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Marcella Rietschel
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100
Nöthen, Markus
80
Maier, Wolfgang
68
Schulze, Thomas
67
Propping, Peter
60
Cichon, Sven
34
Schumacher, Johannes
29
Albus, Margot
26
Müller, Daniel
25
Abou Jamra, Rami
23
Becker, Tim
22
Ohlraun, Stephanie
16
Knapp, Michael
15
Wildenauer, Dieter
14
Krauss, Harald
14
Schmael, Christine
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All Publications
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2009: Perroud Nader; Aitchison Katherine J; Uher Rudolf; Smith Rebecca; Huezo-Diaz Patricia; Marusic Andrej; Maier Wolfgang; Mors Ole; Placentino Anna; Henigsberg Neven; Rietschel Marcella; Hauser Joanna; Souery Daniel; Kapelski Pawel; Bonvicini Cristian; Zobel Astrid; Jorgensen Lisbeth; Petrovic Ana; Kalember Petra; Schulze Thomas G; Gupta Bhanu; Gray Joanna; Lewis Cathryn M; Farmer Anne E; McGuffin Peter; Craig Ian
Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2009;34(12):2517-28.
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2009: Uher Rudolf; Mors Ole; Hauser Joanna; Rietschel Marcella; Maier Wolfgang; Kozel Dejan; Henigsberg Neven; Souery Daniel; Placentino Anna; Perroud Nader; Dernovsek Moica Zvezdana; Strohmaier Jana; Larsen Erik Roj; Zobel Astrid; Leszczynska-Rodziewicz Anna; Kalember Petra; Pedrini Laura; Linotte Sylvie; Gunasinghe Cerisse; Aitchison Katherine J; McGuffin Peter; Farmer Anne
Body weight as a predictor of antidepressant efficacy in the GENDEP project.
Journal of affective disorders 2009;118(1-3):147-54.
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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.
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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.
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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.
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2009: Buchmann Arlette F; Schmid Brigitte; Blomeyer Dorothea; Becker Katja; Treutlein Jens; Zimmermann Ulrich S; Jennen-Steinmetz Christine; Schmidt Martin H; Esser Günter; Banaschewski Tobias; Rietschel Marcella; Schumann Gunter; Laucht Manfred
Impact of age at first drink on vulnerability to alcohol-related problems: testing the marker hypothesis in a prospective study of young adults.
Journal of psychiatric research 2009;43(15):1205-12.
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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.
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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.
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2009: Schmid Brigitte; Blomeyer Dorothea; Becker Katja; Treutlein Jens; Zimmermann Ulrich S; Buchmann Arlette F; Schmidt Martin H; Esser Günter; Banaschewski Tobias; Rietschel Marcella; Laucht Manfred
The interaction between the dopamine transporter gene and age at onset in relation to tobacco and alcohol use among 19-year-olds.
Addiction biology 2009;14(4):489-99.
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2009: Uher Rudolf; Farmer Anne; Henigsberg Neven; Rietschel Marcella; Mors Ole; Maier Wolfgang; Kozel Dejan; Hauser Joanna; Souery Daniel; Placentino Anna; Strohmaier Jana; Perroud Nader; Zobel Astrid; Rajewska-Rager Aleksandra; Dernovsek Moica Z; Larsen Erik Roj; Kalember Petra; Giovannini Caterina; Barreto Mara; McGuffin Peter; Aitchison Katherine J
Adverse reactions to antidepressants.
The British journal of psychiatry : the journal of mental science 2009;195(3):202-10.
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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.
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2009: Uher Rudolf; Huezo-Diaz Patricia; Perroud Nader; Smith Rebecca; Rietschel Marcella; Mors Ole; Hauser Joanna; Maier Wolfgang; Kozel Dejan; Henigsberg Neven; Barreto Mara; Placentino Anna; Dernovsek Mojca Zvezdana; Schulze Thomas G; Kalember Petra; Zobel Astrid; Czerski Piotr M; Larsen Erik Roj; Souery Daniel; Giovannini Caterina; Gray Joanna M; Lewis Cathryn M; Farmer Anne; Aitchison Katherine J; McGuffin Peter; Craig Ian
Genetic predictors of response to antidepressants in the GENDEP project.
The pharmacogenomics journal 2009;9(4):225-33.
