Virpi Töhönen

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith–Wiedemann syndrome

Rolf Ohlsson, A. Nyström, Susan Pfeifer‐Ohlsson et al. · Nature Genetics · 1993 · 296 citations

Developmental Biology, Tissue Development, Genetics +12

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

Henrik Stranneheim, Kristina Lagerstedt‐Robinson, Måns Magnusson et al. · Genome Medicine · 2021 · 253 citations · Full text

PDK1 signaling in oocytes controls reproductive aging and lifespan by manipulating the survival of primordial follicles

Pradeep Reddy, Deepak Adhikari, Wenjing Zheng et al. · Human Molecular Genetics · 2009 · 233 citations

AGC1 Deficiency Associated with Global Cerebral Hypomyelination

Rolf Wibom, Francesco M. Lasorsa, Virpi Töhönen et al. · New England Journal of Medicine · 2009 · 170 citations · Full text

Neurological Disorder, Genetics, Agc1 Deficiency Associated +17

Novel PRD-like homeodomain transcription factors and retrotransposon elements in early human development

Virpi Töhönen, Shintaro Katayama, Liselotte Vesterlund et al. · Nature Communications · 2015 · 126 citations · Full text