Works by Nothnagel, Michael

Results: 64
    1
    2

    Statistical inference of allelic imbalance from transcriptome data.

    Published in:
    Human Mutation, 2011, v. 32, n. 1, p. 98, doi. 10.1002/humu.21396
    By:
    • Nothnagel, Michael;
    • Wolf, Andreas;
    • Herrmann, Alexander;
    • Szafranski, Karol;
    • Vater, Inga;
    • Brosch, Mario;
    • Huse, Klaus;
    • Siebert, Reiner;
    • Platzer, Matthias;
    • Hampe, Jochen;
    • Krawczak, Michael
    Publication type:
    Article
    3
    4
    5

    Development and Evaluation of the Ancestry Informative Marker Panel of the VISAGE Basic Tool.

    Published in:
    Genes, 2021, v. 12, n. 8, p. 1284, doi. 10.3390/genes12081284
    By:
    • de la Puente, María;
    • Ruiz-Ramírez, Jorge;
    • Ambroa-Conde, Adrián;
    • Xavier, Catarina;
    • Pardo-Seco, Jacobo;
    • Álvarez-Dios, Jose;
    • Freire-Aradas, Ana;
    • Mosquera-Miguel, Ana;
    • Gross, Theresa E.;
    • Cheung, Elaine Y. Y.;
    • Branicki, Wojciech;
    • Nothnagel, Michael;
    • Parson, Walther;
    • Schneider, Peter M.;
    • Kayser, Manfred;
    • Carracedo, Ángel;
    • Lareu, Maria Victoria;
    • Phillips, Christopher
    Publication type:
    Article
    6
    7

    An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 7, p. 967, doi. 10.1038/ejhg.2008.266
    By:
    • Lu, Timothy Tehua;
    • Lao, Oscar;
    • Nothnagel, Michael;
    • Junge, Olaf;
    • Freitag-Wolf, Sandra;
    • Caliebe, Amke;
    • Balascakova, Miroslava;
    • Bertranpetit, Jaume;
    • Bindoff, Laurence Albert;
    • Comas, David;
    • Holmlund, Gunilla;
    • Kouvatsi, Anastasia;
    • Macek, Milan;
    • Mollet, Isabelle;
    • Nielsen, Finn;
    • Parson, Walther;
    • Palo, Jukka;
    • Ploski, Rafal;
    • Sajantila, Antti;
    • Tagliabracci, Adriano
    Publication type:
    Article
    8
    9
    10
    11

    De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.

    Published in:
    Nature Genetics, 2015, v. 47, n. 4, p. 393, doi. 10.1038/ng.3239
    By:
    • Syrbe, Steffen;
    • Bertsche, Astrid;
    • Bernhard, Matthias K;
    • Merkenschlager, Andreas;
    • Kiess, Wieland;
    • Serratosa, José M;
    • Nothnagel, Michael;
    • May, Patrick;
    • Krause, Roland;
    • Dorn, Thomas;
    • Vogt, Heinrich;
    • Krämer, Günter;
    • Mullis, Primus E;
    • Linnankivi, Tarja;
    • Lehesjoki, Anna-Elina;
    • Sterbova, Katalin;
    • Craiu, Dana C;
    • Hoffman-Zacharska, Dorota;
    • Hedrich, Ulrike B S;
    • Müller, Stephan
    Publication type:
    Article
    12

    Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1067, doi. 10.1038/ng.2728
    By:
    • Lemke, Johannes R;
    • Lal, Dennis;
    • Reinthaler, Eva M;
    • Steiner, Isabelle;
    • Nothnagel, Michael;
    • Alber, Michael;
    • Geider, Kirsten;
    • Laube, Bodo;
    • Schwake, Michael;
    • Finsterwalder, Katrin;
    • Franke, Andre;
    • Schilhabel, Markus;
    • Jähn, Johanna A;
    • Muhle, Hiltrud;
    • Boor, Rainer;
    • Van Paesschen, Wim;
    • Caraballo, Roberto;
    • Fejerman, Natalio;
    • Weckhuysen, Sarah;
    • De Jonghe, Peter
    Publication type:
    Article
    13
    14

    Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1319, doi. 10.1038/ng.221
    By:
    • Franke, Andre;
    • Balschun, Tobias;
    • Karlsen, Tom H;
    • Sventoraityte, Jurgita;
    • Nikolaus, Susanna;
    • Mayr, Gabriele;
    • Domingues, Francisco S;
    • Albrecht, Mario;
    • Nothnagel, Michael;
    • Ellinghaus, David;
    • Sina, Christian;
    • Onnie, Clive M;
    • Weersma, Rinse K;
    • Stokkers, Pieter C F;
    • Wijmenga, Cisca;
    • Gazouli, Maria;
    • Strachan, David;
    • McArdle, Wendy L;
    • Vermeire, Séverine;
    • Rutgeerts, Paul
    Publication type:
    Article
    15
    16
    17
    18
    19
    20

    Metabolic Signature of Electrosurgical Liver Dissection.

    Published in:
    PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0072022
    By:
    • von Schönfels, Witigo;
    • von Kampen, Oliver;
    • Patsenker, Eleonora;
    • Stickel, Felix;
    • Schniewind, Bodo;
    • Hinz, Sebastian;
    • Ahrens, Markus;
    • Balschun, Katharina;
    • Egberts, Jan-Hendrik;
    • Richter, Klaus;
    • Landrock, Andreas;
    • Sipos, Bence;
    • Will, Olga;
    • Huebbe, Patrizia;
    • Schreiber, Stefan;
    • Nothnagel, Michael;
    • Röcken, Christoph;
    • Rimbach, Gerald;
    • Becker, Thomas;
    • Hampe, Jochen
    Publication type:
    Article
    21

    Pipeline for Large-Scale Microdroplet Bisulfite PCR-Based Sequencing Allows the Tracking of Hepitype Evolution in Tumors.

    Published in:
    PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0021332
    By:
    • Herrmann, Alexander;
    • Haake, Andrea;
    • Ammerpohl, Ole;
    • Martin-Guerrero, Idoia;
    • Szafranski, Karol;
    • Stemshorn, Kathryn;
    • Nothnagel, Michael;
    • Kotsopoulos, Steve K.;
    • Richter, Julia;
    • Warner, Jason;
    • Olson, Jeff;
    • Link, Darren R.;
    • Schreiber, Stefan;
    • Krawczak, Michael;
    • Platzer, Matthias;
    • Nü rnberg, Peter;
    • Siebert, Reiner;
    • Hampe, Jochen
    Publication type:
    Article
    22

    Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 14, p. 3883, doi. 10.1093/hmg/ddu076
    By:
    • Stickel, Felix;
    • Buch, Stephan;
    • Zoller, Heinz;
    • Hultcrantz, Rolf;
    • Gallati, Sabina;
    • Österreicher, Christoph;
    • Finkenstedt, Armin;
    • Stadlmayr, Andreas;
    • Aigner, Elmar;
    • Sahinbegovic, Enijad;
    • Sarrazin, Christoph;
    • Schafmayer, Clemens;
    • Braun, Felix;
    • Erhart, Wiebke;
    • Nothnagel, Michael;
    • Lerch, Markus M.;
    • Mayerle, Julia;
    • Völzke, Henry;
    • Schaller, André;
    • Kratzer, Wolfgang
    Publication type:
    Article
    23
    24

    Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.

    Published in:
    2016
    By:
    • Gardella, Elena;
    • Becker, Felicitas;
    • Møller, Rikke S.;
    • Schubert, Julian;
    • Lemke, Johannes R.;
    • Larsen, Line H. G.;
    • Eiberg, Hans;
    • Nothnagel, Michael;
    • Thiele, Holger;
    • Altmüller, Janine;
    • Syrbe, Steffen;
    • Merkenschlager, Andreas;
    • Bast, Thomas;
    • Steinhoff, Bernhard;
    • Nürnberg, Peter;
    • Mang, Yuan;
    • Bakke Møller, Louise;
    • Gellert, Pia;
    • Heron, Sarah E.;
    • Dibbens, Leanne M.
    Publication type:
    journal article
    25

    A Novel Sarcoidosis Risk Locus for Europeans on Chromosome 11q13.1.

