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1

Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma

Thomsen, Hauke, Chattopadhyay, Subhayan, Weinhold, Niels, Vodicka, Pavel, Vodickova, Ludmila, Hoffmann, Per, Nöthen, Markus M., Jöckel, Karl-Heinz, Langer, Christian, Hajek, Roman, Hallmans, Göran, Pe

Journal:

Year:

2019

Language:

english

File:

PDF, 565 KB

english, 2019

2

Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data

Hochfeld, Lara M., Keller, Andreas, Anhalt, Thomas, Fricker, Nadine, Nöthen, Markus M., Heilmann-Heimbach, Stefanie

Journal:

The Journal of Investigative Dermatology

Year:

2018

Language:

english

File:

PDF, 1.60 MB

english, 2018

3

Durchbrüche im Verständnis der molekularen Ursachen psychiatrischer Störungen; Breakthrough in understanding the molecular causes of psychiatric disorders;

Nöthen, Markus M., Degenhardt, Franziska, Forstner, Andreas J.

Journal:

Year:

2019

Language:

german

File:

PDF, 253 KB

german, 2019

4

Molekulargenetische Erkenntnisse erweitern das Verständnis psychiatrischer Störungen; Molecular genetic knowledge extends the understanding of psychiatric disorders;

Nöthen, Markus M., Degenhardt, Franziska, Forstner, Andreas J.

Journal:

Year:

2019

Language:

german

File:

PDF, 206 KB

german, 2019

5

An interstitial deletion of chromosome 7 at band q21: A case report and review

Winnie Courtens, Stefan Vermeulen, Wim Wuyts, Ludwine Messiaen, Jan Wauters, Lieve Nuytinck, Nils Peeters, Katrien Storm, Frank Speleman, Markus M. Nöthen

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 291 KB

english, 2005

6

Prenatal diagnosis of Pfeiffer syndrome type II

Bettina Blaumeiser, Philip Loquet, Wim Wuyts, Markus M. Nöthen

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 179 KB

english, 2004

7

Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis

Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski-Feder, Markus M. Nöthen, Per Hoffmann, Stefan Aretz

Journal:

Year:

2012

Language:

english

File:

PDF, 213 KB

english, 2012

8

Familial occurrence of the VATER/VACTERL association

Alina Hilger, Charlotte Schramm, Markus Draaken, Sadaf S. Mughal, Gabriel Dworschak, Enrika Bartels, Per Hoffmann, Markus M. Nöthen, Heiko Reutter, Michael Ludwig

Journal:

Pediatric Surgery International

Year:

2012

Language:

english

File:

PDF, 166 KB

english, 2012

9

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

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

Journal:

Year:

2004

Language:

english

File:

PDF, 578 KB

english, 2004

10

Chip-Based Genome-Wide Search for Micro-Aberrations in Patients With the Exstrophy-Epispadias Complex

Markus Draaken, Heiko Reutter, Thomas M. Boemers, Simeon A. Boyadjiev, Per Hoffmann, Markus M. Nöthen, Michael Ludwig

Journal:

Journal of Pediatric Urology

Year:

2009

Language:

english

File:

PDF, 40 KB

english, 2009

11

Chip-Based Genome-Wide Search for Micro-Aberrations in Patients with the Exstrophy-Epispadias Complex

Markus Draaken, Heiko Reutter, Thomas M. Boemers, Simeon A. Boyadjiev, Per Hoffmann, Markus M. Nöthen, Michael LUDWIG

Journal:

Journal of Pediatric Urology

Year:

2009

Language:

english

File:

PDF, 59 KB

english, 2009

12

VEGF Gene Haplotypes Are Associated With Sarcoidosis

Pabst, Stefan, Karpushova, Anna, Diaz-Lacava, Amalia, Herms, Stefan, Walier, Maja, Zimmer, Sebastian, Cichon, Sven, Nickenig, Georg, Nöthen, Markus M., Wienker, Thomas F., Grohé, Christian

Journal:

Year:

2010

Language:

english

File:

