Suzanne Granhøj Lindquist

A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction

Andreas Puschmann, Owen A. Ross, Carles Vilariño‐Güell et al. · Parkinsonism & Related Disorders · 2009 · 99 citations · Full text

Neurodegenerative Diseases, Neurobiology Of Disease, Molecular Neuroscience +14

Alzheimer disease‐like clinical phenotype in a family with FTDP‐17 caused by a <i>MAPT</i> R406W mutation

Suzanne Granhøj Lindquist, Ida E. Holm, M. Schwartz et al. · European Journal of Neurology · 2008 · 82 citations

Further delineation of the 22q13 deletion syndrome

Suzanne Granhøj Lindquist, M. Kirchhoff, Claes Lundsteen et al. · Clinical Dysmorphology · 2005 · 47 citations

Down Syndrome, Karyotype Imaging, Dna Markers +15

Frontotemporal dementia linked to chromosome 3 (FTD‐3) – current concepts and the detection of a previously unknown branch of the Danish FTD‐3 family

Suzanne Granhøj Lindquist, Hans Brændgaard, Kirsten Svenstrup et al. · European Journal of Neurology · 2008 · 42 citations · Full text

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

Viorica Chelban, Sarah Wiethoff, Bjørn K. Fabian‐Jessing et al. · Movement Disorders · 2018 · 35 citations · Full text