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Markus Nöthen

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Physiology

Genes & Molecular Sequences

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Germany

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Publications

TOP 3
Pasternack Sandra M; von Kügelgen Ivar; Müller Melanie; Oji Vinzenz; Traupe Heiko; Sprecher Eli; Nöthen Markus M; Janecke Andreas R; Betz Regina C
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth.
Nikopensius Tiit; Ambrozaityte Laima; Ludwig Kerstin U; Birnbaum Stefanie; Jagomägi Triin; Saag Mare; Matuleviciene Ausra; Linkeviciene Laura; Herms Stefan; Knapp Michael; Hoffmann Per; Nöthen Markus M; Kucinskas Vaidutis; Metspalu Andres; Mangold Elisabeth
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.
Markov V; Krug A; Krach S; Whitney C; Eggermann T; Zerres K; Stöcker T; Shah N J; Nöthen M M; Treutlein J; Rietschel M; Kircher T
Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals.

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All Publications

2009: Pasternack Sandra M; von Kügelgen Ivar; Müller Melanie; Oji Vinzenz; Traupe Heiko; Sprecher Eli; Nöthen Markus M; Janecke Andreas R; Betz Regina C
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth.
The Journal of investigative dermatology 2009;129(12):2772-6.
2009: Nikopensius Tiit; Ambrozaityte Laima; Ludwig Kerstin U; Birnbaum Stefanie; Jagomägi Triin; Saag Mare; Matuleviciene Ausra; Linkeviciene Laura; Herms Stefan; Knapp Michael; Hoffmann Per; Nöthen Markus M; Kucinskas Vaidutis; Metspalu Andres; Mangold Elisabeth
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.
American journal of medical genetics. Part A 2009;149A(11):2551-3.
2009: Markov V; Krug A; Krach S; Whitney C; Eggermann T; Zerres K; Stöcker T; Shah N J; Nöthen M M; Treutlein J; Rietschel M; Kircher T
Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals.
NeuroImage 2009;47(4):2016-22.
2009: Kircher Tilo; Krug Axel; Markov Valentin; Whitney Carin; Krach Sören; Zerres Klaus; Eggermann Thomas; Stöcker Tony; Shah Nadim Jon; Treutlein Jens; Nöthen Markus M; Becker Tim; Rietschel Marcella
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.
Human brain mapping 2009;30(10):3406-16.
2009: Kircher T; Markov V; Krug A; Eggermann T; Zerres K; Nöthen M M; Skowronek M H; Rietschel M
Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects.
Psychological medicine 2009;39(10):1657-65.
2009: Grigoroiu-Serbanescu Maria; Herms Stefan; Mühleisen Thomas W; Georgi Alexander; Diaconu Carmen C; Strohmaier Jana; Czerski Piotr; Hauser Joanna; Leszczynska-Rodziewicz Anna; Jamra Rami Abou; Babadjanova Gulia; Tiganov A; Krasnov V; Kapiletti Sofia; Neagu Ana Iulia; Vollmer Jennifer; Breuer René; Rietschel Marcella; Nöthen Markus M; Cichon Sven; Propping Peter; Nöthen Markus M; Cichon Sven
Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(7):1017-21.
2009: Haenisch Britta; Linsel Karoline; Brüss Michael; Gilsbach Ralf; Propping Peter; Nöthen Markus M; Rietschel Marcella; Fimmers Rolf; Maier Wolfgang; Zobel Astrid; Höfels Susanne; Guttenthaler Vera; Göthert Manfred; Bönisch Heinz
Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(7):1013-6.
2009: 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
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
Bipolar disorders 2009;11(6):610-20.
2009: Ludwig K U; Mattheisen M; Mühleisen T W; Roeske D; Schmäl C; Breuer R; Schulte-Körne G; Müller-Myhsok B; Nöthen M M; Hoffmann P; Rietschel M; Cichon S
Supporting evidence for LRRTM1 imprinting effects in schizophrenia.
Molecular psychiatry 2009;14(8):743-5.
2009: Hillmer Axel M; Freudenberg Jan; Myles Sean; Herms Stefan; Tang Kun; Hughes David A; Brockschmidt Felix F; Ruan Yijun; Stoneking Mark; Nöthen Markus M
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness.
Human genetics 2009;126(2):255-64.
2009: Treutlein Jens; Cichon Sven; Ridinger Monika; Wodarz Norbert; Soyka Michael; Zill Peter; Maier Wolfgang; Moessner Rainald; Gaebel Wolfgang; Dahmen Norbert; Fehr Christoph; Scherbaum Norbert; Steffens Michael; Ludwig Kerstin U; Frank Josef; Wichmann H Erich; Schreiber Stefan; Dragano Nico; Sommer Wolfgang H; Leonardi-Essmann Fernando; Lourdusamy Anbarasu; Gebicke-Haerter Peter; Wienker Thomas F; Sullivan Patrick F; Nöthen Markus M; Kiefer Falk; Spanagel Rainer; Mann Karl; Rietschel Marcella
Genome-wide association study of alcohol dependence.
Archives of general psychiatry 2009;66(7):773-84.
2009: Schumacher Johannes; Laje Gonzalo; Abou Jamra Rami; 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
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
Human molecular genetics 2009;18(14):2719-27.
2009: Reutter Heiko; Bökenkamp Arend; Ebert Anne-Karolin; Rösch Wolfgang; Boemers Thomas M; Nöthen Markus M; Ludwig Michael
Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.
European journal of pediatrics 2009;168(7):881-3.
2009: Treutlein Jens; Mühleisen Thomas W; Frank Josef; Mattheisen Manuel; Herms Stefan; Ludwig Kerstin U; Treutlein Tsendsesmee; Schmael Christine; Strohmaier Jana; Bösshenz Katja Veronika; Breuer René; Paul Torsten; Witt Stephanie H; Schulze Thomas G; Schlösser Ralf G M; Nenadic Igor; Sauer Heinrich; Becker Tim; Maier Wolfgang; Cichon Sven; Nöthen Markus M; Rietschel Marcella
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter.
Schizophrenia research 2009;111(1-3):123-30.
2009: Nahum Sagi; Pasternack Sandra M; Pforr Jana; Indelman Margarita; Wollnik Bernd; Bergman Reuven; Nöthen Markus M; König Arne; Khamaysi Ziyad; Betz Regina C; Sprecher Eli
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.
Archives of dermatological research 2009;301(5):391-3.
2009: Rietschel Marcella; Georgi Alexander; Schmael Christine; Schirmbeck Frederike; Strohmaier Jana; Boesshenz Katja V; Schwarz Markus; Nöthen Markus M; Schulze Thomas G
Premorbid adjustment: a phenotype highlighting a distinction rather than an overlap between schizophrenia and bipolar disorder.
Schizophrenia research 2009;110(1-3):33-9.
2009: Schulze T G; Detera-Wadleigh S D; Akula N; Gupta A; Kassem L; Steele J; Pearl J; Strohmaier J; Breuer R; Schwarz M; Propping P; Nöthen M M; Cichon S; Schumacher J; Rietschel M; McMahon F J
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder.
Molecular psychiatry 2009;14(5):487-91.
2009: Georgi Alexander; Schumacher Johannes; Leon Chady Abboud; Wolf Angela Villela; Klein Katrin; Böhenz Katja V; Schirmbeck Frederike; Strohmaier Jana; Propping Peter; Schulze Thomas G; Rietschel Marcella; Nöthen Markus M; Cichon Sven; Jamra Rami Abou
No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample.
Psychiatric genetics 2009;19(2):104.
2009: 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
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2009;117(2):200-3.
2009: Dahdouh Faten; Anthoni Heidi; Tapia-Páez Isabel; Peyrard-Janvid Myriam; Schulte-Körne Gerd; Warnke Andreas; Remschmidt Helmut; Ziegler Andreas; Kere Juha; Müller-Myhsok Bertram; Nöthen Markus M; Schumacher Johannes; Zucchelli Marco
Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Psychiatric genetics 2009;19(2):59-63.
2009: Jansen Andreas; Krach Sören; Krug Axel; Markov Valentin; Eggermann Thomas; Zerres Klaus; Stöcker Tony; Shah N Jon; Nöthen Markus M; Treutlein Jens; Rietschel Marcella; Kircher Tilo
A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe.
NeuroImage 2009;45(3):1002-8.
2009: Jamra Rami Abou; Georgi Alexander; Suliman Husam; Klein Katrin; Villela Angela Wolf; Schulze Thomas G; Propping Peter; Cichon Sven; Rietschel Marcella; Nöthen Markus M; Schumacher Johannes
No association between the D-aspartate oxidase locus and schizophrenia.
Psychiatric genetics 2009;19(1):56.
2009: Jansen Andreas; Krach Sören; Krug Axel; Markov Valentin; Eggermann Thomas; Zerres Klaus; Thimm Markus; Nöthen Markus M; Treutlein Jens; Rietschel Marcella; Kircher Tilo
Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects.
BMC psychiatry 2009;9():60.
2008: Ludwig Kerstin U; Schumacher Johannes; Schulte-Körne Gerd; König Inke R; Warnke Andreas; Plume Ellen; Anthoni Heidi; Peyrard-Janvid Myriam; Meng Haiying; Ziegler Andreas; Remschmidt Helmut; Kere Juha; Gruen Jeffrey R; Müller-Myhsok Bertram; Nöthen Markus M; Hoffmann Per
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Psychiatric genetics 2008;18(6):310-2.
2008: Hillmer Axel M; Brockschmidt 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; Betz Regina C; Cichon Sven; Propping Peter; Baur Max P; Wienker Thomas F; Kruse Roland; Nöthen Markus M
Susceptibility variants for male-pattern baldness on chromosome 20p11.
Nature genetics 2008;40(11):1279-81.
2008: Ludwig Kerstin U; Roeske Darina; Schumacher Johannes; Schulte-Körne Gerd; König Inke R; Warnke Andreas; Plume Ellen; Ziegler Andreas; Remschmidt Helmut; Müller-Myhsok Bertram; Nöthen Markus M; Hoffmann Per
Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(11):1587-9.
2008: 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
Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.
Journal of autism and developmental disorders 2008;38(10):1977-81.
2008: Grigoroiu-Serbanescu Maria; Diaconu Carmen C; Herms Stefan; Bleotu Coralia; Vollmer Jennifer; Mühleisen Thomas W; Prelipceanu Dan; Priebe Lutz; Mihailescu Radu; Georgescu Marie-Jana; Sima Dorina; Grimberg Mihaela; Nöthen Markus M; Cichon Sven
Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population.
Psychiatric genetics 2008;18(5):240-7.
2008: Krug Axel; Markov Valentin; Eggermann Thomas; Krach Sören; Zerres Klaus; Stöcker Tony; Shah N Jon; Schneider Frank; Nöthen Markus M; Treutlein Jens; Rietschel Marcella; Kircher Tilo
Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals.
NeuroImage 2008;42(4):1569-76.
2008: Jain Mahim; Wallis Deeann; Robin Nathaniel H; De Vrieze Fabienne Wavrant; Hardy John A; Ghadami Mohsen; Bosse Kristin; Betz Regina C; Nöthen Markus M; Arcos-Burgos Mauricio; Muenke Maximilian
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
American journal of medical genetics. Part A 2008;146A(17):2308-11.
2008: Abou Jamra Rami; Gobina Carl Motinda; Becker Tim; Georgi Alexander; Schulze Thomas G; Schmael Christine; Cichon Sven; Propping Peter; Rietschel Marcella; Nöthen Markus M; Schumacher Johannes
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder.
Psychiatric genetics 2008;18(4):199-203.
2008: Krug Axel; Markov Valentin; Leube Dirk; Zerres Klaus; Eggermann Thomas; Nöthen Markus M; Skowronek Markus H; Rietschel Marcella; Kircher Tilo
Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals.
European psychiatry : the journal of the Association of European Psychiatrists 2008;23(5):344-9.
2008: Schumacher Johannes; König Inke R; Schröder Tatjana; Duell Maike; Plume Ellen; Propping Peter; Warnke Andreas; Libertus Claudia; Ziegler Andreas; Müller-Myhsok Bertram; Schulte-Körne Gerd; Nöthen Markus M
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.
Psychiatric genetics 2008;18(3):137-42.
2008: Rietschel Marcella; Beckmann Lars; Strohmaier Jana; Georgi Alexander; Karpushova Anna; Schirmbeck Frederike; Boesshenz Katja V; Schmäl Christine; Bürger Christin; Jamra Rami Abou; Schumacher Johannes; Höfels Susanne; Kumsta Robert; Entringer Sonja; Krug Axel; Markov Valentin; Maier Wolfgang; Propping Peter; Wüst Stefan; Kircher Tilo; Nöthen Markus M; Cichon Sven; Schulze Thomas G
G72 and its association with major depression and neuroticism in large population-based groups from Germany.
The American journal of psychiatry 2008;165(6):753-62.
2008: Hillmer Axel M; Flaquer Antonia; Hanneken Sandra; Eigelshoven Sibylle; Kortüm Anne-Katrin; Brockschmidt Felix F; Golla Astrid; Metzen Christine; Thiele Holger; Kolberg Susanne; Reinartz Roman; Betz Regina C; Ruzicka Thomas; Hennies Hans Christian; Kruse Roland; Nöthen Markus M
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.
American journal of human genetics 2008;82(3):737-43.
2008: Pasternack Sandra M; von Kügelgen Ivar; Aboud Khalid Al; Lee Young-Ae; Rüschendorf Franz; Voss Katrin; Hillmer Axel M; Molderings Gerhard J; Franz Thomas; Ramirez Alfredo; Nürnberg Peter; Nöthen Markus M; Betz Regina C
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.
Nature genetics 2008;40(3):329-34.
2008: Abou Jamra R; Becker T; Georgi A; Feulner T; Schumacher J; Stromaier J; Schirmbeck F; Schulze T G; Propping P; Rietschel M; Nöthen M M; Cichon S
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.
Molecular psychiatry 2008;13(3):277-84.
2008: Betz R C; König K; Flaquer A; Redler S; Eigelshoven S; Kortüm A-K; Hanneken S; Hillmer A; Tüting T; Lambert J; De Weert J; Kruse R; Lutz G; Blaumeiser B; Nöthen M M
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.
The British journal of dermatology 2008;158(2):389-91.
2008: Baum A E; Akula N; Cabanero M; Cardona I; Corona W; Klemens B; Schulze T G; Cichon S; Rietschel M; Nöthen M M; Georgi A; Schumacher J; Schwarz M; Abou Jamra R; Höfels S; Propping P; Satagopan J; Detera-Wadleigh S D; Hardy J; McMahon F J
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
Molecular psychiatry 2008;13(2):197-207.
2008: Cichon Sven; Winge Ingeborg; Mattheisen Manuel; Georgi Alexander; Karpushova Anna; Freudenberg Jan; Freudenberg-Hua Yun; Babadjanova Gulia; Van Den Bogaert Ann; Abramova Lilia I; Kapiletti Sofia; Knappskog Per M; McKinney Jeffrey; Maier Wolfgang; Jamra Rami Abou; Schulze Thomas G; Schumacher Johannes; Propping Peter; Rietschel Marcella; Haavik Jan; Nöthen Markus M
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder.
Human molecular genetics 2008;17(1):87-97.
2008: Reutter Heiko; Birnbaum Stefanie; Mende Meinhard; Lauster Carola; Schmidt Gül; Henschke Henning; Saffar Mitra; Martini Markus; Lauster Roland; Schiefke Franziska; Reich Rudolf H; Braumann Bert; Scheer Martin; Knapp Michael; Nöthen Markus M; Kramer Franz-Josef; Mangold Elisabeth
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate.
Journal of human genetics 2008;53(7):656-61.
2007: Planko Laura; Böhse Karsten; Höhfeld Jörg; Betz Regina C; Hanneken Sandra; Eigelshoven Sibylle; Kruse Roland; Nöthen Markus M; Magin Thomas M
Identification of a keratin-associated protein with a putative role in vesicle transport.
European journal of cell biology 2007;86(11-12):827-39.
2007: Betz Regina C; Pforr Jana; Flaquer Antonia; Redler Silke; Hanneken Sandra; Eigelshoven Sibylle; Kortüm Anne-Katrin; Tüting Thomas; Lambert Julien; De Weert Jozef; Hillmer Axel M; Schmael Christine; Wienker Thomas F; Kruse Roland; Lutz Gerhard; Blaumeiser Bettina; Nöthen Markus M
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.
The Journal of investigative dermatology 2007;127(11):2539-43.
2007: Storm Katrien; Moens Els; Vits Lieve; De Vlieger Haike; Delaere Gino; D'Hollander Maria; Wuyts Wim; Biervliet Martine; Van Schil Lutgardis; Desager Kristine; Nöthen Markus M
High incidence of the CFTR mutations 3272-26A-->G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A-->G, E588V, and 1671insTATCA).
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2007;6(6):371-5.
2007: Martin Ludovic; Raison-Peyron Nadia; Nöthen Markus M; Cichon Sven; Drouet Christian
Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene.
The Journal of allergy and clinical immunology 2007;120(4):975-7.
2007: Georgi Alexander; Jamra Rami Abou; Klein Katrin; Villela Angela Wolf; Schumacher Johannes; Becker Tim; Paul Torsten; Schmael Christine; Höfels Susanne; Klopp Norman; Illig Thomas; Propping Peter; Cichon Sven; Nöthen Markus M; Schulze Thomas G; Rietschel Marcella
Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample.
Psychiatric genetics 2007;17(5):308-10.
2007: Massat I; Lerer B; Souery D; Blackwood D; Muir W; Kaneva R; Nöthen M M; Oruc L; Papadimitriou G N; Dikeos D; Serretti A; Bellivier F; Golmard J L; Milanova V; Del-Favero J; Van Broeckhoven C; Mendlewicz J
HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study.
Molecular psychiatry 2007;12(9):797-8.
2007: Brockschmidt Felix F; Nöthen Markus M; Hillmer Axel M
The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function.
Journal of molecular endocrinology 2007;39(1):1-8.
2007: Betz Regina C; Indelman Margarita; Pforr Jana; Schreiner Felix; Bauer Ralf; Bergman Reuven; Lentze Michael J; Nöthen Markus M; Cichon Sven; Sprecher Eli
Identification of mutations in the human hairless gene in two new families with congenital atrichia.
Archives of dermatological research 2007;299(3):157-61.
2007: Schmael Christine; Georgi Alexander; Krumm Bertram; Buerger Christin; Deschner Monika; Nöthen Markus M; Schulze Thomas G; Rietschel Marcella
Premorbid adjustment in schizophrenia--an important aspect of phenotype definition.
Schizophrenia research 2007;92(1-3):50-62.
2007: Schumacher Johannes; Hoffmann Per; Schmäl Christine; Schulte-Körne Gerd; Nöthen Markus M
Genetics of dyslexia: the evolving landscape.
Journal of medical genetics 2007;44(5):289-97.
