Works by Nöthen, Markus M.

Results: 231
    1

    Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature.

    Published in:
    2011
    By:
    • Schramm, Charlotte;
    • Draaken, Markus;
    • Tewes, Gabriel;
    • Bartels, Enrika;
    • Schmiedeke, Eberhard;
    • Märzheuser, Stefanie;
    • Grasshoff-Derr, Sabine;
    • Hosie, Stuart;
    • Holland-Cunz, Stefan;
    • Priebe, Lutz;
    • Kreiß-Nachtsheim, Martina;
    • Hoffmann, Per;
    • Aretz, Stefan;
    • Nöthen, Markus M.;
    • Reutter, Heiko;
    • Ludwig, Michael;
    • Märzheuser, Stefanie;
    • Kreiss-Nachtsheim, Martina;
    • Nöthen, Markus M
    Publication type:
    journal article
    2
    3

    Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders.

    Published in:
    Translational Psychiatry, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41398-025-03440-1
    By:
    • Federmann, Lydia M.;
    • Sindermann, Lisa;
    • Primus, Sabrina;
    • Raimondo, Federico;
    • Oexle, Konrad;
    • Goltermann, Janik;
    • Winkelmann, Juliane;
    • Nöthen, Markus M.;
    • Amunts, Katrin;
    • Mühleisen, Thomas W.;
    • Cichon, Sven;
    • Eickhoff, Simon B.;
    • Hoffstaedter, Felix;
    • Dannlowski, Udo;
    • Patil, Kaustubh R.;
    • Forstner, Andreas J.
    Publication type:
    Article
    4
    5

    Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes.

    Published in:
    Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0231-5
    By:
    • Went, Molly;
    • Kinnersley, Ben;
    • Sud, Amit;
    • Johnson, David C.;
    • Weinhold, Niels;
    • Försti, Asta;
    • van Duin, Mark;
    • Orlando, Giulia;
    • Mitchell, Jonathan S.;
    • Kuiper, Rowan;
    • Walker, Brian A.;
    • Gregory, Walter M.;
    • Hoffmann, Per;
    • Jackson, Graham H.;
    • Nöthen, Markus M.;
    • da Silva Filho, Miguel Inacio;
    • Thomsen, Hauke;
    • Broyl, Annemiek;
    • Davies, Faith E.;
    • Thorsteinsdottir, Unnur
    Publication type:
    Article
    6
    7

    Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.

    Published in:
    Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0175-x
    By:
    • Hughes, Timothy;
    • Sønderby, Ida E.;
    • Polushina, Tatiana;
    • Hansson, Lars;
    • Holmgren, Asbjørn;
    • Athanasiu, Lavinia;
    • Melbø-Jørgensen, Christian;
    • Hassani, Sahar;
    • Hoeffding, Louise K.;
    • Herms, Stefan;
    • Bergen, Sarah E.;
    • Karlsson, Robert;
    • Song, Jie;
    • Rietschel, Marcella;
    • Nöthen, Markus M.;
    • Forstner, Andreas J.;
    • Hoffmann, Per;
    • Hultman, Christina M.;
    • Landén, Mikael;
    • Cichon, Sven
    Publication type:
    Article
    8
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    10

    Brief Report: No Association Between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin.

    Published in:
    Journal of Autism & Developmental Disorders, 2008, v. 38, n. 10, p. 1977, doi. 10.1007/s10803-008-0582-6
    By:
    • Schirmbeck, Frederike;
    • Georgi, Alexander;
    • Strohmaier, Jana;
    • Schmael, Christine;
    • Boesshenz, Katja V.;
    • Mühleisen, Thomas W.;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Jamra, Rami Abou;
    • Schumacher, Johannes;
    • Maier, Wolfgang;
    • Propping, Peter;
    • Nöthen, Markus M.;
    • Cichon, Sven;
    • Rietschel, Marcella;
    • Schulze, Thomas G.
    Publication type:
    Article
    11
    12

    Influence of obesity-related risk factors in the aetiology of glioma.

