Works by Nöthen, Markus M.

Results: 228

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

Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.

Published in:

2009

By:

Reutter, Heiko;
Bökenkamp, Arend;
Ebert, Anne-Karolin;
Rösch, Wolfgang;
Boemers, Thomas M.;
Nöthen, Markus M.;
Ludwig, Michael;
Bökenkamp, Arend;
Rösch, Wolfgang;
Nöthen, Markus M

Publication type:

journal article

Genetic and environmental contributions to epigenetic aging across adolescence and young adulthood.

Published in:

Clinical Epigenetics, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13148-025-01880-6

By:

Kuznetsov, Dmitry V.;
Liu, Yixuan;
Schowe, Alicia M.;
Czamara, Darina;
Instinske, Jana;
Pahnke, Charlotte K. L.;
Nöthen, Markus M.;
Spinath, Frank M.;
Binder, Elisabeth B.;
Diewald, Martin;
Forstner, Andreas J.;
Kandler, Christian;
Mönkediek, Bastian

Publication type:

Article

Immunochip analysis identifies association of the RAD50/ IL13 region with human longevity.

Published in:

Aging Cell, 2016, v. 15, n. 3, p. 585, doi. 10.1111/acel.12471

By:

Flachsbart, Friederike;
Ellinghaus, David;
Gentschew, Liljana;
Heinsen, Femke‐Anouska;
Caliebe, Amke;
Christiansen, Lene;
Nygaard, Marianne;
Christensen, Kaare;
Blanché, Hélène;
Deleuze, Jean‐François;
Derbois, Céline;
Galan, Pilar;
Büning, Carsten;
Brand, Stephan;
Peters, Anette;
Strauch, Konstantin;
Müller‐Nurasyid, Martina;
Hoffmann, Per;
Nöthen, Markus M.;
Lieb, Wolfgang

Publication type:

Article

Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia.

Published in:

Experimental Dermatology, 2022, v. 31, n. 6, p. 906, doi. 10.1111/exd.14536

By:

Chew, Elaine G. Y.;
Lim, Tze Chiun;
Leong, Meng Fatt;
Liu, Xingliang;
Sia, Yee Yen;
Leong, See Ting;
Yan‐Jiang, Benjamin C.;
Stoecklin, Celine;
Borhan, Rosa;
Heilmann‐Heimbach, Stefanie;
Nöthen, Markus M.;
Viasnoff, Virgile;
Shyh‐Chang, Ng;
Wan, Andrew C. A.;
Philpott, Michael P.;
Hillmer, Axel M.

Publication type:

Article

Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies.

Published in:

Experimental Dermatology, 2020, v. 29, n. 9, p. 814, doi. 10.1111/exd.14130

By:

Heilmann‐Heimbach, Stefanie;
Hochfeld, Lara M.;
Henne, Sabrina K.;
Nöthen, Markus M.

Publication type:

Article

Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.

Published in:

Experimental Dermatology, 2017, v. 26, n. 6, p. 536, doi. 10.1111/exd.13123

By:

Fischer, Johannes;
Degenhardt, Franziska;
Hofmann, Andrea;
Redler, Silke;
Basmanav, F. Buket;
Heilmann‐Heimbach, Stefanie;
Hanneken, Sandra;
Giehl, Kathrin A.;
Wolff, Hans;
Moebus, Susanne;
Kruse, Roland;
Lutz, Gerhard;
Blaumeiser, Bettina;
Böhm, Markus;
Garcia Bartels, Natalie;
Blume‐Peytavi, Ulrike;
Petukhova, Lynn;
Christiano, Angela M.;
Nöthen, Markus M.;
Betz, Regina C.

Publication type:

Article

Hunting the genes in male-pattern alopecia: how important are they, how close are we and what will they tell us?

Published in:

Experimental Dermatology, 2016, v. 25, n. 4, p. 251, doi. 10.1111/exd.12965

By:

Heilmann‐Heimbach, Stefanie;
Hochfeld, Lara M.;
Paus, Ralf;
Nöthen, Markus M.

Publication type:

Article

Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified.

Published in:

Experimental Dermatology, 2012, v. 21, n. 5, p. 390, doi. 10.1111/j.1600-0625.2012.01469.x

By:

Redler, Silke;
Tazi-Ahnini, Rachid;
Drichel, Dmitriy;
Birch, Mary P.;
Brockschmidt, Felix F.;
Dobson, Kathy;
Giehl, Kathrin A.;
Refke, Melanie;
Kluck, Nadine;
Kruse, Roland;
Lutz, Gerhard;
Wolff, Hans;
Böhm, Markus;
Becker, Tim;
Nöthen, Markus M.;
Betz, Regina C.;
Messenger, Andrew

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

Identification of pleiotropy at the gene level between psychiatric disorders and related traits.

Published in:

Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01530-4

By:

Polushina, Tatiana;
Banerjee, Niladri;
Giddaluru, Sudheer;
Bettella, Francesco;
Espeseth, Thomas;
Lundervold, Astri J.;
Djurovic, Srdjan;
Cichon, Sven;
Hoffmann, Per;
Nöthen, Markus M.;
Steen, Vidar M.;
Andreassen, Ole A.;
Le Hellard, Stéphanie

Publication type:

Article

Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder.

Published in:

Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01148-y

By:

Nunes, Abraham;
Stone, William;
Ardau, Raffaella;
Berghöfer, Anne;
Bocchetta, Alberto;
Chillotti, Caterina;
Deiana, Valeria;
Degenhardt, Franziska;
Forstner, Andreas J.;
Garnham, Julie S.;
Grof, Eva;
Hajek, Tomas;
Manchia, Mirko;
Mattheisen, Manuel;
McMahon, Francis;
Müller-Oerlinghausen, Bruno;
Nöthen, Markus M.;
Pinna, Marco;
Pisanu, Claudia;
O'Donovan, Claire

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

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

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

Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall study.

Published in:

PLoS ONE, 2024, v. 19, n. 5, p. 1, doi. 10.1371/journal.pone.0303357

By:

Tannemann, Nico;
Erbel, Raimund;
Nöthen, Markus M.;
Jöckel, Karl-Heinz;
Pechlivanis, Sonali

Publication type:

Article

SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4

By:

Matsson, Hans;
Tammimies, Kristiina;
Zucchelli, Marco;
Anthoni, Heidi;
Onkamo, Päivi;
Nopola-Hemmi, Jaana;
Lyytinen, Heikki;
Leppanen, Paavo H. T.;
Neuhoff, Nina;
Warnke, Andreas;
Schulte-Körne, Gert;
Schumacher, Johannes;
Nöthen, Markus M.;
Kere, Juha;
Peyrard-Janvid, Myriam

Publication type:

Article

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

Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers.

Published in:

BMC Psychiatry, 2004, v. 4, p. 4, doi. 10.1186/1471-244X-4-4

By:

Jönsson, Erik G.;
Bah, Jessica;
Melke, Jonas;
Jamra, Rami Abou;
Schumacher, Johannes;
Westberg, Lars;
Ivo, Roland;
Cichon, Sven;
Propping, Peter;
Nöthen, Markus M.;
Eriksson, Elias;
Sedvall, Göran C.

Publication type:

Article

Pluripotent stem cell-derived radial glia-like cells as stable intermediate for efficient generation of human oligodendrocytes.

Published in:

Glia (0894-1491), 2015, v. 63, n. 12, p. 2152, doi. 10.1002/glia.22882

By:

Gorris, Raphaela;
Fischer, Julia;
Erwes, Kim Lina;
Kesavan, Jaideep;
Peterson, Daniel A.;
Alexander, Michael;
Nöthen, Markus M.;
Peitz, Michael;
Quandel, Tamara;
Karus, Michael;
Brüstle, Oliver

Publication type:

Article

Hyper-Coordinated DNA Methylation is Altered in Schizophrenia and Associated with Brain Function.

Published in:

Schizophrenia Bulletin Open, 2021, n. 1, p. 1, doi. 10.1093/schizbullopen/sgab036

By:

Chen, Junfang;
Schwarz, Kristina;
Zhenxiang Zang;
Braun, Urs;
Harneit, Anais;
Kremer, Thomas;
Ren Ma;
Schweiger, Janina;
Moessnang, Carolin;
Geiger, Lena;
Han Cao;
Degenhardt, Franziska;
Nöthen, Markus M.;
Tost, Heike;
Meyer-Lindenberg, Andreas;
Schwarz, Emanuel

Publication type:

Article

Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma.

Published in:

Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0329-2

By:

Chattopadhyay, Subhayan;
Thomsen, Hauke;
Yadav, Pankaj;
da Silva Filho, Miguel Inacio;
Weinhold, Niels;
Nöthen, Markus M.;
Hoffman, Per;
Bertsch, Uta;
Huhn, Stefanie;
Morgan, Gareth J.;
Goldschmidt, Hartmut;
Houlston, Richard;
Hemminki, Kari;
Försti, Asta

Publication type:

Article

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

Epigenetic Signatures of Smoking in Five Brain Regions.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 566, doi. 10.3390/jpm12040566

By:

Zillich, Lea;
Poisel, Eric;
Streit, Fabian;
Frank, Josef;
Fries, Gabriel R.;
Foo, Jerome C.;
Friske, Marion M.;
Sirignano, Lea;
Hansson, Anita C.;
Nöthen, Markus M.;
Witt, Stephanie H.;
Walss-Bass, Consuelo;
Spanagel, Rainer;
Rietschel, Marcella

Publication type:

Article

Association between urinary iodine excretion, genetic disposition and fluid intelligence in children, adolescents and young adults: the DONALD study.

