Found: 55

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  • Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.

    Published in:
    Addiction Biology, 2012, v. 17, n. 1, p. 171, doi. 10.1111/j.1369-1600.2011.00395.x
    By:
    • Frank, Josef;
    • Cichon, Sven;
    • Treutlein, Jens;
    • Ridinger, Monika;
    • Mattheisen, Manuel;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Wodarz, Norbert;
    • Soyka, Michael;
    • Zill, Peter;
    • Maier, Wolfgang;
    • Mössner, Rainald;
    • Gaebel, Wolfgang;
    • Dahmen, Norbert;
    • Scherbaum, Norbert;
    • Schmäl, Christine;
    • Steffens, Michael;
    • Lucae, Susanne;
    • Ising, Marcus;
    • Müller-Myhsok, Bertram
    Publication type:
    Article

  • Genetic factors influencing a neurobiological substrate for psychiatric disorders.

    Published in:
    Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01317-7
    By:
    • Andlauer, Till F. M.;
    • Mühleisen, Thomas W.;
    • Hoffstaedter, Felix;
    • Teumer, Alexander;
    • Wittfeld, Katharina;
    • Teuber, Anja;
    • Reinbold, Céline S.;
    • Grotegerd, Dominik;
    • Bülow, Robin;
    • Caspers, Svenja;
    • Dannlowski, Udo;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Kircher, Tilo;
    • Minnerup, Heike;
    • Moebus, Susanne;
    • Nenadić, Igor;
    • Teismann, Henning;
    • Völker, Uwe;
    • Etkin, Amit
    Publication type:
    Article

  • Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families.

    Published in:
    Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01146-0
    By:
    • Guzman-Parra, Jose;
    • Streit, Fabian;
    • Forstner, Andreas J.;
    • Strohmaier, Jana;
    • González, Maria José;
    • Gil Flores, Susana;
    • Cabaleiro Fabeiro, Francisco J.;
    • del Río Noriega, Francisco;
    • Perez Perez, Fermin;
    • Haro González, Jesus;
    • Orozco Diaz, Guillermo;
    • de Diego-Otero, Yolanda;
    • Moreno-Kustner, Berta;
    • Auburger, Georg;
    • Degenhardt, Franziska;
    • Heilmann-Heimbach, Stefanie;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Frank, Josef;
    • Foo, Jerome C.
    Publication type:
    Article

  • Investigation of the role of TCF4 rare sequence variants in schizophrenia.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 5, p. 354, doi. 10.1002/ajmg.b.32318
    By:
    • Basmanav, F. Buket;
    • Forstner, Andreas J.;
    • Fier, Heide;
    • Herms, Stefan;
    • Meier, Sandra;
    • Degenhardt, Franziska;
    • Hoffmann, Per;
    • Barth, Sandra;
    • Fricker, Nadine;
    • Strohmaier, Jana;
    • Witt, Stephanie H.;
    • Ludwig, Michael;
    • Schmael, Christine;
    • Moebus, Susanne;
    • Maier, Wolfgang;
    • Mössner, Rainald;
    • Rujescu, Dan;
    • Rietschel, Marcella;
    • Lange, Christoph;
    • Nöthen, Markus M.
    Publication type:
    Article

  • Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 263, doi. 10.1002/ajmg.b.32034
    By:
    • Degenhardt, Franziska;
    • Priebe, Lutz;
    • Herms, Stefan;
    • Mattheisen, Manuel;
    • Mühleisen, Thomas W.;
    • Meier, Sandra;
    • Moebus, Susanne;
    • Strohmaier, Jana;
    • Groß, Magdalena;
    • Breuer, René;
    • Lange, Christoph;
    • Hoffmann, Per;
    • Meyer-Lindenberg, Andreas;
    • Heinz, Andreas;
    • Walter, Henrik;
    • Lucae, Susanne;
    • Wolf, Christiane;
    • Müller-Myhsok, Bertram;
    • Holsboer, Florian;
    • Maier, Wolfgang
    Publication type:
    Article

  • Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 968, doi. 10.1038/ng.2360
    By:
    • Ludwig, Kerstin U;
    • Mangold, Elisabeth;
    • Herms, Stefan;
    • Nowak, Stefanie;
    • Reutter, Heiko;
    • Paul, Anna;
    • Becker, Jessica;
    • Herberz, Ruth;
    • AlChawa, Taofik;
    • Nasser, Entessar;
    • Böhmer, Anne C;
    • Mattheisen, Manuel;
    • Alblas, Margrieta A;
    • Barth, Sandra;
    • Kluck, Nadine;
    • Lauster, Carola;
    • Braumann, Bert;
    • Reich, Rudolf H;
    • Hemprich, Alexander;
    • Pötzsch, Simone
    Publication type:
    Article

  • Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.

