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Nature Genetics, ISSN 1061-4036, 09/2013, Volume 45, Issue 9, pp. 1067 - 1072
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 7, pp. 896 - 901
Journal Article
by Appenzeller, Silke and Balling, Rudi and Barisic, Nina and Baulac, Stéphanie and Caglayan, Hande and Craiu, Dana and De Jonghe, Peter and Depienne, Christel and Dimova, Petia and Djémié, Tania and Gormley, Padhraig and Guerrini, Renzo and Helbig, Ingo and Hjalgrim, Helle and Hoffman-Zacharska, Dorota and Jähn, Johanna and Klein, Karl Martin and Koeleman, Bobby and Komarek, Vladimir and Krause, Roland and Kuhlenbäumer, Gregor and Leguern, Eric and Lehesjoki, Anna-Elina and Lemke, Johannes R and Lerche, Holger and Linnankivi, Tarja and Marini, Carla and May, Patrick and Møller, Rikke S and Muhle, Hiltrud and Pal, Deb and Palotie, Aarno and Pendziwiat, Manuela and Robbiano, Angela and Roelens, Filip and Rosenow, Felix and Selmer, Kaja and Serratosa, Jose M and Sisodiya, Sanjay and Stephani, Ulrich and Sterbova, Katalin and Striano, Pasquale and Suls, Arvid and Talvik, Tiina and von Spiczak, Sarah and Weber, Yvonne and Weckhuysen, Sarah and Zara, Federico and Abou-Khalil, Bassel and Alldredge, Brian K and Andermann, Eva and Andermann, Frederick and Amron, Dina and Bautista, Jocelyn F and Berkovic, Samuel F and Bluvstein, Judith and Boro, Alex and Cascino, Gregory and Consalvo, Damian and Crumrine, Patricia and Devinsky, Orrin and Dlugos, Dennis and Epstein, Michael P and Fiol, Miguel and Fountain, Nathan B and French, Jacqueline and Friedman, Daniel and Geller, Eric B and Glauser, Tracy and Glynn, Simon and Haas, Kevin and Haut, Sheryl R and Hayward, Jean and Helmers, Sandra L and Joshi, Sucheta and Kanner, Andres and Kirsch, Heidi E and Knowlton, Robert C and Kossoff, Eric H and Kuperman, Rachel and Kuzniecky, Ruben and Lowenstein, Daniel H and McGuire, Shannon M and Motika, Paul V and Novotny, Edward J and Ottman, Ruth and Paolicchi, Juliann M and Parent, Jack and Park, Kristen and Poduri, Annapurna and Sadleir, Lynette and Scheffer, Ingrid E and Shellhaas, Renée A and Sherr, Elliott and Shih, Jerry J and Singh, Rani and Sirven, Joseph and Smith, Michael C and Sullivan, Joe and Thio, Liu Lin and ... and Epi4K Consortium and EuroEPINOMICS-RES Consortium and Epilepsy Phenome Genome Project and Epilepsy Phenome/Genome Project
The American Journal of Human Genetics, ISSN 0002-9297, 10/2014, Volume 95, Issue 4, pp. 360 - 370
Journal Article
Neurology, ISSN 0028-3878, 2015, Volume 84, Issue 5, pp. 480 - 489
Journal Article
Journal of Pediatric Epilepsy, ISSN 2146-457X, 2012, Volume 1, Issue 3, pp. 161 - 169
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 6961 - 12
Adaptive laboratory evolution is an important tool to evolve organisms to increased tolerance towards different physical and chemical stress. It is applied to... 
CELL LINEAGE | YEAST | EVOLUTION | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | TRACKING | ANTIBIOTIC-RESISTANCE | POPULATIONS | NEMATODE CAENORHABDITIS-ELEGANS | MUTATIONS | GENOME | Growth rate | Antibiotics | Laboratories | Antibiotic resistance | Phenotyping | Insertion | Evolution | Genomes | Evolution & development | Experiments | Strains (organisms)
Journal Article
by Allen, Anew S and Berkovic, Samuel F and Bridgers, Joshua and Cossette, Patrick and Dlugos, Dennis and Epstein, Michael P and Glauser, Tracy and Goldstein, David B and Heinzen, Erin L and Jiang, Yu and Johnson, Michael R and Kuzniecky, Ruben and Lowenstein, Daniel H and Marson, Anthony G and Mefford, Heather C and O'Brien, Terence J and Ottman, Ruth and Petrou, Steven and Petrovski, Slavé and Poduri, Annapurna and Ren, Zhong and Scheffer, Ingrid E and Sherr, Elliott and Wang, Quanli and Balling, Rudi and Barisic, Nina and Baulac, Stéphanie and Caglayan, Hande and Craiu, Dana and De Jonghe, Peter and Depienne, Christel and Guerrini, Renzo and Helbig, Ingo and Hjalgrim, Helle and Hoffman-Zacharska, Dorota and Jähn, Johanna A and Klein, Karl Martin and Koeleman, Bobby|info:eu-repo/dai/nl/157197468 and Komarek, Vladimir and Krause, Roland and Leguern, Eric and Lehesjoki, Anna-Elina and Lemke, Johannes R and Lerche, Holger and Linnankivi, Tarja and Marini, Carla and May, Patrick and Møller, Rikke S and Muhle, Hiltrud and Pal, Deb and Palotie, Aarno and Rosenow, Felix and Selmer, Kaja and Serratosa, Jose M and Sisodiya, Sanjay M and Stephani, Ulrich and Sterbova, Katalin and Striano, Pasquale and Suls, Arvid and Talvik, Tiina and von Spiczak, Sarah and Weber, Yvonne G and Weckhuysen, Sarah and Zara, Federico and Abou-Khalil, Bassel and Alledge, Brian K and Amrom, Dina and Andermann, Eva and Andermann, Frederick and Bautista, Jocelyn F and Bluvstein, Judith and Cascino, Gregory D and Consalvo, Damian and Crumrine, Patricia and Devinsky, Orrin and Fiol, Miguel E and Fountain, Nathan B and French, Jacqueline and Friedman, Daniel and Haas, Kevin and Haut, Sheryl R and Hayward, Jean and Joshi, Sucheta and Kanner, Anes and Kirsch, Heidi E and Kossoff, Eric H and Kuperman, Rachel and McGuire, Shannon M and Motika, Paul V and Novotny, Edward J and Paolicchi, Juliann M and Parent, Jack and Park, Kristen and Shellhaas, Renée A and Sirven, Joseph and Smith, Michael C and Sullivan, Joseph and Thio, Liu Lin and Venkat, Anu and Vining, Eileen P. G and ... and Epi4K Consortium and Epilepsy Phenome Genome Project and EuroEPINOMICS- RES Consortium and EuroEPINOMICS-RES Consortium
European Journal of Human Genetics, ISSN 1018-4813, 06/2017, Volume 25, Issue 7, pp. 894 - 899
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2018, Volume 102, Issue 4, pp. 557 - 573
Journal Article
by Helbig, Ingo and Helbig, Katherine L and Lopez-Hernandez, Tania and Shor, Oded and Galer, Peter and Ganesan, Shiva and Pendziwiat, Manuela and Rademacher, Annika and Ellis, Colin A and Hümpfer, Nadja and Schwarz, Niklas and Seiffert, Simone and Peeden, Joseph and Shen, Joseph and Štěrbová, Katalin and Hammer, Trine Bjørg and Møller, Rikke S and Shinde, Deepali N and Tang, Sha and Smith, Lacey and Poduri, Annapurna and Krause, Roland and Benninger, Felix and Haucke, Volker and Weber, Yvonne G and Balling, Rudi and Barisic, Nina and Baulac, Stéphanie and Caglayan, Hande and Craiu, Dana and De Jonghe, Peter and Depienne, Christel and Guerrini, Renzo and Hjalgrim, Helle and Hoffman-Zacharska, Dorota and Jähn, Johanna and Klein, Karl Martin and Koeleman, Bobby P.C and Komarek, Vladimir and Leguern, Eric and Lehesjoki, Anna-Elina and Lemke, Johannes R and Lerche, Holger and Linnankivi, Tarja and Marini, Carla and May, Patrick and Muhle, Hiltrud and Pal, Deb K and Palotie, Aarno and Rosenow, Felix and Schubert-Bast, Susanne and Selmer, Kaja and Serratosa, Jose M and Sisodiya, Sanjay and Stephani, Ulrich and Striano, Pasquale and Suls, Arvid and Talvik, Tiina and von Spiczak, Sarah and Weckhuysen, Sarah and Zara, Federico and Avillach, Paul and Bartels, Anna and Biswas, Sawona and Bourgeois, Florence and Devkota, Batsal and Glauser, Tracy and Hallinan, Barbara and Heath, Allison and Hirschhorn, Joel and Kilbourn, Judson and Kong, Sek Won and Krantz, Ian and Lee, In-Hee and Mandl, Kenneth D and Marsh, Eric and Sund, Kristen and Taylor, Deanne and White, Peter
The American Journal of Human Genetics, ISSN 0002-9297, 06/2019, Volume 104, Issue 6, pp. 1060 - 1072
The developmental and epileptic encephalopathies (DEEs) are heterogeneous disorders with a strong genetic contribution, but the underlying genetic etiology... 
computational phenotypes | synaptic transmission | developmental and epileptic encephalopathy | neurodevelopmental disorders | clathrin-mediated endocytosis | Human Phenotype Ontology
Journal Article