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51

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

52

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

53

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)

Markus M. Nöthen, Thomas Eggermann, Jeanette Erdmann, Bernd Eiben, Dieter Hofmann, Peter Propping, Gesa Schwanitz

Journal:

Year:

1993

Language:

english

File:

PDF, 503 KB

english, 1993

54

Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees

Lionel C. C. Lim, Nick Craddock, Mike Owen, Pak Sham, Markus M. Nöthen, Judith Körner, Marcella Rietschel, Rolf Fimmer, Peter Propping, Peter McGuffin, Robin Murray, Michael Gill

Journal:

Behavior Genetics

Year:

1996

Language:

english

File:

PDF, 855 KB

english, 1996

55

Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15

Markus M. Nöthen, G. Schulte-Körne, T. Grimm, S. Cichon, I. R. Vogt, B. Müller-Myhsok, P. Propping, H. Remschmidt

Journal:

European Child & Adolescent Psychiatry

Year:

1999

Language:

english

File:

PDF, 371 KB

english, 1999

56

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

57

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

58

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

59

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

60

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

Axel M. Hillmer, Jan Freudenberg, Sean Myles, Stefan Herms, Kun Tang, David A. Hughes, Felix F. Brockschmidt, Yijun Ruan, Mark Stoneking, Markus M. Nöthen

Journal:

Year:

2009

Language:

english

File:

PDF, 995 KB

english, 2009

61

Achalasia: will genetic studies provide insights?

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

Journal:

Year:

2010

Language:

english

File:

PDF, 351 KB

english, 2010

62

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

63

Investigation of interaction betweenDCDC2andKIAA0319in a large German dyslexia sample

Kerstin U. Ludwig, Darina Roeske, Johannes Schumacher, Gerd Schulte-Körne, Inke R. König, Andreas Warnke, Ellen Plume, Andreas Ziegler, Helmut Remschmidt, Bertram Müller-Myhsok, Markus M. Nöthen, Per

Journal:

Journal of Neural Transmission

Year:

2008

Language:

english

File:

PDF, 143 KB

english, 2008

64

10.1038/90050

Betz, Regina C., Schoser, Benedikt G. H., Kasper, Dagmar, Ricker, Kenneth, Ramírez, Alfredo, Stein, Valentin, Torbergsen, Torberg, Lee, Young-Ae, Nöthen, Markus M., Wienker, Thomas F., Malin, Jean-Pie

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 1.03 MB

english, 2001

65

In Vitro Analysis of LIPH Mutations Causing Hypotrichosis Simplex: Evidence Confirming the Role of Lipase H and Lysophosphatidic Acid in Hair Growth

Pasternack, Sandra M, von Kügelgen, Ivar, Müller, Melanie, Oji, Vinzenz, Traupe, Heiko, Sprecher, Eli, Nöthen, Markus M, Janecke, Andreas R, Betz, Regina C

Journal:

The Journal of Investigative Dermatology

Year:

2009

Language:

english

File:

PDF, 918 KB

english, 2009

66

Reply to “Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression”

McMahon, Francis J, Akula, Nirmala, Cichon, Sven, Detera-Wadleigh, Sevilla D, Edenberg, Howard, Holsboer, Florian, Nöthen, Markus M, Nurnberger, John I, Potash, James, Preisig, Martin

Journal:

Nature Genetics

Year:

2011

Language:

english

File:

PDF, 89 KB

english, 2011

67

CNTF and psychiatric disorders

Knapp, Michael, Maier, Wolfgang, Rietschel, Marcella, Nöthen, Markus M., Cichon, Sven, Eggermann, Katja, Propping, Peter

Journal:

Nature Genetics

Year:

1996

File:

PDF, 302 KB

1996

68

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

Schultz, C Christoph, Nenadic, Igor, Koch, Kathrin, Wagner, Gerd, Roebel, Martin, Schachtzabel, Claudia, Mühleisen, Thomas W, Nöthen, Markus M, Cichon, Sven, Deufel, Thomas

Journal:

Neuropsychopharmacology

Year:

2011

Language:

english

File:

PDF, 304 KB

english, 2011

69

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

Mendlewicz, Julien, Massat, Isabelle, Souery, Daniel, Del-Favero, Jurgen, Oruč, Lilijana, Nöthen, Markus M, Blackwood, Douglas, Muir, Walter, Battersby, Sharon, Lerer, Beny

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 123 KB

english, 2004

70

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

71

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

72

Partial support for ZNF804A genotype-dependent alterations in prefrontal connectivity

Frieder M. Paulus, Sören Krach, Johannes Bedenbender, Martin Pyka, Jens Sommer, Axel Krug, Susanne Knake, Markus M. Nöthen, Stephanie H. Witt, Marcella Rietschel, Tilo Kircher, Andreas Jansen

Journal:

Human Brain Mapping

Year:

2012

Language:

english

File:

PDF, 445 KB

english, 2012

73

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

74

Linkage-Disequilibrium-Based Binning Affects the Interpretation of GWASs

Andrea Christoforou, Michael Dondrup, Morten Mattingsdal, Manuel Mattheisen, Sudheer Giddaluru, Markus M. Nöthen, Marcella Rietschel, Sven Cichon, Srdjan Djurovic, Ole A. Andreassen, Inge Jonassen, Vi

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 111 KB

english, 2012

75

Identification of a keratin-associated protein with a putative role in vesicle transport

Laura Planko, Karsten Böhse, Jörg Höhfeld, Regina C. Betz, Sandra Hanneken, Sibylle Eigelshoven, Roland Kruse, Markus M. Nöthen, Thomas M. Magin

Journal:

European Journal of Cell Biology

Year:

2007

Language:

english

File:

PDF, 2.78 MB

english, 2007

76

Further evidence for age of onset being an indicator for severity in bipolar disorder

Thomas G. Schulze, Daniel J. Müller, Harald Krauss, Magdalena Gross, Heiner Fangerau-Lefèvre, Franciska Ill≐s, Stephanie Ohlraun, Sven Cichon, Tilo Held, Peter Propping, Markus M. Nöthen, Wolfgang Mai

Journal:

Journal of Affective Disorders

Year:

2002

Language:

english

File:

PDF, 46 KB

english, 2002

77

Efficacy and side-effects of clozapine: Testing for association with allelic variation in the dopamine D4 receptor gene

Marcella Rietschel, Dieter Naber, Heinrich Oberländer, Rüdiger Holzbach, Roulf Fimmers, Katja Eggermann, Hans-Jürgen Möller, Peter Propping, Markus M. Nöthen

Journal:

Neuropsychopharmacology

Year:

1996

Language:

english

File:

PDF, 735 KB

english, 1996

78

Serotonin Subtype 2 Receptor Genes and Clinical Response to Clozapine in Schizophrenia Patients

Mario Masellis, Vincenzo Basile, Herbert Y. Meltzer, Jeffrey A. Lieberman, Serge Sevy, Fabio M. Macciardi, Phil Cola, Alfreda Howard, Farideh Badri, Markus M. Nöthen, Werner Kalow, James L. Kennedy

Journal:

Neuropsychopharmacology

Year:

1998

Language:

english

File:

PDF, 159 KB

english, 1998

79

Genetics and Neuroscience in Dyslexia: Perspectives for Education and Remediation

Gerd Schulte-Körne, Kerstin U. Ludwig, Jennifer El Sharkawy, Markus M. Nöthen, Bertram Müller-Myhsok, Per Hoffmann

Journal:

Mind Brain and Education

Year:

2007

Language:

english

File:

PDF, 250 KB

english, 2007

80

TheFUgene and its possible protein isoforms

Torben Østerlund, David B Everman, Regina C Betz, Monica Mosca, Markus M Nöthen, Charles E Schwartz, Peter G Zaphiropoulos, Rune Toftgård

Journal:

Year:

2004

Language:

english

File:

PDF, 572 KB

english, 2004

81

The effects of a DTNBP1 gene variant on attention networks: an fMRI study

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

Journal:

Behavioral and Brain Functions

Year:

2010

Language:

english

File:

PDF, 1.03 MB

english, 2010

82

Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age

Vanessa Nieratschker, Martin Grosshans, Josef Frank, Jana Strohmaier, Christoph von der Goltz, Osman El-Maarri, Stephanie H. Witt, Sven Cichon, Markus M. Nöthen, Falk Kiefer, Marcella Rietschel

Journal:

Addiction Biology

Year:

2012

Language:

english

File:

PDF, 324 KB

english, 2012

83

Dinucleotide repeat polymorphism at the human CD59 locus

Markus M. Nöthen, Georg Dewald

Journal:

Clinical Genetics

Year:

1995

Language:

english

File:

PDF, 220 KB

english, 1995

84

Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region

Daphne Shimron-Abarbanell, Jeanette Erdmann, Ina R. Vogt, Stephen P. Bryant, Nigel K. Spurr, Michael Knapp, Peter Propping, Markus M. Nöthen

Journal:

Biochemical and Biophysical Research Communications

Year:

1997

Language:

english

File:

PDF, 66 KB

english, 1997

85

Localization of the Human Glucosidase I Gene to Chromosome 2p12–p13 by Fluorescencein SituHybridization and PCR Analysis of Somatic Cell Hybrids

Burga Kalz-Füller, Christiane Heidrich-Kaul, Markus Nöthen, Ernst Bause, Gesa Schwanitz

Journal:

Year:

1996

Language:

english

File:

PDF, 169 KB

english, 1996

86

Human complement component C8: Molecular basis of the β-chain polymorphism

Georg Dewald, Susanne Hemmer, Markus M. Nöthen

Journal:

Year:

1994

Language:

english

File:

PDF, 597 KB

english, 1994

87

De novo microduplication at 22q11.21 in a patient with VACTERL association

Charlotte Schramm, Markus Draaken, Enrika Bartels, Thomas M. Boemers, Stefan Aretz, Felix F. Brockschmidt, Markus M. Nöthen, Michael Ludwig, Heiko Reutter

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 660 KB

english, 2011

88

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

89

Genome-Wide Linkage Scan in a Moroccan Family With Autosomal-Recessive Exstrophy of the Bladder Identifies a Novel Susceptibility Locus on Chromosome 3p25.3

Michael Ludwig, Heiko Reutter, Franz Rüschendorf, Markus Draaken, Regina Betz, Norbert Hübner, Kathrin Saar, Niklas Schäfer, Raimund Stein, Katja P. Wolfenbüttel, Markus M. Nöthen

Journal:

Journal of Pediatric Urology

Year:

2009

Language:

english

File:

PDF, 62 KB

english, 2009

90

Microduplications At 22q11.21 are Associated with Classic Bladder Exstrophy

Wolfgang H. Rösch, Markus Draaken, Michael Ludwig, Heiko Reutter, Charlotte Schramm, Enrika Bartels, Thomas M. Boemers, Annette Schröder, Raimund Stein, Markus M. Nöthen, Anne-Karoline Ebert

Journal:

Journal of Pediatric Urology

Year:

2010

Language:

english

File:

PDF, 35 KB

english, 2010

91

Breakthroughs in the genetics of orofacial clefting

Elisabeth Mangold, Kerstin U. Ludwig, Markus M. Nöthen

Journal:

Trends in Molecular Medicine

Year:

2011

Language:

english

File:

PDF, 942 KB

english, 2011

92

DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population

Alessandro Serretti, Cristina Lorenzi, Laura Mandelli, Sven Cichon, Johannes Schumacher, Markus M. Nöthen, Marcella Rietschel, Monja Tullius, Stephanie Ohlraun

Journal:

Neuroscience Letters

Year:

2004

Language:

english

File:

PDF, 73 KB

english, 2004

93

Norepinephrine transporter (NET) promoter and 5′-UTR polymorphisms: association analysis in panic disorder

Yoo J. Lee, Christa Hohoff, Katharina Domschke, Philipp Sand, Gregor Kuhlenbäumer, Anja Schirmacher, Christine M. Freitag, Jobst Meyer, Gerald Stöber, Petra Franke, Markus M. Nöthen, Jürgen Fritze, Ro

Journal:

Neuroscience Letters

Year:

2005

Language:

english

File:

PDF, 68 KB

english, 2005

94

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

Rosie M. Walker, Andrea Christoforou, Pippa A. Thomson, Kevin A. McGhee, Alan Maclean, Thomas W. Mühleisen, Jana Strohmaier, Vanessa Nieratschker, Markus M. Nöthen, Marcella Rietschel, Sven Cichon, St

Journal:

Neuroscience Letters

Year:

2010

Language:

english

File:

PDF, 277 KB

english, 2010

95

Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells

Marc Thier, Philipp Wörsdörfer, Yenal B. Lakes, Raphaela Gorris, Stefan Herms, Thoralf Opitz, Dominic Seiferling, Tamara Quandel, Per Hoffmann, Markus M. Nöthen, Oliver Brüstle, Frank Edenhofer

Journal:

Year:

2012

Language:

english

File:

PDF, 1.18 MB

english, 2012

96

Nonreplication of Linkage Disequilibrium between the Dopamine D4 Receptor Locus and Tourette Syndrome

Johannes Hebebrand, Markus M. Nöthen, Andreas Ziegler, Birgit Klug, Helge Neidt, Katja Eggermann, Gerd Lehmkuhl, Fritz Poustka, Martin H. Schmidt, Peter Propping, Helmut Remschmidt

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 65 KB

english, 1997

97

Pharmacogenetics of clozapine response

Johannes Schumacher, Thomas G Schulze, Thomas F Wienker, Marcella Rietschel, Markus M Nöthen

Journal:

Year:

2000

Language:

english

File:

PDF, 91 KB

english, 2000

98

Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteers

Erik G Jönsson, Markus M Nöthen, J.Petter Gustavsson, Helge Neidt, Roland Bunzel, Peter Propping, Göran C Sedvall

Journal:

Psychiatry Research

Year:

1998

Language:

english

File:

PDF, 93 KB

english, 1998

99

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

100

A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22

Markus M. Nöthen, Sven Cichon, Ina R. Vogt, Susanne Hemmer, Roland Kruse, Michael Knapp, Tobias Höller, Muhammad Faiyaz ul Haque, Sayedul Haque, Peter Propping, Mahmud Ahmad, Marcella Rietschel

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 792 KB

english, 1998