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Markus Nöthen

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Genes & Molecular Sequences

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Stefanie Heilmann; Christine Herold; Axel M Hillmer; David A Hinds; Stavroula Kanoni; Ari Kárason; Amy K Kiefer; Lambertus A Kiemeney; Rui Li; Nicholas G Martin; Vincent Mooser; Tim Becker; Regina C Betz; Felix F Brockschmidt; George Dedoussis; Dmitriy Drichel; Nicholas Eriksson; Nadine Fricker; Dale R Nyholt; Silke Redler; J Brent Richards; Kijoung Song; Kari Stefansson; Joyce Y Tung; Sita H Vermeulen; Markus M Nöthen
Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology.
Niels Weinhold; Mathias Witzens-Harig; Peter Broderick; Bowang Chen; Daniel Chubb; Faith E Davies; Sara E Dobbins; Lewin Eisele; Asta Försti; Hartmut Goldschmidt; Walter A Gregory; Per Hoffmann; Dirk Hose; Fay J Hosking; Richard S Houlston; Graham H Jackson; Anna Jauch; David C Johnson; Martin F Kaiser; Ni L Li; Yussanne P Ma; Gareth J Morgan; Thomas W Mühleisen; Kai Neben; Markus M Nöthen; Fiona M Ross; Brian A Walker; Kari Hemminki
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Britta Haenisch; Stefan Herms; Susanne Lucae; Wolfgang Maier; Manuel Mattheisen; Markus M Nöthen; Marcella Rietschel; Christine Schmäl; Michael Steffens; Jana Strohmaier; Rene Breuer; Franziska Degenhardt; Sven Cichon
Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder.

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All Publications

2013: Stefanie Heilmann; Christine Herold; Axel M Hillmer; David A Hinds; Stavroula Kanoni; Ari Kárason; Amy K Kiefer; Lambertus A Kiemeney; Rui Li; Nicholas G Martin; Vincent Mooser; Tim Becker; Regina C Betz; Felix F Brockschmidt; George Dedoussis; Dmitriy Drichel; Nicholas Eriksson; Nadine Fricker; Dale R Nyholt; Silke Redler; J Brent Richards; Kijoung Song; Kari Stefansson; Joyce Y Tung; Sita H Vermeulen; Markus M Nöthen
Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology.
The Journal of investigative dermatology 2013;133(6):1489-96.
2013: Niels Weinhold; Mathias Witzens-Harig; Peter Broderick; Bowang Chen; Daniel Chubb; Faith E Davies; Sara E Dobbins; Lewin Eisele; Asta Försti; Hartmut Goldschmidt; Walter A Gregory; Per Hoffmann; Dirk Hose; Fay J Hosking; Richard S Houlston; Graham H Jackson; Anna Jauch; David C Johnson; Martin F Kaiser; Ni L Li; Yussanne P Ma; Gareth J Morgan; Thomas W Mühleisen; Kai Neben; Markus M Nöthen; Fiona M Ross; Brian A Walker; Kari Hemminki
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Nature genetics 2013;45(5):522-5.
2013: Britta Haenisch; Stefan Herms; Susanne Lucae; Wolfgang Maier; Manuel Mattheisen; Markus M Nöthen; Marcella Rietschel; Christine Schmäl; Michael Steffens; Jana Strohmaier; Rene Breuer; Franziska Degenhardt; Sven Cichon
Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder.
Journal of affective disorders 2013;146(3):438-40.
2013: Lars Hansen; Taroh Kinoshita; Yusuke Maeda; Yuan Mang; Safia Muhammad; Yoshiko Murakami; Markus M Nöthen; André Reis; Stefanie Schaffer; Hasan Tawamie; Niels Tommerup; Shoaib ur Rehman; Michael Aigner; Shahid Mahmood Baig; Mads Bak; Eric P Bennett; Rebecca Buchert; Rami Abou Jamra
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.
American journal of human genetics 2013;92(4):575-83.
2013: Hassnaa Mahmoudi; Andrew G Messenger; Markus M Nöthen; Silke Redler; Rachid Tazi-Ahnini; Peter Teßmann; Hans Wolff; Tim Becker; Pattie Birch; Ulrike Blume-Peytavi; Markus Böhm; Kathy Dobson; Dmitriy Drichel; Kathrin A Giehl; Sandra Hanneken; Roland Kruse; Gerhard Lutz; Regina C Betz
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss.
Archives of dermatological research 2013;305(3):249-53.
2013: Sandra Meier; Thomas W Mühleisen; Markus M Nöthen; Marcella Rietschel; Thomas G. Schulze; Jana Strohmaier; Rene Breuer; Sven Cichon; Franziska Degenhardt; Manuel Mattheisen; Stefan Wüst
Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2013;16(3):549-56.
2013: Markus Draaken; Anne-Karoline Ebert; Bernhard G Herrmann; Per Hoffmann; Enrika Bartels; Thomas M Boemers; Susanne Moebus; Sadaf S Mughal; Markus M Nöthen; Tracie Pennimpede; Heiko Reutter; Wolfgang Rösch; Dominik Schmidt; Eberhard Schmiedeke; Raimund Stein; Lars Wittler; Stefanie Wolter; Michael Ludwig
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.
Birth defects research. Part A, Clinical and molecular teratology 2013;97(3):133-9.
2013: Franziska Degenhardt; Stefan Herms; Per Hoffmann; Wolfgang Maier; Manuel Mattheisen; Rainald Mössner; Igor Nenadic; Markus M Nöthen; Lutz Priebe; Marcella Rietschel; Dan Rujescu; Heinrich Sauer; Thomas G. Schulze; Jana Strohmaier; Sven Cichon
No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder.
Psychiatric genetics 2013;23(1):45-6.
2013: D T Chen; A Cheng; Sven Cichon; S Jamain; X Jiang; Layla Kassem; M Leboyer; Francis McMajon; P Muglia; Markus M Nöthen; J-H Park; Marcella Rietschel; Thomas G. Schulze; Yin Yao Shugart; C J M Steele; J R Wendland; Judith A Badner; Thomas B Barrett; Wade H Berrettini; Cinnamon S Bloss; William Byerley; David T Chen; William Coryell; David W Craig; Howard J Edenberg; Tatiana Foroud; Elliot S Gershon; Tiffany A Greenwood; Maria Hipolito; John R Kelsoe; Daniel L Koller; William B Lawson; Chunyu Liu; Pamela Lynn Belmonte Mahon; Melvin G McInnis; Rebecca McKinney; Francis J McMahon; Caroline M Nievergelt; John I Nurnberger; Evaristus A Nwulia; James B Potash; John Rice; William A Scheftner; Nicholas J Schork; Paul D Shilling; Erin N Smith; Szabolcs Szelinger; Peter P Zandi; Peng Zhang; Sebastian Zöllner; Nirmala Akula; N Chatterjee; Thomas G Schulze
Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
Molecular psychiatry 2013;18(2):195-205.
2013: Frieder M Paulus; Martin Pyka; Marcella Rietschel; Jens Sommer; Stephanie Witt; Tilo T J Kircher; Susanne Knake; Sören Krach; Axel Krug; Markus M Nöthen; Johannes Bedenbender; Andreas Jansen
Partial support for ZNF804A genotype-dependent alterations in prefrontal connectivity.
Human brain mapping 2013;34(2):304-13.
2013: Sandra M Pasternack; Melanie Refke; Nico Schäfer; Elizabeth Sweeney; Maurice van Steensel; Carlos Ferrándiz; Utz Fischer; Thomas Franz; Alan Fryer; Clemens Grimm; Hans Christian Hennies; Miquel Just; Roland Kruse; Markus M Nöthen; Elham Paknia; Regina C Betz
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.
American journal of human genetics 2013;92(1):81-7.
2013: K U Ludwig; K Moll; B Müller-Myhsok; Markus M Nöthen; R Plomin; Philipp G Sämann; Gerd Schulte-Körne; J Schumacher; D Spieler; A Warnke; M Alexander; J Becker; J Bruder; M Czisch; O S P Davis; S J Docherty; P Hoffmann; Karin Landerl; D Czamara
A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Translational psychiatry 2013;3():e229.
2013: Sonali Pechlivanis; Dirk Schadendorf; André Scherag; Raimund Erbel; Per Hoffmann; Karl-Heinz Jöckel; Susanne Moebus; Stefan Möhlenkamp; Thomas W Mühleisen; Markus M Nöthen
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.
BMC medical genetics 2013;14():23.
2013: Axel Krug; Vanessa Nieratschker; Markus M Nöthen; Marcella Rietschel; N Jon Shah; Stephanie Witt; Andreas Jansen; Sören Krach; Tilo Kircher
The effect of neurogranin on neural correlates of episodic memory encoding and retrieval.
Schizophrenia bulletin 2013;39(1):141-50.
2012: Igor Nenadic; Markus M Nöthen; Jürgen R Reichenbach; Marcella Rietschel; Heinrich Sauer; Claudia Schachtzabel; Sigrid Scherpiet; Sven Cichon; Thomas Deufel; Christian Gaser; Raka Maitra; Thomas W Mühleisen; C Christoph Schultz; Stefan Smesny; Jens Treutlein; Ralf G M Schlösser
Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia.
Journal of psychiatric research 2012;46(12):1531-9.
2012: Markus Draaken; Alina Hilger; Jeanette Latus; Enrika Bartels; Thomas M Boemers; Sadaf S Mughal; Markus M Nöthen; Wiebke Prins; Heiko Reutter; Dominik Schmidt; Eberhard Schmiedeke; Nicole Spychalski; Claudia Zeidler; Michael Ludwig
Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene.
International journal of molecular medicine 2012;30(6):1459-64.
2012: S Redler; H Wolff; F Albert; Tim Becker; Bettina Blaumeiser; M Böhm; Felix F Brockschmidt; Sibylle Eigelshoven; K A Giehl; Sandra Hanneken; C Herold; Roland Kruse; G Lutz; Markus M Nöthen; Regina C Betz
Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata.
The British journal of dermatology 2012;167(6):1360-5.
2012: Entessar Nasser; Markus M Nöthen; Stefanie Nowak; Bernd Pötzsch; Rudolf H Reich; Heiko Reutter; Daniela C Tradowsky; Philipp Wahle; Sandra Barth; Jessica Becker; Anne C Boehmer; Bert Braumann; Heide Fier; Nadine Fricker; Alexander Hemprich; Ruth Herberz; Per Hoffmann; Michael Knapp; Franz-Josef Kramer; Thomas Kreusch; Christoph Lange; Carola Lauster; Elisabeth Mangold; Kerstin U Ludwig
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(11):925-33.
2012: Manuel Mattheisen; Sandra Meier; Thomas W Mühleisen; Igor Nenadic; Markus M Nöthen; Marcella Rietschel; Dan Rujescu; Heinrich Sauer; Thomas G. Schulze; Jana Strohmaier; Jens Treutlein; Stephanie Witt; Franziska Degenhardt; Ina Giegling; Stefan Herms; Per Hoffmann; Margrieta Alblas; Sven Cichon
Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia.
Schizophrenia research 2012;141(2-3):262-5.
2012: Britta Haenisch; Markus M Nöthen; Gerhard J Molderings
Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics.
Immunology 2012;137(3):197-205.
2012: Elisabeth Mangold; Sergio G Muñoz-Jiménez; Markus M Nöthen; Stefanie Nowak; Rocío Ortiz-López; Mario Paredes-Zenteno; Heiko Reutter; Abelardo Arizpe-Cantú; Stefan Herms; Michael Knapp; Franz-Josef Kramer; Rafael B R León-Cachón; Kerstin U Ludwig; Thomas F Wienker; Óscar Chacón-Camacho; Augusto Rojas-Martínez
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2012;120(5):373-7.
2012: Enrika Bartels; Peter Bartmann; Friederike Baudisch; Christoph Berg; Markus Draaken; Gabriel C Dworschak; Annegret Geipel; Ulrich Gembruch; Alina C Hilger; Per Hoffmann; Michael Ludwig; Carlo M Marcelis; Manuel Mattheisen; Nicole W Mora; Andreas Müller; Markus M Nöthen; Daniel E Pineda-Alvarez; Jochen Ritgen; Eberhard Schmiedeke; Anna C Schulz; Benjamin D Solomon; Rüdiger Stressig; Iris A L M van Rooij; Charlotte H W Wijers; Soyhan Bagci; Heiko Reutter
VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis.
Clinical dysmorphology 2012;21(4):191-5.
2012: Lars Wittler; Markus Draaken; Anne-Karoline Ebert; Alina Hilger; Markus M Nöthen; Tracie Pennimpede; Judith Proske; Heiko Reutter; Wolfgang Rösch; Raimund Stein; Michael Ludwig
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias.
Gene 2012;506(2):392-5.
2012: Xavier Miró; Thomas W Mühleisen; Markus M Nöthen; María Teresa Pardo-Olmedilla; Iris Reinhard; Marcella Rietschel; Christine Schmäl; Constanze Seidenbecher; Jana Strohmaier; Andras Bilkei-Gorzo; René Breuer; Sven Cichon; Franziska A Degenhardt; Marie Luise Dreisow; Josef Frank; Manuel Mattheisen; Sandra Meier; Önder Albayram; Andreas Zimmer
Studies in humans and mice implicate neurocan in the etiology of mania.
The American journal of psychiatry 2012;169(9):982-90.
