Gschwendtner, Andreas

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

Gudbjartsson, D. F., Holm, H., Gretarsdottir, S., Thorleifsson, G., Walters, G. B., Thorgeirsson, G., Gulcher, J., Mathiesen, E. B., Njølstad, I., Nyrnes, A., et al. (2009) · Nature Genetics

Atrial Fibrillation Management and OutcomesGenetic Associations and Epidemiology

Cited by 489

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

International Stroke Genetics Consortium, Debette, S., the CADISP group, Kamatani, Y., Metso, T. M., Kloss, M., Chauhan, G., Engelter, S. T., Pezzini, A., Thijs, V., et al. (2015) · Nature Genetics

Cerebrovascular and Carotid Artery DiseasesGenetic Associations and Epidemiology

Cited by 231

Diffusion Magnetic Resonance Histograms as a Surrogate Marker and Predictor of Disease Progression in CADASIL: A Two-Year Follow-Up Study

Holtmannspötter, M., Peters, N., Opherk, C., Martin, D., Herzog, J., Brückmann, H., Sämann, P., Gschwendtner, A., & Dichgans, M. (2005) · Stroke

Cerebrovascular and genetic disordersAdvanced Neuroimaging Techniques and Applications

Cited by 140

Impact of MRI markers in subcortical vascular dementia: A multi-modal analysis in CADASIL

Viswanathan, A., Godin, O., Jouvent, E., O’Sullivan, M., Gschwendtner, A., Peters, N., Duering, M., Guichard, J.-P., Holtmannspötter, M., Dufouil, C., et al. (2010) · Neurobiology of Aging

Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments

Cited by 139

Brain atrophy is related to lacunar lesions and tissue microstructural changes in CADASIL

Jouvent, E., Viswanathan, A., Mangin, J.-F., O’Sullivan, M., Guichard, J.-P., Gschwendtner, A., Cumurciuc, R., Buffon, F., Peters, N., Pachaï, C., et al. (2007) · Stroke

Cerebrovascular and genetic disordersIntracerebral and Subarachnoid Hemorrhage Research

Cited by 109

Identification of a strategic brain network underlying processing speed deficits in vascular cognitive impairment

Duering, M., Gonik, M., Malik, R., Zieren, N., Reyes, S., Jouvent, E., Hervé, D., Gschwendtner, A., Opherk, C., Chabriat, H., et al. (2013) · NeuroImage

Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments

Cited by 89

Hippocampal volume is an independent predictor of cognitive performance in CADASIL

O'Sullivan, M., Ngo, E., Viswanathan, A., Jouvent, E., Gschwendtner, A., Saemann, P. G., Duering, M., Pachai, C., Bousser, M.-G., Chabriat, H., et al. (2009) · Neurobiology of Aging

Neurological Disease Mechanisms and TreatmentsCerebrovascular and genetic disorders

Cited by 85

Education modifies the relation of vascular pathology to cognitive function: cognitive reserve in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Zieren, N., Duering, M., Peters, N., Reyes, S., Jouvent, E., Hervé, D., Gschwendtner, A., Mewald, Y., Opherk, C., Chabriat, H., et al. (2013) · Neurobiology of Aging

Cerebrovascular and genetic disordersDementia and Cognitive Impairment Research

Cited by 65

Extensive White Matter Hyperintensities May Increase Brain Volume in Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

Yao, M., Jouvent, E., During, M., Godin, O., Hervé, D., Guichard, J. P., Zhu, Y.-C., Gschwendtner, A., Opherk, C., Dichgans, M., et al. (2012) · Stroke

Cerebrovascular and genetic disordersIntracerebral and Subarachnoid Hemorrhage Research

Cited by 42