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Olaf Riess

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Martin Kehrer; Olaf Riess; Karin Schäferhoff; Martin Schöning; Sylke Singer; Michael Bonin; Ute Grasshoff; Andreas Tzschach
12q24.33 deletion: Report of a patient with intellectual disability and review of the literature.
A Riess; Olaf Riess; E Rossier; M Alber; S Beck-Woedl; Andreas Dufke; D Gläser; Veronka Horber; R Krüger; Andreas Tzschach
Novel SLC9A6 mutations in two families with Christianson syndrome.
Alexandra Kelp; Arnulf H Koeppen; Claudia Bauer; Peter Bauer; Carsten Calaminus; Elisabeth Petrasch-Parwez; Bernd Pichler; Esteban Portal; Olaf Riess; Libo Yu-Taeger; Huu-Phuc Nguyen
A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers.

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2013: Martin Kehrer; Olaf Riess; Karin Schäferhoff; Martin Schöning; Sylke Singer; Michael Bonin; Ute Grasshoff; Andreas Tzschach
12q24.33 deletion: Report of a patient with intellectual disability and review of the literature.
American journal of medical genetics. Part A 2013;161(6):1409-13.
2013: A Riess; Olaf Riess; E Rossier; M Alber; S Beck-Woedl; Andreas Dufke; D Gläser; Veronka Horber; R Krüger; Andreas Tzschach
Novel SLC9A6 mutations in two families with Christianson syndrome.
Clinical genetics 2013;83(6):596-7.
2013: Alexandra Kelp; Arnulf H Koeppen; Claudia Bauer; Peter Bauer; Carsten Calaminus; Elisabeth Petrasch-Parwez; Bernd Pichler; Esteban Portal; Olaf Riess; Libo Yu-Taeger; Huu-Phuc Nguyen
A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2013;33(21):9068-81.
2013: Anastasia Gazou; Ute Grasshoff; Anna Jauch; Angelika Riess; Olaf Riess; Karin Schäferhoff; Michael Bonin; Andreas Tzschach
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability.
American journal of medical genetics. Part A 2013;161(4):860-4.
2013: Silke Nuber; Bernd J Pichler; Kai Schönig; Ryosuke Takahashi; Peter Teismann; Margaritha Trejo; Juergen Winkler; Hodaka Yamakado; Frank Zimmermann; Anthony Adame; Davide Amato; Claudia Bauer; Carsten Calaminus; Nicolas Casadei; Christiane Giel; Florian Harmuth; Poul H Jensen; Zacharias Kohl; Johannes Kornhuber; Eliezer Masliah; Christian P Müller; Olaf Riess
A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats.
Brain : a journal of neurology 2013;136(Pt 2):412-32.
2013: Arndt Rolfs; Reinhold Schmidt; Christian Tanislav; Turgut Tatlisumak; Ulf Bodechtel; Tobias Böttcher; Martin Dichgans; Christian Enzinger; Franz Fazekas; Anne-Katrin Giese; Ulrike Grittner; Michael G Hennerici; Peter U Heuschmann; Martin Holzhausen; Roman Huber; Gerhard Jan Jungehulsing; Manfred Kaps; Christof Kessler; Edwin Kolodny; Karl Lackner; Christoph Lichy; Peter Martus; Hermann Mascher; Wolfgang Meyer; Bo Norrving; Eduard Paschke; Jukaa Putaala; Olaf Riess
Acute cerebrovascular disease in the young: the Stroke in Young Fabry Patients study.
Stroke; a journal of cerebral circulation 2013;44(2):340-9.
2013: Huu-Phuc Nguyen; Olaf Riess; Jonasz Jeremiasz Weber; Stephan Grueninger; Jeannette Hübener; Andreas Weiss
Cerebellar Soluble Mutant Ataxin-3 Level Decreases during Disease Progression in Spinocerebellar Ataxia Type 3 Mice.
PloS one 2013;8(4):e62043.
2012: Libo Yu-Taeger; Carsten Calaminus; Laura E Clemens; Xiaofeng Gu; David Howland; Silke Metzger; Alexander Osmand; Larry Park; Elisabeth Petrasch-Parwez; Bernd Pichler; Adriana Redensek; Olaf Riess; X William Yang; Huu-Phuc Nguyen
A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012;32(44):15426-38.
2012: Angelika Riess; Olaf Riess; Karin Schäferhoff; Michael Bonin; Ute Grasshoff; Veronka Horber; Andreas Tzschach
Interstitial 3p25.3-p26.1 deletion in a patient with intellectual disability.
American journal of medical genetics. Part A 2012;158A(10):2587-90.
2012: N Brüggemann; Johann Hagenah; P Bauer; W Külper; K Lohmann; Thora Lohnau; Cristian Pattaro; Peter P Pramstaller; Olaf Riess; A Rolfs; R Siebert; Andreas Sprenger; V Tadic; H Tönnies; Peter Vieregge; Susen Winkler; Christine Klein
Autosomal dominant Parkinson's disease in a large German pedigree.
Acta neurologica Scandinavica 2012;126(2):129-37.
2012: Andreas Tzschach; Markus Wolff; Karin Schäferhoff; Andrea Bevot; Michael Bonin; Andreas Dufke; Ute Grasshoff; Karin Haas-Lude; Olaf Riess
Interstitial 9q34.11-q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palate.
American journal of medical genetics. Part A 2012;158A(7):1709-12.
2012: Kathrin Grundmann; Christian Haass; Till-Karsten Hauser; Jasmin Hettich; Giuseppina Martella; Huu-Phuc Nguyen; Brigitte Nuscher; Bernd Pichler; Antonio Pisani; Olaf Riess; Martin Schaller; Giuseppe Sciamanna; Libo Yu; Zhenyu Yue; Salvador Castaneda; Birgit Fehrenbacher; Nicola Glöckle; Thomas Ott
Generation of a novel rodent model for DYT1 dystonia.
Neurobiology of disease 2012;47(1):61-74.
2012: Jeannette Hübener; Maria Björkqvist; Nicolas Casadei; Olaf Riess; Mathias W Seeliger; Peter Teismann; Stephan von Hörsten; Huu-Phuc Nguyen
Automated behavioral phenotyping reveals presymptomatic alterations in a SCA3 genetrap mouse model.
Journal of genetics and genomics = Yi chuan xue bao 2012;39(6):287-99.
2012: Vinko Palada; Olaf Riess; Marta Romani; Sandra Stiern; Krzysztof Szczaluba; Michele Tinazzi; Enza Maria Valente; Domenico Ajena; Peter Bauer; Fatima Carrillo; Nicola Glöckle; Pilar Gómez-Garre; Pablo Mir; Ulrich Müller; Thomas Ott; Kathrin Grundmann
Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.
Movement disorders : official journal of the Movement Disorder Society 2012;27(7):917.
2012: Sandra Martins; António Amorim; Paula Coutinho; Paola Giunti; Laura P W Ranum; Olaf Riess; Hidenao Sasaki; Jorge Sequeiros; Bing-Wen Soong; Giovanni Stevanin; Shoji Tsuji; Virginia C N Wong; Garth A Nicholson
Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala.
Archives of neurology 2012;69(6):746-51.
2012: Juliane Hoyer; Corinna Petsch; Bernt Popp; Gudrun Rappold; Anita Rauch; Andreas Dufke; Arif B Ekici; Sabine Endele; Hartmut Engels; Ina Göhring; Olaf Riess; Eva Rossier; Evelin Schröck; Dagmar Wieczorek; Antje Wiesener; Eva Wohlleber; Alexander M Zink; Christiane Zweier; Markus Zweier; André Reis
Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability.
American journal of human genetics 2012;90(3):565-72.
2012: Peter Bauer; Lubov Blumkin; Tally Lerman-Sagie; Esther Leshinsky-Silver; Dorit Lev; Olaf Riess; Julia Schicks; Nina Schlipf; Christopher Schröder; Ludger Schöls
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) .
Neurogenetics 2012;13(1):73-6.
2012: Yu-Chun Tsai; Olaf Riess; Anne S Soehn; Huu-Phuc Nguyen
The Guanine nucleotide exchange factor kalirin-7 is a novel synphilin-1 interacting protein and modifies synphilin-1 aggregate transport and formation.
PloS one 2012;7(12):e51999.
2012: Yu-Chun Tsai; Silke Metzger; Olaf Riess; Anne S Soehn; Huu-Phuc Nguyen
Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients.
BMC medical genetics 2012;13():48.
2012: Suzana Gispert; Aaron D Gitler; Rejko Krüger; Alexander Kurz; Inga Liepelt; Albert C Ludolph; Olaf Riess; Stefan Waibel; Markus Weber; Peter Bauer; Tim Becker; Daniela Berg; Christof Geisen; Peter M Andersen; Georg Auburger
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect.
Neurobiology of disease 2012;45(1):356-61.
2011: Silke Nuber; Elisabeth Petrasch-Parwez; Anna Samarina; Jacqueline Schneider; Peter Teismann; Thirumalaisamy Palanichamy Velavan; Stephan von Hörsten; Oscar Arias-Carrión; Jana Boy; Carsten Calaminus; Rolf Dermietzel; Markus Fendt; Philipp J Kahle; Leanie Koch; Zacharias Kohl; Rejko Krüger; Huu-Phuc Nguyen; Olaf Riess
Olfactory neuron-specific expression of A30P α-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages.
Neurobiology of disease 2011;44(2):192-204.
2011: N A Schlipf; Sven Klimpe; Olaf Riess; J Schicks; Ludger Schöls; Rebecca Schüle; Matthis Synofzik; K N Karle; Peter Bauer
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients.
Clinical genetics 2011;80(2):148-60.
2011: Jeannette Hübener; Huu-Phuc Nguyen; Hans-Henning Arnold; Stefan Driessen; Claudia Funke; Adriane Gardyan; Thorsten Schmidt; Ina Schmitt; Franz Vauti; Hartwig Wolburg; Karen Wolburg-Buchholz; Yihong Ye; Olaf Riess
N-terminal ataxin-3 causes neurological symptoms with inclusions, endoplasmic reticulum stress and ribosomal dislocation.
Brain : a journal of neurology 2011;134(Pt 7):1925-42.
2011: Matthis Synofzik; Christian Beetz; Claudia Bauer; Michael Bonin; Elena Sanchez-Ferrero; Tanja Schmitz-Hübsch; Ullrich Wüllner; Thomas Nägele; Olaf Riess; Ludger Schöls; Peter Bauer
Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features.
