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Malte Spielmann
Malte Spielmann
Institute of Human Genetics, University of Lübeck
Verified email at uw.edu
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Cited by
Year
The single-cell transcriptional landscape of mammalian organogenesis
J Cao, M Spielmann, X Qiu, X Huang, DM Ibrahim, AJ Hill, F Zhang, ...
Nature 566 (7745), 496-502, 2019
24772019
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions
DG Lupiáñez, K Kraft, V Heinrich, P Krawitz, F Brancati, E Klopocki, ...
Cell 161 (5), 1012-1025, 2015
20632015
Formation of new chromatin domains determines pathogenicity of genomic duplications
M Franke, DM Ibrahim, G Andrey, W Schwarzer, V Heinrich, R Schöpflin, ...
Nature 538 (7624), 265-269, 2016
6682016
Structural variation in the 3D genome
M Spielmann, DG Lupiáñez, S Mundlos
Nature Reviews Genetics 19 (7), 453-467, 2018
6022018
A human cell atlas of fetal gene expression
J Cao, DR O’day, HA Pliner, PD Kingsley, M Deng, RM Daza, MA Zager, ...
Science 370 (6518), eaba7721, 2020
4932020
Breaking TADs: how alterations of chromatin domains result in disease
DG Lupiáñez, M Spielmann, S Mundlos
Trends in Genetics 32 (4), 225-237, 2016
4492016
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome
T Zemojtel, S Köhler, L Mackenroth, M Jäger, J Hecht, P Krawitz, ...
Science translational medicine 6 (252), 252ra123-252ra123, 2014
2782014
A whole-genome analysis framework for effective identification of pathogenic regulatory variants in Mendelian disease
D Smedley, M Schubach, JOB Jacobsen, S Köhler, T Zemojtel, ...
The American Journal of Human Genetics 99 (3), 595-606, 2016
2752016
Deletions, inversions, duplications: engineering of structural variants using CRISPR/Cas in mice
K Kraft, S Geuer, AJ Will, WL Chan, C Paliou, M Borschiwer, I Harabula, ...
Cell reports 10 (5), 833-839, 2015
2382015
Comparison of exome and genome sequencing technologies for the complete capture of protein‐coding regions
SH Lelieveld, M Spielmann, S Mundlos, JA Veltman, C Gilissen
Human mutation 36 (8), 815-822, 2015
2042015
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state
S Smajić, CA Prada-Medina, Z Landoulsi, J Ghelfi, S Delcambre, ...
Brain 145 (3), 964-978, 2022
1892022
Enhanced susceptibility to infections in a diabetic wound healing model
T Hirsch, M Spielmann, B Zuhaili, T Koehler, M Fossum, HU Steinau, ...
BMC surgery 8, 1-8, 2008
1792008
Human beta‐defensin‐3 promotes wound healing in infected diabetic wounds
T Hirsch, M Spielmann, B Zuhaili, M Fossum, M Metzig, T Koehler, ...
The Journal of Gene Medicine: A cross‐disciplinary journal for research on …, 2009
1782009
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesis
BK Kragesteen, M Spielmann, C Paliou, V Heinrich, R Schöpflin, ...
Nature genetics 50 (10), 1463-1473, 2018
1702018
Deletions of chromosomal regulatory boundaries are associated with congenital disease
J Ibn-Salem, S Köhler, MI Love, HR Chung, N Huang, ME Hurles, ...
Genome biology 15, 1-16, 2014
1672014
Deletions of chromosomal regulatory boundaries are associated with congenital disease
J Ibn-Salem, S Köhler, MI Love, HR Chung, N Huang, ME Hurles, ...
Genome biology 15, 1-16, 2014
1672014
Embryo-scale, single-cell spatial transcriptomics
SR Srivatsan, MC Regier, E Barkan, JM Franks, JS Packer, P Grosjean, ...
Science 373 (6550), 111-117, 2021
1602021
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)
E Giorgio, D Robyr, M Spielmann, E Ferrero, E Di Gregorio, D Imperiale, ...
Human molecular genetics 24 (11), 3143-3154, 2015
1562015
Looking beyond the genes: the role of non-coding variants in human disease
M Spielmann, S Mundlos
Human molecular genetics 25 (R2), R157-R165, 2016
1512016
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus
M Spielmann, F Brancati, PM Krawitz, PN Robinson, DM Ibrahim, ...
The American Journal of Human Genetics 91 (4), 629-635, 2012
1412012
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