    Published in:
    Nature Genetics, 2010, v. 42, n. 1, p. 24, doi. 10.1038/ng.506
    By:
    • Mangold, Elisabeth;
    • Ludwig, Kerstin U.;
    • Birnbaum, Stefanie;
    • Baluardo, Carlotta;
    • Ferrian, Melissa;
    • Herms, Stefan;
    • Reutter, Heiko;
    • de Assis, Nilma Almeida;
    • Al Chawa, Taofik;
    • Mattheisen, Manuel;
    • Steffens, Michael;
    • Barth, Sandra;
    • Kluck, Nadine;
    • Paul, Anna;
    • Becker, Jessica;
    • Lauster, Carola;
    • Schmidt, Gül;
    • Braumann, Bert;
    • Scheer, Martin;
    • Reich, Rudolf H.
    Publication type:
    Article

  • Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

    Published in:
    Nature Genetics, 2009, v. 41, n. 4, p. 473, doi. 10.1038/ng.333
    By:
    • Birnbaum, Stefanie;
    • Ludwig, Kerstin U.;
    • Reutter, Heiko;
    • Herms, Stefan;
    • Steffens, Michael;
    • Rubini, Michele;
    • Baluardo, Carlotta;
    • Ferrian, Melissa;
    • Almeida de Assis, Nilma;
    • Alblas, Margrieta A.;
    • Barth, Sandra;
    • Freudenberg, Jan;
    • Lauster, Carola;
    • Schmidt, Gül;
    • Scheer, Martin;
    • Braumann, Bert;
    • Bergé, Stefaan J.;
    • Reich, Rudolf H.;
    • Schiefke, Franziska;
    • Hemprich, Alexander
    Publication type:
    Article

  • Susceptibility variants for male-pattern baldness on chromosome 20p11.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1279, doi. 10.1038/ng.228
    By:
    • Hillmer, Axel M;
    • Brockschmit, Felix F;
    • Hanneken, Sandra;
    • Eigelshoven, Sibylle;
    • Steffens, Michael;
    • Flaquer, Antonia;
    • Herms, Stefan;
    • Becker, Tim;
    • Kortüm, Anne-Katrin;
    • Nyholt, Dale R;
    • Zhao, Zhen Zhen;
    • Montgomery, Grant W;
    • Martin, Nicholas G;
    • Mühleisen, Thomas W;
    • Alblas, Margrieta A;
    • Moebus, Susanne;
    • Jöckel, Karl-Heinz;
    • Bröcker-Preuss, Martina;
    • Erbel, Raimund;
    • Reinartz, Roman
    Publication type:
    Article

  • Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk.

    Published in:
    2014
    By:
    • Figlioli, Gisella;
    • Köhler, Aleksandra;
    • Chen, Bowang;
    • Elisei, Rossella;
    • Romei, Cristina;
    • Cipollini, Monica;
    • Cristaudo, Alfonso;
    • Bambi, Franco;
    • Paolicchi, Elisa;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Kalemba, Michal;
    • Kula, Dorota;
    • Pastor, Susana;
    • Marcos, Ricard;
    • Velázquez, Antonia;
    • Jarzb, Barbara;
    • Landi, Stefano;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    journal article

  • Genome-wide association study on differentiated thyroid cancer.

    Published in:
    2013
    By:
    • Köhler, Aleksandra;
    • Chen, Bowang;
    • Gemignani, Federica;
    • Elisei, Rossella;
    • Romei, Cristina;
    • Figlioli, Gisella;
    • Cipollini, Monica;
    • Cristaudo, Alfonso;
    • Bambi, Franco;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Kalemba, Michal;
    • Kula, Dorota;
    • Harris, Shelley;
    • Broderick, Peter;
    • Houlston, Richard;
    • Pastor, Susana;
    • Marcos, Ricard;
    • Velázquez, Antonia;
    • Jarzab, Barbara
    Publication type:
    Journal Article

  • Small molecules enable highly efficient neuronal conversion of human fibroblasts.

