Comprehensive Noninvasive Fetal Screening by Deep Trio-Exome Sequencing von Miceikaitė, Ieva, Hao, Qin, Brasch-Andersen, Charlotte, Fagerberg, Christina R., Torring, Pernille M., Kristiansen, Britta S., Ousager, Lilian B., Sperling, Lene, Ibsen, Mette H., Löser, Katrin, Larsen, Martin J.

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Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome von Palencia-Campos, Adrian, Aoto, Phillip C., Machal, Erik M.F., Rivera-Barahona, Ana, Soto-Bielicka, Patricia, Bertinetti, Daniela, Baker, Blaine, Vu, Lily, Piceci-Sparascio, Francesca, Torrente, Isabella, Boudin, Eveline, Peeters, Silke, Van Hul, Wim, Huber, Celine, Bonneau, Dominique, Hildebrand, Michael S., Coleman, Matthew, Bahlo, Melanie, Bennett, Mark F., Schneider, Amy L., Scheffer, Ingrid E., Kibæk, Maria, Kristiansen, Britta S., Issa, Mahmoud Y., Mehrez, Mennat I., Ismail, Samira, Tenorio, Jair, Li, Gaoyang, Skålhegg, Bjørn Steen, Otaify, Ghada A., Temtamy, Samia, Aglan, Mona, Jønch, Aia E., De Luca, Alessandro, Mortier, Geert, Cormier-Daire, Valérie, Ziegler, Alban, Wallis, Mathew, Lapunzina, Pablo, Herberg, Friedrich W., Taylor, Susan S., Ruiz-Perez, Victor L.

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Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study von Martin-Brevet, Sandra, Nielsen, Jared A., Maillard, Anne M., Richetin, Sonia, Jønch, Aia E., Zürcher, Nicole R., Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujat, Geneviève, Sloan-Béna, Frédérique, Belfiore, Marco, Bouquillon, Sonia, Brusco, Alfredo, Busa, Tiffany, Cordier, Marie-Pierre, David, Albert, Edery, Patrick, Fagerberg, Christina, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Jacquette, Aurélia, Jaillard, Sylvie, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Pilekær Sørensen, Kristina, Pinson, Lucile, Prieur, Fabienne, Rooryck-Thambo, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Ackerman, Sean, Anwar, Ayesha, Bowe, Alexandra, Berg, Jessica, Berman, Jeffrey, Berry, Leandra N., Blaskey, Lisa, Burko, Jordan, Chang, Yishin, Cheong, Maxwell, Chudnovskaya, Darina, Cornew, Lauren, Dale, Corby, Dempsey, Allison G., Earl, Rachel, Edgar, James, Fischbach, Gerald D., Fregeau, Brieana, Gaetz, Leah, Garza, Silvia, Gerdts, Jennifer, Glenn, Orit, Golembski, Rachel, Greenup, Marion, Hines, Katherine, Jenkins, Julian, Jeremy, Rita J., Kessler, Sudha, Khan, Sarah Y., Ku, Matthew, Laakman, Anna L., Lam, Peter, LaGuerre, Kevin, Llorens, Ashlie V., Campe, Katherine Loftus, Luks, Tracy L., McNally Keehn, Rebecca, Moss, Timothy J., Nagarajan, Srikantan S., Paal, Andrea M., Packer, Alan, Paul, Brianna M., Poduri, Annapurna, Pojman, Nicholas J., Porche, Ken, Proud, Monica B., Ramocki, Melissa B., Reilly, Beau, Roberts, Timothy P.L., Gallagher, Anne Snow, Thieu, Tony, Triantafallou, Christina, Vaughan, Roger, Wakahiro, Mari, Wallace, Arianne, Ward, Tracey, Wenegrat, Julia, Sherr, Elliott H., Spiro, John E., Kherif, Ferath, Hadjikhani, Nouchine, Reymond, Alexandre, Buckner, Randy L.

