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Peter Propping

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Verena Steinke; Reinhard Büttner; Christoph Engel; Hans Konrad Schackert; Wolff H Schmiegel; Peter Propping
Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome.
Christoph Engel; Encarna Gómez García; Timm O Goecke; Heike Goergens; Frederik J Hes; Elke Holinski-Feder; Nicoline Hoogerbrugge; Irma Kluijt; Tom G W Letteboer; Markus Loeffler; Fred H Menko; Gabriela Moeslein; Peter Propping; Nils Rahner; Hans K Schackert; Wolff Schmiegel; Rolf H Sijmons; Verena Steinke; Theo A M van Os; Reinhard Buettner; Wolfgang Dietmaier; Magnus von Knebel Doeberitz; Anja Wagner; Hans F A Vasen
Risks of less common cancers in proven mutation carriers with lynch syndrome.
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.

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All Publications

2013: Verena Steinke; Reinhard Büttner; Christoph Engel; Hans Konrad Schackert; Wolff H Schmiegel; Peter Propping
Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome.
Deutsches Ärzteblatt international 2013;110(3):32-8.
2012: Christoph Engel; Encarna Gómez García; Timm O Goecke; Heike Goergens; Frederik J Hes; Elke Holinski-Feder; Nicoline Hoogerbrugge; Irma Kluijt; Tom G W Letteboer; Markus Loeffler; Fred H Menko; Gabriela Moeslein; Peter Propping; Nils Rahner; Hans K Schackert; Wolff Schmiegel; Rolf H Sijmons; Verena Steinke; Theo A M van Os; Reinhard Buettner; Wolfgang Dietmaier; Magnus von Knebel Doeberitz; Anja Wagner; Hans F A Vasen
Risks of less common cancers in proven mutation carriers with lynch syndrome.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012;30(35):4409-15.
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: Nils Rahner; Johannes Schumacher; Liesbeth Spruijt; Verena Steinke; Susanne Stemmler; Carli J M Tops; Hans F A Vasen; Juul T Wijnen; Tim Becker; Felix F Brockschmidt; Wolfgang Dietmaier; Heike Görgens; Elke Holinski-Feder; Philip Kahl; Matthias Kloor; Marjolijn J L Ligtenberg; Markus M Nöthen; Peter Propping
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
Familial cancer 2012;11(1):19-26.
2011: Lucia Gullotti; Philip Kahl; Jutta Kirfel; Peter Propping; Nils Rahner; Roland Schüle; Verena Steinke; Reinhard Buettner; Jacqueline Czerwitzki; Christoph Engel; Nicolaus Friedrichs
FHL2 expression in peritumoural fibroblasts correlates with lymphatic metastasis in sporadic but not in HNPCC-associated colon cancer.
Laboratory investigation; a journal of technical methods and pathology 2011;91(12):1695-705.
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: Maura Carrai; Christoph Engel; Asta Försti; Heike Görgens; Kari Hemminki; Elke Holinski-Feder; Matthias Kloor; Monika Morak; Alessio Naccarati; Jan Novotny; Barbara Pardini; Peter Propping; Nils Rahner; Hans K Schackert; Angelika Stein; Verena Steinke; Susanne Stemmler; Pavel Vodicka; Ludmila Vodickova; Roberto Barale; Beate Betz; Reinhard Büttner; Federico Canzian; Daniele Campa
Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin.
PloS one 2011;6(6):e20464.
2011: Stefanie Huhn; Dierk Ingelfinger; Justo Lorenzo Bermejo; Melanie Bevier; Barbara Pardini; Alessio Naccarati; Verena Steinke; Nils Rahner; Elke Holinski-Feder; Monika Morak; Hans K Schackert; Heike Görgens; Christian P Pox; Timm Goecke; Matthias Kloor; Markus Loeffler; Reinhard Büttner; Ludmila Vodickova; Jan Novotny; Kubilay Demir; Cristina-Maria Cruciat; Rebecca Renneberg; Wolfgang Huber; Christof Niehrs; Michael Boutros; Peter Propping; Pavel Vodièka; Kari Hemminki; Asta Försti
Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications.
International journal of molecular epidemiology and genetics 2011;2(1):36-50.
2011: Inke R König; Johannes Schumacher; Per Hoffmann; André Kleensang; Kerstin U Ludwig; Tiemo Grimm; Nina Neuhoff; Maike Preis; Darina Roeske; Andreas Warnke; Peter Propping; Helmut Remschmidt; Markus M Nöthen; Andreas Ziegler; Bertram Müller-Myhsok; Gerd Schulte-Körne
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(1):36-43.
2010: Flavie MATHIEU; Marie-Hélène Dizier; Bruno Etain; Stéphane Jamain; Marcella Rietschel; Wolfgang Maier; Margot Albus; Patrick McKeon; Siobhan Roche; Douglas Blackwood; Walter J Muir; Chantal Henry; Alain Malafosse; Martin Preisig; François Ferrero; Sven Cichon; Johannes Schumacher; Stephanie Ohlraun; Peter Propping; Rami Abou Jamra; Thomas G. Schulze; Diana Zelenica; Céline Charon; Andrej Marusic; Mojca C Dernovsek; Hugh Gurling; Markus Nöthen; Mark Lathrop; Marion Leboyer; Frank Bellivier
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(8):1425-33.
2010: Steffen Manekeller; Tilman Sauerbruch; Hans-Peter Fischer; Peter Propping; Andreas Hirner
[Heterozygous alpha-1-antitrypsin deficiency (PiMZ): risk factor in the development of primary liver carcinoma in non-cirrhotic liver?].
Zeitschrift für Gastroenterologie 2010;48(10):1211-4.
