Saana M Mönkäre

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Mönkäre, S., Kuuluvainen, L., Schleutker, J., Myllykangas, L. & Pöyhönen, M., Nov 2022, In: Acta Neurologica Scandinavica. 146, 5, p. 643-651 9 p.

Research output: Contribution to journal › Article › Scientific › peer-review

Open Access

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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., Jul 2022, In: Acta Neurologica Scandinavica. 146, 1, p. 42-50 9 p.

Research output: Contribution to journal › Article › Scientific › peer-review

Open Access

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Genetics of inherited small vessel diseases

Mönkäre, S., 2022, Helsinki: Helsingin yliopisto. 100 p.

Research output: Thesis › Doctoral Thesis › Collection of Articles

Open Access

COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

Kuuluvainen, L., Mönkäre, S., Kokkonen, H., Zhao, F., Verkkoniemi-Ahola, A., Schleutker, J., Hakonen, A. H., Hartikainen, P., Pöyhönen, M. & Myllykangas, L., Oct 2021, In: Stroke. 52, 10, p. E624-E625 2 p.

Research output: Contribution to journal › Letter › Scientific

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., Mueller, S., Bentele, K., Holtgrewe, M., Kun-Rodrigues, C., Alonso, I., Macario, M. D. C., Morgadinho, A. S., Velon, A. G., Santo, G., Santana, I., Mönkäre, S., Kuuluvainen, L., Schleutker, J., Pöyhönen, M., Myllykangas, L., Senatore, A., Berchtold, D., & 14 othersWinek, 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., 16 Mar 2021, In: Scientific Reports. 11, 1, 11 p., 6072.

Research output: Contribution to journal › Article › Scientific › peer-review

Open Access

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Saana M Mönkäre

International and National Collaboration

Dive into details

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Genetic analysis reveals novel variants for vascular cognitive impairment

Genetics of inherited small vessel diseases

COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

Saana M Mönkäre

International and National Collaboration

Publications

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Genetic analysis reveals novel variants for vascular cognitive impairment

Genetics of inherited small vessel diseases

COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice