Nöthen, Markus M.: search on Z-Library

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1

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

2

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

3

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

4

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

5

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

6

No association between serotonin 2A receptor gene variants and personality traits

Jönsson, Erik G., Nöthen, Markus M., Gustavsson, J. Petter, Berggård, Cecilia, Bunzel, Roland, Forslund, Kaj, Rylander, Gunnar, Mattila-Evenden, Marja, Propping, Peter, Åsberg, Marie, Sedvall, Göran

Journal:

Psychiatric Genetics

Year:

2001

Language:

english

File:

PDF, 81 KB

english, 2001

7

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

8

Premorbid adjustment in schizophrenia — An important aspect of phenotype definition

Christine Schmael, Alexander Georgi, Bertram Krumm, Christin Buerger, Monika Deschner, Markus M. Nöthen, Thomas G. Schulze, Marcella Rietschel

Journal:

Schizophrenia Research

Year:

2007

Language:

english

File:

PDF, 215 KB

english, 2007

9

Missing Heritability in the Tails of Quantitative Traits? A Simulation Study on the Impact of Slightly Altered True Genetic Models

Pütter, Carolin, Pechlivanis, Sonali, Nöthen, Markus M., Jöckel, Karl-Heinz, Wichmann, Heinz-Erich, Scherag, André

Journal:

Year:

2011

Language:

english

File:

PDF, 1.17 MB

english, 2011

10

Factor Analysis of Mania

Serretti, Alessandro, Rietschel, Marcella, Lattuada, Enrico, Krauβ, Harald, Held, Tilo, Nöthen, Markus M., Smeraldi, Enrico

Journal:

Archives of General Psychiatry

Year:

1999

Language:

english

File:

PDF, 130 KB

english, 1999

11

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

12

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

13

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

14

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

15

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

16

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

17

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

18

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

19

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

20

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

21

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

22

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

23

Identification of mutations in the humanhairlessgene in two new families with congenital atrichia

Regina C. Betz, Margarita Indelman, Jana Pforr, Felix Schreiner, Ralf Bauer, Reuven Bergman, Michael J. Lentze, Markus M. Nöthen, Sven Cichon, Eli Sprecher

Journal:

Archives of Dermatological Research

Year:

2007

Language:

english

File:

PDF, 299 KB

english, 2007

24

Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder

Cathy L Barr, Chun Xu, Jamie Kroft, Yu Feng, Karen Wigg, Gwyneth Zai, Rosemary Tannock, Russell Schachar, Molly Malone, Wendy Roberts, Markus M Nöthen, Frank Grünhage, David J Vandenbergh, George Uhl,

Journal:

Biological Psychiatry

Year:

2001

Language:

english

File:

PDF, 46 KB

english, 2001

25

An examination of previously reported Alzheimer candidate genes within a large genome-wide association dataset

Gerrish, Amy, Harold, Denise, Sims, Rebecca, Abraham, Richard, Hollingworth, Paul, Hamshere, Marian, Lovestone, Simon, Brayne, Carol, Gill, Michael, Lawlor, Brian, Passmore, Peter, Nothen, Markus, May

Journal:

Alzheimer's & Dementia

Year:

2009

Language:

english

File:

PDF, 47 KB

english, 2009

26

Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen

Aldhorae, Khalid Ahmed, Böhmer, Anne C., Ludwig, Kerstin U., Esmail, Ahlam Hibatulla Ali, Al-Hebshi, Nezar Noor, Lippke, Bärbel, Gölz, Lina, Nöthen, Markus M., Daratsianos, Nikolaos, Knapp, Michael, J

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2014

Language:

english

File:

PDF, 99 KB

english, 2014

27

Dinucleotide repeat polymorphism at the D18S365 locus

Abels, Susanne, Erdmann, Jeanette, Nöthen, Markus

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 80 KB

english, 1993

28

Polygenic risk for depression and the neural correlates of working memory in healthy subjects

Yüksel, Dilara, Dietsche, Bruno, Forstner, Andreas J., Witt, Stephanie H., Maier, Robert, Rietschel, Marcella, Konrad, Carsten, Nöthen, Markus M., Dannlowski, Udo, Baune, Bernhard T., Kircher, Tilo, K

Journal:

Progress in Neuro-Psychopharmacology and Biological Psychiatry

Year:

2017

Language:

english

File:

PDF, 1.25 MB

english, 2017

29

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

30

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

31

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

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

Journal:

European Journal of Pediatrics

Year:

2009

Language:

english

File:

PDF, 76 KB

english, 2009

32

A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci

Winantea, Jane, Hoang, My Ngo, Ohlraun, Stefanie, Rietschel, Marcella, Cichon, Sven, Propping, Peter, Nöthen, Markus M, Freudenberg, Jan, Freudenberg-Hua, Yun

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 125 KB

english, 2006

33

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

Rami Abou Jamra, Orianne Philippe, Annick Raas-Rothschild, Sebastian H. Eck, Elisabeth Graf, Rebecca Buchert, Guntram Borck, Arif Ekici, Felix F. Brockschmidt, Markus M. Nöthen, Arnold Munnich, Tim M.

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 882 KB

english, 2011

34

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Silke Redler, Roland Kruse, Sibylle Eigelshoven, Sandra Hanneken, Melanie Refke, Yaran Wen, Xue Zhang, Sven Cichon, Regina C. Betz, Markus M. Nöthen

Journal:

Journal of the American Academy of Dermatology

Year:

2011

Language:

english

File:

PDF, 838 KB

english, 2011

35

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity

Nöthen, Markus M., Cichon, Sven, Hemmer, Susanne, Hebebrand, Johannes, Remschmidt, Helmut, Lehmkuhl, Gerd, Poustka, Fritz, Schmidt, Martin, Catalano, Marco, Fimmers, Rolf, Kömer, Judith, Rletschel, Ma

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 807 KB

english, 1994

36

SA63METHYLATION PROFILES DURING ACUTE ALCOHOL WITHDRAWAL IN A CLINICAL SAMPLE

Witt, Stephanie, Frank, Josef, Treutlein, Jens, Streit, Fabian, Frischknecht, Ulrich, Foo, Jerome, Degenhardt, Franziska, Adorjan, Kristina, Nöthen, Markus, Spanagel, Rainer, Kiefer, Falk, Rietschel,

Journal:

European Neuropsychopharmacology

Year:

2019

File:

PDF, 49 KB

2019

37

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects

Andreas Jansen, Sören Krach, Axel Krug, Valentin Markov, Thomas Eggermann, Klaus Zerres, Markus Thimm, Markus M Nöthen, Jens Treutlein, Marcella Rietschel, Tilo Kircher

Journal:

Year:

2009

Language:

english

File:

PDF, 853 KB

english, 2009

38

Analysis of the TSC2 gene in human medulloblastoma

Rene Przkora, Birgit Meyer-Puttlitz, Ottmar Schmitt, Frank Berthold, Markus Nöthen, J. Krauss, Jörg C. Tonn, Andreas von Deimling, Otmar D. Wiestler, Torsten Pietsch

Journal:

Acta Neuropathologica

Year:

2001

Language:

english

File:

PDF, 48 KB

english, 2001

39

Mapping of the human adenosine A2areceptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region

J. Deckert, Markus M. Nöthen, Stephan P. Bryant, Simone Schuffenhauer, Peter R. Schofield, Nigel K. Spurr, Peter Propping

Journal:

Year:

1997

Language:

english

File:

PDF, 32 KB

english, 1997

40

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain

Roland Bunzel, Ingmar Blümcke, Sven Cichon, Sabine Normann, Johannes Schramm, Peter Propping, Markus M Nöthen

Journal:

Molecular Brain Research

Year:

1998

Language:

english

File:

PDF, 114 KB

english, 1998

41

A systems medicine research approach for studying alcohol addiction

Spanagel, Rainer, Durstewitz, Daniel, Hansson, Anita, Heinz, Andreas, Kiefer, Falk, Köhr, Georg, Matthäus, Franziska, Nöthen, Markus M., Noori, Hamid R., Obermayer, Klaus, Rietschel, Marcella, Schloss

Journal:

Addiction Biology

Year:

2013

Language:

english

File:

PDF, 235 KB

english, 2013

42

GENETIC FACTORS INFLUENCING THE COMMON NEUROBIOLOGICAL SUBSTRATE FOR MENTAL DISORDERS

Andlauer, Till, Mühleisen, Thomas, Hoffstaedter, Felix, Teumer, Alexander, Teuber, Anja, Reinbold, Céline, Herms, Stefan, Teismann, Henning, Moebus, Susanne, Grabe, Hans J., Nöthen, Markus, Amunts, Ka

Journal:

European Neuropsychopharmacology

Year:

2019

Language:

english

File:

PDF, 46 KB

english, 2019

43

SA63METHYLATION PROFILES DURING ACUTE ALCOHOL WITHDRAWAL IN A CLINICAL SAMPLE

Witt, Stephanie, Frank, Josef, Treutlein, Jens, Streit, Fabian, Frischknecht, Ulrich, Foo, Jerome, Degenhardt, Franziska, Adorjan, Kristina, Nöthen, Markus, Spanagel, Rainer, Kiefer, Falk, Rietschel,

Journal:

European Neuropsychopharmacology

Year:

2019

Language:

english

File:

PDF, 49 KB

english, 2019

44

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

45

Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes

Renate Viersbach, Gesa Schwanitz, Markus M. Nöthen

Journal:

Year:

1994

Language:

english

File:

PDF, 2.46 MB

english, 1994

46

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma

Frampton, Matthew, da Silva Filho, Miguel Inacio, Broderick, Peter, Thomsen, Hauke, Försti, Asta, Vijayakrishnan, Jayaram, Cooke, Rosie, Enciso-Mora, Victor, Hoffmann, Per, Nöthen, Markus M., Lloyd, A

Journal:

Nature Communications

Year:

2013

Language:

english

File:

PDF, 716 KB

english, 2013

47

SA62IDENTIFICATION OF MOLECULAR MECHANISMS FOLLOWING CANNABIS EXPOSURE IN PATIENTS WITH PSYCHOSIS

Stavrum, Anne-Kristin, Polushina, Tatiana, Melle, Ingrid, Lagerberg, Trine V., Ringen, Petter Andreas, Djurovic, Srdjan, Andreassen, Ole, Hoffmann, Per, Nöthen, Markus, Hellard, Stephanie Le

Journal:

European Neuropsychopharmacology

Year:

2019

Language:

english

File:

PDF, 74 KB

english, 2019

48

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

49

A large duplication inLIPHunderlies autosomal recessive hypotrichosis simplex in four Middle Eastern families

Sagi Nahum, Sandra M. Pasternack, Jana Pforr, Margarita Indelman, Bernd Wollnik, Reuven Bergman, Markus M. Nöthen, Arne König, Ziyad Khamaysi, Regina C. Betz, Eli Sprecher

Journal:

Archives of Dermatological Research

Year:

2009

Language:

english

File:

PDF, 303 KB

english, 2009

50

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

Tiit Nikopensius, Stefanie Birnbaum, Kerstin U. Ludwig, Triin Jagomägi, Mare Saag, Stefan Herms, Michael Knapp, Per Hoffmann, Markus M. Nöthen, Andres Metspalu, Elisabeth Mangold

Journal:

European Journal of Oral Sciences

Year:

2010

Language:

english

File:

PDF, 94 KB

english, 2010

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