2007: Schirmbeck Frederike; Georgi Alexander; Strohmaier Jana; Schmael Christine; Knorr Carolin; Jamra Rami Abou; Schumacher Johannes; Becker Tim; Klopp Norman; Illig Thomas; Wulf Maren; Schwarz Markus; Maier Wolfgang; Propping Peter; Cichon Sven; Nöthen Markus M; Schulze Thomas G; Rietschel Marcella
No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample.
Psychiatric genetics 2007;17(2):127.
2007: Strohmaier Jana; Georgi Alexander; Schirmbeck Frederike; Schmael Christine; Jamra Rami Abou; Schumacher Johannes; Becker Tim; Höfels Susanne; Klopp Norman; Illig Thomas; Propping Peter; Cichon Sven; Nöthen Markus M; Rietschel Marcella; Schulze Thomas G
No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample.
Psychiatric genetics 2007;17(2):125.
2007: Anthoni Heidi; Zucchelli Marco; Matsson Hans; Müller-Myhsok Bertram; Fransson Ingegerd; Schumacher Johannes; Massinen Satu; Onkamo Päivi; Warnke Andreas; Griesemann Heide; Hoffmann Per; Nopola-Hemmi Jaana; Lyytinen Heikki; Schulte-Körne Gerd; Kere Juha; Nöthen Markus M; Peyrard-Janvid Myriam
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Human molecular genetics 2007;16(6):667-77.
2007: Schulte-Körne G; Ziegler A; Deimel W; Schumacher J; Plume E; Bachmann C; Kleensang A; Propping P; Nöthen M M; Warnke A; Remschmidt H; König I R
Interrelationship and familiality of dyslexia related quantitative measures.
Annals of human genetics 2007;71(Pt 2):160-75.
2007: Jamra Rami Abou; Becker Tim; Klopp Norman; Dahdouh Faten; Schulze Thomas G; Gross Magdalena; Deschner Monika; Schmäl Christine; Illig Thomas; Rietschel Marcella; Propping Peter; Cichon Sven; Nöthen Markus M; Schumacher Johannes
No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia.
Psychiatric genetics 2007;17(1):43-5.
2006: Cichon Sven; Martin Ludovic; Hennies Hans Christian; Müller Felicitas; Van Driessche Karen; Karpushova Anna; Stevens Wim; Colombo Roberto; Renné Thomas; Drouet Christian; Bork Konrad; Nöthen Markus M
Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III.
American journal of human genetics 2006;79(6):1098-104.
2006: Rietschel Marcella; Propping Peter; Nöthen Markus M
The impact of genetics on psychiatric nosology.
The American journal of psychiatry 2006;163(12):2197-8; author reply 2198.
2006: Schäfer N; Blaumeiser B; Becker T; Freudenberg-Hua Y; Hanneken S; Eigelshoven S; Schmael C; Lambert J; De Weert J; Kruse R; Nöthen M M; Betz R C
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.
International journal of immunogenetics 2006;33(6):393-5.
2006: Skowronek Markus H; Georgi Alexander; Jamra Rami Abou; Schumacher Johannes; Becker Tim; Schmael Christine; Paul Torsten; Deschner Monika; Höfels Susanne; Wulff Maren; Schwarz Markus; Klopp Norman; Illig Thomas; Propping Peter; Cichon Sven; Nöthen Markus M; Schulze Thomas G; Rietschel Marcella
No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample.
Psychiatric genetics 2006;16(6):233-4.
2006: Reutter Heiko; Becker Tim; Ludwig Michael; Schäfer Niklas; Detlefsen Birte; Beaudoin Sylvie; Fisch Margit; Ebert Anne-Karoline; Rösch Wolfgang; Nöthen Markus M; Boemers Thomas M; Betz Regina C
Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex.
American journal of medical genetics. Part A 2006;140(22):2506-9.
2006: Ivo Roland; Schulze Thomas G; Schumacher Johannes; Kesper Kristina; Müller Daniel J; Kremer Ilana; Dobrusin Michael; Mujaheed Mustafa; Murad Ibrahim; Blanaru Monika; Bannoura Isaam; Reshef Alon; Bachner-Melman Rachel; Ebstein Richard P; Propping Peter; Belmaker Robert H; Maier Wolfgang; Rietschel Marcella; Nöthen Markus M; Cichon Sven
No evidence for association between NOTCH4 and schizophrenia in a large family-based and case-control association analysis.
Psychiatric genetics 2006;16(5):197-203.
2006: Georgi Alexander; Jamra Rami A; Schumacher Johannes; Becker Tim; Schmael Christine; Deschner Monika; Höfels Susanne; Wulff Maren; Schwarz Markus; Klopp Norman; Illig Thomas; Propping Peter; Cichon Sven; Nöthen Markus M; Rietschel Marcella; Schulze Thomas G
No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.
Psychiatric genetics 2006;16(5):183-4.
2006: Abou Jamra Rami; Schmael Christine; Cichon Sven; Rietschel Marcella; Schumacher Johannes; Nöthen Markus M
The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries?
Schizophrenia bulletin 2006;32(4):599-608.
2006: Jamra Rami Abou; Klein Katrin; Villela Angela Wolf; Becker Tim; Schulze Thomas G; Schmael Christine; Deschner Monika; Klopp Norman; Illig Thomas; Propping Peter; Cichon Sven; Rietschel Marcella; Nöthen Markus M; Schumacher Johannes
Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(6):663-5.
2006: Winantea Jane; Hoang My Ngo; Ohlraun Stefanie; Rietschel Marcella; Cichon Sven; Propping Peter; Nöthen Markus M; Freudenberg Jan; Freudenberg-Hua Yun
A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.
European journal of human genetics : EJHG 2006;14(9):1037-43.
2006: Dikeos Dimitris G; Papadimitriou George N; Souery Daniel; Del-Favero Jurgen; Massat Isabelle; Blackwood Douglas; Cichon Sven; Daskalopoulou Eugenia; Ivezic Sladjana; Kaneva Radka; Karadima Georgia; Lorenzi Cristina; Milanova Vihra; Muir Walter; Nöthen Markus; Oruc Lilijana; Rietschel Marcella; Serretti Alessandro; Van Broeckhoven Christine; Soldatos Constantin R; Stefanis Costas N; Mendlewicz Julien
Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study.
Psychiatric genetics 2006;16(4):169-71.
2006: Entz Patricia; Blaumeiser Bettina; Betz Regina C; Lambert Julien; Seymons Katia; Eigelshoven Sibylle; Hanneken Sandra; Kruse Roland; Nürnberg Peter; Nagy Marion; Nöthen Markus M
Investigation of the HLA-DRB1 locus in alopecia areata.
European journal of dermatology : EJD 2006;16(4):363-7.
2006: Pforr J; Blaumeiser B; Becker T; Freudenberg-Hua Y; Hanneken S; Eigelshoven S; Cuyt I; De Weert J; Lambert J; Kruse R; Nöthen M M; Betz R C
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.
Tissue antigens 2006;68(1):58-61.
2006: Jamra Rami Abou; Villela Angela Wolf; Klein Katrin; Becker Tim; Schulze Thomas G; Schmael Christine; Deschner Monika; Klopp Norman; Illig Thomas; Propping Peter; Cichon Sven; Rietschel Marcella; Nöthen Markus M; Schumacher Johannes
No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia.
Psychiatric genetics 2006;16(3):91.
2006: Blaumeiser Bettina; van der Goot Ineke; Fimmers Rolf; Hanneken Sandra; Ritzmann Sibylle; Seymons Katia; Betz Regina C; Ruzicka Thomas; Wienker Thomas F; De Weert Jozef; Lambert Julien; Kruse Roland; Nöthen Markus M
Familial aggregation of alopecia areata.
Journal of the American Academy of Dermatology 2006;54(4):627-32.
2006: Courtens Winnie; Wuyts Wim; Poot Martin; Szuhai Karoly; Wauters Jan; Reyniers Edwin; Eleveld Marc; Diaz George; Nöthen Markus M; Parvari Ruti
Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review.
American journal of medical genetics. Part A 2006;140(6):611-7.
2006: Betz Regina C; Planko Laura; Eigelshoven Sibylle; Hanneken Sandra; Pasternack Sandra M; Bussow Heinrich; Van Den Bogaert Kris; Wenzel Joerg; Braun-Falco Markus; Rutten Arno; Rogers Michael A; Ruzicka Thomas; Nöthen Markus M; Magin Thomas M; Kruse Roland
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.
American journal of human genetics 2006;78(3):510-9.
2006: Schumacher J; König I R; Plume E; Propping P; Warnke A; Manthey M; Duell M; Kleensang A; Repsilber D; Preis M; Remschmidt H; Ziegler A; Nöthen M M; Schulte-Körne G
Linkage analyses of chromosomal region 18p11-q12 in dyslexia.
Journal of neural transmission (Vienna, Austria : 1996) 2006;113(3):417-23.
2006: Schumacher Johannes; Anthoni Heidi; Dahdouh Faten; König Inke R; Hillmer Axel M; Kluck Nadine; Manthey Malou; Plume Ellen; Warnke Andreas; Remschmidt Helmut; Hülsmann Jutta; Cichon Sven; Lindgren Cecilia M; Propping Peter; Zucchelli Marco; Ziegler Andreas; Peyrard-Janvid Myriam; Schulte-Körne Gerd; Nöthen Markus M; Kere Juha
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
American journal of human genetics 2006;78(1):52-62.
