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Johannes Schumacher

Research Profile

Physiology

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Germany

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Chromosomes, Human, Pair 6

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Anna Carina Schulz; Johannes Schumacher; Rüdiger Stressig; Jochen Ritgen; Eberhard Schmiedeke; Haitham Bachour; Soyhan Bagci; Enrika Bartels; Peter Bartmann; Christoph Berg; Markus Draaken; Annegret Geipel; Ulrich Gembruch; Andreas Heydweiller; Michael Ludwig; Manuel Mattheisen; Andreas Müller; Markus M Nöthen; Heiko Reutter
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.
Nils Rahner; Johannes Schumacher; Liesbeth Spruijt; Verena Steinke; Susanne Stemmler; Carli J M Tops; Hans F A Vasen; Juul T Wijnen; Tim Becker; Felix F Brockschmidt; Wolfgang Dietmaier; Heike Görgens; Elke Holinski-Feder; Philip Kahl; Matthias Kloor; Marjolijn J L Ligtenberg; Markus M Nöthen; Peter Propping
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
Rami Abou Jamra; Mohammed Ayman Al Khateeb; Arif B Ekici; Mahmoud Fakher; Susanne Giesebrecht; Saber Hamdan; Amina Ismael; Safia Muhammad; Markus M Nöthen; Lutz Priebe; Johannes Schumacher; Steffen Uebe; Sigrun Wohlfart; Markus Zweier; Ahmad Abboud; André Reis
Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.

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All Publications

2012: Anna Carina Schulz; Johannes Schumacher; Rüdiger Stressig; Jochen Ritgen; Eberhard Schmiedeke; Haitham Bachour; Soyhan Bagci; Enrika Bartels; Peter Bartmann; Christoph Berg; Markus Draaken; Annegret Geipel; Ulrich Gembruch; Andreas Heydweiller; Michael Ludwig; Manuel Mattheisen; Andreas Müller; Markus M Nöthen; Heiko Reutter
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(3):182-6.
2012: Nils Rahner; Johannes Schumacher; Liesbeth Spruijt; Verena Steinke; Susanne Stemmler; Carli J M Tops; Hans F A Vasen; Juul T Wijnen; Tim Becker; Felix F Brockschmidt; Wolfgang Dietmaier; Heike Görgens; Elke Holinski-Feder; Philip Kahl; Matthias Kloor; Marjolijn J L Ligtenberg; Markus M Nöthen; Peter Propping
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
Familial cancer 2012;11(1):19-26.
2011: Rami Abou Jamra; Mohammed Ayman Al Khateeb; Arif B Ekici; Mahmoud Fakher; Susanne Giesebrecht; Saber Hamdan; Amina Ismael; Safia Muhammad; Markus M Nöthen; Lutz Priebe; Johannes Schumacher; Steffen Uebe; Sigrun Wohlfart; Markus Zweier; Ahmad Abboud; André Reis
Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.
European journal of human genetics : EJHG 2011;19(11):1161-6.
2011: Johannes Schumacher; Ann Suhl Kristensen; Jens R Wendland; Markus M Nöthen; Ole Mors; Francis McMajon
The genetics of panic disorder.
Journal of medical genetics 2011;48(6):361-8.
2011: Hans Matsson; Kristiina Tammimies; Marco Zucchelli; Heidi Anthoni; Päivi Onkamo; Jaana Nopola-Hemmi; Heikki Lyytinen; Paavo H T Leppanen; Nina Neuhoff; Andreas Warnke; Gerd Schulte-Körne; Johannes Schumacher; Markus M Nöthen; Juha Kere; Myriam Peyrard-Janvid
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Behavior genetics 2011;41(1):134-40.
2011: Inke R König; Johannes Schumacher; Per Hoffmann; André Kleensang; Kerstin U Ludwig; Tiemo Grimm; Nina Neuhoff; Maike Preis; Darina Roeske; Andreas Warnke; Peter Propping; Helmut Remschmidt; Markus M Nöthen; Andreas Ziegler; Bertram Müller-Myhsok; Gerd Schulte-Körne
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(1):36-43.