PDF, 756 KB

english, 2010

13

Polygenic risk for schizophrenia affects working memory and its neural correlates in healthy subjects

Krug, Axel, Dietsche, Bruno, Zöllner, Rebecca, Yüksel, Dilara, Nöthen, Markus M., Forstner, Andreas J., Rietschel, Marcella, Dannlowski, Udo, Baune, Bernhard T., Maier, Robert, Witt, Stephanie H., Kir

Journal:

Schizophrenia Research

Year:

2018

Language:

english

File:

PDF, 829 KB

english, 2018

14

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

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, Lang

Journal:

Molecular Medicine

Year:

2018

Language:

english

File:

PDF, 1.52 MB

english, 2018

15

Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

Foo, Jerome C., Streit, Fabian, Frank, Josef, Witt, Stephanie H., Treutlein, Jens, Baune, Bernhard T., Moebus, Susanne, Jöckel, Karl-Heinz, Forstner, Andreas J., Nöthen, Markus M., Rietschel, Marcella

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2018

Language:

english

File:

PDF, 1.31 MB

english, 2018

16

Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma

Thomsen, Hauke, Chattopadhyay, Subhayan, Weinhold, Niels, Vodicka, Pavel, Vodickova, Ludmila, Hoffmann, Per, Nöthen, Markus M., Jöckel, Karl-Heinz, Langer, Christian, Hajek, Roman, Hallmans, Göran, Pe

Journal:

Year:

2019

File:

PDF, 565 KB

2019

17

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

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, H

Journal:

Communications Biology

Year:

2019

Language:

english

File:

PDF, 1.81 MB

english, 2019

18

Lack of imprinting of the human dopamine D4 receptor (DRD4) gene

Cichon, Sven, Nöthen, Markus M., Wolf, Helmut K., Propping, Peter

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 354 KB

english, 1996

19

Systematic screening for mutations in the 5′-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder

Cichon, Sven, Nöthen, Markus M., Stöber, Gerald, Schroers, Roland, Albus, Margot, Maier, Wolfgang, Rietschel, Marcella, Körner, Judith, Weigelt, Bettina, Franzek, Ernst, Wildenauer, Dieter, Fimmers, R

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 489 KB

english, 1996

20

Systematic search for variation in the human norepinephrine transporter gene: Identification of five naturally occurring missense mutations and study of association with major psychiatric disorders

Stöber, Gerald, Nöthen, Markus M., Pörzgen, Peter, Brüss, Michael, Bönisch, Heinz, Knapp, Michael, Beckmann, Helmut, Propping, Peter

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 981 KB

english, 1996

21

Neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) and panic disorder: An association study

Steinlein, Ortrud K., Deckert, Jürgen, Nöthen, Markus M., Franke, Petra, Maier, Wolfgang, Beckmann, Helmut, Propping, Peter

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 210 KB

english, 1997

22

Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls

Marcella Rietschel, Alexander Schorr, Margot Albus, Ernst Franzek, Roland Kreiner, Tilo Held, Michael Knapp, Daniel J. Müller, Thomas G. Schulze, Peter Propping, Wolfgang Maier, Markus M. Nöthen

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 71 KB

english, 2000

23

Nonreplication of association between μ-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence

Petra Franke, Tao Wang, Markus M. Nöthen, Michael Knapp, Helge Neidt, Susanne Albrecht, Esther Jahnes, Peter Propping, Wolfgang Maier

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 90 KB

english, 2001

24

Different familial transmission patterns in bipolar I disorder with onset before and after age 25

Maria Grigoroiu-Serbanescu, Maria Martinez, Markus M. Nöthen, Mihaela Grinberg, Dorina Sima, Peter Propping, Elvira Marinescu, Mihaela Hrestic

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 127 KB

english, 2001

25

Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder

Daniel J. Müller, Thomas G. Schulze, Esther Jahnes, Sven Cichon, Harald Krauss, Kristina Kesper, Tilo Held, Wolfgang Maier, Peter Propping, Markus M. Nöthen, Marcella Rietschel