    Published in:
    2018
    By:
    • Disney-Hogg, Linden;
    • Sud, Amit;
    • Law, Philip J.;
    • Cornish, Alex J.;
    • Kinnersley, Ben;
    • Ostrom, Quinn T.;
    • Labreche, Karim;
    • Eckel-Passow, Jeanette E.;
    • Armstrong, Georgina N.;
    • Claus, Elizabeth B.;
    • Il’yasova, Dora;
    • Schildkraut, Joellen;
    • Barnholtz-Sloan, Jill S.;
    • Olson, Sara H.;
    • Bernstein, Jonine L.;
    • Lai, Rose K.;
    • Swerdlow, Anthony J.;
    • Simon, Matthias;
    • Hoffmann, Per;
    • Nöthen, Markus M.
    Publication type:
    journal article
    13
    14

    PSY‐PGx: a new intervention for the implementation of pharmacogenetics in psychiatry.

    Published in:
    World Psychiatry, 2025, v. 24, n. 1, p. 141, doi. 10.1002/wps.21289
    By:
    • van Westrhenen, Roos;
    • Young, Allan H.;
    • Heilbronner, Urs;
    • Juruena, Mario;
    • Ingelman‐Sundberg, Magnus;
    • Jukic, Marin;
    • Kaprio, Jaakko;
    • Kas, Martien J.H.;
    • Moldovan, Ramona;
    • Nöthen, Markus M.;
    • Philipsen, Alexandra;
    • Shomron, Noam;
    • Van der Eycken, Erik;
    • Vieta, Eduard;
    • Schulze, Thomas G.
    Publication type:
    Article
    15
    16

    Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.

    Published in:
    International Journal of Bipolar Disorders, 2018, v. 6, n. 1, p. 1, doi. 10.1186/s40345-018-0132-x
    By:
    • Breuer, René;
    • Mattheisen, Manuel;
    • Frank, Josef;
    • Krumm, Bertram;
    • Treutlein, Jens;
    • Kassem, Layla;
    • Strohmaier, Jana;
    • Herms, Stefan;
    • Mühleisen, Thomas W.;
    • Degenhardt, Franziska;
    • Cichon, Sven;
    • Nöthen, Markus M.;
    • Karypis, George;
    • Kelsoe, John;
    • Greenwood, Tiffany;
    • Nievergelt, Caroline;
    • Shilling, Paul;
    • Shekhtman, Tatyana;
    • Edenberg, Howard;
    • Craig, David
    Publication type:
    Article
    17

    Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles.

    Published in:
    Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02228-x
    By:
    • Oraki Kohshour, Mojtaba;
    • Kannaiyan, Nirmal R.;
    • Falk, August Jernbom;
    • Papiol, Sergi;
    • Heilbronner, Urs;
    • Budde, Monika;
    • Kalman, Janos L.;
    • Schulte, Eva C.;
    • Rietschel, Marcella;
    • Witt, Stephanie;
    • Forstner, Andreas J.;
    • Heilmann-Heimbach, Stefanie;
    • Nöthen, Markus M.;
    • Spitzer, Carsten;
    • Malchow, Berend;
    • Müller, Thorsten;
    • Wiltfang, Jens;
    • Falkai, Peter;
    • Schmitt, Andrea;
    • Rossner, Moritz J.
    Publication type:
    Article
    18

    Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum.

    Published in:
    Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01959-1
    By:
    • Zillich, Lea;
    • Poisel, Eric;
    • Frank, Josef;
    • Foo, Jerome C.;
    • Friske, Marion M.;
    • Streit, Fabian;
    • Sirignano, Lea;
    • Heilmann-Heimbach, Stefanie;
    • Heimbach, André;
    • Hoffmann, Per;
    • Degenhardt, Franziska;
    • Hansson, Anita C.;
    • Bakalkin, Georgy;
    • Nöthen, Markus M.;
    • Rietschel, Marcella;
    • Spanagel, Rainer;
    • Witt, Stephanie H.
    Publication type:
    Article
    19

    Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance.

    Published in:
    Blood Cancer Journal, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41408-024-01121-8
    By:
    • Thomsen, Hauke;
    • Chattopadhyay, Subhayan;
    • Weinhold, Niels;
    • Vodicka, Pavel;
    • Vodickova, Ludmila;
    • Hoffmann, Per;
    • Nöthen, Markus M.;
    • Jöckel, Karl-Heinz;
    • Schmidt, Börge;
    • Hajek, Roman;
    • Hallmans, Göran;
    • Pettersson-Kymmer, Ulrika;
    • Späth, Florentin;
    • Goldschmidt, Hartmut;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
    20

    Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6.