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2009: Wüst Stefan; Kumsta Robert; Treutlein Jens; Frank Josef; Entringer Sonja; Schulze Thomas G; Rietschel Marcella
Sex-specific association between the 5-HTT gene-linked polymorphic region and basal cortisol secretion.
Psychoneuroendocrinology 2009;34(7):972-82.
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2009: Ball H A; Samaan Z; Brewster S; Craddock N; Gill M; Korszun A; Maier W; Middleton L; Mors O; Owen M J; Perry J; Preisig M; Rice J; Rietschel M; Jones L; Jones I; Farmer A E; McGuffin P
Depression, migraine with aura and migraine without aura: their familiality and interrelatedness.
Cephalalgia : an international journal of headache 2009;29(8):848-54.
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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.
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2009: Huezo-Diaz Patricia; Uher Rudolf; Smith Rebecca; Rietschel Marcella; Henigsberg Neven; Marusic Andrej; Mors Ole; Maier Wolfgang; Hauser Joanna; Souery Daniel; Placentino Anna; Zobel Astrid; Larsen Erik Roj; Czerski Piotr M; Gupta Bhanu; Hoda Farzana; Perroud Nader; Farmer Anne; Craig Ian; Aitchison Katherine J; McGuffin Peter
Moderation of antidepressant response by the serotonin transporter gene.
The British journal of psychiatry : the journal of mental science 2009;195(1):30-8.
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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.
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2009: Laucht Manfred; Treutlein Jens; Schmid Brigitte; Blomeyer Dorothea; Becker Katja; Buchmann Arlette F; Schmidt Martin H; Esser Günter; Jennen-Steinmetz Christine; Rietschel Marcella; Zimmermann Ulrich S; Banaschewski Tobias
Impact of psychosocial adversity on alcohol intake in young adults: moderation by the LL genotype of the serotonin transporter polymorphism.
Biological psychiatry 2009;66(2):102-9.
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2009: Laucht Manfred; Treutlein Jens; Blomeyer Dorothea; Buchmann Arlette F; Schmid Brigitte; Becker Katja; Zimmermann Ulrich S; Schmidt Martin H; Esser Günter; Rietschel Marcella; Banaschewski Tobias
Interaction between the 5-HTTLPR serotonin transporter polymorphism and environmental adversity for mood and anxiety psychopathology: evidence from a high-risk community sample of young adults.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2009;12(6):737-47.
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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.
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2009: Esslinger Christine; Walter Henrik; Kirsch Peter; Erk Susanne; Schnell Knut; Arnold Claudia; Haddad Leila; Mier Daniela; Opitz von Boberfeld Carola; Raab Kyeon; Witt Stephanie H; Rietschel Marcella; Cichon Sven; Meyer-Lindenberg Andreas
Neural mechanisms of a genome-wide supported psychosis variant.
Science (New York, N.Y.) 2009;324(5927):605.
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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.
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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.
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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.
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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.
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2009: Uher Rudolf; Maier Wolfgang; Hauser Joanna; Marusic Andrej; Schmael Christine; Mors Ole; Henigsberg Neven; Souery Daniel; Placentino Anna; Rietschel Marcella; Zobel Astrid; Dmitrzak-Weglarz Monika; Petrovic Ana; Jorgensen Lisbeth; Kalember Petra; Giovannini Caterina; Barreto Mara; Elkin Amanda; Landau Sabine; Farmer Anne; Aitchison Katherine J; McGuffin Peter
Differential efficacy of escitalopram and nortriptyline on dimensional measures of depression.
The British journal of psychiatry : the journal of mental science 2009;194(3):252-9.
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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.
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2009: Nickl-Jockschat T; Rietschel M; Kircher T
[Correlations between risk gene variants for schizophrenia and brain structure anomalies]
Der Nervenarzt 2009;80(1):40-2, 44-6, 48 passim.
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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.
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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.
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2008: Mössner Rainald; Schuhmacher Anna; Schulze-Rauschenbach Svenja; Kühn Kai-Uwe; Rujescu Dan; Rietschel Marcella; Zobel Astrid; Franke Petra; Wölwer Wolfgang; Gaebel Wolfgang; Häfner Heinz; Wagner Michael; Maier Wolfgang
Further evidence for a functional role of the glutamate receptor gene GRM3 in schizophrenia.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2008;18(10):768-72.
