Zeitschriftenartikel (3055)
421.
Zeitschriftenartikel
35 (6), S. 1009 - 1017 (2019)
The Distance Precision Matrix: computing networks from non-linear relationships. Bioinformatics 422.
Zeitschriftenartikel
9 (9), 4641 (2019)
DMSO induces drastic changes in human cellular processes and epigenetic landscape in vitro. Scientific Reports 423.
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2 (2), e201800283 (2019)
Expanding the repertoire of glucocorticoid receptor target genes by engineering genomic response elements. Life Science Alliance 424.
Zeitschriftenartikel
12, 12:60 (2019)
Mutation p.R356Q in the Collybistin Phosphoinositide Binding Site Is Associated With Mild Intellectual Disability. Frontiers in Molecular Neuroscience 425.
Zeitschriftenartikel
2019, 4:50 (2019)
Variant calling on the GRCh38 assembly with the data from phase three of the 1000 Genomes Project. Wellcome Open Research (open access publishing platform) 426.
Zeitschriftenartikel
21 (2), S. 198 - 213 (2019)
Combined Targeted Re-Sequencing of Cytosine DNA Methylation and Mutations of DNA Repair Genes with Potential Use for PARP1 Inhibitor Sensitivity Testing. The Journal of Molecular Diagnostics 427.
Zeitschriftenartikel
21 (2), S. 198 - 213 (2019)
Combined Targeted Resequencing of Cytosine DNA Methylation and Mutations of DNA Repair Genes with Potential Use for Poly(ADP-Ribose) Polymerase 1 Inhibitor Sensitivity Testing. The Journal of Molecular Diagnostics 428.
Zeitschriftenartikel
39 (3), S. 540 - 556 (2019)
Genetic determinants of steatosis and fibrosis progression in paediatric non‐alcoholic fatty liver disease. Liver International 429.
Zeitschriftenartikel
21 (3), S. 305 - 310 (2019)
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations. Nature Cell Biology 430.
Zeitschriftenartikel
12, S. 27 - 40 (2019)
Tissue-Specific Chk1 Activation Determines Apoptosis by Regulating the Balance of p53 and p21. iScience 431.
Zeitschriftenartikel
28 (4), S. 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 432.
Zeitschriftenartikel
28 (4), S. 615 - 627 (2019)
Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution. Human Molecular Genetics 433.
Zeitschriftenartikel
35 (2), S. 330 - 332 (2019)
KDM5 Histone Demethylase Activity Links Cellular Transcriptomic Heterogeneity to Therapeutic Resistance. Cancer Cell 434.
Zeitschriftenartikel
23 (4), S. 2526 - 2535 (2019)
An integrative systems approach identifies novel candidates in Marfan syndrome-related pathophysiology. Journal of Cellular and Molecular Medicine 435.
Zeitschriftenartikel
179 (1), S. 13 - 19 (2019)
GPR126: A novel candidate gene implicated in autosomal recessive intellectual disability. Am J Med Genet A 436.
Zeitschriftenartikel
95 (1), S. 151 - 159 (2019)
Effect of inbreeding on intellectual disability revisited by Trio sequencing. Clinical Genetics: an international journal of genetics in medicine 437.
Zeitschriftenartikel
22 (1), S. 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 438.
Zeitschriftenartikel
115 (51), S. 13021 - 13026 (2018)
Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice. Proceedings of the National Academy of Sciences of the United States of America 439.
Zeitschriftenartikel
34 (6), S. 996 - 1011 (2018)
Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories. Cancer Cell 440.
Zeitschriftenartikel
23 (6), S. 900 - 904 (2018)
Esrrb Unlocks Silenced Enhancers for Reprogramming to Naive Pluripotency - Correction. Cell Stem Cell