Kathrin Reetz

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Davina J. Hensman Moss, Antonio F. Pardiñas, Douglas R. Langbehn et al. · The Lancet Neurology · 2017 · 332 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data

Kathrin Reetz, Imis Dogan, Ana Sofia Costa et al. · The Lancet Neurology · 2015 · 211 citations

Life Sciences, Neurology, Neuroscience +11

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data

Heike Jacobi, Kathrin Reetz, Sophie Tézenas du Montcel et al. · The Lancet Neurology · 2013 · 191 citations

Life Sciences, Neurology, Neuroscience +17

The Montreal Cognitive Assessment (MoCA) - A Sensitive Screening Instrument for Detecting Cognitive Impairment in Chronic Hemodialysis Patients

Frances Tiffin-Richards, Ana Sofia Costa, Bernhard Holschbach et al. · PLoS ONE · 2014 · 187 citations · Full text

Medicine, Nephrology, Neurology +17

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6

Kathrin Reetz, Ana Sofia Costa, Shahram Mirzazade et al. · Brain · 2013 · 160 citations · Full text

Medicine, Neurology, Radiology +17