COGNITION: a prospective precision oncology trial for patients with early breast cancer at high risk following neoadjuvant chemotherapy by Pixberg, C., Zapatka, M., Hlevnjak, M., Benedetto, S., Suppelna, J.P., Heil, J., Smetanay, K., Michel, L., Fremd, C., Körber, V., Rübsam, M., Buschhorn, L., Heublein, S., Schäfgen, B., Golatta, M., Gomez, C., von Au, A., Wallwiener, M., Wolf, S., Dikow, N., Schaaf, C., Gutjahr, E., Allgäuer, M., Stenzinger, A., Pfütze, K., Kirsten, R., Hübschmann, D., Sinn, H.-P., Jäger, D., Trumpp, A., Schlenk, R., Höfer, T., Thewes, V., Schneeweiss, A., Lichter, P.

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3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior by Dikow, Nicola, Maas, Bianca, Karch, Stephanie, Granzow, Martin, Janssen, Johannes W.G., Jauch, Anna, Hinderhofer, Katrin, Sutter, Christian, Schubert-Bast, Susanne, Anderlid, Britt Marie, Dallapiccola, Bruno, Van der Aa, Nathalie, Moog, Ute

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Referral practice for genetic counseling and patients' expectation over time – a prospective monocenter study by Schott, S, Fischer, C, Dikow, N, Moog, U, Evers, C

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The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1: Is it really a reversed sotos syndrome? by Dikow, Nicola, Maas, Bianca, Gaspar, Harald, Kreiss-Nachtsheim, Martina, Engels, Hartmut, Kuechler, Alma, Garbes, Lutz, Netzer, Christian, Neuhann, Teresa M., Koehler, Udo, Casteels, Kristina, Devriendt, Koen, Janssen, Johannes W.G., Jauch, Anna, Hinderhofer, Katrin, Moog, Ute

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Prophylactic surgery among germline TP53 mutation carriers in Germany – a multicentric observational study by Rippinger, N, Haun, MW, Fischer, C, Rhiem, K, Hübbel, A, Grill, S, Kiechle, M, Cremer, FW, Kast, K, Nguyen, HP, Ditsch, N, Kratz, P, Pfister, S, Pajtler, KW, Speiser, D, Seitz, S, Glimm, H, Maatouk, I, Hahne, A, Sutter, C, Schmutzler, RK, Dikow, N, Sohn, C, Schott, S

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Intensiviertes Früherkennungs- und Nachsorgeprogramm oder prophylaktische Operation? Entscheidungen von Frauen aus Familien mit familiärem Brust- und Eierstockkrebs by Vetter, L, Keller, M, Bruckner, T, Dikow, N, Golatta, M, Sohn, C, Heil, J, Schott, S

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Klinisch-pathologische Charakterisierung von 1078 Ratsuchenden mit pathogener CHEK2 Mutation aus dem Deutschen Konsortium Familiärer Brust- und Eierstockkrebs (DK-FBREK) by Bosse, K, Faust, U, Gruber, I, Habhab, W, Günther, G, Siebers-Renelt, U, Kiechle, M, Speiser, D, Dikow, N, Kast, K, Arnold, N, Vesper, A-S, Harbeck, N, Briest, S, Thomssen, C, Gehrig, A, Wallaschek, H, Solbach, C, Wolf, M, Witzel, I, Holzhauser, I, Kaulfuß, S, Janni, W, Engel, C, Rieß, O, Schmutzler, R, Schroeder, C

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Akzeptanz des intensivierten Früherkennungs- und Nachsorgeprogramms (IFNP) für familiären Brust- und Eierstockkrebs an der Universitätsfrauenklinik Heidelberg – Erste Ergebnisse... by Vetter, L, Keller, M, Bruckner, T, Evers, C, Dikow, N, Sohn, C, Heil, J, Schott, S

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Akzeptanz des intensivierten Früherkennungs- und Nachsorgeprogramms (IFNP) für familiären Brust- und Eierstockkrebs an der Universitätsfrauenklinik Heidelberg – erste Ergebnisse... by Vetter, L, Keller, M, Bruckner, T, Evers, C, Dikow, N, Sohn, C, Heil, J, Schott, S

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Warty skin changes, chronic scrotal lymphoedema, and facial dysmorphism by Felcht, Moritz, Dikow, Nicola, Goebeler, Matthias, Stroebel, Philipp, Booken, Nina, Voßmerbäumer, Urs, Merx, Kirsten, Henzler, Thomas, Marx, Alexander, Moog, Ute, Goerdt, Sergij, Klemke, Claus-Detlev

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Humangenetische Diagnostik und Beratung by Moog, U, Dikow, N, Gaspar, H, Behnecke, A, Schenk, J.P, Flechtenmacher, C, Beedgen, B, Elsässer, M

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Alpha-Thalassämie-Retardierungs-Syndrom: ATRX-Syndrom bei 2 Jungen mit mentaler Retardierung und Muskelhypotonie by Dikow, N., Junge, C., Karch, S., Hinderhofer, K., Froster, U.G., Moog, U.

