| Gut microbiota in Parkinson disease in a northern German cohort F Hopfner, A Künstner, SH Müller, S Künzel, KE Zeuner, NG Margraf, ... Brain research 1667, 41-45, 2017 | 303 | 2017 |
| Genetic predisposition in anti‐LGI1 and anti‐NMDA receptor encephalitis SH Mueller, A Färber, H Prüss, N Melzer, KS Golombeck, T Kümpfel, ... Annals of neurology 83 (4), 863-869, 2018 | 124 | 2018 |
| Genome-wide association study in essential tremor identifies three new loci SH Müller, SL Girard, F Hopfner, ND Merner, CV Bourassa, D Lorenz, ... Brain 139 (12), 3163-3169, 2016 | 93 | 2016 |
| Febrile infection‐related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations S Appenzeller, I Helbig, U Stephani, M Haeusler, G Kluger, M Bungeroth, ... Developmental Medicine & Child Neurology 54 (12), 1144-1148, 2012 | 75 | 2012 |
| Comparing clinical trial population representativeness to real-world populations: an external validity analysis encompassing 43 895 trials and 5 685 738 individuals across 989 … YY Tan, V Papez, WH Chang, SH Mueller, S Denaxas, AG Lai The Lancet Healthy Longevity 3 (10), e674-e689, 2022 | 71 | 2022 |
| Rare variants in specific lysosomal genes are associated with Parkinson's disease F Hopfner, SH Mueller, S Szymczak, O Junge, L Tittmann, S May, ... Movement Disorders 35 (7), 1245-1248, 2020 | 44 | 2020 |
| Topography of essential tremor W Chen, F Hopfner, S Szymczak, O Granert, SH Müller, G Kuhlenbäumer, ... Parkinsonism & Related Disorders 40, 58-63, 2017 | 35 | 2017 |
| Late effects of cancer in children, teenagers and young adults: population-based study on the burden of 183 conditions, in-patient and critical care admissions and years of … WH Chang, M Katsoulis, YY Tan, SH Mueller, K Green, AG Lai The Lancet Regional Health-Europe 12, 100248, 2022 | 27 | 2022 |
| Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis C Liao, CE Castonguay, K Heilbron, V Vuokila, M Medeiros, G Houle, ... JAMA neurology 79 (2), 185-193, 2022 | 19 | 2022 |
| Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome I Helbig, G Barcia, M Pendziwiat, S Ganesan, SH Mueller, KL Helbig, ... Annals of clinical and translational neurology 7 (8), 1429-1435, 2020 | 19 | 2020 |
| Increased burden of cardiovascular disease in people with liver disease: unequal geographical variations, risk factors and excess years of life lost WH Chang, SH Mueller, SC Chung, GR Foster, AG Lai Journal of translational medicine 20 (1), 1-13, 2022 | 17 | 2022 |
| c. 207C> G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia AS Shalash, TW Rösler, SH Müller, M Salama, G Deuschl, U Müller, ... Neurology Genetics 3 (6), 2017 | 17 | 2017 |
| Antithrombotic therapy in patients with liver disease: Population-based insights on variations in prescribing trends, adherence, persistence and impact on stroke and bleeding WH Chang, SH Mueller, YY Tan, AG Lai The Lancet Regional Health-Europe 10, 100222, 2021 | 15 | 2021 |
| The impact of rare variants in FUS in essential tremor F Hopfner, G Stevanin, SH Müller, E Mundwiller, M Bungeroth, A Durr, ... Movement Disorders 30 (5), 721-724, 2015 | 15 | 2015 |
| Multiomics analyses identify genes and pathways relevant to essential tremor C Liao, F Sarayloo, D Rochefort, G Houle, F Akçimen, Q He, AD Laporte, ... Movement Disorders 35 (7), 1153-1162, 2020 | 14 | 2020 |
| No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors F Hopfner, SH Müller, D Steppat, J Miller, N Schmidt, KP Wandinger, ... Translational neurodegeneration 8 (1), 1-7, 2019 | 14 | 2019 |
| Cloning, sequencing and recombinant expression of the open reading frame encoding a novel member of the Sarcocystis muris (Apicomplexa) microneme lectin family H Klein, S Mueller, B Loeschner, RR Toenjes, G Braun, EC Mueller, ... Parasitology research 90 (1), 84-86, 2003 | 10 | 2003 |
| Mendelian randomization analyses implicate biogenesis of translation machinery in human aging S Javidnia, S Cranwell, SH Mueller, C Selman, JMA Tullet, ... Genome research 32 (2), 258-265, 2022 | 8 | 2022 |
| An international consensus on an approach to the diagnosis and management of psychosis of suspected autoimmune origin: the concept of autoimmune psychosis TA Pollak, B Lennox, S Müller, ME Benros, H Prüss, L Tebartz van Elst, ... Lancet Psychiatry 7 (1), 93-108, 2020 | 8 | 2020 |
| Multimorbidity patterns and risk of hospitalisation in children: A population cohort study of 3.6 million children in England, with illustrative examples from childhood cancer … SC Chung, S Mueller, K Green, WH Chang, D Hargrave, AG Lai The Lancet Regional Health-Europe 20, 100433, 2022 | 7 | 2022 |