2012: Dagny Jagielska; Roland Kruse; Gerhard Lutz; Markus M Nöthen; Sandra M Pasternack; Silke Redler; Melanie Refke; Hans Wolff; Bettina Blaumeiser; Ulrike Blume-Peytavi; Markus Böhm; Felix F Brockschmidt; Sibylle Eigelshoven; Natalie Garcia Bartels; Kathrin A Giehl; Sandra Hanneken; Christine Herold; Sandra Barth; Tim Becker; Regina C Betz
Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance.
The Journal of investigative dermatology 2012;132(9):2192-7.
2012: Inti Pedroso; Marcella Rietschel; Ammar Al-Chalabi; Michael R Barnes; Sven Cichon; Anbarasu Lourdusamy; Peter McGuffin; Markus M Nöthen; Gerome Breen
Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes.
Biological psychiatry 2012;72(4):311-7.
2012: Enrika Bartels; Sabine Grasshoff-Derr; Stefan Holland-Cunz; Stuart Hosie; Ekkehart Jenetzky; Christina Kujath; Johannes Leonhardt; Michael Ludwig; Stefanie Märzheuser; Markus M Nöthen; Markus Palta; Heiko Reutter; Anke Rissmann; Mattias Schäfer; Dominik Schmidt; Eberhard Schmiedeke; Benjamin D Solomon; Sandra Weih; Nadine Zwink
Inheritance of the VATER/VACTERL association.
Pediatric surgery international 2012;28(7):681-5.
2012: Ofer Sarig; Enno Schmidt; Karl Skorecki; Henri Trau; Detlef Zillikens; Lilach Zoller; Aviv Barzilai; Sharon Baum; Sivan Bercovici; Reuven Bergman; Ariel Darvasi; Dan Geiger; Ilan Goldberg; Michael Hertl; Saleh M Ibrahim; Margarita Indelman; Shirli Israeli; Oren Katz; Helena Martinez de Morentin; Dedee F Murrell; Sagi Nahum; Markus M Nöthen; Shai Rosenberg; Saharon Rosset; Nadav Sagiv; Eli Sprecher
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.
The Journal of investigative dermatology 2012;132(7):1798-805.
2012: Isabel Spier; Dietlinde Stienen; Siegfried Uhlhaas; Stefanie Vogt; Markus Draaken; Per Hoffmann; Elke Holinski-Feder; Sukanya Horpaopan; Michael Ludwig; Monika Morak; Markus M Nöthen; Stefan Aretz
Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis.
Human mutation 2012;33(7):1045-50.
2012: Alina Hilger; Per Hoffmann; Enrika Bartels; Markus Draaken; Gabriel Dworschak; Sadaf S Mughal; Markus M Nöthen; Heiko Reutter; Charlotte Schramm; Michael Ludwig
Familial occurrence of the VATER/VACTERL association.
Pediatric surgery international 2012;28(7):725-9.
2012: S Redler; M Refke; Rachid Tazi-Ahnini; H Wolff; Tim Becker; M P Birch; M Böhm; Felix F Brockschmidt; K Dobson; D Drichel; K A Giehl; S Herms; Nadine Kluck; Roland Kruse; G Lutz; Andrew G Messenger; Markus M Nöthen; Regina C Betz
Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss.
The British journal of dermatology 2012;166(6):1314-8.
2012: Silke Redler; Melanie Refke; Rachid Tazi-Ahnini; Hans Wolff; Markus M Nöthen; Tim Becker; Regina C Betz; Mary P Birch; Markus Böhm; Felix F Brockschmidt; Kathy Dobson; Dmitriy Drichel; Kathrin A Giehl; Nadine Kluck; Roland Kruse; Gerhard Lutz; Andrew Messenger
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identified.
Experimental dermatology 2012;21(5):390-3.
2012: M Thier; Philipp Wörsdörfer; Oliver Brüstle; Raphaela Gorris; Stefan Herms; Per Hoffmann; Yenal B Lakes; Markus M Nöthen; Thoralf Opitz; Tamara Quandel; Dominic Seiferling; Frank Edenhofer
Direct conversion of fibroblasts into stably expandable neural stem cells.
Cell stem cell 2012;10(4):473-9.
2012: Andrea Christoforou; Sven Cichon; Srdjan Djurovic; Michael Dondrup; Sudheer Giddaluru; Inge Jonassen; Manuel Mattheisen; Morten Mattingsdal; Markus M Nöthen; Pål Puntervoll; Marcella Rietschel; Vidar M Steen; Ole A Andreassen; Stéphanie Le Hellard
Linkage-disequilibrium-based binning affects the interpretation of GWASs.
American journal of human genetics 2012;90(4):727-33.
2012: Thomas Nickl-Jockschat; Markus M Nöthen; Marcella Rietschel; Frank Schneider; N Jon Shah; Tony Stöcker; Jens Treutlein; Klaus Zerres; Ute Habel; Ruihuang Huang; Axel Krug; Valentin Markov; Tilo Kircher
The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: a TBSS-based diffusion tensor imaging study.
NeuroImage 2012;60(2):847-53.
2012: Franziska Degenhardt; Magdalena Gross; Andreas Heinz; Stefan Herms; Per Hoffmann; Florian Holsboer; Christoph Lange; Susanne Lucae; Wolfgang Maier; Manuel Mattheisen; Sandra Meier; Andreas Meyer-Lindenberg; Susanne Moebus; Thomas W Mühleisen; Bertram Müller-Myhsok; Markus M Nöthen; Lutz Priebe; Marcella Rietschel; Jana Strohmaier; Henrik Walter; Christiane Wolf; René Breuer; Sven Cichon
Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012;159B(3):263-73.
2012: L Priebe; Peter Propping; Marcella Rietschel; S Schreiber; M Weingarten; S Witt; V Nieratschker; Markus M Nöthen; T Paul; M Alblas; R Breuer; Sven Cichon; F A Degenhardt; Maria Grigoroiu-Serbanescu; B Haenisch; S Herms; M Lathrop; M Leboyer; Wolfgang Maier; Manuel Mattheisen; Susanne Moebus; T W Mühleisen
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
Molecular psychiatry 2012;17(4):421-32.
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.
2012: C Hammer; J Hauser; Manuel Mattheisen; T W Mühleisen; G Babadjanova; R Breuer; Sven Cichon; F Degenhardt; Maria Grigoroiu-Serbanescu; B Haenisch; Markus M Nöthen; L Oruc; Gudrun Rappold; Marcella Rietschel; F Rivas; Ralph Röth; J Strohmaier; Stephanie Witt; Beate Niesler
Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study.
Translational psychiatry 2012;2():e103.
2012: Thomas E Gladwin; Douglas Levinson; Manuel Mattheisen; Markus M Nöthen; René Breuer; Sven Cichon; Eske Derks; Pablo V Gejman; Marcella Rietschel; Thomas G. Schulze; Jianxin Shi; Roel A Ophoff
Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples.
PloS one 2012;7(6):e38828.
2012: Robert Keers; Patrick M Nolan; Markus M Nöthen; Inti Pedroso; Marcella Rietschel; Leonard C Schalkwyk; KJ Aitchison; Gerome Breen; Sven Cichon; Cathy Fernandes
Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
PloS one 2012;7(6):e38263.
2012: Kari M Ersland; Thomas Espeseth; Carla P D Fernandes; Sudheer Giddaluru; Thomas Hansen; Gudmundur A Hardarson; Ole A Andreassen; René Breuer; Andrea Christoforou; Sven Cichon; Srdjan Djurovic; Astri J Lundervold; Manuel Mattheisen; Morten Mattingsdal; Markus M Nöthen; Ivar Reinvang; Marcella Rietschel; Christine Stansberg; Vidar M Steen; Jana Strohmaier; Thomas Werge; Stéphanie Le Hellard
Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders.
PloS one 2012;7(2):e31687.
2012: Josef Frank; Wolfgang Gaebel; Stefan Herms; Per Hoffmann; Marcus Ising; Falk Kiefer; Susanne Lucae; Wolfgang Maier; Karl Mann; Manuel Mattheisen; Rainald Mössner; Bertram Müller-Myhsok; Markus M Nöthen; Monika Ridinger; Norbert Scherbaum; Christine Schmäl; Michael Soyka; Michael Steffens; Jens Treutlein; Norbert Wodarz; Peter Zill; Sven Cichon; Norbert Dahmen; Marcella Rietschel
Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.
Addiction biology 2012;17(1):171-80.
2011: Susanne Erk; Christine Esslinger; Peter Kirsch; Manuel Mattheisen; Andreas Meyer-Lindenberg; Thomas W Mühleisen; Markus M Nöthen; Carola Opitz von Boberfeld; Marcella Rietschel; Knut Schnell; Sven Cichon; Stephanie Witt; Henrik Walter
Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2011;31(49):18180-4.
2011: Elisabeth Mangold; Kerstin U Ludwig; Markus M Nöthen
Breakthroughs in the genetics of orofacial clefting.
Trends in molecular medicine 2011;17(12):725-33.
2011: M Refke; M M Seyger; S Wenzel; B Fiebig; B C Hamel; N Ishorst; M Ludwig; Markus M Nöthen; S M Pasternack; Regina C Betz
Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay.
The British journal of dermatology 2011;165(5):1127-32.
2011: Stefan Boehringer; Monique M B Breteler; Manuel Günther; Ruth Herberz; Albert Hofman; Bernhard Horsthemke; Stefan Klein; Fan Liu; Kerstin U Ludwig; Elisabeth Mangold; Wiro J Niessen; Markus M Nöthen; Stefanie Nowak; Stella Sinigerova; Andre G Uitterlinden; Fedde van der Lijn; Aad van Der Lugt; Dagmar Wieczorek; Rolf P Würtz; Manfred Kayser
Genetic determination of human facial morphology: links between cleft-lips and normal variation.
European journal of human genetics : EJHG 2011;19(11):1192-7.
2011: Heiko Reutter; Sebastian Rogenhofer; Wolfgang H Rösch; Annette Schröder; Raimund Stein; Boris Utsch; Hannes Vogt; Nadine Zwink; Enrika Bartels; Goedele M A Beckers; Thomas M Boemers; Arend Bökenkamp; Simeon Boyd; Birte Detlefsen; Markus Draaken; Anne-Karoline Ebert; Lisa Gambhir; John P Gearhart; Rita Gobet; Enrique Jaureguizar; Abdol-Mohammad Kajbafzadeh; Yegappan Lakshmanan; Michael Ludwig; Martin Müller; Markus M Nöthen; Ekkehart Jenetzky
Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and Europe.
The Journal of pediatrics 2011;159(5):825-831.e1.
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: Falk Kiefer; T Lemenager; A Batra; M Berner; Sven Cichon; J Frank; A Heinz; Markus M Nöthen; A Richter; Marcella Rietschel; M N Smolka; Rainer Spanagel; Jens Treutlein; Klaus Wiedemann; Stephanie Witt; N Wodarz; U S Zimmermann; K Mann
Involvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosate.
The pharmacogenomics journal 2011;11(5):368-74.
2011: Sara E Dobbins; Lewin Eisele; Maria Feychting; Roger Henriksson; Sarah J Hepworth; Per Hoffmann; Fay J Hosking; Christoffer Johansen; Michael Kosteljanetz; Amy Lloyd; Stefan Lönn; Yussanne P Ma; Beatrice Melin; Susanne Moebus; Thomas W Mühleisen; K Muir; Markus M Nöthen; Bianca Olver; Minouk J Schoemaker; Johannes Schramm; Matthias Simon; Anthony Swerdlow; Anders Ahlbom; Ulrika Andersson; Thomas Brännström; Peter Broderick; Richard S Houlston
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
Nature genetics 2011;43(9):825-7.
2011: C Christoph Schultz; Gerd Wagner; Sven Cichon; Thomas Deufel; Michael Kiehntopf; Kathrin Koch; Thomas W Mühleisen; Igor Nenadic; Markus M Nöthen; Jürgen R Reichenbach; Marcella Rietschel; Martin Roebel; Heinrich Sauer; Claudia Schachtzabel; Ralf Schlösser
Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2011;36(8):1747-53.
2011: Bjarte Håvik; Stephanie Le Hellard; Helle Lybaek; Wolfgang Maier; Manuel Mattheisen; Ingrid Melle; Thomas W Mühleisen; Markus M Nöthen; Lutz Priebe; Marcella Rietschel; Thomas G. Schulze; Ingrid Agartz; Ole A Andreassen; Clive R Bramham; Rene Breuer; Sven Cichon; Franziska Degenhardt; Srdjan Djurovic; Thomas Hansen; Beth Stevens; Thomas Werge; Vidar M Steen
The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia.
Biological psychiatry 2011;70(1):35-42.
2011: Markus Thimm; Tilo T J Kircher; Thilo Kellermann; V Markov; Sören Krach; Andreas Jansen; Klaus Zerres; Thomas Eggermann; Tony Stöcker; N Jon Shah; Markus M Nöthen; Marcella Rietschel; Stephanie Witt; Klaus Mathiak; A Krug
Effects of a CACNA1C genotype on attention networks in healthy individuals.
Psychological medicine 2011;41(7):1551-61.
2011: Rami Abou Jamra; Guntram Borck; Felix F Brockschmidt; Rebecca Buchert; Sebastian H Eck; Arif B Ekici; Elisabeth Graf; Arnold Munnich; Markus M Nöthen; Orianne Philippe; Annick Raas-Rothschild; Andre Reis; Tim M Strom; Laurence Colleaux
Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature.
American journal of human genetics 2011;88(6):788-95.
