby P C
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- LeGuern, Eric
- Depienne, Christel
2014
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Brain (London, England : 1878), 2019-01, Vol.142 (1), p.80-92
- Strehlow, Vincent
- Heyne, Henrike O
- Vlaskamp, Danique R M
- Marwick, Katie F M
- Rudolf, Gabrielle
- de Bellescize, Julitta
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- Hirsch, Edouard
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- Lesca, Gaetan
- Lemke, Johannes R
2019
Link zum Volltext
Nature (London), 2020-11, Vol.587 (7834), p.377-386
- Rajewsky, Nikolaus
- Almouzni, Geneviève
- Gorski, Stanislaw A
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- De Strooper, Bart
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- Figlerowicz, Marek
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- Hubner, Norbert
- Kjems, Jørgen
- Knoblich, Jürgen A
- Krabbe, Grietje
- Lichter, Peter
- Linnarsson, Sten
- Marine, Jean-Christophe
- Marioni, John C
- Marti-Renom, Marc A
- Netea, Mihai G
- Nickel, Dörthe
- Nollmann, Marcelo
- Novak, Halina R
- Parkinson, Helen
- Piccolo, Stefano
- Pinheiro, Inês
- Pombo, Ana
- Popp, Christian
- Reik, Wolf
- Roman-Roman, Sergio
- Rosenstiel, Philip
- Schultze, Joachim L
- Stegle, Oliver
- Tanay, Amos
- Testa, Giuseppe
- Thanos, Dimitris
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- Torres-Padilla, Maria-Elena
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- van Oudenaarden, Alexander
- Vidal, Marie
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2020
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American journal of human genetics, 2014-10, Vol.95 (4), p.360-370
- Appenzeller, Silke
- Balling, Rudi
- Barisic, Nina
- Baulac, Stéphanie
- Caglayan, Hande
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- Depienne, Christel
- Dimova, Petia
- Djémié, Tania
- Gormley, Padhraig
- Guerrini, Renzo
- Helbig, Ingo
- Hjalgrim, Helle
- Jähn, Johanna
- Klein, Karl Martin
- Koeleman, Bobby
- Komarek, Vladimir
- Krause, Roland
- Kuhlenbäumer, Gregor
- Lemke, Johannes R.
- Lerche, Holger
- Linnankivi, Tarja
- Marini, Carla
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- Muhle, Hiltrud
- Palotie, Aarno
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- Roelens, Filip
- Rosenow, Felix
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- Kossoff, Eric H.
- Kuperman, Rachel
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- Delanty, Norman
- Eichler, Evan E.
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- Han, Yujun
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- Petrou, Stephen
- Petrovski, Slavé
- Ruzzo, Elizabeth K.
2014
Link zum Volltext
European journal of paediatric neurology, 2009, Vol.13, p.S4-S4
2009
Link zum Volltext
Nature genetics, 2015-04, Vol.47 (4), p.393-399
- Syrbe, Steffen
- Hedrich, Ulrike B S
- Riesch, Erik
- Djémié, Tania
- Müller, Stephan
- Møller, Rikke S
- Maher, Bridget
- Hernandez-Hernandez, Laura
- Synofzik, Matthis
- Caglayan, Hande S
- Arslan, Mutluay
- Serratosa, José M
- Nothnagel, Michael
- May, Patrick
- Krause, Roland
- Löffler, Heidrun
- Detert, Katja
- Dorn, Thomas
- Vogt, Heinrich
- Krämer, Günter
- Schöls, Ludger
- Mullis, Primus E
- Linnankivi, Tarja
- Lehesjoki, Anna-Elina
- Sterbova, Katalin
- Craiu, Dana C
- Hoffman-Zacharska, Dorota
- Korff, Christian M
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2015
Link zum Volltext
Epilepsia (Copenhagen), 2020-05, Vol.61 (5), p.995-1007
- Tang, Shan
- Addis, Laura
- Smith, Anna
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2020
Link zum Volltext
American journal of human genetics, 2019-06, Vol.104 (6), p.1060-1072
- Helbig, Ingo
- Lopez-Hernandez, Tania
- Shor, Oded
- Galer, Peter
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- Krause, Roland
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- Weber, Yvonne G.
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- Barisic, Nina
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- Craiu, Dana
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- Jähn, Johanna
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- Koeleman, Bobby P.C.
- Komarek, Vladimir
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- Lemke, Johannes R.
- Lerche, Holger
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- May, Patrick
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- Stephani, Ulrich
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2019
Link zum Volltext
Epilepsy & behavior, 2021-03, Vol.116, p.107791-107791, Article 107791
- Gulcebi, Medine I.
- Bartolini, Emanuele
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- Martins Custodio, Helena
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- Katsarou, Anna
- Koeleman, Bobby P.C.
- Krause, Roland
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2021
Link zum Volltext
The New England journal of medicine, 2019-04, Vol.380 (16), p.e24-1028
2019
Link zum Volltext
Lancet neurology, 2018-08, Vol.17 (8), p.699
- May, Patrick
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2018
Link zum Volltext
Genome medicine, 2020-03, Vol.12 (1), p.28-28, Article 28
- Lal, Dennis
- May, Patrick
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- Weber, Yvonne G
- Helbig, Ingo
- Majithia, Amit R
- Palotie, Aarno
- Daly, Mark J
2020
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