Sirkku Peltonen

- Docent,
Faculty of Medicine (University of Turku)
- ,
Dermatology and Venereology (Department of Clinical Medicine)

sipelto@utu.fi

Kiinamyllynkatu 4-8

Turku

: https://orcid.org/orcid.org/0000-0003-0990-1430

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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
Complement Factor D Is a Novel Biomarker and Putative Therapeutic Target in Cutaneous Squamous Cell Carcinoma (2022)
- Cancers
Nezhad Pegah Rahmati, Riihilä Pilvi, Knuutila Jaakko S., Viiklepp Kristiina, Peltonen Sirkku, Kallajoki Markku, Meri Seppo, Nissinen Liisa, Kähäri Veli-Matti
Mast Cells in Human Cutaneous Neurofibromas: Density, Subtypes, and Association with Clinical Features in Neurofibromatosis 1 (2022)
- Dermatology
Kallionpää Roope A, Ahramo Kaisa, Martikkala Eija, Fazeli Elnaz, Haapaniemi Pekka, Rokka Anne, Leivo Ilmo, Harvima Ilkka T, Peltonen Juha, Peltonen Sirkku
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
Treatment of cutaneous neurofibromas with carbon dioxide laser: Technique and patient experience (2022)
- European Journal of Medical Genetics
Peltonen Sirkku, Jannic Arnaud, Wolkenstein Pierre
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis (2022)
- Journal of Allergy and Clinical Immunology
Sliz Eeva, Huilaja Laura, Pasanen Anu, Laisk Triin, Reimann Ene, Mägi Reedik; FinnGen; Estonian Biobank Research Team, Hannula-Jouppi Katariina, Peltonen Sirkku, Salmi Teea, Koulu Leena, Tasanen Kaisa, Kettunen Johannes
A rare disease and education: Neurofibromatosis type 1 decreases educational attainment (2021)
- Clinical Genetics
Johansson Edvard, Kallionpää Roope A, Böckerman Petri, Peltonen Juha, Peltonen Sirkku
Circulating free DNA in the plasma of individuals with neurofibromatosis type 1 (2021)
- American Journal of Medical Genetics Part A
Kallionpää Roope A, Ahramo Kaisa, Aaltonen Marianna, Pennanen Paula, Peltonen Juha, Peltonen Sirkku
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries (2021)
- Nature Communications
Gharahkhani Puya, Jorgenson Eric, Hysi Pirro, Khawaja Anthony P., Pendergrass Sarah, Han Xikun, Ong Jue Sheng, Hewitt Alex W., Segrè Ayellet V., Rouhana John M., Hamel Andrew R., Igo Jr Robert P., Choquet Helene, Qassim Ayub, Josyula Navya S., Bailey Jessica N. Cooke, Bonnemaijer Pieter W. M., Iglesias Adriana, Siggs Owen M., Young Terri L., Vitart Veronique, Thiadens Alberta A. H. J., Karjalainen Juha, Uebe Steffen, Melles Ronald B., Nair K. Saidas, Luben Robert, Simcoe Mark, Amersinghe Nishani, Cree Angela J., Hohn Rene, Poplawski Alicia, Chen Li Jia, Rong Shi-Song, Aung Tin, Eranga Nishanthie Vithana, NEIGHBORHOOD consortium, ANZRAG consortium, Biobank Japan project, UK Biobank Eye and Vision Consortium, GIGA study group, 23 and Me Research Team, Tamiya Gen, Shiga Yukihiro, Yamamoto Masayuki, Nakazawa Toru, Currant Hannah, Birney Ewan, Wang Xin, Auton Adam, Lupton Michelle K., Martin Nicholas G., Ashaye Adeyinka, Olawoye Olusola, Williams Susan E., Akafo Stephen, Ramsay Michele, Hashimoto Kazuki, Kamatani Yoichiro, Akiyama Masato, Momozawa Yukihide, Foster Paul J., Khaw Peng T., Morgan James E., Strouthidis Nicholas G., Kraft Peter, Kang Jae H., Pang Chi Pui, Pasutto Francesca, Mitchell Paul, Lotery Andrew J., Palotie Aarno, van Duijn Cornelia, Haines Jonathan L., Hammond Chris, Pasquale Louis R., Klaver Caroline C. W., Hauser Michael, Khor Chiea Chuen, Mackey David A., Kubo Michiaki, Cheng Ching-Yu, Craig Jamie E., MacGregor Stuart, Wiggs Janey L.; FinnGen Study
Haploinsufficiency of the NF1 gene is associated with protection against diabetes (2021)
- Journal of Medical Genetics
Kallionpää RA, Peltonen S, Leppävirta J, Pöyhönen M, Auranen K, Järveläinen H, Peltonen J