Search Results - Michael Nothnagel

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  1. 1
    Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans

    Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans by Michael Nothnagel, Timothy T. Lu, Manfred Kayser, Michael Krawczak

    Published 2010
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  2. 2
    Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics

    Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics by Corinna Ernst, Eric Hahnen, Christoph Engel, Michael Nothnagel, Jonas Weber, Rita K. Schmutzler, Jan Hauke

    Published 2018
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  3. 3
    Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting

    Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting by Claudia Fritsch, Alexander Herrmann, Michael Nothnagel, Karol Szafranski, Klaus Huse, Frank Schumann, Stefan Schreiber, Matthias Platzer, Michael Krawczak, Jochen Hampe, Mario Brosch

    Published 2012
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  4. 4
    Identification of a Shared Genetic Susceptibility Locus for Coronary Heart Disease and Periodontitis

    Identification of a Shared Genetic Susceptibility Locus for Coronary Heart Disease and Periodontitis by Arne S. Schäefer, G. Richter, Birte Groessner‐Schreiber, Barbara Noack, Michael Nothnagel, N. E. El Mokhtari, Bruno G. Loos, Søren Jepsen, Stefan Schreiber

    Published 2009
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  5. 5
    Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes

    Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes by Andrew Fischer, Michael Nothnagel, Andreas Franke, Gunnar Jacobs, Hamidreza Saadati, KI Gaede, Philip Rosenstiel, Martin Schürmann, Joachim Müller‐Quernheim, Stefanie Schreiber, Sylvia Hofmann

    Published 2010
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  6. 6
    Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing

    Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing by Dennis Lal, Bernd A. Neubauer, Mohammad R. Toliat, Janine Altmüller, Holger Thiele, Peter Nürnberg, Clemens Kamrath, Anne Schänzer, Thomas Sander, Andreas Hahn, Michael Nothnagel

    Published 2016
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  7. 7
    A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1

    A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1 by Sylvia Hofmann, Annegret Fischer, Andreas Till, Joachim Müller‐Quernheim, Robert Häsler, André Franke, Katrin Gade, Heidi Schaarschmidt, Philip Rosenstiel, Almut Nebel, Martin Schürmann, Michael Nothnagel, Stefan Schreiber

    Published 2011
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  8. 8
    CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection

    CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection by Arne S. Schäefer, G. M. Richter, Henrik Dommisch, Michael Reinartz, Michael Nothnagel, Barbara Noack, Marja L. Laine, Mathias Folwaczny, Birte Groessner‐Schreiber, Bruno G. Loos, Søren Jepsen, Stefan Schreiber

    Published 2010
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  9. 9
    A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis

    A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis by Arne S. Schäefer, G. Richter, Michael Nothnagel, Thomas Manke, Henrik Dommisch, Gunnar Jacobs, Alexander Arlt, Philip Rosenstiel, Barbara Noack, Birte Groessner‐Schreiber, Søren Jepsen, Bruno G. Loos, Stefan Schreiber

    Published 2009
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  10. 10
    A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease

    A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease by Sophie A. Riesmeijer, Zoha Kamali, Michael Ng, Dmitriy Drichel, Bram Piersma, Kerstin Becker, T. B. Layton, Jagdeep Nanchahal, Michael Nothnagel, Ahmad Vaez, Hans Christian Hennies, Paul M. N. Werker, Dominic Furniss, Ilja M. Nolte

    Published 2024
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  11. 11
    A 3′ UTR transition within DEFB1 is associated with chronic and aggressive periodontitis

    A 3′ UTR transition within DEFB1 is associated with chronic and aggressive periodontitis by Arne S. Schäefer, G. Richter, Michael Nothnagel, Marja L. Laine, Andreas Rühling, Christine Schäfer, Nils Cordes, Barbara Noack, Mathias Folwaczny, J Glas, Christoph E. Dörfer, Henrik Dommisch, Birte Groessner‐Schreiber, Søren Jepsen, Bruno G. Loos, S Schreiber

    Published 2009
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  12. 12
    A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis

    A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis by Michael Ng, Dipti Thakkar, Lorraine Southam, Paul M. N. Werker, Roel A. Ophoff, Kerstin Becker, Michael Nothnagel, André Franke, Peter Nürnberg, Ana Isabel Espirito-Santo, David Izadi, Hans Christian Hennies, Jagdeep Nanchahal, Eleftheria Zeggini, Dominic Furniss

    Published 2017
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  13. 13
    Polymorphisms in the glial glutamate transporter <i>SLC1A2</i> are associated with essential tremor

    Polymorphisms in the glial glutamate transporter <i>SLC1A2</i> are associated with essential tremor by Sandra Thier, Delia Lorenz, Michael Nothnagel, Caroline Poremba, Frank Papengut, Silke Appenzeller, Steffen Paschen, Frank Hofschulte, Anna-Christina Hussl, Sascha Hering, Werner Poewe, Friedrich Asmus, Thomas Gasser, Lüdger Schöls, Kaare Christensen, Almut Nebel, Stefan Schreiber, Stephan Klebe, Günther Deuschl, Gregor Kuhlenbäumer

