Satu‐Leena Sallinen

Genetic spectrum of hereditary neuropathies with onset in the first year of life

Jonathan Baets, Tine Deconinck, Els De Vriendt et al. · Brain · 2011 · 133 citations · Full text

Life Sciences, Genetics, Neurology +16

Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals

Kirsi M. Kuusisto, Aleksandra Bebel, Mauno Vihinen et al. · Breast Cancer Research · 2011 · 123 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Large genomic rearrangements and germline epimutations in Lynch syndrome

Annette Gylling, Maaret Ridanpää, Outi Vierimaa et al. · International Journal of Cancer · 2008 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Cyclin D1 expression in astrocytomas is associated with cell proliferation activity and patient prognosis

Satu‐Leena Sallinen, P Sallinen, Juha Kononen et al. · The Journal of Pathology · 1999 · 58 citations

Medicine, Oncology, Pathology +16

Genetic Aberrations in Sporadic and Neurofibromatosis 2 (NF2)-Associated Schwannomas Studied by Comparative Genomic Hybridization (CGH)

J. Antinheimo, Satu‐Leena Sallinen, P Sallinen et al. · Acta Neurochirurgica · 2000 · 55 citations

Medicine, Genetics, Molecular Genetics +16