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: 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: Christoph Engel; Nils Rahner; Karsten Schulmann; Elke Holinski-Feder; Timm O Goecke; Hans K Schackert; Matthias Kloor; Verena Steinke; Holger Vogelsang; Gabriela Möslein; Heike Görgens; Stefan Dechant; Magnus von Knebel Doeberitz; Josef Rüschoff; Nicolaus Friedrichs; Reinhard Büttner; Markus Loeffler; Peter Propping; Wolff Schmiegel
Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2010;8(2):174-82.
2010: Daniele Campa; Barbara Pardini; Alessio Naccarati; Ludmila Vodickova; Jan Novotny; Verena Steinke; Nils Rahner; Elke Holinski-Feder; Monika Morak; Hans K Schackert; Heike Görgens; Judith Kötting; Beate Betz; Matthias Kloor; Christoph Engel; Reinhard Büttner; Peter Propping; Asta Försti; Kari Hemminki; Roberto Barale; Pavel Vodicka; Federico Canzian
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study.
BMC gastroenterology 2010;10():112.
2009: Stefanie Vogt; Natalie Jones; Daria Christian; Christoph Engel; Maartje Nielsen; Astrid Kaufmann; Verena Steinke; Hans F Vasen; Peter Propping; Julian R Sampson; Frederik J Hes; Stefan Aretz
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.
Gastroenterology 2009;137(6):1976-85.e1-10.
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: Karsten Haug; Maike Warnstedt; Alexi K. Alekov; Thomas Sander; Alfredo Ramírez; Barbara Poser; Snezana Maljevic; Simon Hebeisen; Christian Kubisch; Johannes Rebstock; Steve Horvath; Kerstin Hallmann; Joern S Dullinger; Birgit Rau; Fritz Haverkamp; Stefan Beyenburg; Herbert Schulz; Dieter Janz; Bernd Giese; Gerhard Müller-Newen; Peter Propping; Christian E Elger; Christoph Fahlke; Holger Lerche
Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Nature genetics 2009;41(9):1043.
2009: Ailing Kleefuss-Lie; Waltraut Friedl; Sven Cichon; Karsten Haug; Maike Warnstedt; Alexi Alekov; Thomas Sander; Alfredo Ramirez; Barbara Poser; Snezana Maljevic; Simon Hebeisen; Christian Kubisch; Johannes Rebstock; Steve Horvath; Kerstin Hallmann; Jörn S Dullinger; Birgit Rau; Fritz Haverkamp; Stefan Beyenburg; Herbert Schulz; Dieter Janz; Bernd Giese; Gerhard Müller-Newen; Peter Propping; Christian E Elger; Christoph Fahlke; Holger Lerche
CLCN2 variants in idiopathic generalized epilepsy.
Nature genetics 2009;41(9):954-5.
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: 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: Thomas G. Schulze; Sevilla D Detera-Wadleigh; Nirmala Akula; A Gupta; L Kassem; Jo Steele; J Pearl; J Strohmaier; R Breuer; M Schwarz; Peter Propping; Markus M Nöthen; Sven Cichon; Johannes Schumacher; Marcella Rietschel; Francis McMajon
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder.
Molecular psychiatry 2009;14(5):487-91.
2009: Alexander Georgi; Johannes Schumacher; Chady Abboud Leon; Angela Villela Wolf; Katrin Klein; Katja V Böhenz; Frederike Schirmbeck; Jana Strohmaier; Peter Propping; Thomas G. Schulze; Marcella Rietschel; Markus M Nöthen; Sven Cichon; Rami Abou Jamra
No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample.
Psychiatric genetics 2009;19(2):104.
2009: R Hüneburg; Frank Lammert; Christian Rabe; Nils Rahner; Philip Kahl; Reinhard Büttner; Peter Propping; Tilman Sauerbruch; Christof Lamberti
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening.
Endoscopy 2009;41(4):316-22.
2009: Jan-Willem Koten; Guilherme Wood; Peter Hagoort; Rainer Goebel; Peter Propping; Klaus Willmes; Dorret I Boomsma
Genetic contribution to variation in cognitive function: an FMRI study in twins.
Science (New York, N.Y.) 2009;323(5922):1737-40.
2009: Astrid Kaufmann; Stefanie Vogt; Siegfried Uhlhaas; Dietlinde Stienen; Ingo Kurth; Horst Hameister; Elisabeth Mangold; Judith Kötting; Elke Kaminsky; Peter Propping; Waltraut Friedl; Stefan Aretz
Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review.
The Journal of molecular diagnostics : JMD 2009;11(2):131-9.
2009: Rami Abou Jamra; Alexander Georgi; Husam Suliman; Katrin Klein; Angela Wolf Villela; Thomas G. Schulze; Peter Propping; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
No association between the D-aspartate oxidase locus and schizophrenia.
Psychiatric genetics 2009;19(1):56.
2008: Eli Papaemmanuil; Luis Carvajal Carmona; Gabrielle S Sellick; Zoe Kemp; Emily Webb; Sarah Spain; Kate Sullivan; Ella Barclay; Steven Lubbe; Emma Jaeger; Jayaram Vijayakrishnan; Peter Broderick; Maggie Gorman; Lynn Martin; Anneke Lucassen; D Timothy Bishop; D Gareth Evans; Eamonn R Maher; Verena Steinke; Nils Rahner; Hans K Schackert; Timm O Goecke; Elke Holinski-Feder; Peter Propping; Tom van Wezel; Juul Wijnen; Jean-Baptiste Cazier; Huw Thomas; Richard S Houlston; Ian Tomlinson
Deciphering the genetics of hereditary non-syndromic colorectal cancer.
European journal of human genetics : EJHG 2008;16(12):1477-86.