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2008: Ebner Florian; Tepest Ralf; Dani Indra; Pfeiffer Ute; Schulze Thomas G; Rietschel Marcella; Maier Wolfgang; Träber Frank; Block Wolfgang; Schild Hans H; Wagner Michael; Steinmetz Helmuth; Gaebel Wolfgang; Honer William G; Schneider-Axmann Thomas; Falkai Peter
The hippocampus in families with schizophrenia in relation to obstetric complications.
Schizophrenia research 2008;104(1-3):71-8.
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2008: Zobel Astrid; Jessen Frank; von Widdern Olrik; Schuhmacher Anna; Höfels Susanne; Metten Martin; Rietschel Marcella; Scheef Lukas; Block Wolfgang; Becker Tim; Schild Hans H; Maier Wolfgang; Schwab Sibylle G
Unipolar depression and hippocampal volume: impact of DNA sequence variants of the glucocorticoid receptor gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(6):836-43.
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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.
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2008: Schumann Gunter; Johann Monika; Frank Josef; Preuss Ulrich; Dahmen Norbert; Laucht Manfred; Rietschel Marcella; Rujescu Dan; Lourdusamy Anbarasu; Clarke Toni-Kim; Krause Kristina; Dyer Anne; Depner Martin; Wellek Stefan; Treutlein Jens; Szegedi Armin; Giegling Ina; Cichon Sven; Blomeyer Dorothea; Heinz Andreas; Heath Simon; Lathrop Mark; Wodarz Norbert; Soyka Michael; Spanagel Rainer; Mann Karl
Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior.
Archives of general psychiatry 2008;65(7):826-38.
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2008: Rietschel Marcella
Environment is important.
Current opinion in psychiatry 2008;21(4):323-4.
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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.
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2008: Sobanski Esther; Brüggemann Daniel; Alm Barbara; Kern Sebastian; Philipsen Alexandra; Schmalzried Hannah; Hesslinger Bernd; Waschkowski H; Rietschel Marcella
Subtype differences in adults with attention-deficit/hyperactivity disorder (ADHD) with regard to ADHD-symptoms, psychiatric comorbidity and psychosocial adjustment.
European psychiatry : the journal of the Association of European Psychiatrists 2008;23(2):142-9.
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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.
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2008: Clarke Toni-Kim; Treutlein Jens; Zimmermann Ulrich S; Kiefer Falk; Skowronek Markus H; Rietschel Marcella; Mann Karl; Schumann Gunter
HPA-axis activity in alcoholism: examples for a gene-environment interaction.
Addiction biology 2008;13(1):1-14.
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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.
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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.
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2008: Wobrock Thomas; Kamer Thomas; Roy Anand; Vogeley Kai; Schneider-Axmann Thomas; Wagner Michael; Maier Wolfgang; Rietschel Marcella; Schulze Thomas G; Scherk Harald; Schild Hans H; Block Wolfgang; Träber Frank; Tepest Ralf; Honer William G; Falkai Peter
Reduction of the internal capsule in families affected with schizophrenia.
Biological psychiatry 2008;63(1):65-71.
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2007: Abou Jamra Rami; Fuerst Robert; Kaneva Radka; Orozco Diaz Guillermo; Rivas Fabio; Mayoral Fermin; Gay Eudoxia; Sans Sebastian; Gonzalez Maria Jose; Gil Susana; Cabaleiro Francisco; Del Rio Francisco; Perez Fermin; Haro Jesus; Auburger Georg; Milanova Vihra; Kostov Christian; Chorbov Vesselin; Stoyanova Vessela; Nikolova-Hill Amelia; Onchev George; Kremensky Ivo; Jablensky Assen; Schulze Thomas G; Propping Peter; Rietschel Marcella; Nothen Markus M; Cichon Sven; Wienker Thomas F; Schumacher Johannes
The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.
American journal of human genetics 2007;81(5):974-86.
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2007: Falkai Peter; Honer William G; Kamer Thomas; Dustert Simone; Vogeley Kai; Schneider-Axmann Thomas; Dani Indra; Wagner Michael; Rietschel Marcella; Müller Daniel J; Schulze Thomas G; Gaebel Wolfgang; Cordes Joachim; Schönell Helmut; Schild Hans H; Block Wolfgang; Träber Frank; Steinmetz Helmuth; Maier Wolfgang; Tepest Ralf
Disturbed frontal gyrification within families affected with schizophrenia.
Journal of psychiatric research 2007;41(10):805-13.
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2007: Sobanski Esther; Brüggemann Daniel; Alm Barbara; Kern Sebastian; Deschner Monika; Schubert Thomas; Philipsen Alexandra; Rietschel Marcella
Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD).
