Burkhard Gess

Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update

Angela Dispenzieri, Teresa Coelho, Isabel Conceição et al. · Orphanet Journal of Rare Diseases · 2022 · 89 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies

Maike F. Dohrn, Nicola Glöckle, Lejla Mulahasanovic et al. · Journal of Neurochemistry · 2017 · 79 citations

Life Sciences, Genetics, Neurology +17

Caveolin-1–mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotype

Camila C. Portugal, Renato Socodato, Teresa Canedo et al. · Science Signaling · 2017 · 78 citations · Full text

Life Sciences, Neurobiology, Neuroscience +12

Charcot-Marie-Tooth disease: Frequency of genetic subtypes in a German neuromuscular center population

Burkhard Gess, Anja Schirmacher, Matthias Boentert et al. · Neuromuscular Disorders · 2013 · 74 citations

Medicine, Genetics, Neurology +14

Prognostic factors in ALS: a comparison between Germany and China

Johannes Dorst, Lu Chen, Angela Rosenbohm et al. · Journal of Neurology · 2019 · 71 citations

Medicine, Neurology, Neurodegeneration +10