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Caspar Gross
Caspar Gross
Institute of Medicinal Genetics and Applied Genomics
Verified email at med.uni-tuebingen.de
Title
Cited by
Cited by
Year
Tracking of antibiotic resistance transfer and rapid plasmid evolution in a hospital setting by Nanopore sequencing
S Peter, M Bosio, C Gross, D Bezdan, J Gutierrez, P Oberhettinger, ...
Msphere 5 (4), 10.1128/msphere. 00525-20, 2020
632020
Identification of drug resistance determinants in a clinical isolate of Pseudomonas aeruginosa by high-density transposon mutagenesis
MS Sonnabend, K Klein, S Beier, A Angelov, R Kluj, C Mayer, C Groß, ...
Antimicrobial Agents and Chemotherapy 64 (3), 10.1128/aac. 01771-19, 2020
292020
Tracking of antibiotic resistance transfer and rapid plasmid evolution in a hospital setting by nanopore sequencing. mSphere. 2020: 5
S Peter, M Bosio, C Gross, D Bezdan, J Gutierrez, P Oberhettinger, ...
Hu X, Xu H, Shang Y, Guo L, Song L, Zhang H, Yue F, Jiang H, Zheng B. First …, 2018
212018
Multisystemic neurodegeneration caused by biallelic pentanucleotide expansions in RFC1
L Herrmann, M Gelderblom, M Bester, N Deininger, T Schütze, U Hidding, ...
Parkinsonism & related disorders 95, 54-56, 2022
102022
Exome sequencing and optical genome mapping in molecularly unsolved cases of duchenne muscular dystrophy: Identification of a causative X-chromosomal inversion disrupting the …
LS Erbe, S Hoffjan, S Janßen, M Kneifel, K Krause, WM Gerding, K Döring, ...
International Journal of Molecular Sciences 24 (19), 14716, 2023
92023
Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study
S Pachchek, Z Landoulsi, L Pavelka, C Schulte, E Buena-Atienza, ...
npj Parkinson's Disease 9 (1), 156, 2023
82023
GGC expansion in ZFHX3 causes SCA4 and impairs autophagy
KP Figueroa, C Gross, EB Atienza, S Paul, M Gandelman, T Haack, ...
MedRxiv, 2023.10. 26.23297560, 2023
72023
Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17
JJ Weber, SC Anger, P Pereira Sena, RD Incebacak Eltemur, C Huridou, ...
Cellular and Molecular Life Sciences 79 (5), 262, 2022
72022
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy
KP Figueroa, C Gross, E Buena-Atienza, S Paul, M Gandelman, N Kakar, ...
Nature Genetics, 1-10, 2024
62024
Whole genome analysis of two sympatric human Mansonella: Mansonella perstans and Mansonella sp “DEUX”
M Rodi, C Gross, TL Sandri, L Berner, M Marcet-Houben, E Kocak, ...
Frontiers in Cellular and Infection Microbiology 13, 1159814, 2023
32023
Author Correction: Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study
S Pachchek, Z Landoulsi, L Pavelka, C Schulte, E Buena-Atienza, ...
npj Parkinson's Disease 9 (1), 168, 2023
12023
Limited reciprocal surrogacy of bird and habitat diversity and inconsistencies in their representation in Romanian protected areas
JC Geue, PJ Rotter, C Gross, Z Benkő, I Kovács, C Fântână, ...
Plos one 17 (2), e0251950, 2022
12022
A rainfall-manipulation experiment with 517 Arabidopsis thaliana accessions
M Exposito-Alonso, R Gómez Rodríguez, C Barragán, G Capovilla, ...
bioRxiv, 186767, 2017
12017
Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects
B Wissinger, B Baumann, E Buena-Atienza, C Gross, S Kohl
NPJ Genomic Medicine 9 (1), 28, 2024
2024
Exome sequencing and optical genome mapping in molecularly unsolved cases of duchenne muscular dystrophy
LS Erbe, S Hoffjan, S Janßen, M Kneifel, K Krause, WM Gerding, K Döring, ...
2023
Accurate long-read sequencing identified GBA variants as a major genetic risk factor in the Luxembourg Parkinson’s study
R Krüger, S Pachchek, Z Landoulsi, L Pavelka, C Schulte, ...
Methods 1354, 38, 2023
2023
Accurate long-read sequencing identified GBA variants as a major genetic risk factor in the Luxembourg Parkinson\textquoterights study 2023.03. 29.23287880
S Peiris, Z Landoulsi, L Pavelka, C Schulte, E Buena-Atienza, C Gross, ...
medRxiv 2023.03. 29.23287880, 2023
2023
Accurate long-read sequencing identified GBA variants as a major genetic risk factor in the Luxembourg Parkinson’s study
SP Peiris, Z Landoulsi, L Pavelka, C Schulte, E Buena-Atienza, C Gross, ...
medRxiv, 2023.03. 29.23287880, 2023
2023
A35 Calpains contribute to the molecular pathogenesis of spinocerebellar ataxia type 17
JJ Weber, SC Anger, PP Sena, RDI Eltemur, C Huridou, F Fath, C Gross, ...
Journal of Neurology, Neurosurgery & Psychiatry 93 (Suppl 1), A12-A13, 2022
2022
Identification and clinical characterization of GBA variants in the Luxembourg Parkinson's Study
S Pachchek, Z Landoulsi, DR Bobbili, L Pavelka, O Terwindt, J Torre, ...
MOVEMENT DISORDERS 37, S572-S572, 2022
2022
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