Suzanne Granhøj Lindquist
Clinical Associate Professor
- 2023
- 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
- 2022
- Published
Arvelige neurologiske sygdomme
Lindquist, Suzanne Granhøj, 2022, Medicinsk genetik. FADL's Forlag, p. 229-244Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication
- Published
Arvelige ændringer i koagulationssystemet og hæmoglobinsygdomme
Hvass, A. M. F. & Lindquist, Suzanne Granhøj, 2022, Medicinsk genetik. FADL's Forlag, p. 331-335Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication
- Published
Demens og arvelighed
Lindquist, Suzanne Granhøj & Hasselbalch, Steen, 2022, Forstå demens. 3 ed. Hans Reitzels Forlag, p. 129-135Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Communication
- 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
- Published
Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival
Roos, P., Johannsen, P., Lindquist, Suzanne Granhøj, Brown, J. M., Waldemar, Gunhild, Duno, M., Nielsen, T. T., Budtz-Joergensen, Esben, Gydesen, S., Holm, I. E., Collinge, J., Isaacs, A. M. & Nielsen, Jørgen Erik, 2022, In: Acta Neurologica Scandinavica. 145, 5, p. 529-540 12 p.Research output: Contribution to journal › Review › Research › peer-review
- Published
Widening the spectrum of spinocerebellar ataxia autosomal recessive type 10 (SCAR10)
Ásbjörnsdóttir, B., Henriksen, O. M., Lindquist, Suzanne Granhøj, Møller, L. B., Sidaros, A. & Nielsen, Jørgen Erik, 2022, In: BMJ Case Reports. 15, 3, e248228.Research output: Contribution to journal › Journal article › Research › peer-review
- 2018
- 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
- Published
Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism
Areškeviciute, A., Melchior, L. C., Broholm, H., Krarup, L., Lindquist, Suzanne Granhøj, Johansen, P., McKenzie, N., Green, A., Nielsen, Jørgen Erik, Laursen, H. & Lund, Eva Løbner, 2018, In: Journal of Neuropathology and Experimental Neurology. 77, 8, p. 673-684 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2012
- 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
- 2010
- Published
Transthyretin as a potential CSF biomarker for Alzheimer's disease and dementia with Lewy bodies: effects of treatment with cholinesterase inhibitors
Schultz, K., Nilsson, K., Nielsen, Jørgen Erik, Lindquist, Suzanne Granhøj, Hjermind, L. E., Andersen, B. B., Wallin, A., Nilsson, C. & Petersén, A., 2010, In: European Journal of Neurology. 17, 3, p. 456-60 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2009
- 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
- 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
- Published
Reduced CSF CART in dementia with Lewy bodies
Schultz, K., Wiehager, S., Nilsson, K., Nielsen, Jørgen Erik, Lindquist, Suzanne Granhøj, Hjermind, L. E., Andersen, B. B., Wallin, A., Nilsson, C. & Petersén, A., 2009, In: Neuroscience Letters. 453, 2, p. 104-6 2 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2008
- 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 › Research
ID: 212552772