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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations von Cárdenas-de-la-Parra, Alonso, Martin-Brevet, Sandra, Moreau, Clara, Rodriguez-Herreros, Borja, Fonov, Vladimir S., Maillard, Anne M., Zürcher, Nicole R., Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujatm, Geneviève, Sloan-Bénan, Frédérique, Belfiore, Marco, Bonneau, Dominique, Bouquillon, Sonia, Boute, Odile, Brusco, Alfredo, Busa, Tiffany, Caberg, Jean-Hubert, Campion, Dominique, Colombert, Vanessa, Cordier, Marie-Pierre, David, Albert, Debray, François-Guillaume, Delrue, Marie-Ange, Doco-Fenzy, Martine, Dunkhase-Heinl, Ulrike, Edery, Patrick, Fagerberg, Christina, Faivre, Laurence, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Héron, Delphine, Isidor, Bertrand, Jacquette, Aurélia, Jaillard, Sylvie, Journel, Hubert, Keren, Boris, Lacombe, Didier, Lebon, Sébastien, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Mathieu-Dramart, Michèle, Mercier, Sandra, Mignot, Cyril, Missirian, Chantal, Petit, Florence, Pilekær Sørensen, Kristina, Pinson, Lucile, Plessis, Ghislaine, Prieur, Fabienne, Rooryck-Thambo, Caroline, Rossi, Massimiliano, Sanlaville, Damien, Schlott Kristiansen, Britta, Schluth-Bolard, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Hadjikhani, Nouchine, Beckmann, Jacques S., Reymond, Alexandre, Draganski, Bogdan, Jacquemont, Sébastien, Collins, D. Louis

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Effects of eight neuropsychiatric copy number variants on human brain structure von Modenato, Claudia, Kumar, Kuldeep, Moreau, Clara, Martin-Brevet, Sandra, Huguet, Guillaume, Schramm, Catherine, Jean-Louis, Martineau, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Douard, Elise, Thébault-Dagher, Fanny, Côté, Valérie, Charlebois, Audrey-Rose, Deguire, Florence, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, Melie-Garcia, Lester, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Chakravarty, Mallar, Bzdok, Danilo, Bearden, Carrie E., Draganski, Bogdan, Jacquemont, Sébastien

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Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome von Palencia-Campos, Adrian, Aoto, Phillip C, Machal, Erik M.F, Rivera-Barahona, Ana, Soto-Bielicka, Patricia, Bertinetti, Daniela, Baker, Blaine, Vu, Lily, Piceci-Sparascio, Francesca, Torrente, Isabella, Boudin, Eveline, Peeters, Silke, Hul, Wim Van, Huber, Celine, Bonneau, Dominique, Hildebrand, Michael S, Coleman, Matthew, Bahlo, Melanie, Bennett, Mark F, Schneider, Amy L, Scheffer, Ingrid E, Kibaek, Maria, Kristiansen, Britta S, Issa, Mahmoud Y, Mehrez, Mennat, Ismail, Samira, Tenorio, Jair, Li, Gaoyang, Skalhegg, Bjorn Steen, Otaify, Ghada A, Temtamy, Samia, Aglan, Mona, Jonch, Aia E, De Luca, Alessandro, Mortier, Geert, Cormier-Daire, Valerie, Ziegler, Alban, Wallis, Mathew, Lapunzina, Pablo, Herberg, Friedrich W, Taylor, Susan S, Ruiz-Perez, Victor L

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Data from: Neurologic phenotypes associated with COL4A1/2 mutations: expanding the spectrum of disease von Zagaglia, Sara, Selch, Christina, Nisevic, Jelena R., Mei, Davide, Michalak, Zuzanna, Hernandez-Hernandez, Laura, Krithika, S., Vezyroglou, Katharina, Varadkar, Sophia M., Pepler, Alexander, Biskup, Saskia, Leao, Miguel, Gartner, Jutta, Merkenschlanger, Andreas, Jaksch, Michaela, Moller, Rikke S., Gardella, Elena, Kristiansen, Britta S., Hansen, Lars K., Vari, Maria Stella, Helbig, Katherine L., Desai, Sonal, Smith-Hicks, Constance L., Hino-Fukuyo, Naomi, Talvik, Tiina, Laugesaar, Rael, Ilves, Pilvi, Õunap, Katrin, Körber, Ingrid, Hartlieb, Till, Kudernatsch, Manfred, Winkler, Peter, Schimmel, Mareike, Hasse, Anette, Knuf, Markus, Heinemeyer, Jan, Makowski, Christine, Ghedia, Sondhya, Subramanian, Gopinath M., Striano, Pasquale, Thomas, Rhys H., Micallef, Caroline, Thom, Maria, Werring, David J., Kluger, Gerhard Josef, Cross, J. Helen, Guerrini, Renzo, Balestrini, Simona, Sisodiya, Sanjay M.

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The HILUS-Trial—a Prospective Nordic Multicenter Phase 2 Study of Ultracentral Lung Tumors Treated With Stereotactic Body Radiotherapy von Lindberg, Karin, Grozman, Vitali, Karlsson, Kristin, Lindberg, Sara, Lax, Ingmar, Wersäll, Peter, Persson, Gitte Fredberg, Josipovic, Mirjana, Khalil, Azza Ahmed, Moeller, Ditte Sloth, Nyman, Jan, Drugge, Ninni, Bergström, Per, Olofsson, Jörgen, Rogg, Lotte Victoria, Ramberg, Christina, Kristiansen, Charlotte, Jeppesen, Stefan Starup, Nielsen, Tine Bjørn, Lödén, Britta, Rosenbrand, Hans-Olov, Engelholm, Silke, Haraldsson, André, Billiet, Charlotte, Lewensohn, Rolf

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Comprehensive prenatal diagnostics: Exome versus genome sequencing von Miceikaite, Ieva, Fagerberg, Christina, Brasch‐Andersen, Charlotte, Torring, Pernille Mathiesen, Kristiansen, Britta Schlott, Hao, Qin, Sperling, Lene, Ibsen, Mette Holm, Löser, Katrin, Bendsen, Eske Alf, Ousager, Lilian Bomme, Larsen, Martin Jakob

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Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease von Zagaglia, Sara, Selch, Christina, Nisevic, Jelena Radic, Mei, Davide, Michalak, Zuzanna, Hernandez-Hernandez, Laura, Krithika, S, Vezyroglou, Katharina, Varadkar, Sophia M, Pepler, Alexander, Biskup, Saskia, Leão, Miguel, Gärtner, Jutta, Merkenschlager, Andreas, Jaksch, Michaela, Møller, Rikke S, Gardella, Elena, Kristiansen, Britta Schlott, Hansen, Lars Kjærsgaard, Vari, Maria Stella, Helbig, Katherine L, Desai, Sonal, Smith-Hicks, Constance L, Hino-Fukuyo, Naomi, Talvik, Tiina, Laugesaar, Rael, Ilves, Pilvi, Õunap, Katrin, Körber, Ingrid, Hartlieb, Till, Kudernatsch, Manfred, Winkler, Peter, Schimmel, Mareike, Hasse, Anette, Knuf, Markus, Heinemeyer, Jan, Makowski, Christine, Ghedia, Sondhya, Subramanian, Gopinath M, Striano, Pasquale, Thomas, Rhys H, Micallef, Caroline, Thom, Maria, Werring, David J, Kluger, Gerhard Josef, Cross, J Helen, Guerrini, Renzo, Balestrini, Simona, Sisodiya, Sanjay M

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Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome von Brinch, Heidi Hesselø, Byrjalsen, Anna, Lohse, Zuzana, Rasmussen, Andreas Ørslev, Karstensen, John Gásdal, Kristiansen, Britta Schlott, Jelsig, Anne Marie

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Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling von Boonsawat, Paranchai, Asadollahi, Reza, Niedrist, Dunja, Steindl, Katharina, Begemann, Anaïs, Joset, Pascal, Bhoj, Elizabeth J., Li, Dong, Zackai, Elaine, Vetro, Annalisa, Barba, Carmen, Guerrini, Renzo, Whalen, Sandra, Keren, Boris, Khan, Amjad, Jing, Duan, Palomares Bralo, María, Rikeros Orozco, Emi, Hao, Qin, Schlott Kristiansen, Britta, Zheng, Bixia, Donnelly, Deirdre, Clowes, Virginia, Zweier, Markus, Papik, Michael, Siegel, Gabriele, Sabatino, Valeria, Mocera, Martina, Horn, Anselm H.C., Sticht, Heinrich, Rauch, Anita

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Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling von Boonsawat, Paranchai, Asadollahi, Reza, Niedrist Baumann, Dunja, Steindl, Katharina, Begemann, Anaïs, Joset, Pascal, Bhoj, Elizabeth J, Li, Dong, Zackai, Elaine, Vetro, Annalisa, Barba, Carmen, Guerrini, Renzo, Whalen, Sandra, Keren, Boris, Khan, Amjad, Jing, Duan, Palomares Bralo, María, Rikeros Orozco, Emi, Hao, Qin, Schlott Kristiansen, Britta, Zheng, Bixia, Donnelly, Deirdre, Clowes, Virginia, Zweier, Markus, Papik, Michael, Siegel, Gabriele, Sabatino, Valeria, Mocera, Martina, Horn, Anselm H C, Sticht, Heinrich, Rauch, Anita