European archives of psychiatry and clinical neuroscience 2007;257(7):371-7.
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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.
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2007: Amar Shirly; Shamir Alon; Ovadia Ofer; Blanaru Monica; Reshef Alon; Kremer Ilana; Rietschel Marcella; Schulze Thomas G; Maier Wolfgang; Belmaker R H; Ebstein Richard P; Agam Galila; Mishmar Dan
Mitochondrial DNA HV lineage increases the susceptibility to schizophrenia among Israeli Arabs.
Schizophrenia research 2007;94(1-3):354-8.
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2007: Laucht Manfred; Skowronek Markus H; Becker Katja; Schmidt Martin H; Esser Günter; Schulze Thomas G; Rietschel Marcella
Interacting effects of the dopamine transporter gene and psychosocial adversity on attention-deficit/hyperactivity disorder symptoms among 15-year-olds from a high-risk community sample.
Archives of general psychiatry 2007;64(5):585-90.
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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.
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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.
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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.
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2007: Brüggemann Daniel; Sobanski Esther; Alm Barbara; Schubert Thomas; Schmalzried Hannah; Philipsen Alexandra; Breen Gerome; Becker Tim; Georgi Alexander; Skowronek Markus H; Schulze Thomas G; Treutlein Jens; Rietschel Marcella
No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder.
Psychiatric genetics 2007;17(2):121.
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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.
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2007: Partonen Timo; Treutlein Jens; Alpman Asude; Frank Josef; Johansson Carolina; Depner Martin; Aron Liviu; Rietschel Marcella; Wellek Stefan; Soronen Pia; Paunio Tiina; Koch Andreas; Chen Ping; Lathrop Mark; Adolfsson Rolf; Persson Maj-Liz; Kasper Siegfried; Schalling Martin; Peltonen Leena; Schumann Gunter
Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression.
Annals of medicine 2007;39(3):229-38.
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2006: Schulze Thomas G; Hedeker Donald; Zandi Peter; Rietschel Marcella; McMahon Francis J
What is familial about familial bipolar disorder? Resemblance among relatives across a broad spectrum of phenotypic characteristics.
Archives of general psychiatry 2006;63(12):1368-76.
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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.
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2006: Tost Heike; Meyer-Lindenberg Andreas; Klein Sabine; Schmitt Andrea; Höhn Fabian; Tenckhoff Amrei; Ruf Matthias; Ende Gabriele; Rietschel Marcella; Henn Fritz A; Braus Dieter F
D2 antidopaminergic modulation of frontal lobe function in healthy human subjects.
Biological psychiatry 2006;60(11):1196-205.
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2006: Todt U; Freudenberg J; Goebel I; Heinze A; Heinze-Kuhn K; Rietschel M; Göbel H; Kubisch C
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura.
Neurology 2006;67(9):1707-9.
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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.
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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.
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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.
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2006: Schneider-Axmann Thomas; Kamer Thomas; Moroni Manuel; Maric Nadja; Tepest Ralf; Dani Indra; Honer William G; Scherk Harald; Rietschel Marcella; Schulze Thomas G; Müller Daniel J; Cordes Joachim; Schönell Helmut; Steinmetz Helmuth; Gaebel Wofgang; Vogeley Kai; Kühn Kai-Uwe; Wagner Michael; Maier Wolfgang; Träber Frank; Block Wolfgang; Schild Hans H; Falkai Peter
Relation between cerebrospinal fluid, gray matter and white matter changes in families with schizophrenia.
Journal of psychiatric research 2006;40(7):646-55.
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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.
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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.
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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.
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2006: Mössner Rainald; Freitag Christine M; Gutknecht Lise; Reif Andreas; Tauber Ralf; Franke Petra; Fritze Jürgen; Wagner Gerd; Peikert Gregor; Wenda Berit; Sand Philipp; Rietschel Marcella; Garritsen Henk; Jacob Christian; Lesch K Peter; Deckert Jürgen
The novel brain-specific tryptophan hydroxylase-2 gene in panic disorder.
Journal of psychopharmacology (Oxford, England) 2006;20(4):547-52.
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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.
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2006: Treutlein J; Kissling C; Frank J; Wiemann S; Dong L; Depner M; Saam C; Lascorz J; Soyka M; Preuss U W; Rujescu D; Skowronek M H; Rietschel M; Spanagel R; Heinz A; Laucht M; Mann K; Schumann G
Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples.
Molecular psychiatry 2006;11(6):594-602.
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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.
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2006: Korostishevsky M; Kremer I; Kaganovich M; Cholostoy A; Murad I; Muhaheed M; Bannoura I; Rietschel M; Dobrusin M; Bening-Abu-Shach U; Belmaker R H; Maier W; Ebstein R P; Navon Ruth
Transmission disequilibrium and haplotype analyses of the G72/G30 locus: suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(1):91-5.
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2005: Horschitz S; Hummerich R; Lau T; Rietschel M; Schloss P
A dopamine transporter mutation associated with bipolar affective disorder causes inhibition of transporter cell surface expression.
Molecular psychiatry 2005;10(12):1104-9.
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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.
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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.
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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.
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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.
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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.
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2005: Maier Wolfgang; Höfgen Barbara; Zobel Astrid; Rietschel Marcella
Genetic models of schizophrenia and bipolar disorder: overlapping inheritance or discrete genotypes?
European archives of psychiatry and clinical neuroscience 2005;255(3):159-66.
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2005: Massat I; Souery D; Del-Favero J; Nothen M; Blackwood D; Muir W; Kaneva R; Serretti A; Lorenzi C; Rietschel M; Milanova V; Papadimitriou G N; Dikeos D; Van Broekhoven C; Mendlewicz J
Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study.
Molecular psychiatry 2005;10(6):598-605.
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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.
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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.
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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.
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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.
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2004: Falkai Peter; Tepest Ralf; Honer William G; Dani Indra; Ahle Guido; Pfeiffer Ute; Vogeley Kai; Schulze Thomas G; Rietschel Marcella; Cordes Joachim; Schönell Helmut; Gaebel Wolfgang; Kühn Kai-Uwe; Maier Wolfgang; Träber Frank; Block Wolfgang; Schild Hans H; Schneider-Axmann Thomas
Shape changes in prefrontal, but not parieto-occipital regions: brains of schizophrenic patients come closer to a circle in coronal and sagittal view.
Psychiatry research 2004;132(3):261-71.
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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.
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2004: Falkai P; Tepest R; Schulze T G; Müller D J; Rietschel M; Maier W; Träber F; Block W; Schild H H; Steinmetz H; Gaebel W; Honer W G; Schneider-Axmann T; Wagner M
Etiopathogenetic mechanisms in long-term course of schizophrenia.
Pharmacopsychiatry 2004;37 Suppl 2():S136-40.
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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.
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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.
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2004: Grasmäder Katja; Verwohlt Petra Louise; Kühn Kai-Uwe; Dragicevic Aleksandra; von Widdern Olrik; Zobel Astrid; Hiemke Christoph; Rietschel Marcella; Maier Wolfgang; Jaehde Ulrich; Rao Marie Luise
Population pharmacokinetic analysis of mirtazapine.
European journal of clinical pharmacology 2004;60(7):473-80.
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2004: Grasmäder Katja; Verwohlt Petra Louise; Rietschel Marcella; Dragicevic Aleksandra; Müller Matthias; Hiemke Christoph; Freymann Nikolaus; Zobel Astrid; Maier Wolfgang; Rao Marie Luise
Impact of polymorphisms of cytochrome-P450 isoenzymes 2C9, 2C19 and 2D6 on plasma concentrations and clinical effects of antidepressants in a naturalistic clinical setting.
European journal of clinical pharmacology 2004;60(5):329-36.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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2003: Schwab Sibylle G; Mondabon Stephanie; Knapp Michael; Albus Margot; Hallmayer Joachim; Borrmann-Hassenbach Margitta; Trixler Matyas; Gross Magdalena; Schulze Thomas G; Rietschel Marcella; Lerer Bernard; Maier Wolfgang; Wildenauer Dieter B
Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia.
Schizophrenia research 2003;65(1):19-25.
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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.
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2003: Maier W; Zobel A; Rietschel M
Genetics of schizophrenia and affective disorders.
Pharmacopsychiatry 2003;36 Suppl 3():S195-202.
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2003: Kremer I; Pinto M; Murad I; Muhaheed M; Bannoura I; Muller D J; Schulze T G; Reshef A; Blanaru M; Gathas S; Goichman R; Rietschel M; Dobrusin M; Bachner-Melman R; Nemanov L; Belmaker R H; Maier W; Ebstein R P
Family-based and case-control study of catechol-O-methyltransferase in schizophrenia among Palestinian Arabs.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;119B(1):35-9.
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2003: Lohmann P L; Bagli M; Krauss H; Müller D J; Schulze T G; Fangerau H; Ludwig M; Barkow K; Held T; Heun R; Maier W; Rietschel M; Rao M L
CYP2D6 polymorphism and tardive dyskinesia in schizophrenic patients.
Pharmacopsychiatry 2003;36(2):73-8.
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2003: Schwab Sibylle G; Knapp Michael; Mondabon Stephanie; Hallmayer Joachim; Borrmann-Hassenbach Margitta; Albus Margot; Lerer Bernard; Rietschel Marcella; Trixler Matyas; Maier Wolfgang; Wildenauer Dieter B
Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.
American journal of human genetics 2003;72(1):185-90.
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2002: Maier Wolfgang; Lichtermann Dirk; Franke Petra; Heun Reinhard; Falkai Peter; Rietschel Marcella
The dichotomy of schizophrenia and affective disorders in extended pedigrees.
Schizophrenia research 2002;57(2-3):259-66.
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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.
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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.
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2002: Lerer Bernard; Segman Ronnen H; Fangerau Heiner; Daly Ann K; Basile Vincenzo S; Cavallaro Roberto; Aschauer Harald N; McCreadie Robin G; Ohlraun Stephanie; Ferrier Nicol; Masellis Mario; Verga Massimiliano; Scharfetter Joachim; Rietschel Marcella; Lovlie Roger; Levy Uriel Heresco; Meltzer Herbert Y; Kennedy James L; Steen Vidar M; Macciardi Fabio
Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2002;27(1):105-19.
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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.
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2002: Schwab Sibylle G; Hallmayer Joachim; Freimann Julia; Lerer Bernard; Albus Margot; Borrmann-Hassenbach Margitta; Segman Ronnen H; Trixler Matyas; Rietschel Marcella; Maier Wolfgang; Wildenauer Dieter B
Investigation of linkage and association/linkage disequilibrium of HLA A-, DQA1-, DQB1-, and DRB1-alleles in 69 sib-pair- and 89 trio-families with schizophrenia.
American journal of medical genetics 2002;114(3):315-20.
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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.
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2002: Massat I; Souery D; Del-Favero J; Oruc L; Noethen M M; Blackwood D; Thomson M; Muir W; Papadimitriou G N; Dikeos D G; Kaneva R; Serretti A; Lilli R; Smeraldi E; Jakovljevic M; Folnegovic V; Rietschel M; Milanova V; Valente F; Van Broeckhoven C; Mendlewicz J
Excess of allele1 for alpha3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association study.
Molecular psychiatry 2002;7(2):201-7.
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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.
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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.
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2001: Rietschel M
[Pharmacogenetic strategies]
Fortschritte der Neurologie-Psychiatrie 2001;69 Suppl 2():S62-4.
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2001: Lerer B; Macciardi F; Segman R H; Adolfsson R; Blackwood D; Blairy S; Del Favero J; Dikeos D G; Kaneva R; Lilli R; Massat I; Milanova V; Muir W; Noethen M; Oruc L; Petrova T; Papadimitriou G N; Rietschel M; Serretti A; Souery D; Van Gestel S; Van Broeckhoven C; Mendlewicz J
Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder.
Molecular psychiatry 2001;6(5):579-85.
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2001: Serretti A; Rietschel M; Lattuada E; Krauss H; Schulze T G; Müller D J; Maier W; Smeraldi E
Major psychoses symptomatology: factor analysis of 2241 psychotic subjects.
European archives of psychiatry and clinical neuroscience 2001;251(4):193-8.
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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.
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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.
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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.
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2001: Dobrusin M; Corbex M; Kremer I; Murad I; Muhaheed M; Bannoura I; Müller D J; Schulze T G; Reshef A; Blanaru M; Gathas S; Rietschel M; Belmaker R H; Maier W; Ebstein R P
No evidence for linkage by transmission disequilibrium test analysis of microsatellite marker D22S278 and schizophrenia in a Palestinian Arab and in a German population.
American journal of medical genetics 2001;105(4):328-31.
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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.