Journal of medical genetics 2011;48(6):407-12.
2011: Francis Odeh; Trygve B Leergaard; Jana Boy; Thorsten Schmidt; Olaf Riess; Jan G Bjaalie
Atlas of transgenic Tet-Off Ca2+/calmodulin-dependent protein kinase II and prion protein promoter activity in the mouse brain.
NeuroImage 2011;54(4):2603-11.
2011: Katharina Rall; Olaf Riess; Karin Schaeferhoff; Birgitt Schoenfisch; Diethelm Wallwiener; Michael Walter; Gianmaria Barresi; Michael Bonin; Karina Haebig; Sven Poths; Sara Brucker
A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients.
Orphanet journal of rare diseases 2011;6():32.
2011: Hong Van B Che; Silke Metzger; Esteban Portal; Carolin Deyle; Olaf Riess; Huu-Phuc Nguyen
Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease.
Molecular neurodegeneration 2011;6(1):1.
2011: Arndt Rolfs; Peter Martus; Peter U Heuschmann; Ulrike Grittner; Martin Holzhausen; Turgut Tatlisumak; Tobias Böttcher; Franz Fazekas; Christian Enzinger; Stefan Ropele; Reinhold Schmidt; Olaf Riess; Bo Norrving
Protocol and methodology of the Stroke in Young Fabry Patients (sifap1) study: a prospective multicenter European study of 5,024 young stroke patients aged 18-55 years.
Cerebrovascular diseases (Basel, Switzerland) 2011;31(3):253-62.
2010: Lena F Burbulla; Carina Schelling; Hiroki Kato; Doron Rapaport; Dirk Woitalla; Carola Schiesling; Claudia Schulte; Manu Sharma; Thomas Illig; Peter Bauer; Stephan Jung; Alfred Nordheim; Ludger Schöls; Olaf Riess; Rejko Krüger
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis.
Human molecular genetics 2010;19(22):4437-52.
2010: Denise Horn; Johannes Kapeller; Núria Rivera-Brugués; Ute Moog; Bettina Lorenz-Depiereux; Sebastian Eck; Maja Hempel; Janine Wagenstaller; Alex Gawthrope; Anthony P Monaco; Michael Bonin; Olaf Riess; Eva Wohlleber; Thomas Illig; Connie R Bezzina; Andre Franke; Stephanie Spranger; Pablo Villavicencio-Lorini; Wenke Seifert; Jochen Rosenfeld; Eva Klopocki; Gudrun A Rappold; Tim M Strom
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Human mutation 2010;31(11):E1851-60.
2010: Peter Bauer; Giovanni Stevanin; Christian Beetz; Matthis Synofzik; Tanja Schmitz-Hübsch; Ullrich Wüllner; Eric Berthier; Elisabeth Ollagnon-Roman; Olaf Riess; Sylvie Forlani; Emeline Mundwiller; Alexandra Durr; Ludger Schöls; Alexis Brice
Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.
Journal of neurology, neurosurgery, and psychiatry 2010;81(11):1229-32.
2010: Silke Metzger; Meiju Saukko; Hong Van Che; Liang Tong; Yvonne Puder; Olaf Riess; Huu-Phuc Nguyen
Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7.
Human genetics 2010;128(4):453-9.
2010: Anne S Söhn; Nicola Glöckle; Andrea Duarte Doetzer; Günther Deuschl; Ute Felbor; Helge Topka; Ludger Schöls; Olaf Riess; Peter Bauer; Ulrich Müller; Kathrin Grundmann
Prevalence of THAP1 sequence variants in German patients with primary dystonia.
Movement disorders : official journal of the Movement Disorder Society 2010;25(12):1982-6.
2010: K Schaeferhoff; S Michalakis; N Tanimoto; M Dominik Fischer; E Becirovic; S C Beck; G Huber; N Rieger; Olaf Riess; Bernd Wissinger; Martin Biel; Mathias W Seeliger; Michael Bonin
Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice.
Cellular and molecular life sciences : CMLS 2010;67(18):3173-86.
2010: Nina A Schlipf; Christian Beetz; Rebecca Schüle; Giovanni Stevanin; Anne Kjersti Erichsen; Sylvie Forlani; Cécile Zaros; Kathrin Karle; Stephan Klebe; Sven Klimpe; Alexandra Durr; Susanne Otto; Chantal M E Tallaksen; Olaf Riess; Alexis Brice; Peter Bauer; Ludger Schöls
A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42).
European journal of human genetics : EJHG 2010;18(9):1065-7.
2010: Marta Valenza; Valerio Leoni; Joanna M Karasinska; Lara Petricca; Jianjia Fan; Jeffrey Carroll; Mahmoud A Pouladi; Elisa Fossale; Huu-Phuc Nguyen; Olaf Riess; Marcy E MacDonald; Cheryl L Wellington; Stefano DiDonato; Michael R Hayden; Elena Cattaneo
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2010;30(32):10844-50.
2010: Mahesh Kandasamy; Sebastien Couillard-Despres; Kerstin A Raber; Michael Stephan; Bernadette Lehner; Beate Winner; Zacharias Kohl; Francisco J Rivera; Huu-Phuc Nguyen; Olaf Riess; Ulrich Bogdahn; Jürgen Winkler; Stephan von Hörsten; Ludwig Aigner
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington disease.
Journal of neuropathology and experimental neurology 2010;69(7):717-28.
2010: Christopher Schroeder; Fanny Stutzmann; Bernhard H F Weber; Olaf Riess; Michael Bonin
High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays.
Breast cancer research and treatment 2010;122(1):287-97.
2010: Kay Seidel; Ludger Schöls; Silke Nuber; Elisabeth Petrasch-Parwez; Kristin Gierga; Zbigniew Wszolek; dennis dickson; WP Gai; Antje Bornemann; Olaf Riess; Abdelhaq Rami; Wilfried F A Den Dunnen; Thomas Deller; Udo Rüb; Rejko Krüger
First appraisal of brain pathology owing to A30P mutant alpha-synuclein.
Annals of neurology 2010;67(5):684-9.
2010: M Walter; Michael Bonin; Rachel Saunders-Pullman; E M Valente; M Loi; M Gambarin; D Raymond; M Tinazzi; Christoph Kamm; N Glöckle; Sven Poths; Thomas Gasser; Susan Bressman; Christine Klein; L J Ozelius; Olaf Riess; Kathrin Grundmann
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia.
Neurobiology of disease 2010;38(2):192-200.
2010: Anne S Soehn; Thomas Franck; Saskia Biskup; Emilie Giaime; Christian Melle; Ruth Rott; Daniel Cebo; Hubert Kalbacher; Erwin Ott; Jens Pahnke; Thomas Meitinger; Rejko Krüger; Thomas Gasser; Daniela Berg; Ferdinand von Eggeling; Simone Engelender; Cristine Alves da Costa; Olaf Riess
Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease.
Neurogenetics 2010;11(2):203-15.
2010: Jeannette Hübener; Olaf Riess
Polyglutamine-induced neurodegeneration in SCA3 is not mitigated by non-expanded ataxin-3: conclusions from double-transgenic mouse models.
Neurobiology of disease 2010;38(1):116-24.
2010: Silke Nuber; Thomas Franck; Hartwig Wolburg; Ulrike Schumann; Nicolas Casadei; Kristina Fischer; Carsten Calaminus; Bernd J Pichler; Sittinan Chanarat; Peter Teismann; Jörg B Schulz; Andreas R Luft; Jürgen Tomiuk; Johannes Wilbertz; Antje Bornemann; Rejko Krüger; Olaf Riess
Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in mice.
Neurogenetics 2010;11(1):107-20.
2010: Jana Boy; Thorsten Schmidt; Ulrike Schumann; Ute Grasshoff; Samy Unser; Carsten Holzmann; Ina Schmitt; Tim Karl; Franco Laccone; Hartwig Wolburg; Saleh Ibrahim; Olaf Riess
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats.
Neurobiology of disease 2010;37(2):284-93.
2010: Karina Haebig; Christian Johannes Gloeckner; Marta Garcia Miralles; Frank Gillardon; Claudia Schulte; Olaf Riess; Marius Ueffing; Saskia Biskup; Michael Bonin
ARHGEF7 (Beta-PIX) acts as guanine nucleotide exchange factor for leucine-rich repeat kinase 2.
PloS one 2010;5(10):e13762.
2010: M Dominik Fischer; Naoyuki Tanimoto; Susanne C Beck; Gesine Huber; Karin Schaeferhoff; Stylianos Michalakis; Olaf Riess; Bernd Wissinger; Martin Biel; Michael Bonin; Mathias W Seeliger
Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies.
Advances in experimental medicine and biology 2010;664():593-9.
2010: Guido Krebiehl; Sabine Ruckerbauer; Lena F Burbulla; Nicole Kieper; Brigitte Maurer; Jens Waak; Hartwig Wolburg; Zemfira Gizatullina; Frank N Gellerich; Dirk Woitalla; Olaf Riess; Philipp J Kahle; Tassula Proikas-Cezanne; Rejko Krüger
Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1.
PloS one 2010;5(2):e9367.
2010: Yvonne K Urbach; Felix J Bode; Huu-Phuc Nguyen; Olaf Riess; Stephan von Hörsten
Neurobehavioral tests in rat models of degenerative brain diseases.
Methods in molecular biology (Clifton, N.J.) 2010;597():333-56.
2010: Susanne C Beck; Karin Schaeferhoff; Stylianos Michalakis; M Dominik Fischer; Gesine Huber; Norman Rieger; Olaf Riess; Bernd Wissinger; Martin Biel; Michael Bonin; Mathias W Seeliger; Naoyuki Tanimoto
In vivo analysis of cone survival in mice.
Investigative ophthalmology & visual science 2010;51(1):493-7.
2009: Rebecca Schüle; N Schlipf; Matthis Synofzik; S Klebe; Sven Klimpe; U Hehr; Beate Winner; T Lindig; A Dotzer; Olaf Riess; Jürgen Winkler; Ludger Schöls; Peter Bauer
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.
Journal of neurology, neurosurgery, and psychiatry 2009;80(12):1402-4.
2009: Martin Regensburger; Zacharias Kohl; Kathrin Grundmann; Beate Winner; Olaf Riess; Jürgen Winkler
Adult neural precursor cells unaffected in animal models of DYT1 dystonia.
Neuroreport 2009;20(17):1529-33.
