Pauli Ylikotila

- Doctoral Researcher,
Department of Clinical Medicine (Faculty of Medicine)

pauli.ylikotila@utu.fi

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Obesity and the Risk of Cryptogenic Ischemic Stroke in Young Adults (2022)
- Journal of Stroke and Cerebrovascular Diseases
Jaakonmäki Nina, Zedde Marialuisa, Sarkanen Tomi, Martinez-Majander Nicolas, Tuohinen Suvi, Sinisalo Juha, Ryödi Essi, Autere Jaana, Hedman Marja, Junttola Ulla, Huhtakangas Jaana K, Grimaldi Teresa, Pascarella Rosario, Nordanstig Annika, Bech-Hanssen Odd, Holbe Christine, Busch Raila, Fromm Annette, Ylikotila Pauli, Turgut Esme Ekizoglu, Amorim Isabel, Ryliskiene Kristina, Tulkki Lauri, Pascasio Laura Amaya, Licenik Radim, Ferdinand Phillip, Tsivgoulis Georgios, Jatužis Dalius, Kõrv Liisa, Kõrv Janika, Pezzini Alessandro, Fonseca Ana Catarina, Yesilot Nilufer, Roine Risto O, Waje-Andreassen Ulrike, von Sarnowski Bettina, Redfors Petra, Huhtakangas Juha, Numminen Heikki, Jäkälä Pekka, Putaala Jukka; SECRETO Study Group
Association between Migraine and Cryptogenic Ischemic Stroke in Young Adults (2021)
- Annals of Neurology
Martinez-Majander Nicolas Artto Ville, Ylikotila Pauli, von Sarnowski Bettina, Waje-Andreassen Ulrike, Yesilot Nilufer, Zedde Marialuise, Huhtakangas Juha, Numminen Heikki, Jäkälä Pekka, Fonseca Ana Catarina, Redfors Petra, Wermer MariekeJH, Pezzini Alessandro, Putaala Jukka
Rivaroxaban versus aspirin for secondary prevention of ischaemic stroke in patients with cancer: a subgroup analysis of the NAVIGATE ESUS randomized trial (2020)
- European Journal of Neurology
N. Martinez‐Majander, G. Ntaios, Y. Y. Liu , P. Ylikotila, H. Joensuu, J. Saarinen, K. S. Perera, J. Marti‐Fabregas, A. Chamorro, S. Rudilosso, L. Prats‐Sanchez , S. D. Berkowitz, H. Mundl, E. Themeles, M. Tiainen, A. Demchuk, S. E. Kasner, R. G Hart, T. Tatlisumak; on behalf of the NAVIGATE ESUS investigators
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis (2019)
- Scientific Reports
Ari Siitonen, Laura Kytövuori, Mike A. Nalls, Raphael Gibbs, Dena G. Hernandez, Pauli Ylikotila, Markku Peltonen, Andrew B. Singleton, Kari Majamaa
Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy (2018)
- Epilepsia
Hynynen J., Pokka T., Komulainen-Ebrahim J., Myllynen P., Kärppä M., Pylvänen L., Kälviäinen R., Sokka A., Jyrkilä A., Lähdetie J., Haataja L., Mäkitalo A., Ylikotila P., Eriksson K., Haapala P., Ansakorpi H., Hinttala R., Vieira P., Majamaa K., Rantala H., Uusimaa J.
Genetic risk factors in Finnish patients with Parkinson's disease (2017)
- Parkinsonism and Related Disorders
Susanna Ylönen, Ari Siitonen, Michael A. Nalls, Pauli Ylikotila, Jaana Autere, Johanna Eerola-Rautio, Raphael Gibbs, Mikko Hiltunen, Pentti J. Tienari, Hilkka Soininen, Andrew B. Singleton, Kari Majamaa
Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study (2017)
- Neurobiology of Aging
Siitonen A, Nalls MA, Hernandez D, Gibbs JR, Ding JH, Ylikotila P, Edsall C, Singleton A, Majamaa K
Leaving A Legacy Of Stroke In Europe: A Community Of Dedicated Professionals Is Changing The Face Of Stroke In Europe (2017)
- Oruen - The CNS Journal
Robert Mikulik, Pauli Ylikotila, Risto Roine, Miroslav Brozman, Sandy Middleton
Searching for Explanations for Cryptogenic Stroke in the Young: Revealing the Triggers, Causes, and Outcome (SECRETO): Rationale and design (2017)
- European Stroke Journal
Jukka Putaala, Nicolas Martinez-Majander, Sahrai Saeed, Nilufer Yesilot, Pekka Jäkälä, Ossi Nerg, Georgios Tsivgoulis, Heikki Numminen, Daniel Gordin, Bettina von Sarnowski, Ulrike Waje-Andreassen, Pauli Ylikotila, Risto O Roine, Marialuisa Zedde, Juha Huhtakangas, Catarina Fonseca, Petra Redfors, Frank-Erik de Leeuw, Alessandro Pezzini, Janika Kõrv, Siim Schneider, Christian Tanislav, Christian Enzinger, Dalius Jatuzis, Bob Siegerink,
Patricia Martínez-Sánchez, Armin J Grau, Frederick Palm, Per-Henrik Groop, Sylvain Lanthier, Hugo Ten Cate, Pirkko Pussinen, Susanna Paju, Juha Sinisalo, Mika Lehto, Arne Lindgren, José Ferro, Steven Kittne, Franz Fazekas,
Eva Gerdts, Turgut Tatlisumak
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012)
- Human Molecular Genetics
KELLER MF, SAAD M, BRAS J, Bettella F, NICOLAOU N, Simon-Sanchez J, Mittag F, BUCHEL F, SHARMA M, GIBBS JR, SCHULTE C, Moskvina V, DURR A, HOLMANS P, Kilarski LL, Guerreiro R, HERNANDEZ DG, BRICE A, Ylikotila P, STEFANSSON H, MAJAMAA K, MORRIS HR, WILLIAMS N, GASSER T, HEUTINK P, WOOD NW, HARDY J, MARTINEZ M, Singleton AB, Nalls MA