Crew–Mission Control Communicative Behaviour in Sirius-17 Experiment von Supolkina, N. S., Yusupova, A. K., Shved, D. M., Chekalina, A. I., Sarantsev, S. V., Gushin, V. I., Feichtinger, E. L.

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ORGANIZATION OF COMMUNICATIONS BETWEEN ISOLATED MULTINATIONAL CREW AND EXTERNAL CALLERS TOWARDS THE PSYCHOLOGICAL SUPPORT OPTIMIZATION von Feichtinger, Е.L.

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Non-invasive preimplantation genetic screening using array comparative genomic hybridization on spent culture media: a proof-of-concept pilot study von Feichtinger, M, Vaccari, E, Carli, L, Wallner, E, Mädel, U, Figl, K, Palini, S, Feichtinger, W

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Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency von Alston, Charlotte L., Heidler, Juliana, Dibley, Marris G., Kremer, Laura S., Taylor, Lucie S., Fratter, Carl, French, Courtney E., Glasgow, Ruth I.C., Feichtinger, René G., Delon, Isabelle, Pagnamenta, Alistair T., Dolling, Helen, Lemonde, Hugh, Aiton, Neil, Bjørnstad, Alf, Henneke, Lisa, Gärtner, Jutta, Thiele, Holger, Tauchmannova, Katerina, Quaghebeur, Gerardine, Houstek, Josef, Sperl, Wolfgang, Raymond, F. Lucy, Prokisch, Holger, Mayr, Johannes A., McFarland, Robert, Poulton, Joanna, Ryan, Michael T., Wittig, Ilka, Henneke, Marco, Taylor, Robert W.

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Bioactive molecules for regenerative pulp capping von Whitehouse, L L, Thomson, N H, Do, T, Feichtinger, G A

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Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype von Alston, Charlotte L., Compton, Alison G., Formosa, Luke E., Strecker, Valentina, Oláhová, Monika, Haack, Tobias B., Smet, Joél, Stouffs, Katrien, Diakumis, Peter, Ciara, Elżbieta, Cassiman, David, Romain, Nadine, Yarham, John W., He, Langping, De Paepe, Boel, Vanlander, Arnaud V., Seneca, Sara, Feichtinger, René G., Płoski, Rafal, Rokicki, Dariusz, Pronicka, Ewa, Haller, Ronald G., Van Hove, Johan L.K., Bahlo, Melanie, Mayr, Johannes A., Van Coster, Rudy, Prokisch, Holger, Wittig, Ilka, Ryan, Michael T., Thorburn, David R., Taylor, Robert W.

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Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency von Olsen, Rikke K.J., Koňaříková, Eliška, Giancaspero, Teresa A., Mosegaard, Signe, Boczonadi, Veronika, Mataković, Lavinija, Veauville-Merllié, Alice, Terrile, Caterina, Schwarzmayr, Thomas, Haack, Tobias B., Auranen, Mari, Leone, Piero, Galluccio, Michele, Imbard, Apolline, Gutierrez-Rios, Purificacion, Palmfeldt, Johan, Graf, Elisabeth, Vianey-Saban, Christine, Oppenheim, Marcus, Schiff, Manuel, Pichard, Samia, Rigal, Odile, Pyle, Angela, Chinnery, Patrick F., Konstantopoulou, Vassiliki, Möslinger, Dorothea, Feichtinger, René G., Talim, Beril, Topaloglu, Haluk, Coskun, Turgay, Gucer, Safak, Botta, Annalisa, Pegoraro, Elena, Malena, Adriana, Vergani, Lodovica, Mazzà, Daniela, Zollino, Marcella, Ghezzi, Daniele, Acquaviva, Cecile, Tyni, Tiina, Boneh, Avihu, Meitinger, Thomas, Strom, Tim M., Gregersen, Niels, Mayr, Johannes A., Horvath, Rita, Barile, Maria, Prokisch, Holger

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How to proceed after “negative” exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques von Wortmann, Saskia B., Oud, Machteld M., Alders, Mariëlle, Coene, Karlien L. M., Crabben, Saskia N., Feichtinger, René G., Garanto, Alejandro, Hoischen, Alex, Langeveld, Mirjam, Lefeber, Dirk, Mayr, Johannes A., Ockeloen, Charlotte W., Prokisch, Holger, Rodenburg, Richard, Waterham, Hans R., Wevers, Ron A., Warrenburg, Bart P. C., Willemsen, Michel A. A. P., Wolf, Nicole I., Vissers, Lisenka E. L. M., Karnebeek, Clara D. M.

