Magnetic Resonance Enteroclysis in the Diagnosis of Small-Intestinal Crohn's Disease: Diagnostic Accuracy and Inter- and Intra-observer Agreement von Negaard, A., Sandvik, L., Mulahasanovic, A., Berstad, A. E., Klöw, N.-E.

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Crohn's Disease Evaluated with Magnetic Resonance Enteroclysis: Diagnostic Performance of Experienced and Inexperienced Readers before and after Training von Negaard, A., Mulahasanovic, A., Reisaeter, L. A., Aasekjaer, K., Sandvik, L., Klow, N.-E.

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CDHR1 mutations in retinal dystrophies von Stingl, Katarina, Mayer, Anja K., Llavona, Pablo, Mulahasanovic, Lejla, Rudolph, Günther, Jacobson, Samuel G., Zrenner, Eberhart, Kohl, Susanne, Wissinger, Bernd, Weisschuh, Nicole

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Heterozygous POLG variant Ser1181Asn is associated with autosomal dominant neuro-myopathy in one family with no further specific manifestations of mitochondrial syndrome von Dohrn, Maike F, Beijer, Danique, Mulahasanovic, Lejla

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BLS-MT-ZKP: A novel approach to selective disclosure of claims from digital credentials von Ramic, Seila Becirovic, Prazina, Irfan, Pozderac, Damir, Mulahasanovic, Razija Turcinhodzic, Mrdovic, Sasa

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Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutation von Nasser, F., Mulahasanovic, L., Alkhateeb, M., Biskup, S., Stingl, K., Zrenner, E.

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P15 Idiopathic dancing dens syndrome – A new disease entity associated with (hereditary) disorders of connective tissue? von Toteva, B., Mulahasanovic, L., Förg, A., Megahed, M., Dafotakis, M., Dohrn, M.F.

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Clinical characterization and therapy discussion of the p.Asp313Tyr variant in GLA von Dumke, Christina, Zengeler, Diana, Mulahasanovic, Lejla, Schulz, Jörg B., Gess, Burkhard, Dohrn, Maike F.

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Genomic analyses inform on migration events during the peopling of Eurasia von Pagani, Luca, Lawson, Daniel John, Jagoda, Evelyn, Mörseburg, Alexander, Eriksson, Anders, Mitt, Mario, Clemente, Florian, Hudjashov, Georgi, DeGiorgio, Michael, Saag, Lauri, Wall, Jeffrey D., Cardona, Alexia, Mägi, Reedik, Sayres, Melissa A. Wilson, Kaewert, Sarah, Inchley, Charlotte, Scheib, Christiana L., Järve, Mari, Karmin, Monika, Jacobs, Guy S., Antao, Tiago, Iliescu, Florin Mircea, Kushniarevich, Alena, Ayub, Qasim, Tyler-Smith, Chris, Xue, Yali, Yunusbayev, Bayazit, Tambets, Kristiina, Mallick, Chandana Basu, Saag, Lehti, Pocheshkhova, Elvira, Andriadze, George, Muller, Craig, Westaway, Michael C., Lambert, David M., Zoraqi, Grigor, Turdikulova, Shahlo, Dalimova, Dilbar, Sabitov, Zhaxylyk, Sultana, Gazi Nurun Nahar, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Isakova, Jainagul, Damba, Larisa D., Gubina, Marina, Nymadawa, Pagbajabyn, Evseeva, Irina, Atramentova, Lubov, Utevska, Olga, Ricaut, François-Xavier, Brucato, Nicolas, Sudoyo, Herawati, Letellier, Thierry, Cox, Murray P., Barashkov, Nikolay A., Škaro, Vedrana, Mulahasanovic´, Lejla, Primorac, Dragan, Sahakyan, Hovhannes, Mormina, Maru, Eichstaedt, Christina A., Lichman, Daria V., Abdullah, Syafiq, Chaubey, Gyaneshwer, Wee, Joseph T. S., Mihailov, Evelin, Karunas, Alexandra, Litvinov, Sergei, Khusainova, Rita, Ekomasova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Marjanović, Damir, Yepiskoposyan, Levon, Behar, Doron M., Balanovska, Elena, Metspalu, Andres, Derenko, Miroslava, Malyarchuk, Boris, Voevoda, Mikhail, Fedorova, Sardana A., Osipova, Ludmila P., Lahr, Marta Mirazón, Gerbault, Pascale, Leavesley, Matthew, Migliano, Andrea Bamberg, Petraglia, Michael, Balanovsky, Oleg, Khusnutdinova, Elza K., Metspalu, Ene, Thomas, Mark G., Manica, Andrea, Nielsen, Rasmus, Villems, Richard, Willerslev, Eske, Kivisild, Toomas, Metspalu, Mait