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: Jessica E Van Schijndel; Martine Van Zweeden; Thomas Werge; Rolf Adolfsson; Ole A Andreassen; Anders D Børglum; Sven Cichon; Stephan Claes; marc de hert; Jurgen Del-Favero; Srdjan Djurovic; Thomas Hansen; Pekka Kallunki; Ole Mors; Preben B Mortensen; Merete Nordentoft; Karl-Fredrik Norrback; Markus M Nöthen; Mette Nyegaard; Jan Torleif Pedersen; Marcella Rietschel; Karina Meden Sørensen; Karen van Loo; Gerard J M Martens
Dual association of a TRKA polymorphism with schizophrenia.
Psychiatric genetics 2011;21(3):125-31.
2011: Charlotte Schramm; Gabriel Tewes; Stefanie Märzheuser; Markus M Nöthen; Lutz Priebe; Heiko Reutter; Eberhard Schmiedeke; Stefan Aretz; Enrika Bartels; Markus Draaken; Sabine Grasshoff-Derr; Per Hoffmann; Stefan Holland-Cunz; Stuart Hosie; Martina Kreiss-Nachtsheim; Michael Ludwig
Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature.
European journal of pediatrics 2011;170(6):741-6.
2011: R Breuer; M L Hamshere; J Strohmaier; M Mattheisen; F Degenhardt; S Meier; T Paul; M C O'Donovan; T W Mühleisen; Thomas G. Schulze; Markus M Nöthen; Sven Cichon; N Craddock; Marcella Rietschel
Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype.
Molecular psychiatry 2011;16(6):587-9.
2011: Karsten K-G John; Felix F Brockschmidt; Silke Redler; Christine Herold; Sandra Hanneken; Sibylle Eigelshoven; Kathrin A Giehl; Jozef De Weert; Gerhard Lutz; Roland Kruse; Hans Wolff; Bettina Blaumeiser; Markus Böhm; Tim Becker; Markus M Nöthen; Regina C Betz
Genetic variants in CTLA4 are strongly associated with alopecia areata.
The Journal of investigative dermatology 2011;131(5):1169-72.
2011: Stefan Pabst; M Golebiewski; S Herms; A Karpushova; A Díaz-Lacava; M Walier; S Zimmer; Sven Cichon; Thomas F Wienker; Markus M Nöthen; Georg Nickenig; R Meyer; Dirk Skowasch; Christian Grohé
Caspase recruitment domain 15 gene haplotypes in sarcoidosis.
Tissue antigens 2011;77(4):333-7.
2011: Thomas W Mühleisen; F Buket Basmanav; Andreas J Forstner; Manuel Mattheisen; Lutz Priebe; Stefan Herms; Rene Breuer; Susanne Moebus; Igor Nenadic; Heinrich Sauer; Rainald Mössner; Wolfgang Maier; Dan Rujescu; Michael Ludwig; Marcella Rietschel; Markus M Nöthen; Sven Cichon
Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients.
Schizophrenia research 2011;127(1-3):35-40.
2011: Chady Abboud Leon; Markus M Nöthen; Peter Propping; Marcella Rietschel; Thomas G. Schulze; Johannes Schumacher; Sven Cichon; Christine Herold; Nadine Kluck; Rami Abou Jamra
Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample.
Psychiatric genetics 2011;21(2):114.
2011: Silke Redler; Roland Kruse; Sibylle Eigelshoven; Sandra Hanneken; Melanie Refke; Yaran Wen; Xue Zhang; Sven Cichon; Regina C Betz; Markus M Nöthen
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.
Journal of the American Academy of Dermatology 2011;64(4):e45-50.
2011: Henrik Walter; K Schnell; Susanne Erk; C Arnold; Peter Kirsch; C Esslinger; D Mier; M M Schmitgen; Marcella Rietschel; Stephanie Witt; Markus M Nöthen; Sven Cichon; Andreas Meyer-Lindenberg
Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task.
Molecular psychiatry 2011;16(4):462-70.
2011: Charlotte Schramm; Markus Draaken; Enrika Bartels; Thomas M Boemers; Eberhard Schmiedeke; Sabine Grasshoff-Derr; Stefanie Märzheuser; Stuart Hosie; Stefan Holland-Cunz; Friederike Baudisch; Lutz Priebe; Per Hoffmann; Alexander M Zink; Hartmut Engels; Felix F Brockschmidt; Stefan Aretz; Markus M Nöthen; Michael Ludwig; Heiko Reutter
De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation.
American journal of medical genetics. Part A 2011;155A(2):445-9.
2011: Carolin Pütter; Karl-Heinz Jöckel; Markus M Nöthen; Sonali Pechlivanis; Heinz-Erich Wichmann; André Scherag
Missing heritability in the tails of quantitative traits? A simulation study on the impact of slightly altered true genetic models.
Human heredity 2011;72(3):173-81.
2011: E Bartels; F Baudisch; M Draaken; B Kazmierczak; Michael Ludwig; Markus M Nöthen; E Schmiedeke; C Schramm; S Spranger; Heiko Reutter
De novo partial trisomy 18p and partial monosomy 18q in a patient with anorectal malformation.
Cytogenetic and genome research 2011;134(3):243-8.
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.
2011: Nilma Almeida de Assis; Stefanie Nowak; Kerstin U Ludwig; Heiko Reutter; Jennifer Vollmer; Stefanie Heilmann; Nadine Kluck; Carola Lauster; Bert Braumann; Rudolf H Reich; Alexander Hemprich; Michael Knapp; Thomas F Wienker; Franz-Josef Kramer; Per Hoffmann; Markus M Nöthen; Elisabeth Mangold
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients.
International journal of pediatric otorhinolaryngology 2011;75(1):49-52.
2011: Charlotte Schramm; Markus Draaken; Enrika Bartels; Thomas M Boemers; Stefan Aretz; Felix F Brockschmidt; Markus M Nöthen; Michael Ludwig; Heiko Reutter
De novo microduplication at 22q11.21 in a patient with VACTERL association.
European journal of medical genetics 2011;54(1):9-13.
2011: Axel Krug; Valentin Markov; Sören Krach; Andreas Jansen; Klaus Zerres; Thomas Eggermann; Tony Stöcker; N Jon Shah; Markus M Nöthen; Alexander Georgi; Jana Strohmaier; Marcella Rietschel; Tilo T J Kircher
Genetic variation in G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals.
Human brain mapping 2011;32(1):118-26.
2010: Axel Krug; Valentin Markov; Sören Krach; Andreas Jansen; Klaus Zerres; Thomas Eggermann; Tony Stöcker; N Jon Shah; Markus M Nöthen; Jens Treutlein; Marcella Rietschel; Tilo T J Kircher
The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval.
NeuroImage 2010;53(3):985-91.
2010: Andreas Jansen; Sören Krach; Axel Krug; Valentin Markov; Markus Thimm; Frieder M Paulus; Klaus Zerres; Tony Stöcker; N Jon Shah; Markus M Nöthen; Jens Treutlein; Marcella Rietschel; Tilo T J Kircher
The effect of G72 genotype on neural correlates of memory encoding and retrieval.
NeuroImage 2010;53(3):1001-6.
2010: Dina M Schardt; Susanne Erk; Corinna Nüsser; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Jens Treutlein; Thomas Goschke; Henrik Walter
Volition diminishes genetically mediated amygdala hyperreactivity.
NeuroImage 2010;53(3):943-51.
2010: Henning R Gockel; Johannes Schumacher; Ines Gockel; Hauke Lang; Thomas Haaf; Markus M Nöthen
Achalasia: will genetic studies provide insights?
Human genetics 2010;128(4):353-64.
2010: Heiko Reutter; Franz Rüschendorf; Manuel Mattheisen; Markus Draaken; Enrika Bartels; Norbert Hübner; Per Hoffmann; Seyedmedhi Payabvash; Kathrin Saar; Markus M Nöthen; Abdol-Mohammad Kajbafzadeh; Michael Ludwig
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(9):757-61.
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: Sonali Pechlivanis; André Scherag; Thomas W Mühleisen; Stefan Möhlenkamp; Bernhard Horsthemke; Tanja Boes; Martina Bröcker-Preuss; Klaus Mann; Raimund Erbel; Karl-Heinz Jöckel; Markus M Nöthen; Susanne Moebus
Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort.
Arteriosclerosis, thrombosis, and vascular biology 2010;30(9):1867-72.
2010: Alistair T Pagnamenta; Elena Bacchelli; Maretha V de Jonge; Ghazala Mirza; Thomas Scerri; Fiorella Minopoli; Andreas Chiocchetti; Kerstin U Ludwig; Per Hoffmann; Silvia Paracchini; Ernesto Lowy; Denise H Harold; Jade A Chapman; Sabine M Klauck; Fritz Poustka; Renske H Houben; Wouter G Staal; Roel A Ophoff; Michael C O'Donovan; Julie Williams; Markus M Nöthen; Gerd Schulte-Körne; Panos Deloukas; Jiannis Ragoussis; Anthony J Bailey; Elena Maestrini; Anthony P Monaco
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.
Biological psychiatry 2010;68(4):320-8.
2010: Susanne Erk; Andreas Meyer-Lindenberg; Knut Schnell; Carola Opitz von Boberfeld; Christine Esslinger; Peter Kirsch; Oliver Grimm; Claudia Arnold; Leila Haddad; Stephanie Witt; Sven Cichon; Markus M Nöthen; Marcella Rietschel; Henrik Walter
Brain function in carriers of a genome-wide supported bipolar disorder variant.
Archives of general psychiatry 2010;67(8):803-11.
2010: Markus Draaken; Judith Proske; Charlotte Schramm; Lars Wittler; Enrika Bartels; Markus M Nöthen; Heiko Reutter; Michael Ludwig
Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(7):546-50.
2010: Augusto Rojas-Martinez; Heiko Reutter; Oscar Chacon-Camacho; Rafael B R Leon-Cachon; Sergio G Munoz-Jimenez; Stefanie Nowak; Jessica Becker; Ruth Herberz; Kerstin U Ludwig; Mario Paredes-Zenteno; Abelardo Arizpe-Cantú; Susanne Raeder; Stefan Herms; Rocio Ortiz-Lopez; Michael Knapp; Per Hoffmann; Markus M Nöthen; Elisabeth Mangold
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(7):535-7.
2010: Antònia Flaquer; Rami Abou Jamra; Karolin Etterer; Guillermo Orozco Díaz; Fabio Rivas; Marcella Rietschel; Sven Cichon; Markus M Nöthen; Konstantin Strauch
A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(5):1110-4.
2010: Rosie M Walker; Andrea Christoforou; Pippa A Thomson; Kevin A McGhee; Alan Maclean; Thomas W Mühleisen; Jana Strohmaier; Vanessa Nieratschker; Markus M Nöthen; Marcella Rietschel; Sven Cichon; Stewart W Morris; Omer Jilani; David Stclair; Douglas H Blackwood; Walter J Muir; David J Porteous; Kathryn L Evans
Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder.
Neuroscience letters 2010;478(1):9-13.
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: Tiit Nikopensius; Stefanie Birnbaum; Kerstin U Ludwig; Triin Jagomägi; Mare Saag; Stefan Herms; Michael Knapp; Per Hoffmann; Markus M Nöthen; Andres Metspalu; Elisabeth Mangold
Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.
European journal of oral sciences 2010;118(3):317-9.
2010: Maria Grigoroiu-Serbanescu; Stefan Herms; Carmen C Diaconu; Rami Abou Jamra; Sandra Meier; Coralia Bleotu; Ana Iulia Neagu; Dan Prelipceanu; Dorina Sima; Mihail Gherghel; Radu Mihailescu; Marcella Rietschel; Markus M Nöthen; Sven Cichon; Thomas W Mühleisen
Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients.
Progress in neuro-psychopharmacology & biological psychiatry 2010;34(4):657-63.
2010: Roy H Perlis; Jordan W Smoller; Jayalakshmi Mysore; Mei Sun; Tammy Gillis; Shaun Purcell; Marcella Rietschel; Markus M Nöthen; Stephanie Witt; Wolfgang Maier; Dan V Iosifescu; Patrick Sullivan; A John Rush; Maurizio Fava; Hans C Breiter; Marcy E MacDonald; James Gusella
Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorder.
The American journal of psychiatry 2010;167(5):574-9.
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: Felix F Brockschmidt; Axel M Hillmer; Sibylle Eigelshoven; Sandra Hanneken; S Heilmann; S Barth; C Herold; Tim Becker; Roland Kruse; Markus M Nöthen
Fine mapping of the human AR/EDA2R locus in androgenetic alopecia.
The British journal of dermatology 2010;162(4):899-903.
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: S Redler; Felix F Brockschmidt; L Forstbauer; K A Giehl; C Herold; Sibylle Eigelshoven; Sandra Hanneken; Jozef De Weert; G Lutz; H Wolff; Roland Kruse; Bettina Blaumeiser; M Böhm; Tim Becker; Markus M Nöthen; Regina C Betz
The TRAF1/C5 locus confers risk for familial and severe alopecia areata.
The British journal of dermatology 2010;162(4):866-9.
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: Markus Draaken; Heiko Reutter; Charlotte Schramm; Enrika Bartels; Thomas M Boemers; Anne-Karoline Ebert; Wolfgang Rösch; Annette Schröder; Raimund Stein; Susanne Moebus; Dietlinde Stienen; Per Hoffmann; Markus M Nöthen; Michael Ludwig
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
European journal of medical genetics 2010;53(2):55-60.