Published in:

European Journal of Nutrition, 2023, v. 62, n. 6, p. 2375, doi. 10.1007/s00394-023-03152-6

By:

Schulz, Christina-Alexandra;
Weinhold, Leonie;
Schmid, Matthias;
Nöthen, Markus M.;
Nöthlings, Ute

Publication type:

Article

Analysis of associations between dietary patterns, genetic disposition, and cognitive function in data from UK Biobank.

Published in:

European Journal of Nutrition, 2023, v. 62, n. 1, p. 511, doi. 10.1007/s00394-022-02976-y

By:

Schulz, Christina-Alexandra;
Weinhold, Leonie;
Schmid, Matthias;
Nöthen, Markus M.;
Nöthlings, Ute

Publication type:

Article

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.

Published in:

Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03178-z

By:

Vijayakrishnan, Jayaram;
Studd, James;
Broderick, Peter;
Kinnersley, Ben;
Holroyd, Amy;
Law, Philip J.;
Kumar, Rajiv;
Allan, James M.;
Harrison, Christine J.;
Moorman, Anthony V.;
Vora, Ajay;
Roman, Eve;
Rachakonda, Sivaramakrishna;
Kinsey, Sally E.;
Sheridan, Eamonn;
Thompson, Pamela D.;
Irving, Julie A.;
Koehler, Rolf;
Hoffmann, Per;
Nöthen, Markus M.

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

Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy.

Published in:

Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01220-0

By:

Marenholz, Ingo;
Grosche, Sarah;
Kalb, Birgit;
Rüschendorf, Franz;
Blümchen, Katharina;
Schlags, Rupert;
Harandi, Neda;
Price, Mareike;
Hansen, Gesine;
Seidenberg, Jürgen;
Röblitz, Holger;
Yürek, Songül;
Tschirner, Sebastian;
Xiumei Hong;
Xiaobin Wang;
Homuth, Georg;
Schmidt, Carsten O.;
Nöthen, Markus M.;
Hübner, Norbert;
Niggemann, Bodo

Publication type:

Article

Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.

Published in:

Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00366-1

By:

Kim-Hellmuth, Sarah;
Bechheim, Matthias;
Pütz, Benno;
Mohammadi, Pejman;
Nédélec, Yohann;
Giangreco, Nicholas;
Becker, Jessica;
Kaiser, Vera;
Fricker, Nadine;
Beier, Esther;
Boor, Peter;
Castel, Stephane E.;
Nöthen, Markus M.;
Barreiro, Luis B.;
Pickrell, Joseph K.;
Müller-Myhsok, Bertram;
Lappalainen, Tuuli;
Schumacher, Johannes;
Hornung, Veit

Publication type:

Article

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.

Published in:

Bipolar Disorders, 2014, v. 16, n. 7, p. 764, doi. 10.1111/bdi.12207

By:

Hammer, Christian;
Degenhardt, Franziska;
Priebe, Lutz;
Stütz, Adrian M;
Heilmann, Stefanie;
Waszak, Sebastian M;
Schlattl, Andreas;
Mangold, Elisabeth;
Hoffmann, Per;
Nöthen, Markus M;
Rietschel, Marcella;
Rappold, Gudrun;
Korbel, Jan;
Cichon, Sven;
Niesler, Beate

Publication type:

Article

Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.

Published in:

Bipolar Disorders, 2009, v. 11, n. 6, p. 610, doi. 10.1111/j.1399-5618.2009.00736.x

By:

Hamshere, Marian L;
Schulze, Thomas G;
Schumacher, Johannes;
Corvin, Aiden;
Owen, Michael J;
Jamra, Rami Abou;
Propping, Peter;
Maier, Wolfgang;
Orozco y Diaz, Guillermo;
Mayoral, Fermin;
Rivas, Fabio;
Jones, Ian;
Jones, Lisa;
Kirov, George;
Gill, Michael;
Holmans, Peter A;
Nöthen, Markus M;
Cichon, Sven;
Rietschel, Marcella;
Craddock, Nick

Publication type:

Article

MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review.