2006: Jönsson Erik G; Cichon Sven; Schumacher Johannes; Abou Jamra Rami; Schulze Thomas G; Deschner Monica; Forslund Kaj; Hall Håkan; Propping Peter; Czerski Piotr M; Dmitrak-Weglarz Monica; Kapelski Pawel; Driessen Martin; Maier Wolfgang; Hauser Joanna; Rietschel Marcella; Nöthen Markus M
Association study of a functional promoter polymorphism in the XBP1 gene and schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(1):71-5.
2005: Dávalos N O; García-Vargas A; Pforr J; Dávalos I P; Picos-Cárdenas V J; García-Cruz D; Kruse R; Figuera L E; Nöthen M M; Betz R C
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.
The British journal of dermatology 2005;153(6):1216-9.
2005: Schulze Thomas G; Ohlraun Stephanie; Czerski Piotr M; Schumacher Johannes; Kassem Layla; Deschner Monika; Gross Magdalena; Tullius Monja; Heidmann Vivien; Kovalenko Svetlana; Jamra Rami Abou; Becker Tim; Leszczynska-Rodziewicz Anna; Hauser Joanna; Illig Thomas; Klopp Norman; Wellek Stefan; Cichon Sven; Henn Fritz A; McMahon Francis J; Maier Wolfgang; Propping Peter; Nöthen Markus M; Rietschel Marcella
Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.
The American journal of psychiatry 2005;162(11):2101-8.
2005: Abou Jamra Rami; Schumacher Johannes; Becker Tim; Dahdouh Faten; Ohlraun Stephanie; Suliman Husam; Schulze Thomas G; Tullius Monja; Kovalenko Svetlana; Maier Wolfgang; Rietschel Marcella; Propping Peter; Nöthen Markus M; Cichon Sven
No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder.
Psychiatric genetics 2005;15(3):195-8.
2005: Schumacher Johannes; Jamra Rami Abou; Becker Tim; Ohlraun Stephanie; Klopp Norman; Binder Elisabeth B; Schulze Thomas G; Deschner Monika; Schmäl Christine; Höfels Susanne; Zobel Astrid; Illig Thomas; Propping Peter; Holsboer Florian; Rietschel Marcella; Nöthen Markus M; Cichon Sven
Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression.
Biological psychiatry 2005;58(4):307-14.
2005: Glaser Beate; Schumacher Johannes; Williams Hywel J; Jamra Rami Abou; Ianakiev Nikolai; Milev Radoi; Ohlraun Stephanie; Schulze Thomas G; Czerski Piotr M; Hauser Joanna; Jönsson Erick G; Sedvall Göran C; Klopp Norman; Illig Thomas; Becker Tim; Propping Peter; Williams Nigel M; Cichon Sven; Kirov George; Rietschel Marcella; Murphy Kieran C; O'Donovan Michael C; Nöthen Markus M; Owen Michael J
No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.
Biological psychiatry 2005;58(1):78-80.
2005: Abou Jamra R; Sircar I; Becker T; Freudenberg-Hua Y; Ohlraun S; Freudenberg J; Brockschmidt F; Schulze T G; Gross M; Spira F; Deschner M; Schmäl C; Maier W; Propping P; Rietschel M; Cichon S; Nöthen M M; Schumacher J
A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.
Molecular psychiatry 2005;10(7):618-20.
2005: Schumacher J; Abou Jamra R; Becker T; Klopp N; Franke P; Jacob C; Sand P; Fritze J; Ohlraun S; Schulze T G; Rietschel M; Illig T; Propping P; Cichon S; Deckert J; Nöthen M M
Investigation of the DAOA/G30 locus in panic disorder.
Molecular psychiatry 2005;10(5):428-9.
2005: Courtens Winnie; Vermeulen Stefan; Wuyts Wim; Messiaen Ludwine; Wauters Jan; Nuytinck Lieve; Peeters Nils; Storm Katrien; Speleman Frank; Nöthen Markus M
An interstitial deletion of chromosome 7 at band q21: a case report and review.
American journal of medical genetics. Part A 2005;134A(1):12-23.
2005: Lee Yoo J; Hohoff Christa; Domschke Katharina; Sand Philipp; Kuhlenbäumer Gregor; Schirmacher Anja; Freitag Christine M; Meyer Jobst; Stöber Gerald; Franke Petra; Nöthen Markus M; Fritze Jürgen; Fimmers Rolf; Garritsen Henk S; Stögbauer Florian; Deckert Jürgen
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder.
Neuroscience letters 2005;377(1):40-3.
2005: Hoefgen Barbara; Schulze Thomas G; Ohlraun Stephanie; von Widdern Olrik; Höfels Susanne; Gross Magdalena; Heidmann Vivien; Kovalenko Svetlana; Eckermann Anita; Kölsch Heike; Metten Martin; Zobel Astrid; Becker Tim; Nöthen Markus M; Propping Peter; Heun Reinhard; Maier Wolfgang; Rietschel Marcella
The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder.
Biological psychiatry 2005;57(3):247-51.
2005: Grigoroiu-Serbanescu Maria; Nöthen Markus M; Ohlraun Stephanie; Propping Peter; Maier Wolfgang; Wickramaratne Priya; Georgescu Marie-Jana; Prelipceanu Dan; Grimberg Mihaela; Sima Dorina; Rietschel Marcella
Family history influences age of onset in bipolar I disorder in females but not in males.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;133B(1):6-11.
2005: Müller Daniel J; Barkow Katrin; Kovalenko Svetlana; Ohlraun Stephanie; Fangerau Heiner; Kölsch Heike; Lemke Matthias R; Held Tilo; Nöthen Markus M; Maier Wofgang; Heun Reinhard; Rietschel Marcella
Suicide attempts in schizophrenia and affective disorders with relation to some specific demographical and clinical characteristics.
European psychiatry : the journal of the Association of European Psychiatrists 2005;20(1):65-9.
2005: Ziegler Andreas; König Inke R; Deimel Wolfgang; Plume Ellen; Nöthen Markus M; Propping Peter; Kleensang André; Müller-Myhsok Bertram; Warnke Andreas; Remschmidt Helmut; Schulte-Körne Gerd
Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design.
Human heredity 2005;59(3):136-43.
2005: Bygum Anette; Betz Regina C; Kragballe Knud; Steiniche Torben; Peeters Nils; Wuyts Wim; Nöthen Markus M
KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation.
Acta dermato-venereologica 2005;85(2):152-5.
2005: Freudenberg-Hua Y; Freudenberg J; Winantea J; Kluck N; Cichon S; Brüss M; Propping P; Nöthen M M
Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.
The pharmacogenomics journal 2005;5(3):183-92.
2004: Paus Sebastian; Rietschel Marcella; Schulze Thomas G; Ohlraun Stephanie; Diaconu Carmen C; Van Den Bogaert Ann; Maier Wolfgang; Propping Peter; Cichon Sven; Nöthen Markus M
Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population.
Psychiatric genetics 2004;14(4):233-4.
2004: Frank Bernd; Niesler Beate; Nöthen Markus M; Neidt Helge; Propping Peter; Bondy Brigitta; Rietschel Marcella; Maier Wolfgang; Albus Margot; Rappold Gudrun
Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;131B(1):1-5.
2004: Serretti Alessandro; Lorenzi Cristina; Mandelli Laura; Cichon Sven; Schumacher Johannes; Nöthen Markus M; Rietschel Marcella; Tullius Monja; Ohlraun Stephanie
DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population.
Neuroscience letters 2004;368(3):269-73.
2004: Blaumeiser Bettina; Loquet Philip; Wuyts Wim; Nöthen Markus M
Prenatal diagnosis of Pfeiffer syndrome type II.
Prenatal diagnosis 2004;24(8):644-6.
2004: Østerlund Torben; Everman David B; Betz Regina C; Mosca Monica; Nöthen Markus M; Schwartz Charles E; Zaphiropoulos Peter G; Toftgård Rune
The FU gene and its possible protein isoforms.
BMC genomics 2004;5(1):49.
2004: Paus Sebastian; Seeger Gert; Brecht Hans M; Köster Jürgen; El-Faddagh Mahha; Nöthen Markus M; Klockgether Thomas; Wüllner Ullrich
Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2004;19(6):705-7.
2004: Domschke Katharina; Freitag Christine M; Kuhlenbäumer Gregor; Schirmacher Anja; Sand Philipp; Nyhuis Peter; Jacob Christian; Fritze Jürgen; Franke Petra; Rietschel Marcella; Garritsen Henk S; Fimmers Rolf; Nöthen Markus M; Lesch Klaus-Peter; Stögbauer Florian; Deckert Jürgen
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2004;7(2):183-8.
2004: Rothe Claudia; Gutknecht Lise; Freitag Christine; Tauber Ralf; Mössner Rainald; Franke Petra; Fritze Jrgen; Wagner Gerd; Peikert Gregor; Wenda Berit; Sand Philipp; Jacob Christian; Rietschel Marcella; Nöthen Markus M; Garritsen Henk; Fimmers Rolf; Deckert Jürgen; Lesch Klaus-Peter
Association of a functional 1019C>G 5-HT1A receptor gene polymorphism with panic disorder with agoraphobia.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2004;7(2):189-92.
2004: Gadzicki Dorothea; Müller-Vahl Kirsten R; Heller Daniela; Ossege Sebastian; Nöthen Markus M; Hebebrand Johannes; Stuhrmann Manfred
Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;127B(1):97-103.
