Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)
Journal Article (128)
41.
Journal Article
15, pp. 33 - 40 (2015)
Network and systems biology: essential steps in virtualising drug discovery and development. Drug Discovery Today: Technology 42.
Journal Article
524 (7563), pp. 47 - 53 (2015)
Comprehensive genomic profiles of small cell lung cancer. Nature 43.
Journal Article
97 (2), pp. 302 - 310 (2015)
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability. The American Journal of Human Genetics 44.
Journal Article
97 (2), pp. 343 - 352 (2015)
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. The American Journal of Human Genetics 45.
Journal Article
112 (31), pp. E4236 - E4245 (2015)
Simultaneous deletion of the methylcytosine oxidases Tet1 and Tet3 increases transcriptome variability in early embryogenesis. Proceedings of the National Academy of Sciences of the United States of America 46.
Journal Article
58 (8), pp. 376 - 380 (2015)
FGFR2 mutation in a patient without typical features of Pfeiffer syndrome--The emerging role of combined NGS and phenotype based strategies. European Journal of Medical Genetics 47.
Journal Article
25 (8), pp. 1215 - 1228 (2015)
Quantification of GC-biased gene conversion in the human genome. Genome Research 48.
Journal Article
36 (8), pp. 815 - 822 (2015)
Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions. Human Mutations 49.
Journal Article
40 (4), pp. 402 - 423 (2015)
Visualizing confidence bands for semiparametrically estimated nonlinear relations among latent variables. Journal of Educational and Behavioral Statistics 50.
Journal Article
469 (3), pp. 409 - 420 (2015)
Cyclin Y phosphorylation- and 14-3-3-binding-dependent activation of PCTAIRE-1/CDK16. Biochemical Journal 51.
Journal Article
60 (8), pp. 419 - 425 (2015)
Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations? JOURNAL OF HUMAN GENETICS 52.
Journal Article
9, 202 (2015)
The impact of perceived similarity on tacit coordination: Propensity for matching and aversion to decoupling choices. Frontiers in Behavioral Neuroscience 53.
Journal Article
52 (7), pp. 476 - 483 (2015)
Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type. Journal of Medical Genetics 54.
Journal Article
47 (7), pp. 822 - 826 (2015)
Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics 55.
Journal Article
26 (7), pp. 1144 - 1146 (2015)
Evidence for the upward spiral stands steady: A response to Heathers, Brown, Coyne, & Friedman. Psychological Science 56.
Journal Article
97 (1), pp. 38 - 45 (2015)
Is meditation always relaxing?: Investigating heart rate, heart rate variability, experienced effort and likeability during training of three types of meditation. International Journal of Psychophysiology 57.
Journal Article
29 (7), pp. 1037 - 1054 (2015)
miR-22 and miR-29a are members of the androgen receptor cistrome modulating LAMC1 and Mcl-1 in prostate cancer. Molecular Endocrinology 58.
Journal Article
10 (6), e0132209 (2015)
Shaped by the past: The default mode network supports cognition that is independent of immediate perceptual input. PLoS One 59.
Journal Article
24 (12), pp. 3335 - 3347 (2015)
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain. Human Molecular Genetics 60.
Journal Article
112 (22), pp. 7009 - 7014 (2015)
Structural rearrangements in the phage head-to-tail interface during assembly and infection. Proceedings of the National Academy of Sciences of the United States of America