2009: Paul Michel Aloyse Antony; Simone Mäntele; Phillip Mollenkopf; Jana Boy; Ralph H Kehlenbach; Olaf Riess; Thorsten Schmidt
Identification and functional dissection of localization signals within ataxin-3.
Neurobiology of disease 2009;36(2):280-92.
2009: Anne S Soehn; Thu-Trang Pham; Karin Schaeferhoff; Thomas Floss; Daniela Vogt Weisenhorn; Wolfgang Wurst; Michael Bonin; Olaf Riess
Periphilin is strongly expressed in the murine nervous system and is indispensable for murine development.
Genesis (New York, N.Y. : 2000) 2009;47(10):697-707.
2009: Manu Sharma; Peter Lichtner; Rejko Kruger; Daniela Berg; Claudia Schulte; Thomas Illig; Olaf Riess; Thomas Gasser
Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease.
Neurobiology of aging 2009;30(10):1706-9.
2009: Claudia Funke; Jürgen Tomiuk; Olaf Riess; Daniela Berg; Anne S Soehn
Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patients.
Journal of neural transmission (Vienna, Austria : 1996) 2009;116(7):853-9.
2009: Dominic J McMullan; Michael Bonin; Jayne Y Hehir-Kwa; Bert B A de Vries; Andreas Dufke; Eleanor Rattenberry; Marloes Steehouwer; Luminita Moruz; Rolph Pfundt; Nicole de Leeuw; Angelika Riess; Ozge Altug-Teber; Herbert Enders; Sylke Singer; Ute Grasshoff; Michael Walter; Judith M Walker; Catherine V Lamb; E Val Davison; Louise Brueton; Olaf Riess; Joris Veltman
Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
Human mutation 2009;30(7):1082-92.
2009: Sonja W Scholz; Henry Houlden; Claudia Schulte; Manu Sharma; Abi Li; Daniela Berg; Anna Melchers; Reema Paudel; J Raphael Gibbs; Javier Simon-Sanchez; Coro Paisan-Ruiz; Jose Bras; Jinhui Ding; Honglei Chen; Bryan Joseph Traynor; Sampath Arepalli; Ryan R Zonozi; Tamas Revesz; Janice Holton; Nicholas W Wood; Andrew Lees; Wolfgang H Oertel; Ullrich Wüllner; Stefano Goldwurm; Maria Teresa Pellecchia; Thomas Illig; Olaf Riess; Hubert H Fernandez; Ramon L Rodriguez; Michael S Okun; Werner Poewe; Gregor K Wenning; John Hardy; Andrew Singleton; Francesca Del Sorbo; Susanne Schneider; Kailash P Bhatia; Thomas Gasser
SNCA variants are associated with increased risk for multiple system atrophy.
Annals of neurology 2009;65(5):610-4.
2009: Claudia Funke; Anne S Soehn; Jürgen Tomiuk; Olaf Riess; Daniela Berg
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patients.
Journal of neural transmission (Vienna, Austria : 1996) 2009;116(4):443-50.
2009: K Seidel; Rob A I de Vos; L Derksen; P Bauer; Olaf Riess; W den Dunnen; Thomas Deller; G Hageman; Udo Rüb
Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP).
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 2009;191(2):203-11.
2009: Franz Marxreiter; Silke Nuber; Mahesh Kandasamy; Jochen Klucken; Robert Aigner; Ralf Burgmayer; Sebastien Couillard-Despres; Olaf Riess; Jürgen Winkler; Beate Winner
Changes in adult olfactory bulb neurogenesis in mice expressing the A30P mutant form of alpha-synuclein.
The European journal of neuroscience 2009;29(5):879-90.
2009: Karina Häbig; Michael Walter; Heike Stappert; Olaf Riess; Michael Bonin
Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA--a key player in the pathogenesis of Parkinson's disease.
Brain research 2009;1256():19-33.
2009: Peter Bauer; Beate Winner; Rebecca Schüle; Claudia Bauer; Veronika Häfele; Ute Hehr; Michael Bonin; Michael Walter; Kathrin Karle; Thomas M Ringer; Olaf Riess; Jürgen Winkler; Ludger Schöls
Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization.
Neurogenetics 2009;10(1):43-8.
2008: Huu-Phuc Nguyen; Silke Metzger; Carsten Holzmann; Dirk Koczan; Hans-Jürgen Thiesen; Stephan von Hörsten; Olaf Riess; Michael Bonin
Age-dependent gene expression profile and protein expression in a transgenic rat model of Huntington's disease.
Proteomics. Clinical applications 2008;2(12):1638-50.
2008: B Zirn; K Grundmann; P Huppke; J Puthenparampil; H Wolburg; Olaf Riess; U Müller
Novel TOR1A mutation p.Arg288Gln in early-onset dystonia (DYT1).
Journal of neurology, neurosurgery, and psychiatry 2008;79(12):1327-30.
2008: Frank N Gellerich; Zemfira Gizatullina; Huu P Nguyen; Sonata Trumbeckaite; Stefan Vielhaber; Enn Seppet; Stephan Zierz; Bernhard Landwehrmeyer; Olaf Riess; Stephan von Hörsten; Frank Striggow
Impaired regulation of brain mitochondria by extramitochondrial Ca2+ in transgenic Huntington disease rats.
The Journal of biological chemistry 2008;283(45):30715-24.
2008: Paola Conforti; Catarina Ramos; Barbara L Apostol; Danielle A Simmons; Huu-Phuc Nguyen; Olaf Riess; Leslie Michels Thompson; Chiara Zuccato; Elena Cattaneo
Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: restoration by the neuroprotective compound CEP-1347.
Molecular and cellular neurosciences 2008;39(1):1-7.
2008: Felix J Bode; Michael Stephan; Hendrik Suhling; Reinhard Pabst; Rainer H Straub; Kerstin A Raber; Michael Bonin; Huu-Phuc Nguyen; Olaf Riess; Andreas Bauer; Charlotte Sjoberg; Asa Petersén; Stephan von Hörsten
Sex differences in a transgenic rat model of Huntington's disease: decreased 17beta-estradiol levels correlate with reduced numbers of DARPP32+ neurons in males.
Human molecular genetics 2008;17(17):2595-609.
2008: Hans-Hermann Hoepken; Suzana Gispert; Mekhman Azizov; Michael Klinkenberg; Filomena Ricciardi; Alexander Kurz; Blas Morales-Gordo; Michael Bonin; Olaf Riess; Thomas Gasser; Donat Kögel; Helmuth Steinmetz; Georg Auburger
Parkinson patient fibroblasts show increased alpha-synuclein expression.
Experimental neurology 2008;212(2):307-13.
2008: Claudia Wahl; Sabine Kautzmann; Guido Krebiehl; Karsten Strauss; Dirk Woitalla; Thomas Müller; Peter Bauer; Olaf Riess; Rejko Krüger
A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson's disease patients.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(8):1141-8.
2008: Michael Bonin; Frank P Marx; S Kautzmann; Olaf Riess; Rejko Krüger
Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(7):941-58.
2008: Kathrin Grundmann; Jeannette Hübener; Karina Häbig; Bettina Reischmann; Sven Poths; Till-Karsten Hauser; Janine Magg; Olaf Riess; Michael Bonin; Huu-Phuc Nguyen
Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinA.
Proteomics. Clinical applications 2008;2(5):720-36.
2008: Christopher Schroeder; Michael Walter; Daniela Berg; Petra Leitner; Peter Bauer; Zacharias Kohl; Jürgen Winkler; Olaf Riess; Michael Bonin
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease.
The Journal of molecular diagnostics : JMD 2008;10(3):217-24.
2008: K Häbig; M Walter; Sven Poths; Olaf Riess; Michael Bonin
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player.
Neurogenetics 2008;9(2):83-94.
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: Silke Nuber; Elisabeth Petrasch-Parwez; Beate Winner; Jürgen Winkler; Stephan von Hörsten; Thorsten Schmidt; Jana Boy; Melanie Kuhn; Huu-Phuc Nguyen; Peter Teismann; Jörg B Schulz; Manuela Neumann; Bernd J Pichler; Gerald Reischl; Carsten Holzmann; Ina Schmitt; Antje Bornemann; Wilfried Kuhn; Frank Zimmermann; Antonio Servadio; Olaf Riess
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(10):2471-84.
2008: Olaf Riess; Udo Rüb; Annalisa Pastore; Peter Bauer; Ludger Schöls
SCA3: neurological features, pathogenesis and animal models.
Cerebellum (London, England) 2008;7(2):125-37.
2008: Bernhard T Baune; Gerald Ponath; Matthias Rothermundt; Olaf Riess; Harald Funke; Klaus Berger
Association between genetic variants of IL-1beta, IL-6 and TNF-alpha cytokines and cognitive performance in the elderly general population of the MEMO-study.
Psychoneuroendocrinology 2008;33(1):68-76.
2007: Ute Hehr; Peter Bauer; Beate Winner; Rebecca Schüle; Akgün Olmez; Wolfgang Koehler; Gökhan Uyanik; Anna Engel; Daniela Lenz; Andrea Seibel; Andreas Hehr; Sonja Ploetz; Josep Gamez; Arndt Rolfs; Joachim Weis; Thomas M Ringer; Michael Bonin; Gerhard Schuierer; Jörg Marienhagen; Ulrich Bogdahn; Bernhard H F Weber; Haluk Topaloglu; Ludger Schols; Olaf Riess; Jürgen Winkler
Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
Annals of neurology 2007;62(6):656-65.
2007: Sandra Martins; Francesc Calafell; Claudia Gaspar; Virginia C N Wong; Isabel Silveira; Garth A Nicholson; Ewout R Brunt; Lisbeth Tranebjaerg; Giovanni Stevanin; Mingli Hsieh; bing-wen soong; Leal Loureiro; Alexandra Dürr; Shoji Tsuji; Mitsunori Watanabe; Laura B Jardim; Paola Giunti; Olaf Riess; Laura P W Ranum; Alexis Brice; Guy Rouleau; Paula Coutinho; António Amorim; Jorge Sequeiros
Asian origin for the worldwide-spread mutational event in Machado-Joseph disease.
Archives of neurology 2007;64(10):1502-8.
2007: Kathrin Grundmann; B Reischmann; Greetje Vanhoutte; J Hübener; Peter Teismann; Till-Karsten Hauser; Michael Bonin; Johannes Wilbertz; S Horn; H P Nguyen; M Kuhn; S Chanarat; Hartwig Wolburg; Annemie Van der Linden; Olaf Riess
Overexpression of human wildtype torsinA and human DeltaGAG torsinA in a transgenic mouse model causes phenotypic abnormalities.