2008: Bernd Frank; Barbara Burwinkel; Justo Lorenzo Bermejo; Asta Försti; Kari Hemminki; Richard Houlston; Elisabeth Mangold; Nils Rahner; Waltraut Friedl; Nicolaus Friedrichs; Reinhard Buettner; Christoph Engel; Markus Loeffler; Elke Holinski-Feder; Monika Morak; Gisela Keller; Hans K Schackert; Stefan Krüger; Timm Goecke; Gabriela Moeslein; Matthias Kloor; Johannes Gebert; Erdmute Kunstmann; Karsten Schulmann; Josef Rüschoff; Peter Propping
Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families.
Cancer letters 2008;271(1):153-7.
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: 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: Peter Propping
[Genetic analysis in oncology--contra].
Deutsche medizinische Wochenschrift (1946) 2008;133(41):2085.
2008: Rami Abou Jamra; Carl Motinda Gobina; Tim Becker; Alexander Georgi; Thomas G. Schulze; Christine Schmael; Sven Cichon; Peter Propping; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder.
Psychiatric genetics 2008;18(4):199-203.
2008: Johannes Schumacher; Inke R König; Tatjana Schröder; Maike Duell; Ellen Plume; Peter Propping; Andreas Warnke; Claudia Libertus; Andreas Ziegler; Bertram Müller-Myhsok; Gerd Schulte-Körne; Markus M Nöthen
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.
Psychiatric genetics 2008;18(3):137-42.
2008: Marcella Rietschel; Lars Beckmann; Jana Strohmaier; Alexander Georgi; Anna Karpushova; Frederike Schirmbeck; Katja V Boesshenz; Christine Schmäl; Christin Bürger; Rami Abou Jamra; Johannes Schumacher; Susanne Höfels; Robert Kumsta; Sonja Entringer; Axel Krug; Valentin Markov; Wolfgang Maier; Peter Propping; Stefan Wüst; Tilo Kircher; Markus M Nöthen; Sven Cichon; Thomas G. Schulze
G72 and its association with major depression and neuroticism in large population-based groups from Germany.
The American journal of psychiatry 2008;165(6):753-62.
2008: Nils Rahner; Gerald Höefler; Christoph Högenauer; Caroline Lackner; Verena Steinke; Marlies Sengteller; Waltraut Friedl; Stefan Aretz; Peter Propping; Elisabeth Mangold; Constanze Walldorf
Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus.
American journal of medical genetics. Part A 2008;146A(10):1314-9.
2008: Verena Steinke; Nils Rahner; Monika Morak; Gisela Keller; Hans K Schackert; Heike Görgens; Wolff Schmiegel; Brigitte Royer-Pokora; Wolfgang Dietmaier; Matthias Kloor; Christoph Engel; Peter Propping; Stefan Aretz
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
European journal of human genetics : EJHG 2008;16(5):587-92.
2008: Silke Metzger; Juan Rong; Huu-Phuc Nguyen; Austin Cape; Jürgen Tomiuk; Anne S Soehn; Peter Propping; Yun Freudenberg-Hua; Jan Freudenberg; Liang Tong; Shi-Hua Li; Xiao-Jiang Li; Olaf Riess
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.
Human molecular genetics 2008;17(8):1137-46.
2008: Peter Propping
The optimization of polar body diagnosis: a consequence of the german embryo protection act.
Deutsches Ärzteblatt international 2008;105(11):189.
2008: Rami Abou Jamra; Tim Becker; Alexander Georgi; T Feulner; Johannes Schumacher; J Stromaier; F Schirmbeck; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Markus M Nöthen; Sven Cichon
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.
Molecular psychiatry 2008;13(3):277-84.
2008: A E Baum; Nirmala Akula; M Cabanero; I Cardona; Winston Corona; B Klemens; Thomas G. Schulze; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Alexander Georgi; Johannes Schumacher; M Schwarz; Rami Abou Jamra; Susanne Höfels; Peter Propping; Jaya M Satagopan; Sevilla D Detera-Wadleigh; John Hardy; Francis McMajon
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
Molecular psychiatry 2008;13(2):197-207.
2008: Peter Propping
Genetic analysis for early diagnosis of otorhinolaryngeal diseases.
GMS current topics in otorhinolaryngology, head and neck surgery 2008;7():Doc02.
2008: Peter Propping
Assisted reproduction: an important review of the literature on the risk of malformation after in vitro fertilization and intracytoplasmic sperm injection.
Deutsches Ärzteblatt international 2008;105(1-2):9-10.
2008: Nils Rahner; Nicolaus Friedrichs; V Steinke; Stefan Aretz; Waltraut Friedl; Reinhard Buettner; Elisabeth Mangold; Peter Propping; Constanze Walldorf
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome.
The Journal of pathology 2008;214(1):10-6.
2008: Sven Cichon; Ingeborg Winge; Manuel Mattheisen; Alexander Georgi; Anna Karpushova; Jan Freudenberg; Yun Freudenberg-Hua; Gulia Babadjanova; Ann Van Den Bogaert; Lilia I Abramova; Sofia Kapiletti; Per M Knappskog; Jeffrey McKinney; Wolfgang Maier; Rami Abou Jamra; Thomas G. Schulze; Johannes Schumacher; Peter Propping; Marcella Rietschel; Jan Haavik; Markus M Nöthen
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder.
Human molecular genetics 2008;17(1):87-97.
2007: Rami Abou Jamra; Robert Fuerst; RAdka Kaneva; Guillermo Orozco Diaz; Fabio Rivas; Fermin Mayoral; Eudoxia Gay; Sebastian Sans; Maria Jose Gonzalez; Susana Gil; Francisco Cabaleiro; Francisco Del Rio; Fermin Perez; Jesus Haro; Georg Auburger; vihra milanova; Christian Kostov; Vesselin Chorbov; Vessela Stoyanova; Amelia Nikolova-Hill; Georgi Onchev; Ivo Kremensky; Assen Jablensky; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Markus M Nothen; Sven Cichon; Thomas F Wienker; Johannes Schumacher
The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.
American journal of human genetics 2007;81(5):974-86.