Published in:

Frontiers in Molecular Neuroscience, 2013, v. 6, p. 1, doi. 10.3389/fnmol.2013.00047

By:

Forstner, Andreas J.;
Degenhardt, Franziska;
Schratt, Gerhard;
Nöthen, Markus M.

Publication type:

Article

Schizotypy, Psychosis Proneness, and the Polygenic Risk for Schizophrenia and Resilience.

Published in:

Schizophrenia Bulletin, 2025, v. 51, p. S85, doi. 10.1093/schbul/sbae161

By:

Meller, Tina;
Lundberg, Clara;
Maj, Carlo;
Hoffmann, Per;
Forstner, Andreas J;
Nöthen, Markus M;
Nenadić, Igor

Publication type:

Article

Differential Association of Schizotypy Dimensions With Brain Structural Connectivity and Moderation by Schizophrenia Polygenic Risk.

Published in:

Schizophrenia Bulletin, 2025, v. 51, p. S149, doi. 10.1093/schbul/sbae160

By:

Hoffmann, Jonas;
Meller, Tina;
Maj, Carlo;
Hoffmann, Per;
Forstner, Andreas J;
Nöthen, Markus M;
Nenadić, Igor

Publication type:

Article

IMPACT OF POLYGENIC AND POLYENVIRONMENTAL RISK FACTORS ON AÂ PSYCHOSIS RISK PHENOTYPE EXPLAINED THROUGH BRAIN STRUCTURE.

Published in:

Schizophrenia Bulletin, 2020, v. 46, p. S35, doi. 10.1093/schbul/sbaa031.079

By:

Meller, Tina;
Schmitt, Simon;
Stein, Frederike;
Brosch, Katharina;
Grotegerd, Dominik;
Dohm, Katharina;
Meinert, Susanne;
Andlauer, Till F. M.;
Rietschel, Marcella;
Müller-Myhsok, Bertram;
Nöthen, Markus M.;
Dannlowski, Udo;
Krug, Axel;
Kircher, Tilo;
Nenadić, Igor

Publication type:

Article

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

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

Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.

Published in:

Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0031-8

By:

Chattopadhyay, Subhayan;
Thomsen, Hauke;
da Silva Filho, Miguel Inacio;
Weinhold, Niels;
Hoffmann, Per;
Nöthen, Markus M.;
Marina, Arendt;
Jöckel, Karl-Heinz;
Schmidt, Börge;
Pechlivanis, Sonali;
Langer, Christian;
Goldschmidt, Hartmut;
Hemminki, Kari;
Försti, Asta

Publication type:

Article

Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors —results of the Heinz Nixdorf Recall Study.

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Naunyn-Schmiedeberg's Archives of Pharmacology, 2021, v. 394, n. 8, p. 1713, doi. 10.1007/s00210-021-02100-7

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Pechlivanis, Sonali;
Jung, Dominik;
Moebus, Susanne;
Lehmann, Nils;
Mahabadi, Amir A.;
Hoffmann, Per;
Erbel, Raimund;
Nöthen, Markus M.;
Bachmann, Hagen S.

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Article

Dysfunctional nitric oxide signalling increases risk of myocardial infarction.

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Nature, 2013, v. 504, n. 7480, p. 432, doi. 10.1038/nature12722

By:

Erdmann, Jeanette;
Stark, Klaus;
Esslinger, Ulrike B.;
Rumpf, Philipp Moritz;
Koesling, Doris;
de Wit, Cor;
Kaiser, Frank J.;
Braunholz, Diana;
Medack, Anja;
Fischer, Marcus;
Zimmermann, Martina E.;
Tennstedt, Stephanie;
Graf, Elisabeth;
Eck, Sebastian;
Aherrahrou, Zouhair;
Nahrstaedt, Janja;
Willenborg, Christina;
Bruse, Petra;
Brænne, Ingrid;
Nöthen, Markus M.

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Article

Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample.

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Birth Defects Research, 2018, v. 110, n. 10, p. 871, doi. 10.1002/bdr2.1213

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Ishorst, Nina;
Francheschelli, Paola;
Böhmer, Anne C.;
Khan, Mohammad Faisal J.;
Heilmann‐Heimbach, Stefanie;
Fricker, Nadine;
Little, Julian;
Steegers‐Theunissen, Regine P. M.;
Peterlin, Borut;
Nowak, Stefanie;
Martini, Markus;
Kruse, Teresa;
Dunsche, Anton;
Kreusch, Thomas;
Gölz, Lina;
Aldhorae, Khalid;
Halboub, Esam;
Reutter, Heiko;
Mossey, Peter;
Nöthen, Markus M.

