Որոնման արդյունքները - Michael Nothnagel
- Ցուցադրվում են 1 - 20 արդյունքները 33
- Գնացեք Հաջորդ էջ
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2
Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics Corinna Ernst, Eric Hahnen, Christoph Engel, Michael Nothnagel, Jonas Weber, Rita K. Schmutzler, Jan Hauke
Հրապարակվել է 2018Artigo -
3
Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting Claudia Fritsch, Alexander Herrmann, Michael Nothnagel, Karol Szafranski, Klaus Huse, Frank Schumann, Stefan Schreiber, Matthias Platzer, Michael Krawczak, Jochen Hampe, Mario Brosch
Հրապարակվել է 2012Artigo -
4
Identification of a Shared Genetic Susceptibility Locus for Coronary Heart Disease and Periodontitis Arne S. Schäefer, G. Richter, Birte Groessner‐Schreiber, Barbara Noack, Michael Nothnagel, N. E. El Mokhtari, Bruno G. Loos, Søren Jepsen, Stefan Schreiber
Հրապարակվել է 2009Artigo -
5
Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes Andrew Fischer, Michael Nothnagel, Andreas Franke, Gunnar Jacobs, Hamidreza Saadati, KI Gaede, Philip Rosenstiel, Martin Schürmann, Joachim Müller‐Quernheim, Stefanie Schreiber, Sylvia Hofmann
Հրապարակվել է 2010Artigo -
6
Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing Dennis Lal, Bernd A. Neubauer, Mohammad R. Toliat, Janine Altmüller, Holger Thiele, Peter Nürnberg, Clemens Kamrath, Anne Schänzer, Thomas Sander, Andreas Hahn, Michael Nothnagel
Հրապարակվել է 2016Artigo -
7
A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1 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
Հրապարակվել է 2011Artigo -
8
CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection 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
Հրապարակվել է 2010Artigo -
9
A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis 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
Հրապարակվել է 2009Artigo -
10
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease 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
Հրապարակվել է 2024Revisão -
11
A 3′ UTR transition within DEFB1 is associated with chronic and aggressive periodontitis 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
Հրապարակվել է 2009Artigo -
12
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis 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
Հրապարակվել է 2017Artigo -
13
Polymorphisms in the glial glutamate transporter <i>SLC1A2</i> are associated with essential tremor 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
Հրապարակվել է 2012Artigo -
14
Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis 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
Հրապարակվել է 2012Revisão -
15
Genome-Wide Association Analysis in Sarcoidosis and Crohn's Disease Unravels a Common Susceptibility Locus on 10p12.2 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
Հրապարակվել է 2008Artigo -
16
Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition 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
Հրապարակվել է 2010Artigo -
17
Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome 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
Հրապարակվել է 2012Artigo -
18
Wnt Signaling and Dupuytren's Disease 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
Հրապարակվել է 2011Artigo -
19
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans 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
Հրապարակվել է 2018Artigo -
20
Schizophrenia risk polymorphisms in the <i>TCF4</i> gene interact with smoking in the modulation of auditory sensory gating 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
Հրապարակվել է 2012Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Genotype
Medicine
Single-nucleotide polymorphism
Internal medicine
Genome-wide association study
Allele
Computational biology
Genetic association
Locus (genetics)
Population
Haplotype
Disease
Evolutionary biology
Odds ratio
SNP
Bioinformatics
Environmental health
Genome
Mutation
Neuroscience
Phenotype
Genetic variation
Pathology
Periodontitis
Sarcoidosis
Demography
Exome