    Published in:
    American Journal of Respiratory & Critical Care Medicine, 2012, v. 186, n. 9, p. 877, doi. 10.1164/rccm.201204-0708OC
    By:
    • Fischer, Annegret;
    • Schmid, Benjamin;
    • Ellinghaus, David;
    • Nothnagel, Michael;
    • Gaede, Karoline I.;
    • Schürmann, Manfred;
    • Lipinski, Simone;
    • Rosenstiel, Philip;
    • Zissel, Gernot;
    • Höhne, Kerstin;
    • Petrek, Martin;
    • Kolek, Vitezslav;
    • Pabst, Stefan;
    • Grohé, Christian;
    • Grunewald, Johan;
    • Ronninger, Marcus;
    • Eklund, Anders;
    • Padyukov, Leonid;
    • Gieger, Christian;
    • Wichmann, H.-Erich
    Publication type:
    Article
    26
    27
    28
    29

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

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03857-x
    By:
    • Krause-Kyora, Ben;
    • Nutsua, Marcel;
    • Boehme, Lisa;
    • Pierini, Federica;
    • Pedersen, Dorthe Dangvard;
    • Kornell, Sabin-Christin;
    • Drichel, Dmitriy;
    • Bonazzi, Marion;
    • Möbus, Lena;
    • Tarp, Peter;
    • Susat, Julian;
    • Bosse, Esther;
    • Willburger, Beatrix;
    • Schmidt, Alexander H.;
    • Sauter, Jürgen;
    • Franke, Andre;
    • Wittig, Michael;
    • Caliebe, Amke;
    • Nothnagel, Michael;
    • Schreiber, Stefan
    Publication type:
    Article
    30

    Identification and characterization of two functional variants in the human longevity gene FOXO3.

    Published in:
    Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-02183-y
    By:
    • Flachsbart, Friederike;
    • Dose, Janina;
    • Gentschew, Liljana;
    • Badarinarayan, Nandini;
    • May, Sandra;
    • Luzius, Anne;
    • Torres, Guillermo G.;
    • Jentzsch, Marlene;
    • Forster, Michael;
    • Häsler, Robert;
    • Rosenstiel, Philip;
    • Franke, Andre;
    • Nebel, Almut;
    • Till, Andreas;
    • Krause-Kyora, Ben;
    • Schreiber, Stefan;
    • ElSharawy, Abdou;
    • Drichel, Dmitriy;
    • Nothnagel, Michael;
    • Blanché, Hélène
    Publication type:
    Article
    31
    32
    33
    34

    Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19265-z
    By:
    • Quach, Bryan C.;
    • Bray, Michael J.;
    • Gaddis, Nathan C.;
    • Liu, Mengzhen;
    • Palviainen, Teemu;
    • Minica, Camelia C.;
    • Zellers, Stephanie;
    • Sherva, Richard;
    • Aliev, Fazil;
    • Nothnagel, Michael;
    • Young, Kendra A.;
    • Marks, Jesse A.;
    • Young, Hannah;
    • Carnes, Megan U.;
    • Guo, Yuelong;
    • Waldrop, Alex;
    • Sey, Nancy Y. A.;
    • Landi, Maria T.;
    • McNeil, Daniel W.;
    • Drichel, Dmitriy
    Publication type:
    Article
    35
    36
    37

    Role of NOD2/CARD15 in coronary heart disease.