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Humangenetische Diagnostik und Beratung: Seltene Erkrankungen in der Pränatalmedizin by Moog, U., Dikow, N., Gaspar, H., Behnecke, A., Schenk, J.P., Flechtenmacher, C., Beedgen, B., Elsässer, M.

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First Genome Sequence of the Gunnison’s Prairie Dog (Cynomys gunnisoni), a Keystone Species and Player in the Transmission of Sylvatic Plague by Tsuchiya, Mirian T N, Dikow, Rebecca B, Cassin-Sackett, Loren

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Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer by Rebbeck, Timothy R, Mitra, Nandita, Wan, Fei, Sinilnikova, Olga M, Healey, Sue, McGuffog, Lesley, Mazoyer, Sylvie, Chenevix-Trench, Georgia, Nathanson, Katherine L, Kushnir, Anya, Zidan, Jamal, Ehrencrona, Hans, Stenmark-Askmalm, Marie, Melin, Beatrice, Huo, Dezheng, Olopade, Olufunmilayo I, Odunsi, Kunle, Domchek, Susan M, Karlan, Beth Y, Walsh, Christine, Chung, Wendy K, Janavicius, Ramunas, Steele, Linda, Ejlertsen, Bent, Hansen, Thomas v. O, Benitez, Javier, Godino, Javier, Duran, Mercedes, Weitzel, Jeffrey N, Bobolis, Kristie A, Peissel, Bernard, Genuardi, Maurizio, Manoukian, Siranoush, Pensotti, Valeria, Gismondi, Viviana, Fostira, Florentia, Frost, Debra, Platte, Radka, Davidson, Rosemarie, Eccles, Diana, Hodgson, Shirley, Porteous, Mary E, Izatt, Louise, Donaldson, Alan, Ellis, Steve, Schmutzler, Rita Katharina, Becker, Alexandra, Engel, Christoph, Mundhenke, Christoph, Niederacher, Dieter, Fleisch, Markus, Sutter, Christian, Gadzicki, Dorothea, Varon-Mateeva, Raymonda, Gehrig, Andrea, Weber, Bernhard H, Mazoyer, Sylvie, Gauthier-Villars, Marion, Peyrat, Jean-Philippe, Muller, Danièle, De Paepe, Anne, De Leeneer, Kim, Piedmonte, Marion, Rodriguez, Gustavo, Blank, Stephanie V, Azodi, Masoud, Phillips, Kelly-Anne, de la Hoya, Miguel, Romero, Atocha, Aittomäki, Kristiina, Oosterwijk, Jan C, Wijnen, Juul T, Ausems, Margreet G. E. M, Aalfs, Cora M, Kwong, Ava, Darder, Esther, Blanco, Ignacio, Durda, Katarzyna, Sukiennicki, Grzegorz, Byrski, Tomasz, Toloczko-Grabarek, Aleksandra, Arason, Adalgeir, Laframboise, Rachel, Agata, Simona, Lee, Min Hyuk, Park, Sue K, Lindor, Noralane M, Tischkowitz, Marc, Vijai, Joseph, Offit, Kenneth, Rau-Murthy, Rohini, Fink-Retter, Anneliese, Singer, Christian F, Pfeiler, Georg, Senter, Leigha, Pedersen, Inge Sokilde, Sunde, Lone, Thomassen, Mads, Teo, Soo-Hwang, Hulick, Peter J

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High-risk breast cancer surveillance with MRI: 10-year experience from the German consortium for hereditary breast and ovarian cancer by Bick, Ulrich, Engel, Christoph, Krug, Barbara, Heindel, Walter, Fallenberg, Eva M., Rhiem, Kerstin, Maintz, David, Golatta, Michael, Speiser, Dorothee, Rjosk-Dendorfer, Dorothea, Lämmer-Skarke, Irina, Dietzel, Frederic, Schäfer, Karl Werner Fritz, Leinert, Elena, Weigel, Stefanie, Sauer, Stephanie, Pertschy, Stefanie, Hofmockel, Thomas, Hagert-Winkler, Anne, Kast, Karin, Quante, Anne, Meindl, Alfons, Kiechle, Marion, Loeffler, Markus, Schmutzler, Rita K.

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Whole-Genome Sequencing of Procyonids Reveals Distinct Demographic Histories in Kinkajou (Potos flavus) and Northern Raccoon (Procyon lotor) by Tsuchiya, Mirian T N, Dikow, Rebecca B, Koepfli, Klaus-Peter, Frandsen, Paul B, Rockwood, Larry L, Maldonado, Jesús E

