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Christian Mertes
Christian Mertes
在 in.tum.de 的电子邮件经过验证
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Severe COVID-19 is marked by a dysregulated myeloid cell compartment
J Schulte-Schrepping, N Reusch, D Paclik, K Baßler, S Schlickeiser, ...
Cell 182 (6), 1419-1440. e23, 2020
13382020
Genetic diagnosis of Mendelian disorders via RNA sequencing
LS Kremer, DM Bader, C Mertes, R Kopajtich, G Pichler, A Iuso, TB Haack, ...
Nature communications 8 (15824), 2017
5452017
Longitudinal multi-omics analyses identify responses of megakaryocytes, erythroid cells, and plasmablasts as hallmarks of severe COVID-19
JP Bernardes, N Mishra, F Tran, T Bahmer, L Best, JI Blase, D Bordoni, ...
Immunity 53 (6), 1296-1314. e9, 2020
3202020
Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19
B Krämer, R Knoll, L Bonaguro, M ToVinh, J Raabe, ...
Immunity 54 (11), 2650-2669. e14, 2021
1922021
OUTRIDER: a statistical method for detecting aberrantly expressed genes in RNA sequencing data
F Brechtmann, C Mertes, A Matusevičiūtė, VA Yépez, Ž Avsec, M Herzog, ...
The American Journal of Human Genetics 103 (6), 907-917, 2018
1562018
Clinical implementation of RNA sequencing for Mendelian disease diagnostics
VA Yépez, M Gusic, R Kopajtich, C Mertes, NH Smith, CL Alston, R Ban, ...
Genome medicine 14 (1), 38, 2022
1252022
Detection of aberrant splicing events in RNA-seq data with FRASER
C Mertes, I Scheller, VA Yépez, MH Çelik, Y Liang, LS Kremer, M Gusic, ...
Nature communications 12 (529), 2021
1182021
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes
M Witzel, D Petersheim, Y Fan, E Bahrami, T Racek, M Rohlfs, J Puchałka, ...
Nature genetics 49 (5), 742-752, 2017
1112017
Detection of aberrant gene expression events in RNA sequencing data
VA Yépez, C Mertes, MF Müller, D Klaproth-Andrade, L Wachutka, ...
Nature Protocols 16, 1276-1296, 2021
982021
Mutations in MDH2, encoding a Krebs cycle enzyme, cause early-onset severe encephalopathy
S Ait-El-Mkadem, M Dayem-Quere, M Gusic, A Chaussenot, S Bannwarth, ...
The American Journal of Human Genetics 100 (1), 151-159, 2017
932017
Aberrant splicing prediction across human tissues
N Wagner, MH Çelik, FR Hölzlwimmer, C Mertes, H Prokisch, VA Yépez, ...
Nature genetics 55 (5), 861-870, 2023
332023
Integration of proteomics with genomics and transcriptomics increases the diagnostic rate of Mendelian disorders
R Kopajtich, D Smirnov, SL Stenton, S Loipfinger, C Meng, IF Scheller, ...
MedRxiv, 2021.03. 09.21253187, 2021
302021
Cloud prediction of protein structure and function with PredictProtein for Debian
L Kaján, G Yachdav, E Vicedo, M Steinegger, M Mirdita, C Angermüller, ...
BioMed Research International 2013 (1), 398968, 2013
242013
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
B Hagl, BD Spielberger, S Thoene, S Bonnal, C Mertes, C Winter, ...
Scientific Reports 8 (1), 16719, 2018
162018
Improved detection of aberrant splicing with FRASER 2.0 and the intron Jaccard index
IF Scheller, K Lutz, C Mertes, VA Yépez, J Gagneur
The American Journal of Human Genetics 110 (12), 2056-2067, 2023
11*2023
Towards real-time machine learning
A Hapfelmeier, C Mertes, J Schmidt, S Kramer
Proceedings of the ECML PKDD 2012 Workshop on Instant Interactive Data Mining, 2012
72012
NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling
F Hanssen, G Gabernet, F Bäuerle, B Stöcker, F Wiegand, NH Smith, ...
F1000Research 12, 1125, 2024
32024
Evaluation of input data modality choices on functional gene embeddings
F Brechtmann, T Bechtler, S Londhe, C Mertes, J Gagneur
NAR Genomics and Bioinformatics 5 (4), lqad095, 2023
32023
FRASER: Find RAre Splicing Events in RNA-seq Data
C Mertes, I Scheller, J Gagneur
2024
Splicing control by PHF5A is crucial for melanoma cell survival
T Meißgeier, M Kappelmann‐Fenzl, S Staebler, AJ Ahari, C Mertes, ...
Cell Proliferation, e13741, 2024
2024
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