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The Genomic Impact of European Colonization of the Americas von Ongaro, Linda, Scliar, Marilia O., Flores, Rodrigo, Raveane, Alessandro, Marnetto, Davide, Sarno, Stefania, Gnecchi-Ruscone, Guido A., Alarcón-Riquelme, Marta E., Patin, Etienne, Wangkumhang, Pongsakorn, Hellenthal, Garrett, Gonzalez-Santos, Miguel, King, Roy J., Kouvatsi, Anastasia, Balanovsky, Oleg, Balanovska, Elena, Atramentova, Lubov, Turdikulova, Shahlo, Mastana, Sarabjit, Marjanovic, Damir, Mulahasanovic, Lejla, Leskovac, Andreja, Lima-Costa, Maria F., Pereira, Alexandre C., Barreto, Mauricio L., Horta, Bernardo L., Mabunda, Nédio, May, Celia A., Moreno-Estrada, Andrés, Achilli, Alessandro, Olivieri, Anna, Semino, Ornella, Tambets, Kristiina, Kivisild, Toomas, Luiselli, Donata, Torroni, Antonio, Capelli, Cristian, Tarazona-Santos, Eduardo, Metspalu, Mait, Pagani, Luca, Montinaro, Francesco

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Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers von Dohrn, Maike F, Heller, Corina, Zengeler, Diana, Obermaier, Carolin D, Biskup, Saskia, Weis, Joachim, Nikolin, Stefan, Claeys, Kristl G, Schöne, Ulrike, Beijer, Danique, Winter, Natalie, Achenbach, Pascal, Gess, Burkhard, Schulz, Jörg B, Mulahasanovic, Lejla

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Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies von Dohrn, Maike F., Glöckle, Nicola, Mulahasanovic, Lejla, Heller, Corina, Mohr, Julia, Bauer, Christine, Riesch, Erik, Becker, Andrea, Battke, Florian, Hörtnagel, Konstanze, Hornemann, Thorsten, Suriyanarayanan, Saranya, Blankenburg, Markus, Schulz, Jörg B., Claeys, Kristl G., Gess, Burkhard, Katona, Istvan, Ferbert, Andreas, Vittore, Debora, Grimm, Alexander, Wolking, Stefan, Schöls, Ludger, Lerche, Holger, Korenke, G. Christoph, Fischer, Dirk, Schrank, Bertold, Kotzaeridou, Urania, Kurlemann, Gerhard, Dräger, Bianca, Schirmacher, Anja, Young, Peter, Schlotter‐Weigel, Beate, Biskup, Saskia

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Genetic Heritage of the Balto-Slavic Speaking Populations: A Synthesis of Autosomal, Mitochondrial and Y-Chromosomal Data von Kushniarevich, Alena, Utevska, Olga, Chuhryaeva, Marina, Agdzhoyan, Anastasia, Dibirova, Khadizhat, Uktveryte, Ingrida, Möls, Märt, Mulahasanovic, Lejla, Pshenichnov, Andrey, Frolova, Svetlana, Shanko, Andrey, Metspalu, Ene, Reidla, Maere, Tambets, Kristiina, Tamm, Erika, Koshel, Sergey, Zaporozhchenko, Valery, Atramentova, Lubov, Kučinskas, Vaidutis, Davydenko, Oleg, Goncharova, Olga, Evseeva, Irina, Churnosov, Michail, Pocheshchova, Elvira, Yunusbayev, Bayazit, Khusnutdinova, Elza, Marjanović, Damir, Rudan, Pavao, Rootsi, Siiri, Yankovsky, Nick, Endicott, Phillip, Kassian, Alexei, Dybo, Anna, Tyler-Smith, Chris, Balanovska, Elena, Metspalu, Mait, Kivisild, Toomas, Villems, Richard, Balanovsky, Oleg

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P 44 Brisk jerk reflexes in a CMT case – novel heterozygous variant c.785T>C; p.Leu262Pro in KIF5A explaining the mixed phenotype von Dohrn, M.F., Glöckle, N., Mulahasanovic, L., Sprecher, A., Biskup, S., Claeys, K.G., Schulz, J.B., Gess, B.

