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Year Number of Results
2017 2
2018 1
2019 2
2020 2
2021 3
2022 1
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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: kuuluvainen l. 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.
PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice.
Messerschmidt C, Foddis M, Blumenau S, Müller S, Bentele K, Holtgrewe M, Kun-Rodrigues C, Alonso I, do Carmo Macario M, Morgadinho AS, Velon AG, Santo G, Santana I, Mönkäre S, Kuuluvainen L, Schleutker J, Pöyhönen M, Myllykangas L, Senatore A, Berchtold D, Winek K, Meisel A, Pavlovic A, Kostic V, Dobricic V, Lohmann E, Hanagasi H, Guven G, Bilgic B, Bras J, Guerreiro R, Beule D, Dirnagl U, Sassi C. Messerschmidt C, et al. Among authors: kuuluvainen l. Sci Rep. 2021 Mar 16;11(1):6072. doi: 10.1038/s41598-021-84919-x. Sci Rep. 2021. PMID: 33727568 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: kuuluvainen l. 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.
Oligogenic basis of sporadic ALS: The example of SOD1 p.Ala90Val mutation.
Kuuluvainen L, Kaivola K, Mönkäre S, Laaksovirta H, Jokela M, Udd B, Valori M, Pasanen P, Paetau A, Traynor BJ, Stone DJ, Schleutker J, Pöyhönen M, Tienari PJ, Myllykangas L. Kuuluvainen L, et al. Neurol Genet. 2019 Apr 23;5(3):e335. doi: 10.1212/NXG.0000000000000335. eCollection 2019 Jun. Neurol Genet. 2019. PMID: 31086828 Free PMC article.