    Published in:
    Nature Methods, 2012, v. 9, n. 6, p. 575, doi. 10.1038/nmeth.1972
    By:
    • Ladewig, Julia;
    • Mertens, Jerome;
    • Kesavan, Jaideep;
    • Doerr, Jonas;
    • Poppe, Daniel;
    • Glaue, Finnja;
    • Herms, Stefan;
    • Wernet, Peter;
    • Kögler, Gesine;
    • Müller, Franz-Josef;
    • Koch, Philipp;
    • Brüstle, Oliver
    Publication type:
    Article

  • 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

  • Inbreeding and homozygosity in breast cancer survival.

    Published in:
    Scientific Reports, 2015, p. 16467, doi. 10.1038/srep16467
    By:
    • Thomsen, Hauke;
    • Filho, Miguel Inacio da Silva;
    • Woltmann, Andrea;
    • Johansson, Robert;
    • Eyfjörd, Jorunn E.;
    • Hamann, Ute;
    • Manjer, Jonas;
    • Enquist-Olsson, Kerstin;
    • Henriksson, Roger;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Chen, Bowang;
    • Huhn, Stefanie;
    • Hemminki, Kari;
    • Lenner, Per;
    • Försti, Asta
    Publication type:
    Article

  • Systematic Pathway Enrichment Analysis of a Genome-Wide Association Study on Breast Cancer Survival Reveals an Influence of Genes Involved in Cell Adhesion and Calcium Signaling on the Patients’ Clinical Outcome.

    Published in:
    PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0098229
    By:
    • Woltmann, Andrea;
    • Chen, Bowang;
    • Lascorz, Jesús;
    • Johansson, Robert;
    • Eyfjörd, Jorunn E.;
    • Hamann, Ute;
    • Manjer, Jonas;
    • Enquist-Olsson, Kerstin;
    • Henriksson, Roger;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Hemminki, Kari;
    • Lenner, Per;
    • Försti, Asta
    Publication type:
    Article

  • Copy Number Variants in German Patients with Schizophrenia.

    Published in:
    PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0064035
    By:
    • Priebe, Lutz;
    • Degenhardt, Franziska;
    • Strohmaier, Jana;
    • Breuer, René;
    • Herms, Stefan;
    • Witt, Stephanie H.;
    • Hoffmann, Per;
    • Kulbida, Rebecca;
    • Mattheisen, Manuel;
    • Moebus, Susanne;
    • Meyer-Lindenberg, Andreas;
    • Walter, Henrik;
    • Mössner, Rainald;
    • Nenadic, Igor;
    • Sauer, Heinrich;
    • Rujescu, Dan;
    • Maier, Wolfgang;
    • Rietschel, Marcella;
    • Nöthen, Markus M.;
    • Cichon, Sven
    Publication type:
    Article

  • Research Paper. Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.

    Published in:
    Journal of Psychiatry & Neuroscience, 2014, v. 39, n. 6, p. 386, doi. 10.1503/jpn.130189
    By:
    • Forstner, Andreas J.;
    • Basmanav, F. Buket;
    • Mattheisen, Manuel;
    • Böhmer, Anne C.;
    • Hollegaard, Mads V.;
    • Janson, Esther;
    • Strengman, Eric;
    • Priebe, Lutz;
    • Degenhardt, Franziska;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Maier, Wolfgang;
    • Mössner, Rainald;
    • Rujescu, Dan;
    • Ophoff, Roel A.;
    • Moebus, Susanne;
    • Mortensen, Preben B.;
    • Børglum, Anders D.;
    • Hougaard, David M.;
    • Frank, Josef
    Publication type:
    Article

  • Runs of homozygosity and inbreeding in thyroid cancer.

    Published in:
    2016
    By:
    • Thomsen, Hauke;
    • Chen, Bowang;
    • Figlioli, Gisella;
    • Elisei, Rossella;
    • Romei, Cristina;
    • Cipollini, Monica;
    • Cristaudo, Alfonso;
    • Bambi, Franco;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Landi, Stefano;
    • Hemminki, Kari;
    • Gemignani, Federica;
    • Försti, Asta
    Publication type:
    journal article

  • Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness.

