Anri Hurme‐Niiranen

Biallelic expansion in RFC1 as a rare cause of Parkinson’s disease

Laura Kytövuori, Jussi Sipilä, Hiroshi Doi et al. · npj Parkinson s Disease · 2022 · 37 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel non‐neutral mitochondrial <scp>DNA</scp> mutations found in childhood acute lymphoblastic leukemia

Tekla Järviaho, Anri Hurme‐Niiranen, Heidi K. Soini et al. · Clinical Genetics · 2017 · 26 citations

Life Sciences, Genetics, Oncology +16

Association of biallelic <scp><i>RFC1</i></scp> expansion with early‐onset Parkinson's disease

Pauli Ylikotila, Jussi Sipilä, Tiina Alapirtti et al. · European Journal of Neurology · 2023 · 24 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Cognitive impairment is not uncommon in patients with biallelic RFC1 AAGGG repeat expansion, but the expansion is rare in patients with cognitive disease

Anita Korpioja, Johanna Krüger, Anri Hurme‐Niiranen et al. · Parkinsonism & Related Disorders · 2022 · 10 citations · Full text

Medicine, Neurology, Neuroscience +17