2004: Mendlewicz Julien; Massat Isabelle; Souery Daniel; Del-Favero Jurgen; Oruc Lilijana; Nöthen Markus M; Blackwood Douglas; Muir Walter; Battersby Sharon; Lerer Beny; Segman Ronen H; Kaneva Radka; Serretti Alessandro; Lilli Roberta; Lorenzi Christian; Jakovljevic Miro; Ivezic Sladana; Rietschel Marcella; Milanova Vihra; Van Broeckhoven Christine
Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study.
European journal of human genetics : EJHG 2004;12(5):377-82.
2004: Abou Jamra Rami; Schumacher Johannes; Golla Astrid; Richter Carola; Otte Andreas C J; Schulze Thomas G; Ohlraun Stephanie; Maier Wolfgang; Rietschel Marcella; Cichon Sven; Propping Peter; Nöthen Markus M
Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;126B(1):79-81.
2004: Jönsson Erik G; Bah Jessica; Melke Jonas; Abou Jamra Rami; Schumacher Johannes; Westberg Lars; Ivo Roland; Cichon Sven; Propping Peter; Nöthen Markus M; Eriksson Elias; Sedvall Göran C
Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers.
BMC psychiatry 2004;4():4.
2004: Schumacher J; Jamra R Abon; Freudenberg J; Becker T; Ohlraun S; Otte A C J; Tullius M; Kovalenko S; Bogaert A Van Den; Maier W; Rietschel M; Propping P; Nöthen M M; Cichon S
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder.
Molecular psychiatry 2004;9(2):203-7.
2004: Fangerau Heiner; Ohlraun Stephanie; Granath Ralf O; Nöthen Markus M; Rietschel Marcella; Schulze Thomas G
Computer-assisted phenotype characterization for genetic research in psychiatry.
Human heredity 2004;58(3-4):122-30.
2004: Hösing V G; Schirmacher A; Kuhlenbäumer G; Freitag C; Sand P; Schlesiger C; Jacob C; Fritze J; Franke P; Rietschel M; Garritsen H; Nöthen M M; Fimmers R; Stögbauer F; Deckert J
Cholecystokinin- and cholecystokinin-B-receptor gene polymorphisms in panic disorder.
Journal of neural transmission. Supplementum 2004;(68):147-56.
2003: Papadimitriou George N; Dikeos Dimitris G; Souery Daniel; Del-Favero Jurgen; Massat Isabelle; Avramopoulos Dimitrios; Blairy Sylvie; Cichon Sven; Ivezic Sladjana; Kaneva Radka; Karadima Georgia; Lilli Roberta; Milanova Vihra; Nöthen Markus; Oruc Lilijana; Rietschel Marcella; Serretti Alessandro; Van Broeckhoven Christine; Stefanis Costas N; Mendlewicz Julien
Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study.
Psychiatric genetics 2003;13(4):211-20.
2003: Van Den Bogaert Ann; Schumacher Johannes; Schulze Thomas G; Otte Andreas C; Ohlraun Stephanie; Kovalenko Svetlana; Becker Tim; Freudenberg Jan; Jönsson Erik G; Mattila-Evenden Marja; Sedvall Göran C; Czerski Piotr M; Kapelski Pawel; Hauser Joanna; Maier Wolfgang; Rietschel Marcella; Propping Peter; Nöthen Markus M; Cichon Sven
The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease.
American journal of human genetics 2003;73(6):1438-43.
2003: Schumacher Johannes; Otte Andreas C J; Becker Tim; Sun Yuli; Wienker Thomas F; Wirth Brunhilde; Franke Petra; Abou Jamra Rami; Propping Peter; Deckert Jürgen; Nöthen Markus M; Cichon Sven
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.
Human genetics 2003;114(1):115-7.
2003: Freudenberg-Hua Yun; Freudenberg Jan; Kluck Nadine; Cichon Sven; Propping Peter; Nöthen Markus M
Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.
Genome research 2003;13(10):2271-6.
2003: Jönsson Erik G; Abou Jamra Rami; Schumacher Johannes; Flyckt Lena; Edman Gunnar; Forslund Kaj; Mattila-Evenden Marja; Rylander Gunnar; Asberg Marie; Bjerkenstedt Lars; Wiesel Frits-Axel; Propping Peter; Cichon Sven; Nöthen Markus M; Sedvall Göran C
No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia.
Psychiatric genetics 2003;13(3):175-8.
2003: Hanneken S; Ritzmann S; Nöthen M M; Kruse R
[Androgenetic alopecia. Current aspects of a common phenotype]
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2003;54(8):703-12.
2003: Levy-Nissenbaum Etgar; Betz Regina C; Frydman Moshe; Simon Michel; Lahat Hadas; Bakhan Tengiz; Goldman Boleslaw; Bygum Anette; Pierick Monika; Hillmer Axel M; Jonca Nathalie; Toribio Jaime; Kruse Roland; Dewald Georg; Cichon Sven; Kubisch Christian; Guerrin Marina; Serre Guy; Nöthen Markus M; Pras Elon
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.
Nature genetics 2003;34(2):151-3.
2003: Jönsson Erik G; Sedvall Göran C; Nöthen Markus M; Cichon Sven
Dopamine D4 receptor gene (DRD4) variants and schizophrenia: meta-analyses.
Schizophrenia research 2003;61(1):111-9.
2003: Jönsson Erik G; Cichon Sven; Gustavsson J Petter; Grünhage Frank; Forslund Kaj; Mattila-Evenden Marja; Rylander Gunnar; Asberg Marie; Farde Lars; Propping Peter; Nöthen Markus M
Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment.
Biological psychiatry 2003;53(7):577-84.
2003: Schulze Thomas G; Cichon Sven; Nöthen Markus M; Propping Peter; Maier Wolfgang; Rietschel Marcella
Is there a phenotypic difference between probands in case-control versus family-based association studies?
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;118B(1):25-6; author reply 27-8.
2003: Domschke K; Kuhlenbäumer G; Schirmacher A; Lorenzi C; Armengol L; DiBella D; Gratacos M; Garritsen H S; Nöthen M M; Franke P; Sand P; Fritze J; Perez G; Maier W; Sibrowski W; Estivill X; Bellodi L; Ringelstein E B; Arolt V; Martin-Santos R; Catalano M; Stögbauer F; Deckert J
Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):70-8.
2002: Sand P G; Mori T; Godau C; Stöber G; Flachenecker P; Franke P; Nöthen M M; Fritze J; Maier W; Lesch K-P; Riederer P; Beckmann H; Deckert J
Norepinephrine transporter gene (NET) variants in patients with panic disorder.
Neuroscience letters 2002;333(1):41-4.
2002: Müller Daniel J; Schulze T G; Macciardi F; Ohlraun S; Gross M M; Scherk H; Neidt H; Syagailo Y V; Grässle M; Nöthen M M; Maier W; Lesch K-P; Rietschel M
Moclobemide response in depressed patients: association study with a functional polymorphism in the monoamine oxidase A promoter.
Pharmacopsychiatry 2002;35(4):157-8.
2002: Jahnes Esther; Müller Daniel J; Schulze Thomas G; Windemuth Christine; Cichon Sven; Ohlraun Stephanie; Fangerau Heiner; Held Tilo; Maier Wolfgang; Propping Peter; Nöthen Markus M; Rietschel Marcella
Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder.
American journal of medical genetics 2002;114(5):519-22.
2002: Schulze Thomas G; Chen Yu-Sheng; Akula Nirmala; Hennessy Kathleen; Badner Judith A; McInnis Melvin G; DePaulo J Raymond; Schumacher Johannes; Cichon Sven; Propping Peter; Maier Wolfgang; Rietschel Marcella; Nöthen Markus M; McMahon Francis J
Can long-range microsatellite data be used to predict short-range linkage disequilibrium?
Human molecular genetics 2002;11(12):1363-72.
2002: Sand P G; Schlurmann K; Luckhaus C; Götz M; Stöber G; Lesch K-P; Riederer P; Franke P; Maier W; Nöthen M M; Propping P; Fritze J; Deckert J
Estrogen receptor 1 gene (ESR1) variants in panic disorder.
American journal of medical genetics 2002;114(4):426-8.
2002: Schulze Thomas G; Müller Daniel J; Krauss Harald; Gross Magdalena; Fangerau-Lefèvre Heiner; Illes Franciska; Ohlraun Stephanie; Cichon Sven; Held Tilo; Propping Peter; Nöthen Markus M; Maier Wolfgang; Rietschel Marcella
Further evidence for age of onset being an indicator for severity in bipolar disorder.
Journal of affective disorders 2002;68(2-3):343-5.
2002: Hillmer A M; Kruse R; Macciardi F; Heyn U; Betz R C; Ruzicka T; Propping P; Nöthen M M; Cichon S
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.
The British journal of dermatology 2002;146(4):601-8.
2002: Nöthen Markus M; Cichon Sven
Linking single nucleotide polymorphisms.
Pharmacogenetics 2002;12(2):89-90.
2002: Müller Daniel J; Schulze Thomas G; Jahnes Esther; Cichon Sven; Krauss Harald; Kesper Kristina; Held Tilo; Maier Wolfgang; Propping Peter; Nöthen Markus M; Rietschel Marcella
Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder.
American journal of medical genetics 2002;114(1):74-8.
2002: Martí Sylvia Bort; Cichon Sven; Propping Peter; Nöthen Markus
Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population.
American journal of medical genetics 2002;114(1):46-50.
2002: Martí Sylvia Bort; Cichon Sven; Propping Peter; Nöthen Markus
Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization.
American journal of medical genetics 2002;114(1):12-4.
2002: Jönsson E G; Ivo R; Gustavsson J P; Geijer T; Forslund K; Mattila-Evenden M; Rylander G; Cichon S; Propping P; Bergman H; sberg M; Nöthen M M
No association between dopamine D4 receptor gene variants and novelty seeking.
