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  1. 1

    The GENESIS database and tools: A decade of discovery in Mendelian genomics by Danzi, Matt (Author) , Powell, Eric (Author) , Rebelo, Adriana P. (Author) , Dohrn, Maike F. (Author) , Beijer, Danique (Author) , Fazal, Sarah (Author) , Xu, Isaac R. L. (Author) , Medina, Jessica (Author) , Chen, Sitong (Author) , Arcia de Jesus, Yeisha (Author) , Schatzman, Jacquelyn (Author) , Hershberger, Ray E. (Author) , Saporta, Mario (Author) , Baets, Jonathan (Author) , Falk, Marni (Author) , Herrmann, David N. (Author) , Scherer, Steven S. (Author) , Reilly, Mary M. (Author) , Cortese, Andrea (Author) , Marques, Wilson (Author) , Cornejo-Olivas, Mario R. (Author) , Sanmaneechai, Oranee (Author) , Kennerson, Marina L. (Author) , Jordanova, Albena (Author) , Silva, Thiago Y. T. (Author) , Pedroso, Jose Luiz (Author) , Schierbaum, Luca (Author) , Ebrahimi-Fakhari, Darius (Author) , Peric, Stojan (Author) , Lee, Yi-Chung (Author) , Synofzik, Matthis (Author) , Tekin, Mustafa (Author) , Ravenscroft, Gianina (Author) , Shy, Mike (Author) , Basak, Nazli (Author) , Schüle-Freyer, Rebecca (Author) , Zuchner, Stephan (Author) ,


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  2. 2

    The Medaka Inbred Kiyosu-Karlsruhe (MIKK) panel by Fitzgerald, Tomas (Author) , Brettell, Ian (Author) , Leger, Adrien (Author) , Wolf, Nadeshda (Author) , Kusminski, Natalja (Author) , Monahan, Jack (Author) , Barton, Carl (Author) , Herder, Cathrin (Author) , Aadepu, Narendar (Author) , Gierten, Jakob (Author) , Becker, Clara (Author) , Hammouda, Omar (Author) , Hasel, Eva Mareike (Author) , Lischik, Colin Q. (Author) , Lust, Katharina (Author) , Sokolova, Natalia (Author) , Suzuki, Risa (Author) , Tsingos, Erika (Author) , Tavhelidse-Suck, Tinatini (Author) , Thumberger, Thomas (Author) , Watson, Philip (Author) , Welz, Bettina (Author) , Khouja, Nadia (Author) , Naruse, Kiyoshi (Author) , Birney, Ewan (Author) , Wittbrodt, Joachim (Author) , Loosli, Felix (Author) ,


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  3. 3

    Return of individual research results from genomic research: a systematic review of stakeholder perspectives by Vears, Danya F. (Author) , Minion, Joel T. (Author) , Roberts, Stephanie J. (Author) , Cummings, James (Author) , Machirori, Mavis (Author) , Blell, Mwenza (Author) , Budin-Ljøsne, Isabelle (Author) , Cowley, Lorraine (Author) , Dyke, Stephanie O. M. (Author) , Gaff, Clara (Author) , Green, Robert (Author) , Hall, Alison (Author) , Johns, Amber L. (Author) , Knoppers, Bartha M. (Author) , Mulrine, Stephanie (Author) , Patch, Christine (Author) , Winkler, Eva C. (Author) , Murtagh, Madeleine J. (Author) ,


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  4. 4

    Familial cancer: how to successfully recruit families for germline mutations studies? Multiple myeloma as an example by Blocka, Joanna (Author) , Durie, Brian G. M. (Author) , Huhn, Stefanie (Author) , Müller-Tidow, Carsten (Author) , Försti, Asta (Author) , Hemminki, Kari (Author) , Goldschmidt, Hartmut (Author) ,


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  5. 5

    Findings made in gene panel to whole genome sequencing: data, knowledge, ethics - and consequences? by Winkler, Eva C. (Author) , Wiemann, Stefan (Author) ,


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  6. 6

    KIT mutation and loss of 14q may be sufficient for the development of clinically symptomatic very low-risk GIST by Klinke, Olaf (Author) , Mizani, Tuba (Author) , Baldwin, Gouri (Author) , Bancel, Brigitte (Author) , Devouassoux-Shisheboran, Mojgan (Author) , Scoazec, Jean-Yves (Author) , Bringuier, Pierre-Paul (Author) , Feederle, Regina (Author) , Jauch, Anna (Author) , Hinderhofer, Katrin (Author) , Taniere, Philippe (Author) , Delecluse, Henri-Jacques (Author) ,


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  7. 7

    Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation by Blake, Jonathon (Author) , Riddell, Andrew (Author) , Theiß, Susanne (Author) , Gonzalez, Alexis Perez (Author) , Haase, Bettina (Author) , Jauch, Anna (Author) , Janssen, Johannes W. G. (Author) , Ibberson, David (Author) , Pavlinic, Dinko (Author) , Moog, Ute (Author) , Benes, Vladimir (Author) , Runz, Heiko (Author) ,


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  8. 8

    Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies by Rieber, Nora (Author) , Zapatka, Marc (Author) , Lasitschka, Bärbel (Author) , Jones, David T. W. (Author) , Northcott, Paul (Author) , Hutter, Barbara (Author) , Jäger, Natalie (Author) , Kool, Marcel (Author) , Taylor, Michael (Author) , Lichter, Peter (Author) , Pfister, Stefan (Author) , Wolf, Stephan (Author) , Brors, Benedikt (Author) , Eils, Roland (Author) ,


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