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A Survey of Procedural Modelling Methods for Layout Generation of Virtual Scenes von Cogo, Emir, Krupalija, Ehlimana, Prazina, Irfan, Bećirović, Šeila, Okanović, Vensada, Rizvić, Selma, Mulahasanović, Razija Turčinhodžić

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Conventional surgical repair and endovascular treatment of acute traumatic aortic rupture von Buz, Semih, Zipfel, Burkhart, Mulahasanovic, Sead, Pasic, Miralem, Weng, Yuguo, Hetzer, Roland

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Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants von Schwarz, Niklas, Seiffert, Simone, Pendziwiat, Manuela, Rademacher, Annika Verena, Brünger, Tobias, Hedrich, Ulrike B S, Augustijn, Paul B, Baier, Hartmut, Bayat, Allan, Bisulli, Francesca, Buono, Russell J, Bruria, Ben Zeev, Doyle, Michael G, Guerrini, Renzo, Heimer, Gali, Iacomino, Michele, Kearney, Hugh, Klein, Karl Martin, Kousiappa, Ioanna, Kunz, Wolfram S, Lerche, Holger, Licchetta, Laura, Lohmann, Ebba, Minardi, Raffaella, McDonald, Marie, Montgomery, Sarah, Mulahasanovic, Lejla, Oegema, Renske, Ortal, Barel, Papacostas, Savvas S, Ragona, Francesca, Granata, Tiziana, Reif, Phillip S, Rosenow, Felix, Rothschild, Annick, Scudieri, Paolo, Striano, Pasquale, Tinuper, Paolo, Tanteles, George A, Vetro, Annalisa, Zahnert, Felix, Goldberg, Ethan M, Zara, Federico, Lal, Dennis, May, Patrick, Muhle, Hiltrud, Helbig, Ingo, Weber, Yvonne

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Stx4 is required to regulate cardiomyocyte Ca2+ handling during vertebrate cardiac development von Perl, Eliyahu, Ravisankar, Padmapriyadarshini, Beerens, Manu E., Mulahasanovic, Lejla, Smallwood, Kelly, Sasso, Marion Bermúdez, Wenzel, Carina, Ryan, Thomas D., Komár, Matej, Bove, Kevin E., MacRae, Calum A., Weaver, K. Nicole, Prada, Carlos E., Waxman, Joshua S.

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Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants von Schwarz, Niklas, Seiffert, Simone, Pendziwiat, Manuela, Rademacher, Annika Verena, Brà Nger, Tobias, Hedrich, Ulrike B S, Augustijn, Paul B, Baier, Hartmut, Bayat, Allan, Bisulli, Francesca, Buono, Russell J, Bruria, Ben Zeev, Doyle, Michael G, Guerrini, Renzo, Heimer, Gali, Iacomino, Michele, Kearney, Hugh, Klein, Karl Martin, Kousiappa, Ioanna, Kunz, Wolfram S, Lerche, Holger, Licchetta, Laura, Lohmann, Ebba, Minardi, Raffaella, McDonald, Marie, Montgomery, Sarah, Mulahasanovic, Leijla, Oegema, Renske, Ortal, Barel, Papacostas, Savvas S, Ragona, Francesca, Granata, Tiziana, Reif, Phillip S, Rosenow, Felix, Rothschild, Annick, Scudieri, Paolo, Striano, Pasquale, Tinuper, Paolo, Tanteles, George A, Vetro, Annalisa, Zahnert, Felix, Goldberg, Ethan M, Zara, Federico, Lal, Dennis, May, Patrick, Muhle, Hiltrud, Helbig, Ingo, Weber, Yvonne

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A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C von Suriyanarayanan, Saranya, Othman, Alaa, Dräger, Bianca, Schirmacher, Anja, Young, Peter, Mulahasanovic, Lejla, Hörtnagel, Konstanze, Biskup, Saskia, von Eckardstein, Arnold, Hornemann, Thorsten, Lone, Museer A.

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