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Journal Article

Bobbili, Dheeraj R., Lal, Dennis, May, Patrick ORCID: 0000-0001-8698-3770, Reinthaler, Eva M., Jabbari, Kamel, Thiele, Holger, Nothnagel, Michael ORCID: 0000-0001-8305-7114, Jurkowski, Wiktor, Feucht, Martha, Nuernberg, Peter, Lerche, Holger, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Krause, Roland ORCID: 0000-0001-9938-7126, Neubauer, Bernd A., Reinthaler, Eva M., Zimprich, Fritz ORCID: 0000-0002-6998-5480, Feucht, Martha, Steinboeck, Hannelore, Neophytou, Birgit, Geldner, Julia, Gruber-Sedlmayr, Ursula, Haberlandt, Edda, Ronen, Gabriel M., Altmueller, Janine, Lal, Dennis, Nrnberg, Peter, Sander, Thomas, Thiele, Holger, Krause, Roland ORCID: 0000-0001-9938-7126, May, Patrick ORCID: 0000-0001-8698-3770, Balling, Rudi ORCID: 0000-0003-2902-5650, Lerche, Holger and Neubauer, Bernd A. (2018). Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. Eur. J. Hum. Genet., 26 (2). S. 258 - 265. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Chalhoub, Boulos, Denoeud, France ORCID: 0000-0001-8819-7634, Liu, Shengyi, Parkin, Isobel A. P., Tang, Haibao ORCID: 0000-0002-3460-8570, Wang, Xiyin, Chiquet, Julien ORCID: 0000-0002-3629-3429, Belcram, Harry, Tong, Chaobo, Samans, Birgit, Correa, Margot, Da Silva, Corinne, Just, Jeremy ORCID: 0000-0003-0842-9808, Falentin, Cyril, Koh, Chu Shin, Le Clainche, Isabelle, Bernard, Maria ORCID: 0000-0001-9005-5563, Bento, Pascal, Noel, Benjamin ORCID: 0000-0002-5830-3253, Labadie, Karine ORCID: 0000-0001-7467-8509, Alberti, Adriana ORCID: 0000-0003-3372-9423, Charles, Mathieu, Arnaud, Dominique, Guo, Hui, Daviaud, Christian, Alamery, Salman, Jabbari, Kamel, Zhao, Meixia, Edger, Patrick P., Chelaifa, Houda, Tack, David, Lassalle, Gilles, Mestiri, Imen ORCID: 0000-0002-7528-2781, Schnel, Nicolas, Le Paslier, Marie-Christine, Fan, Guangyi, Renault, Victor, Bayer, Philippe E., Golicz, Agnieszka A., Manoli, Sahana, Lee, Tae-Ho, Chalabi, Smahane, Hu, Qiong, Fan, Chuchuan ORCID: 0000-0001-8443-7194, Tollenaere, Reece, Lu, Yunhai, Battail, Christophe ORCID: 0000-0001-6849-7824, Shen, Jinxiong, Sidebottom, Christine H. D., Wang, Xinfa, Canaguier, Aurelie, Chauveau, Aurelie, Berard, Aurelie, Deniot, Gwenaelle, Guan, Mei, Liu, Zhongsong, Sun, Fengming, Lim, Yong Pyo, Lyons, Eric ORCID: 0000-0002-3348-8845, Town, Christopher D., Bancroft, Ian ORCID: 0000-0001-7707-1171, Wang, Xiaowu, Meng, Jinling, Ma, Jianxin, Pires, J. Chris ORCID: 0000-0001-9682-2639, King, Graham J., Brunel, Dominique, Delourme, Regine, Renard, Michel, Aury, Jean-Marc ORCID: 0000-0003-1718-3010, Adams, Keith L., Batley, Jacqueline ORCID: 0000-0002-5391-5824, Snowdon, Rod J., Tost, Jorg, Edwards, David ORCID: 0000-0001-7599-6760, Zhou, Yongming, Hua, Wei, Sharpe, Andrew G., Paterson, Andrew H., Guan, Chunyun and Wincker, Patrick (2014). Early allopolyploid evolution in the post-Neolithic Brassica napus oilseed genome. Science, 345 (6199). S. 950 - 954. WASHINGTON: AMER ASSOC ADVANCEMENT SCIENCE. ISSN 1095-9203