2010: Vanessa Nieratschker; Josef Frank; Thomas W Mühleisen; Jana Strohmaier; Jens R Wendland; Johannes Schumacher; Jens Treutlein; René Breuer; Rami Abou Jamra; Manuel Mattheisen; Stefan Herms; Christine Schmäl; Wolfgang Maier; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Thomas G. Schulze
The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample.
Schizophrenia research 2010;122(1-3):24-30.
2010: Rami Abou Jamra; Thomas G. Schulze; Tim Becker; Felix F Brockschmidt; Elaine Green; Margrieta A Alblas; Jens R Wendland; Mazda Adli; Detelina Grozeva; Jana Strohmeier; Alexander Georgi; Nick Craddock; Peter Propping; Marcella Rietschel; Markus M Nöthen; Sven Cichon; Johannes Schumacher
A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(4):878-84.
2010: Jana Strohmaier; Josef Frank; Jens R Wendland; Johannes Schumacher; Rami Abou Jamra; Jens Treutlein; Vanessa Nieratschker; René Breuer; Manuel Mattheisen; Stefan Herms; Thomas W Mühleisen; Wolfgang Maier; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Thomas G. Schulze
A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry.
Schizophrenia research 2010;118(1-3):98-105.
2010: Husam Suliman; Johannes Schumacher; Tim Becker; Sven Cichon; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Markus M Nöthen; Rami Abou Jamra
Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia.
Psychiatric genetics 2010;20(2):82-3.
2010: Kerstin U Ludwig; Darina Roeske; Stefan Herms; Johannes Schumacher; Andreas Warnke; Ellen Plume; Nina Neuhoff; Jennifer Bruder; Helmut Remschmidt; Gerd Schulte-Körne; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(2):503-11.
2010: Johannes Schumacher; Jürgen Deckert
Serotonin transporter polymorphisms and panic disorder.
Genome medicine 2010;2(6):40.
2009: Johannes Schumacher; Gonzalo Laje; Rami Abou Jamra; Tim Becker; Thomas W Mühleisen; Catalina Vasilescu; Manuel Mattheisen; Stefan Herms; Per Hoffmann; Axel M Hillmer; Alexander Georgi; Christine Herold; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Francis McMajon; Markus M Nöthen; Sven Cichon
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: David M Otte; Andras Bilkei-Gorzó; Michaela D Filiou; Christoph W Turck; Oznur Yilmaz; Martin Ingo Holst; Karl Schilling; Rami Abou Jamra; Johannes Schumacher; Isabel Benzel; Wolfram S Kunz; Heinz Beck; Andreas Zimmer
Behavioral changes in G72/G30 transgenic mice.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2009;19(5):339-48.
2009: Thomas G. Schulze; Sevilla D Detera-Wadleigh; Nirmala Akula; A Gupta; L Kassem; Jo Steele; J Pearl; J Strohmaier; R Breuer; M Schwarz; Peter Propping; Markus M Nöthen; Sven Cichon; Johannes Schumacher; Marcella Rietschel; Francis McMajon
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder.
Molecular psychiatry 2009;14(5):487-91.
2009: Alexander Georgi; Johannes Schumacher; Chady Abboud Leon; Angela Villela Wolf; Katrin Klein; Katja V Böhenz; Frederike Schirmbeck; Jana Strohmaier; Peter Propping; Thomas G. Schulze; Marcella Rietschel; Markus M Nöthen; Sven Cichon; Rami Abou Jamra
No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample.
Psychiatric genetics 2009;19(2):104.
2009: Faten Dahdouh; Heidi Anthoni; Isabel Tapia-Páez; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Andreas Warnke; Helmut Remschmidt; Andreas Ziegler; Juha Kere; Bertram Müller-Myhsok; Markus M Nöthen; Johannes Schumacher; Marco Zucchelli
Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Psychiatric genetics 2009;19(2):59-63.
2009: Rami Abou Jamra; Alexander Georgi; Husam Suliman; Katrin Klein; Angela Wolf Villela; Thomas G. Schulze; Peter Propping; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
No association between the D-aspartate oxidase locus and schizophrenia.
