Tobias Lindig

Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta

Lutz Garbes, Kyung‐Ho Kim, Angelika Rieß et al. · The American Journal of Human Genetics · 2015 · 175 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Comparison of three clinical rating scales in Friedreich ataxia (FRDA)

Katrin Bürk, Ulrike Mälzig, Stefanie Wolf et al. · Movement Disorders · 2009 · 147 citations

Life Sciences, Genetics, Neurology +13

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

Martina Minnerop, Delia Kurzwelly, Holger Wagner et al. · Brain · 2017 · 121 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The anterior and medial thalamic nuclei and the human limbic system: tracing the structural connectivity using diffusion-weighted imaging

Wolfgang Grodd, Vinod Kumar, Almut Schüz et al. · Scientific Reports · 2020 · 113 citations · Full text

Medicine, Neurobiology, Neuroscience +17

DeepCEST 3T: Robust MRI parameter determination and uncertainty quantification with neural networks—application to CEST imaging of the human brain at 3T

Felix Glang, A Deshmane, Sergey Prokudin et al. · Magnetic Resonance in Medicine · 2019 · 93 citations · Full text

Medicine, Computer Science, Radiology +17