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2001: Murad I; Kremer I; Dobrusin M; Muhaheed M; Bannoura I; Müller D J; Schulze T G; Reshef A; Blanaru M; Gathas S; Tsenter V; Rietschel M; Belmaker R H; Maier W; Ebstein R P
A family-based study of the Cys23Ser 5HT2C serotonin receptor polymorphism in schizophrenia.
American journal of medical genetics 2001;105(3):236-8.
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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.
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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.
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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: Kremer I; Rietschel M; Dobrusin M; Mujaheed M; Murad I; Blanaru M; Bannoura I; Müller D J; Schulze T G; Reshef A; Gathas S; Schwab S; Wildenauer D; Bachner-Melman R; Belmaker R H; Maier W; Ebstein R P
No association between the dopamine D3 receptor Bal I polymorphism and schizophrenia in a family-based study of a Palestinian Arab population.
American journal of medical genetics 2000;96(6):778-80.
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2000: Schwab S G; Hallmayer J; Albus M; Lerer B; Eckstein G N; Borrmann M; Segman R H; Hanses C; Freymann J; Yakir A; Trixler M; Falkai P; Rietschel M; Maier W; Wildenauer D B
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6.
Molecular psychiatry 2000;5(6):638-49.
-
2000: Block W; Bayer T A; Tepest R; Träber F; Rietschel M; Müller D J; Schulze T G; Honer W G; Maier W; Schild H H; Falkai P
Decreased frontal lobe ratio of N-acetyl aspartate to choline in familial schizophrenia: a proton magnetic resonance spectroscopy study.
Neuroscience letters 2000;289(2):147-51.
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2000: Held T; Weber T; Krausz H; Ahle G; Hager B; Alfter D; Schulze T; Knapp M; Maier W; Rietschel M
[Clinical characteristics of patients with tardive dyskinesias]
Fortschritte der Neurologie-Psychiatrie 2000;68(7):321-31.
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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.
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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: Krauss H; Marwinski K; Schulze T; Mueller D J; Held T; Rietschel M; Maier W; Freyberger H J
[Reliability and validity of the German version of the Premorbid Adjustment Scale (PAS)]
Der Nervenarzt 2000;71(3):188-94.
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2000: Hranilovic D; Schwab S G; Jernej B; Knapp M; Lerer B; Albus M; Rietschel M; Kanyas K; Borrmann M; Lichtermann D; Maier W; Wildenauer D B
Serotonin transporter gene and schizophrenia: evidence for association/linkage disequilibrium in families with affected siblings.
Molecular psychiatry 2000;5(1):91-5.
-
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.
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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: Maier W; Lichtermann D; Rietschel M; Held T; Falkai P; Wagner M; Schwab S
[Genetics of schizophrenic disorders. New concepts and findings]
Der Nervenarzt 1999;70(11):955-69.
-
1999: Serretti A; Rietschel M; Lattuada E; Krauss H; Held T; Nöthen M M; Smeraldi E
Factor analysis of mania.
Archives of general psychiatry 1999;56(7):671-2.
-
1999: Wittekindt O; Schwab S G; Burgert E; Knapp M; Albus M; Lerer B; Hallmayer J; Rietschel M; Segman R; Borrmann M; Lichtermann D; Crocq M A; Maier W; Morris-Rosendahl D J; Wildenauer D B
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios.
Molecular psychiatry 1999;4(3):267-70.
-
1999: Rietschel M; Kennedy J L; Macciardi F; Meltzer H Y
Application of pharmacogenetics to psychotic disorders: the first consensus conference. The Consensus Group for Outcome Measures in Psychoses for Pharmacological Studies.
Schizophrenia research 1999;37(2):191-6.
-
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: Maier W; Rietschel M; Lichtermann D; Wildenauer D B
Family and genetic studies on the relationship of schizophrenia to affective disorders.
European archives of psychiatry and clinical neuroscience 1999;249 Suppl 4():57-61.
-
1998: Krauss H; Knapp M; Schulze T; Rietschel M
Premorbid adjustment and schizophrenia.
The British journal of psychiatry : the journal of mental science 1998;173():536.
-
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.
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1998: Schwab S G; Hallmayer J; Albus M; Lerer B; Hanses C; Kanyas K; Segman R; Borrman M; Dreikorn B; Lichtermann D; Rietschel M; Trixler M; Maier W; Wildenauer D B
Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.
American journal of medical genetics 1998;81(4):302-7.
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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.
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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: Przkora R; Falkai P; von Deimling A; Wiestler O D; Albus M; Rietschel M; Maier W; Bayer T A
Analysis of a polymorphism in the tuberous sclerosis (TSC2) gene does not predispose to schizophrenia.
European archives of psychiatry and clinical neuroscience 1998;248(6):314-5.
-
1998: Krauss H; Marwinski K; Held T; Rietschel M; Freyberger H J
Reliability and validity of the premorbid adjustment scale (PAS) in a German sample of schizophrenic and schizoaffective patients.
European archives of psychiatry and clinical neuroscience 1998;248(6):277-81.
-
1997: Rietschel M; Krauss H; Müller D J; Nöthen M M; Macciardi F
Apolipoprotein E epsilon 4 and clinical phenotype in schizophrenia.
Lancet 1997;350(9094):1857-8.
-
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.
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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: Goldin L R; Gershon E S; Berrettini W H; Stine O C; DePaulo R; McMahon F; Meyers D; Nothen M; Propping P; Cichon S; Fimmers R; Baur M; Albus M; Franzek E; Kreiner R; Maier W; Rietschel M; Baron M; Knowles J; Gilliam C; Endicott J; Gurling H; Curtis D; Smyth C; Kelsoe J
Description of the Genetic Analysis Workshop 10 bipolar disorder linkage data sets.
Genetic epidemiology 1997;14(6):563-8.
-
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: 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.
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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.
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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: 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.
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1996: Körner J; Rietschel M; Nöthen M M; Propping P
[Genetic counseling in psychiatric diseases]
Der Nervenarzt 1996;67(1):3-14.
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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.
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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.
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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.
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1995: Nöthen M M; Rietschel M; Erdmann J; Oberländer H; Möller H J; Nober D; Propping P
Genetic variation of the 5-HT2A receptor and response to clozapine.
Lancet 1995;346(8979):908-9.
-
1995: Rietschel M; Nöthen M M; Maier W; Albus M; Franzek E; Propping P
Tyrosine hydroxylase gene and manic-depressive illness.
Lancet 1995;345(8961):1368.
-
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: 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.
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1994: Wilk M; Rietschel M; Körner J; Möller H J; Nöthen M M; Bauer R; Kreysel H W
[Pemphigus chronicus benignus familiaris (Hailey-Hailey disease) and bipolar affective disease in 3 members of a family]
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1994;45(5):313-7.
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1994: Nöthen M M; Wildenauer D; Cichon S; Albus M; Maier W; Minges J; Lichtermann D; Bondy B; Rietschel M; Körner J
Dopamine D2 receptor molecular variant and schizophrenia.
Lancet 1994;343(8908):1301-2.
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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: 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: Körner J; Rietschel M; Nöthen M M; Wilk C M; Bauer R; Propping P; Möller H J
Familial cosegregation of affective disorder and Hailey-Hailey disease.
The British journal of psychiatry : the journal of mental science 1993;163():109-10.
-
1993: Nöthen M M; Cichon S; Erdmann J; Körner J; Rietschel M; Rappold G A; Fritze J; Propping P
Pseudoautosomal marker DXYS20 and manic depression.
American journal of human genetics 1993;52(4):841-2.
-
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.
-
1992: Rietschel M; Rudnik-Schöneborn S; Zerres K
Clinical variability of autosomal dominant spinal muscular atrophy.
Journal of the neurological sciences 1992;107(1):65-73.
-
1992: Rudnik-Schöneborn S; Zerres K; Ignatius J; Rietschel M
Pregnancy and spinal muscular atrophy.
Journal of neurology 1992;239(1):26-30.
-
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.
-
1992: Kress W; Müller E; Kausch K; Kullmann F; Mostacciuolo M L; Rietschel M; Rotthauwe H W; Schmalenberger B; Siciliano G; Voit T
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene.
Neuromuscular disorders : NMD 1992;2(2):111-5.
-
1991: Rietschel M; Friedl W; Uhlhaas S; Neugebauer M; Heimann D; Zerres K
MASA syndrome: clinical variability and linkage analysis.
American journal of medical genetics 1991;41(1):10-4.
-
1991: Kausch K; Müller C R; Grimm T; Ricker K; Rietschel M; Rudnik-Schöneborn S; Zerres K
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.
Human genetics 1991;86(3):317-8.
-
1990: Zerres K; Rudnik-Schöneborn S; Rietschel M
Heterogeneity in proximal spinal muscular atrophy.
Lancet 1990;336(8717):749-50.
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