Molecular psychiatry 2002;7(1):18-20.
2001: Grigoroiu-Serbanescu M; Martinez M; Nöthen M M; Grinberg M; Sima D; Propping P; Marinescu E; Hrestic M
Different familial transmission patterns in bipolar I disorder with onset before and after age 25.
American journal of medical genetics 2001;105(8):765-73.
2001: Cichon S; Schumacher J; Müller D J; Hürter M; Windemuth C; Strauch K; Hemmer S; Schulze T G; Schmidt-Wolf G; Albus M; Borrmann-Hassenbach M; Franzek E; Lanczik M; Fritze J; Kreiner R; Reuner U; Weigelt B; Minges J; Lichtermann D; Lerer B; Kanyas K; Baur M P; Wienker T F; Maier W; Rietschel M; Propping P; Nöthen M M
A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.
Human molecular genetics 2001;10(25):2933-44.
2001: Müller D J; Schulze T G; Knapp M; Held T; Krauss H; Weber T; Ahle G; Maroldt A; Alfter D; Maier W; Nöthen M M; Rietschel M
Familial occurrence of tardive dyskinesia.
Acta psychiatrica Scandinavica 2001;104(5):375-9.
2001: Przkora R; Meyer-Puttlitz B; Schmitt O; Berthold F; Nöthen M; Krauss J; Tonn J C; von Deimling A; Wiestler O D; Pietsch T
Analysis of the TSC2 gene in human medulloblastoma.
Acta neuropathologica 2001;102(4):380-4.
2001: Niesler B; Flohr T; Nöthen M M; Fischer C; Rietschel M; Franzek E; Albus M; Propping P; Rappold G A
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder.
Pharmacogenetics 2001;11(6):471-5.
2001: Jönsson E G; Ivo R; Forslund K; Mattila-Evenden M; Rylander G; Cichon S; Propping P; Nöthen M M; Asberg M; Sedvall G C
No association between a promoter dopamine D(4) receptor gene variant and schizophrenia.
American journal of medical genetics 2001;105(6):525-8.
2001: Schulze T G; Schumacher J; Müller D J; Krauss H; Alfter D; Maroldt A; Ahle G; Maroldt A O; Novo y Fernández A; Weber T; Held T; Propping P; Maier W; Nöthen M M; Rietschel M
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.
American journal of medical genetics 2001;105(6):498-501.
2001: Betz R C; Schoser B G; Kasper D; Ricker K; Ramírez A; Stein V; Torbergsen T; Lee Y A; Nöthen M M; Wienker T F; Malin J P; Propping P; Reis A; Mortier W; Jentsch T J; Vorgerd M; Kubisch C
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.
Nature genetics 2001;28(3):218-9.
2001: Hillmer A M; Kruse R; Betz R C; Schumacher J; Heyn U; Propping P; Nöthen M M; Cichon S
Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia.
American journal of human genetics 2001;69(1):235-7.
2001: Schulze T G; Müller D J; Krauss H; Gross M; Bauer I; Fangerau-Lefèvre H; Illes F; Ohlraun S; Fimmers R; Cichon S; Held T; Propping P; Nöthen M M; Maier W; Rietschel M
Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios.
American journal of medical genetics 2001;105(4):351-3.
2001: Cichon S; Schmidt-Wolf G; Schumacher J; Müller D J; Hürter M; Schulze T G; Albus M; Borrmann-Hassenbach M; Franzek E; Lanczik M; Fritze J; Kreiner R; Weigelt B; Minges J; Lichtermann D; Lerer B; Kanyas K; Strauch K; Windemuth C; Baur M P; Wienker T F; Maier W; Rietschel M; Propping P; Nöthen M M
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26.
Molecular psychiatry 2001;6(3):342-9.
2001: Becker A J; Löbach M; Klein H; Normann S; Nöthen M M; von Deimling A; Mizuguchi M; Elger C E; Schramm J; Wiestler O D; Blümcke I
Mutational analysis of TSC1 and TSC2 genes in gangliogliomas.
Neuropathology and applied neurobiology 2001;27(2):105-14.
2001: Jönsson E G; Nöthen M M; Gustavsson J P; Berggård C; Bunzel R; Forslund K; Rylander G; Mattila-Evenden M; Propping P; Asberg M; Sedvall G
No association between serotonin 2A receptor gene variants and personality traits.
Psychiatric genetics 2001;11(1):11-7.
2001: Souery D; Van Gestel S; Massat I; Blairy S; Adolfsson R; Blackwood D; Del-Favero J; Dikeos D; Jakovljevic M; Kaneva R; Lattuada E; Lerer B; Lilli R; Milanova V; Muir W; Nöthen M; Oruc L; Papadimitriou G; Propping P; Schulze T; Serretti A; Shapira B; Smeraldi E; Stefanis C; Thomson M; Van Broeckhoven C; Mendlewicz J
Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study.
Biological psychiatry 2001;49(5):405-9.
2001: Schulze T G; Müller D J; Krauss H; Marwinski K; Maroldt A O; Novo Y Fernández A; Fimmers R; Held T; Maier W; Nöthen M M; Rietschel M
Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?
European psychiatry : the journal of the Association of European Psychiatrists 2001;16(1):71-4.
2001: Niesler B; Weiss B; Fischer C; Nöthen M M; Propping P; Bondy B; Rietschel M; Maier W; Albus M; Franzek E; Rappold G A
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.
Pharmacogenetics 2001;11(1):21-7.
2001: Franke P; Wang T; Nöthen M M; Knapp M; Neidt H; Albrecht S; Jahnes E; Propping P; Maier W
Nonreplication of association between mu-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence.
American journal of medical genetics 2001;105(1):114-9.
2001: Wang T; Franke P; Neidt H; Cichon S; Knapp M; Lichtermann D; Maier W; Propping P; Nöthen M M
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach.
Molecular psychiatry 2001;6(1):109-11.
2000: Sand P G; Godau C; Riederer P; Peters C; Franke P; Nöthen M M; Stöber G; Fritze J; Maier W; Propping P; Lesch K P; Riess O; Sander T; Beckmann H; Deckert J
Exonic variants of the GABA(B) receptor gene and panic disorder.
Psychiatric genetics 2000;10(4):191-4.
2000: Schulze T G; Müller D J; Krauss H; Scherk H; Ohlraun S; Syagailo Y V; Windemuth C; Neidt H; Grässle M; Papassotiropoulos A; Heun R; Nöthen M M; Maier W; Lesch K P; Rietschel M
Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder.
American journal of medical genetics 2000;96(6):801-3.
2000: Cichon S; Kruse R; Hillmer A M; Kukuk G; Anker M; Altland K; Knapp M; Propping P; Nöthen M M
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
The British journal of dermatology 2000;143(4):811-4.
2000: Bosse K; Betz R C; Lee Y A; Wienker T F; Reis A; Kleen H; Propping P; Cichon S; Nöthen M M
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.
American journal of human genetics 2000;67(2):492-7.
2000: Sand P; Lesch K P; Catalano M; Bosi M; Syagailo Y V; Okladnova O; Di Bella D; Maffei P; Heils A; Friess F; Politi E; Nöthen M M; Franke P; Stöber G; Fritze J; Maier W; Propping P; Beckmann H; Bellodi L; Riederer P; Deckert J
Polymorphic MAO-A and 5-HT-transporter genes: analysis of interactions in panic disorder.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2000;1(3):147-50.
2000: Runkel F; Brüss M; Nöthen M M; Stöber G; Propping P; Bönisch H
Pharmacological properties of naturally occurring variants of the human norepinephrine transporter.
Pharmacogenetics 2000;10(5):397-405.
2000: Rietschel M; Schorr A; Albus M; Franzek E; Kreiner R; Held T; Knapp M; Müller D J; Schulze T G; Propping P; Maier W; Nöthen M M
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls.
American journal of medical genetics 2000;96(3):310-1.
2000: Betz R C; Lee Y A; Bygum A; Brandrup F; Bernal A I; Toribio J; Alvarez J I; Kukuk G M; Ibsen H H; Rasmussen H B; Wienker T F; Reis A; Propping P; Kruse R; Cichon S; Nöthen M M
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
American journal of human genetics 2000;66(6):1979-83.
2000: Grünhage F; Schulze T G; Müller D J; Lanczik M; Franzek E; Albus M; Borrmann-Hassenbach M; Knapp M; Cichon S; Maier W; Rietschel M; Propping P; Nöthen M M
Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1).
Molecular psychiatry 2000;5(3):275-82.
2000: Vogt I R; Shimron-Abarbanell D; Neidt H; Erdmann J; Cichon S; Schulze T G; Müller D J; Maier W; Albus M; Borrmann-Hassenbach M; Knapp M; Rietschel M; Propping P; Nöthen M M
Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia.
American journal of medical genetics 2000;96(2):217-21.
2000: Geijer T; Frisch A; Persson M L; Wasserman D; Rockah R; Michaelovsky E; Apter A; Jönsson E G; Nöthen M M; Weizman A
Search for association between suicide attempt and serotonergic polymorphisms.
Psychiatric genetics 2000;10(1):19-26.
2000: Franke P; Nöthen M M; Wang T; Knapp M; Lichtermann D; Neidt H; Sander T; Propping P; Maier W
DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.
Molecular psychiatry 2000;5(1):101-4.
2000: Rietschel M; Krauss H; Müller D J; Schulze T G; Knapp M; Marwinski K; Maroldt A O; Paus S; Grünhage F; Propping P; Maier W; Held T; Nöthen M M
Dopamine D3 receptor variant and tardive dyskinesia.