Neurobiology of disease 2007;27(2):190-206.
2007: Ulrike Bichelmeier; Thorsten Schmidt; Jeannette Hübener; Jana Boy; Lukas Rüttiger; Karina Häbig; Sven Poths; Michael Bonin; Marlies Knipper; Werner J Schmidt; Johannes Wilbertz; Hartwig Wolburg; Franco Laccone; Olaf Riess
Nuclear localization of ataxin-3 is required for the manifestation of symptoms in SCA3: in vivo evidence.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(28):7418-28.
2007: Frank P Marx; Anne S Soehn; Daniela Berg; Christian Melle; Carola Schiesling; Mira Lang; Sabine Kautzmann; Karsten M Strauss; Thomas Franck; Simone Engelender; Jens Pahnke; Simon Dawson; Ferdinand von Eggeling; Jörg B Schulz; Olaf Riess; Rejko Krüger
The proteasomal subunit S6 ATPase is a novel synphilin-1 interacting protein--implications for Parkinson's disease.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007;21(8):1759-67.
2007: Elisabeth Petrasch-Parwez; Huu-Phuc Nguyen; Marlen Löbbecke-Schumacher; Hans-Werner Habbes; Stefan Wieczorek; Olaf Riess; Karl-Hermann Andres; Rolf Dermietzel; Stephan von Hörsten
Cellular and subcellular localization of Huntingtin [corrected] aggregates in the brain of a rat transgenic for Huntington disease.
The Journal of comparative neurology 2007;501(5):716-30.
2007: Melanie Kuhn; Karina Haebig; Michael Bonin; Natalia Ninkina; Vladimir L Buchman; Sven Poths; Olaf Riess
Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein.
Neurogenetics 2007;8(2):71-81.
2007: Nadine Abahuni; Suzana Gispert; Peter Bauer; Olaf Riess; Rejko Krüger; Tim Becker; Georg Auburger
Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease.
Neuroscience letters 2007;414(2):126-9.
2007: O Altug-Teber; Michael Bonin; M Walter; Ulrike Angelika Mau-Holzmann; Andreas Dufke; H Stappert; Ismail Tekesin; H Heilbronner; Kay Nieselt; Olaf Riess
Specific transcriptional changes in human fetuses with autosomal trisomies.
Cytogenetic and genome research 2007;119(3-4):171-84.
2007: Jürgen Tomiuk; Lutz Bachmann; Claudia Bauer; Arndt Rolfs; Ludger Schöls; Christian Roos; Hans Zischler; Mathias M Schuler; Silke Bruntner; Olaf Riess; Peter Bauer
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach.
European journal of human genetics : EJHG 2007;15(1):81-7.
2006: Thomas Franck; R Krueger; Dirk Woitalla; Thomas Müller; Simone Engelender; Olaf Riess
Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2006;113(12):1903-8.
2006: Huu-Phuc Nguyen; Philipp Kobbe; Henning Rahne; Till Wörpel; Burkard Jäger; Michael Stephan; Reinhard Pabst; Carsten Holzmann; Olaf Riess; Hubert Korr; Orsolya Kántor; Elisabeth Petrasch-Parwez; Ronald B. Wetzel; Alexander Osmand; Stephan von Hörsten
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease.
Human molecular genetics 2006;15(21):3177-94.
2006: Jana Boy; Trygve B Leergaard; Thorsten Schmidt; Francis Odeh; Ulrike Bichelmeier; Silke Nuber; Carsten Holzmann; Andreas Wree; Stanley B Prusiner; Hermann Bujard; Olaf Riess; Jan G Bjaalie
Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease models.
NeuroImage 2006;33(2):449-62.
2006: Nilgün Akbas; Helmine Hochstrasser; Joelle Deplazes; Jürgen Tomiuk; Peter Bauer; Uwe Walter; Stefanie Behnke; Olaf Riess; Daniela Berg
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra.
Neuroscience letters 2006;407(1):16-9.
2006: Peter Bauer; Friedmar R Kreuz; Katrin Bürk; Carsten Saft; Jürgen Andrich; Hubert Heilemann; Olaf Riess; Ludger Schöls
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
Movement disorders : official journal of the Movement Disorder Society 2006;21(10):1734-7.
2006: Silke Metzger; Peter Bauer; Jürgen Tomiuk; Franco Laccone; Stefano Didonato; Cinzia Gellera; Caterina Mariotti; Herwig W Lange; Helga Weirich-Schwaiger; Gregor K Wenning; Klaus Seppi; Béla Melegh; Viktoria Havasi; Laszlo Balikó; Stefan Wieczorek; Jacek Zaremba; Dorota Hoffman-Zacharska; Anna Sulek; A Nazli Basak; Esra Soydan; Jana Zidovska; Vera Kebrdlova; Massimo Pandolfo; Pascale Ribaï; Ludovit Kadasi; Marta Kvasnicova; Bernhard H F Weber; Friedmar Kreuz; Matthias Dose; Manfred Stuhrmann; Olaf Riess
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease.
Human genetics 2006;120(2):285-92.
2006: Demetrius M Maraganore; Mariza de Andrade; Alexis Elbaz; Matthew J Farrer; John Ioannidis; Rejko Krüger; Walter A Rocca; Nicole K Schneider; Timothy G Lesnick; Sarah J Lincoln; Mary Hulihan; Jan Aasly; Tetsuo Ashizawa; Marie-Christine Chartier-Harlin; Harvey Checkoway; Carlo Ferrarese; Georgios M Hadjigeorgiou; Nobutaka Hattori; Hideshi Kawakami; jean-charles lambert; Timothy Lynch; George D Mellick; Spiridon Papapetropoulos; Abbas Parsian; Aldo Quattrone; Olaf Riess; Eng-King Tan; Christine Van Broeckhoven
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
JAMA : the journal of the American Medical Association 2006;296(6):661-70.
2006: Peter Bauer; Ludger Schöls; Olaf Riess
Spectrin mutations in spinocerebellar ataxia (SCA).
BioEssays : news and reviews in molecular, cellular and developmental biology 2006;28(8):785-7.
2006: Orsolya Kántor; Yasin Temel; Carsten Holzmann; Kerstin Raber; Huu-Phuc Nguyen; Chunyan Cao; Hatice Ozen Türkoglu; Bart P F Rutten; Veerle Visser-Vandewalle; Harry W M Steinbusch; Arjan Blokland; Hubert Korr; Olaf Riess; Stephan von Hörsten; Christoph Schmitz
Selective striatal neuron loss and alterations in behavior correlate with impaired striatal function in Huntington's disease transgenic rats.
Neurobiology of disease 2006;22(3):538-47.
2006: Christina S Schuetz; Michael Bonin; Susan E Clare; Kay Nieselt; Karl Sotlar; Michael Walter; Tanja Fehm; Erich Solomayer; Olaf Riess; Diethelm Wallwiener; Raffael Kurek; Hans Neubauer
Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysis.
Cancer research 2006;66(10):5278-86.
2006: C Winkler; Joana M A C Gil; Inês M Araújo; Olaf Riess; Thomas Skripuletz; Stephan von Hörsten; Asa Petersén
Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat.
Brain research bulletin 2006;69(3):306-10.
2006: Markus Konieczny; Peter Bauer; Jürgen Tomiuk; Gabriele Weisser; Jean Haan; Klaus Berger; Olaf Riess; Ludger Schöls
CAG repeats in Restless Legs syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(2):173-6.
2006: Silke Metzger; Peter Bauer; Juergen Tomiuk; Franco Laccone; Stefano Didonato; Cinzia Gellera; Paola Soliveri; Herwig W Lange; Helga Weirich-Schwaiger; Gregor K Wenning; Béla Melegh; Viktoria Havasi; Lazlo Balikó; Stefan Wieczorek; Larissa Arning; Jacek Zaremba; Anna Sulek; Dorota Hoffman-Zacharska; A Nazli Basak; Nagehan Ersoy; Jana Zidovska; Vera Kebrdlova; Massimo Pandolfo; Pascale Ribaï; Ludovit Kadasi; Marta Kvasnicova; Bernhard H F Weber; Friedmar Kreuz; Matthias Dose; Manfred Stuhrmann; Olaf Riess
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease.
Neurogenetics 2006;7(1):27-30.
2006: Olaf Riess; Rejko Krüger; Helmine Hochstrasser; Anne S Soehn; S Nuber; Thomas Franck; Daniela Berg
Genetic causes of Parkinson's disease: extending the pathway.
Journal of neural transmission. Supplementum 2006;(70):181-9.
2006: Daniela Berg; Helmine Hochstrasser; Katherine J Schweitzer; Olaf Riess
Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarker.
Neurotoxicity research 2006;9(1):1-13.
2006: Robert Hering; Rosario Frade-Martinez; Thomas Bajanowski; Christian F Poets; Frank Tschentscher; Olaf Riess
Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(1):55-8.
2005: Stephan Klebe; Alexandra Durr; Alexander Rentschler; Valerie Hahn-Barma; Michael Abele; Naima Bouslam; Ludger Schöls; Pierre Jedynak; Sylvie Forlani; Elodie Denis; Christel Dussert; Yves Agid; Peter Bauer; Christoph Globas; Ullrich Wüllner; Alexis Brice; Olaf Riess; Giovanni Stevanin
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
Annals of neurology 2005;58(5):720-9.
2005: Helmine Hochstrasser; Jürgen Tomiuk; Uwe Walter; Stefanie Behnke; Jörg Spiegel; Rejko Krüger; Georg Becker; Olaf Riess; Daniela Berg
Functional relevance of ceruloplasmin mutations in Parkinson's disease.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(13):1851-3.
2005: Christine Klein; Ana Djarmati; Katja Hedrich; Nora Schäfer; Cesa Scaglione; Roberta Marchese; Norman Kock; Birgitt Schuele; Anja Hiller; Thora Lohnau; Susen Winkler; Karin Wiegers; Robert Hering; Peter Bauer; Olaf Riess; Giovanni Abbruzzese; Paolo Martinelli; Peter P Pramstaller
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.
European journal of human genetics : EJHG 2005;13(9):1086-93.
2005: Daniela Berg; Marc Niwar; Sylvia Maass; Alexander Zimprich; J Carsten Möller; Ullrich Wüllner; Tanja Schmitz-Hübsch; Christine Klein; Eng-King Tan; Ludger Schöls; Laura Marsh; Ted M Dawson; Bernd Janetzky; Thomas Müller; Dirk Woitalla; Vladimir Kostic; Peter P Pramstaller; Wolfgang H Oertel; Peter Bauer; Rejko Krueger; Thomas Gasser; Olaf Riess
Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patients.
Movement disorders : official journal of the Movement Disorder Society 2005;20(9):1191-4.
2005: Anne Hofer; Daniela Berg; Friedrich Asmus; M Niwar; Gerhard Ransmayr; M Riemenschneider; Silvia Beatrice Bonelli; Michaela Steffelbauer; A Ceballos-Baumann; Peter Haussermann; Stefanie Behnke; Rejko Krüger; Jürgen Prestel; Manu Sharma; Alexander Zimprich; Olaf Riess; Thomas Gasser
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies.
Journal of neural transmission (Vienna, Austria : 1996) 2005;112(9):1249-54.
2005: Andreas Bauer; Karl Zilles; Andreas Matusch; Carsten Holzmann; Olaf Riess; Stephan von Hörsten
Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation.
Journal of neurochemistry 2005;94(3):639-50.
2005: Ozge Altug-Teber; Andreas Dufke; Sven Poths; Ulrike Angelika Mau-Holzmann; Murat Bastepe; Laurence Colleaux; Valérie Cormier-Daire; Thomas Eggermann; Gabriele Gillessen-Kaesbach; Michael Bonin; Olaf Riess
A rapid microarray based whole genome analysis for detection of uniparental disomy.
Human mutation 2005;26(2):153-9.
2005: Sabine Stahl; Carina Ittrich; Philip Marx-Stoelting; Christoph Köhle; Ozge Altug-Teber; Olaf Riess; Michael Bonin; Jürgen Jobst; Stephan Kaiser; Albrecht Buchmann; Michael Schwarz
Genotype-phenotype relationships in hepatocellular tumors from mice and man.
Hepatology (Baltimore, Md.) 2005;42(2):353-61.
2005: Karsten M Strauss; L Miguel Martins; Helene Plun-Favreau; Frank P Marx; Sabine Kautzmann; Daniela Berg; Thomas Gasser; Zbigniew K Wszolek; Thomas Müller; Antje Bornemann; Hartwig Wolburg; Julian Downward; Olaf Riess; Jörg B Schulz; Rejko Krüger
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.
Human molecular genetics 2005;14(15):2099-111.
2005: Jochen Reiss; Michael Bonin; Herbert Schwegler; Jörn Oliver Sass; Enrico Garattini; Silke Wagner; Heon-Jin Lee; Wolfgang Engel; Olaf Riess; Günter Schwarz
The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis.
Molecular genetics and metabolism 2005;85(1):12-20.
2005: Maike Jaworski; Albrecht Buchmann; Peter Bauer; Olaf Riess; Michael Schwarz
B-raf and Ha-ras mutations in chemically induced mouse liver tumors.
Oncogene 2005;24(7):1290-5.
2005: Georg Lamprecht; Ulrike A Mau; Christian Kortum; Armin Raible; Martin Stern; Olaf Riess; Michael Gregor
Relapsing pancreatitis due to a novel compound heterozygosity in the CFTR gene involving the second most common mutation in central and eastern Europe [CFTRdele2,3(21 kb)].
Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2005;5(1):92-6; discussion 95-6.
2004: Andreas Lazar; U A Mau-Holzmann; H Kolb; H E Reichenmiller; Olaf Riess; Edgar Schömig
Multiple organ failure due to 5-fluorouracil chemotherapy in a patient with a rare dihydropyrimidine dehydrogenase gene variant.
Onkologie 2004;27(6):559-62.
2004: Helmine Hochstrasser; Peter Bauer; Uwe Walter; Stefanie Behnke; Jörg Spiegel; Ilona Csoti; B Zeiler; A Bornemann; Jens Pahnke; Georg Becker; Olaf Riess; Daniela Berg
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease.
Neurology 2004;63(10):1912-7.
2004: Kathrin Grundmann; Ulrike Laubis-Herrmann; Dirk Dressler; Juliane Vollmer-Haase; Peter Bauer; Manfred Stuhrmann; Thorsten Schulte; Ludger Schöls; Helge Topka; Olaf Riess
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias.
Movement disorders : official journal of the Movement Disorder Society 2004;19(11):1294-7.
2004: Kathrin Grundmann; Ulrike Laubis-Herrmann; Dirk Dressler; Juliane Vollmer-Haase; Peter Bauer; Manfred Stuhrmann; Thorsten Schulte; Ludger Schöls; Helge Topka; Olaf Riess
Mutation at the SCA17 locus is not a common cause of primary dystonia.
Journal of neurology 2004;251(10):1232-4.
2004: Robert Hering; Karsten M Strauss; Xiao Tao; Andreas Bauer; Dirk Woitalla; Eva-Maria Mietz; Slobodanka Petrovic; Peter Bauer; Wilhelm Schaible; Thomas Müller; Ludger Schöls; Christine Klein; Daniela Berg; Philipp T Meyer; Jörg B Schulz; Bernd Wollnik; Liang Tong; Rejko Krüger; Olaf Riess
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).
Human mutation 2004;24(4):321-9.
2004: Michael Bonin; Sven Poths; H Osaka; Y-L Wang; K Wada; Olaf Riess
Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathways.
Brain research. Molecular brain research 2004;126(1):88-97.
2004: Ana Djarmati; Katja Hedrich; Marina Svetel; Nora Schäfer; Vladislava Juric; Slobodanka Vukosavic; Robert Hering; Olaf Riess; Stanka Romac; Christine Klein; Vladimir Kostic
Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.
Human mutation 2004;23(5):525.
2004: Ludger Schöls; Peter Bauer; Thorsten Schmidt; Thorsten Schulte; Olaf Riess
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Lancet neurology 2004;3(5):291-304.
2004: Robert Hering; S Petrovic; E-M Mietz; Carsten Holzmann; Daniela Berg; Peter Bauer; Dirk Woitalla; Thomas Müller; Klaus Berger; Rejko Krüger; Olaf Riess
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.
Neurology 2004;62(7):1231-2.
2004: Esti Liani; Allon Eyal; Eyal Avraham; Revital Shemer; Raymonde Szargel; Daniela Berg; Antje Bornemann; Olaf Riess; Christopher A Ross; Ruth Rott; Simone Engelender
Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(15):5500-5.
2004: J Deplazes; K Schöbel; Helmine Hochstrasser; Peter Bauer; Uwe Walter; Stefanie Behnke; Jörg Spiegel; Georg Becker; Olaf Riess; Daniela Berg
Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra.
Journal of neural transmission (Vienna, Austria : 1996) 2004;111(4):515-21.
2004: P Bauer; Franco Laccone; Arndt Rolfs; Ullrich Wüllner; S Bösch; Hartmut Peters; S Liebscher; M Scheible; J T Epplen; Bernhard H F Weber; E Holinski-Feder; H Weirich-Schwaiger; Deborah J Morris-Rosendahl; J Andrich; Olaf Riess
Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype.
Journal of medical genetics 2004;41(3):230-2.
2004: Katja Hedrich; Ana Djarmati; Nora Schäfer; Robert Hering; Claudia Wellenbrock; Peter H Weiss; Rüdiger Hilker; Peter Vieregge; Laurie J Ozelius; Peter Heutink; Vincenzo Bonifati; Eberhard Schwinger; Anthony E Lang; J Noth; Susan Bressman; Peter P Pramstaller; Olaf Riess; Christine Klein
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
Neurology 2004;62(3):389-94.
2004: A S Glass; duong huynh; Thomas Franck; Dirk Woitalla; Thomas Müller; Stef pulst; Daniela Berg; Rejko Krüger; Olaf Riess
Screening for mutations in synaptotagmin XI in Parkinson's disease.
Journal of neural transmission. Supplementum 2004;(68):21-8.
2004: Katja Hedrich; Nora Schäfer; Robert Hering; Johann Hagenah; Andrea J Lanthaler; Eberhard Schwinger; Patricia L Kramer; Laurie J Ozelius; Susan Bressman; Giovanni Abbruzzese; Paolo Martinelli; Vladimir Kostic; Peter P Pramstaller; Peter Vieregge; Olaf Riess; Christine Klein
The R98Q variation in DJ-1 represents a rare polymorphism.
Annals of neurology 2004;55(1):145; author reply 145-6.
2003: Bettina Felletschin; Peter Bauer; Uwe Walter; Stefanie Behnke; Jörg Spiegel; Ilona Csoti; Ulrike Sommer; Björn Zeiler; Georg Becker; Olaf Riess; Daniela Berg
Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra.
Neuroscience letters 2003;352(1):53-6.
2003: Rejko Krüger; Christian Fischer; Thorsten Schulte; Karsten M Strauss; Thomas Müller; Dirk Woitalla; Daniela Berg; Marcel Hungs; René Gobbele; Klaus Berger; Jörg T Epplen; Olaf Riess; Ludger Schöls
Mutation analysis of the neurofilament M gene in Parkinson's disease.
Neuroscience letters 2003;351(2):125-9.
2003: Kathrin Grundmann; Ulrike Laubis-Herrmann; Ingrid Bauer; Dirk Dressler; Juliane Vollmer-Haase; Peter Bauer; Manfred Stuhrmann; Thorsten Schulte; Ludger Schöls; Helge Topka; Olaf Riess
Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.
Archives of neurology 2003;60(9):1266-70.
2003: Arndt Rolfs; Arnulf H Koeppen; Ingrid Bauer; Peter Bauer; Sven Buhlmann; Helge Topka; Ludger Schöls; Olaf Riess
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
Annals of neurology 2003;54(3):367-75.
2003: Daniela Berg; Carsten Holzmann; Olaf Riess
14-3-3 proteins in the nervous system.
Nature reviews. Neuroscience 2003;4(9):752-62.
2003: Daniela Berg; Olaf Riess; Antje Bornemann
Specification of 14-3-3 proteins in Lewy bodies.
Annals of neurology 2003;54(1):135.
2003: Ludger Schöls; Ingrid Bauer; Christine Zühlke; Thorsten Schulte; Christina Kölmel; Katrin Bürk; Helge Topka; Peter Bauer; Horst Przuntek; Olaf Riess
Do CTG expansions at the SCA8 locus cause ataxia?
Annals of neurology 2003;54(1):110-5.
2003: T Schulte; Stefan Boehringer; Ludger Schöls; Thomas Müller; C Fischer; Olaf Riess; Horst Przuntek; K Berger; Jörg T Epplen; Rejko Krüger
Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2003;110(7):749-55.
2003: Frank P Marx; Carsten Holzmann; Karsten M Strauss; Lei Li; Olaf Eberhardt; Ellen Gerhardt; Mark Cookson; Dena Hernandez; Matthew J Farrer; Jennifer Kachergus; Simone Engelender; Christopher A Ross; Klaus Berger; Ludger Schöls; Jörg B Schulz; Olaf Riess; Rejko Krüger
Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.
Human molecular genetics 2003;12(11):1223-31.
2003: Stephan von Hörsten; Ina Schmitt; Huu-Phuc Nguyen; Carsten Holzmann; Thorsten Schmidt; Thomas Walther; Michael Bader; Reinhard Pabst; Philipp Kobbe; Jana Krotova; Detlef Stiller; Ants Kask; Annika Vaarmann; Silvia Rathke-Hartlieb; Jörg B Schulz; Ute Grasshoff; Ingrid Bauer; Ana Maria Menezes Vieira-Saecker; Martin Paul; Lesley Jones; Katrin S Lindenberg; Bernhard G Landwehrmeyer; Andreas Bauer; Xiao-Jiang Li; Olaf Riess
Transgenic rat model of Huntington's disease.
Human molecular genetics 2003;12(6):617-24.
2003: Olaf Riess; Daniela Berg; Rejko Krüger; Jörg B Schulz
Therapeutic strategies for Parkinson's disease based on data derived from genetic research.
Journal of neurology 2003;250 Suppl 1():I3-10.
2003: Carsten Holzmann; Rejko Krüger; A M M Vieira Saecker; Ina Schmitt; Ludger Schöls; Klaus Berger; Olaf Riess
Polymorphisms of the alpha-synuclein promoter: expression analyses and association studies in Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2003;110(1):67-76.
2003: Hirokazu Kobayashi; Rejko Krüger; Katerina Markopoulou; Zbigniew K Wszolek; Bruce Chase; Hikari Taka; Reiko Mineki; Kimie Murayama; Olaf Riess; Yoshikuni Mizuno; Nobutaka Hattori
Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
Brain : a journal of neurology 2003;126(Pt 1):32-42.
2002: Andreas Ubl; Daniela Berg; Carsten Holzmann; Rejko Krüger; Klaus Berger; Thomas Arzberger; Antje Bornemann; Olaf Riess
14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 eta.
Brain research. Molecular brain research 2002;108(1-2):33-9.
2002: Peter Riederer; Gabriele Gille; Thomas Müller; Horst Przuntek; Heinz Reichmann; Olaf Riess; A Schwartz; Johannes Schwarz; T Vogt
Practical importance of neuroprotection in Parkinson's disease.
Journal of neurology 2002;249 Suppl 3():III/53-6.
2002: Olaf Riess; Rejko Krüger; Jörg B Schulz
Spectrum of phenotypes and genotypes in Parkinson's disease.
Journal of neurology 2002;249 Suppl 3():III/15-20.
2002: Nils Rahner; Carsten Holzmann; Rejko Krüger; Ludger Schöls; Klaus Berger; Olaf Riess
Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease.
Brain research 2002;951(1):82-6.
2002: P Wintermeyer; Olaf Riess; Ludger Schöls; Horst Przuntek; Bianca Miterski; Jörg T Epplen; Rejko Krüger
Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patients.
Journal of neural transmission (Vienna, Austria : 1996) 2002;109(9):1181-8.
2002: Ingrid Bauer; Martin Gencik; Franco Laccone; Hartmut Peters; Bernhard H F Weber; Elke Holinski Feder; Helga Weirich; Deborah J Morris-Rosendahl; Arndt Rolfs; Alexandra Gencikova; Peter Bauer; Gregor Wenning; Jörg T Epplen; Susan E Holmes; Russell L Margolis; Christopher A Ross; Olaf Riess
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype.
Annals of neurology 2002;51(5):662.
2002: Rejko Krüger; Olaf Eberhardt; Olaf Riess; Jörg B Schulz
Parkinson's disease: one biochemical pathway to fit all genes?
Trends in molecular medicine 2002;8(5):236-40.
2002: Michael Abele; Katrin Bürk; Ludger Schöls; S Schwartz; I Besenthal; Johannes Dichgans; Christine Zühlke; Olaf Riess; Thomas Klockgether
The aetiology of sporadic adult-onset ataxia.
Brain : a journal of neurology 2002;125(Pt 5):961-8.
2002: Thorsten Schmidt; Katrin S Lindenberg; Antje Krebs; Ludger Schöls; Franco Laccone; Jochen Herms; Martin Rechsteiner; Olaf Riess; G Bernhard Landwehrmeyer
Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions.
Annals of neurology 2002;51(3):302-10.
2001: Karla P Figueroa; P Chan; L Schöls; Caroline M Tanner; Olaf Riess; Susan L Perlman; Daniel Geschwind; Stef pulst
Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia.
Archives of neurology 2001;58(10):1649-53.
2001: Rejko Krüger; Ludger Schöls; Thomas Müller; Wilfried Kuhn; Dirk Woitalla; Horst Przuntek; Jörg T Epplen; Olaf Riess
Evaluation of the gamma-synuclein gene in German Parkinson's disease patients.
Neuroscience letters 2001;310(2-3):191-3.
2001: Carsten Holzmann; Thorsten Schmidt; G Thiel; Jörg T Epplen; Olaf Riess
Functional characterization of the human Huntington's disease gene promoter.
Brain research. Molecular brain research 2001;92(1-2):85-97.
2001: Linda B Moran; Siegfried Kösel; Christoph Spitzer; Franz-Werner Schwaiger; Olaf Riess; Georg W Kreutzberg; Manuel B Graeber
Expression of alpha-synuclein in non-apoptotic, slowly degenerating facial motoneurones.
Journal of neurocytology 2001;30(6):515-21.
2001: Rejko Krüger; Wilfried Kuhn; Klaus L Leenders; Reiner Sprengelmeyer; Thomas Müller; Dirk Woitalla; Axel T Portman; R P Maguire; L Veenma; U Schröder; Ludger Schöls; Jörg T Epplen; Olaf Riess; Horst Przuntek
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.
Neurology 2001;56(10):1355-62.
2001: Christine Zühlke; Yorck Hellenbroich; Andreas Dalski; N Kononowa; Johann Hagenah; Peter Vieregge; Olaf Riess; Christine Klein; Eberhard Schwinger
Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia.
European journal of human genetics : EJHG 2001;9(3):160-4.
2001: Claudia Gaspar; Iscia Lopes-Cendes; S Hayes; Jun Goto; K Arvidsson; Adelaide Dias; Isabel Silveira; Patrícia Maciel; Paula Coutinho; M Lima; Y X Zhou; bing-wen soong; Masahiko Watanabe; Paola Giunti; Giovanni Stevanin; Olaf Riess; H Sasaki; M Hsieh; G A Nicholson; E Brunt; J J Higgins; M Lauritzen; Lisbeth Tranebjaerg; V Volpini; Nicholas W Wood; Laura P W Ranum; Shoji Tsuji; Alexis Brice; Jorge Sequeiros; Guy Rouleau
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
American journal of human genetics 2001;68(2):523-8.
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: Anil Batra; G Gelfort; Mathias Bartels; H Smoltczyk; Gerhard Buchkremer; Olaf Riess; L Schöls
The dopamine D2 receptor (DRD2) gene-a genetic risk factor in heavy smoking?
Addiction biology 2000;5(4):429-36.
2000: Dagmar Wieczorek; M Krause; Frank Majewski; Beate Albrecht; Peter Meinecke; Olaf Riess; Gabriele Gillessen-Kaesbach
Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).
Journal of medical genetics 2000;37(10):798-804.
2000: Ludger Schöls; S Peters; Sandra Szymanski; Rejko Krüger; S Lange; Cornelia Hardt; Olaf Riess; Horst Przuntek
Extrapyramidal motor signs in degenerative ataxias.
Archives of neurology 2000;57(10):1495-500.
2000: Rejko Krüger; AM Menezes Saecker; Ludger Schöls; Wilfried Kuhn; Thomas Müller; Dirk Woitalla; Daniela Berg; K Berger; Horst Przuntek; Jörg T Epplen; Olaf Riess
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.
Neuroreport 2000;11(11):2439-42.
2000: Ludger Schöls; Sandra Szymanski; S Peters; Horst Przuntek; J T Epplen; Cornelia Hardt; Olaf Riess
Genetic background of apparently idiopathic sporadic cerebellar ataxia.
Human genetics 2000;107(2):132-7.
2000: S Hayes; Gustavo Turecki; Kateri Brisebois; Iscia Lopes-Cendes; Claudia Gaspar; Olaf Riess; Laura P W Ranum; Stef pulst; Guy Rouleau
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).
Human molecular genetics 2000;9(12):1753-8.
2000: P Wintermeyer; Rejko Krüger; Wilfried Kuhn; Thomas Müller; Dirk Woitalla; Daniela Berg; G Becker; E Leroy; Mihael H Polymeropoulos; K Berger; Horst Przuntek; Ludger Schöls; Jörg T Epplen; Olaf Riess
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.
Neuroreport 2000;11(10):2079-82.
2000: Dagmar Wieczorek; M Krause; Frank Majewski; Beate Albrecht; Denise Horn; Olaf Riess; Gabriele Gillessen-Kaesbach
Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
European journal of human genetics : EJHG 2000;8(7):519-26.
2000: Melvin G McInnis; T Swift-Scanlanl; Amy Mahoney; J Vincent; Greta Verheyen; Tsuo-Hung Lan; Lilijana Oruc; Olaf Riess; Christine Van Broeckhoven; H Chen; James L Kennedy; Dean F MacKinnon; Russell L Margolis; Sylvia G Simpson; Francis McMajon; Elliot S Gershon; John Nurnberger; Theodore Reich; J. Raymond DePaulo; Christopher A Ross
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia.
Molecular psychiatry 2000;5(4):439-42.
2000: Thomas Sander; Herbert Schulz; Kathrin Saar; Elena Gennaro; M C Riggio; Amedeo Bianchi; Federico Zara; D Luna; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; F Picard; Jean-François Prud'homme; Louise Bate; A Sundquist; R Mark Gardiner; Guus A M A J Janssen; Gerrit-Jan de Haan; Dorothée G A Kasteleijn-Nolst Trenité; Adri Bader; Dick Lindhout; Olaf Riess; Thomas F Wienker; Dieter Janz; A Reis
Genome search for susceptibility loci of common idiopathic generalised epilepsies.