Psychiatric genetics 2009;19(1):56.
2008: Kerstin U Ludwig; Johannes Schumacher; Gerd Schulte-Körne; Inke R König; Andreas Warnke; Ellen Plume; Heidi Anthoni; Myriam Peyrard-Janvid; Haiying Meng; Andreas Ziegler; Helmut Remschmidt; Juha Kere; Jeffrey R Gruen; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
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: Kerstin U Ludwig; Darina Roeske; Johannes Schumacher; Gerd Schulte-Körne; Inke R König; Andreas Warnke; Ellen Plume; Andreas Ziegler; Helmut Remschmidt; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
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: Frederike Schirmbeck; Alexander Georgi; Jana Strohmaier; Christine Schmael; Katja V Boesshenz; Thomas W Mühleisen; Stefan Herms; Per Hoffmann; Rami Abou Jamra; Johannes Schumacher; Wolfgang Maier; Peter Propping; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Thomas G. Schulze
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: Rami Abou Jamra; Carl Motinda Gobina; Tim Becker; Alexander Georgi; Thomas G. Schulze; Christine Schmael; Sven Cichon; Peter Propping; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder.
Psychiatric genetics 2008;18(4):199-203.
2008: Johannes Schumacher; Inke R König; Tatjana Schröder; Maike Duell; Ellen Plume; Peter Propping; Andreas Warnke; Claudia Libertus; Andreas Ziegler; Bertram Müller-Myhsok; Gerd Schulte-Körne; Markus M Nöthen
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.
Psychiatric genetics 2008;18(3):137-42.
2008: Marcella Rietschel; Lars Beckmann; Jana Strohmaier; Alexander Georgi; Anna Karpushova; Frederike Schirmbeck; Katja V Boesshenz; Christine Schmäl; Christin Bürger; Rami Abou Jamra; Johannes Schumacher; Susanne Höfels; Robert Kumsta; Sonja Entringer; Axel Krug; Valentin Markov; Wolfgang Maier; Peter Propping; Stefan Wüst; Tilo Kircher; Markus M Nöthen; Sven Cichon; Thomas G. Schulze
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: Rami Abou Jamra; Tim Becker; Alexander Georgi; T Feulner; Johannes Schumacher; J Stromaier; F Schirmbeck; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Markus M Nöthen; Sven Cichon
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.
Molecular psychiatry 2008;13(3):277-84.
2008: A E Baum; Nirmala Akula; M Cabanero; I Cardona; Winston Corona; B Klemens; Thomas G. Schulze; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Alexander Georgi; Johannes Schumacher; M Schwarz; Rami Abou Jamra; Susanne Höfels; Peter Propping; Jaya M Satagopan; Sevilla D Detera-Wadleigh; John Hardy; Francis McMajon
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: Sven Cichon; Ingeborg Winge; Manuel Mattheisen; Alexander Georgi; Anna Karpushova; Jan Freudenberg; Yun Freudenberg-Hua; Gulia Babadjanova; Ann Van Den Bogaert; Lilia I Abramova; Sofia Kapiletti; Per M Knappskog; Jeffrey McKinney; Wolfgang Maier; Rami Abou Jamra; Thomas G. Schulze; Johannes Schumacher; Peter Propping; Marcella Rietschel; Jan Haavik; Markus M Nöthen
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.
2007: Rami Abou Jamra; Robert Fuerst; RAdka Kaneva; Guillermo Orozco Diaz; Fabio Rivas; Fermin Mayoral; Eudoxia Gay; Sebastian Sans; Maria Jose Gonzalez; Susana Gil; Francisco Cabaleiro; Francisco Del Rio; Fermin Perez; Jesus Haro; Georg Auburger; vihra milanova; Christian Kostov; Vesselin Chorbov; Vessela Stoyanova; Amelia Nikolova-Hill; Georgi Onchev; Ivo Kremensky; Assen Jablensky; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Markus M Nothen; Sven Cichon; Thomas F Wienker; Johannes Schumacher
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.
2007: Alexander Georgi; Rami Abou Jamra; Katrin Klein; Angela Wolf Villela; Johannes Schumacher; Tim Becker; Torsten Paul; Christine Schmael; Susanne Höfels; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
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: Johannes Schumacher; Per Hoffmann; Christine Schmäl; Gerd Schulte-Körne; Markus M Nöthen
Genetics of dyslexia: the evolving landscape.
Journal of medical genetics 2007;44(5):289-97.
2007: Frederike Schirmbeck; Alexander Georgi; Jana Strohmaier; Christine Schmael; Carolin Knorr; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Norman Klopp; Thomas Illig; Maren Wulf; Markus Schwarz; Wolfgang Maier; Peter Propping; Sven Cichon; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample.
Psychiatric genetics 2007;17(2):127.
2007: Jana Strohmaier; Alexander Georgi; Frederike Schirmbeck; Christine Schmael; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Susanne Höfels; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Marcella Rietschel; Thomas G. Schulze
No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample.
Psychiatric genetics 2007;17(2):125.
2007: Heidi Anthoni; Marco Zucchelli; Hans Matsson; Bertram Müller-Myhsok; Ingegerd Fransson; Johannes Schumacher; Satu Massinen; Päivi Onkamo; Andreas Warnke; Heide Griesemann; Per Hoffmann; Jaana Nopola-Hemmi; Heikki Lyytinen; Gerd Schulte-Körne; Juha Kere; Markus M Nöthen; Myriam Peyrard-Janvid
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: Gerd Schulte-Körne; Andreas Ziegler; Wolfgang Deimel; Johannes Schumacher; Ellen Plume; C Bachmann; André Kleensang; Peter Propping; Markus M Nöthen; Andreas Warnke; Helmut Remschmidt; Inke R König
Interrelationship and familiality of dyslexia related quantitative measures.
Annals of human genetics 2007;71(Pt 2):160-75.
2007: Rami Abou Jamra; Tim Becker; Norman Klopp; Faten Dahdouh; Thomas G. Schulze; Magdalena Gross; Monika Deschner; Christine Schmäl; Thomas Illig; Marcella Rietschel; Peter Propping; Sven Cichon; Markus M Nöthen; Johannes Schumacher
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: Markus H Skowronek; Alexander Georgi; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Christine Schmael; Torsten Paul; Monika Deschner; Susanne Höfels; Maren Wulff; Markus Schwarz; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
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: Roland Ivo; Thomas G. Schulze; Johannes Schumacher; Kristina Kesper; Daniel J Müller; Ilana Kremer; Michael Dobrusin; Mustafa Mujaheed; Ibrahim Murad; Monika Blanaru; Isaam Bannoura; Alon Reshef; Rachel Bachner-Melman; Richard P Ebstein; Peter Propping; Robert H Belmaker; Wolfgang Maier; Marcella Rietschel; Markus M Nöthen; Sven Cichon
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: Alexander Georgi; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Christine Schmael; Monika Deschner; Susanne Höfels; Maren Wulff; Markus Schwarz; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Marcella Rietschel; Thomas G. Schulze
No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.
Psychiatric genetics 2006;16(5):183-4.
2006: Rami Abou Jamra; Christine Schmael; Sven Cichon; Marcella Rietschel; Johannes Schumacher; Markus M Nöthen
The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries?
Schizophrenia bulletin 2006;32(4):599-608.
2006: Rami Abou Jamra; Katrin Klein; Angela Wolf Villela; Tim Becker; Thomas G. Schulze; Christine Schmael; Monika Deschner; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
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: Rami Abou Jamra; Angela Wolf Villela; Katrin Klein; Tim Becker; Thomas G. Schulze; Christine Schmael; Monika Deschner; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia.
Psychiatric genetics 2006;16(3):91.
2006: Johannes Schumacher; Inke R König; Ellen Plume; Peter Propping; Andreas Warnke; M Manthey; M Duell; André Kleensang; Dirk Repsilber; M Preis; Helmut Remschmidt; Andreas Ziegler; Markus M Nöthen; Gerd Schulte-Körne
Linkage analyses of chromosomal region 18p11-q12 in dyslexia.
Journal of neural transmission (Vienna, Austria : 1996) 2006;113(3):417-23.
2006: Erik G Jönsson; Sven Cichon; Johannes Schumacher; Rami Abou Jamra; Thomas G. Schulze; Monika Deschner; Kaj Forslund; Håkan Hall; Peter Propping; Piotr M Czerski; Monica Dmitrak-Weglarz; Pawel Kapelski; Martin Driessen; Wolfgang Maier; Joanna Hauser; Marcella Rietschel; Markus M Nöthen
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.
2006: Johannes Schumacher; Heidi Anthoni; Faten Dahdouh; Inke R König; Axel M Hillmer; Nadine Kluck; Malou Manthey; Ellen Plume; Andreas Warnke; Helmut Remschmidt; Jutta Hülsmann; Sven Cichon; Cecilia M Lindgren; Peter Propping; Marco Zucchelli; Andreas Ziegler; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Markus M Nöthen; Juha Kere
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
American journal of human genetics 2006;78(1):52-62.
2005: Tim Becker; Johannes Schumacher; Sven Cichon; Max P Baur; Michael Knapp
Haplotype interaction analysis of unlinked regions.
Genetic epidemiology 2005;29(4):313-22.
2005: Thomas G. Schulze; Stephanie Ohlraun; Piotr M Czerski; Johannes Schumacher; Layla Kassem; Monika Deschner; Magdalena Gross; Monja Tullius; Vivien Heidmann; Svetlana Kovalenko; Rami Abou Jamra; Tim Becker; Anna Leszczynska-Rodziewicz; Joanna Hauser; Thomas Illig; Norman Klopp; Stefan Wellek; Sven Cichon; Fritz A Henn; Francis McMajon; Wolfgang Maier; Peter Propping; Markus M Nöthen; Marcella Rietschel
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: Rami Abou Jamra; Johannes Schumacher; Tim Becker; Faten Dahdouh; Stephanie Ohlraun; Husam Suliman; Thomas G. Schulze; Monja Tullius; Svetlana Kovalenko; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen; Sven Cichon
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: Johannes Schumacher; Rami Abou Jamra; Tim Becker; Stephanie Ohlraun; Norman Klopp; Elisabeth B Binder; Thomas G. Schulze; Monika Deschner; Christine Schmäl; Susanne Höfels; Astrid Zobel; Thomas Illig; Peter Propping; Florian Holsboer; Marcella Rietschel; Markus M Nöthen; Sven Cichon
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: Beate Glaser; Johannes Schumacher; Hywel J Williams; Rami Abou Jamra; Nikolai Ianakiev; Radoi Milev; Stephanie Ohlraun; Thomas G. Schulze; Piotr M Czerski; Joanna Hauser; Erik G Jönsson; Göran C Sedvall; Norman Klopp; Thomas Illig; Tim Becker; Peter Propping; Nigel M Williams; Sven Cichon; George Kirov; Marcella Rietschel; Kieran C Murphy; Michael C O'Donovan; Markus M Nöthen; Michael J Owen
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: Axel M Hillmer; Sandra Hanneken; Sibylle Ritzmann; Tim Becker; Jan Freudenberg; Felix F Brockschmidt; Antonia Flaquer; Yun Freudenberg-Hua; Rami Abou Jamra; Christine Metzen; Uwe Heyn; Nadine Schweiger; Regina C Betz; Bettina Blaumeiser; Jochen Hampe; Stefan Schreiber; Thomas G. Schulze; Hans Christian Hennies; Johannes Schumacher; Peter Propping; Thomas Ruzicka; Sven Cichon; Thomas F Wienker; Roland Kruse; Markus M Nothen
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
American journal of human genetics 2005;77(1):140-8.
2005: Rami Abou Jamra; I Sircar; Tim Becker; Yun Freudenberg-Hua; Stephanie Ohlraun; Jan Freudenberg; Felix F Brockschmidt; Thomas G. Schulze; Magdalena Gross; F Spira; Monika Deschner; Christine Schmäl; Wolfgang Maier; Peter Propping; Marcella Rietschel; Sven Cichon; Markus M Nöthen; Johannes Schumacher
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: Johannes Schumacher; Rami Abou Jamra; Tim Becker; Norman Klopp; Petra Franke; Christian Jacob; Philipp Sand; Jürgen Fritze; Stephanie Ohlraun; Thomas G. Schulze; Marcella Rietschel; Thomas Illig; Peter Propping; Sven Cichon; Jürgen Deckert; Markus M Nöthen
Investigation of the DAOA/G30 locus in panic disorder.