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 96 KB

english, 2002

26

Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder

Esther Jahnes, Daniel J. Müller, Thomas G. Schulze, Christine Windemuth, Sven Cichon, Stephanie Ohlraun, Heiner Fangerau, Tilo Held, Wolfgang Maier, Peter Propping, Markus M. Nöthen, Marcella Rietsche

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 56 KB

english, 2002

27

Steinfeld syndrome: Report of a second family and further delineation of a rare autosomal dominant disorder

Dr. Markus M. Nöthen, Gisela Knöpfle, Hans-Jörg Födisch, Klaus Zerres

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 397 KB

english, 1993

28

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method

Dr. Markus M. Nöthen, Johannes Hebebrand, Michael Knapp, Kathrin Hebebrand, Astrid Camps, Alexander von Gontard, Roswitha Wettke-Schäfer, Sonja Lisch, Sven Cichon, Fritz Poustka, Martin Schmidt, Gerd

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 540 KB

english, 1994

29

No evidence of association between dopamine D4 receptor variants and bipolar affective disorder

Dr. Lionel C. C. Lim, Markus M. Nöthen, Judith Körner, Marcella Rietschel, David Castle, Neil Hunt, Peter Propping, Robin Murray, Michael Gill

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 575 KB

english, 1994

30

Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1

Elisabeth Dawson, Elizabeth Parfitt, Queta Roberts, Jo Daniels, Lionel Lim, Pak Sham, Markus Nöthen, Peter Propping, Mario Lanczik, Wolfgang Maier, Ulrike Reuner, Jean Weissenbach, Michael Gill, John

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 939 KB

english, 1995

31

No association between a promoter dopamine D4 receptor gene variant and schizophrenia

Erik G. Jönsson, Roland Ivo, Kaj Forslund, Marja Mattila-Evenden, Gunnar Rylander, Sven Cichon, Peter Propping, Markus M. Nöthen, Marie Åsberg, Göran C. Sedvall

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 81 KB

english, 2001

32

Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population

Sylvia Bort Martí, Sven Cichon, Peter Propping, Markus Nöthen

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 85 KB

english, 2002

33

Human metabotropic glutamate receptor 2 gene (GRM2): Chromosomal sublocalization (3p21.1–p21.2) and genomic organization

Sylvia Bort Martí, Sven Cichon, Peter Propping, Markus Nöthen

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 91 KB

english, 2002

34

Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation—clinical report and review

Winnie Courtens, Wim Wuyts, Martin Poot, Karoly Szuhai, Jan Wauters, Edwin Reyniers, Marc Eleveld, George Diaz, Markus M. Nöthen, Ruti Parvari

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 155 KB

english, 2006

35

Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex

Heiko Reutter, Tim Becker, Michael Ludwig, Niklas Schäfer, Birte Detlefsen, Sylvie Beaudoin, Margit Fisch, Anne-Karoline Ebert, Wolfgang Rösch, Markus M. Nöthen, Thomas M. Boemers, Regina C. Betz

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 83 KB

english, 2006

36

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?

Mahim Jain, Deeann Wallis, Nathaniel H. Robin, Fabienne Wavrant De Vrieze, John A. Hardy, Mohsen Ghadami, Kristin Bosse, Regina C. Betz, Markus M. Nöthen, Mauricio Arcos-Burgos, Maximilian Muenke

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 262 KB

english, 2008

37

Is there a phenotypic difference between probands in case-control versus family-based association studies?

Thomas G. Schulze, Sven Cichon, Markus M. Nöthen, Peter Propping, Wolfgang Maier, Marcella Rietschel

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2003

Language:

english

File:

PDF, 35 KB

english, 2003

38

Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene

Dorothea Gadzicki, Kirsten R. Müller-Vahl, Daniela Heller, Sebastian Ossege, Markus M. Nöthen, Johannes Hebebrand, Manfred Stuhrmann

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 180 KB

english, 2004

39

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

Bernd Frank, Beate Niesler, Markus M. Nöthen, Helge Neidt, Peter Propping, Brigitta Bondy, Marcella Rietschel, Wolfgang Maier, Margot Albus, Gudrun Rappold

