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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 ORCID: 0000-0002-8932-2772
(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