Roope Kallionpää

- Docent,
Faculty of Medicine (University of Turku)
- Senior Research Fellow,
Institute of Biomedicine (Faculty of Medicine)

roope.kallionpaa@utu.fi

+358 29 450 4565

+358 50 321 5982

Kiinamyllynkatu 10

Turku

: https://orcid.org/0000-0002-7512-2980

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Dentofacial Malocclusion in Neurofibromatosis 1 in FinlandIncreased incidence of melanoma in children and adolescents in Finland in 1990-2014: nationwide re-evaluation of histopathological characteristics (2025)
- American Journal of Medical Genetics Part AAnnals of Medicine
Reinhold, Vivian; Valtanen, Mikko; Auranen, Kari; Syrjänen, Stina; Peltonen, Sirkku; Peltonen, Juha; Kallionpää, Roope A.
Hospital Visits Associated With Oral Infections in Patients With Neurofibromatosis Type 1: A Register-Based Analysis (2025)
- American Journal of Medical Genetics Part ADermatology
Reinhold, Vivian; Kallionpää, Roope; Valtanen, Mikko; Auranen, Kari; Syrjänen, Stina; Peltonen, Sirkku; Peltonen, Juha
Mass spectrometric insights into the protein composition of human cutaneous neurofibromas: comparison of neurofibromas with the overlying skin.Morbidity in neurofibromatosis 1: Epidemiological perspectives on breast cancer and diabetes (2025)
- British Journal of Cancer
Kallionpää, Roope A.; Martikkala, Eija; Haapaniemi, Pekka; Karppinen, Sanna-Maria; Riihilä, Pilvi; Rokka, Anne; Leivo, Ilmo; Pihlajaniemi, Taina; Peltonen, Sirkku; Peltonen, Juha
Pregnancy and the Risk for Cancer in Neurofibromatosis 1 (2025)
- Genes, Chromosomes and Cancer
Kallionpää, Roope A.; Määttanen, Juha; Leppävirta, Jussi; Peltonen, Sirkku; Peltonen, Juha
Risk and prognosis of myocardial infarction in patients with neurofibromatosis type 1: Evidence of compromised survival (2025)
- Genetics in MedicineClinical Genetics
Loponen, Niina; Kallionpää, Roope A.; Ylä-Outinen, Heli; Valtanen, Mikko; Auranen, Kari; Järveläinen, Hannu; Peltonen, Sirkku; Peltonen, Juha
Characterization of Immune Cell Populations of Cutaneous Neurofibromas in Neurofibromatosis 1Circulating free DNA in the plasma of individuals with neurofibromatosis type 1 (2024)
- Laboratory InvestigationAmerican Journal of Medical Genetics Part A
Kallionpää Roope A., Peltonen Sirkku, Le Kim My, Martikkala Eija, Jääskeläinen Mira, Fazeli Elnaz, Riihilä Pilvi, Haapaniemi Pekka, Rokka Anne, Salmi Marko, Leivo Ilmo, Peltonen Juha
Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causesHaploinsufficiency of the NF1 gene is associated with protection against diabetes (2024)
- Molecular Genetics and Genomic MedicineJournal of Medical Genetics
Loponen Niina, Yla-Outinen Heli, Kallionpää Roope A., Valtanen Mikko, Auranen Kari, Järveläinen Hannu, Peltonen Sirkku, Peltonen Juha
Patients with Darier disease have an increased risk of keratinocyte carcinoma: a Swedish registry-based nationwide cohort study (2024)
- Orphanet Journal of Rare Diseases
Inci, Rahime; Gillstedt, Martin; Kallionpää, Roope A.; Peltonen, Sirkku; Polesie, Sam
The contribution of morbidity and unemployment for the reduced labor market participation of individuals with neurofibromatosis 1 in Finland (2023)
- European Journal of Human Genetics
Kallionpää Roope A., Johansson Edvard, Böckerman Petri, Peltonen Juha, Peltonen Sirkku
(2022)
Rousi Emma K., Kallionpää Roope A., Kallionpää Roosa E., Juteau Susanna M., Talve Lauri A., Hernberg Micaela M., Vihinen Pia P., Kähäri Veli-Matti, Koskivuo Ilkka O.
Mast Cells in Human Cutaneous Neurofibromas: Density, Subtypes, and Association with Clinical Features in Neurofibromatosis 1Breast cancer in neurofibromatosis 1: survival and risk of contralateral breast cancer in a five country cohort study (2022)
Kallionpää Roope A, Ahramo Kaisa, Martikkala Eija, Fazeli Elnaz, Haapaniemi Pekka, Rokka Anne, Leivo Ilmo, Harvima Ilkka T, Peltonen Juha, Peltonen Sirkku
Breast cancer risk in Neurofibromatosis type 1 is a function of the type of NF1 gene mutation: a new genotype-phenotype correlation (2022) Kallionpää Roope
The rare disease neurofibromatosis 1 as a source of hereditary economic inequality: evidence from Finland (2022)
- Genetics in Medicine
Johansson Edvard, Kallionpää Roope A, Böckerman Petri, Peltonen Sirkku, Peltonen Juha
A rare disease and education: Neurofibromatosis type 1 decreases educational attainment (2021)
Johansson Edvard, Kallionpää Roope A, Böckerman Petri, Peltonen Juha, Peltonen Sirkku
(2021)
Kallionpää Roope A, Ahramo Kaisa, Aaltonen Marianna, Pennanen Paula, Peltonen Juha, Peltonen Sirkku
(2021)
Kallionpää RA, Peltonen S, Leppävirta J, Pöyhönen M, Auranen K, Järveläinen H, Peltonen J
Increased risk for dementia in neurofibromatosis type 1 (2021)
- Genetics in Medicine
Kallionpää Roope A, Valtanen Mikko, Auranen Kari, Uusitalo Elina, Rinne Juha O, Peltonen Sirkku, Peltonen Juha
Signaling pathways in human osteoclasts differentiation: ERK1/2 as a key player (2021)
- Molecular Biology Reports
Pennanen Paula, Kallionpää Roope A, Peltonen Sirkku, Nissinen Liisa, Kähäri Veli-Matti, Heervä Eetu, Peltonen Juha
(2020)
- Genetics in Medicine
Evans DGR, Kallionpää RA, Clementi M, Trevisson E, Mautner V, Howell SJ, Lewis L, Zehou O, Peltonen S, Brunello A, Harkness EF, Wolkenstein P, Peltonen J
(2019)
- Journal of Medical Genetics
Frayling IM, Mautner V-F, van Minkelen R, Kallionpää RA, Aktas S, Baralle D, Ben-Shachar S, Callaway A, Cox H, Eccles DM, Ferkal S, LaDuca H, Lazaro C, Rogers MT, Stuenkel AJ, Summerour P, Varan A, Yap Y-S, Peltonen J, Evans DG, Wolkenstein P, Upadhyaya M