Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nella Junna"'
Autor:
Anniina Tervi, Nella Junna, Martin Broberg, Samuel E. Jones, null FinnGen, Satu Strausz, Hanna-Riikka Kreivi, Caroline A. Heckman, Hanna M. Ollila
Publikováno v:
Human Molecular Genetics. 32:161-171
Tuberculosis is a significant public health concern resulting in the death of over 1 million individuals each year worldwide. While treatment options and vaccines exist, a substantial number of infections still remain untreated or are caused by treat
Autor:
Elisabeth Widén, Nella Junna, Sanni Ruotsalainen, Ida Surakka, Nina Mars, Pietari Ripatti, Juulia J. Partanen, Johanna Aro, Pekka Mustonen, Tiinamaija Tuomi, Aarno Palotie, Veikko Salomaa, Jaakko Kaprio, Jukka Partanen, Kristina Hotakainen, Pasi Pöllänen, Samuli Ripatti
Publikováno v:
Circulation. Genomic and precision medicine. 15(2)
Background: Prediction tools that combine polygenic risk scores with clinical factors provide a new opportunity for improved prediction and prevention of atherosclerotic cardiovascular disease, but the clinical utility of polygenic risk score has rem
Autor:
Aarno Palotie, Elisabeth Widen, Kristina Hotakainen, Samuli Ripatti, Ida Surakka, Veikko Salomaa, Johanna Aro, Nina Mars, Jukka Partanen, Sanni Ruotsalainen, Nella Junna, Pekka Mustonen, Tiinamaija Tuomi, Pietari Ripatti, Juulia Partanen, Pasi Pöllänen, Jaakko Kaprio
BackgroundAlgorithms including both traditional risk factors and polygenic risk scores (PRS) can significantly improve prediction of atherosclerotic cardiovascular disease (ASCVD). However, the clinical benefit of adding PRS to clinical risk evaluati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36f4f388db5554bb5e4db2bcb9a8fef0
https://doi.org/10.1101/2020.09.18.20197137
https://doi.org/10.1101/2020.09.18.20197137
Autor:
Aurora Djupsjöbacka, Federica Dagradi, Maria Christina Kotta, Jaakko T. Leinonen, Elisabeth Widen, Alice Ghidoni, Annukka M. Tuiskula, Kimmo Kontula, Lia Crotti, Peter J. Schwartz, Nella Junna, Silvia Castelletti, Heikki Swan, Matti Viitasalo, Carla Spazzolini
Publikováno v:
International Journal of Cardiology. 250:139-145
Background: Ventricular fibrillation (VF) is a major cause of sudden cardiac death. In some cases clinical investigations fail to identify the underlying cause and the event is classified as idiopathic (IVF). Since mutations in arrhythmia-associated
Autor:
Fadi F. Hamdan, Karin M E J Oberndorff, Eunjoon Kim, Randal Richardson, Guy A. Rouleau, Jae-Ran Lee, Rocio Moran, Henna Tyynismaa, Elisa Rahikkala, Nienke E. Verbeek, Doyoun Kim, Catherine Brunel-Guitton, So Hee Lim, Joost Nicolai, Tjitske Kleefstra, Sonja A. de Munnik, Michèl A.A.P. Willemsen, Connie T.R.M. Stumpel, Allison Schreiber, Kym M. Boycott, Justin D. Wagner, Jean Claude Décarie, Grant A. Mitchell, Elsa Rossignol, Jacques L. Michaud, Nella Junna, Inge Cuppen, Keith Van Haren, Myriam Srour, Erik-Jan Kamsteeg
Publikováno v:
Human Mutation, 36, 1, pp. 69-78
Human Mutation, 36(1), 69. Wiley-Liss Inc.
Human Mutation, 36, 69-78
Human Mutation, 36(1), 69-78. Wiley
Human Mutation, 36(1), 69. Wiley-Liss Inc.
Human Mutation, 36, 69-78
Human Mutation, 36(1), 69-78. Wiley
Item does not contain fulltext KIF1A is a neuron-specific motor protein that plays important roles in cargo transport along neurites. Recessive mutations in KIF1A were previously described in families with spastic paraparesis or sensory and autonomic