Kerstin Berg

Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene

Tommy Martinsson, Anders Oldfors, Niklas Darín et al. · Proceedings of the National Academy of Sciences · 2000 · 154 citations

Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy

Eva Lagberg Arkblad, Niklas Darín, Kerstin Berg et al. · Neuromuscular Disorders · 2006 · 116 citations

Muscle Function, Skeletal Muscle, Medicine +7

Age-Dependent Levels of Select Immunological Mediators in Sera of Healthy Children

Ulrich Sack, U Burkhardt, Michael Borte et al. · Clinical and Diagnostic Laboratory Immunology · 1998 · 107 citations · Full text

Evaluation of the cytotoxic and mutagenic potential of three ginkgolic acids

Kerstin Berg, Christine Braun, Isabel Krug et al. · Toxicology · 2014 · 51 citations

Polyphenolics, Biochemistry, Medicine +6

Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families

Cecilia Bjursell, Jan Wahlström, Kerstin Berg et al. · European Journal of Human Genetics · 1998 · 33 citations · Full text

Scandinavian Cdg Type, Genetic Analysis, Genetic Disorder +13