Whole-exome sequencing of Finnish patients with vascular cognitive impairment
Mönkäre, Saana, Kuuluvainen, Liina, Kun-Rodrigues, Celia, Carmona, Susana, Schleutker, Johanna, Bras, Jose, Pöyhönen, Minna, Guerreiro, Rita, Myllykangas, Liisa
Published in European journal of human genetics : EJHG (01.04.2021)
Published in European journal of human genetics : EJHG (01.04.2021)
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COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes
Kuuluvainen, Liina, Mönkäre, Saana, Kokkonen, Hannaleena, Zhao, Fang, Verkkoniemi-Ahola, Auli, Schleutker, Johanna, Hakonen, Anna H, Hartikainen, Päivi, Pöyhönen, Minna, Myllykangas, Liisa
Published in Stroke (1970) (01.10.2021)
Published in Stroke (1970) (01.10.2021)
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Oligogenic basis of sporadic ALS: The example of SOD1 p.Ala90Val mutation
Kuuluvainen, Liina, Kaivola, Karri, Mönkäre, Saana, Laaksovirta, Hannu, Jokela, Manu, Udd, Bjarne, Valori, Miko, Pasanen, Petra, Paetau, Anders, Traynor, Bryan J, Stone, David J, Schleutker, Johanna, Pöyhönen, Minna, Tienari, Pentti J, Myllykangas, Liisa
Published in Neurology. Genetics (01.06.2019)
Published in Neurology. Genetics (01.06.2019)
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Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Myllykangas, Liisa, Pöyhönen, Minna
Published in Acta neurologica Scandinavica (01.11.2022)
Published in Acta neurologica Scandinavica (01.11.2022)
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Journal Article
PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice
Messerschmidt, Clemens, Foddis, Marco, Blumenau, Sonja, Müller, Susanne, Bentele, Kajetan, Holtgrewe, Manuel, Kun-Rodrigues, Celia, Alonso, Isabel, do Carmo Macario, Maria, Morgadinho, Ana Sofia, Velon, Ana Graça, Santo, Gustavo, Santana, Isabel, Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Pöyhönen, Minna, Myllykangas, Liisa, Senatore, Assunta, Berchtold, Daniel, Winek, Katarzyna, Meisel, Andreas, Pavlovic, Aleksandra, Kostic, Vladimir, Dobricic, Valerija, Lohmann, Ebba, Hanagasi, Hasmet, Guven, Gamze, Bilgic, Basar, Bras, Jose, Guerreiro, Rita, Beule, Dieter, Dirnagl, Ulrich, Sassi, Celeste
Published in Scientific reports (16.03.2021)
Published in Scientific reports (16.03.2021)
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TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients
Foddis, Marco, Blumenau, Sonja, Holtgrewe, Manuel, Paquette, Kimberly, Westra, Kaitlyn, Alonso, Isabel, Macario, Maria do Carmo, Morgadinho, Ana Sofia, Velon, Ana Graça, Santo, Gustavo, Santana, Isabel, Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Pöyhönen, Minna, Myllykangas, Liisa, Pavlovic, Aleksandra, Kostic, Vladimir, Dobricic, Valerija, Lohmann, Ebba, Hanagasi, Hasmet, Santos, Mariana, Guven, Gamze, Bilgic, Basar, Bras, Jose, Beule, Dieter, Dirnagl, Ulrich, Guerreiro, Rita, Sassi, Celeste
Published in Neurobiology of aging (01.03.2023)
Published in Neurobiology of aging (01.03.2023)
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Oligogenic basis of sporadic ALS: The example of
Kuuluvainen, Liina, Kaivola, Karri, Mönkäre, Saana, Laaksovirta, Hannu, Jokela, Manu, Udd, Bjarne, Valori, Miko, Pasanen, Petra, Paetau, Anders, Traynor, Bryan J., Stone, David J., Schleutker, Johanna, Pöyhönen, Minna, Tienari, Pentti J., Myllykangas, Liisa
Published in Neurology. Genetics (23.04.2019)
Published in Neurology. Genetics (23.04.2019)
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