Suzanne Granhøj Lindquist

Research output

Research output per year 2008 2009 2022 2023

• 217 Citations
• 10 Journal article
• 3 Book chapter
• 1 Ph.D. thesis
• 1 Review

Research output per year

Research output per year

Search results

• 2023

  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, L., 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, S. G., Hammer, T. B. & Diness, B. R., 2023, In: European Journal of Medical Genetics. 66, 12, 5 p., 104872.

  Research output: Contribution to journal › Journal article › Research › peer-review
  1 Citation (Scopus)
• 2022

  Arvelige ændringer i koagulationssystemet og hæmoglobinsygdomme

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

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

• Arvelige neurologiske sygdomme

  Lindquist, S. G., 2022, Medicinsk genetik. FADL's Forlag, p. 229-244

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

• Demens og arvelighed

  Lindquist, S. G. & Hasselbalch, S., 2022, Forstå demens. 3 ed. Hans Reitzels Forlag, p. 129-135

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

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

  Nielsen, E. N., Ásbjörnsdóttir, B., Møller, L. B., Nielsen, J. E. & Lindquist, S. G., 2022, In: Cold Spring Harbor molecular case studies. 8, 6, a006236.

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

  Open Access

  File
  16 Downloads (Pure)

• Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival

  Roos, P., Johannsen, P., Lindquist, S. G., Brown, J. M., Waldemar, G., Duno, M., Nielsen, T. T., Budtz-Jorgensen, E., Gydesen, S., Holm, I. E., Collinge, J., Isaacs, A. M. & Nielsen, J. E., 2022, In: Acta Neurologica Scandinavica. 145, 5, p. 529-540 12 p.

  Research output: Contribution to journal › Review › Research › peer-review
  4 Citations (Scopus)

• Widening the spectrum of spinocerebellar ataxia autosomal recessive type 10 (SCAR10)

  Ásbjörnsdóttir, B., Henriksen, O. M., Lindquist, S., Møller, L. B., Sidaros, A. & Nielsen, J. E., 2022, In: BMJ Case Reports. 15, 3, e248228.

  Research output: Contribution to journal › Journal article › Research › peer-review
  1 Citation (Scopus)
• 2018

  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, S. G., Petersen, M. B., Nielsen, J. E., 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

  Open Access
  27 Citations (Scopus)

• 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-H., Lindquist, S. G., Johansen, P., McKenzie, N., Green, A., Nielsen, J. E., Laursen, H. & Lund, E. L., 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
  6 Citations (Scopus)
• 2012

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

  Ravn, K., Lindquist, S. G., Nielsen, K., Dahm, T. & Tümer, Z., Sep 2012, In: Clinical Genetics. 82, 3, p. 292-294 3 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  22 Citations (Scopus)
• 2010

  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, J. E., Lindquist, S. G., 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
  22 Citations (Scopus)
• 2009

  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, S. G., Nielsen, J. E., 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
  88 Citations (Scopus)

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

  Lindquist, S. G., Schwartz, M., Batbayli, M., Waldemar, G. & Nielsen, J. E., 2009, In: Clinical Genetics. 76, 2, p. 205-9 4 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  21 Citations (Scopus)

• Reduced CSF CART in dementia with Lewy bodies

  Schultz, K., Wiehager, S., Nilsson, K., Nielsen, J. E., Lindquist, S. G., 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
  25 Citations (Scopus)
• 2008

  Autosomal dominant inherited dementia - clinical and molecular genetic aspects

  Lindquist, SG., 2008, København: Museum Tusculanum. 39 p.

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