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448: National consensus-based bespoke automatic delineation of thoracic organs at risk von Thorsen, Lise B.J., Mortensen, Hanna R., Hoffmann, Lone, Aagaard, Torben, Knap, Marianne M., Nyeng, Tine B., Szejniuk, Weronika M., Persson, Gitte, Pøhl, Mette, Nordsmark, Marianne, Weber, Britta, Kristiansen, Charlotte, Land, Lotte H., Borissova, Svetlana, Larsen, Irene D., Khalil, Azza A., Mortensen, Lise S., Schmidt, Hjørdis H, Korreman, Stine S., Kyndt, Martin, Møller, Ditte S.

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1984: Cox-based prediction model of grade 5 bleeding after SBRT of ultra-centrally located lung tumors von Karlsson, Kristin, Rancati, Tiziana, Lindberg, Sara, Grozman, Vitali, Hoffmann, Lone, Khalil, Azza, Knap, Marianne Marquard, Nielsen, Tine Bjørn, Jeppesen, Stefan Starup, Kristiansen, Charlotte, Ramberg, Christina, Rogg, Lotte Victoria, Drugge, Ninni, Nyman, Jan, Josipovic, Mirjana, Persson, Gitte Fredberg, Olofsson, Jörgen, Bergström, Per, Rosenbrand, Hans-Olov, Lödén, Britta, Haraldsson, André, Engelholm, Silke, Billiet, Charlotte, Lindberg, Karin, Onjukka, Eva

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Implication of the Receptor Tyrosine Kinase AXL in Head and Neck Cancer Progression von von Mässenhausen, Anne, Brägelmann, Johannes, Billig, Hannah, Thewes, Britta, Queisser, Angela, Vogel, Wenzel, Kristiansen, Glen, Schröck, Andreas, Bootz, Friedrich, Brossart, Peter, Kirfel, Jutta, Perner, Sven

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Cyclin K dependent regulation of Aurora B affects apoptosis and proliferation by induction of mitotic catastrophe in prostate cancer von Schecher, Sabrina, Walter, Britta, Falkenstein, Michael, Macher‐Goeppinger, Stephan, Stenzel, Philipp, Krümpelmann, Kristina, Hadaschik, Boris, Perner, Sven, Kristiansen, Glen, Duensing, Stefan, Roth, Wilfried, Tagscherer, Katrin E.

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Expanded HILUS Trial: A Pooled Analysis of Risk Factors for Toxicity From Stereotactic Body Radiation Therapy of Central and Ultracentral Lung Tumors von Lindberg, Sara, Grozman, Vitali, Karlsson, Kristin, Onjukka, Eva, Lindbäck, Elias, Jirf, Karam Al, Lax, Ingmar, Wersäll, Peter, Persson, Gitte Fredberg, Josipovic, Mirjana, Khalil, Azza Ahmed, Møller, Ditte Sloth, Hoffmann, Lone, Knap, Marianne Marquard, Nyman, Jan, Drugge, Ninni, Bergström, Per, Olofsson, Jörgen, Rogg, Lotte Victoria, Hagen, Rebecca Knoph, Frøland, Anne-Sofie, Ramberg, Christina, Kristiansen, Charlotte, Jeppesen, Stefan Starup, Nielsen, Tine Bjørn, Lödén, Britta, Rosenbrand, Hans-Olov, Engelholm, Silke, Haraldsson, André, Billiet, Charlotte, Lewensohn, Rolf, Lindberg, Karin

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Prenatal cases with rare RIT1 variants causing severe fetal hydrops and death von Miceikaite, Ieva, Bak, Geske Sidsel, Larsen, Martin Jakob, Kristiansen, Britta Schlott, Torring, Pernille Mathiesen

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OA24.05 The Nordic HILUS-Trial - First Report of a Phase II Trial of SBRT of Centrally Located Lung Tumors von Lindberg, Karin, Bergström, Per, Brustugun, Odd Terje, Engelholm, Silke, Grozman, Vitali, Hoyer, Morten, Karlsson, Kristin, Khalil, Azza, Kristiansen, Charlotte, Lax, Ingmar, Löden, Britta, Nyman, Jan, Persson, Gitte, Rogg, Lotte, Wersäll, Peter, Lewensohn, Rolf

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