Human molecular genetics 2000;9(10):1465-72.
2000: Olaf Riess; W Kuhn; Rejko Krüger
Genetic influence on the development of Parkinson's disease.
Journal of neurology 2000;247 Suppl 2():II69-74.
2000: Rejko Krüger; Cornelia Hardt; F Tschentscher; S Jäckel; W Kuhn; Thomas Müller; J Werner; Dirk Woitalla; Daniela Berg; N Kühnl; G A Fuchs; Eduardo J M Santos; Horst Przuntek; Jörg T Epplen; Ludger Schöls; Olaf Riess
Genetic analysis of immunomodulating factors in sporadic Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2000;107(5):553-62.
2000: Rejko Krüger; Thomas Müller; Olaf Riess
Involvement of alpha-synuclein in Parkinson's disease and other neurodegenerative disorders.
Journal of neural transmission (Vienna, Austria : 1996) 2000;107(1):31-40.
1999: Susan E Holmes; Elizabeth O'Hearn; Melvin G McInnis; D A Gorelick-Feldman; John Kleiderlein; Colleen Callahan; N G Kwak; R G Ingersoll-Ashworth; M Sherr; A J Sumner; Alan H Sharp; U Ananth; William K Seltzer; MA Boss; A M Vieria-Saecker; J T Epplen; Olaf Riess; Christopher A Ross; Russell L Margolis
Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.
Nature genetics 1999;23(4):391-2.
1999: Franco Laccone; U Engel; E Holinski-Feder; M Weigell-Weber; K Marczinek; D Nolte; Deborah J Morris-Rosendahl; Christine Zühlke; K Fuchs; H Weirich-Schwaiger; Gregor Schlüter; G Von Beust; AM Vieira-Saecker; Bernhard H F Weber; Olaf Riess
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland.
Neurology 1999;53(4):801-6.
1999: Thomas Sander; C Peters; G Kämmer; Jerzy Samochowiec; M Zirra; Dietmar Mischke; Andreas Ziegler; Klemens Kaupmann; B Bettler; JT Epplen; Olaf Riess
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.
American journal of medical genetics 1999;88(4):305-10.
1999: Thomas Sander; Jerzy Samochowiec; M Ladehoff; Michael N Smolka; C Peters; Olaf Riess; Hans Rommelspacher; Lutz G Schmidt
Association analysis of exonic variants of the gene encoding the GABAB receptor and alcohol dependence.
Psychiatric genetics 1999;9(2):69-73.
1999: Rejko Krüger; AM Vieira-Saecker; Wilfried Kuhn; Daniela Berg; Thomas Müller; N Kühnl; G A Fuchs; A Storch; Marcel Hungs; Dirk Woitalla; Horst Przuntek; Jörg T Epplen; Ludger Schöls; Olaf Riess
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype.
Annals of neurology 1999;45(5):611-7.
1999: Thomas Sander; Herbert Schulz; A M Vieira-Saeker; A Bianchi; U Sailer; Gerhard Bauer; A Scaramelli; Thomas F Wienker; Kathrin Saar; André Reis; Dieter Janz; JT Epplen; Olaf Riess
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.
American journal of medical genetics 1999;88(2):182-7.
1999: Martin Dichgans; L Schöls; Jürgen Herzog; Giovanni Stevanin; H Weirich-Schwaiger; G Rouleau; Katrin Bürk; Thomas Klockgether; Christine Zühlke; Franco Laccone; Olaf Riess; Thomas Gasser
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families.
Neurology 1999;52(4):849-51.
1999: Eva Grasbon-Frodl; Siegfried Kösel; Olaf Riess; U Müller; Parviz Mehraein; Manuel B Graeber
Analysis of mitochondrial targeting sequence and coding region polymorphisms of the manganese superoxide dismutase gene in German Parkinson disease patients.
Biochemical and biophysical research communications 1999;255(3):749-52.
1999: Thomas Sander; L Schölz; Dieter Janz; J T Epplen; Olaf Riess
Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy.
Epilepsy research 1999;33(2-3):227-33.
1999: Thomas Klockgether; Ludger Schöls; Michael Abele; Katrin Bürk; Helge Topka; Frank Andres; Georgios Amoiridis; R Lüdtke; Olaf Riess; Franco Laccone; Johannes Dichgans
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD).
Journal of neurology, neurosurgery, and psychiatry 1999;66(2):222-4.
1999: Eva Grasbon-Frodl; Rupert Egensperger; Siegfried Kösel; R Krüger; Olaf Riess; Parviz Mehraein; Manuel B Graeber
The alpha1-antichymotrypsin A-allele in German Parkinson disease patients.
Journal of neural transmission (Vienna, Austria : 1996) 1999;106(7-8):729-36.
1999: Olaf Riess; Rejko Krüger
Parkinson's disease--a multifactorial neurodegenerative disorder.
Journal of neural transmission. Supplementum 1999;56():113-25.
1999: Rejko Krüger; A M Vieira-Säcker; Wilfried Kuhn; Thomas Müller; Dirk Woitalla; Ludger Schöls; Horst Przuntek; Jörg T Epplen; Olaf Riess
Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication.
Journal of neural transmission (Vienna, Austria : 1996) 1999;106(2):159-63.
1998: H C Peters; G Kämmer; A Volz; Klemens Kaupmann; Andreas Ziegler; B Bettler; Jörg T Epplen; T Sander; Olaf Riess
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy.
Neurogenetics 1998;2(1):47-54.
1998: Ludger Schöls; J Haan; Olaf Riess; Georgios Amoiridis; Horst Przuntek
Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?
Neurology 1998;51(6):1603-7.
1998: Carsten Holzmann; W Mäueler; D Petersohn; T Schmidt; G Thiel; Jörg T Epplen; Olaf Riess
Isolation and characterization of the rat huntingtin promoter.
The Biochemical journal 1998;336 ( Pt 1)():227-34.
1998: T Schmidt; G Bernhard Landwehrmeyer; Iris Schmitt; Yvon Trottier; Georg Auburger; Franco Laccone; Thomas Klockgether; M Völpel; Jörg T Epplen; Ludger Schöls; Olaf Riess
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.
Brain pathology (Zurich, Switzerland) 1998;8(4):669-79.
1998: Olaf Riess; R Jakes; Rejko Krüger
Genetic dissection of familial Parkinson's disease.
Molecular medicine today 1998;4(10):438-44.
1998: Thomas Sander; R Kretz; Herbert Schulz; U Sailer; Gerhard Bauer; A Scaramelli; JT Epplen; Olaf Riess; Dieter Janz
Replication analysis of a putative susceptibility locus (EGI) for idiopathic generalized epilepsy on chromosome 8q24.
Epilepsia 1998;39(7):715-20.
1998: Thomas Klockgether; R Lüdtke; B Kramer; Michael Abele; Katrin Bürk; Ludger Schöls; Olaf Riess; Franco Laccone; Sylvia Boesch; I Lopes-Cendes; Alexis Brice; R Inzelberg; Nelly Zilber; Johannes Dichgans
The natural history of degenerative ataxia: a retrospective study in 466 patients.
Brain : a journal of neurology 1998;121 ( Pt 4)():589-600.
1998: R Krüger; W Kuhn; Thomas Müller; D Woitalla; Manuel B Graeber; Siegfried Kösel; H Przuntek; J T Epplen; L Schöls; Olaf Riess
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.
Nature genetics 1998;18(2):106-8.
1998: Thomas Sander; C Peters; Dieter Janz; A Bianchi; Gerhard Bauer; Thomas F Wienker; T Hildmann; JT Epplen; Olaf Riess
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.
Epilepsy research 1998;29(2):115-22.
1998: Ludger Schöls; R Krüger; Georgios Amoiridis; Horst Przuntek; Jörg T Epplen; Olaf Riess
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
Journal of neurology, neurosurgery, and psychiatry 1998;64(1):67-73.
1997: Ludger Schöls; Georgios Amoiridis; T h Büttner; Horst Przuntek; Jörg T Epplen; Olaf Riess
Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
Annals of neurology 1997;42(6):924-32.
1997: Y Y Fang; S Bain; Eric A Haan; Helen Eyre; M MacDonald; TJ Wright; Michael R Altherr; Olaf Riess; Grant R Sutherland; David F Callen
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
American journal of medical genetics 1997;71(4):453-7.
1997: Iris Schmitt; T Brattig; M Gossen; Olaf Riess
Characterization of the rat spinocerebellar ataxia type 3 gene.
Neurogenetics 1997;1(2):103-12.
1997: Ludger Schöls; Suzana Gispert; M Vorgerd; A M Menezes Vieira-Saecker; P Blanke; Georg Auburger; Georgios Amoiridis; S Meves; Jörg T Epplen; Horst Przuntek; Stef pulst; Olaf Riess
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
Archives of neurology 1997;54(9):1073-80.
1997: Thomas Sander; B Bockenkamp; T Hildmann; R Blasczyk; R Kretz; Thomas F Wienker; Armin Volz; Bettina Schmitz; G Beck-Mannagetta; Olaf Riess; JT Epplen; Dieter Janz; Andreas Ziegler
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
Neurology 1997;49(3):842-7.
1997: Olaf Riess; Ludger Schöls; H Bottger; D Nolte; AM Vieira-Saecker; C Schimming; Friedmar R Kreuz; Milan Macek Jr.; A Krebsová; Thomas Klockgether; Christine Zühlke; Franco Laccone
SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.
Human molecular genetics 1997;6(8):1289-93.
1997: Olaf Riess; Franco Laccone; Suzana Gispert; Ludger Schöls; Christine Zühlke; AM Vieira-Saecker; S Herlt; Karl Wessel; Jörg T Epplen; Bernhard H F Weber; Friedmar R Kreuz; S Chahrokh-Zadeh; A Meindl; A Lunkes; J Aguiar; M Macek; A Krebsová; Milan Macek Jr.; Katrin Bürk; S Tinschert; I Schreyer; Stef pulst; Georg Auburger
SCA2 trinucleotide expansion in German SCA patients.
Neurogenetics 1997;1(1):59-64.
1997: Carsten Holzmann; A M Saecker; Jörg T Epplen; Olaf Riess
Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene.
Journal of medical genetics 1997;34(3):264.
1997: Ludger Schöls; Olaf Riess; Georgios Amoiridis; A Riess; Horst Przuntek; Jörg T Epplen
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities].