    Published in:
    Human Genetics, 2009, v. 126, n. 2, p. 255, doi. 10.1007/s00439-009-0668-z
    By:
    • Hillmer, Axel M.;
    • Freudenberg, Jan;
    • Myles, Sean;
    • Herms, Stefan;
    • Tang, Kun;
    • Hughes, David A.;
    • Brockschmidt, Felix F.;
    • Yijun Ruan;
    • Stoneking, Mark;
    • Nöthen, Markus M.
    Publication type:
    Article

  • Genetic and functional analyses implicate microRNA 499A in bipolar disorder development.

    Published in:
    Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02176-6
    By:
    • Tielke, Aileen;
    • Martins, Helena;
    • Pelzl, Michael A.;
    • Maaser-Hecker, Anna;
    • David, Friederike S.;
    • Reinbold, Céline S.;
    • Streit, Fabian;
    • Sirignano, Lea;
    • Schwarz, Markus;
    • Vedder, Helmut;
    • Kammerer-Ciernioch, Jutta;
    • Albus, Margot;
    • Borrmann-Hassenbach, Margitta;
    • Hautzinger, Martin;
    • Hünten, Karola;
    • Degenhardt, Franziska;
    • Fischer, Sascha B.;
    • Beins, Eva C.;
    • Herms, Stefan;
    • Hoffmann, Per
    Publication type:
    Article

  • Polygenic risk scores across the extended psychosis spectrum.

    Published in:
    Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01720-0
    By:
    • Smigielski, Lukasz;
    • Papiol, Sergi;
    • Theodoridou, Anastasia;
    • Heekeren, Karsten;
    • Gerstenberg, Miriam;
    • Wotruba, Diana;
    • Buechler, Roman;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Adorjan, Kristina;
    • Anderson-Schmidt, Heike;
    • Budde, Monika;
    • Comes, Ashley L.;
    • Gade, Katrin;
    • Heilbronner, Maria;
    • Heilbronner, Urs;
    • Kalman, Janos L.;
    • Klöhn-Saghatolislam, Farahnaz;
    • Reich-Erkelenz, Daniela;
    • Schaupp, Sabrina K.
    Publication type:
    Article

  • 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

  • IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.

    Published in:
    European Journal of Oral Sciences, 2009, v. 117, n. 6, p. 766, doi. 10.1111/j.1600-0722.2009.00680.x
    By:
    • Birnbaum, Stefanie;
    • Ludwig, Kerstin U.;
    • Reutter, Heiko;
    • Herms, Stefan;
    • De Assis, Nilma A.;
    • Diaz‐Lacava, Amalia;
    • Barth, Sandra;
    • Lauster, Carola;
    • Schmidt, Gül;
    • Scheer, Martin;
    • Saffar, Mitra;
    • Martini, Markus;
    • Reich, Rudolf H.;
    • Schiefke, Franziska;
    • Hemprich, Alexander;
    • Pötzsch, Simone;
    • Pötzsch, Bernd;
    • Wienker, Thomas F.;
    • Hoffmann, Per;
    • Knapp, Michael
    Publication type:
    Article

  • Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.

    Published in:
    European Journal of Oral Sciences, 2009, v. 117, n. 2, p. 200, doi. 10.1111/j.1600-0722.2008.00604.x
    By:
    • Birnbaum, Stefanie;
    • Reutter, Heiko;
    • Mende, Meinhard;
    • De Assis, Nilma A.;
    • Diaz‐Lacava, Amalia;
    • Herms, Stefan;
    • Scheer, Martin;
    • Lauster, Carola;
    • Braumann, Bert;
    • Schmidt, Gül;
    • Martini, Markus;
    • Hemprich, Alexander;
    • Pötzsch, Simone;
    • Knapp, Michael;
    • Nöthen, Markus M.;
    • Kramer, Franz‐Josef;
    • Mangold, Elisabeth
    Publication type:
    Article

  • Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.

    Published in:
    European Journal of Human Genetics, 2015, v. 23, n. 6, p. 824, doi. 10.1038/ejhg.2014.184
    By:
    • Thomsen, Hauke;
    • da Silva Filho, Miguel Inacio;
    • Försti, Asta;
    • Fuchs, Michael;
    • Ponader, Sabine;
    • von Strandmann, Elke Pogge;
    • Eisele, Lewin;
    • Herms, Stefan;
    • Hofmann, Per;
    • Sundquist, Jan;
    • Engert, Andreas;
    • Hemminki, Kari
    Publication type:
    Article

  • Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome.