2007: Stefan Aretz; Dietlinde Stienen; Siegfried Uhlhaas; Manfred Stolte; M M Entius; Steffan Loff; Walter Back; A Kaufmann; Klaus-Michael Keller; S H Blaas; R Siebert; S Vogt; S Spranger; E Holinski-Feder; Lone Sunde; Peter Propping; Waltraut Friedl
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome.
Journal of medical genetics 2007;44(11):702-9.
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: Stefan Aretz; Dietlinde Stienen; Nicolaus Friedrichs; Susanne Stemmler; Siegfried Uhlhaas; Nils Rahner; Peter Propping; Waltraut Friedl
Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).
Human mutation 2007;28(10):985-92.
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: Hartmut Engels; A Brockschmidt; Alexander Hoischen; C Landwehr; Kristin Bosse; Constanze Walldorf; Grischa Toedt; Bernhard Radlwimmer; Peter Propping; Peter Lichter; Ruthild G Weber
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation.
Neurology 2007;68(10):743-50.
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: Constanze Pagenstecher; Dorothea Gadzicki; Dietlinde Stienen; Siegfried Uhlhaas; Elisabeth Mangold; Nils Rahner; Mine Arslan-Kirchner; Peter Propping; Waltraut Friedl; Stefan Aretz
A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification.
The Journal of molecular diagnostics : JMD 2007;9(1):122-6.
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.
2007: Nils Rahner; Nicolaus Friedrichs; Maria Wehner; Verena Steinke; Stefan Aretz; Waltraut Friedl; Reinhard Buettner; Elisabeth Mangold; Peter Propping; Constanze Walldorf
Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.
Acta oncologica (Stockholm, Sweden) 2007;46(6):763-9.
2007: Xiaorong Liu; Xiangnian Shan; Waltraut Friedl; Siegfried Uhlhaas; Peter Propping; Jintian Li; Yaping Wang
May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers?
Acta oncologica (Stockholm, Sweden) 2007;46(6):757-62.
2007: Elisabeth Mangold; Nils Rahner; Nicolaus Friedrichs; Reinhard Buettner; Constanze Pagenstecher; Stefan Aretz; Waltraut Friedl; Thomas Ruzicka; Peter Propping; Arno Rütten; Roland Kruse
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
The British journal of dermatology 2007;156(1):158-62.
2007: Christian H Brenk; Eva-Christina Prott; Detlef Trost; Alexander Hoischen; Constanze Walldorf; Bernhard Radlwimmer; Dagmar Wieczorek; Peter Propping; Gabriele Gillessen-Kaesbach; Ruthild G Weber; Hartmut Engels
Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
European journal of human genetics : EJHG 2007;15(1):35-44.
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: 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: Stefan Aretz; Arend Koch; Siegfried Uhlhaas; Waltraut Friedl; Peter Propping; Dietrich von Schweinitz; Torsten Pietsch
Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
Pediatric blood & cancer 2006;47(6):811-8.
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: Timm Goecke; Karsten Schulmann; Christoph Engel; Elke Holinski-Feder; Constanze Pagenstecher; Hans K Schackert; Matthias Kloor; Erdmute Kunstmann; Holger Vogelsang; Gisela Keller; Wolfgang Dietmaier; Elisabeth Mangold; Nicolaus Friedrichs; Peter Propping; Stefan Krüger; Johannes Gebert; Wolff Schmiegel; Josef Rueschoff; Markus Loeffler; Gabriela Moeslein
Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2006;24(26):4285-92.
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: Stefan Aretz; Siegfried Uhlhaas; Heike Goergens; Kirsten Siberg; Matthias Vogel; Constanze Pagenstecher; Elisabeth Mangold; Reiner Caspari; Peter Propping; Waltraut Friedl
MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.
International journal of cancer. Journal international du cancer 2006;119(4):807-14.
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: Constanze Pagenstecher; Maria Wehner; Waltraut Friedl; Nils Rahner; Stefan Aretz; Nicolaus Friedrichs; Marlies Sengteller; Wolfram Henn; Reinhard Buettner; Peter Propping; Elisabeth Mangold
Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.
Human genetics 2006;119(1-2):9-22.
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: Christof Lamberti; Elisabeth Mangold; Constanze Pagenstecher; Matthias Jungck; D Schwering; Magdolna Bollmann; J Vogel; D Kindermann; R Nikorowitsch; Nicolaus Friedrichs; B Schneider; Farzad Houshdaran; Ingo G H Schmidt-Wolf; Waltraut Friedl; Peter Propping; Tilman Sauerbruch; Reinhard Büttner; Micaela Mathiak
Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany.
Digestion 2006;74(1):58-67.
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: Stefan Aretz; Dietlinde Stienen; Siegfried Uhlhaas; Steffan Loff; Walter Back; Constanze Pagenstecher; D Ross McLeod; Gail E Graham; Elisabeth Mangold; René Santer; Peter Propping; Waltraut Friedl
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Human mutation 2005;26(6):513-9.
2005: Elisabeth Mangold; Constanze Pagenstecher; Waltraut Friedl; Hans-Peter Fischer; Sabine Merkelbach-Bruse; Maike Ohlendorf; Nicolaus Friedrichs; Stefan Aretz; Reinhard Buettner; Peter Propping; Micaela Mathiak
Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining.
The Journal of pathology 2005;207(4):385-95.
2005: Susanne Zahn; Antje Ehrbrecht; Kristin Bosse; Vera Kalscheuer; Peter Propping; Gesa Schwanitz; Beate Albrecht; Hartmut Engels
Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1).
American journal of medical genetics. Part A 2005;139(1):19-24.
