Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)
Journal Article (94)
81.
Journal Article
21 (3), pp. 305 - 310 (2019)
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations. Nature Cell Biology 82.
Journal Article
15 (2), e1007964 (2019)
Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype. PLOS Genetics 83.
Journal Article
12, pp. 27 - 40 (2019)
Tissue-Specific Chk1 Activation Determines Apoptosis by Regulating the Balance of p53 and p21. iScience 84.
Journal Article
124, pp. 117 - 124 (2019)
Inter-brain synchrony in mother-child dyads during cooperation: An fNIRS hyperscanning study. Neuropsychologia 85.
Journal Article
28 (4), pp. 598 - 614 (2019)
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation. Human Molecular Genetics 86.
Journal Article
28 (4), pp. 615 - 627 (2019)
Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution. Human Molecular Genetics 87.
Journal Article
6, 180307 (2019)
A functional connectome phenotyping dataset including cognitive state and personality measures. Scientific Data 88.
Journal Article
35 (2), pp. 330 - 332 (2019)
KDM5 Histone Demethylase Activity Links Cellular Transcriptomic Heterogeneity to Therapeutic Resistance. Cancer Cell 89.
Journal Article
9, 1492 (2019)
Neural mechanisms of affective matching across faces and scenes. Scientific Reports 90.
Journal Article
23 (4), pp. 2526 - 2535 (2019)
An integrative systems approach identifies novel candidates in Marfan syndrome-related pathophysiology. Journal of Cellular and Molecular Medicine 91.
Journal Article
26 (4), pp. 1059 - 1069 (2019)
Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes. Cell Reports 92.
Journal Article
179 (1), pp. 13 - 19 (2019)
GPR126: A novel candidate gene implicated in autosomal recessive intellectual disability. Am J Med Genet A 93.
Journal Article
95 (1), pp. 151 - 159 (2019)
Effect of inbreeding on intellectual disability revisited by Trio sequencing. Clinical Genetics: an international journal of genetics in medicine 94.
Journal Article
22 (1), pp. 37 - 46 (2019)
Epigenome-wide study uncovers large-scale changes in histone acetylation driven by tau pathology in aging and Alzheimer's human brains. Nature Neuroscience Conference Paper (2)
95.
Conference Paper
LNBI 11773, pp. 96 - 119 (Eds. Bortolussi, L.; Sanguinetti, G.). 17th International Conference, CMSB 2019: Computational Methods in Systems Biology, Trieste, Italy, September 18, 2019 - September 20, 2019. Springer Nature Switzerland AG, Cham, Switzerland (2019)
Designing Distributed Cell Classifier Circuits Using a Genetic Algorithm. In: CMSB 2019, part of Lecture Notes in Computer Science 11773, Vol. 96.
Conference Paper
Nanopore SimulatION – a raw data simulator for Nanopore Sequencing. In: 2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), pp. 1536 - 1543. 2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), Madrid, Spain, December 03, 2018 - December 06, 2018. (2019)
Thesis - PhD (6)
97.
Thesis - PhD
Bioinformatic Reconstruction of Gene Regulatory Networks Controlling EMT and Mesoderm Formation. Dissertation (2019)
98.
Thesis - PhD
De novo and haplotype assembly of polyploid genomes. Dissertation, vii, 157 pp. (2019)
99.
Thesis - PhD
Dissecting the genetic basis of transcriptional and translational regulation in heart and liver. Dissertation, V, 108 pp. (2019)
100.
Thesis - PhD
Enhancer Prediction Based on Epigenomic Data. Dissertation, iv, 186 pp. (2019)