Olaf Riess
TMB and BRAF mutation status are independent predictive factors in high-risk melanoma patients with adjuvant anti-PD-1 therapy.
Eckardt J, Schroeder C, Martus P, Armeanu-Ebinger S, Kelemen O, Gschwind A, Bonzheim I, Eigentler T, Amaral T, Ossowski S, Riess O, Flatz L, Garbe C, Forschner A. TMB and BRAF mutation status are independent predictive factors in high-risk melanoma patients with adjuvant anti-PD-1 therapy. J Cancer Res Clin Oncol 2022; 149:833-840.
Feb 22, 2022TMB and BRAF mutation status are independent predictive factors in high-risk melanoma patients with adjuvant anti-PD-1 therapy.
Feb 22, 2022J Cancer Res Clin Oncol 2022; 149:833-840
Eckardt Julia, Schroeder Christopher, Martus Peter, Armeanu-Ebinger Sorin, Kelemen Olga, Gschwind Axel, Bonzheim Irina, Eigentler Thomas Kurt, Amaral Teresa, Ossowski Stephan, Riess Olaf, Flatz Lukas, Garbe Claus, Forschner Andrea
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect
Gispert S, Ludolph A, Riess O, Krüger R, Andersen P, Berg D, Weber M, Becker T, Gitler A, Geisen C, Liepelt I, Bauer P, Waibel S, Kurz A, Auburger G. The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiol Dis 2011; 45:356-61.
Aug 25, 2011The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect
Aug 25, 2011Neurobiol Dis 2011; 45:356-61
Gispert Suzana, Ludolph Albert C, Riess Olaf, Krüger Rejko, Andersen Peter M, Berg Daniela, Weber Markus, Becker Tim, Gitler Aaron D, Geisen Christof, Liepelt Inga, Bauer Peter, Waibel Stefan, Kurz Alexander, Auburger Georg
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Horn D, Illig T, Bezzina C, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold G, Wohlleber E, Riess O, Bonin M, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco A, Strom T. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat 2010; 31:E1851-60.
Nov 1, 2010Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Nov 1, 2010Hum Mutat 2010; 31:E1851-60
Horn Denise, Illig Thomas, Bezzina Connie R, Franke Andre, Spranger Stephanie, Villavicencio-Lorini Pablo, Seifert Wenke, Rosenfeld Jochen, Klopocki Eva, Rappold Gudrun A, Wohlleber Eva, Riess Olaf, Bonin Michael, Kapeller Johannes, Rivera-Brugués Núria, Moog Ute, Lorenz-Depiereux Bettina, Eck Sebastian, Hempel Maja, Wagenstaller Janine, Gawthrope Alex, Monaco Anthony P, Strom Tim M