Roope A Kallionpää

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 11

Top Topics

Top Venues

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

European journal of human genetics : EJHG

Annals of medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Niina Loponen, Heli Ylä-Outinen, Roope A Kallionpää, Mikko Valtanen, Kari Auranen, Hannu Järveläinen, Sirkku Peltonen, Juha Peltonen
Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causes. Molecular genetics & genomic medicine 12 (1) (2023)
Roope A Kallionpää, Edvard Johansson, Petri Böckerman, Juha Peltonen, Sirkku Peltonen
The contribution of morbidity and unemployment for the reduced labor market participation of individuals with neurofibromatosis 1 in Finland. European journal of human genetics : EJHG (2023)
Niina Loponen, Heli Ylä-Outinen, Roope A Kallionpää, Mikko Valtanen, Kari Auranen, Hannu Järveläinen, Sirkku Peltonen, Juha Peltonen
Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causes. Molecular genetics & genomic medicine 12 (1) (2023)
Niina Loponen, Heli Ylä-Outinen, Roope A Kallionpää, Mikko Valtanen, Kari Auranen, Hannu Järveläinen, Sirkku Peltonen, Juha Peltonen
Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causes. Molecular genetics & genomic medicine (2023)
Niina Loponen, Heli Ylä-Outinen, Roope A Kallionpää, Mikko Valtanen, Kari Auranen, Hannu Järveläinen, Sirkku Peltonen, Juha Peltonen
Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causes. Molecular genetics & genomic medicine (2023)
Niina Loponen, Heli Ylä-Outinen, Roope A Kallionpää, Mikko Valtanen, Kari Auranen, Hannu Järveläinen, Sirkku Peltonen, Juha Peltonen
Hypertension in NF1: A closer look at the primacy of essential hypertension versus secondary causes. Molecular genetics & genomic medicine (2023)
Emma K Rousi, Roope A Kallionpää, Roosa E Kallionpää, Susanna M Juteau, Lauri A I Talve, Micaela M Hernberg, Pia P Vihinen, Veli-Matti Kähäri, Ilkka O Koskivuo
Increased incidence of melanoma in children and adolescents in Finland in 1990-2014: nationwide re-evaluation of histopathological characteristics. Annals of medicine 54 (1) (2022)
Roope A Kallionpää, Kaisa Ahramo, Marianna Aaltonen, Paula Pennanen, Juha Peltonen, Sirkku Peltonen
Circulating free DNA in the plasma of individuals with neurofibromatosis type 1. American journal of medical genetics. Part A 185 (4) (2021)
Edvard Johansson, Roope A Kallionpää, Petri Böckerman, Juha Peltonen, Sirkku Peltonen
A rare disease and education: Neurofibromatosis type 1 decreases educational attainment. Clinical genetics 99 (4) (2021)
D Gareth R Evans, Roope A Kallionpää, Maurizio Clementi, Eva Trevisson, Victor-Felix Mautner, Sacha J Howell, Lauren Lewis, Ouidad Zehou, Sirkku Peltonen, Antonella Brunello, Elaine F Harkness, Pierre Wolkenstein, Juha Peltonen
Breast cancer in neurofibromatosis 1: survival and risk of contralateral breast cancer in a five country cohort study. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Heli Ylä-Outinen, Niina Loponen, Roope A Kallionpää, Sirkku Peltonen, Juha Peltonen
Intestinal tumors in neurofibromatosis 1 with special reference to fatal gastrointestinal stromal tumors (GIST). Molecular genetics & genomic medicine 7 (9) (2019)