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: Elisabeth Mangold; Constanze Pagenstecher; Waltraut Friedl; Micaela Mathiak; Reinhard Buettner; Christoph Engel; Markus Loeffler; Elke Holinski-Feder; Yvonne Müller-Koch; Gisela Keller; Hans K Schackert; Stefan Krüger; Timm Goecke; Gabriela Moeslein; Matthias Kloor; Johannes Gebert; Erdmute Kunstmann; Karsten Schulmann; Josef Rüschoff; Peter Propping
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
International journal of cancer. Journal international du cancer 2005;116(5):692-702.
2005: Xiao-rong Liu; Xiang-Nian Shan; Waltraut Friedl; Siegfried Uhlhaas; Jin-Tian Li; Peter Propping; Ya-Ping Wang
[Detection of germline mutations in the APC gene with the protein truncation test].
Yi chuan xue bao = Acta genetica Sinica 2005;32(9):903-8.
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: Maria Wehner; Elisabeth Mangold; Marlies Sengteller; Nicolaus Friedrichs; Stefan Aretz; Waltraut Friedl; Peter Propping; Constanze Pagenstecher
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.
European journal of human genetics : EJHG 2005;13(8):983-6.
2005: Peter Propping
The biography of psychiatric genetics: from early achievements to historical burden, from an anxious society to critical geneticists.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;136B(1):2-7.
2005: Peter Propping
ISPG Lifetime Achievement Award 2004.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;136B(1):1.
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: Ming Zhu; Jintian Li; Xiaomei Zhang; Xiaorong Liu; Waltraut Friedl; Yuanying Zhang; Xiaoliu Wu; Peter Propping; Yaping Wang
Large genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancer.
Cancer genetics and cytogenetics 2005;160(1):61-7.
2005: Axel M Hillmer; Sandra Hanneken; Sibylle Ritzmann; Tim Becker; Jan Freudenberg; Felix F Brockschmidt; Antonia Flaquer; Yun Freudenberg-Hua; Rami Abou Jamra; Christine Metzen; Uwe Heyn; Nadine Schweiger; Regina C Betz; Bettina Blaumeiser; Jochen Hampe; Stefan Schreiber; Thomas G. Schulze; Hans Christian Hennies; Johannes Schumacher; Peter Propping; Thomas Ruzicka; Sven Cichon; Thomas F Wienker; Roland Kruse; Markus M Nothen
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
American journal of human genetics 2005;77(1):140-8.
2005: Rami Abou Jamra; I Sircar; Tim Becker; Yun Freudenberg-Hua; Stephanie Ohlraun; Jan Freudenberg; Felix F Brockschmidt; Thomas G. Schulze; Magdalena Gross; F Spira; Monika Deschner; Christine Schmäl; Wolfgang Maier; Peter Propping; Marcella Rietschel; Sven Cichon; Markus M Nöthen; Johannes Schumacher
A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.
Molecular psychiatry 2005;10(7):618-20.
2005: Stefan Aretz; Ruth Raff; Joachim Woelfle; Klaus Zerres; Marianne Esser; Peter Propping; Thomas Eggermann
Maternal uniparental disomy 14 in a 15-year-old boy with normal karyotype and no evidence of precocious puberty.
American journal of medical genetics. Part A 2005;135(3):336-8.
2005: Xiao-rong Liu; Xiang-Nian Shan; Waltraut Friedl; Siegfried Uhlhaas; Peter Propping; Ya-ping Wang
Analysis of germline mutations in the APC gene in familial adenomatous polyposis patients.
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005;22(3):261-4.
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: 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: Stefan Aretz; Dietlinde Stienen; Siegfried Uhlhaas; Constanze Pagenstecher; Elisabeth Mangold; Reiner Caspari; Peter Propping; Waltraut Friedl
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis.
Journal of medical genetics 2005;42(2):185-92.
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: 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.
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: Thomas G. Schulze; Heiner Fangerau; Peter Propping
From degeneration to genetic susceptibility, from eugenics to genethics, from Bezugsziffer to LOD score: the history of psychiatric genetics.
International review of psychiatry (Abingdon, England) 2004;16(4):246-59.
2004: Stefan Aretz; Siegfried Uhlhaas; Yuli Sun; Constanze Pagenstecher; Elisabeth Mangold; Reiner Caspari; Gabriela Möslein; Karsten Schulmann; Peter Propping; Waltraut Friedl
Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
Human mutation 2004;24(5):370-80.
2004: Elisabeth Mangold; Constanze Pagenstecher; M Leister; Micaela Mathiak; Arno Rütten; Waltraut Friedl; Peter Propping; T Ruzicka; Roland Kruse
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.
Journal of medical genetics 2004;41(7):567-72.
2004: Peter Propping; Stefan Aretz
[The genetic revolution-impact on therapy and prevention].
Der Internist 2004;45 Suppl 1():S6-14.
2004: Dagmar von Bubnoff; Martina Kreiss-Nachtsheim; Natalija Novak; Eva Engels; Hartmut Engels; Claudia Behrend; Peter Propping; Henri de la Salle; Thomas Bieber
Primary immunodeficiency in combination with transverse upper limb defect and anal atresia in a 34-year-old patient with Jacobsen syndrome.
American journal of medical genetics. Part A 2004;126A(3):293-8.
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: Stefan Aretz; Siegfried Uhlhaas; Reiner Caspari; Elisabeth Mangold; Constanze Pagenstecher; Peter Propping; Waltraut Friedl
Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.
European journal of human genetics : EJHG 2004;12(1):52-8.
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: Hartmut Engels; Antje Ehrbrecht; Susanne Zahn; Kristin Bosse; Hans Vrolijk; Stefan White; Vera Kalscheuer; Jan M N Hoovers; Gesa Schwanitz; Peter Propping; Hans J Tanke; Joop Wiegant; Anton K Raap
Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.
European journal of human genetics : EJHG 2003;11(9):643-51.
2003: Roland Kruse; Arno Rütten; Nadine Schweiger; Eva Jakob; Micaela Mathiak; Peter Propping; Elisabeth Mangold; Michele Bisceglia; Thomas Ruzicka
Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias.