    Published in:
    2022
    By:
    • Clay-Gilmour, Alyssa;
    • Chattopadhyay, Subhayan;
    • Hildebrandt, Michelle A. T.;
    • Thomsen, Hauke;
    • Weinhold, Niels;
    • Vodicka, Pavel;
    • Vodickova, Ludmila;
    • Hoffmann, Per;
    • Nöthen, Markus M.;
    • Jöckel, Karl-Heinz;
    • Schmidt, Börge;
    • Langer, Christian;
    • Hajek, Roman;
    • Hallmans, Göran;
    • Pettersson-Kymmer, Ulrika;
    • Ohlsson, Claes;
    • Späth, Florentin;
    • Houlston, Richard;
    • Goldschmidt, Hartmut;
    • Manasanch, Elisabet E.
    Publication type:
    Letter
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    Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.

    Published in:
    Journal of Human Genetics, 2015, v. 60, n. 7, p. 399, doi. 10.1038/jhg.2015.37
    By:
    • Matsson, Hans;
    • Huss, Mikael;
    • Persson, Helena;
    • Einarsdottir, Elisabet;
    • Tiraboschi, Ettore;
    • Nopola-Hemmi, Jaana;
    • Schumacher, Johannes;
    • Neuhoff, Nina;
    • Warnke, Andreas;
    • Lyytinen, Heikki;
    • Schulte-Körne, Gert;
    • Nöthen, Markus M;
    • Leppänen, Paavo HT;
    • Peyrard-Janvid, Myriam;
    • Kere, Juha
    Publication type:
    Article
    24

    A New Intervention for Implementation of Pharmacogenetics in Psychiatry: A Description of the PSY-PGx Clinical Study.

    Published in:
    Pharmaceuticals (14248247), 2024, v. 17, n. 2, p. 151, doi. 10.3390/ph17020151
    By:
    • Pelgrim, Teuntje A. D.;
    • Philipsen, Alexandra;
    • Young, Allan H.;
    • Juruena, Mario;
    • Jimenez, Ester;
    • Vieta, Eduard;
    • Jukić, Marin;
    • Van der Eycken, Erik;
    • Heilbronner, Urs;
    • Moldovan, Ramona;
    • Kas, Martien J. H.;
    • Jagesar, Raj R.;
    • Nöthen, Markus M.;
    • Hoffmann, Per;
    • Shomron, Noam;
    • Kilarski, Laura L.;
    • van Amelsvoort, Thérèse;
    • Campforts, Bea;
    • van Westrhenen, Roos
    Publication type:
    Article
    25
    26

    Genetic determination of human facial morphology: links between cleft-lips and normal variation.

    Published in:
    European Journal of Human Genetics, 2011, v. 19, n. 11, p. 1192, doi. 10.1038/ejhg.2011.110
    By:
    • Boehringer, Stefan;
    • van der Lijn, Fedde;
    • Liu, Fan;
    • Günther, Manuel;
    • Sinigerova, Stella;
    • Nowak, Stefanie;
    • Ludwig, Kerstin U;
    • Herberz, Ruth;
    • Klein, Stefan;
    • Hofman, Albert;
    • Uitterlinden, Andre G;
    • Niessen, Wiro J;
    • Breteler, Monique M B;
    • van der Lugt, Aad;
    • Würtz, Rolf P;
    • Nöthen, Markus M;
    • Horsthemke, Bernhard;
    • Wieczorek, Dagmar;
    • Mangold, Elisabeth;
    • Kayser, Manfred
    Publication type:
    Article
    27

    Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.

    Published in:
    European Journal of Human Genetics, 2011, v. 19, n. 11, p. 1161, doi. 10.1038/ejhg.2011.98
    By:
    • Abou Jamra, R;
    • Wohlfart, Sigrun;
    • Zweier, Markus;
    • Uebe, Steffen;
    • Priebe, Lutz;
    • Ekici, Arif;
    • Giesebrecht, Susanne;
    • Abboud, Ahmad;
    • Al Khateeb, Mohammed Ayman;
    • Fakher, Mahmoud;
    • Hamdan, Saber;
    • Ismael, Amina;
    • Muhammad, Safia;
    • Nöthen, Markus M;
    • Schumacher, Johannes;
    • Reis, André
    Publication type:
    Article
    28
    29

    Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study.

