Sirkku Peltonen
sipelto@utu.fi Kiinamyllynkatu 4-8 Turku |
- Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes (2019)
- Familial Cancer
- Genetic architecture of human plasma lipidome and its link to cardiovascular disease (2019)
- Nature Communications
- Intestinal tumors in neurofibromatosis 1 with special reference to fatal gastrointestinal stromal tumors (GIST) (2019)
- Molecular Genetics and Genomic Medicine
- Neurofibromatosis type 1 of the child increases birth weight (2019)
- American Journal of Medical Genetics Part A
- Pediatric malignancies in neurofibromatosis type 1: A population‐based cohort study (2019)
- International Journal of Cancer
- Tumour-cell-derived complement components C1r and C1s promote growth of cutaneous squamous cell carcinoma (2019)
- British Journal of Dermatology
- Congenital anomalies in neurofibromatosis 1: a retrospective register-based total population study (2018)
- Orphanet Journal of Rare Diseases
- Craniofacial and oral alterations in patients with Neurofibromatosis 1 (2018)
- Orphanet Journal of Rare Diseases
- Prevalence of neurofibromatosis type 1 in the Finnish population (2018)
- Genetics in Medicine
- The effect of estradiol, testosterone, and human chorionic gonadotropin on the proliferation of Schwann cells with NF1 +/− or NF1 −/− genotype derived from human cutaneous neurofibromas (2018)
- Molecular and Cellular Biochemistry