2010: Francis McMajon; Nirmala Akula; Thomas G. Schulze; Pierandrea Muglia; Federica Tozzi; Sevilla D Detera-Wadleigh; C J M Steele; René Breuer; Jana Strohmaier; Jens R Wendland; Manuel Mattheisen; Thomas W Mühleisen; Wolfgang Maier; Markus M Nöthen; Sven Cichon; Anne Farmer; John B Vincent; Florian Holsboer; Martin Preisig; Marcella Rietschel
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
Nature genetics 2010;42(2):128-31.
2010: Valentin Markov; Axel Krug; Sören Krach; Andreas Jansen; Thomas Eggermann; Karl Zerres; Tony Stöcker; N Jon Shah; Markus M Nöthen; Jens Treutlein; Marcella Rietschel; Tilo T J Kircher
Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals.
Human brain mapping 2010;31(2):266-75.
2010: Markus Thimm; Axel Krug; Valentin Markov; Sören Krach; Andreas Jansen; Klaus Zerres; Thomas Eggermann; Tony Stöcker; N Jon Shah; Markus M Nöthen; Marcella Rietschel; Tilo T J Kircher
The impact of dystrobrevin-binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval.
Human brain mapping 2010;31(2):203-9.
2010: Markus Thimm; Axel Krug; Thilo Kellermann; Valentin Markov; Sören Krach; Andreas Jansen; Klaus Zerres; Thomas Eggermann; Tony Stöcker; N Jon Shah; Markus M Nöthen; Marcella Rietschel; Tilo T J Kircher
The effects of a DTNBP1 gene variant on attention networks: an fMRI study.
Behavioral and brain functions : BBF 2010;6():54.
2010: Vanessa Nieratschker; Markus M Nöthen; Marcella Rietschel
New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?
Frontiers in behavioral neuroscience 2010;4():23.
2010: Markus M Nöthen; Vanessa Nieratschker; Sven Cichon; Marcella Rietschel
New findings in the genetics of major psychoses.
Dialogues in clinical neuroscience 2010;12(1):85-93.
2010: Michael Steffens; Tim Becker; Thomas Sander; Rolf Fimmers; Christine Herold; Daniela A Holler; Costin Leu; Stefan Herms; Sven Cichon; Bastian Bohn; Thomas Gerstner; Michael Griebel; Markus M Nöthen; Thomas F Wienker; Max P Baur
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.
Human heredity 2010;69(4):268-84.
2010: Soyhan Bağci; Andreas Müller; Axel Franz; Andreas Heydweiller; Christoph Berg; Markus M Nöthen; Peter Bartmann; Heiko Reutter
Intestinal atresia, encephalocele, and cardiac malformations in infants with 47,XXX: Expansion of the phenotypic spectrum and a review of the literature.
Fetal diagnosis and therapy 2010;27(2):113-7.
2010: Stefan Pabst; Anna Karpushova; Amalia Diaz-Lacava; Stefan Herms; Maja Walier; Sebastian Zimmer; Sven Cichon; Georg Nickenig; Markus M Nöthen; Thomas F Wienker; Christian Grohé
VEGF gene haplotypes are associated with sarcoidosis.
Chest 2010;137(1):156-63.
2009: Stefanie Birnbaum; Kerstin U Ludwig; Heiko Reutter; Stefan Herms; Nilma A de Assis; Amalia Diaz-Lacava; Sandra Barth; Carola Lauster; Gül Schmidt; Martin Scheer; Mitra Saffar; Markus Martini; Rudolf H Reich; Franziska Schiefke; Alexander Hemprich; Simone Pötzsch; Bernd Pötzsch; Thomas F Wienker; Per Hoffmann; Michael Knapp; Franz-Josef Kramer; Markus M Nöthen; Elisabeth Mangold
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2009;117(6):766-9.
2009: Elisabeth Mangold; Heiko Reutter; Stefanie Birnbaum; Maja Walier; Manuel Mattheisen; Henning Henschke; Carola Lauster; Gül Schmidt; Franziska Schiefke; Rudolf H Reich; Martin Scheer; Alexander Hemprich; Markus Martini; Bert Braumann; Michael Krimmel; Charlotte Opitz; Jan-Hendrik Lenz; Franz-Josef Kramer; Thomas F Wienker; Markus M Nöthen; Amalia Diaz-Lacava
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin.
American journal of medical genetics. Part A 2009;149A(12):2680-94.
2009: Sandra M Pasternack; Ivar von Kügelgen; Melanie Müller; Vinzenz Oji; Heiko Traupe; Eli Sprecher; Markus M Nöthen; Andreas R Janecke; Regina C Betz
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth.
The Journal of investigative dermatology 2009;129(12):2772-6.
2009: Tiit Nikopensius; Laima Ambrozaityte; Kerstin U Ludwig; Stefanie Birnbaum; Triin Jagomägi; Mare Saag; Ausra Matuleviciene; Laura Linkeviciene; Stefan Herms; Michael Knapp; Per Hoffmann; Markus M Nöthen; Vaidutis Kucinskas; Andres Metspalu; Elisabeth Mangold
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.
American journal of medical genetics. Part A 2009;149A(11):2551-3.
2009: Maria Grigoroiu-Serbanescu; Stefan Herms; Thomas W Mühleisen; Alexander Georgi; Carmen C Diaconu; Jana Strohmaier; Piotr M Czerski; Joanna Hauser; Anna Leszczynska-Rodziewicz; Rami Abou Jamra; Gulia Babadjanova; A Tiganov; V Krasnov; Sofia Kapiletti; Ana Iulia Neagu; Jennifer Vollmer; René Breuer; Marcella Rietschel; Markus M Nöthen; Sven Cichon; Peter Propping; Markus M Nöthen; Sven Cichon
Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(7):1017-21.
2009: Britta Haenisch; Karoline Linsel; Michael Brüss; Ralf Gilsbach; Peter Propping; Markus M Nöthen; Marcella Rietschel; Rolf Fimmers; Wolfgang Maier; Astrid Zobel; Susanne Höfels; Vera Guttenthaler; Manfred Göthert; Heinz Bönisch
Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(7):1013-6.
2009: Heiko Reutter; Stefanie Birnbaum; Meinhard Mende; Nilma Almeida de Assis; Per Hoffmann; Amalia Diaz Lacava; Stefan Herms; Bert Braumann; Martin Scheer; Carola Lauster; Gül Schmidt; Franziska Schiefke; Anton Dunsche; Markus Martini; Michael Knapp; Franz-Josef Kramer; Markus M Nöthen; Elisabeth Mangold
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent.
International journal of pediatric otorhinolaryngology 2009;73(10):1334-8.
2009: V Markov; A Krug; Sören Krach; C Whitney; Thomas Eggermann; Klaus Zerres; Tony Stöcker; N Jon Shah; Markus M Nöthen; J Treutlein; Marcella Rietschel; Tilo T J Kircher
Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals.
NeuroImage 2009;47(4):2016-22.
2009: Tilo T J Kircher; Axel Krug; Valentin Markov; Carin Whitney; Sören Krach; Klaus Zerres; Thomas Eggermann; Tony Stöcker; N Jon Shah; Jens Treutlein; Markus M Nöthen; Tim Becker; Marcella Rietschel
Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals.
Human brain mapping 2009;30(10):3406-16.
2009: Tilo T J Kircher; V Markov; A Krug; Thomas Eggermann; Klaus Zerres; Markus M Nöthen; M H Skowronek; Marcella Rietschel
Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects.
Psychological medicine 2009;39(10):1657-65.
2009: Marian L Hamshere; Thomas G. Schulze; Johannes Schumacher; Aiden Corvin; Michael J Owen; Rami Abou Jamra; Peter Propping; Wolfgang Maier; Guillermo Orozco y Diaz; Fermin Mayoral; Fabio Rivas; Ian Jones; Lisa Jones; George Kirov; Michael Gill; Peter A Holmans; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Nick Craddock
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
Bipolar disorders 2009;11(6):610-20.
2009: K U Ludwig; Manuel Mattheisen; T W Mühleisen; D Roeske; C Schmäl; R Breuer; Gerd Schulte-Körne; Bertram Müller-Myhsok; Markus M Nöthen; P Hoffmann; Marcella Rietschel; Sven Cichon
Supporting evidence for LRRTM1 imprinting effects in schizophrenia.
Molecular psychiatry 2009;14(8):743-5.
2009: Axel M Hillmer; Jan Freudenberg; Sean Myles; Stefan Herms; Kun Tang; David A Hughes; Felix F Brockschmidt; Yijun Ruan; Mark Stoneking; Markus M Nöthen
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness.
Human genetics 2009;126(2):255-64.
2009: 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: Jens Treutlein; Sven Cichon; Monika Ridinger; Norbert Wodarz; Michael Soyka; Peter Zill; Wolfgang Maier; Rainald Moessner; Wolfgang Gaebel; Norbert Dahmen; Christoph Fehr; Norbert Scherbaum; Michael Steffens; Kerstin U Ludwig; Josef Frank; H-Erich Wichmann; Stefan Schreiber; Nico Dragano; Wolfgang Sommer; Fernando Leonardi-Essmann; Anbarasu Lourdusamy; Peter J Gebicke-Haerter; Thomas F Wienker; Patrick F Sullivan; Markus M Nöthen; Falk Kiefer; Rainer Spanagel; Karl Mann; Marcella Rietschel
Genome-wide association study of alcohol dependence.
Archives of general psychiatry 2009;66(7):773-84.
2009: Heiko Reutter; Arend Bökenkamp; Anne-Karolin Ebert; Wolfgang Rösch; Thomas M Boemers; Markus M Nöthen; Michael Ludwig
Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.
European journal of pediatrics 2009;168(7):881-3.
2009: Jens Treutlein; Thomas W Mühleisen; Josef Frank; Manuel Mattheisen; Stefan Herms; Kerstin U Ludwig; Tsendsesmee Treutlein; Christine Schmael; Jana Strohmaier; Katja Veronika Bösshenz; René Breuer; Torsten Paul; Stephanie Witt; Thomas G. Schulze; Ralf Schlösser; Igor Nenadic; Heinrich Sauer; Tim Becker; Wolfgang Maier; Sven Cichon; Markus M Nöthen; Marcella Rietschel
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter.
Schizophrenia research 2009;111(1-3):123-30.
2009: Sagi Nahum; Sandra M Pasternack; Jana Pforr; Margarita Indelman; Bernd Wollnik; Reuven Bergman; Markus M Nöthen; Arne König; Ziad Khamaysi; Regina C Betz; Eli Sprecher
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.
Archives of dermatological research 2009;301(5):391-3.
2009: Marcella Rietschel; Alexander Georgi; Christine Schmael; Frederike Schirmbeck; Jana Strohmaier; Katja V Boesshenz; Markus Schwarz; Markus M Nöthen; Thomas G. Schulze
Premorbid adjustment: a phenotype highlighting a distinction rather than an overlap between schizophrenia and bipolar disorder.
Schizophrenia research 2009;110(1-3):33-9.
2009: 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: Andreas Jansen; Sören Krach; Axel Krug; Valentin Markov; Thomas Eggermann; Klaus Zerres; Tony Stöcker; N Jon Shah; Markus M Nöthen; Jens Treutlein; Marcella Rietschel; Tilo T J Kircher
A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe.
NeuroImage 2009;45(3):1002-8.
2009: 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: Stefanie Birnbaum; Heiko Reutter; Meinhard Mende; Nilma A de Assis; Amalia Diaz-Lacava; Stefan Herms; Martin Scheer; Carola Lauster; Bert Braumann; Gül Schmidt; Markus Martini; Alexander Hemprich; Simone Pötzsch; Michael Knapp; Markus M Nöthen; Franz-Josef Kramer; Elisabeth Mangold
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2009;117(2):200-3.
2009: 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.
2009: Andreas Jansen; Sören Krach; Axel Krug; Valentin Markov; Thomas Eggermann; Klaus Zerres; Markus Thimm; Markus M Nöthen; Jens Treutlein; Marcella Rietschel; Tilo Kircher
Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects.
BMC psychiatry 2009;9():60.
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: Axel M Hillmer; Felix F Brockschmidt; Sandra Hanneken; Sibylle Eigelshoven; Michael Steffens; Antonia Flaquer; Stefan Herms; Tim Becker; Anne-Katrin Kortüm; Dale R Nyholt; Zhen Zhen Zhao; Grant W Montgomery; Nicholas G Martin; Thomas W Mühleisen; Margrieta A Alblas; Susanne Moebus; Karl-Heinz Jöckel; Martina Bröcker-Preuss; Raimund Erbel; Roman Reinartz; Regina C Betz; Sven Cichon; Peter Propping; Max P Baur; Thomas F Wienker; Roland Kruse; Markus M Nöthen
Susceptibility variants for male-pattern baldness on chromosome 20p11.
Nature genetics 2008;40(11):1279-81.
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: Maria Grigoroiu-Serbanescu; Carmen C Diaconu; Stefan Herms; Coralia Bleotu; Jennifer Vollmer; Thomas W Mühleisen; Dan Prelipceanu; Lutz Priebe; Radu Mihailescu; Marie-Jana Georgescu; Dorina Sima; Mihaela Grimberg; Markus M Nöthen; Sven Cichon
Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population.
Psychiatric genetics 2008;18(5):240-7.
2008: Axel Krug; Valentin Markov; Thomas Eggermann; Sören Krach; Klaus Zerres; Tony Stöcker; N Jon Shah; Frank Schneider; Markus M Nöthen; Jens Treutlein; Marcella Rietschel; Tilo T J Kircher
Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals.
NeuroImage 2008;42(4):1569-76.
