Prof. Dr. André Wiesmann da Silva Reis

Lehrstuhl für Humangenetik

KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility (2017) Cascella R, Strafella C, Ragazzo M, Manzo L, Costanza G, Bowes J, Hueffmeier U, et al. Journal article Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2 (2017) Kraus C, Hoyer J, Vasileiou G, Wunderle M, Lux MP, Fasching P, Krumbiegel M, et al. Journal article Clinical validation of genetic variants associated with in vitro chemotherapy-related lymphoblastoid cell toxicity (2017) Fasching P, Häberle L, Rack B, Li L, Hein A, Ekici AB, Reis A, et al. Journal article Alternative splicing and nonsense-mediated mRNA decay contribute to regulation of LOXL1 expression in response to cellular stress in pseudoexfoliation (2017) Berner D, Zenkel M, Pasutto F, Schoedel J, Reis A, Kruse F, Schlötzer-Schrehardt U Conference contribution Genetic Breast Cancer Susceptibility Variants and Prognosis in the Prospectively Randomized SUCCESS A Study (2017) Hein A, Rack B, Li L, Ekici AB, Reis A, Lux MP, Cunningham JM, et al. Journal article Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairment (2017) Reuter M, Krumbiegel M, Schlueter G, Ekici AB, Reis A, Zweier C Journal article AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability (2017) Brechet A, Buchert R, Schwenk J, Boudkkazi S, Zolles G, Siquier-Pernet K, Schaber I, et al. Journal article Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly (2017) Tawamie H, Martianov I, Wohlfahrt N, Buchert R, Mengus G, Uebe S, Janiri L, et al. Journal article Cost-effectiveness of risk-reducing surgeries in preventing hereditary breast and ovarian cancer (2017) Schrauder MG, Brunel-Geuder L, Häberle L, Wunderle M, Hoyer J, Wiesmann da Silva Reis A, Schulz-Wendtland R, et al. Journal article FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum (2017) Reuter M, Riess A, Moog U, Briggs TA, Chandler KE, Rauch A, Stampfer M, et al. Journal article