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1.
GBD 2021 Stroke Risk Factor Collaborators (Breitner-Busch, S.*): Global, regional, and national burden of stroke and its risk factors, 1990-2021: A systematic analysis for the Global Burden of Disease Study 2021. Lancet Neurol. 23, 973-1003 (2024)
2.
Morenas-Rodríguez, E.* et al.: Soluble TREM2 in CSF and its association with other biomarkers and cognition in autosomal-dominant Alzheimer's disease: A longitudinal observational study. Lancet Neurol. 21, 329-341 (2022)
3.
Miglis, M.G.* et al.: Biomarkers of conversion to α-synucleinopathy in isolated rapid-eye-movement sleep behaviour disorder. Lancet Neurol. 20, 671-684 (2021)
4.
Zech, M. et al.: Monogenic variants in dystonia: An exome-wide sequencing study. Lancet Neurol. 19, 908-918 (2020)
5.
Pottier, C.* et al.: Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: A genome-wide association study. Lancet Neurol. 17, 548-558 (2018)
6.
Trenkwalder, C.* et al.: Comorbidities, treatment, and pathophysiology in restless legs syndrome. Lancet Neurol. 17, 994-1005 (2018)
7.
Moss, D.J.H.* et al.: Identification of genetic variants associated with Huntington's disease progression: A genome-wide association study. Lancet Neurol. 16, 701-711 (2017)
8.
Schormair, B. et al.: Identification of novel risk loci for restless legs syndrome: A meta-analysis of genome-wide association studies in individuals of European ancestry: A meta-analysis. Lancet Neurol. 16, 898–907 (2017)
9.
Mok, K.Y.* et al.: Deletions at 22q11.2 in idiopathic Parkinson's disease: A combined analysis of genome-wide association data. Lancet Neurol. 15, 585-596 (2016)
10.
International Stroke Genetics Consortium (Pulit, S.L.* ; McArdle, P.F.* ; Wong, Q.* ; Malik, R.* ; Gieger, C. ; Meisinger, C. ; Müller-Nurasyid, M. ; Peters, A. ; Strauch, K. ; Waldenberger, M. ; Rosand, J.*): Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study. Lancet Neurol. 15, 174-184 (2016)
11.
Jansen, I.E.* et al.: CHCHD2 and Parkinson's disease. Lancet Neurol. 14, 678-679 (2015)
12.
International League Against Epilepsy Consortium on Complex Epilepsies (Gieger, C. ; Grallert, H. ; Heinrich, J. ; Holle, R. ; Leidl, R. ; Meisinger, C. ; Peters, A. ; Strauch, K.): Genetic determinants of common epilepsies: A meta-analysis of genome-wide association studies. Lancet Neurol. 13, 893-903 (2014)
13.
Trenkwalder, C.* et al.: Prolonged release oxycodone-naloxone for treatment of severe restless legs syndrome after failure of previous treatment: A double-blind, randomised, placebo-controlled trial with an open-label extension. Lancet Neurol. 12, 1141-1150 (2013)
14.
Kretzschmar, H.* & Illig, T.: Are further genetic factors associated with the risk of developing variant Creutzfeldt-Jakob disease? Lancet Neurol. 8, 25-26 (2009)
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