2008: Mahim Jain; Deeann Wallis; Nathaniel H Robin; Fabienne Wavrant De Vrieze; John Hardy; Mohsen Ghadami; Kristin Bosse; Regina C Betz; Markus M Nöthen; Mauricio Arcos-Burgos; Maximilian Muenke
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
American journal of medical genetics. Part A 2008;146A(17):2308-11.
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: Axel Krug; Valentin Markov; Dirk Leube; Klaus Zerres; Thomas Eggermann; Markus M Nöthen; Markus H Skowronek; Marcella Rietschel; Tilo Kircher
Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals.
European psychiatry : the journal of the Association of European Psychiatrists 2008;23(5):344-9.
2008: 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: Axel M Hillmer; Antonia Flaquer; Sandra Hanneken; Sibylle Eigelshoven; Anne-Katrin Kortüm; Felix F Brockschmidt; Astrid Golla; Christine Metzen; Holger Thiele; Susanne Kolberg; Roman Reinartz; Regina C Betz; Thomas Ruzicka; Hans Christian Hennies; Roland Kruse; Markus M Nöthen
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.
American journal of human genetics 2008;82(3):737-43.
2008: Sandra M Pasternack; Ivar von Kügelgen; YA Lee; Franz Rüschendorf; Katrin Voss; Axel M Hillmer; Gerhard J Molderings; Thomas Franz; Alfredo Ramirez; Peter Nürnberg; Markus M Nöthen; Khalid Al Aboud; Regina C Betz
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.
Nature genetics 2008;40(3):329-34.
2008: 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: Regina C Betz; K König; Antonia Flaquer; S Redler; Sibylle Eigelshoven; Anne-Katrin Kortüm; Sandra Hanneken; Axel M Hillmer; Thomas Tüting; Julien Lambert; Jozef De Weert; Roland Kruse; G Lutz; Bettina Blaumeiser; Markus M Nöthen
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.
The British journal of dermatology 2008;158(2):389-91.
2008: 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: Heiko Reutter; Stefanie Birnbaum; Meinhard Mende; Carola Lauster; Gül Schmidt; Henning Henschke; Mitra Saffar; Markus Martini; Roland Lauster; Franziska Schiefke; Rudolf H Reich; Bert Braumann; Martin Scheer; Michael Knapp; Markus M Nöthen; Franz-Josef Kramer; Elisabeth Mangold
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate.
Journal of human genetics 2008;53(7):656-61.
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: Laura Planko; Karsten Böhse; Jörg Höhfeld; Regina C Betz; Sandra Hanneken; Sibylle Eigelshoven; Roland Kruse; Markus M Nöthen; Thomas M Magin
Identification of a keratin-associated protein with a putative role in vesicle transport.
European journal of cell biology 2007;86(11-12):827-39.
2007: Katrien Storm; Els Moens; Lieve Vits; Haike De Vlieger; Gino Delaere; Maria D'Hollander; Wim Wuyts; Martine Biervliet; Lutgardis Van Schil; Kristine N Desager; Markus M Nöthen
High incidence of the CFTR mutations 3272-26A-->G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A-->G, E588V, and 1671insTATCA).
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2007;6(6):371-5.
2007: Regina C Betz; Jana Pforr; Antonia Flaquer; Silke Redler; Sandra Hanneken; Sibylle Eigelshoven; Anne-Katrin Kortüm; Thomas Tüting; Julien Lambert; Jozef De Weert; Axel M Hillmer; Christine Schmael; Thomas F Wienker; Roland Kruse; Gerhard Lutz; Bettina Blaumeiser; Markus M Nöthen
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.
The Journal of investigative dermatology 2007;127(11):2539-43.
2007: Ludovic Martin; Nadia Raison-Peyron; Markus M Nöthen; Sven Cichon; Christian Drouet
Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene.
The Journal of allergy and clinical immunology 2007;120(4):975-7.
2007: 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: Isabelle Massat; Bernard Lerer; Daniel Souery; Douglas Blackwood; Walter Muir; RAdka Kaneva; Markus M Nöthen; Lilijana Oruc; George N Papadimitriou; Dimitris G Dikeos; Alessandro Serretti; Frank Bellivier; J L Golmard; vihra milanova; Jurgen Del-Favero; Christine Van Broeckhoven; Julien Mendlewicz
HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study.
Molecular psychiatry 2007;12(9):797-8.
2007: Felix F Brockschmidt; Markus M Nöthen; Axel M Hillmer
The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function.
Journal of molecular endocrinology 2007;39(1):1-8.
2007: Regina C Betz; Margarita Indelman; Jana Pforr; Felix Schreiner; Ralf Bauer; Reuven Bergman; Michael J Lentze; Markus M Nöthen; Sven Cichon; Eli Sprecher
Identification of mutations in the human hairless gene in two new families with congenital atrichia.
Archives of dermatological research 2007;299(3):157-61.
2007: Christine Schmael; Alexander Georgi; Bertram Krumm; Christin Buerger; Monika Deschner; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
Premorbid adjustment in schizophrenia--an important aspect of phenotype definition.
Schizophrenia research 2007;92(1-3):50-62.
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: Sven Cichon; Ludovic Martin; Hans Christian Hennies; Felicitas Müller; Karen Van Driessche; Anna Karpushova; Wim Stevens; Roberto Colombo; Thomas Renné; Christian Drouet; Konrad Bork; Markus M Nöthen
Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III.
American journal of human genetics 2006;79(6):1098-104.
2006: Marcella Rietschel; Peter Propping; Markus M Nöthen
The impact of genetics on psychiatric nosology.
The American journal of psychiatry 2006;163(12):2197-8; author reply 2198.
2006: Nico Schäfer; Bettina Blaumeiser; Tim Becker; Yun Freudenberg-Hua; Sandra Hanneken; Sibylle Eigelshoven; Christine Schmael; Julien Lambert; Jozef De Weert; Roland Kruse; Markus M Nöthen; Regina C Betz
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.
International journal of immunogenetics 2006;33(6):393-5.
2006: 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: Heiko Reutter; Tim Becker; Michael Ludwig; Nico Schäfer; Birte Detlefsen; Sylvie Beaudoin; Margit Fisch; Anne-Karoline Ebert; Wolfgang Rösch; Markus M Nöthen; Thomas M Boemers; Regina C Betz
Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex.
American journal of medical genetics. Part A 2006;140(22):2506-9.
2006: 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: Jane Winantea; My Ngo Hoang; Stephanie Ohlraun; Marcella Rietschel; Sven Cichon; Peter Propping; Markus M Nöthen; Jan Freudenberg; Yun Freudenberg-Hua
A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.
European journal of human genetics : EJHG 2006;14(9):1037-43.
2006: Dimitris G Dikeos; George N Papadimitriou; Daniel Souery; Jurgen Del-Favero; Isabelle Massat; Douglas Blackwood; Sven Cichon; Eugenia G Daskalopoulou; Sladjana Ivezic; RAdka Kaneva; GEORGIA KARADIMA; Cristina Lorenzi; vihra milanova; Walter Muir; Markus M Nöthen; Lilijana Oruc; Marcella Rietschel; Alessandro Serretti; Christine Van Broeckhoven; Constantin R Soldatos; Costas N Stefanis; Julien Mendlewicz
Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study.
Psychiatric genetics 2006;16(4):169-71.
2006: Patricia Entz; Bettina Blaumeiser; Regina C Betz; Julien Lambert; Katia Seymons; Sibylle Eigelshoven; Sandra Hanneken; Roland Kruse; Peter Nürnberg; Marion Nagy; Markus M Nöthen
Investigation of the HLA-DRB1 locus in alopecia areata.
European journal of dermatology : EJD 2006;16(4):363-7.
2006: Jana Pforr; Bettina Blaumeiser; Tim Becker; Yun Freudenberg-Hua; Sandra Hanneken; Sibylle Eigelshoven; I Cuyt; Jozef De Weert; Julien Lambert; Roland Kruse; Markus M Nöthen; Regina C Betz
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.
Tissue antigens 2006;68(1):58-61.
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: Bettina Blaumeiser; Ineke van der Goot; Rolf Fimmers; Sandra Hanneken; Sibylle Ritzmann; Katia Seymons; Regina C Betz; Thomas Ruzicka; Thomas F Wienker; Jozef De Weert; Julien Lambert; Roland Kruse; Markus M Nöthen
Familial aggregation of alopecia areata.
Journal of the American Academy of Dermatology 2006;54(4):627-32.
2006: Winnie Courtens; Wim Wuyts; Martin Poot; Karoly Szuhai; Jan Wauters; Edwin Reyniers; Marc J Eleveld; George Diaz; Markus M Nöthen; Ruti Parvari
Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review.
American journal of medical genetics. Part A 2006;140(6):611-7.
2006: Regina C Betz; Laura Planko; Sibylle Eigelshoven; Sandra Hanneken; Sandra M Pasternack; Heinrich Bussow; Kris Van Den Bogaert; Joerg Wenzel; Markus Braun-Falco; Arno Rutten; Michael A Rogers; Thomas Ruzicka; Markus M Nöthen; Thomas M Magin; Roland Kruse
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.
American journal of human genetics 2006;78(3):510-9.
2006: 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: NO Dávalos; A García-Vargas; Jana Pforr; Ingrid Patricia Dávalos; V J Picos-Cárdenas; Diana García-Cruz; Roland Kruse; Luis Figuera; Markus M Nöthen; Regina C Betz
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.
The British journal of dermatology 2005;153(6):1216-9.
2005: 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: 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.
2005: Winnie Courtens; Stefan Vermeulen; Wim Wuyts; Ludwine MESSIAEN; Jan Wauters; Lieve Nuytinck; Nils Peeters; Katrien Storm; Frank Speleman; Markus M Nöthen
An interstitial deletion of chromosome 7 at band q21: a case report and review.
American journal of medical genetics. Part A 2005;134A(1):12-23.
2005: Yoo J Lee; Carsten Hohoff; Katharina Domschke; Philipp Sand; Gregor Kuhlenbäumer; Anja Schirmacher; Christine M Freitag; Jobst Meyer; Gerald Stöber; Petra Franke; Markus M Nöthen; Jürgen Fritze; Rolf Fimmers; Henk Garritsen; Florian Stögbauer; Jürgen Deckert
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder.
Neuroscience letters 2005;377(1):40-3.
2005: Maria Grigoroiu-Serbanescu; Markus M Nöthen; Stephanie Ohlraun; Peter Propping; Wolfgang Maier; Priya Wickramaratne; Marie-Jana Georgescu; Dan Prelipceanu; Mihaela Grimberg; Dorina Sima; Marcella Rietschel
Family history influences age of onset in bipolar I disorder in females but not in males.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;133B(1):6-11.
2005: Barbara Hoefgen; Thomas G. Schulze; Stephanie Ohlraun; Olrik von Widdern; Susanne Höfels; Magdalena Gross; Vivien Heidmann; Svetlana Kovalenko; Anita Eckermann; Heike Kölsch; Martin Metten; Astrid Zobel; Tim Becker; Markus M Nöthen; Peter Propping; Reinhard Heun; Wolfgang Maier; Marcella Rietschel
The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder.
Biological psychiatry 2005;57(3):247-51.
2005: Andreas Ziegler; Inke R König; Wolfgang Deimel; Ellen Plume; Markus M Nöthen; Peter Propping; André Kleensang; Bertram Müller-Myhsok; Andreas Warnke; Helmut Remschmidt; Gerd Schulte-Körne
Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design.
Human heredity 2005;59(3):136-43.
2005: Anette Bygum; Regina C Betz; Knud Kragballe; Torben Steiniche; Nils Peeters; Wim Wuyts; Markus M Nöthen
KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation.
Acta dermato-venereologica 2005;85(2):152-5.
2005: Yun Freudenberg-Hua; Jan Freudenberg; J Winantea; Nadine Kluck; Sven Cichon; M Brüss; Peter Propping; Markus M Nöthen
Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.
The pharmacogenomics journal 2005;5(3):183-92.
2005: Daniel J Müller; Katrin Barkow; Svetlana Kovalenko; Stephanie Ohlraun; Heiner Fangerau; Heike Kölsch; Matthias R Lemke; Tilo Held; Markus M Nöthen; Wofgang Maier; Reinhard Heun; Marcella Rietschel
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.
2004: Sebastian Paus; Marcella Rietschel; Thomas G. Schulze; Stephanie Ohlraun; Carmen C Diaconu; Ann Van Den Bogaert; Wolfgang Maier; Peter Propping; Sven Cichon; Markus M Nöthen
Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population.
Psychiatric genetics 2004;14(4):233-4.
2004: Bernd Frank; Beate Niesler; Markus M Nöthen; Helge Neidt; Peter Propping; Brigitta Bondy; Marcella Rietschel; Wolfgang Maier; Margot Albus; Gudrun Rappold
Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;131B(1):1-5.
2004: 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: Bettina Blaumeiser; Philip Loquet; Wim Wuyts; Markus M Nöthen
Prenatal diagnosis of Pfeiffer syndrome type II.
Prenatal diagnosis 2004;24(8):644-6.
2004: Torben Østerlund; David B Everman; Regina C Betz; Monica Mosca; Markus M Nöthen; Charles E Schwartz; Peter G Zaphiropoulos; Rune Toftgård
The FU gene and its possible protein isoforms.
BMC genomics 2004;5(1):49.
2004: Sebastian Paus; Gert Seeger; H Michael Brecht; Jürgen Köster; Mahha El-Faddagh; Markus M Nöthen; Thomas Klockgether; Ullrich Wüllner
Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2004;19(6):705-7.
