Massive parallelization of divide-and-conquer algorithms over powerlists von Achatz, Klaus, Schulte, Wolfram

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Determining the point of minimum error for 6DOF pose uncertainty representation von Pustka, D, Willneff, J, Wenisch, O, Lukewille, P, Achatz, K, Keitler, P, Klinker, G

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endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield von Waller, F, Achatz, B, Baltruschat, H, Fodor, J, Becker, K, Fischer, M, Heier, T, Huckelhoven, R, Neumann, C, Wettstein, D. von

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Proterodiplostomid no longer: Molecular phylogeny reveals the true position of Proalarioides (Digenea: Diplostomoidea) von Achatz, Tyler J., Chacko, Sherin, Prasadan, Puthanpurayil K., Tkach, Vasyl V.

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Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients von Santiago, K.M., Castro, L.P., Neto, J.P.D., Nóbrega, A.F., Pinto, C.A.L., Ashton‐Prolla, P., Pinto e Vairo, F., Medeiros, P.F.V., Ribeiro, E.M., Ribeiro, B.F.R., Valle, F.F., Doriqui, M.J.R., Leite, C.H.B., Rocha, R.M., Moura, L.M.S., Munford, V., Galante, P.A.F., Menck, C.F.M., Rogatto, S.R., Achatz, M.I.

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Copper transporters and chaperones CTR1, CTR2, ATOX1, and CCS as determinants of cisplatin sensitivity von Bompiani, Kristin M, Tsai, Cheng-Yu, Achatz, Felix P, Liebig, Janika K, Howell, Stephen B

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Digital Transformation at thyssenkrupp: Challenges, Strategies and Examples von Achatz, Reinhold

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Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood von Achatz, Maria Isabel, Porter, Christopher C, Brugières, Laurence, Druker, Harriet, Frebourg, Thierry, Foulkes, William D, Kratz, Christian P, Kuiper, Roland P, Hansford, Jordan R, Hernandez, Hector Salvador, Nathanson, Katherine L, Kohlmann, Wendy K, Doros, Leslie, Onel, Kenan, Schneider, Kami Wolfe, Scollon, Sarah R, Tabori, Uri, Tomlinson, Gail E, Evans, D Gareth R, Plon, Sharon E

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Patterns of Clinostomum marginatum infection in fishes and amphibians: integration of field, genetic, and experimental approaches von Calhoun, D M, Leslie, K L, Riepe, T B, Achatz, T J, McDevitt-Galles, T, Tkach, V V, Johnson, P T J

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Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome von Kratz, Christian P, Achatz, Maria Isabel, Brugières, Laurence, Frebourg, Thierry, Garber, Judy E, Greer, Mary-Louise C, Hansford, Jordan R, Janeway, Katherine A, Kohlmann, Wendy K, McGee, Rose, Mullighan, Charles G, Onel, Kenan, Pajtler, Kristian W, Pfister, Stefan M, Savage, Sharon A, Schiffman, Joshua D, Schneider, Katherine A, Strong, Louise C, Evans, D Gareth R, Wasserman, Jonathan D, Villani, Anita, Malkin, David

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HAX1 deficiency: Impact on lymphopoiesis and B‐cell development von Peckl‐Schmid, Doris, Wolkerstorfer, Susanne, Königsberger, Sebastian, Achatz‐Straussberger, Gertrude, Feichtner, Stefan, Schwaiger, Elisabeth, Zaborsky, Nadja, Huemer, Michael, Gratz, Iris K, Schibli, Roger, Lamers, Marinus, Crameri, Reto, Moser, Katrin, Luger, Elke O, Achatz, Gernot

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Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants von Fortuno, Cristina, Lee, Kristy, Olivier, Magali, Pesaran, Tina, Mai, Phuong L., Andrade, Kelvin C., Attardi, Laura D., Crowley, Stephanie, Evans, D. Gareth, Feng, Bing‐Jian, Foreman, Ann K. M., Frone, Megan N., Huether, Robert, James, Paul A., McGoldrick, Kelly, Mester, Jessica, Seifert, Bryce A., Slavin, Thomas P., Witkowski, Leora, Zhang, Liying, Plon, Sharon E., Spurdle, Amanda B., Savage, Sharon A.

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Whole-genome sequencing analysis of phenotypic heterogeneity and anticipation in Li–Fraumeni cancer predisposition syndrome von Ariffin, Hany, Hainaut, Pierre, Puzio-Kuter, Anna, Choong, Soo Sin, Chan, Adelyne Sue Li, Tolkunov, Denis, Rajagopal, Gunaretnam, Kang, Wenfeng, Lim, Leon Li Wen, Krishnan, Shekhar, Chen, Kok-Siong, Achatz, Maria Isabel, Karsa, Mawar, Shamsani, Jannah, Levine, Arnold J., Chan, Chang S.