European archives of psychiatry and clinical neuroscience 2000;250(1):31-5.
1999: Rohrmeier T; Putzhammer A; Schoeler A; Sartor H; Dallinger P; Nöthen M M; Propping P; Knapp M; Albus M; Borrmann M; Knothe K; Kreiner R; Franzek E; Lichtermann D; Rietschel M; Maier W; Klein H E; Eichhammer P
hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia.
Psychiatric genetics 1999;9(4):169-75.
1999: Kruse R; Cichon S; Anker M; Hillmer A M; Barros-Núñez P; Cantú J M; Leal E; Weinlich G; Schmuth M; Fritsch P; Ruzicka T; Propping P; Nöthen M M
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.
The Journal of investigative dermatology 1999;113(6):954-9.
1999: Jönsson E G; Nöthen M M; Neidt H; Forslund K; Rylander G; Mattila-Evenden M; Asberg M; Propping P; Sedvall G C
Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia.
Schizophrenia research 1999;40(1):31-6.
1999: Franke P; Nöthen M M; Wang T; Neidt H; Knapp M; Lichtermann D; Weiffenbach O; Mayer P; Höllt V; Propping P; Maier W
Human delta-opioid receptor gene and susceptibility to heroin and alcohol dependence.
American journal of medical genetics 1999;88(5):462-4.
1999: Gustavsson J P; Nöthen M M; Jönsson E G; Neidt H; Forslund K; Rylander G; Mattila-Evenden M; Sedvall G C; Propping P; Asberg M
No association between serotonin transporter gene polymorphisms and personality traits.
American journal of medical genetics 1999;88(4):430-6.
1999: Jönsson E G; Nöthen M M; Grünhage F; Farde L; Nakashima Y; Propping P; Sedvall G C
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers.
Molecular psychiatry 1999;4(3):290-6.
1999: Kühn K U; Meyer K; Nöthen M M; Gänsicke M; Papassotiropoulos A; Maier W
Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: replication tests.
American journal of medical genetics 1999;88(2):168-72.
1999: Stöber G; Hebebrand J; Cichon S; Brüss M; Bönisch H; Lehmkuhl G; Poustka F; Schmidt M; Remschmidt H; Propping P; Nöthen M M
Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.
American journal of medical genetics 1999;88(2):158-63.
1999: Deckert J; Catalano M; Syagailo Y V; Bosi M; Okladnova O; Di Bella D; Nöthen M M; Maffei P; Franke P; Fritze J; Maier W; Propping P; Beckmann H; Bellodi L; Lesch K P
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder.
Human molecular genetics 1999;8(4):621-4.
1999: Brüss M; Bönisch H; Bühlen M; Nöthen M M; Propping P; Göthert M
Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptor.
Pharmacogenetics 1999;9(1):95-102.
1999: Nöthen M M; Cichon S; Rohleder H; Hemmer S; Franzek E; Fritze J; Albus M; Borrmann-Hassenbach M; Kreiner R; Weigelt B; Minges J; Lichtermann D; Maier W; Craddock N; Fimmers R; Höller T; Baur M P; Rietschel M; Propping P
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.
Molecular psychiatry 1999;4(1):76-84.
1999: Nöthen M M; Schulte-Körne G; Grimm T; Cichon S; Vogt I R; Müller-Myhsok B; Propping P; Remschmidt H
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.
European child & adolescent psychiatry 1999;8 Suppl 3():56-9.
1998: Göthert M; Propping P; Bönisch H; Brüss M; Nöthen M M
Genetic variation in human 5-HT receptors: potential pathogenetic and pharmacological role.
Annals of the New York Academy of Sciences 1998;861():26-30.
1998: Cichon S; Anker M; Vogt I R; Rohleder H; Pützstück M; Hillmer A; Farooq S A; Al-Dhafri K S; Ahmad M; Haque S; Rietschel M; Propping P; Kruse R; Nöthen M M
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.
Human molecular genetics 1998;7(11):1671-9.
1998: Grigoroiu-Serbanescu M; Martinez M; Nöthen M M; Propping P; Milea S; Mihailescu R; Marinescu E
Patterns of parental transmission and familial aggregation models in bipolar affective disorder.
American journal of medical genetics 1998;81(5):397-404.
1998: Bunzel R; Blümcke I; Cichon S; Normann S; Schramm J; Propping P; Nöthen M M
Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain.
Brain research. Molecular brain research 1998;59(1):90-2.
1998: Jönsson E G; Nöthen M M; Gustavsson J P; Neidt H; Forslund K; Mattila-Evenden M; Rylander G; Propping P; Asberg M
Lack of association between dopamine D4 receptor gene and personality traits.
Psychological medicine 1998;28(4):985-9.
1998: Schulte-Körne G; Grimm T; Nöthen M M; Müller-Myhsok B; Cichon S; Vogt I R; Propping P; Remschmidt H
Evidence for linkage of spelling disability to chromosome 15.
American journal of human genetics 1998;63(1):279-82.
1998: Jönsson E G; Nöthen M M; Gustavsson J P; Neidt H; Bunzel R; Propping P; Sedvall G C
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteers.
Psychiatry research 1998;79(1):1-9.
1998: Cichon S; Kesper K; Propping P; Nöthen M M
Assignment of the human serotonin 4 receptor gene (HTR4) to the long arm of chromosome 5 (5q31-q33).
Molecular membrane biology 1998;15(2):75-8.
1998: Wang Y; Friedl W; Lamberti C; Nöthen M M; Kruse R; Propping P
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among Europeans.
Human heredity 1998;48(2):87-91.
1998: Deckert J; Nöthen M M; Albus M; Franzek E; Rietschel M; Ren H; Stiles G L; Knapp M; Weigelt B; Maier W; Beckmann H; Propping P
Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies.
American journal of medical genetics 1998;81(1):18-23.
1998: Nöthen M M; Cichon S; Vogt I R; Hemmer S; Kruse R; Knapp M; Höller T; Faiyaz ul Haque M; Haque S; Propping P; Ahmad M; Rietschel M
A gene for universal congenital alopecia maps to chromosome 8p21-22.
American journal of human genetics 1998;62(2):386-90.
1998: Deckert J; Nöthen M M; Franke P; Delmo C; Fritze J; Knapp M; Maier W; Beckmann H; Propping P
Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease.
Molecular psychiatry 1998;3(1):81-5.
1997: Schroers R; Nöthen M M; Rietschel M; Albus M; Maier W; Schwab S; Wildenauer D; Fimmers R; Propping P; Dewald G
Investigation of complement C4B deficiency in schizophrenia.
Human heredity 1997;47(5):279-82.
1997: Erdmann J; Shimron-Abarbanell D; Shridhar V; Smith D I; Propping P; Nöthen M M
Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1).
Molecular membrane biology 1997;14(3):133-5.
1997: Platten M; Meyer-Puttlitz B; Blümcke I; Waha A; Wolf H K; Nöthen M M; Louis D N; Sampson J R; von Deimling A
A novel splice site associated polymorphism in the tuberous sclerosis 2 (TSC2) gene may predispose to the development of sporadic gangliogliomas.
Journal of neuropathology and experimental neurology 1997;56(7):806-10.
1997: Jönsson E G; Nöthen M M; Gustavsson J P; Neidt H; Brené S; Tylec A; Propping P; Sedvall G C
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms.
The American journal of psychiatry 1997;154(5):697-9.
1997: Shimron-Abarbanell D; Erdmann J; Vogt I R; Bryant S P; Spurr N K; Knapp M; Propping P; Nöthen M M
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region.
Biochemical and biophysical research communications 1997;233(1):6-9.
1997: Steinlein O K; Deckert J; Nöthen M M; Franke P; Maier W; Beckmann H; Propping P
Neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and panic disorder: an association study.
American journal of medical genetics 1997;74(2):199-201.
1997: Arranz M J; Erdmann J; Kirov G; Rietschel M; Sodhi M; Albus M; Ball D; Maier W; Davies N; Franzek E; Abusaad I; Weigelt B; Murray R; Shimron-Abarbanell D; Kerwin R; Propping P; Sham P; Nöthen M M; Collier D A
5-HT2A receptor and bipolar affective disorder: association studies in affected patients.
Neuroscience letters 1997;224(2):95-8.
1997: Deckert J; Nöthen M M; Bryant S P; Schuffenhauer S; Schofield P R; Spurr N K; Propping P
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region.
Human genetics 1997;99(3):326-8.
1997: Nobile M; Maffei P; Nöthen M M; Rietschel M; Smeraldi E; Catalano M
Association study of schizophrenia and the histidase gene.
Psychiatric genetics 1997;7(3):107-9.
1997: Deckert J; Catalano M; Heils A; Di Bella D; Friess F; Politi E; Franke P; Nöthen M M; Maier W; Bellodi L; Lesch K P
Functional promoter polymorphism of the human serotonin transporter: lack of association with panic disorder.
Psychiatric genetics 1997;7(1):45-7.
1996: Erdmann J; Nöthen M M; Shimron-Abarbanell D; Rietschel M; Albus M; Borrmann M; Maier W; Franzek E; Körner J; Weigelt B; Fimmers R; Propping P
The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.
Molecular psychiatry 1996;1(5):392-7.
1996: Stöber G; Nöthen M M; Pörzgen P; Brüss M; Bönisch H; Knapp M; Beckmann H; Propping P
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.
American journal of medical genetics 1996;67(6):523-32.