The Journal of investigative dermatology 2003;120(5):858-64.
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: Karsten Haug; Maike Warnstedt; Alexi K. Alekov; Thomas Sander; Alfredo Ramírez; Barbara Poser; Snezana Maljevic; Simon Hebeisen; Christian Kubisch; Johannes Rebstock; Steve Horvath; Kerstin Hallmann; Joern S Dullinger; Birgit Rau; Fritz Haverkamp; Stefan Beyenburg; Herbert Schulz; Dieter Janz; Bernd Giese; Gerhard Müller-Newen; Peter Propping; Christian E Elger; Christoph Fahlke; Holger Lerche; Armin Heils
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Nature genetics 2003;33(4):527-32.
2003: Yaping Wang; Waltraut Friedl; Christof Lamberti; Matthias Jungck; Micaela Mathiak; Constanze Pagenstecher; Peter Propping; Elisabeth Mangold
Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes.
International journal of cancer. Journal international du cancer 2003;103(5):636-41.
2003: Nikola Tilgen; Johannes Rebstock; Steve Horvath; Peter Propping; Christian Erich Elger; Armin Heils
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Annals of neurology 2003;53(2):280-1; author reply 281-2.
2002: Nikola Tilgen; Heike Pfeiffer; Joana Cobilanschi; Birgit Rau; Steve Horvath; Christian E Elger; Peter Propping; Armin Heils
Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions.
Neuroscience letters 2002;334(1):68-70.
2002: Hartmut Engels; Kristin Bosse; Antje Ehrbrecht; Susanne Zahn; Alexander Hoischen; Peter Propping; Lutz Bindl; Heiko Reutter
Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
American journal of medical genetics 2002;111(2):205-9.
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: Waltraut Friedl; Siegfried Uhlhaas; Karsten Schulmann; Manfred Stolte; Steffan Loff; Walter Back; Elisabeth Mangold; Martin Stern; Hanns-Peter Knaebel; Christian Sutter; Ruthild G Weber; Steffen Pistorius; Bettina Burger; Peter Propping
Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers.
Human genetics 2002;111(1):108-11.
2002: Bettina Burger; Siegfried Uhlhaas; Elisabeth Mangold; Peter Propping; Waltraut Friedl; Dieter E Jenne; Gerhard Dockter; Walter Back
Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis.
American journal of medical genetics 2002;110(3):289-91.
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: Pascal Duijf; Kaate R J Vanmolkot; Peter Propping; Waltraut Friedl; Elmar Krieger; Frank McKeon; Volker Dötsch; Han G Brunner; Hans van Bokhoven
Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63.
Human molecular genetics 2002;11(7):799-804.
2002: Micaela Mathiak; Arno Rütten; Elisabeth Mangold; Hans-Peter Fischer; Thomas Ruzicka; Waltraut Friedl; Peter Propping; Roland Kruse
Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test.
The American journal of surgical pathology 2002;26(3):338-43.
2002: Yaping Wang; Waltraut Friedl; Marlies Sengteller; Matthias Jungck; Isabel Filges; Peter Propping; Elisabeth Mangold
A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1.
Human mutation 2002;19(3):279-86.
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.
2002: Christof Lamberti; Matthias Jungck; Michael Laarmann; Michael Knapp; Reiner Caspari; Waltraut Friedl; Tilman Sauerbruch; Peter Propping; Roland Kruse
Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis.
Pharmacogenetics 2002;12(1):49-54.
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: Karsten Haug; Kerstin Hallmann; Johannes Rebstock; Joern S Dullinger; S Muth; Fritz Haverkamp; H Pfeiffer; Birgit Rau; Christian E Elger; Peter Propping; Armin Heils
The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy.
Epilepsy research 2001;47(3):243-6.
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: Waltraut Friedl; Elisabeth Mangold; Reiner Caspari; Christof Lamberti; Peter Propping
Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis.
Gastroenterology 2001;121(2):503-4.
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: Waltraut Friedl; Reiner Caspari; Marlies Sengteller; Siegfried Uhlhaas; Christof Lamberti; Matthias Jungck; Martina Kadmon; M Wolf; J Fahnenstich; Johannes Gebert; Gabriela Möslein; Elisabeth Mangold; Peter Propping
Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.
Gut 2001;48(4):515-21.
2001: Elisabeth Mangold; Waltraut Friedl; Peter Propping
[Hereditary colorectal carcinoma: predictive diagnosis and genetic counseling].
Praxis 2001;90(12):490-6.
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: Roland Kruse; Arno Rütten; HR Hosseiny-Malayeri; Michele Bisceglia; Waltraut Friedl; Peter Propping; Thomas Ruzicka; Elisabeth Mangold
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation.
The Journal of investigative dermatology 2001;116(3):463-5.
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: Holger Lauschke; Reiner Caspari; Waltraut Friedl; B Schwarz; Micaela Mathiak; Peter Propping; Andreas Hirner
Detection of APC and k-ras mutations in the serum of patients with colorectal cancer.
Cancer detection and prevention 2001;25(1):55-61.
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: 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: Armin Heils; K Haug; Wolfram S Kunz; G Fernandez; Steve Horvath; Johannes Rebstock; Peter Propping; Christian E Elger
Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis.
Annals of neurology 2000;48(6):948-50.
2000: Karsten Haug; Kerstin Hallmann; Steve Horvath; Thomas Sander; Christian Kubisch; Birgit Rau; Joern S Dullinger; Stefan Beyenburg; Christian E Elger; Peter Propping; Armin Heils
No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.
Epilepsy research 2000;42(1):57-62.
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: Karsten Haug; Thomas Sander; Kerstin Hallmann; Birgit Rau; Joern S Dullinger; Christian E Elger; Peter Propping; Armin Heils
The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy.
Neuroreport 2000;11(12):2687-9.
