141 EXTENDED TREATMENT DURATION IN CHRONIC HEPATITIS C GENOTYPE 1-INFECTED SLOW RESPONDERS: FINAL RESULTS OF THE SUCCESS STUDY von Buti, M, Lurie, Y, Zakharova, N.G, Blokhina, N.P, Horban, A, Sarrazin, C, Balciuniene, L, Chen, R, Yu, X, Faruqi, R, Esteban, R

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[448] CORRELATES OF INNATE AND ADAPTIVE IMMUNITY DURING ACUTE HCV INFECTION: IMPLICATIONS FOR CHRONIC VIRAL PERSISTENCE von Chokshi, S, Guobuzaite, A, Bonetto, S, Balciuniene, L, Ambrozaitis, A, Naoumov, N.V

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Glycyrrhizin in patients who failed previous interferon alpha-based therapies: biochemical and histological effects after 52 weeks von Manns, M. P., Wedemeyer, H., Singer, A., Khomutjanskaja, N., Dienes, H. P., Roskams, T., Goldin, R., Hehnke, U., Inoue, H.

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Rabies post-exposure prophylaxis vaccination with purified chick embryo cell vaccine (PCECV) and purified vero cell rabies vaccine (PVRV) in a four-site intradermal schedule (4-0-2... von Ambrozaitis, Arvydas, Laiškonis, Alvydas, Balčiuniene, Ligita, Banzhoff, Angelika, Malerczyk, Claudius

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Polymorphism of response to cobalt excess in individual Vicia faba plants von Rancelis, Vytautas, Cesniene, Tatjana, Zvingila, Donatas, Barysas, Dainius, Balciuniene, Laimute, Dapkuniene, Stase

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Combination of IFNa2b and isoprinosine in treatment of CHC: A pilotstudy von Osna, N., Hagina, E., Viulgert, N., Sochnev, A., Kuse, V., Silonova, G., Viksna, L., Zvirbliena, A., Mauricas, M., Balciuniene, L., Ambrozaitis, A., Schalm, S.W.

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Hepatitis C Virus RNA Levels During Initial Induction or Standard Interferon Therapy: Influence of Continued Treatment on Sustained Response von Balciuniene, Ligita, Carlsson, Tony, Ambrozaitis, Arvydas, Reichard, Olle, Weiland, Ola

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Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities von Balciuniene, Jorune, Feng, Ningping, Iyadurai, Kelly, Hirsch, Betsy, Charnas, Lawrence, Bill, Brent R., Easterday, Mathew C., Staaf, Johan, Oseth, LeAnn, Czapansky-Beilman, Desiree, Avramopoulos, Dimitri, Thomas, George H., Borg, Åke, Valle, David, Schimmenti, Lisa A., Selleck, Scott B.

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The significance of amniotic fluid immunological analysis for the prediction of intrauterine infection von G. Balciuniene, L. Jakubauskiene, G.S. Drasutiene, A. Meskauskiene, D. Ramasauskaite

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Allele-Specific Droplet Digital PCR Combined with a Next-Generation Sequencing-Based Algorithm for Diagnostic Copy Number Analysis in Genes with High Homology: Proof of Concept Usi... von Amr, Sami S, Murphy, Elissa, Duffy, Elizabeth, Niazi, Rojeen, Balciuniene, Jorune, Luo, Minjie, Rehm, Heidi L, Abou Tayoun, Ahmad N

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Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior von Harris, Holly K., Nakayama, Tojo, Lai, Jenny, Zhao, Boxun, Argyrou, Nikoleta, Gubbels, Cynthia S., Soucy, Aubrie, Genetti, Casie A., Suslovitch, Victoria, Rodan, Lance H., Tiller, George E., Lesca, Gaetan, Gripp, Karen W., Asadollahi, Reza, Hamosh, Ada, Applegate, Carolyn D., Turnpenny, Peter D., Simon, Marleen E.H., Volker-Touw, Catharina M.L., Gassen, Koen L.I. van, Binsbergen, Ellen van, Pfundt, Rolph, Gardeitchik, Thatjana, Vries, Bert B.A. de, Immken, LaDonna L., Buchanan, Catherine, Willing, Marcia, Toler, Tomi L., Fassi, Emily, Baker, Laura, Vansenne, Fleur, Wang, Xiadong, Ambrus, Julian L., Fannemel, Madeleine, Posey, Jennifer E., Agolini, Emanuele, Novelli, Antonio, Rauch, Anita, Boonsawat, Paranchai, Fagerberg, Christina R., Larsen, Martin J., Kibaek, Maria, Labalme, Audrey, Poisson, Alice, Payne, Katelyn K., Walsh, Laurence E., Aldinger, Kimberly A., Balciuniene, Jorune, Skraban, Cara, Gray, Christopher, Murrell, Jill, Bupp, Caleb P., Pascolini, Giulia, Grammatico, Paola, Broly, Martin, Küry, Sébastien, Nizon, Mathilde, Rasool, Iqra Ghulam, Zahoor, Muhammad Yasir, Kraus, Cornelia, Reis, André, Iqbal, Muhammad, Uguen, Kevin, Audebert-Bellanger, Severine, Ferec, Claude, Redon, Sylvia, Baker, Janice, Wu, Yunhong, Zampino, Guiseppe, Syrbe, Steffan, Brosse, Ines, Jamra, Rami Abou, Dobyns, William B., Cohen, Lilian L., Blomhoff, Anne, Mignot, Cyril, Keren, Boris, Courtin, Thomas, Agrawal, Pankaj B., Beggs, Alan H., Yu, Timothy W.

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Variation in eye care professional distribution across Europe, a survey von Arnould, Louis, Varsanyi, Balazs, Dervan, Edward, Posarelli, Chiara, Filipe, Helena Prior, Bourcier, Tristan, Wedrich, Andreas, Ivekovic, Renata, Petrovski, Goran, Porro, Giorgio L., Laganovska, Guna, Balciuniene, Vilma Jurate, Mrukwa-Kominek, Ewa, Paust, Karsten, Roemer, Segolene, Haefliger, Ivan O., Atilla, Huban, Ursell, Paul, Cvenkel, Barba, Kiilgaard, Jens, Grupcheva, Christina, Furdova, Alena, Claeys, Marnix, Maresova, Klara, Mercieca, Franco, Sepp, Toomas, Parikakis, Efstratios, Burcea, Marian, Aclimandos, Wagih, Khawaja, Anthony P.

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Mutagenesis Screen Identifies agtpbp1 and eps15L1 as Essential for T lymphocyte Development in Zebrafish von Seiler, Christoph, Gebhart, Nichole, Zhang, Yong, Shinton, Susan A, Li, Yue-sheng, Ross, Nicola L, Liu, Xingjun, Li, Qin, Bilbee, Alison N, Varshney, Gaurav K, LaFave, Matthew C, Burgess, Shawn M, Balciuniene, Jorune, Balciunas, Darius, Hardy, Richard R, Kappes, Dietmar J, Wiest, David L, Rhodes, Jennifer

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Investigation of the functional effect of monoamine oxidase polymorphisms in human brain von BALCIUNIENE, J, EMILSSON, L, ORELAND, L, PETTERSSON, U, JAZIN, E. E

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Automated Clinical Exome Reanalysis Reveals Novel Diagnoses von Baker, Samuel W., Murrell, Jill R., Nesbitt, Addie I., Pechter, Kieran B., Balciuniene, Jorune, Zhao, Xiaonan, Yu, Zhenming, Denenberg, Elizabeth H., DeChene, Elizabeth T., Wilkens, Alisha B., Bhoj, Elizabeth J., Guan, Qiaoning, Dulik, Matthew C., Conlin, Laura K., Abou Tayoun, Ahmad N., Luo, Minjie, Wu, Chao, Cao, Kajia, Sarmady, Mahdi, Bedoukian, Emma C., Tarpinian, Jennifer, Medne, Livija, Skraban, Cara M., Deardorff, Matthew A., Krantz, Ian D., Krock, Bryan L., Santani, Avni B.

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ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy von Mattison, Kari A, Tossing, Gilles, Mulroe, Fred, Simmons, Callum, Butler, Kameryn M, Schreiber, Alison, Alsadah, Adnan, Neilson, Derek E, Naess, Karin, Wedell, Anna, Wredenberg, Anna, Sorlin, Arthur, McCann, Emma, Burghel, George J, Menendez, Beatriz, Hoganson, George E, Botto, Lorenzo D, Filloux, Francis M, Aledo-Serrano, Ángel, Gil-Nagel, Antonio, Tatton-Brown, Katrina, Verbeek, Nienke E, van der Zwaag, Bert, Aleck, Kyrieckos A, Fazenbaker, Andrew C, Balciuniene, Jorune, Dubbs, Holly A, Marsh, Eric D, Garber, Kathryn, Ek, Jakob, Duno, Morten, Hoei-Hansen, Christina E, Deardorff, Matthew A, Raca, Gordana, Quindipan, Catherine, van Hirtum-Das, Michele, Breckpot, Jeroen, Hammer, Trine Bjørg, Møller, Rikke S, Whitney, Andrea, Douglas, Andrew G L, Kharbanda, Mira, Brunetti-Pierri, Nicola, Morleo, Manuela, Nigro, Vincenzo, May, Halie J, Tao, James X, Argilli, Emanuela, Sherr, Elliot H, Dobyns, William B, Baines, Richard A, Warwicker, Jim, Parker, J Alex, Banka, Siddharth, Campeau, Philippe M, Escayg, Andrew

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Global increases in both common and rare copy number load associated with autism von Girirajan, Santhosh, Johnson, Rebecca L, Tassone, Flora, Balciuniene, Jorune, Katiyar, Neerja, Fox, Keolu, Baker, Carl, Srikanth, Abhinaya, Yeoh, Kian Hui, Khoo, Su Jen, Nauth, Therese B, Hansen, Robin, Ritchie, Marylyn, Hertz-Picciotto, Irva, Eichler, Evan E, Pessah, Isaac N, Selleck, Scott B

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The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene von Stevens, Servi J. C., Stumpel, Constance T. R. M., Diderich, Karin E. M., Slegtenhorst, Marjon A., Abbott, Mary‐Alice, Manning, Courtney, Balciuniene, Jorune, Pyle, Louise C., Leonard, Jacqueline, Murrell, Jill R., Putte, Romy, Rooij, Iris A. L. M., Hoischen, Alexander, Lasko, Paul, Brunner, Han G.

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Randomized trial of peginterferon alfa‐2b and ribavirin for 48 or 72 weeks in patients with hepatitis C virus genotype 1 and slow virologic response von Buti, Maria, Lurie, Yoav, Zakharova, Natalia G., Blokhina, Natalia P., Horban, Andrzej, Teuber, Gerlinde, Sarrazin, Christoph, Balciuniene, Ligita, Feinman, Saya V., Faruqi, Rab, Pedicone, Lisa D., Esteban, Rafael

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PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanism von Romasko, Edward J., DeChene, Elizabeth T., Balciuniene, Jorune, Akgumus, Gozde T., Helbig, Ingo, Tarpinian, Jennifer M., Keena, Beth A., Vogiatzi, Maria G., Zackai, Elaine H., Izumi, Kosuke, Massey, Shavonne L., Tayoun, Ahmad N. Abou

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