    Published in:
    BMC Genetics, 2007, v. 8, p. 76, doi. 10.1186/1471-2156-8-76
    By:
    • Eddine El Mokhtari, Nour;
    • Ott, Stephan J.;
    • Nebel, Almut;
    • Schäfer, Arne;
    • Rosenstiel, Philip;
    • Förster, Matti;
    • Nothnagel, Michael;
    • Simon, Rüdiger;
    • Schreiber, Stefan
    Publication type:
    Article
    38

    Meta-Analysis of Genome-Wide Association Studies and Network Analysis-Based Integration with Gene Expression Data Identify New Suggestive Loci and Unravel a Wnt-Centric Network Associated with Dupuytren’s Disease.

    Published in:
    PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0158101
    By:
    • Becker, Kerstin;
    • Siegert, Sabine;
    • Toliat, Mohammad Reza;
    • Du, Juanjiangmeng;
    • Casper, Ramona;
    • Dolmans, Guido H.;
    • Werker, Paul M.;
    • Tinschert, Sigrid;
    • Franke, Andre;
    • Gieger, Christian;
    • Strauch, Konstantin;
    • Nothnagel, Michael;
    • Nürnberg, Peter;
    • Hennies, Hans Christian;
    • null, null
    Publication type:
    Article
    39
    40
    41
    42
    43

    Prognostic relevance of gastric cancer staging by endoscopic ultrasound.

    Published in:
    Surgical Endoscopy & Other Interventional Techniques, 2013, v. 27, n. 4, p. 1124, doi. 10.1007/s00464-012-2558-z
    By:
    • Jürgensen, Christian;
    • Brand, Jana;
    • Nothnagel, Michael;
    • Arlt, Alexander;
    • Neser, Frank;
    • Habeck, Jörg-Olaf;
    • Schreiber, Stefan;
    • Stölzel, Ulrich;
    • Zeitz, Martin;
    • Hampe, Jochen
    Publication type:
    Article
    44
    45
    46

    CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online.

    Published in:
    Bioinformatics, 2023, v. 39, n. 5, p. 1, doi. 10.1093/bioinformatics/btad290
    By:
    • Macnee, Marie;
    • Pérez-Palma, Eduardo;
    • Brünger, Tobias;
    • Klöckner, Chiara;
    • Platzer, Konrad;
    • Stefanski, Arthur;
    • Montanucci, Ludovica;
    • Bayat, Allan;
    • Radtke, Maximilian;
    • Collins, Ryan L;
    • Talkowski, Michael;
    • Blankenberg, Daniel;
    • Møller, Rikke S;
    • Lemke, Johannes R;
    • Nothnagel, Michael;
    • May, Patrick;
    • Lal, Dennis
    Publication type:
    Article
    47

    Polymorphisms in NACHT-LRR ( NLR) genes in atopic dermatitis.

    Published in:
    Experimental Dermatology, 2007, v. 16, n. 8, p. 692, doi. 10.1111/j.1600-0625.2007.00589.x
    By:
    • Macaluso, Filippina;
    • Nothnagel, Michael;
    • Parwez, Qumar;
    • Petrasch-Parwez, Elisabeth;
    • Bechara, Falk Georges;
    • Epplen, Joerg Thomas;
    • Hoffjan, Sabine
    Publication type:
    Article
    48

    Exploring Paleogene Tibet's warm temperate environments through target enrichment and phylogenetic niche modelling of Himalayan spiny frogs (Paini, Dicroglossidae).

    Published in:
    Molecular Ecology, 2024, v. 33, n. 15, p. 1, doi. 10.1111/mec.17446
    By:
    • Hofmann, Sylvia;
    • Rödder, Dennis;
    • Andermann, Tobias;
    • Matschiner, Michael;
    • Riedel, Jendrian;
    • Baniya, Chitra B.;
    • Flecks, Morris;
    • Yang, Jianhuan;
    • Jiang, Ke;
    • Jianping, Jiang;
    • Litvinchuk, Spartak N.;
    • Martin, Sebastian;
    • Masroor, Rafaqat;
    • Nothnagel, Michael;
    • Vershinin, Vladimir;
    • Zheng, Yuchi;
    • Jablonski, Daniel;
    • Schmidt, Joachim;
    • Podsiadlowski, Lars
    Publication type:
    Article
    49
    50