MAOA gene hypomethylation in panic disorder—reversibility of an epigenetic risk pattern by psychotherapy von Ziegler, C, Richter, J, Mahr, M, Gajewska, A, Schiele, M A, Gehrmann, A, Schmidt, B, Lesch, K-P, Lang, T, Helbig-Lang, S, Pauli, P, Kircher, T, Reif, A, Rief, W, Vossbeck-Elsebusch, A N, Arolt, V, Wittchen, H-U, Hamm, A O, Deckert, J, Domschke, K

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Mimicry of surgical site infection – Case report von Bretschneider, H., Helbig, S., Kleber, C., de With, K., Stiehler, M.

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Calcium-binding protein expression in peritoneal endometriosis-associated nerve fibres von Barcena de Arellano, M. L., Münch, S., Arnold, J., Helbig, S., Schneider, A., Mechsner, S.

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Diagnosis and inflammatory response of patients with candiduria von Helbig, S., Achkar, J. M., Jain, N., Wang, X., Gialanella, P., Levi, M., Fries, B. C.

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Navigation-Supported and Sonographically-Controlled Fine-Needle Puncture in Soft Tissues of the Neck von Helbig, M, Krysztoforski, K, Kroll, T, Kucharski, J, Popek, M, Helbig, S, Gstoettner, W, May, A, Kozak, J

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The 2017 Update of the German Clinical Guideline on Epidemiology, Diagnostics, Therapy, Prevention, and Management of Uncomplicated Urinary Tract Infections in Adult Patients. Part... von Kranz, Jennifer, Schmidt, Stefanie, Lebert, Cordula, Schneidewind, Laila, Mandraka, Falitsa, Kunze, Mirjam, Helbig, Sina, Vahlensieck, Winfried, Naber, Kurt, Schmiemann, Guido, Wagenlehner, Florian M.

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Navigation-assisted sonography for soft tissues in the head and neck region von Helbig, M, Krysztoforski, K, Kucharski, J, Popek, M, Kroll, T, Helbig, S, May, A, Gstoettner, W, Kozak, J

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GRIN2A-related disorders: genotype and functional consequence predict phenotype von Strehlow, Vincent, Heyne, Henrike O, Vlaskamp, Danique R M, Marwick, Katie F M, Rudolf, Gabrielle, de Bellescize, Julitta, Biskup, Saskia, Brilstra, Eva H, Brouwer, Oebele F, Callenbach, Petra M C, Hentschel, Julia, Hirsch, Edouard, Kind, Peter C, Mignot, Cyril, Platzer, Konrad, Rump, Patrick, Skehel, Paul A, Wyllie, David J A, Hardingham, Giles E, van Ravenswaaij-Arts, Conny M A, Lesca, Gaetan, Lemke, Johannes R

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A functional genetic variation of SLC6A2 repressor hsa-miR-579-3p upregulates sympathetic noradrenergic processes of fear and anxiety von Hommers, L. G., Richter, J., Yang, Y., Raab, A., Baumann, C., Lang, K., Schiele, M. A., Weber, H., Wittmann, A., Wolf, C., Alpers, G. W., Arolt, V., Domschke, K., Fehm, L., Fydrich, T., Gerlach, A., Gloster, A. T., Hamm, A. O., Helbig-Lang, S., Kircher, T., Lang, T., Pané-Farré, C. A., Pauli, P., Pfleiderer, B., Reif, A., Romanos, M., Straube, B., Ströhle, A., Wittchen, H.-U., Frantz, S., Ertl, G., Lohse, M. J., Lueken, U., Deckert, J.

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Quality management: reduced waiting time and enhanced efficiency in a university ear, nose, and throat outpatient department von Helbig, M, Helbig, S, Knecht, R, Kahla-Witzsch, H A, Gstöttner, W

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PROBLEMS WITH HOMEWORK IN CBT: RARE EXCEPTION OR RATHER FREQUENT? von Helbig, Sylvia, Fehm, Lydia

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Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies von 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., Weckhuysen, Sarah, Meisler, Miriam, Berkovic, Samuel F., De Jonghe, Peter, Scheffer, Ingrid E., Myers, Richard M., Cooper, Gregory M., Mefford, Heather C.

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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy von 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, Weber, Yvonne G, Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K, Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M, Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R

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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

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Robot Intelligence Technology and Applications 7: Results from the 10th International Conference on Robot Intelligence Technology and Applications von Jo, Jun, Choi, Han-Lim, Helbig, Marde, Oh, Hyondong, Hwangbo, Jemin, Lee, Chang-Hun, Stantic, Bela

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Genetic generalized epilepsies von Mullen, Saul A., Berkovic, Samuel F., Berkovic, Samuel F, Lowenstein, Daniel H, Kato, Mitsuhiro, Cross, Helen, Satishchandra, Parthasathy, Jonghe, Peter, Goldman, Alica, Petrou, Steve, Tan, Nigel CK, Helbig, Ingo, Mefford, Heather C, Jiang, Yuwu

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Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders von Lal, Dennis, May, Patrick, Perez-Palma, Eduardo, Samocha, Kaitlin E., Kosmicki, Jack A., Robinson, Elise B., Moller, Rikke S., Krause, Roland, Nuernberg, Peter, Weckhuysen, Sarah, De Jonghe, Peter, Guerrini, Renzo, Niestroj, Lisa M., Du, Juliana, Marini, Carla, Ware, James S., Kurki, Mitja, Gormley, Padhraig, Tang, Sha, Wu, Sitao, Biskup, Saskia, Poduri, Annapurna, Neubauer, Bernd A., Koeleman, Bobby P. C., Helbig, Katherine L., Weber, Yvonne G., Helbig, Ingo, Majithia, Amit R., Palotie, Aarno, Daly, Mark J.

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The phenotypic spectrum of SCN8A encephalopathy von Larsen, Jan, Carvill, Gemma L, Gardella, Elena, Kluger, Gerhard, Schmiedel, Gudrun, Barisic, Nina, Depienne, Christel, Brilstra, Eva, Mang, Yuan, Nielsen, Jens Erik Klint, Kirkpatrick, Martin, Goudie, David, Goldman, Rebecca, Jähn, Johanna A, Jepsen, Birgit, Gill, Deepak, Döcker, Miriam, Biskup, Saskia, McMahon, Jacinta M, Koeleman, Bobby, Harris, Mandy, Braun, Kees, de Kovel, Carolien G F, Marini, Carla, Specchio, Nicola, Djémié, Tania, Weckhuysen, Sarah, Tommerup, Niels, Troncoso, Monica, Troncoso, Ledia, Bevot, Andrea, Wolff, Markus, Hjalgrim, Helle, Guerrini, Renzo, Scheffer, Ingrid E, Mefford, Heather C, Møller, Rikke S

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First release of Teretriosoma nigrescens Lewis (Col., Histeridae), the predator of Prostephanus truncatus (Horn) (Col. Bostrichidae), and follow-up investigations in southern Togo von Richter, J., Biliwa, A., Helbig, J., Henning-Helbig, S.

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals von Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L., Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Brünger, Tobias, Thomas, Rhys H., Talkowski, Michael, Helbig, Ingo, Leu, Costin, Lal, Dennis

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