    Published in:
    Breast Cancer Research & Treatment, 2011, v. 130, n. 3, p. 905, doi. 10.1007/s10549-011-1600-5
    By:
    • Shi, Hong;
    • Bevier, Melanie;
    • Johansson, Robert;
    • Grzybowska, Ewa;
    • Chen, Bowang;
    • Eyfjörd, Jorunn;
    • Hamann, Ute;
    • Manjer, Jonas;
    • Enquist, Kerstin;
    • Henriksson, Roger;
    • Carlson, Joyce;
    • Brandt, Andreas;
    • Lascorz, Jesús;
    • Butkiewicz, Dorota;
    • Pamula-Pilat, Jolanta;
    • Tecza, Karolina;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Hemminki, Kari;
    • Lenner, Per
    Publication type:
    Article

  • XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans.

    Published in:
    Neuropsychopharmacology, 2015, v. 40, n. 2, p. 361, doi. 10.1038/npp.2014.178
    By:
    • Juraeva, Dilafruz;
    • Treutlein, Jens;
    • Scholz, Henrike;
    • Frank, Josef;
    • Degenhardt, Franziska;
    • Cichon, Sven;
    • Ridinger, Monika;
    • Mattheisen, Manuel;
    • Witt, Stephanie H;
    • Lang, Maren;
    • Sommer, Wolfgang H;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Wodarz, Norbert;
    • Soyka, Michael;
    • Zill, Peter;
    • Maier, Wolfgang;
    • Jünger, Elisabeth;
    • Gaebel, Wolfgang;
    • Dahmen, Norbert
    Publication type:
    Article

  • 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

  • Acquisition of chromosome 1q duplication in parental and genome‐edited human‐induced pluripotent stem cell‐derived neural stem cells results in their higher proliferation rate in vitro and in vivo.

    Published in:
    Cell Proliferation, 2020, v. 53, n. 10, p. 1, doi. 10.1111/cpr.12892
    By:
    • Mehrjardi, Narges Zare;
    • Molcanyi, Marek;
    • Hatay, Firuze Fulya;
    • Timmer, Marco;
    • Shahbazi, Ebrahim;
    • Ackermann, Justus P.;
    • Herms, Stefan;
    • Heilmann‐Heimbach, Stefanie;
    • Wunderlich, Thomas F.;
    • Prochnow, Nora;
    • Haghikia, Aiden;
    • Lampert, Angelika;
    • Hescheler, Jürgen;
    • Neugebauer, Edmund A. M.;
    • Baharvand, Hossein;
    • Šarić, Tomo
    Publication type:
    Article

  • HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum.

    Published in:
    Birth Defects Research, 2019, v. 111, n. 10, p. 591, doi. 10.1002/bdr2.1493
    By:
    • Kause, Franziska;
    • Zhang, Rong;
    • Ludwig, Michael;
    • Schmiedeke, Eberhard;
    • Rissmann, Anke;
    • Thiele, Holger;
    • Altmueller, Janine;
    • Herms, Stefan;
    • Hilger, Alina C.;
    • Hildebrandt, Friedhelm;
    • Reutter, Heiko
    Publication type:
    Article

  • Genome-wide association study identifies multiple susceptibility loci for glioma.

    Published in:
    Nature Communications, 2015, v. 6, n. 10, p. 8559, doi. 10.1038/ncomms9559
    By:
    • Kinnersley, Ben;
    • Labussière, Marianne;
    • Holroyd, Amy;
    • Di Stefano, Anna-Luisa;
    • Broderick, Peter;
    • Vijayakrishnan, Jayaram;
    • Mokhtari, Karima;
    • Delattre, Jean-Yves;
    • Gousias, Konstantinos;
    • Schramm, Johannes;
    • Schoemaker, Minouk J.;
    • Fleming, Sarah J.;
    • Herms, Stefan;
    • Heilmann, Stefanie;
    • Schreiber, Stefan;
    • Wichmann, Heinz-Erich;
    • Nöthen, Markus M.;
    • Swerdlow, Anthony;
    • Lathrop, Mark;
    • Simon, Matthias
    Publication type:
    Article

  • Genome-wide association study reveals two new risk loci for bipolar disorder.

