Talya Dor

Exome sequencing and disease-network analysis of a single family implicate a mutation in <i>KIF1A</i> in hereditary spastic paraparesis

Yaniv Erlich, Simon Edvardson, Emily Hodges et al. · Genome Research · 2011 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia

Veronika Boczonadi, Juliane Müller, Angela Pyle et al. · Nature Communications · 2014 · 158 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Monitoring liver damage using hepatocyte-specific methylation markers in cell-free circulating DNA

Roni Lehmann‐Werman, Judith Magenheim, Joshua Moss et al. · JCI Insight · 2018 · 145 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

<i>KIF1C</i> mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction

Talya Dor, Yuval Cinnamon, Laure Raymond et al. · Journal of Medical Genetics · 2013 · 83 citations

Life Sciences, Genetics, Molecular Genetics +15

Safety and clinical outcome of tamoxifen in Duchenne muscular dystrophy

Reuven Tsabari, Elana Simchovitz, Eran Lavi et al. · Neuromuscular Disorders · 2021 · 22 citations

Medicine, Endocrinology, Oncology +13