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Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies von Feichtinger, René G., Oláhová, Monika, Kishita, Yoshihito, Garone, Caterina, Kremer, Laura S., Yagi, Mikako, Uchiumi, Takeshi, Jourdain, Alexis A., Thompson, Kyle, D’Souza, Aaron R., Kopajtich, Robert, Alston, Charlotte L., Koch, Johannes, Sperl, Wolfgang, Mastantuono, Elisa, Strom, Tim M., Wortmann, Saskia B., Meitinger, Thomas, Pierre, Germaine, Chinnery, Patrick F., Chrzanowska-Lightowlers, Zofia M., Lightowlers, Robert N., DiMauro, Salvatore, Calvo, Sarah E., Mootha, Vamsi K., Moggio, Maurizio, Sciacco, Monica, Comi, Giacomo P., Ronchi, Dario, Murayama, Kei, Ohtake, Akira, Rebelo-Guiomar, Pedro, Kohda, Masakazu, Kang, Dongchon, Mayr, Johannes A., Taylor, Robert W., Okazaki, Yasushi, Minczuk, Michal, Prokisch, Holger

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Impact of maternally derived meiotic aneuploidies on early embryonic development in vitro von Tschare, Lena, Ennemoser, Anna, Carli, Luca, Vaccari, Enrico, Feichtinger, Michael

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Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2 von Kennedy, Hannah, Haack, Tobias B., Hartill, Verity, Mataković, Lavinija, Baumgartner, E. Regula, Potter, Howard, Mackay, Richard, Alston, Charlotte L., O’Sullivan, Siobhan, McFarland, Robert, Connolly, Grainne, Gannon, Caroline, King, Richard, Mead, Scott, Crozier, Ian, Chan, Wandy, Florkowski, Chris M., Sage, Martin, Höfken, Thomas, Alhaddad, Bader, Kremer, Laura S., Kopajtich, Robert, Feichtinger, René G., Sperl, Wolfgang, Rodenburg, Richard J., Minet, Jean Claude, Dobbie, Angus, Strom, Tim M., Meitinger, Thomas, George, Peter M., Johnson, Colin A., Taylor, Robert W., Prokisch, Holger, Doudney, Kit, Mayr, Johannes A.

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Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy von Feichtinger, René G., Mucha, Bettina E., Hengel, Holger, Orfi, Zakaria, Makowski, Christine, Dort, Junio, D'Anjou, Guy, Nguyen, Thi Tuyet Mai, Buchert, Rebecca, Juenger, Hendrik, Freisinger, Peter, Baumeister, Sarah, Schoser, Benedikt, Ahting, Uwe, Keimer, Reinhard, Nguyen, Cam-Tu Emilie, Fabre, Paul, Gauthier, Julie, Miguet, Marguerite, Lopes, Fátima, AlHakeem, Afnan, AlHashem, Amal, Tabarki, Brahim, Kandaswamy, Krishna Kumar, Bauer, Peter, Steinbacher, Peter, Prokisch, Holger, Sturm, Marc, Strom, Tim M., Ellezam, Benjamin, Mayr, Johannes A., Schöls, Ludger, Michaud, Jacques L., Campeau, Philippe M., Haack, Tobias B., Dumont, Nicolas A.

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In‐depth comparison of N‐glycosylation of human plasma‐derived factor VIII and different recombinant products: from structure to clinical implications von Canis, K., Anzengruber, J., Garenaux, E., Feichtinger, M., Benamara, K., Scheiflinger, F., Savoy, L.‐A., Reipert, B. M., Malisauskas, M.

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Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants von Vogel, Georg F., Mozer-Glassberg, Yael, Landau, Yuval E., Schlieben, Lea D., Prokisch, Holger, Feichtinger, René G., Mayr, Johannes A., Brennenstuhl, Heiko, Schröter, Julian, Pechlaner, Agnes, Alkuraya, Fowzan S., Baker, Joshua J., Barcia, Giulia, Baric, Ivo, Braverman, Nancy, Burnyte, Birute, Christodoulou, John, Ciara, Elzbieta, Coman, David, Das, Anibh M., Darin, Niklas, Della Marina, Adela, Distelmaier, Felix, Eklund, Erik A., Ersoy, Melike, Fang, Weiyan, Gaignard, Pauline, Ganetzky, Rebecca D., Gonzales, Emmanuel, Howard, Caoimhe, Hughes, Joanne, Konstantopoulou, Vassiliki, Kose, Melis, Kerr, Marina, Khan, Aneal, Lenz, Dominic, McFarland, Robert, Margolis, Merav Gil, Morrison, Kevin, Müller, Thomas, Murayama, Kei, Nicastro, Emanuele, Pennisi, Alessandra, Peters, Heidi, Piekutowska-Abramczuk, Dorota, Rötig, Agnès, Santer, René, Scaglia, Fernando, Schiff, Manuel, Shagrani, Mohmmad, Sharrard, Mark, Soler-Alfonso, Claudia, Staufner, Christian, Storey, Imogen, Stormon, Michael, Taylor, Robert W., Thorburn, David R., Teles, Elisa Leao, Wang, Jian-She, Weghuber, Daniel, Wortmann, Saskia

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Punzi-loss: a non-differentiable metric approximation for sensitivity optimisation in the search for new particles von Abudinén, F., Bertemes, M., Bilokin, S., Campajola, M., Casarosa, G., Cunliffe, S., Corona, L., De Nuccio, M., De Pietro, G., Dey, S., Eliachevitch, M., Feichtinger, P., Ferber, T., Gemmler, J., Goldenzweig, P., Gottmann, A., Graziani, E., Haigh, H., Hohmann, M., Humair, T., Inguglia, G., Kahn, J., Keck, T., Komarov, I., Krohn, J.-F., Kuhr, T., Lacaprara, S., Lieret, K., Maiti, R., Martini, A., Meier, F., Metzner, F., Milesi, M., Park, S.-H., Prim, M., Pulvermacher, C., Ritter, M., Sato, Y., Schwanda, C., Sutcliffe, W., Tamponi, U., Tenchini, F., Urquijo, P., Zani, L., Žlebčík, R., Zupanc, A.

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Punzi-loss von Abudinén, F, Bertemes, M, Bilokin, S, Campajola, M, Casarosa, G, Cunliffe, S, Corona, L

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Combined analysis of Belle and Belle II data to determine the CKM angle ϕ 3 using B + → D( K S 0 $$ {K}_S^0 $$ h + h − )h + decays von The Belle and Belle II collaborations, F. Abudinén, L. Aggarwal, H. Ahmed, H. Aihara, N. Akopov, S. Al Said, A. Aloisio, N. Anh Ky, D. M. Asner, H. Atmacan, V. Aushev, R. Ayad, V. Babu, S. Bacher, S. Baehr, S. Bahinipati, P. Bambade, Sw. Banerjee, S. Bansal, J. Baudot, J. Becker, P. K. Behera, K. Belous, J. V. Bennett, F. U. Bernlochner, M. Bertemes, E. Bertholet, M. Bessner, S. Bettarini, F. Bianchi, T. Bilka, D. Biswas, A. Bobrov, D. Bodrov, G. Bonvicini, J. Borah, A. Bozek, M. Bračko, P. Branchini, R. A. Briere, T. E. Browder, A. Budano, S. Bussino, M. Campajola, L. Cao, G. Casarosa, C. Cecchi, D. Červenkov, P. Cheema, V. Chekelian, A. Chen, B. G. Cheon, K. Chilikin, K. Chirapatpimol, H.-E. Cho, S.-J. Cho, S.-K. Choi, Y. Choi, S. Choudhury, D. Cinabro, L. Corona, S. Cunliffe, T. Czank, S. Das, F. Dattola, E. De La Cruz-Burelo, G. de Marino, S. K. Maurya, G. De Nardo, M. De Nuccio, G. De Pietro, R. de Sangro, M. Destefanis, S. Dey, A. De Yta-Hernandez, R. Dhamija, A. Di Canto, Z. Doležal, I. Domínguez Jiménez, T. V. Dong, M. Dorigo, D. Dossett, S. Dubey, G. Dujany, M. Eliachevitch, D. Epifanov, P. Feichtinger, D. Ferlewicz, T. Fillinger, S. Fiore, A. Fodor, F. Forti, B. G. Fulsom, A. Gabrielli, E. Ganiev, M. Garcia-Hernandez, V. Gaur, A. Gaz, R. Giordano

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The Chromosomes of Terraranan Frogs. Insights into Vertebrate Cytogenetics von Schmid, M., Steinlein, C., Bogart, J.P., Feichtinger, W., León, P., La Marca, E., Diaz, L.M., Sanz, A., Chen, S.-H-, Hedges, S.B.

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Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder von Yoon, Wan Hee, Jangam, Sharayu, Davidson, Jean M., Grove, Megan E., Kohler, Jennefer N., Holmes, Matthew, Zhao, Chunli, Contrepois, Kévin, Heyman, Heino M., Webb-Robertson, Bobbie-Jo M., Alejandro, Mercedes E., Allard, Patrick, Balasubramanyam, Ashok, Barseghyan, Hayk, Bican, Anna, Birch, Camille L., Bostwick, Bret L., Briere, Lauren C., Brown, Donna M., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dayal, Jyoti G., Dell’Angelica, Esteban C., Dorset, Daniel C., Draper, David D., Eckstein, David J., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Ferreira, Carlos, Glanton, Emily, Godfrey, Rena A., Goldstein, David B., Gould, Sarah E., Gourdine, Jean-Philippe F., Hanchard, Neil A., Herzog, Matthew R., Hom, Jason, Howerton, Ellen M., Huang, Yong, Jacob, Howard J., Jiang, Yong-hui, Johnston, Jean M., Jones, Angela L., Kohane, Isaac S., Krier, Joel B., Lazar, Jozef, Lee, Hane, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, May, Thomas, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo M., Novacic, Donna, Orange, Jordan S., Palmer, Christina G.S., Potocki, Lorraine, Pusey, Barbara N., Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Samson, Susan L., Schoch, Kelly, Schroeder, Molly C., Shashi, Vandana, Silverman, Edwin K., Sinsheimer, Janet S., Spillmann, Rebecca C., Stong, Nicholas, Tifft, Cynthia J., Tran, Alyssa A., Valivullah, Zaheer M., Ward, Patricia A., Yamamoto, Shinya, Snyder, Michael, Merker, Jason D., Fisher, Paul G., Mayr, Johannes A., Morris, Andrew A., Schelley, Susan, Friederich, Marisa W., Yamamoto, Shinya, Wangler, Michael F., Taylor, Robert W., Bernstein, Jonathan A.

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Tests of Light-Lepton Universality in Angular Asymmetries of B0→D-ℓν Decays von Adachi, I., Adamczyk, K., Aggarwal, L., Aihara, H., Akopov, N., Aloisio, A., Anh Ky, N., Asner, D. M., Atmacan, H., Aushev, T., Aushev, V., Aversano, M., Babu, V., Bae, H., Bahinipati, S., Bambade, P., Banerjee, Sw, Barrett, M., Baudot, J., Bauer, M., Baur, A., Beaubien, A., Becherer, F., Becker, J., Behera, P. K., Bennett, J. V., Bernlochner, F. U., Bertacchi, V., Bertemes, M., Bertholet, E., Bessner, M., Bettarini, S., Bhuyan, B., Bianchi, F., Bilka, T., Biswas, D., Bobrov, A., Bodrov, D., Bolz, A., Bondar, A., Borah, J., Bozek, A., Bračko, M., Branchini, P., Briere, R. A., Browder, T. E., Budano, A., Bussino, S., Campajola, M., Cao, L., Casarosa, G., Cecchi, C., Cerasoli, J., Chang, M. -C., Chang, P., Cheaib, R., Cheema, P., Chekelian, V., Cheon, B. G., Chilikin, K., Chirapatpimol, K., Cho, H. -E., Cho, K., Choi, S. -K., Choudhury, S., Cochran, J., Corona, L., Cremaldi, L. M., Das, S., Dattola, F., De La Cruz-Burelo, E., de la Motte, S. A., De Nardo, G., de Nuccio, M., de Pietro, G., de Sangro, R., Destefanis, M., Dey, S., Dhamija, R., Di Canto, A., Di Capua, F., Dingfelder, J., Doležal, Z., Domínguez Jiménez, I., Dong, T. V., Dorigo, M., Dort, K., Dossett, D., Dreyer, S., Dubey, S., Dujany, G., Ecker, P., Eliachevitch, M., Epifanov, D., Feichtinger, P., Ferber, T., Ferlewicz, D., Fillinger, T., Finck, C., Finocchiaro, G.

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