Fortschritte der Neurologie-Psychiatrie 1997;65(2):79-89.
1997: Olaf Riess; Jörg T Epplen; Georgios Amoiridis; Horst Przuntek; Ludger Schöls
Transmission distortion of the mutant alleles in spinocerebellar ataxia.
Human genetics 1997;99(2):282-4.
1996: Ludger Schöls; Georgios Amoiridis; J T Epplen; M Langkafel; Horst Przuntek; Olaf Riess
Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.
Journal of neurology, neurosurgery, and psychiatry 1996;61(5):466-70.
1996: K Witter; Thomas Werner; J H Blusch; E M Schneider; Olaf Riess; I Ziegler; W Rödl; Adelbert Bacher; M Gütlich
Cloning, sequencing and functional studies of the gene encoding human GTP cyclohydrolase I.
Gene 1996;171(2):285-90.
1996: M Gossen; Iris Schmitt; K Obst; Petra Wahle; J T Epplen; Olaf Riess
cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 gene.
Human molecular genetics 1996;5(3):381-9.
1996: Yuko Ota; Robert N Haire; Chris T Amemiya; Ronda T Litman; T Träger; Olaf Riess; Gary W Litman
Human Txk: genomic organization, structure and contiguous physical linkage with the Tec gene.
Oncogene 1996;12(4):937-42.
1996: G Lucotte; N Gérard; P Roubertoux; Iris Schmitt; Olaf Riess
Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the disease.
Genetic counseling (Geneva, Switzerland) 1996;7(4):297-302.
1996: Olaf Riess; C Kozak; G J van Ommen
Report of the Fourth International Workshop on Human Chromosome 4 Mapping 1996.
Cytogenetics and cell genetics 1996;74(1-2):57-69.
1995: Ludger Schöls; Olaf Riess; S Schöls; S Zeck; Georgios Amoiridis; M Langkafel; J T Epplen; Horst Przuntek
Spinocerebellar ataxia type 1: Clinical and neurophysiological characteristics in German kindreds.
Acta neurologica Scandinavica 1995;92(6):478-85.
1995: Y Y Fang; H J Eyre; S K Bohlander; Anna Estop; E McPherson; T Träger; Olaf Riess; David F Callen
Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.
American journal of human genetics 1995;57(5):1137-42.
1995: Ludger Schöls; Georgios Amoiridis; M Langkafel; T Büttner; Horst Przuntek; Olaf Riess; AM Vieira-Saecker; J T Epplen
Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany.
Journal of neurology, neurosurgery, and psychiatry 1995;59(4):449-50.
1995: Iris Schmitt; J T Epplen; Olaf Riess
Predominant neuronal expression of the gene responsible for dentatorubral-pallidoluysian atrophy (DRPLA) in rat.
Human molecular genetics 1995;4(9):1619-24.
1995: Iris Schmitt; D Bächner; D Megow; P Henklein; H Hameister; J T Epplen; Olaf Riess
Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during development.
Human molecular genetics 1995;4(7):1173-82.
1995: Ludger Schöls; AM Vieira-Saecker; S Schöls; Horst Przuntek; J T Epplen; Olaf Riess
Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients.
Human molecular genetics 1995;4(6):1001-5.
1995: J T Epplen; Johannes Buitkamp; C Epplen; W Mäueler; Olaf Riess
Indirect DNA/gene diagnoses via electrophoresis--an obsolete principle?
Electrophoresis 1995;16(5):683-90.
1995: Olaf Riess; H Schulz; T Träger; Iris Schmitt; J T Epplen
Molecular genetics of inherited diseases involving human chromosome 4.
Casopís lékar̆ů c̆eských 1995;134(4):108-16.
1995: Gérard Lucotte; J C Turpin; Olaf Riess; J T Epplen; I Siedlaczk; France Loirat; Serge Hazout
Confidence intervals for predicted age of onset, given the size of (CAG)n repeat, in Huntington's disease.
Human genetics 1995;95(2):231-2.
1994: M S Corbett; Iris Schmitt; Olaf Riess; A Walz
Characterization of the gene for human neutrophil-activating peptide 78 (ENA-78).
Biochemical and biophysical research communications 1994;205(1):612-7.
1994: Olaf Riess; B Winkelmann; J T Epplen
Toward the complete genomic map and molecular pathology of human chromosome 4.
Human genetics 1994;94(1):1-18.
1994: Bernhard H F Weber; Heidi Stöhr; I Siedlaczck; Jonathan L Longmire; LL Deaven; A M Duncan; Olaf Riess
Characterization of a cosmid library from flow-sorted chromosomes 11.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1994;2(3):201-7.
1994: Olaf Riess; U Thies; I Siedlaczck; S Potisek; Graham Kyrenia Rona; J Theilmann; T Grimm; J T Epplen; Michael R Hayden
Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16.
Genomics 1994;19(2):298-302.
1994: Olaf Riess; I Siedlaczck; S Kredtke; G Melmer; J T Epplen; LL Deaven
Characterization of a human chromosome 4 flow-sorted cosmid library.
Cytogenetics and cell genetics 1994;65(4):238-42.
1993: Olaf Riess; C Epplen; I Siedlaczck; J T Epplen
Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25.
Human genetics 1993;92(6):629-30.
1993: Christine Zühlke; Olaf Riess; B Bockel; H Lange; U Thies
Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene.
Human molecular genetics 1993;2(12):2063-7.
1993: I Siedlaczck; C Epplen; Olaf Riess; J T Epplen
Simple repetitive (GAA)n loci in the human genome.
Electrophoresis 1993;14(10):973-7.
1993: Olaf Riess; A Noerremoelle; S A Soerensen; J T Epplen
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease.
Human molecular genetics 1993;2(9):1523.
1993: A Nørremølle; Olaf Riess; J T Epplen; Kirsten Fenger; Lis Hasholt; Sven Asger Sørensen
Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families.
Human molecular genetics 1993;2(9):1475-6.
1993: Christine Zühlke; Olaf Riess; K Schröder; I Siedlaczck; J T Epplen; W Engel; U Thies
Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin.
Human molecular genetics 1993;2(9):1467-9.
1993: B Weber; Olaf Riess; H Daneshvar; Graham Kyrenia Rona; Michael R Hayden
(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3.
Human molecular genetics 1993;2(6):827.
1993: Olaf Riess; A Noerremoelle; S A Soerensen; J T Epplen
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease.
Human molecular genetics 1993;2(6):637.
1992: B Weber; Olaf Riess; G Wolff; S Andrew; C Collins; Graham Kyrenia Rona; J Theilmann; Michael R Hayden
Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease.
Nature genetics 1992;2(3):216-22.
1992: Olaf Riess; A Noerremoelle; B Weber; Maria A Musarella; Michael R Hayden
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa.
American journal of human genetics 1992;51(4):755-62.
1992: Olaf Riess; B Weber; Michael R Hayden
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16.
Human molecular genetics 1992;1(6):452.
1992: C Collins; G Hutchinson; D Kowbel; Olaf Riess; B Weber; Michael R Hayden
The human beta-subunit of rod photoreceptor cGMP phosphodiesterase: complete retinal cDNA sequence and evidence for expression in brain.
Genomics 1992;13(3):698-704.
1992: Olaf Riess; A Noerremoelle; C Collins; D Mah; B Weber; Michael R Hayden
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease.
Nature genetics 1992;1(2):104-8.
1992: B Weber; A Hedrick; S Andrew; Olaf Riess; C Collins; D Kowbel; Michael R Hayden
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.
American journal of human genetics 1992;50(2):382-93.
1992: Olaf Riess; B Weber; A Noeremolle; R A Shaikh; Michael R Hayden; Maria A Musarella
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosis.
Human mutation 1992;1(6):478-85.
1991: B Weber; C Collins; D Kowbel; Olaf Riess; Michael R Hayden
Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene.
Genomics 1991;11(4):1113-24.
1991: B Weber; Olaf Riess; G Hutchinson; C Collins; B Y Lin; D Kowbel; S Andrew; K Schappert; Michael R Hayden
Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3.
Nucleic acids research 1991;19(22):6263-8.
1991: B Weber; Olaf Riess; C N Kreklywich; S Wood; Michael R Hayden
A polymorphic DNA marker at the D8S131 locus.
Nucleic acids research 1991;19(7):1725.
1991: B Weber; Olaf Riess; Michael R Hayden
A polymorphic DNA marker at the D10S106 locus.
Nucleic acids research 1991;19(7):1725.
1991: Lutz Roewer; Olaf Riess; O Prokop
Hybridization and polymerase chain reaction amplification of simple repeated DNA sequences for the analysis of forensic stains.
Electrophoresis 1991;12(2-3):181-6.
1991: Jadwiga Jaruzelska; K F Henriksen; F Güttler; Olaf Riess; K Borski; N Blin; Ryszard Slomski
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria.
Human genetics 1991;86(3):247-50.
1990: Olaf Riess; C Kammerbauer; Lutz Roewer; V Steimle; A Andreas; E Albert; T Nagai; J T Epplen
Hypervariability of intronic simple (gt)n(ga)m repeats in HLA-DRB genes.
Immunogenetics 1990;32(2):110-6.
1989: Olaf Riess; A Michel; W Berger; Peter Nürnberg; J T Epplen; Astrid Speer; Charles Coutelle
RFLP-discordance within the human phenylalanine hydroxylase locus.
Human genetics 1989;83(2):199-201.
1989: Manfred Stuhrmann; Olaf Riess; E Mönch; G Kurdoglu
Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.
Clinical genetics 1989;36(2):117-21.
1989: Jadwiga Jaruzelska; K Borski; Olaf Riess; N Blin; R Słomski
Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria.
Acta biochimica Polonica 1989;36(3-4):323-32.
1988: Olaf Riess; A Michel; Astrid Speer; W Meiske; G Cobet; Charles Coutelle
Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic.
Human genetics 1988;78(4):343-6.
1987: Olaf Riess; A Michel; Astrid Speer; G Cobet; Charles Coutelle
Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic Republic.
Clinical genetics 1987;32(4):209-15.
1986: Astrid Speer; R Bollman; A Michel; R Neumann; C Bommer; R Hanke; Olaf Riess; G Cobet; Charles Coutelle
Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysis.
Prenatal diagnosis 1986;6(6):447-50.
1986: Astrid Speer; H H Dahl; Olaf Riess; G Cobet; R Hanke; R G Cotton; Charles Coutelle
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.
Clinical genetics 1986;29(6):491-5.