1996: Rietschel M; Naber D; Oberländer H; Holzbach R; Fimmers R; Eggermann K; Möller H J; Propping P; Nöthen M M
Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor gene.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 1996;15(5):491-6.
1996: Dewald G; Cichon S; Bryant S P; Hemmer S; Nöthen M M; Spurr N K
The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.
Annals of human genetics 1996;60(Pt 4):281-91.
1996: Cichon S; Nöthen M M; Stöber G; Schroers R; Albus M; Maier W; Rietschel M; Körner J; Weigelt B; Franzek E; Wildenauer D; Fimmers R; Propping P
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.
American journal of medical genetics 1996;67(4):424-8.
1996: Rietschel M; Nöthen M M; Albus M; Maier W; Minges J; Bondy B; Körner J; Hemmer S; Fimmers R; Möller H J; Wildenauer D; Propping P
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases.
Schizophrenia research 1996;20(1-2):181-6.
1996: Erdmann J; Shimron-Abarbanell D; Rietschel M; Albus M; Maier W; Körner J; Bondy B; Chen K; Shih J C; Knapp M; Propping P; Nöthen M M
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia.
Human genetics 1996;97(5):614-9.
1996: Eggermann T; Engels H; Moskalonek B; Nöthen M M; Müller-Navia J; Schleiermacher E; Schwanitz G; Stengel-Rutkowski S
Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.
Human genetics 1996;97(5):568-72.
1996: Cichon S; Nöthen M M; Wolf H K; Propping P
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.
American journal of medical genetics 1996;67(2):229-31.
1996: Shimron-Abarbanell D; Harms H; Erdmann J; Albus M; Maier W; Rietschel M; Körner J; Weigelt B; Franzek E; Sander T; Knapp M; Propping P; Nöthen M M
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.
American journal of medical genetics 1996;67(2):225-8.
1996: Lim L C; Craddock N; Owen M; Sham P; Nöthen M M; Körner J; Rietschel M; Fimmer R; Propping P; McGuffin P; Murray R; Gill M
Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees.
Behavior genetics 1996;26(2):113-22.
1996: Eggermann T; Nöthen M M; Eiben B; Hofmann D; Hinkel K; Fimmers R; Schwanitz G
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.
Human genetics 1996;97(2):218-23.
1996: Körner J; Rietschel M; Nöthen M M; Propping P
[Genetic counseling in psychiatric diseases]
Der Nervenarzt 1996;67(1):3-14.
1996: Deckert J; Nöthen M M; Rietschel M; Wildenauer D; Bondy B; Ertl M A; Knapp M; Schofield P R; Albus M; Maier W; Propping P
Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia.
Journal of neural transmission (Vienna, Austria : 1996) 1996;103(12):1447-55.
1996: Zhu S; Nöthen M M; Uhlhaas S; Rietschel M; Körner J; Lanczik M; Fimmers R; Propping P
Apolipoprotein E genotype distribution in schizophrenia.
Psychiatric genetics 1996;6(2):75-9.
1995: Dawson E; Powell J F; Sham P C; Nöthen M; Crocq M A; Propping P; Körner J; Rietschel M; van Os J; Wright P
An association study of a neurotrophin-3 (NT-3) gene polymorphism with schizophrenia.
Acta psychiatrica Scandinavica 1995;92(6):425-8.
1995: Propping P; Nöthen M M
Genetic variation of CNS receptors--a new perspective for pharmacogenetics.
Pharmacogenetics 1995;5(5):318-25.
1995: Nöthen M M; Eggermann K; Albus M; Borrmann M; Rietschel M; Körner J; Maier W; Minges J; Lichtermann D; Franzek E
Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls.
American journal of human genetics 1995;57(4):975-8.
1995: Deckert J; Nöthen M M; Bryant S P; Ren H; Wolf H K; Stiles G L; Spurr N K; Propping P
Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding region.
Biochemical and biophysical research communications 1995;214(2):614-21.
1995: Shimron-Abarbanell D; Nöthen M M; Erdmann J; Propping P
Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation.
Brain research. Molecular brain research 1995;29(2):387-90.
1995: Dawson E; Parfitt E; Roberts Q; Daniels J; Lim L; Sham P; Nöthen M; Propping P; Lanczik M; Maier W
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1.
American journal of medical genetics 1995;60(2):94-102.
1995: Nöthen M M; Dewald G
Dinucleotide repeat polymorphism at the human CD59 locus.
Clinical genetics 1995;47(3):165-6.
1995: Hebebrand J; Nöthen M M; Klug B; Wettke-Schäfer R; Camps A; Lisch S; Hemmer S; von Gontard A; Poustka F; Lehmkuhl G
No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndrome.
Biological psychiatry 1995;37(3):209-11.
1995: Cichon S; Nöthen M M; Catalano M; Di Bella D; Maier W; Lichtermann D; Minges J; Albus M; Borrmann M; Franzek E
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene.
Psychiatric genetics 1995;5(3):97-103.
1994: Cichon S; Nöthen M M; Rietschel M; Körner J; Propping P
Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression.
Biological psychiatry 1994;36(12):850-3.
1994: Nöthen M M; Cichon S; Hemmer S; Hebebrand J; Remschmidt H; Lehmkuhl G; Poustka F; Schmidt M; Catalano M; Fimmers R
Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.
Human molecular genetics 1994;3(12):2207-12.
1994: Nöthen M M; Erdmann J; Shimron-Abarbanell D; Propping P
Identification of genetic variation in the human serotonin 1D beta receptor gene.
Biochemical and biophysical research communications 1994;205(2):1194-200.
1994: Dewald G; Nöthen M M; Rüther K
A common Ser/Thr polymorphism in the perforin-homologous region of human complement component C7.
Human heredity 1994;44(6):301-4.
1994: Propping P; Nöthen M M; Körner J; Rietschel M; Maier W
[Genetic association in psychiatric diseases. Concepts and findings]
Der Nervenarzt 1994;65(11):725-40.
1994: Lim L C; Nöthen M M; Körner J; Rietschel M; Castle D; Hunt N; Propping P; Murray R; Gill M
No evidence of association between dopamine D4 receptor variants and bipolar affective disorder.
American journal of medical genetics 1994;54(3):259-63.
1994: Nöthen M M; Hebebrand J; Knapp M; Hebebrand K; Camps A; von Gontard A; Wettke-Schäfer R; Lisch S; Cichon S; Poustka F
Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method.
American journal of medical genetics 1994;54(3):249-52.
1994: Viersbach R; Schwanitz G; Nöthen M M
Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes.
Human genetics 1994;93(6):663-7.
1994: Dewald G; Hemmer S; Nöthen M M
Human complement component C8. Molecular basis of the beta-chain polymorphism.
FEBS letters 1994;340(3):211-5.
1994: Nöthen M M; Dewald G
A common amino acid polymorphism in complement component C1R.
Human molecular genetics 1994;3(1):217.
1994: Cichon S; Nöthen M M; Erdmann J; Propping P
Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).
Human molecular genetics 1994;3(1):209.
1994: Körner J; Rietschel M; Hunt N; Castle D; Gill M; Nöthen M M; Craddock N; Daniels J; Owen M; Fimmers R
Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls.
Psychiatric genetics 1994;4(3):167-75.
1994: Dawson E; Powell J F; Nöthen M M; Crocq M A; Lanczik M; Körner J; Rietschel M; van Os J; Wright P; Gill M
An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia.
Psychiatric genetics 1994;4(4):215-8.
1993: Abels S; Erdmann J; Nöthen M M
Dinucleotide repeat polymorphism at the D18S365 locus.
Human molecular genetics 1993;2(10):1747.
1993: Nöthen M M; Erdmann J; Propping P; Lanczik M; Rietschel M; Körner J; Maier W; Albus M; Ertl M A; Wildenauer D B
Mutation in the beta amyloid precursor protein gene and schizophrenia.
Biological psychiatry 1993;34(7):502.
1993: Nöthen M M; Eggermann T; Erdmann J; Eiben B; Hofmann D; Propping P; Schwanitz G
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome).
Human genetics 1993;92(4):347-9.
1993: Dewald G; Nöthen M M; Cichon S
Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.
Biochemical and biophysical research communications 1993;194(1):458-64.
1993: Nöthen M M; Knöpfle G; Födisch H J; Zerres K
Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder.
American journal of medical genetics 1993;46(4):467-70.
1993: Rietschel M; Nöthen M M; Lannfelt L; Sokoloff P; Schwartz J C; Lanczik M; Fritze J; Cichon S; Fimmers R; Körner J
A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder.
Psychiatry research 1993;46(3):253-9.
1993: Erdmann J; Nöthen M M
Dinucleotide repeat polymorphism at the D18S99 locus.
Human molecular genetics 1993;2(1):91.
1993: Erdmann J; Nöthen M M; Stratmann M; Fimmers R; Franzek E; Propping P
The use of microsatellites in zygosity diagnosis of twins.
Acta geneticae medicae et gemellologiae 1993;42(1):45-51.
1993: Eggermann T; Nöthen M M; Propping P; Schwanitz G
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling.
Annales de génétique 1993;36(4):214-6.
1992: Nöthen M M; Erdmann J; Körner J; Lanczik M; Fritze J; Fimmers R; Grandy D K; O'Dowd B; Propping P
Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder.
The American journal of psychiatry 1992;149(2):199-201.
1992: Lanczik M; Nöthen M; Körner J; Rietschel M; Erdmann J; Stratmann M; Cichon S; Lichtermann D; Maier W; Propping P
Association and linkage studies in bipolar affective disorder.
Clinical neuropharmacology 1992;15 Suppl 1 Pt A():580A-581A.

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