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Regime of Validity of Soundproof Atmospheric Flow Models von KLEIN, Rupert, ACHATZ, Ulrich, BRESCH, Didier, KNIO, Omar M, SMOLARKIEWICZ, Piotr K

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Genomic profile of Li-Fraumeni syndrome patients with adrenocortical carcinoma in childhood von Fortes, F., Canto, L., Kuasne, H., Marchi, F., Miranda, P., Andrade, K., Santiago, K., Rogatto, S., Achatz, M.I.

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Gastric cancer in individuals with Li-Fraumeni syndrome von Masciari, Serena, Dewanwala, Akriti, Stoffel, Elena M., Lauwers, Gregory Y., Zheng, Hui, Achatz, Maria Isabel, Riegert-Johnson, Douglas, Foretova, Lenka, Silva, Edaise M., Digianni, Lisa, Verselis, Sigitas J., Schneider, Katherine, Li, Frederick P., Fraumeni, Joseph, Garber, Judy E., Syngal, Sapna

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Brazilian health-care policy for targeted oncology therapies and companion diagnostic testing von Ferreira, Carlos Gil, Dr, Achatz, Maria Isabel, MD, Ashton-Prolla, Patricia, MD, Begnami, Maria Dirlei, MD, Marchini, Fabricio K, PhD, Stefani, Stephen Doral, MD

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Low-temperature transport in highly boron-doped nanocrystalline diamond von Achatz, P., Gajewski, W., Bustarret, E., Marcenat, C., Piquerel, R., Chapelier, C., Dubouchet, T., Williams, O. A., Haenen, K., Garrido, J. A., Stutzmann, M.

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ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk von Stolarova, Lenka, Kleiblova, Petra, Zemankova, Petra, Stastna, Barbora, Janatova, Marketa, Soukupova, Jana, Achatz, Maria Isabel, Ambrosone, Christine, Apostolou, Paraskevi, Arun, Banu K, Auer, Paul, Barnard, Mollie, Bertelsen, Birgitte, Blok, Marinus J, Boddicker, Nicholas, Brunet, Joan, Burnside, Elizabeth S, Calvello, Mariarosaria, Campbell, Ian, Chan, Sock Hoai, Chen, Fei, Chiang, Jian Bang, Coppa, Anna, Cortesi, Laura, Crujeiras-González, Ana, De Leeneer, Kim, De Putter, Robin, DePersia, Allison, Devereux, Lisa, Domchek, Susan, Efremidis, Anna, Engel, Christoph, Ernst, Corinna, Evans, D Gareth R, Feliubadaló, Lidia, Fostira, Florentia, Fuentes-Ríos, Olivia, Gómez-García, Encarna B, González, Sara, Haiman, Christopher, Hansen, Thomas van Overeem, Hauke, Jan, Hodge, James, Hu, Chunling, Huang, Hongyan, Ishak, Nur Diana Binte, Iwasaki, Yusuke, Konstantopoulou, Irene, Kraft, Peter, Lacey, James, Lázaro, Conxi, Li, Na, Lim, Weng Khong, Lindstrom, Sara, Lori, Adriana, Martinez, Elana, Martins, Alexandra, Matsuda, Koichi, Matullo, Giuseppe, McInerny, Simone, Michailidou, Kyriaki, Montagna, Marco, Monteiro, Alvaro N A, Mori, Luigi, Nathanson, Katherine, Neuhausen, Susan L, Nevanlinna, Heli, Olson, Janet E, Palmer, Julie, Pasini, Barbara, Patel, Alpa, Piane, Maria, Poppe, Bruce, Radice, Paolo, Renieri, Alessandra, Resta, Nicoletta, Richardson, Marcy E, Rosseel, Toon, Ruddy, Kathryn J, Santamariña, Marta, Dos Santos, Elizabeth Santana, Teras, Lauren, Toland, Amanda E, Trentham-Dietz, Amy, Vachon, Celine M, Volk, Alexander E, Weber-Lassalle, Nana, Weitzel, Jeffrey N, Wiesmuller, Lisa, Winham, Stacey, Yadav, Siddhartha, Yannoukakos, Drakoulis, Yao, Song, Zampiga, Valentina, Zethoven, Magnus, Zhang, Ze Wen, Zima, Tomas, Spurdle, Amanda B, Vega, Ana, Rossing, Maria

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein von Meindl, Alfons, Pusch, Carsten M, Zeitz, Christina, Brandau, Oliver, Pesch, Katrin, Achatz, Helene, Feil, Silke, Scharfe, Curt, Maurer, Johannes, Jacobi, Felix K, Pinckers, Alfred, Andreasson, Sten, Hardcastle, Alison, Wissinger, Bernd, Berger, Wolfgang

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