P
Peter Geisler
Researcher at University of Regensburg
Publications - 73
Citations - 2647
Peter Geisler is an academic researcher from University of Regensburg. The author has contributed to research in topics: Narcolepsy & Sleep disorder. The author has an hindex of 26, co-authored 71 publications receiving 2345 citations. Previous affiliations of Peter Geisler include Max Planck Society & University Hospital Regensburg.
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Journal ArticleDOI
ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy
Juliette Faraco,Ling Lin,Birgitte Rahbek Kornum,Birgitte Rahbek Kornum,Eimear E. Kenny,Gosia Trynka,Mali Einen,Tom Rico,Peter Lichtner,Yves Dauvilliers,Isabelle Arnulf,Michel Lecendreux,Sirous Javidi,Peter Geisler,Geert Mayer,Fabio Pizza,Francesca Poli,Giuseppe Plazzi,Giuseppe Plazzi,Sebastiaan Overeem,Gert Jan Lammers,David Kemlink,Karel Sonka,Sona Nevsimalova,Guy A. Rouleau,Alex Desautels,Jacques Montplaisir,Birgit Frauscher,Laura Ehrmann,Birgit Högl,Poul Jennum,Patrice Bourgin,Rosa Peraita-Adrados,Alex Iranzo,Claudio L. Bassetti,Wei-Min Chen,Patrick Concannon,Susan D. Thompson,Vincent Damotte,Bertrand Fontaine,Maxime Breban,Maxime Breban,Christian Gieger,Norman Klopp,Panos Deloukas,Cisca Wijmenga,Joachim Hallmayer,Suna Onengut-Gumuscu,Stephen S. Rich,Juliane Winkelmann,Emmanuel Mignot +50 more
TL;DR: For example, the authors found that three loci located outside the Human Leukocyte Antigen (HLA) region on chromosome 6 were significantly associated with disease risk, including Cathepsin H (CTSH), Tumor necrosis factor (ligand) superfamily member 4 (TNFSF4), and OX40L.
Book ChapterDOI
Tinnitus and insomnia.
TL;DR: Similarities between the results from these two groups suggest that sleep specific psychotherapeutic methods, which are established for treating insomnia, should be further developed for the use in patients with insomnia and tinnitus.
Journal ArticleDOI
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy
Hyun Hor,Hyun Hor,Zoltán Kutalik,Zoltán Kutalik,Yves Dauvilliers,Armand Valsesia,Armand Valsesia,Armand Valsesia,Gert J. Lammers,Claire E H M Donjacour,Alex Iranzo,Joan Santamaria,Rosa Peraita Adrados,José L. Vicario,Sebastiaan Overeem,Isabelle Arnulf,Ioannis Theodorou,Poul Jennum,Stine Knudsen,Claudio L. Bassetti,Johannes Mathis,Michel Lecendreux,Geert Mayer,Peter Geisler,Antonio Benetó,Brice Petit,Corinne Pfister,Julie Vienne Bürki,Gérard Didelot,Michel Billiard,Guadalupe Ercilla,Willem Verduijn,Frans H.J. Claas,Peter Vollenweider,Gérard Waeber,Dawn M. Waterworth,Vincent Mooser,Raphael Heinzer,Jacques S. Beckmann,Jacques S. Beckmann,Sven Bergmann,Sven Bergmann,Mehdi Tafti,Mehdi Tafti +43 more
TL;DR: An unexpected protective HLA haplotype is found near HLA-DQA2, which suggests a virtually causal involvement of the HLA region in narcolepsy susceptibility.
Journal ArticleDOI
Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study
Gianina Luca,José Haba-Rubio,Yves Dauvilliers,Gert Jan Lammers,Sebastiaan Overeem,C. Donjacour,Geert Mayer,Sirous Javidi,Alex Iranzo,Joan Santamaria,Rosa Peraita-Adrados,Hyun Hor,Zoltán Kutalik,Zoltán Kutalik,Giuseppe Plazzi,Francesca Poli,Fabio Pizza,Isabelle Arnulf,Michel Lecendreux,Claudio L. Bassetti,Johannes Mathis,Raphael Heinzer,Poul Jennum,Stine Knudsen,Peter Geisler,Aleksandra Wierzbicka,Eva Feketeova,Corinne Pfister,Ramin Khatami,Christian R. Baumann,Mehdi Tafti,Mehdi Tafti +31 more
TL;DR: The results indicate that the diagnostic delay remains extremely long, age and gender substantially affect symptoms, and that a genetic predisposition affects the age at onset of symptoms.
Journal ArticleDOI
DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe.
Mehdi Tafti,Mehdi Tafti,Hyun Hor,Hyun Hor,Yves Dauvilliers,Gert J. Lammers,Sebastiaan Overeem,Geert Mayer,Sirous Javidi,Alex Iranzo,Joan Santamaria,Rosa Peraita-Adrados,José L. Vicario,Isabelle Arnulf,Giuseppe Plazzi,Sophie Bayard,Francesca Poli,Fabio Pizza,Peter Geisler,Aleksandra Wierzbicka,Claudio L. Bassetti,Johannes Mathis,Michel Lecendreux,Claire E H M Donjacour,Astrid van der Heide,Raphael Heinzer,José Haba-Rubio,Eva Feketeova,Birgit Högl,Birgit Frauscher,Antonio Benetó,Ramin Khatami,Francesca Canellas,Corinne Pfister,Sabine Scholz,Michel Billiard,Christian R. Baumann,Guadalupe Ercilla,Willem Verduijn,Frans H.J. Claas,Valérie Dubois,Jacek Nowak,Hans Peter Eberhard,Sylvain Pradervand,Sylvain Pradervand,Charlotte N. Hor,Manuela Testi,Jean-Marie Tiercy,Zoltán Kutalik,Zoltán Kutalik,Zoltán Kutalik +50 more
TL;DR: An overwhelming portion of genetic risk for narcolepsy with cataplexy is found at DQB1 locus and may be relevant to public health policy.