2000: Reiner Caspari; Siegfried Uhlhaas; Waltraut Friedl; Michael Knapp; Peter Propping
Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26.
American journal of medical genetics 2000;93(4):290-3.
2000: Karsten Haug; Joachim Kremerskothen; Kerstin Hallmann; Thomas Sander; Joern S Dullinger; Birgit Rau; Stefan Beyenburg; M J Lentze; Angelika Barnekow; Christian E Elger; Peter Propping; Armin Heils
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
Molecular and cellular probes 2000;14(4):255-60.
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: Petra Franke; T Wang; M M Möthen; Michael Knapp; H Neith; Dirk Lichtermann; K M Capellen; Thomas Sander; Peter Propping; Wolfgang Maier
Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach.
Addiction biology 2000;5(3):289-95.
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: Karsten Haug; Thomas Sander; Kerstin Hallmann; M J Lentze; Peter Propping; Christian E Elger; Armin Heils
Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy.
Epilepsy research 2000;39(2):127-32.
2000: Reiner Caspari; Matthias Jungck; Christof Lamberti; Ingo G H Schmidt-Wolf; Waltraut Friedl; Peter Propping
[The diagnosis of hereditary colorectal carcinomas].
Deutsche medizinische Wochenschrift (1946) 2000;125(6):153-8.
2000: Peter Propping; Waltraut Friedl; Thomas F Wienker; Siegfried Uhlhaas; Klaus Zerres
ADULT syndrome allelic to limb mammary syndrome (LMS)?
American journal of medical genetics 2000;90(2):179-82.
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: Arno Rütten; Walter Burgdorf; Heino Hügel; Heinz Kutzner; HR Hosseiny-Malayeri; Waltraut Friedl; Peter Propping; Roland Kruse
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study.
The American Journal of dermatopathology 1999;21(5):405-13.
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: Waltraut Friedl; Roland Kruse; Siegfried Uhlhaas; Manfred Stolte; B Schartmann; Klaus-Michael Keller; Matthias Jungck; M Stern; Steffan Loff; Walter Back; Peter Propping; Dieter E Jenne
Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients.
Genes, chromosomes & cancer 1999;25(4):403-6.
1999: Christof Lamberti; Roland Kruse; C Ruelfs; Reiner Caspari; Yaping Wang; Matthias Jungck; Micaela Mathiak; H R Malayeri; Waltraut Friedl; Tilman Sauerbruch; Peter Propping
Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer.
Gut 1999;44(6):839-43.
1999: Matthias Jungck; Waltraut Friedl; Peter Propping
[Hereditary gastrointestinal tumors].
Der Internist 1999;40(5):502-12.
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: 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: Roland Kruse; Siegfried Uhlhaas; Christof Lamberti; Klaus-Michael Keller; C Jackisch; Johannes Steinhard; Gisela Knöpfle; Steffan Loff; Walter Back; Manfred Stolte; Matthias Jungck; Peter Propping; Waltraut Friedl; Dieter E Jenne
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Human mutation 1999;13(3):257-8.
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: Roland Kruse; Arno Rütten; Christof Lamberti; HR Hosseiny-Malayeri; Yaping Wang; C Ruelfs; Matthias Jungck; Micaela Mathiak; Thomas Ruzicka; W Hartschuh; M Bisceglia; Waltraut Friedl; Peter Propping
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.
American journal of human genetics 1998;63(1):63-70.
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: Roland Kruse; M Guttenbach; B Schartmann; Regine Schubert; Hans van der Ven; M Schmid; Peter Propping
Genetic counseling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection.
Fertility and sterility 1998;69(3):482-5.
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: Roland Kruse; Peter Propping
[Skin diseases and genetic instability. II. Genetic dermatoses with genetic instability].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1998;49(2):W153-63.
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: C Biervert; Björn C Schroeder; Christian Kubisch; SF Berkovic; Peter Propping; Thomas J Jentsch; Ortrud K Steinlein
A potassium channel mutation in neonatal human epilepsy.
Science (New York, N.Y.) 1998;279(5349):403-6.
1998: Roland Kruse; Peter Propping
[Skin diseases and genetic instability. I: Basic principles of genetic instability].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1998;49(1):65-71.
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: Yaping Wang; Waltraut Friedl; Christof Lamberti; C Ruelfs; Roland Kruse; Peter Propping
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue.
Human genetics 1997;100(3-4):362-4.
1997: Ortrud K Steinlein; Thomas Sander; J Stoodt; R Kretz; Dieter Janz; Peter Propping
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies.
American journal of medical genetics 1997;74(4):445-9.
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: C Esche; Roland Kruse; C Lamberti; Waltraut Friedl; Peter Propping; Percy Lehmann; Thomas Ruzicka
Muir-Torre syndrome: clinical features and molecular genetic analysis.
The British journal of dermatology 1997;136(6):913-7.
1997: Ortrud K Steinlein; A Magnusson; J Stoodt; S Bertrand; S Weiland; SF Berkovic; Karl O Nakken; Peter Propping; Daniel Bertrand
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy.
Human molecular genetics 1997;6(6):943-7.
1997: M Rietschel; D Naber; R Fimmers; Hans-Jürgen Möller; Peter Propping; M M Nöthen
Efficacy and side-effects of clozapine not associated with variation in the 5-HT2C receptor.
Neuroreport 1997;8(8):1999-2003.
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: LR Goldin; Elliot S Gershon; Wade H Berrettini; O Colin Stine; J. Raymond DePaulo; Francis McMajon; Deborah A Meyers; Markus M Nothen; Peter Propping; Sven Cichon; Rolf Fimmers; Max P Baur; Margot Albus; E Franzek; R Kreiner; Wolfgang Maier; Marcella Rietschel; M Baron; J Knowles; C Gilliam; J Endicott; Hugh M D Gurling; D Curtis; C Smyth; John R Kelsoe
Description of the Genetic Analysis Workshop 10 bipolar disorder linkage data sets.
