Jean Marie Baptiste Vianney de Jong (1937-2024)

Baas, F., van der Kooi, A., Stam, J. & de Visser, M., 1 Feb 2025, In: Amyotrophic lateral sclerosis and frontotemporal degeneration. 26, 1-2, p. 186-187 2 p.

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

Neurovascular Decoupling Is Associated With Lobar Intracerebral Hemorrhages and White Matter Hyperintensities

van Dijk, S. E., Drenth, N., Hafkemeijer, A., Labadie, G., Witjes-Ané, M.-N. W., Baas, F., Vreijling, J. P., Blauw, G. J., Rombouts, S. A. R. B., van der Grond, J. & van Rooden, S., 18 Feb 2025, In: J. Am. Heart Assoc.. 14, 4, p. e038819 e038819.

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Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel SUPT5H Variants

Nik Mohd Hasan, N. F. F., Achour, A., Koopmann, T., Gammeren, A. V., van der Leeuw, J., Ceelie, H., Stieber, D., Baas, F. & Harteveld, C. L., 2025, (E-pub ahead of print) In: Hemoglobin.

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

A framework for sharing of clinical and genetic data for precision medicine applications

Elhussein, A., Baymuradov, U. & NYGC ALS Consortium, Dec 2024, In: Nature medicine. 30, 12, p. 3578-3589 12 p., 134.

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

Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage

Rutten, J. W., Cerfontaine, M. N., Dijkstra, K. L., Mulder, A. A., Vreijling, J., Kruit, M., Koning, R. I., de Bot, S. T., van Nieuwenhuizen, K. M., Baelde, H. J., Berendse, H. W., Mei, L. H., Ruijter, G. J. G., Baas, F., Jost, C. R., van Duinen, S. G., Nibbeling, E. A. R., Gravesteijn, G. & Lesnik Oberstein, S. A. J., 1 Jun 2024, In: Genetics in medicine. 26, 6, 101105.

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