Jabbari, Kamel, Bobbili, Dheeraj R., Lal, Dennis, Reinthaler, Eva M., Schubert, Julian, Wolking, Stefan ORCID: 0000-0002-1460-6623, Sinha, Vishal, Motameny, Susanne, Thiele, Holger, Kawalia, Amit, Altmueller, Janine, Toliat, Mohammad Reza, Kraaij, Robert, van Rooij, Jeroen, Uitterlinden, Andre G., Ikram, M. Arfan, Zara, Federico, Lehesjoki, Anna-Elina, Krause, Roland, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Sander, Thomas, Neubauer, Bernd A., May, Patrick ORCID: 0000-0001-8698-3770, Lerche, Holger and Nuernberg, Peter (2018). Rare gene deletions in genetic generalized and Rolandic epilepsies. PLoS One, 13 (8). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Jabbari, Kamel, Chakraborty, Maharshi and Wiehe, Thomas ORCID: 0000-0002-8932-2772 (2019). DNA sequence-dependent chromatin architecture and nuclear hubs formation. Sci Rep, 9. LONDON: NATURE PUBLISHING GROUP. ISSN 2045-2322

Jabbari, Kamel, Heger, Peter ORCID: 0000-0003-2583-2981, Sharma, Ranu and Wiehe, Thomas ORCID: 0000-0002-8932-2772 (2018). The Diverging Routes of BORIS and CTCF: An Interactomic and Phylogenomic Analysis. Life-Basel, 8 (1). BASEL: MDPI. ISSN 2075-1729

Jabbari, Kamel and Nuernberg, Peter (2016). A genomic view on epilepsy and autism candidate genes. Genomics, 108 (1). S. 31 - 37. SAN DIEGO: ACADEMIC PRESS INC ELSEVIER SCIENCE. ISSN 1089-8646

Jabbari, Kamel, Wirtz, Johannes, Rauscher, Martina and Wiehe, Thomas (2019). A common genomic code for chromatin architecture and recombination landscape. PLoS One, 14 (3). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Lal, Dennis, Reinthaler, Eva M., Schubert, Julian, Muhle, Hiltrud, Riesch, Erik, Kluger, Gerhard, Jabbari, Kamel, Kawalia, Amit, Baeumel, Christine, Holthausen, Hans, Hahn, Andreas, Feucht, Martha, Neophytou, Birgit, Haberlandt, Edda, Becker, Felicitas, Altmueller, Janine, Thiele, Holger, Lemke, Johannes R., Lerche, Holger, Nuernberg, Peter, Sander, Thomas, Weber, Yvonne, Zimprich, Fritz ORCID: 0000-0002-6998-5480 and Neubauer, Bernd A. (2014). DEPDC5 Mutations in Genetic Focal Epilepsies of Childhood. Ann. Neurol., 75 (5). S. 788 - 793. HOBOKEN: WILEY-BLACKWELL. ISSN 1531-8249

May, Patrick ORCID: 0000-0001-8698-3770, Girard, Simon ORCID: 0000-0002-4089-2280, Harrer, Merle, Bobbili, Dheeraj R., Schubert, Julian, Wolking, Stefan ORCID: 0000-0002-1460-6623, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline, Niturad, Cristina E., Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-Lopez, Rosa, Baulac, Stephanie ORCID: 0000-0001-6430-4693, Marini, Carla, Thiele, Holger, Altmueller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestele, Sandrine ORCID: 0000-0002-5982-1562, Terragni, Benedetta, Coombs, Ian D., Reid, Christopher A., Striano, Pasquale ORCID: 0000-0002-6065-1476, Caglayan, Hande, Siren, Auli, Everett, Kate ORCID: 0000-0001-6700-1698, Moller, Rikke S., Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S. ORCID: 0000-0003-1113-3493, Weber, Yvonne G., Weckhuysen, Sarah ORCID: 0000-0003-2878-1147, De Jonghe, Peter, Sisodiya, Sanjay M., Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S., Trenite, Dorothee Kasteleijn-Nolst, Baykan, Betul, Ozbek, Ugur ORCID: 0000-0001-5319-0547, Bebek, Nerses, Klein, Karl M., Rosenow, Felix, Nguyen, Dang K., Dubeau, Francois, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clement, Jean-Francois, Cieuta-Walti, Cecile, Sills, Graeme J., Auce, Pauls, Francis, Ben, Johnson, Michael R., Marson, Anthony G., Berghuis, Bianca, Sander, Josemir W., Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L., Delanty, Norman, Depondt, Chantal, Krenn, Martin ORCID: 0000-0003-3026-3082, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi ORCID: 0000-0003-2902-5650, Ikram, M. Arfan, Uitterlinden, Andre G., Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven ORCID: 0000-0002-4960-6375, Mantegazza, Massimo ORCID: 0000-0002-1070-7929, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M., Koeleman, Bobby P. C., Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael ORCID: 0000-0001-8305-7114, Nuernberg, Peter, Maljevic, Snezana ORCID: 0000-0003-1876-5872, Zara, Federico, Cossette, Patrick, Krause, Roland ORCID: 0000-0001-9938-7126 and Lerche, Holger (2018). Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies: an exome-based case-control study. Lancet Neurol., 17 (8). S. 699 - 709. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1474-4465