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 105 KB

english, 2004

40

Family history influences age of onset in bipolar I disorder in females but not in males

Maria Grigoroiu-Serbanescu, Markus M. Nöthen, Stephanie Ohlraun, Peter Propping, Wolfgang Maier, Priya Wickramaratne, Marie-Jana Georgescu, Dan Prelipceanu, Mihaela Grimberg, Dorina Sima, Marcella Rie

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2005

Language:

english

File:

PDF, 88 KB

english, 2005

41

Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes

Britta Haenisch, Karoline Linsel, Michael Brüss, Ralf Gilsbach, Peter Propping, Markus M. Nöthen, Marcella Rietschel, Rolf Fimmers, Wolfgang Maier, Astrid Zobel, Susanne Höfels, Vera Guttenthaler, Man

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2009

Language:

english

File:

PDF, 85 KB

english, 2009

42

A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3

Antònia Flaquer, Rami Abou Jamra, Karolin Etterer, Guillermo Orozco Díaz, Fabio Rivas, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Konstantin Strauch

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2010

Language:

english

File:

PDF, 94 KB

english, 2010

43

Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias

Markus Draaken, Judith Proske, Charlotte Schramm, Lars Wittler, Enrika Bartels, Markus M. Nöthen, Heiko Reutter, Michael Ludwig

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2010

Language:

english

File:

PDF, 152 KB

english, 2010

44

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous iranian family

Heiko Reutter, Franz Rüschendorf, Manuel Mattheisen, Markus Draaken, Enrika Bartels, Norbert Hübner, Per Hoffmann, Seyedmedhi Payabvash, Kathrin Saar, Markus M. Nöthen, Abdol-Mohammad Kajbafzadeh, Mic

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2010

Language:

english

File:

PDF, 206 KB

english, 2010

45

Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

Tilo Kircher, Axel Krug, Valentin Markov, Carin Whitney, Sören Krach, Klaus Zerres, Thomas Eggermann, Tony Stöcker, Nadim Jon Shah, Jens Treutlein, Markus M. Nöthen, Tim Becker, Marcella Rietschel

Journal:

Human Brain Mapping

Year:

2009

Language:

english

File:

PDF, 257 KB

english, 2009

46

Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals

Valentin Markov, Axel Krug, Sören Krach, Andreas Jansen, Thomas Eggermann, Karl Zerres, Tony Stöcker, N. Jon Shah, Markus M. Nöthen, Jens Treutlein, Marcella Rietschel, Tilo Kircher

Journal:

Human Brain Mapping

Year:

2010

Language:

english

File:

PDF, 208 KB

english, 2010

47

The impact of dystrobrevin-binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval

Markus Thimm, Axel Krug, Valentin Markov, Sören Krach, Andreas Jansen, Klaus Zerres, Thomas Eggermann, Tony Stöcker, Nadim Jon Shah, Markus M. Nöthen, Marcella Rietschel, Tilo Kircher

Journal:

Human Brain Mapping

Year:

2010

Language:

english

File:

PDF, 148 KB

english, 2010

48

Genetic variation in G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals

Axel Krug, Valentin Markov, Sören Krach, Andreas Jansen, Klaus Zerres, Thomas Eggermann, Tony Stöcker, N Jon Shah, Markus M Nöthen, Alexander Georgi, Jana Strohmaier, Marcella Rietschel, Tilo Kircher

Journal:

Human Brain Mapping

Year:

2011

Language:

english

File:

PDF, 154 KB

english, 2011

49

Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease

Sebastian Paus, Gert Seeger, Hans M. Brecht, Jürgen Köster, Mahha El-Faddagh, Markus M. Nöthen, Thomas Klockgether, Ullrich Wüllner

Journal:

Movement Disorders

Year:

2004

Language:

english

File:

PDF, 47 KB

english, 2004

50

Reply

Cichon, Sven, Kruse, Roland, Nothen, Markus M.

Journal:

The Journal of Investigative Dermatology

Year:

2000

Language:

english

File:

PDF, 54 KB

english, 2000