    Published in:
    Nature Communications, 2014, v. 5, n. 3, p. 3339, doi. 10.1038/ncomms4339
    By:
    • Mühleisen, Thomas W.;
    • Leber, Markus;
    • Schulze, Thomas G.;
    • Strohmaier, Jana;
    • Degenhardt, Franziska;
    • Treutlein, Jens;
    • Mattheisen, Manuel;
    • Forstner, Andreas J.;
    • Schumacher, Johannes;
    • Breuer, René;
    • Meier, Sandra;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Lacour, André;
    • Witt, Stephanie H.;
    • Reif, Andreas;
    • Müller-Myhsok, Bertram;
    • Lucae, Susanne;
    • Maier, Wolfgang;
    • Schwarz, Markus
    Publication type:
    Article

  • Gene expression is stable in a complete CIB1 knockout keratinocyte model.

    Published in:
    Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71889-9
    By:
    • Imahorn, Elias;
    • Aushev, Magomet;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Cichon, Sven;
    • Reichelt, Julia;
    • Itin, Peter H.;
    • Burger, Bettina
    Publication type:
    Article

  • 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 22, p. 6069, doi. 10.1093/hmg/ddu306
    By:
    • Reinthaler, Eva M.;
    • Lal, Dennis;
    • Lebon, Sebastien;
    • Hildebrand, Michael S.;
    • Dahl, Hans-Henrik M.;
    • Regan, Brigid M.;
    • Feucht, Martha;
    • Steinböck, Hannelore;
    • Neophytou, Birgit;
    • Ronen, Gabriel M.;
    • Roche, Laurian;
    • Gruber-Sedlmayr, Ursula;
    • Geldner, Julia;
    • Haberlandt, Edda;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Gieger, Christian;
    • Waldenberger, Melanie;
    • Franke, Andre;
    • Wittig, Michael
    Publication type:
    Article

  • Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.

    Published in:
    Cerebral Cortex, 2020, v. 30, n. 2, p. 801, doi. 10.1093/cercor/bhz127
    By:
    • Caspers, Svenja;
    • Röckner, Melanie E;
    • Jockwitz, Christiane;
    • Bittner, Nora;
    • Teumer, Alexander;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Nöthen, Markus M;
    • Moebus, Susanne;
    • Amunts, Katrin;
    • Cichon, Sven;
    • Mühleisen, Thomas W
    Publication type:
    Article

  • Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.

    Published in:
    International Journal of Cancer, 2018, v. 143, n. 11, p. 2800, doi. 10.1002/ijc.31725
    By:
    • Kayser, Katrin;
    • Degenhardt, Franziska;
    • Holzapfel, Stefanie;
    • Horpaopan, Sukanya;
    • Peters, Sophia;
    • Spier, Isabel;
    • Morak, Monika;
    • Vangala, Deepak;
    • Rahner, Nils;
    • Knebel‐Doeberitz, Magnus;
    • Schackert, Hans K.;
    • Engel, Christoph;
    • Büttner, Reinhard;
    • Wijnen, Juul;
    • Doerks, Tobias;
    • Bork, Peer;
    • Moebus, Susanne;
    • Herms, Stefan;
    • Fischer, Sascha;
    • Hoffmann, Per
    Publication type:
    Article

  • Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate.

    Published in:
    European Journal of Oral Sciences, 2012, v. 120, n. 5, p. 373, doi. 10.1111/j.1600-0722.2012.00991.x
    By:
    • Mangold, Elisabeth;
    • Reutter, Heiko;
    • León‐Cachón, Rafael B. R.;
    • Ludwig, Kerstin U.;
    • Herms, Stefan;
    • Chacón‐Camacho, Óscar;
    • Ortiz‐López, Rocío;
    • Paredes‐Zenteno, Mario;
    • Arizpe‐Cantú, Abelardo;
    • Muñoz‐Jiménez, Sergio G.;
    • Nowak, Stefanie;
    • Kramer, Franz‐Josef;
    • Wienker, Thomas F.;
    • Nöthen, Markus M.;
    • Knapp, Michael;
    • Rojas‐Martínez, Augusto
    Publication type:
    Article

  • Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.

    Published in:
    European Journal of Oral Sciences, 2010, v. 118, n. 3, p. 317, doi. 10.1111/j.1600-0722.2010.00741.x
    By:
    • Nikopensius, Tiit;
    • Birnbaum, Stefanie;
    • Ludwig, Kerstin U.;
    • Jagomägi, Triin;
    • Saag, Mare;
    • Herms, Stefan;
    • Knapp, Michael;
    • Hoffmann, Per;
    • Nöthen, Markus M.;
    • Metspalu, Andres;
    • Mangold, Elisabeth
    Publication type:
    Article

  • Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.

    Published in:
    PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171595
    By:
    • Forstner, Andreas J.;
    • Hecker, Julian;
    • Hofmann, Andrea;
    • Maaser, Anna;
    • Reinbold, Céline S.;
    • Mühleisen, Thomas W.;
    • Leber, Markus;
    • Strohmaier, Jana;
    • Degenhardt, Franziska;
    • Treutlein, Jens;
    • Mattheisen, Manuel;
    • Schumacher, Johannes;
    • Streit, Fabian;
    • Meier, Sandra;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Lacour, André;
    • Witt, Stephanie H.;
    • Reif, Andreas;
    • Müller-Myhsok, Bertram
    Publication type:
    Article

  • Evidence of Inbreeding in Hodgkin Lymphoma.

    Published in:
    PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0154259
    By:
    • Thomsen, Hauke;
    • Inacio da Silva Filho, Miguel;
    • Fuchs, Michael;
    • Ponader, Sabine;
    • Pogge von Strandmann, Elke;
    • Eisele, Lewin;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Engert, Andreas;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article

  • Stimulation of MMP-1 and CCL2 by NAMPT in PDL Cells.

    Published in:
    Mediators of Inflammation, 2013, v. 2013, p. 1, doi. 10.1155/2013/437123
    By:
    • Nokhbehsaim, Marjan;
    • Eick, Sigrun;
    • Vilas Boas Nogueira, Andressa;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Fröhlich, Holger;
    • Jepsen, Søren;
    • Jäger, Andreas;
    • Cirelli, Joni Augusto;
    • Deschner, James
    Publication type:
    Article

  • Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.

    Published in:
    Scientific Reports, 2015, p. 8922, doi. 10.1038/srep08922
    By:
    • Figlioli, Gisella;
    • Chen, Bowang;
    • Elisei, Rossella;
    • Romei, Cristina;
    • Campo, Chiara;
    • Cipollini, Monica;
    • Cristaudo, Alfonso;
    • Bambi, Franco;
    • Paolicchi, Elisa;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Kalemba, Michał;
    • Kula, Dorota;
    • Pastor, Susana;
    • Marcos, Ricard;
    • Velázquez, Antonia;
    • Jarząb, Barbara;
    • Landi, Stefano;
    • Hemminki, Kari;
    • Gemignani, Federica
    Publication type:
    Article

  • Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.

    Published in:
    Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01818-4
    By:
    • Schulz, Herbert;
    • Ruppert, Ann-Kathrin;
    • Herms, Stefan;
    • Wolf, Christiane;
    • Mirza-Schreiber, Nazanin;
    • Stegle, Oliver;
    • Czamara, Darina;
    • Forstner, Andreas J.;
    • Sivalingam, Sugirthan;
    • Schoch, Susanne;
    • Moebus, Susanne;
    • Pütz, Benno;
    • Hillmer, Axel;
    • Fricker, Nadine;
    • Vatter, Hartmut;
    • Müller-Myhsok, Bertram;
    • Nöthen, Markus M.;
    • Becker, Albert J.;
    • Hoffmann, Per;
    • Sander, Thomas
    Publication type:
    Article

  • Evidence for contribution of epigenetic mechanisms in the pathogenesis of systemic mast cell activation disease.

    Published in:
    Immunogenetics, 2014, v. 66, n. 5, p. 287, doi. 10.1007/s00251-014-0768-3
    By:
    • Haenisch, Britta;
    • Fröhlich, Holger;
    • Herms, Stefan;
    • Molderings, Gerhard
    Publication type:
    Article

  • Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients.

    Published in:
    Psychopharmacology, 2024, v. 241, n. 4, p. 727, doi. 10.1007/s00213-023-06505-5
    By:
    • Sakrajda, Kosma;
    • Bilska, Karolina;
    • Czerski, Piotr M.;
    • Narożna, Beata;
    • Dmitrzak-Węglarz, Monika;
    • Heilmann-Heimbach, Stefanie;
    • Brockschmidt, Felix F.;
    • Herms, Stefan;
    • Nöthen, Markus M.;
    • Cichon, Sven;
    • Więckowska, Barbara;
    • Rybakowski, Janusz K.;
    • Pawlak, Joanna;
    • Szczepankiewicz, Aleksandra
    Publication type:
    Article

  • The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 14, p. 2719, doi. 10.1093/hmg/ddp204
    By:
    • Schumacher, Johannes;
    • Laje, Gonzalo;
    • Jamra, Rami Abou;
    • Becker, Tim;
    • Mühleisen, Thomas W.;
    • Vasilescu, Catalina;
    • Mattheisen, Manuel;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Hillmer, Axel M.;
    • Georgi, Alexander;
    • Herold, Christine;
    • Schulze, Thomas G.;
    • Propping, Peter;
    • Rietschel, Marcella;
    • McMahon, Francis J.;
    • Nöthen, Markus M.;
    • Cichon, Sven
    Publication type:
    Article

  • Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study.

    Published in:
    Molecular Autism, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13229-020-00345-2
    By:
    • Krug, Axel;
    • Wöhr, Markus;
    • Seffer, Dominik;
    • Rippberger, Henrike;
    • Sungur, A. Özge;
    • Dietsche, Bruno;
    • Stein, Frederike;
    • Sivalingam, Sugirthan;
    • Forstner, Andreas J.;
    • Witt, Stephanie H.;
    • Dukal, Helene;
    • Streit, Fabian;
    • Maaser, Anna;
    • Heilmann-Heimbach, Stefanie;
    • Andlauer, Till F. M.;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Rietschel, Marcella;
    • Nöthen, Markus M.;
    • Lackinger, Martin
    Publication type:
    Article

  • Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment.

    Published in:
    Science Translational Medicine, 2023, v. 15, n. 705, p. 1, doi. 10.1126/scitranslmed.adg1659
    By:
    • Lechner, Lara;
    • Opitz, Robert;
    • Silver, Matt J.;
    • Krabusch, Philipp M.;
    • Prentice, Andrew M.;
    • Field, Martha S.;
    • Stachelscheid, Harald;
    • Leitão, Elsa;
    • Schröder, Christopher;
    • Fernandez Vallone, Valeria;
    • Horsthemke, Bernhard;
    • Jöckel, Karl-Heinz;
    • Schmidt, Börge;
    • Nöthen, Markus M.;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Kleyn, Patrick W.;
    • Megges, Matthias;
    • Blume-Peytavi, Ulrike;
    • Weiss, Katja
    Publication type:
    Article

  • Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO).

    Published in:
    Genes, 2021, v. 12, n. 9, p. 1449, doi. 10.3390/genes12091449
    By:
    • Schierbaum, Luca M.;
    • Schneider, Sophia;
    • Herms, Stefan;
    • Sivalingam, Sugirthan;
    • Fabian, Julia;
    • Reutter, Heiko;
    • Weber, Stefanie;
    • Merz, Waltraut M.;
    • Tkaczyk, Marcin;
    • Miklaszewska, Monika;
    • Sikora, Przemyslaw;
    • Szmigielska, Agnieszka;
    • Krzemien, Grazyna;
    • Zachwieja, Katarzyna;
    • Szczepanska, Maria;
    • Taranta-Janusz, Katarzyna;
    • Kroll, Pawel;
    • Polok, Marcin;
    • Zaniew, Marcin;
    • Hilger, Alina C.
    Publication type:
    Article

  • Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis.

    Published in:
    Genes, 2017, v. 8, n. 7, p. 183, doi. 10.3390/genes8070183
    By:
    • Treutlein, Jens;
    • Frank, Josef;
    • Streit, Fabian;
    • Reinbold, Céline S.;
    • Juraeva, Dilafruz;
    • Degenhardt, Franziska;
    • Rietschel, Liz;
    • Witt, Stephanie H.;
    • Forstner, Andreas J.;
    • Ridinger, Monika;
    • Strohmaier, Jana;
    • Wodarz, Norbert;
    • Dukal, Helene;
    • Foo, Jerome C.;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Heilmann-Heimbach, Stefanie;
    • Soyka, Michael;
    • Maier, Wolfgang;
    • Gaebel, Wolfgang
    Publication type:
    Article