    Published in:
    European Journal of Human Genetics, 2004, v. 12, n. 5, p. 377, doi. 10.1038/sj.ejhg.5201149
    By:
    • Mendlewicz, Julien;
    • Massat, Isabelle;
    • Souery, Daniel;
    • Del-Favero, Jurgen;
    • Oruč, Lilijana;
    • Nöthen, Markus M.;
    • Blackwood, Douglas;
    • Muir, Walter;
    • Battersby, Sharon;
    • Lerer, Beny;
    • Segman, Ronen H.;
    • Kaneva, Radka;
    • Serretti, Alessandro;
    • Lilli, Roberta;
    • Lorenzi, Christian;
    • Jacovljevič, Miro;
    • Ivezič, Sladana;
    • Rietschel, Marcella;
    • Milanova, Vihra
    Publication type:
    Article
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    Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
    By:
    • Broderick, Peter;
    • Chubb, Daniel;
    • Johnson, David C;
    • Weinhold, Niels;
    • Försti, Asta;
    • Lloyd, Amy;
    • Olver, Bianca;
    • Ma, Yussanne P;
    • Dobbins, Sara E;
    • Walker, Brian A;
    • Davies, Faith E;
    • Gregory, Walter A;
    • Child, J Anthony;
    • Ross, Fiona M;
    • Jackson, Graham H;
    • Neben, Kai;
    • Jauch, Anna;
    • Hoffmann, Per;
    • Mühleisen, Thomas W;
    • Nöthen, Markus M
    Publication type:
    Article
    34

    Common variation at 10p12.31 near MLLT10 influences meningioma risk.

    Published in:
    Nature Genetics, 2011, v. 43, n. 9, p. 825, doi. 10.1038/ng.879
    By:
    • Dobbins, Sara E.;
    • Broderick, Peter;
    • Melin, Beatrice;
    • Feychting, Maria;
    • Johansen, Christoffer;
    • Andersson, Ulrika;
    • Brännström, Thomas;
    • Schramm, Johannes;
    • Olver, Bianca;
    • Lloyd, Amy;
    • Ma, Yussanne P;
    • Hosking, Fay J.;
    • Lönn, Stefan;
    • Ahlbom, Anders;
    • Henriksson, Roger;
    • Schoemaker, Minouk J.;
    • Hepworth, Sarah J.;
    • Hoffmann, Per;
    • Mühleisen, Thomas W.;
    • Nöthen, Markus M.
    Publication type:
    Article
    35
    36

    Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

    Published in:
    Nature Genetics, 2010, v. 42, n. 2, p. 128, doi. 10.1038/ng.523
    By:
    • McMahon, Francis J.;
    • Akula, Nirmala;
    • Schulze, Thomas G.;
    • Muglia, Pierandrea;
    • Tozzi, Federica;
    • Detera-Wadleigh, Sevilla D.;
    • Steele, C. J. M.;
    • Breuer, René;
    • Strohmaier, Jana;
    • Wendland, Jens R.;
    • Mattheisen, Manuel;
    • Mühleisen, Thomas W.;
    • Maier, Wolfgang;
    • Nöthen, Markus M.;
    • Cichon, Sven;
    • Farmer, Anne;
    • Vincent, John B.;
    • Holsboer, Florian;
    • Preisig, Martin;
    • Rietschel, Marcella
    Publication type:
    Article
    37
    38

    Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.

    Published in:
    Nature Genetics, 2009, v. 41, n. 2, p. 228, doi. 10.1038/ng.276
    By:
    • Yaran Wen;
    • Yang Liu;
    • Yiming Xu;
    • Yiwei Zhao;
    • Rui Hua;
    • Kaibo Wang;
    • Miao Sun;
    • Yuanhong Li;
    • Sen Yang;
    • Xue-Jun Zhang;
    • Kruse, Roland;
    • Cichon, Sven;
    • Betz, Regina C.;
    • Nöthen, Markus M.;
    • van Steensel, Maurice A. M.;
    • van Geel, Michel;
    • Steijlen, Peter M.;
    • Hohl, Daniel;
    • Huber, Marcel;
    • Dunnill, Giles S.
    Publication type:
    Article
    39
    40

    Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.