2004: Katharina Domschke; Christine M Freitag; Gregor Kuhlenbäumer; Anja Schirmacher; Philipp Sand; Peter Nyhuis; Christian Jacob; Jürgen Fritze; Petra Franke; Marcella Rietschel; Henk Garritsen; Rolf Fimmers; Markus M Nöthen; Klaus-Peter Lesch; Florian Stögbauer; Jürgen Deckert
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2004;7(2):183-8.
2004: Claudia Rothe; Lise Gutknecht; Christine M Freitag; Ralf Tauber; Rainald Mössner; Petra Franke; Jürgen Fritze; Gerd Wagner; Gregor Peikert; Berit Wenda; Philipp Sand; Christian Jacob; Marcella Rietschel; Markus M Nöthen; Henk Garritsen; Rolf Fimmers; Jürgen Deckert; Klaus-Peter Lesch
Association of a functional 1019C>G 5-HT1A receptor gene polymorphism with panic disorder with agoraphobia.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2004;7(2):189-92.
2004: Dorothea Gadzicki; Kirsten R Müller-Vahl; Daniela Heller; Sebastian Ossege; Markus M Nöthen; Johannes Hebebrand; Manfred Stuhrmann
Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;127B(1):97-103.
2004: Julien Mendlewicz; Isabelle Massat; Daniel Souery; Jurgen Del-Favero; Lilijana Oruc; Markus M Nöthen; Douglas Blackwood; Walter Muir; Sharon Battersby; Bernard Lerer; Ronnen Segman; RAdka Kaneva; Alessandro Serretti; Roberta Lilli; Cristina Lorenzi; Miro Jakovljevic; Sladana Ivezic; Marcella Rietschel; vihra milanova; Christine Van Broeckhoven
Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study.
European journal of human genetics : EJHG 2004;12(5):377-82.
2004: 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.
2004: Heiner Fangerau; Stephanie Ohlraun; Ralf O Granath; Markus M Nöthen; Marcella Rietschel; Thomas G. Schulze
Computer-assisted phenotype characterization for genetic research in psychiatry.
Human heredity 2004;58(3-4):122-30.
2004: V G Hösing; Anja Schirmacher; Gregor Kuhlenbäumer; Christine M Freitag; Philipp Sand; C Schlesiger; Christian Jacob; Jürgen Fritze; Petra Franke; Marcella Rietschel; Henk Garritsen; Markus M Nöthen; Rolf Fimmers; Florian Stögbauer; Jürgen Deckert
Cholecystokinin- and cholecystokinin-B-receptor gene polymorphisms in panic disorder.
Journal of neural transmission. Supplementum 2004;(68):147-56.
2003: George N Papadimitriou; Dimitris G Dikeos; Daniel Souery; Jurgen Del-Favero; Isabelle Massat; Dimitrios Avramopoulos; Sylvie Blairy; Sven Cichon; Sladjana Ivezic; RAdka Kaneva; GEORGIA KARADIMA; Roberta Lilli; vihra milanova; Markus M Nöthen; Lilijana Oruc; Marcella Rietschel; Alessandro Serretti; Christine Van Broeckhoven; Costas N Stefanis; Julien Mendlewicz
Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study.
Psychiatric genetics 2003;13(4):211-20.
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: Yun Freudenberg-Hua; Jan Freudenberg; Nadine Kluck; Sven Cichon; Peter Propping; Markus M Nöthen
Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.
Genome research 2003;13(10):2271-6.
2003: 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.
2003: Sandra Hanneken; Sibylle Ritzmann; Markus M Nöthen; Roland Kruse
[Androgenetic alopecia. Current aspects of a common phenotype].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2003;54(8):703-12.
2003: Etgar Levy-Nissenbaum; Regina C Betz; Moshe Frydman; Michel Simon; Hadas Lahat; Tangiz Bakhan; Boleslaw Goldman; Anette Bygum; Monika Pierick; Axel M Hillmer; Nathalie Jonca; Jaime Toribio; Roland Kruse; Georg Dewald; Sven Cichon; Christian Kubisch; Marina Guerrin; Guy Serre; Markus M Nöthen; Elon Pras
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.
Nature genetics 2003;34(2):151-3.
2003: Erik G Jönsson; Göran C Sedvall; Markus M Nöthen; Sven Cichon
Dopamine D4 receptor gene (DRD4) variants and schizophrenia: meta-analyses.
Schizophrenia research 2003;61(1):111-9.
2003: Erik G Jönsson; Sven Cichon; J Petter Gustavsson; Frank Grünhage; Kaj Forslund; Marja Mattila-Evenden; Gunnar Rylander; Marie Asberg; Lars Farde; Peter Propping; Markus M Nöthen
Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment.
Biological psychiatry 2003;53(7):577-84.
2003: Thomas G. Schulze; Sven Cichon; Markus M Nöthen; Peter Propping; Wolfgang Maier; Marcella Rietschel
Is there a phenotypic difference between probands in case-control versus family-based association studies?
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;118B(1):25-6; author reply 27-8.
2003: Katharina Domschke; Gregor Kuhlenbäumer; Anja Schirmacher; Cristina Lorenzi; Lluis Armengol; D DiBella; M Gratacos; Henk Garritsen; Markus M Nöthen; Petra Franke; Philipp Sand; Jürgen Fritze; G Perez; Wolfgang Maier; Walter Sibrowski; Xavier Estivill; laura bellodi; E Bernd Ringelstein; Volker Arolt; R Martin-Santos; Marco Catalano; Florian Stögbauer; Jürgen Deckert
Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):70-8.
2002: Philipp Sand; T Mori; C Godau; Gerald Stöber; Peter Flachenecker; Petra Franke; Markus M Nöthen; Jürgen Fritze; Wolfgang Maier; Klaus-Peter Lesch; Peter Riederer; Helmut Beckmann; Jürgen Deckert
Norepinephrine transporter gene (NET) variants in patients with panic disorder.
Neuroscience letters 2002;333(1):41-4.
2002: Esther Jahnes; Daniel J Müller; Thomas G. Schulze; Christine Windemuth; Sven Cichon; Stephanie Ohlraun; Heiner Fangerau; Tilo Held; Wolfgang Maier; Peter Propping; Markus M Nöthen; Marcella Rietschel
Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder.
American journal of medical genetics 2002;114(5):519-22.
2002: Daniel J Müller; Thomas G. Schulze; F Macciardi; Stephanie Ohlraun; M M Gross; Harald Scherk; Helge Neidt; Yana V Syagailo; Marcus Grässle; Markus M Nöthen; Wolfgang Maier; Klaus-Peter Lesch; Marcella Rietschel
Moclobemide response in depressed patients: association study with a functional polymorphism in the monoamine oxidase A promoter.
Pharmacopsychiatry 2002;35(4):157-8.
2002: Thomas G. Schulze; Yu-Sheng Chen; Nirmala Akula; Kathy Hennessy; Judith A Badner; Melvin G McInnis; J. Raymond DePaulo; Johannes Schumacher; Sven Cichon; Peter Propping; Wolfgang Maier; Marcella Rietschel; Markus M Nöthen; Francis McMajon
Can long-range microsatellite data be used to predict short-range linkage disequilibrium?
Human molecular genetics 2002;11(12):1363-72.
2002: Philipp Sand; K Schlurmann; Christian Luckhaus; M Götz; Gerald Stöber; Klaus-Peter Lesch; Peter Riederer; Petra Franke; Wolfgang Maier; Markus M Nöthen; Peter Propping; Jürgen Fritze; Jürgen Deckert
Estrogen receptor 1 gene (ESR1) variants in panic disorder.
American journal of medical genetics 2002;114(4):426-8.
2002: Thomas G. Schulze; Daniel J Müller; Harald Krauss; Magdalena Gross; Heiner Fangerau-Lefèvre; Franciska Illes; Stephanie Ohlraun; Sven Cichon; Tilo Held; Peter Propping; Markus M Nöthen; Wolfgang Maier; Marcella Rietschel
Further evidence for age of onset being an indicator for severity in bipolar disorder.
Journal of affective disorders 2002;68(2-3):343-5.
2002: Axel M Hillmer; Roland Kruse; F Macciardi; Uwe Heyn; Regina C Betz; Thomas Ruzicka; Peter Propping; Markus M Nöthen; Sven Cichon
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.
The British journal of dermatology 2002;146(4):601-8.
2002: Markus M Nöthen; Sven Cichon
Linking single nucleotide polymorphisms.
Pharmacogenetics 2002;12(2):89-90.
2002: Daniel J Müller; Thomas G. Schulze; Esther Jahnes; Sven Cichon; Harald Krauss; Kristina Kesper; Tilo Held; Wolfgang Maier; Peter Propping; Markus M Nöthen; Marcella Rietschel
Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder.
American journal of medical genetics 2002;114(1):74-8.
2002: Sylvia Bort Martí; Sven Cichon; Peter Propping; Markus M Nöthen
Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population.
American journal of medical genetics 2002;114(1):46-50.
2002: Sylvia Bort Martí; Sven Cichon; Peter Propping; Markus M Nöthen
Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization.
American journal of medical genetics 2002;114(1):12-4.
2002: Erik G Jönsson; Roland Ivo; J Petter Gustavsson; Thomas Geijer; Kaj Forslund; Marja Mattila-Evenden; Gunnar Rylander; Sven Cichon; Peter Propping; H Bergman; M sberg; Markus M Nöthen
No association between dopamine D4 receptor gene variants and novelty seeking.
Molecular psychiatry 2002;7(1):18-20.
2001: Maria Grigoroiu-Serbanescu; M Martinez; Markus M Nöthen; M Grinberg; D Sima; Peter Propping; Elvira Marinescu; M Hrestic
Different familial transmission patterns in bipolar I disorder with onset before and after age 25.
American journal of medical genetics 2001;105(8):765-73.
2001: 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: Daniel J Müller; Thomas G. Schulze; Michael Knapp; Tilo Held; Harald Krauss; T Weber; Guido Ahle; AO Maroldt; Daniela Alfter; Wolfgang Maier; Markus M Nöthen; Marcella Rietschel
Familial occurrence of tardive dyskinesia.
Acta psychiatrica Scandinavica 2001;104(5):375-9.
2001: R Przkora; Birgit Meyer-Puttlitz; Ottmar Schmitt; Frank Berthold; Markus M Nöthen; J Krauss; Jörg-Christian Tonn; Andreas von Deimling; Otmar D Wiestler; Torsten Pietsch
Analysis of the TSC2 gene in human medulloblastoma.
Acta neuropathologica 2001;102(4):380-4.
2001: Erik G Jönsson; Roland Ivo; Kaj Forslund; Marja Mattila-Evenden; Gunnar Rylander; Sven Cichon; Peter Propping; Markus M Nöthen; Marie Asberg; Göran C Sedvall
No association between a promoter dopamine D(4) receptor gene variant and schizophrenia.
American journal of medical genetics 2001;105(6):525-8.
2001: Thomas G. Schulze; J Schumacher; Daniel J Müller; Harald Krauss; Daniela Alfter; AO Maroldt; Guido Ahle; A O Maroldt; A Novo y Fernández; T Weber; Tilo Held; Peter Propping; Wolfgang Maier; Markus M Nöthen; Marcella Rietschel
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.
American journal of medical genetics 2001;105(6):498-501.
2001: Beate Niesler; T Flohr; Markus M Nöthen; Christine Fischer; Marcella Rietschel; E Franzek; Margot Albus; Peter Propping; Gudrun A Rappold
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder.
Pharmacogenetics 2001;11(6):471-5.
2001: Regina C Betz; Benedikt Schoser; D Kasper; Kenneth Ricker; A Ramírez; Valentin Stein; Torberg Torbergsen; YA Lee; Markus M Nöthen; Thomas F Wienker; Jean-Pierre Malin; Peter Propping; A Reis; Wilhelm Mortier; Thomas J Jentsch; Matthias Vorgerd; Christian Kubisch
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.
Nature genetics 2001;28(3):218-9.
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: Thomas G. Schulze; Daniel J Müller; Harald Krauss; M Gross; I Bauer; H Fangerau-Lefèvre; F Illes; Stephanie Ohlraun; R Fimmers; Sven Cichon; Tilo Held; Peter Propping; Markus M Nöthen; Wolfgang Maier; Marcella Rietschel
Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios.
American journal of medical genetics 2001;105(4):351-3.
2001: 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.
2001: Albert J Becker; M Löbach; H Klein; Sabine Normann; Markus M Nöthen; Andreas von Deimling; M Mizuguchi; Christian E Elger; Johannes Schramm; Otmar D Wiestler; Ingmar Blümcke
Mutational analysis of TSC1 and TSC2 genes in gangliogliomas.
Neuropathology and applied neurobiology 2001;27(2):105-14.
2001: Erik G Jönsson; Markus M Nöthen; J Petter Gustavsson; Cecilia Berggård; R Bunzel; Kaj Forslund; Gunnar Rylander; Marja Mattila-Evenden; Peter Propping; Marie Asberg; Göran C Sedvall
No association between serotonin 2A receptor gene variants and personality traits.
Psychiatric genetics 2001;11(1):11-7.
2001: Daniel Souery; S Van Gestel; Isabelle Massat; Sylvie Blairy; Rolf Adolfsson; Douglas Blackwood; Jurgen Del-Favero; Dimitris G Dikeos; Miro Jakovljevic; RAdka Kaneva; Enrico Lattuada; Bernard Lerer; Roberta Lilli; vihra milanova; Walter Muir; Markus M Nöthen; Lilijana Oruc; George N Papadimitriou; Peter Propping; Thomas G. Schulze; Alessandro Serretti; Baruch Shapira; Enrico Smeraldi; Costas N Stefanis; M Thomson; Christine Van Broeckhoven; Julien Mendlewicz
Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study.