Molecular psychiatry 2005;10(5):428-9.
2004: Alessandro Serretti; Cristina Lorenzi; Laura Mandelli; Sven Cichon; Johannes Schumacher; Markus M Nöthen; Marcella Rietschel; Monja Tullius; Stephanie Ohlraun
DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population.
Neuroscience letters 2004;368(3):269-73.
2004: Rami Abou Jamra; Johannes Schumacher; Astrid Golla; Carola Richter; Andreas C J Otte; Thomas G. Schulze; Stephanie Ohlraun; Wolfgang Maier; Marcella Rietschel; Sven Cichon; Peter Propping; Markus M Nöthen
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: Erik G Jönsson; Jessica Bah; Jonas Melke; Rami Abou Jamra; Johannes Schumacher; Lars Westberg; Roland Ivo; Sven Cichon; Peter Propping; Markus M Nöthen; Elias Eriksson; Göran C Sedvall
Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers.
BMC psychiatry 2004;4():4.
2004: Johannes Schumacher; Rami Abou Jamra; Jan Freudenberg; Tim Becker; Stephanie Ohlraun; Andreas C J Otte; Monja Tullius; Svetlana Kovalenko; A Van Den Bogaert; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen; Sven Cichon
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.
2003: Ann Van Den Bogaert; Johannes Schumacher; Thomas G. Schulze; Andreas C Otte; Stephanie Ohlraun; Svetlana Kovalenko; Tim Becker; Jan Freudenberg; Erik G Jönsson; Marja Mattila-Evenden; Göran C Sedvall; Piotr M Czerski; Pawel Kapelski; Joanna Hauser; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen; Sven Cichon
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: Johannes Schumacher; Andreas C J Otte; Tim Becker; Yuli Sun; Thomas F Wienker; Brunhilde Wirth; Petra Franke; Rami Abou Jamra; Peter Propping; Jürgen Deckert; Markus M Nöthen; Sven Cichon
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.
Human genetics 2003;114(1):115-7.
2003: Erik G Jönsson; Rami Abou Jamra; Johannes Schumacher; Lena Flyckt; Gunnar Edman; Kaj Forslund; Marja Mattila-Evenden; Gunnar Rylander; Marie Asberg; Lars Bjerkenstedt; Frits-Axel Wiesel; Peter Propping; Sven Cichon; Markus M Nöthen; Göran C Sedvall
No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia.
Psychiatric genetics 2003;13(3):175-8.
2001: Sven Cichon; Johannes Schumacher; Daniel J Müller; M Hürter; Christine Windemuth; Konstantin Strauch; S Hemmer; Thomas G. Schulze; Gabriele D Schmidt-Wolf; Margot Albus; Margitta Borrmann-Hassenbach; E Franzek; Mario Lanczik; J Fritze; R Kreiner; U Reuner; B Weigelt; J Minges; Dirk Lichtermann; Bernard Lerer; Kyra Sarner Kanyas; Max P Baur; Thomas F Wienker; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen
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: Axel M Hillmer; Roland Kruse; Regina C Betz; Johannes Schumacher; Uwe Heyn; Peter Propping; Markus M Nöthen; Sven Cichon
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: Sven Cichon; Gabriele D Schmidt-Wolf; Johannes Schumacher; Daniel J Müller; M Hürter; Thomas G. Schulze; Margot Albus; Margitta Borrmann-Hassenbach; E Franzek; Mario Lanczik; J Fritze; R Kreiner; B Weigelt; J Minges; Dirk Lichtermann; Bernard Lerer; Kyra Sarner Kanyas; Konstantin Strauch; Christine Windemuth; Max P Baur; Thomas F Wienker; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26.
Molecular psychiatry 2001;6(3):342-9.