    Published in:
    Nature Genetics, 2001, v. 28, n. 3, p. 218, doi. 10.1038/90050
    By:
    • Betz, Regina C.;
    • Schoser, Benedikt G. H.;
    • Kasper, Dagmar;
    • Ricker, Kenneth;
    • Ramírez, Alfredo;
    • Stein, Valentin;
    • Torbergsen, Torberg;
    • Lee, Young-Ae;
    • Nöthen, Markus M.;
    • Wienker, Thomas F.;
    • Malin, Jean-Pierre;
    • Propping, Peter;
    • Reis, André;
    • Mortier, Wilhelm;
    • Jentsch, Thomas J.;
    • Vorgerd, Matthias;
    • Kubisch, Christian
    Publication type:
    Article
    41

    High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.

    Published in:
    2016
    By:
    • Rivera, Natalia V.;
    • Ronninger, Marcus;
    • Shchetynsky, Klementy;
    • Franke, Andre;
    • Nöthen, Markus M.;
    • Müller-Quernheim, Joachim;
    • Schreiber, Stefan;
    • Adrianto, Indra;
    • Karakaya, Bekir;
    • van Moorsel, Coline H. M.;
    • Navratilova, Zdenka;
    • Kolek, Vitezslav;
    • Rybicki, Benjamin A.;
    • Iannuzzi, Michael C.;
    • Petrek, Martin;
    • Grutters, Jan C.;
    • Montgomery, Courtney;
    • Fischer, Annegret;
    • Eklund, Anders;
    • Padyukov, Leonid
    Publication type:
    journal article
    42

    Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.

    Published in:
    2015
    By:
    • Fischer, Annegret;
    • Ellinghaus, David;
    • Nutsua, Marcel;
    • Hofmann, Sylvia;
    • Montgomery, Courtney G.;
    • Iannuzzi, Michael C.;
    • Rybicki, Benjamin A.;
    • Petrek, Martin;
    • Mrazek, Frantisek;
    • Pabst, Stefan;
    • Grohé, Christian;
    • Grunewald, Johan;
    • Ronninger, Marcus;
    • Eklund, Anders;
    • Padyukov, Leonid;
    • Mihailovic-Vucinic, Violeta;
    • Jovanovic, Dragana;
    • Sterclova, Martina;
    • Homolka, Jiri;
    • Nöthen, Markus M.
    Publication type:
    journal article
    43

    Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005024
    By:
    • Draaken, Markus;
    • Knapp, Michael;
    • Pennimpede, Tracie;
    • Schmidt, Johanna M.;
    • Ebert, Anne-Karolin;
    • Rösch, Wolfgang;
    • Stein, Raimund;
    • Utsch, Boris;
    • Hirsch, Karin;
    • Boemers, Thomas M.;
    • Mangold, Elisabeth;
    • Heilmann, Stefanie;
    • Ludwig, Kerstin U.;
    • Jenetzky, Ekkehart;
    • Zwink, Nadine;
    • Moebus, Susanne;
    • Herrmann, Bernhard G.;
    • Mattheisen, Manuel;
    • Nöthen, Markus M.;
    • Ludwig, Michael
    Publication type:
    Article
    44
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    Deeplasia: deep learning for bone age assessment validated on skeletal dysplasias.

    Published in:
    Pediatric Radiology, 2024, v. 54, n. 1, p. 82, doi. 10.1007/s00247-023-05789-1
    By:
    • Rassmann, Sebastian;
    • Keller, Alexandra;
    • Skaf, Kyra;
    • Hustinx, Alexander;
    • Gausche, Ruth;
    • Ibarra-Arrelano, Miguel A.;
    • Hsieh, Tzung-Chien;
    • Madajieu, Yolande E. D.;
    • Nöthen, Markus M.;
    • Pfäffle, Roland;
    • Attenberger, Ulrike I.;
    • Born, Mark;
    • Mohnike, Klaus;
    • Krawitz, Peter M.;
    • Javanmardi, Behnam
    Publication type:
    Article
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