| Age-specific CT and MRI templates for spatial normalization C Rorden, L Bonilha, J Fridriksson, B Bender, HO Karnath Neuroimage 61 (4), 957-965, 2012 | 665 | 2012 |
| Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study CD Whelan, A Altmann, JA Botía, N Jahanshad, DP Hibar, J Absil, ... Brain 141 (2), 391-408, 2018 | 412 | 2018 |
| Nigral stimulation for resistant axial motor impairment in Parkinson’s disease? A randomized controlled trial D Weiss, M Walach, C Meisner, M Fritz, M Scholten, S Breit, C Plewnia, ... Brain 136 (7), 2098-2108, 2013 | 225 | 2013 |
| Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum M Synofzik, AS Soehn, J Gburek-Augustat, J Schicks, KN Karle, R Schüle, ... Orphanet journal of rare diseases 8 (1), 41, 2013 | 181 | 2013 |
| Iterative reconstruction in head CT: image quality of routine and low-dose protocols in comparison with standard filtered back-projection A Korn, M Fenchel, B Bender, S Danz, TK Hauser, D Ketelsen, T Flohr, ... American journal of neuroradiology 33 (2), 218-224, 2012 | 160 | 2012 |
| Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study EL van der Ende, LH Meeter, JM Poos, JL Panman, LC Jiskoot, ... The Lancet Neurology 18 (12), 1103-1111, 2019 | 157 | 2019 |
| White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study SN Hatton, KH Huynh, L Bonilha, E Abela, S Alhusaini, A Altmann, ... Brain 143 (8), 2454-2473, 2020 | 146 | 2020 |
| The in vivo influence of white matter fiber orientation towards B0 on T2* in the human brain B Bender, U Klose NMR in Biomedicine 23 (9), 1071-1076, 2010 | 137 | 2010 |
| Distribution and prognostic relevance of tumor-infiltrating lymphocytes (TILs) and PD-1/PD-L1 immune checkpoints in human brain metastases PN Harter, S Bernatz, A Scholz, PS Zeiner, J Zinke, M Kiyose, S Blasel, ... Oncotarget 6 (38), 40836, 2015 | 128 | 2015 |
| In vivo molecular profiling of human glioma using diffusion kurtosis imaging JM Hempel, S Bisdas, J Schittenhelm, C Brendle, B Bender, H Wassmann, ... Journal of neuro-oncology 131, 93-101, 2017 | 82 | 2017 |
| Outcome after whole brain radiotherapy alone in intracranial leptomeningeal carcinomatosis from solid tumors C Gani, AC Müller, F Eckert, C Schroeder, B Bender, G Pantazis, ... Strahlentherapie und Onkologie 188 (2), 148, 2012 | 82 | 2012 |
| Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1 AV Strickland, M Schabhüttl, H Offenbacher, M Synofzik, NS Hauser, ... Journal of neurology 262, 2124-2134, 2015 | 76 | 2015 |
| 3D gradient echo snapshot CEST MRI with low power saturation for human studies at 3T A Deshmane, M Zaiss, T Lindig, K Herz, M Schuppert, C Gandhi, ... Magnetic resonance in medicine 81 (4), 2412-2423, 2019 | 75 | 2019 |
| PI3K Pathway Inhibition Achieves Potent Antitumor Activity in Melanoma Brain Metastases In Vitro and In Vivo H Niessner, J Schmitz, G Tabatabai, AM Schmid, C Calaminus, ... Clinical Cancer Research 22 (23), 5818-5828, 2016 | 75 | 2016 |
| De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) KN Karle, S Biskup, R Schüle, KJ Schweitzer, R Krüger, P Bauer, ... Neurology 81 (23), 2039-2044, 2013 | 71 | 2013 |
| Metabolic mapping of gliomas using hybrid MR-PET imaging: feasibility of the method and spatial distribution of metabolic changes S Bisdas, R Ritz, B Bender, C Braun, C Pfannenberg, M Reimold, ... Investigative radiology 48 (5), 295-301, 2013 | 71 | 2013 |
| Glioma Grading and Determination of IDH Mutation Status and ATRX loss by DCE and ASL Perfusion C Brendle, JM Hempel, J Schittenhelm, M Skardelly, G Tabatabai, ... Clinical Neuroradiology 28, 421-428, 2018 | 70 | 2018 |
| DeepCEST 3T: Robust MRI parameter determination and uncertainty quantification with neural networks—application to CEST imaging of the human brain at 3T F Glang, A Deshmane, S Prokudin, F Martin, K Herz, T Lindig, B Bender, ... Magnetic resonance in medicine 84 (1), 450-466, 2020 | 68 | 2020 |
| Motor protein mutations cause a new form of hereditary spastic paraplegia A Caballero Oteyza, E Battaloğlu, L Ocek, T Lindig, J Reichbauer, ... Neurology 82 (22), 2007-2016, 2014 | 68 | 2014 |
| STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations SN Hayer, T Deconinck, B Bender, K Smets, S Züchner, S Reich, L Schöls, ... Orphanet journal of rare diseases 12, 1-8, 2017 | 67 | 2017 |
