Anna Melchers

<i>SNCA</i> variants are associated with increased risk for multiple system atrophy

Sonja W. Scholz, Henry Houlden, Claudia Schulte et al. · Annals of Neurology · 2009 · 283 citations

Life Sciences, Genetics, Molecular Genetics +16

<i>THAP1</i> mutations (DYT6) are an additional cause of early-onset dystonia

Henry Houlden, Susanne A. Schneider, Reema Paudel et al. · Neurology · 2010 · 105 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability

Ilja Demuth, Pierre‐Olivier Frappart, Gabriele Hildebrand et al. · Human Molecular Genetics · 2004 · 75 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Familial paroxysmal exercise‐induced dystonia: atypical presentation of autosomal dominant GTP‐cyclohydrolase 1 deficiency

Russell C. Dale, Anna Melchers, Victor SC Fung et al. · Developmental Medicine & Child Neurology · 2010 · 58 citations · Full text

Medicine, Genetics, Neurology +16

Mutational analysis of parkin and PINK1 in multiple system atrophy

Janet Brooks, Henry Houlden, Anna Melchers et al. · Neurobiology of Aging · 2010 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14