Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1991 2
1992 1
1993 4
1994 2
1995 1
1996 2
1997 3
1998 5
1999 2
2000 8
2001 2
2002 1
2003 2
2004 8
2005 3
2006 3
2007 3
2009 3
2010 1
2011 2
2012 6
2013 3
2014 6
2015 3
2016 6
2017 10
2018 5
2019 5
2020 4
2021 5
2022 4
2023 2
Text availability
Article attribute
Article type
Publication date

Search Results

104 results
Results by year
Filters applied: . Clear all
Page 1
CADASIL and CARASIL.
Tikka S, Baumann M, Siitonen M, Pasanen P, Pöyhönen M, Myllykangas L, Viitanen M, Fukutake T, Cognat E, Joutel A, Kalimo H. Tikka S, et al. Among authors: poyhonen m. Brain Pathol. 2014 Sep;24(5):525-44. doi: 10.1111/bpa.12181. Brain Pathol. 2014. PMID: 25323668 Free PMC article. Review.
APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study.
Kurki SN, Kantonen J, Kaivola K, Hokkanen L, Mäyränpää MI, Puttonen H; FinnGen; Martola J, Pöyhönen M, Kero M, Tuimala J, Carpén O, Kantele A, Vapalahti O, Tiainen M, Tienari PJ, Kaila K, Hästbacka J, Myllykangas L. Kurki SN, et al. Among authors: poyhonen m. Acta Neuropathol Commun. 2021 Dec 23;9(1):199. doi: 10.1186/s40478-021-01302-7. Acta Neuropathol Commun. 2021. PMID: 34949230 Free PMC article.
Genetic analysis reveals novel variants for vascular cognitive impairment.
Mönkäre S, Kuuluvainen L, Schleutker J, Bras J, Roine S, Pöyhönen M, Guerreiro R, Myllykangas L. Mönkäre S, et al. Among authors: poyhonen m. Acta Neurol Scand. 2022 Jul;146(1):42-50. doi: 10.1111/ane.13613. Epub 2022 Mar 20. Acta Neurol Scand. 2022. PMID: 35307828 Free PMC article.
Genetics of dementia in a Finnish cohort.
Pasanen P, Myllykangas L, Pöyhönen M, Kiviharju A, Siitonen M, Hardy J, Bras J, Paetau A, Tienari PJ, Guerreiro R, Verkkoniemi-Ahola A. Pasanen P, et al. Among authors: poyhonen m. Eur J Hum Genet. 2018 Jun;26(6):827-837. doi: 10.1038/s41431-018-0117-3. Epub 2018 Feb 23. Eur J Hum Genet. 2018. PMID: 29476165 Free PMC article.
[How to recognize neurofibromatosis?].
Peltonen S, Pöyhönen M, Koillinen H, Valanne L, Peltonen J. Peltonen S, et al. Among authors: poyhonen m. Duodecim. 2014;130(6):619-25. Duodecim. 2014. PMID: 24724460 Review. Finnish.
Whole-exome sequencing of Finnish patients with vascular cognitive impairment.
Mönkäre S, Kuuluvainen L, Kun-Rodrigues C, Carmona S, Schleutker J, Bras J, Pöyhönen M, Guerreiro R, Myllykangas L. Mönkäre S, et al. Among authors: poyhonen m. Eur J Hum Genet. 2021 Apr;29(4):663-671. doi: 10.1038/s41431-020-00775-9. Epub 2020 Dec 2. Eur J Hum Genet. 2021. PMID: 33268848 Free PMC article.
CADASIL: hereditary disease of arteries causing brain infarcts and dementia.
Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Pöyhönen M, Rinne JO, Savontaus M, Tuisku S, Winblad B. Kalimo H, et al. Among authors: poyhonen m. Neuropathol Appl Neurobiol. 1999 Aug;25(4):257-65. doi: 10.1046/j.1365-2990.1999.00198.x. Neuropathol Appl Neurobiol. 1999. PMID: 10476042 Review.
104 results