Works by Lange, Lukas

Results: 12
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    Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.

    Published in:
    Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01240-0
    By:
    • Pagnamenta, Alistair T.;
    • Camps, Carme;
    • Giacopuzzi, Edoardo;
    • Taylor, John M.;
    • Hashim, Mona;
    • Calpena, Eduardo;
    • Kaisaki, Pamela J.;
    • Hashimoto, Akiko;
    • Yu, Jing;
    • Sanders, Edward;
    • Schwessinger, Ron;
    • Hughes, Jim R.;
    • Lunter, Gerton;
    • Dreau, Helene;
    • Ferla, Matteo;
    • Lange, Lukas;
    • Kesim, Yesim;
    • Ragoussis, Vassilis;
    • Vavoulis, Dimitrios V.;
    • Allroggen, Holger
    Publication type:
    Article
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    Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods.

    Published in:
    Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.01150
    By:
    • Shields, Adrian M.;
    • Pagnamenta, Alistair T.;
    • Pollard, Andrew J.;
    • Taylor, Jenny C.;
    • Allroggen, Holger;
    • Patel, Smita Y.;
    • Knight, Samantha J. L.;
    • Popitsch, Niko;
    • Camps, Carme;
    • Pentony, Melissa M.;
    • Kvikstad, Erika M.;
    • Lange, Lukas;
    • Hashim, Mona;
    • Harris, Steve;
    • Tilley, Mark;
    • Vavoulis, Dimitris;
    • Kaisaki, Pamela;
    • Ragoussis, Vassilis;
    • Feral, Matteo;
    • Schuh, Anna H.
    Publication type:
    Article
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