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Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition by Palmer, Elizabeth E., Pusch, Michael, Picollo, Alessandra, Forwood, Caitlin, Nguyen, Matthew H., Suckow, Vanessa, Gibbons, Jessica, Hoff, Alva, Sigfrid, Lisa, Megarbane, Andre, Nizon, Mathilde, Cogné, Benjamin, Beneteau, Claire, Alkuraya, Fowzan S., Chedrawi, Aziza, Hashem, Mais O., Stamberger, Hannah, Weckhuysen, Sarah, Vanlander, Arnaud, Ceulemans, Berten, Rajagopalan, Sulekha, Nunn, Kenneth, Arpin, Stéphanie, Raynaud, Martine, Motter, Constance S., Ward-Melver, Catherine, Janssens, Katrien, Meuwissen, Marije, Beysen, Diane, Dikow, Nicola, Grimmel, Mona, Haack, Tobias B., Clement, Emma, McTague, Amy, Hunt, David, Townshend, Sharron, Ward, Michelle, Richards, Linda J., Simons, Cas, Costain, Gregory, Dupuis, Lucie, Mendoza-Londono, Roberto, Dudding-Byth, Tracy, Boyle, Jackie, Saunders, Carol, Fleming, Emily, El Chehadeh, Salima, Spitz, Marie-Aude, Piton, Amelie, Gerard, Bénédicte, Abi Warde, Marie-Thérèse, Rea, Gillian, McKenna, Caoimhe, Douzgou, Sofia, Banka, Siddharth, Akman, Cigdem, Bain, Jennifer M., Sands, Tristan T., Wilson, Golder N., Silvertooth, Erin J., Miller, Lauren, Lederer, Damien, Sachdev, Rani, Macintosh, Rebecca, Monestier, Olivier, Karadurmus, Deniz, Collins, Felicity, Carter, Melissa, Rohena, Luis, Willemsen, Marjolein H., Ockeloen, Charlotte W., Pfundt, Rolph, Kroft, Sanne D., Field, Michael, Laranjeira, Francisco E. R., Fortuna, Ana M., Soares, Ana R., Michaud, Vincent, Naudion, Sophie, Golla, Sailaja, Weaver, David D., Bird, Lynne M., Friedman, Jennifer, Clowes, Virginia, Joss, Shelagh, Pölsler, Laura, Campeau, Philippe M., Blazo, Maria, Bijlsma, Emilia K., Rosenfeld, Jill A., Beetz, Christian, Powis, Zöe, McWalter, Kirsty, Brandt, Tracy, Torti, Erin, Mathot, Mikaël, Mohammad, Shekeeb S., Armstrong, Ruth, Kalscheuer, Vera M.

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Partial loss of USP9X function leads to a male neurodevelopmental and behavioural disorder converging on TGFβ signalling by Johnson, Brett V., Kumar, Raman, Oishi, Sabrina, Alexander, Suzy, Kasherman, Maria, Vega, Michelle Sanchez, Ivancevic, Atma, Gardner, Alison, Domingo, Deepti, Corbett, Mark, Parnell, Euan, Yoon, Sehyoun, Oh, Tracey, Lines, Matthew, Lefroy, Henrietta, Kini, Usha, Van Allen, Margot, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Bézieau, Stéphane, Pasquier, Laurent, Raynaud, Martine, Afenjar, Alexandra, de Villemeur, Thierry Billette, Keren, Boris, Désir, Julie, Van Maldergem, Lionel, Marangoni, Martina, Dikow, Nicola, Koolen, David A., VanHasselt, Peter M., Weiss, Marjan, Zwijnenburg, Petra, Sa, Joaquim, Reis, Claudia Falcao, López-Otín, Carlos, Santiago-Fernández, Olaya, Fernández-Jaén, Alberto, Rauch, Anita, Steindl, Katharina, Joset, Pascal, Goldstein, Amy, Madan-Khetarpal, Suneeta, Infante, Elena, Zackai, Elaine, Mcdougall, Carey, Narayanan, Vinodh, Ramsey, Keri, Mercimek-Andrews, Saadet, Pena, Loren, Shashi, Vandana, Schoch, Kelly, Sullivan, Jennifer A., Pinto e Vairo, Filippo, Pichurin, Pavel N., Ewing, Sarah A., Barnett, Sarah S., Klee, Eric W., Perry, M. Scott, Koenig, Mary Kay, Keegan, Catherine E., Schuette, Jane L., Asher, Stephanie, Perilla-Young, Yezmin, Smith, Laurie D., Rosenfeld, Jill A., Bhoj, Elizabeth, Kaplan, Paige, Li, Dong, Oegema, Renske, van Binsbergen, Ellen, van der Zwaag, Bert, Smeland, Marie Falkenberg, Cutcutache, Ioana, Page, Matthew, Armstrong, Martin, Lin, Angela E., Steeves, Marcie A., den Hollander, Nicolette, Hoffer, Mariëtte J V, Reijnders, Margot R.F., Demirda, Serwet, Koboldt, Daniel C., Bartholomew, Dennis, Mosher, Theresa Mihalic, Hickey, Scott E., Shieh, Christine, Sanchez-Lara, Pedro A., Graham, John M., Tezcan, Kamer, Schaefer, G. B., Danylchuk, Noelle R., Asamoah, Alexander, Jackson, Kelly E., Yachelevich, Naomi, Au, Margaret, Pérez-Jurado, Luis A., Kleefstra, Tjitske

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Sodium citrate anticoagulation during sustained low efficiency dialysis (SLED) in patients with acute renal failure and severely impaired liver function by Morath, Christian, Miftari, Nexhat, Dikow, Ralf, Hainer, Christian, Zeier, Martin, Morgera, Stanislao, Weigand, Markus A., Schwenger, Vedat

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