    Published 2012
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  14. 14
    Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis

    Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis by Sylvia Hofmann, Annegret Fischer, Michael Nothnagel, Gunnar Jacobs, Benjamin Schmid, Michael Wittig, André Franke, Karoline I. Gaede, Manfred Schürmann, Martin Petřek, František Mrázek, Stefan Pabst, Christian Grohé, Johan Grünewald, Marcus Ronninger, Anders Eklúnd, Philip Rosenstiel, Kerstin Höhne, Gernot Zissel, Joachim Müller‐Quernheim, Stefan Schreiber

    Published 2012
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  15. 15
    Genome-Wide Association Analysis in Sarcoidosis and Crohn's Disease Unravels a Common Susceptibility Locus on 10p12.2

    Genome-Wide Association Analysis in Sarcoidosis and Crohn's Disease Unravels a Common Susceptibility Locus on 10p12.2 by André Franke, Annegret Fischer, Michael Nothnagel, Christian Becker, Nils Grabe, Andreas Till, Tim Lu, Joachim Müller‐Quernheim, Michael Wittig, Alexander Hermann, Tobias Balschun, Sylvia Hofmann, Regina Niemiec, Sabrina Schulz, Jochen Hampe, Susanna Nikolaus, Peter Nürnberg, Michael Krawczak, Manfred Schürmann, Philip Rosenstiel, Almut Nebel, Stefan Schreiber

    Published 2008
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  16. 16
    Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition

    Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition by Stephan Buch, Clemens Schafmayer, Henry Völzke, Marcus Seeger, Juan Francisco Miquel, Silvia Sookoian, Jan Egberts, Alexander Arlt, Carlos J. Pirola, Markus M. Lerch, Ulrich John, André Franke, Oliver von Kampen, Mario Brosch, Michael Nothnagel, Wolfgang Kratzer, Bernhard O. Boehm, D. C. Bröring, Stefan Schreiber, Michael Krawczak, Jochen Hampe

    Published 2010
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  17. 17
    Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome

    Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome by Michael Nothnagel, R. Szibor, Oliver Vollrath, Christa Augustin, Jeanett Edelmann, M. Geppert, Cı́ntia Alves, Leonor Gusmão, Marielle Vennemann, Yiping Hou, Uta‐Dorothee Immel, S. Inturri, Haibo Luo, Sabine Lutz‐Bonengel, Carlo Robino, Lutz Roewer, Burkhard Rolf, Juliane Sanft, Kyoung‐Jin Shin, Jeong Eun Sim, Peter Wiegand, Christian Winkler, Michael Krawczak, Sandra Hering

    Published 2012
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  18. 18
    Wnt Signaling and Dupuytren's Disease

    Wnt Signaling and Dupuytren's Disease by Guido H. Dolmans, Paul M. N. Werker, Hans Christian Hennies, Dominic Furniss, Eleonora A. Festen, Lude Franke, Kerstin Becker, Pieter van der Vlies, Bruce H. R. Wolffenbuttel, Sigrid Tinschert, Mohammad R. Toliat, Michael Nothnagel, André Franke, Norman Klopp, H. E. Wichmann, Peter Nürnberg, Henk Giele, Roel A. Ophoff, Cisca Wijmenga

    Published 2011
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  19. 19
    Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans

    Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans by Ben Krause‐Kyora, Marcel Nutsua, Lisa Boehme, Federica Pierini, Dorthe Dangvard Pedersen, Sabin-Christin Kornell, Dmitriy Drichel, Marion Bonazzi, Lena Mӧbus, Peter Tarp, Julian Susat, Esther Bosse, Beatrix Willburger, Alexander H. Schmidt, Jürgen Sauter, André Franke, Michael Wittig, Amke Caliebe, Michael Nothnagel, Stefan Schreiber, Jesper L. Boldsen, Tobias L. Lenz, Almut Nebel

    Published 2018
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  20. 20
    Schizophrenia risk polymorphisms in the <i>TCF4</i> gene interact with smoking in the modulation of auditory sensory gating

    Schizophrenia risk polymorphisms in the <i>TCF4</i> gene interact with smoking in the modulation of auditory sensory gating by Boris B. Quednow, Jürgen Brinkmeyer, Arian Mobascher, Michael Nothnagel, Francesco Musso, Gerhard Gründer, Noah Savary, Nadine Petrovsky, Ingo Frommann, Leonhard Lennertz, Katja N. Spreckelmeyer, Thomas F. Wienker, Norbert Dahmen, Norbert Thuerauf, Marion Clepce, Falk Kiefer, Tomislav Majić, Rainald Mößner, Wolfgang Maier, Jürgen Gallinat, Amalia Díaz‐Lacava, Mohammad R. Toliat, Hölger Thiele, Peter Nürnberg, Michael Wagner, Georg Winterer

    Published 2012
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