Genetic epidemiology 1997;14(6):563-8.
1997: Maria Wehner; L Buschhausen; Christof Lamberti; Roland Kruse; Reiner Caspari; Peter Propping; Waltraut Friedl
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.
Human mutation 1997;10(3):241-4.
1996: Roland Kruse; Christof Lamberti; Yaping Wang; C Ruelfs; A Bruns; C Esche; Percy Lehmann; Thomas Ruzicka; Arno Rütten; Waltraut Friedl; Peter Propping
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
Human genetics 1996;98(6):747-50.
1996: S Weiland; Veit Witzemann; Alfredo Villarroel; Peter Propping; Ortrud K Steinlein
An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics.
FEBS letters 1996;398(1):91-6.
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: M M Nöthen; Sven Cichon; K Eggermann; Peter Propping; M Knapp; W Maier; M Rietschel
CNTF and psychiatric disorders.
Nature genetics 1996;13(2):142-3; author reply 144.
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: Waltraut Friedl; S Meuschel; Reiner Caspari; Christof Lamberti; S Krieger; M Sengteller; Peter Propping
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC protein.
Human genetics 1996;97(5):579-84.
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: Ortrud K Steinlein; S Weiland; J Stoodt; Peter Propping
Exon-intron structure of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4).
Genomics 1996;32(2):289-94.
1996: M Mandl; Reiner Caspari; A Jauch; T Böker; Heidrun Raschke; M Sengteller; Peter Propping; Waltraut Friedl
Familial adenomatous polyposis: a submicroscopic deletion at the APC locus in a family with mentally normal patients.
Human genetics 1996;97(2):204-8.
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.
1995: Peter Propping; Markus M Nöthen
Genetic variation of CNS receptors--a new perspective for pharmacogenetics.
Pharmacogenetics 1995;5(5):318-25.
1995: Ortrud K Steinlein; John C Mulley; Peter Propping; Robyn H Wallace; Hilary A Phillips; G R Sutherland; Ingrid E Scheffer; S F Berkovic
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
Nature genetics 1995;11(2):201-3.
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: 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.
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: R Paffenholz; M Mandl; Reiner Caspari; M Sengteller; Peter Propping; Waltraut Friedl
Eleven novel germline mutations in the adenomatous polyposis coli (APC) gene.
Human molecular genetics 1994;3(9):1703-4.
1994: M Mandl; Martina Kadmon; M Sengteller; Reiner Caspari; Peter Propping; Waltraut Friedl
A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosis.
Human molecular genetics 1994;3(6):1009-11.
1994: Waltraut Friedl; Reiner Caspari; Peter Propping
[Diagnosis of familial adenomatosis polyposis].
Deutsche medizinische Wochenschrift (1946) 1994;119(1-2):27-30.
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: M Mandl; R Paffenholz; Waltraut Friedl; Reiner Caspari; M Sengteller; Peter Propping
Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.
Human molecular genetics 1994;3(1):181-4.
1993: Waltraut Friedl; Peter Propping
[Progress in molecular genetic diagnosis].
Versicherungsmedizin / herausgegeben von Verband der Lebensversicherungs-Unternehmen e.V. und Verband der Privaten Krankenversicherung e.V 1993;45(6):179-84.
1993: Reiner Caspari; Waltraut Friedl; T Böker; A Augustin; M Mandl; K Jaeger; K Gallkowski; Peter Propping
Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods.
Zeitschrift für Gastroenterologie 1993;31(11):646-52.
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: Peter Propping; Klaus Zerres
ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
American journal of medical genetics 1993;45(5):642-8.
1993: M Faiyaz ul Haque; Siegfried Uhlhaas; Michael Knapp; H Schüler; Waltraut Friedl; M Ahmad; Peter Propping
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.
Human genetics 1993;91(1):17-9.
1993: J M Penzien; J Kappler; Norbert Herschkowitz; B Schuknecht; P Leinekugel; Peter Propping; T Tønnesen; H Lou; H Moser; S Zierz
Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease.
American journal of human genetics 1993;52(3):557-64.
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.
1991: J Kappler; P Leinekugel; Ernst Conzelmann; W J Kleijer; Alfried Kohlschuetter; T Tønnesen; M Rochel; F Freycon; Peter Propping
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.
Human genetics 1991;86(5):463-70.
1991: J Kappler; R W Watts; Ernst Conzelmann; D A Gibbs; Peter Propping; V Gieselmann
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy.
European journal of pediatrics 1991;150(4):287-90.
1991: J Kappler; W Pötter; V Gieselmann; W Kiessling; Waltraut Friedl; Peter Propping
Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis?
Developmental neuroscience 1991;13(4-5):228-31.
1990: J Körner; J Fritze; Peter Propping
RFLP alleles at the tyrosine hydroxylase locus: no association found to affective disorders.
Psychiatry research 1990;32(3):275-80.
1989: C Hohenschutz; P Eich; Waltraut Friedl; A Waheed; Ernst Conzelmann; Peter Propping
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications.
Human genetics 1989;82(1):45-8.
1988: J Körner; Siegfried Uhlhaas; J Mallet; Peter Propping; Andreas Gal
Further RFLPs at the human tyrosine hydroxylase locus.
Nucleic acids research 1988;16(18):9078.
1988: C Hohenschutz; Waltraut Friedl; K H Schlör; A Waheed; Ernst Conzelmann; Konrad Sandhoff; Peter Propping
Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology.
American journal of medical genetics 1988;31(1):169-75.
1986: Peter Propping; Waltraut Friedl; M Huschka; K H Schlör; F Reimer; M Lee-Vaupel; Ernst Conzelmann; Konrad Sandhoff
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patients.
Human genetics 1986;74(3):244-8.