Suzanne Granhøj Lindquist

Suzanne Granhøj Lindquist

Clinical Associate Professor

Member of:

  • Clinical Genetics


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  1. Published

    A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction

    Puschmann, A., Ross, O. A., Vilariño-Güell, C., Lincoln, S. J., Kachergus, J. M., Cobb, S. A., Lindquist, Suzanne Granhøj, Nielsen, Jørgen Erik, Wszolek, Z. K., Farrer, M., Widner, H., van Westen, D., Hägerström, D., Markopoulou, K., Chase, B. A., Nilsson, K., Reimer, J. & Nilsson, C., 2009, In: Parkinsonism & Related Disorders. 15, 9, p. 627-32 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  2. Published

    Arvelige neurologiske sygdomme

    Lindquist, Suzanne Granhøj, 2022, Medicinsk genetik. FADL's Forlag, p. 229-244

    Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication

  3. Published

    Arvelige ændringer i koagulationssystemet og hæmoglobinsygdomme

    Hvass, A. M. F. & Lindquist, Suzanne Granhøj, 2022, Medicinsk genetik. FADL's Forlag, p. 331-335

    Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication

  4. Published

    Autosomal dominant inherited dementia - clinical and molecular genetic aspects

    Lindquist, Suzanne Granhøj, 2008, København: Museum Tusculanum. 39 p.

    Research output: Book/Report › Ph.D. thesis

  5. Published

    Deletion of CUL4B leads to concordant phenotype in a monozygotic twin pair

    Ravn, K., Lindquist, Suzanne Granhøj, Nielsen, K., Dahm, T. & Tümer, Asuman Zeynep, Sep 2012, In: Clinical Genetics. 82, 3, p. 292-294 3 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    Demens og arvelighed

    Lindquist, Suzanne Granhøj & Hasselbalch, Steen, 2022, Forstå demens. 3 ed. Hans Reitzels Forlag, p. 129-135

    Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication

  7. Published

    Episodic ataxia type 2 (EA2) with interictal myokymia and focal dystonia

    Nielsen, E. N., Ásbjörnsdóttir, B., Møller, L. B., Nielsen, Jørgen Erik & Lindquist, Suzanne Granhøj, 2022, In: Cold Spring Harbor molecular case studies. 8, 6, a006236.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    Genetic testing in familial AD and FTD: mutation and phenotype spectrum in a Danish cohort

    Lindquist, Suzanne Granhøj, Schwartz, M., Batbayli, M., Waldemar, Gunhild & Nielsen, Jørgen Erik, 2009, In: Clinical Genetics. 76, 2, p. 205-9 4 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14

    Chelban, V., Wiethoff, S., Fabian-Jessing, B. K., Haridy, N. A., Khan, A., Efthymiou, S., Becker, E. B. E., O'Connor, E., Hersheson, J., Newland, K., Hojland, A. T., Gregersen, P. A., Lindquist, Suzanne Granhøj, Petersen, M. B., Nielsen, Jørgen Erik, Nielsen, M., Wood, N. W., Giunti, P. & Houlden, H., 2018, In: Movement Disorders. 33, 7, p. 1119-1129 11 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

    National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark

    Lildballe, D. L., Frederiksen, A. L., Schönewolf-Greulich, B., Brasch-Andersen, C., Lautrup, C. K., Karstensen, H. G., Pedersen, I. S., Sunde, Lone, Risom, L., Rasmussen, M., Bertelsen, M., Andersen, M. K., Rendtorff, N. D., Gregersen, P. A., Tørring, P. M., Hammer-Hansen, S., Boonen, S. E., Lindquist, Suzanne Granhøj, Hammer, T. B. & Diness, Birgitte Rode, 2023, In: European Journal of Medical Genetics. 66, 12, 5 p., 104872.

    Research output: Contribution to journal › Journal article › Research › peer-review

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