Biological psychiatry 2001;49(5):405-9.
2001: Thomas G. Schulze; Daniel J Müller; Harald Krauss; K Marwinski; AO Maroldt; A Novo Y Fernández; R Fimmers; Tilo Held; Wolfgang Maier; Markus M Nöthen; Marcella Rietschel
Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?
European psychiatry : the journal of the Association of European Psychiatrists 2001;16(1):71-4.
2001: Beate Niesler; Birgit Weiss; Christine Fischer; Markus M Nöthen; Peter Propping; Brigitta Bondy; Marcella Rietschel; Wolfgang Maier; Margot Albus; E Franzek; Gudrun A Rappold
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.
Pharmacogenetics 2001;11(1):21-7.
2001: Petra Franke; T Wang; Markus M Nöthen; Michael Knapp; Helge Neidt; S Albrecht; Esther Jahnes; Peter Propping; Wolfgang Maier
Nonreplication of association between mu-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence.
American journal of medical genetics 2001;105(1):114-9.
2001: T Wang; Petra Franke; Helge Neidt; Sven Cichon; Michael Knapp; Dirk Lichtermann; Wolfgang Maier; Peter Propping; Markus M Nöthen
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach.
Molecular psychiatry 2001;6(1):109-11.
2000: Thomas G. Schulze; Daniel J Müller; Harald Krauss; Harald Scherk; Stephanie Ohlraun; Yana V Syagailo; Christine Windemuth; Helge Neidt; Marcus Grässle; Andreas Papassotiropoulos; Reinhard Heun; Markus M Nöthen; Wolfgang Maier; Klaus-Peter Lesch; Marcella Rietschel
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: Philipp Sand; C Godau; Peter Riederer; C Peters; Petra Franke; Markus M Nöthen; Gerald Stöber; Jürgen Fritze; Wolfgang Maier; Peter Propping; Klaus-Peter Lesch; Olaf Riess; T Sander; Helmut Beckmann; Jürgen Deckert
Exonic variants of the GABA(B) receptor gene and panic disorder.
Psychiatric genetics 2000;10(4):191-4.
2000: Sven Cichon; Roland Kruse; Axel M Hillmer; Guido Kukuk; M Anker; K Altland; Michael Knapp; Peter Propping; Markus M Nöthen
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
The British journal of dermatology 2000;143(4):811-4.
2000: Kristin Bosse; Regina C Betz; YA Lee; Thomas F Wienker; A Reis; H Kleen; Peter Propping; Sven Cichon; Markus M Nöthen
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.
American journal of human genetics 2000;67(2):492-7.
2000: Philipp Sand; Klaus-Peter Lesch; Marco Catalano; Monica Francesca Bosi; Yana V Syagailo; Olga Okladnova; Daniela Di Bella; P Maffei; A Heils; F Friess; E Politi; Markus M Nöthen; Petra Franke; Gerald Stöber; Jürgen Fritze; Wolfgang Maier; Peter Propping; Helmut Beckmann; laura bellodi; Peter Riederer; Jürgen Deckert
Polymorphic MAO-A and 5-HT-transporter genes: analysis of interactions in panic disorder.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2000;1(3):147-50.
2000: Fabian Runkel; Michael Brüss; Markus M Nöthen; Gerald Stöber; Peter Propping; Heinz Bönisch
Pharmacological properties of naturally occurring variants of the human norepinephrine transporter.
Pharmacogenetics 2000;10(5):397-405.
2000: Marcella Rietschel; A Schorr; Margot Albus; E Franzek; R Kreiner; Tilo Held; Michael Knapp; Daniel J Müller; Thomas G. Schulze; Peter Propping; Wolfgang Maier; Markus M Nöthen
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls.
American journal of medical genetics 2000;96(3):310-1.
2000: Regina C Betz; YA Lee; Anette Bygum; Flemming Brandrup; A I Bernal; J Toribio; J I Alvarez; Guido Kukuk; H H Ibsen; H B Rasmussen; Thomas F Wienker; A Reis; Peter Propping; Roland Kruse; Sven Cichon; Markus M Nöthen
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
American journal of human genetics 2000;66(6):1979-83.
2000: Frank Grünhage; Thomas G. Schulze; Daniel J Müller; Mario Lanczik; E Franzek; Margot Albus; Margitta Borrmann-Hassenbach; Michael Knapp; Sven Cichon; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen
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: Ina R Vogt; D Shimron-Abarbanell; Helge Neidt; Jeanette Erdmann; Sven Cichon; Thomas G. Schulze; Daniel J Müller; Wolfgang Maier; Margot Albus; Margitta Borrmann-Hassenbach; Michael Knapp; Marcella Rietschel; Peter Propping; Markus M Nöthen
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: Thomas Geijer; Amos Frisch; ML Persson; Danuta Wasserman; Rivka Rockah; Elena Michaelovsky; Alan Apter; Erik G Jönsson; Markus M Nöthen; Abraham Weizman
Search for association between suicide attempt and serotonergic polymorphisms.
Psychiatric genetics 2000;10(1):19-26.
2000: Marcella Rietschel; Harald Krauss; Daniel J Müller; Thomas G. Schulze; Michael Knapp; K Marwinski; AO Maroldt; Sebastian Paus; Frank Grünhage; Peter Propping; Wolfgang Maier; Tilo Held; Markus M Nöthen
Dopamine D3 receptor variant and tardive dyskinesia.
European archives of psychiatry and clinical neuroscience 2000;250(1):31-5.
2000: Petra Franke; Markus M Nöthen; T Wang; Michael Knapp; Dirk Lichtermann; Helge Neidt; Thomas Sander; Peter Propping; Wolfgang Maier
DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.
Molecular psychiatry 2000;5(1):101-4.
1999: Thomas Rohrmeier; Albert Putzhammer; Anja Schoeler; Heino Sartor; P Dallinger; Markus M Nöthen; Peter Propping; Michael Knapp; Margot Albus; M Borrmann; K Knothe; R Kreiner; E Franzek; Dirk Lichtermann; Marcella Rietschel; Wolfgang Maier; Helmfried E Klein; Peter Eichhammer
hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia.
Psychiatric genetics 1999;9(4):169-75.
1999: Roland Kruse; Sven Cichon; M Anker; Axel M Hillmer; Patricio Barros-Núñez; JM Cantú; Evelia Leal; Georg Weinlich; Matthias Schmuth; Peter Fritsch; Thomas Ruzicka; Peter Propping; Markus M Nöthen
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.
The Journal of investigative dermatology 1999;113(6):954-9.
1999: Erik G Jönsson; Markus M Nöthen; H Neidt; Kaj Forslund; Gunnar Rylander; Marja Mattila-Evenden; Marie Asberg; Peter Propping; Göran C Sedvall
Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia.
Schizophrenia research 1999;40(1):31-6.
1999: Petra Franke; Markus M Nöthen; T Wang; Helge Neidt; Michael Knapp; Dirk Lichtermann; O Weiffenbach; P Mayer; V Höllt; Peter Propping; Wolfgang Maier
Human delta-opioid receptor gene and susceptibility to heroin and alcohol dependence.
American journal of medical genetics 1999;88(5):462-4.
1999: J Petter Gustavsson; Markus M Nöthen; Erik G Jönsson; H Neidt; Kaj Forslund; Gunnar Rylander; Marja Mattila-Evenden; Göran C Sedvall; Peter Propping; Marie Asberg
No association between serotonin transporter gene polymorphisms and personality traits.
American journal of medical genetics 1999;88(4):430-6.
1999: Erik G Jönsson; Markus M Nöthen; Frank Grünhage; Lars Farde; Y Nakashima; Peter Propping; Göran C Sedvall
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers.
Molecular psychiatry 1999;4(3):290-6.
1999: Kai-Uwe Kühn; K Meyer; Markus M Nöthen; Michael Gänsicke; Andreas Papassotiropoulos; Wolfgang Maier
Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: replication tests.
American journal of medical genetics 1999;88(2):168-72.
1999: Gerald Stöber; Johannes Hebebrand; Sven Cichon; Michael Brüss; Heinz Bönisch; Gerd Lehmkuhl; Fritz Poustka; M Schmidt; Helmut Remschmidt; Peter Propping; Markus M Nöthen
Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.
American journal of medical genetics 1999;88(2):158-63.
1999: Jürgen Deckert; Marco Catalano; Yana V Syagailo; Monica Francesca Bosi; Olga Okladnova; Daniela Di Bella; Markus M Nöthen; P Maffei; Petra Franke; Jürgen Fritze; Wolfgang Maier; Peter Propping; Helmut Beckmann; laura bellodi; Klaus-Peter Lesch
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder.
Human molecular genetics 1999;8(4):621-4.
1999: Michael Brüss; Heinz Bönisch; M Bühlen; Markus M Nöthen; Peter Propping; Manfred Göthert
Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptor.
Pharmacogenetics 1999;9(1):95-102.
1999: Markus M Nöthen; Gerd Schulte-Körne; Tiemo Grimm; Sven Cichon; Ina R Vogt; Bertram Müller-Myhsok; Peter Propping; Helmut Remschmidt
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.
European child & adolescent psychiatry 1999;8 Suppl 3():56-9.
1999: Markus M Nöthen; Sven Cichon; H Rohleder; S Hemmer; E Franzek; J Fritze; Margot Albus; Margitta Borrmann-Hassenbach; R Kreiner; B Weigelt; J Minges; Dirk Lichtermann; Wolfgang Maier; N Craddock; Rolf Fimmers; Tobias Höller; Max P Baur; Marcella Rietschel; Peter Propping
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.
Molecular psychiatry 1999;4(1):76-84.
1998: Manfred Göthert; Peter Propping; Heinz Bönisch; Michael Brüss; Markus M Nöthen
Genetic variation in human 5-HT receptors: potential pathogenetic and pharmacological role.
Annals of the New York Academy of Sciences 1998;861():26-30.
1998: Sven Cichon; M Anker; Ina R Vogt; H Rohleder; M Pützstück; Axel M Hillmer; S A Farooq; K S Al-Dhafri; M Ahmad; Sayedul Haque; Marcella Rietschel; Peter Propping; Roland Kruse; Markus M Nöthen
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.
Human molecular genetics 1998;7(11):1671-9.
1998: Maria Grigoroiu-Serbanescu; M Martinez; Markus M Nöthen; Peter Propping; Stefan Milea; R Mihailescu; Elvira Marinescu
Patterns of parental transmission and familial aggregation models in bipolar affective disorder.
American journal of medical genetics 1998;81(5):397-404.
1998: R Bunzel; Ingmar Blümcke; Sven Cichon; Sabine Normann; Johannes Schramm; Peter Propping; Markus M Nöthen
Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain.
Brain research. Molecular brain research 1998;59(1):90-2.
1998: Erik G Jönsson; Markus M Nöthen; J Petter Gustavsson; H Neidt; Kaj Forslund; Marja Mattila-Evenden; Gunnar Rylander; Peter Propping; Marie Asberg
Lack of association between dopamine D4 receptor gene and personality traits.
Psychological medicine 1998;28(4):985-9.
1998: Gerd Schulte-Körne; Tiemo Grimm; Markus M Nöthen; Bertram Müller-Myhsok; Sven Cichon; Ina R Vogt; Peter Propping; Helmut Remschmidt
Evidence for linkage of spelling disability to chromosome 15.
American journal of human genetics 1998;63(1):279-82.
1998: Erik G Jönsson; Markus M Nöthen; J Petter Gustavsson; H Neidt; R Bunzel; Peter Propping; Göran C Sedvall
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteers.
Psychiatry research 1998;79(1):1-9.
1998: Sven Cichon; Kristina Kesper; Peter Propping; Markus M Nöthen
Assignment of the human serotonin 4 receptor gene (HTR4) to the long arm of chromosome 5 (5q31-q33).
Molecular membrane biology 1998;15(2):75-8.
1998: Yaping Wang; Waltraut Friedl; Christof Lamberti; Markus M Nöthen; Roland Kruse; Peter Propping
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among Europeans.
Human heredity 1998;48(2):87-91.
1998: Jürgen Deckert; Markus M Nöthen; Margot Albus; E Franzek; Marcella Rietschel; H Ren; G L Stiles; Michael Knapp; B Weigelt; Wolfgang Maier; Helmut Beckmann; Peter Propping
Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies.
American journal of medical genetics 1998;81(1):18-23.
1998: Markus M Nöthen; Sven Cichon; Ina R Vogt; S Hemmer; Roland Kruse; Michael Knapp; Tobias Höller; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Peter Propping; M Ahmad; Marcella Rietschel
A gene for universal congenital alopecia maps to chromosome 8p21-22.
American journal of human genetics 1998;62(2):386-90.
1998: Jürgen Deckert; Markus M Nöthen; Petra Franke; CD Delmo; Jürgen Fritze; Michael Knapp; Wolfgang Maier; Helmut Beckmann; Peter Propping
Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease.
Molecular psychiatry 1998;3(1):81-5.
1997: R Schroers; Markus M Nöthen; Marcella Rietschel; Margot Albus; W Maier; S Schwab; Dieter B Wildenauer; Rolf Fimmers; Peter Propping; G Dewald
Investigation of complement C4B deficiency in schizophrenia.
Human heredity 1997;47(5):279-82.
1997: Jeanette Erdmann; D Shimron-Abarbanell; V Shridhar; David I Smith; Peter Propping; Markus M Nöthen
Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1).
Molecular membrane biology 1997;14(3):133-5.
1997: Michael Platten; Birgit Meyer-Puttlitz; Ingmar Blümcke; Andreas Waha; HK Wolf; Markus M Nöthen; David N Louis; J R Sampson; Andreas von Deimling
A novel splice site associated polymorphism in the tuberous sclerosis 2 (TSC2) gene may predispose to the development of sporadic gangliogliomas.
Journal of neuropathology and experimental neurology 1997;56(7):806-10.
1997: Erik G Jönsson; Markus M Nöthen; J Petter Gustavsson; H Neidt; Stefan Brené; A Tylec; Peter Propping; Göran C Sedvall
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms.
The American journal of psychiatry 1997;154(5):697-9.
1997: Ortrud K Steinlein; Jürgen Deckert; Markus M Nöthen; Petra Franke; Wolfgang Maier; Helmut Beckmann; Peter Propping
Neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and panic disorder: an association study.
American journal of medical genetics 1997;74(2):199-201.
1997: D Shimron-Abarbanell; Jeanette Erdmann; Ina R Vogt; SP Bryant; Nigel K Spurr; Michael Knapp; Peter Propping; Markus M Nöthen
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region.
Biochemical and biophysical research communications 1997;233(1):6-9.
1997: Maria J Arranz; Jeanette Erdmann; G Kirov; Marcella Rietschel; Monsheel Sodhi; M Albus; D Ball; Wolfgang Maier; N Davies; E Franzek; I Abusaad; B Weigelt; Robin Murray; D Shimron-Abarbanell; Robert Kerwin; Peter Propping; Pak Sham; Markus M Nöthen; David A Collier
5-HT2A receptor and bipolar affective disorder: association studies in affected patients.
Neuroscience letters 1997;224(2):95-8.
1997: Jürgen Deckert; Markus M Nöthen; SP Bryant; S Schuffenhauer; P R Schofield; Nigel K Spurr; Peter Propping
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region.
Human genetics 1997;99(3):326-8.
1997: M Nobile; P Maffei; Markus M Nöthen; M Rietschel; E Smeraldi; Marco Catalano
Association study of schizophrenia and the histidase gene.
Psychiatric genetics 1997;7(3):107-9.
1997: Jürgen Deckert; Marco Catalano; A Heils; Daniela Di Bella; F Friess; E Politi; Petra Franke; Markus M Nöthen; Wolfgang Maier; laura bellodi; Klaus-Peter Lesch
Functional promoter polymorphism of the human serotonin transporter: lack of association with panic disorder.
Psychiatric genetics 1997;7(1):45-7.
1996: Gerald Stöber; Markus M Nöthen; P Pörzgen; Michael Brüss; Heinz Bönisch; Michael Knapp; Helmut Beckmann; Peter Propping
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.
American journal of medical genetics 1996;67(6):523-32.
1996: Jeanette Erdmann; Markus M Nöthen; D Shimron-Abarbanell; Marcella Rietschel; Margot Albus; M Borrmann; W Maier; E Franzek; J Körner; B Weigelt; Rolf Fimmers; Peter Propping
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: Marcella Rietschel; D Naber; H Oberländer; R Holzbach; R Fimmers; K Eggermann; Hans-Jürgen Möller; Peter Propping; Markus M Nöthen
Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor gene.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 1996;15(5):491-6.
1996: Sven Cichon; Markus M Nöthen; Gerald Stöber; R Schroers; Margot Albus; W Maier; Marcella Rietschel; J Körner; B Weigelt; E Franzek; Dieter B Wildenauer; Rolf Fimmers; Peter Propping
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.
American journal of medical genetics 1996;67(4):424-8.
1996: G Dewald; Sven Cichon; S P Bryant; S Hemmer; Markus M Nöthen; Nigel K Spurr
The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.
Annals of human genetics 1996;60(Pt 4):281-91.
1996: Marcella Rietschel; Markus M Nöthen; Margot Albus; W Maier; J Minges; Brigitta Bondy; J Körner; S Hemmer; Rolf Fimmers; Hans-Jürgen Möller; Dieter B Wildenauer; Peter Propping
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: Jeanette Erdmann; D Shimron-Abarbanell; Marcella Rietschel; Margot Albus; W Maier; J Körner; Brigitta Bondy; K Chen; J C Shih; Michael Knapp; Peter Propping; Markus M Nöthen
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: Thomas Eggermann; Hartmut Engels; B Moskalonek; Markus M Nöthen; J Müller-Navia; E Schleiermacher; Gesa Schwanitz; S Stengel-Rutkowski
Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.
Human genetics 1996;97(5):568-72.
1996: Sven Cichon; Markus M Nöthen; H K Wolf; Peter Propping
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.
American journal of medical genetics 1996;67(2):229-31.
1996: D Shimron-Abarbanell; H Harms; Jeanette Erdmann; Margot Albus; W Maier; Marcella Rietschel; J Körner; B Weigelt; E Franzek; Thomas Sander; Michael Knapp; Peter Propping; Markus M Nöthen
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: L C Lim; Nick Craddock; Michael J Owen; Pak Sham; Markus M Nöthen; J Körner; Marcella Rietschel; R Fimmer; P Propping; Peter McGuffin; Robin Murray; M Gill
Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees.
Behavior genetics 1996;26(2):113-22.
1996: Thomas Eggermann; Markus M Nöthen; B Eiben; D Hofmann; K Hinkel; Rolf Fimmers; Gesa Schwanitz
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.
Human genetics 1996;97(2):218-23.
1996: Jürgen Deckert; Markus M Nöthen; Marcella Rietschel; Dieter B Wildenauer; Brigitta Bondy; M A Ertl; Michael Knapp; P R Schofield; Margot Albus; W Maier; Peter Propping
Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia.
Journal of neural transmission (Vienna, Austria : 1996) 1996;103(12):1447-55.
1996: S Zhu; Markus M Nöthen; Siegfried Uhlhaas; Marcella Rietschel; J Körner; Mario Lanczik; Rolf Fimmers; Peter Propping
Apolipoprotein E genotype distribution in schizophrenia.
Psychiatric genetics 1996;6(2):75-9.
1996: J Körner; Marcella Rietschel; Markus M Nöthen; P Propping
[Genetic counseling in psychiatric diseases].
Der Nervenarzt 1996;67(1):3-14.
1995: E Dawson; John F Powell; P C Sham; Markus M Nöthen; Marc-Antoine Crocq; P Propping; J Körner; Marcella Rietschel; J van Os; P Wright
An association study of a neurotrophin-3 (NT-3) gene polymorphism with schizophrenia.
Acta psychiatrica Scandinavica 1995;92(6):425-8.
1995: Peter Propping; Markus M Nöthen
Genetic variation of CNS receptors--a new perspective for pharmacogenetics.
Pharmacogenetics 1995;5(5):318-25.
1995: Markus M Nöthen; K Eggermann; Margot Albus; M Borrmann; Marcella Rietschel; J Körner; W Maier; J Minges; Dirk Lichtermann; E Franzek
Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls.
American journal of human genetics 1995;57(4):975-8.
1995: Jürgen Deckert; Markus M Nöthen; S P Bryant; H Ren; H K Wolf; G L Stiles; Nigel K Spurr; Peter Propping
Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding region.
Biochemical and biophysical research communications 1995;214(2):614-21.
1995: E Dawson; E Parfitt; Q Roberts; J Daniels; L Lim; Pak Sham; Markus M Nöthen; P Propping; Mario Lanczik; W Maier
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1.
American journal of medical genetics 1995;60(2):94-102.
1995: D Shimron-Abarbanell; Markus M Nöthen; Jeanette Erdmann; Peter Propping
Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation.
Brain research. Molecular brain research 1995;29(2):387-90.
1995: Markus M Nöthen; G Dewald
Dinucleotide repeat polymorphism at the human CD59 locus.
Clinical genetics 1995;47(3):165-6.
1995: J Hebebrand; Markus M Nöthen; B Klug; R Wettke-Schäfer; A Camps; S Lisch; S Hemmer; Alexander Von Gontard; Fritz Poustka; Gerd Lehmkuhl
No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndrome.
Biological psychiatry 1995;37(3):209-11.
1995: Sven Cichon; Markus M Nöthen; M Catalano; D Di Bella; W Maier; Dirk Lichtermann; J Minges; Margot Albus; M Borrmann; E Franzek
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene.
Psychiatric genetics 1995;5(3):97-103.
1994: Sven Cichon; Markus M Nöthen; Marcella Rietschel; J Körner; P Propping
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: Markus M Nöthen; Jeanette Erdmann; D Shimron-Abarbanell; Peter Propping
Identification of genetic variation in the human serotonin 1D beta receptor gene.
Biochemical and biophysical research communications 1994;205(2):1194-200.
1994: Markus M Nöthen; Sven Cichon; S Hemmer; J Hebebrand; H Remschmidt; Gerd Lehmkuhl; Fritz Poustka; M Schmidt; M Catalano; Rolf Fimmers
Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.
Human molecular genetics 1994;3(12):2207-12.
1994: G Dewald; Markus M Nöthen; K Rüther
A common Ser/Thr polymorphism in the perforin-homologous region of human complement component C7.
Human heredity 1994;44(6):301-4.
1994: P Propping; Markus M Nöthen; J Körner; Marcella Rietschel; W Maier
[Genetic association in psychiatric diseases. Concepts and findings].
Der Nervenarzt 1994;65(11):725-40.
1994: L C Lim; Markus M Nöthen; J Körner; Marcella Rietschel; D Castle; N Hunt; P Propping; Robin Murray; M Gill
No evidence of association between dopamine D4 receptor variants and bipolar affective disorder.
American journal of medical genetics 1994;54(3):259-63.
1994: Markus M Nöthen; J Hebebrand; Michael Knapp; K Hebebrand; A Camps; Alexander Von Gontard; R Wettke-Schäfer; S Lisch; Sven Cichon; Fritz Poustka
Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method.
American journal of medical genetics 1994;54(3):249-52.
1994: R Viersbach; Gesa Schwanitz; Markus M Nöthen
Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes.
Human genetics 1994;93(6):663-7.
1994: G Dewald; S Hemmer; Markus M Nöthen
Human complement component C8. Molecular basis of the beta-chain polymorphism.
FEBS letters 1994;340(3):211-5.
1994: Markus M Nöthen; G Dewald
A common amino acid polymorphism in complement component C1R.
Human molecular genetics 1994;3(1):217.
1994: Sven Cichon; Markus M Nöthen; Jeanette Erdmann; Peter Propping
Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).
Human molecular genetics 1994;3(1):209.
1994: J Körner; Marcella Rietschel; N Hunt; D Castle; M Gill; Markus M Nöthen; Nick Craddock; J Daniels; Michael J Owen; Rolf Fimmers
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: E Dawson; John F Powell; Markus M Nöthen; Marc-Antoine Crocq; Mario Lanczik; J Körner; Marcella Rietschel; J van Os; P Wright; M Gill
An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia.
Psychiatric genetics 1994;4(4):215-8.
1993: S Abels; J Erdmann; Markus M Nöthen
Dinucleotide repeat polymorphism at the D18S365 locus.
Human molecular genetics 1993;2(10):1747.
1993: Markus M Nöthen; Jeanette Erdmann; P Propping; Mario Lanczik; Marcella Rietschel; J Körner; W Maier; Margot Albus; M A Ertl; Dieter B Wildenauer
Mutation in the beta amyloid precursor protein gene and schizophrenia.
Biological psychiatry 1993;34(7):502.
1993: Markus M Nöthen; Thomas Eggermann; Jeanette Erdmann; B Eiben; D Hofmann; Peter Propping; Gesa Schwanitz
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome).
Human genetics 1993;92(4):347-9.
1993: G Dewald; Markus M Nöthen; Sven Cichon
Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.
Biochemical and biophysical research communications 1993;194(1):458-64.
1993: Markus M Nöthen; Gisela Knöpfle; H J Födisch; Klaus Zerres
Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder.
American journal of medical genetics 1993;46(4):467-70.
1993: Marcella Rietschel; Markus M Nöthen; Lars Lannfelt; Pierre Sokoloff; J C Schwartz; Mario Lanczik; J Fritze; Sven Cichon; Rolf Fimmers; J Körner
A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder.
Psychiatry research 1993;46(3):253-9.
1993: J Erdmann; Markus M Nöthen
Dinucleotide repeat polymorphism at the D18S99 locus.
Human molecular genetics 1993;2(1):91.
1993: Jeanette Erdmann; Markus M Nöthen; M Stratmann; Rolf Fimmers; E Franzek; Peter Propping
The use of microsatellites in zygosity diagnosis of twins.
Acta geneticae medicae et gemellologiae 1993;42(1):45-51.
1993: Thomas Eggermann; Markus M Nöthen; Peter Propping; Gesa Schwanitz
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling.
Annales de génétique 1993;36(4):214-6.
1992: Markus M Nöthen; Jeanette Erdmann; J Körner; Mario Lanczik; J Fritze; Rolf Fimmers; David K Grandy; B O'Dowd; Peter Propping
Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder.
The American journal of psychiatry 1992;149(2):199-201.
1992: Mario Lanczik; Markus M Nöthen; J Körner; Marcella Rietschel; Jeanette Erdmann; M Stratmann; Sven Cichon; Dirk Lichtermann; W Maier; Peter Propping
Association and linkage studies in bipolar affective disorder.
Clinical neuropharmacology 1992;15 Suppl 1 Pt A():580A-581A.