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Article

Investigation of dominant and recessive inheritance models in genome-wide association studies data of nonsyndromic cleft lip with or without cleft palate.

Published in:

Birth Defects Research, 2018, v. 110, n. 4, p. 336, doi. 10.1002/bdr2.1144

By:

Böhmer, Anne C.;
Golz, Lina;
Kreusch, Thomas;
Kramer, Franz-Josef;
Pötzsch, Bernd;
Nöthen, Markus M.;
Jäger, Andreas;
Mangold, Elisabeth;
Knapp, Michael;
Ludwig, Kerstin U.

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Article

Achalasia: will genetic studies provide insights?

Published in:

Human Genetics, 2010, v. 128, n. 4, p. 353, doi. 10.1007/s00439-010-0874-8

By:

Gockel, Henning R.;
Schumacher, Johannes;
Gockel, Ines;
Lang, Hauke;
Haaf, Thomas;
Nöthen, Markus M.

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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.

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Article

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

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Human Genetics, 2003, v. 114, n. 1, p. 115, doi. 10.1007/s00439-003-1022-5

By:

Schumacher, Johannes;
Otte, Andreas C. J.;
Becker, Tim;
Sun, Yuli;
Wienker, Thomas F.;
Wirth, Brunhilde;
Franke, Petra;
Abou Jamra, Rami;
Propping, Peter;
xFC;rgen#Deckert, J&;
Nöthen, Markus M.;
Cichon, Sven

Publication type:

Article

NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression.

Published in:

Neuropsychopharmacology, 2015, v. 40, n. 11, p. 2510, doi. 10.1038/npp.2015.86

By:

Dannlowski, Udo;
Kugel, Harald;
Grotegerd, Dominik;
Redlich, Ronny;
Suchy, Janina;
Opel, Nils;
Suslow, Thomas;
Konrad, Carsten;
Ohrmann, Patricia;
Bauer, Jochen;
Kircher, Tilo;
Krug, Axel;
Jansen, Andreas;
Baune, Bernhard T;
Heindel, Walter;
Domschke, Katharina;
Forstner, Andreas J;
Nöthen, Markus M;
Treutlein, Jens;
Arolt, Volker

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Article

Further Evidence for the Impact of a Genome-Wide-Supported Psychosis Risk Variant in ZNF804A on the Theory of Mind Network.

Published in:

Neuropsychopharmacology, 2014, v. 39, n. 5, p. 1196, doi. 10.1038/npp.2013.321

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Mohnke, Sebastian;
Erk, Susanne;
Schnell, Knut;
Schütz, Claudia;
Romanczuk-Seiferth, Nina;
Grimm, Oliver;
Haddad, Leila;
Pöhland, Lydia;
Garbusow, Maria;
Schmitgen, Mike M;
Kirsch, Peter;
Esslinger, Christine;
Rietschel, Marcella;
Witt, Stephanie H;
Nöthen, Markus M;
Cichon, Sven;
Mattheisen, Manuel;
Mühleisen, Thomas;
Jensen, Jimmy;
Schott, Björn H

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Article

Reduced Cortical Thickness is Associated with the Glutamatergic Regulatory Gene Risk Variant DAOA Arg30Lys in Schizophrenia.

Published in:

Neuropsychopharmacology, 2011, v. 36, n. 8, p. 1747, doi. 10.1038/npp.2011.56

By:

Schultz, C. Christoph;
Nenadic, Igor;
Koch, Kathrin;
Wagner, Gerd;
Roebel, Martin;
Schachtzabel, Claudia;
Mühleisen, Thomas W.;
Nöthen, Markus M.;
Cichon, Sven;
Deufel, Thomas;
Kiehntopf, Michael;
Rietschel, Marcella;
Reichenbach, Jürgen R.;
Sauer, Heinrich;
Schlösser, Ralf G M.

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Article

Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.

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Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2021, v. 76, n. 5, p. 786, doi. 10.1093/gerona/glab023

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Torres, Guillermo G.;
Nygaard, Marianne;
Caliebe, Amke;
Blanché, Hélène;
Chantalat, Sophie;
Galan, Pilar;
Lieb, Wolfgang;
Christiansen, Lene;
Deleuze, Jean-François;
Christensen, Kaare;
Strauch, Konstantin;
Müller-Nurasyid, Martina;
Peters, Annette;
Nöthen, Markus M.;
Hoffmann, Per;
Flachsbart, Friederike;
Schreiber, Stefan;
Ellinghaus, David;
Franke, Andre;
Dose, Janina

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Article