Max Planck Publications of Lastname Lab
The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.
Journal Article (102)
Journal Article
18 (1), 1:240 (2017)
PureCLIP: Capturing target-specific protein-RNA interaction footprints from single-nucleotide CLIP-seq data. Genome Biology
Journal Article
2, pp. 45 - 51 (2017)
Preschool children and chimpanzees incur costs to watch punishment of antisocial others. Nature Human Behaviour
Journal Article
33 (24), pp. 3929 - 3937 (2017)
An improved compound Poisson model for the number of motif hits in DNA sequences. Bioinformatics
Journal Article
21 (10), pp. 2813 - 2828 (2017)
Non-Canonical Hedgehog Signaling Is a Positive Regulator of the WNT Pathway and Is Required for the Survival of Colon Cancer Stem Cells. Cell Reports
Journal Article
3 (6), e200 (2017)
CDKL5 variants: Improving our understanding of a rare neurologic disorder. Neurology Genetics
Journal Article
8 (6), pp. 1488 - 1512 (2017)
Differential effects of attention-, compassion- and socio-cognitively based mental practices on self-reports of mindfulness and compassion. Mindfulness
Journal Article
17 (8), pp. 1156 - 1165 (2017)
Influences of oxytocin and respiratory sinus arrhythmia on emotions and social behavior in daily life. Emotion
Journal Article
2017, 8:105882-105904 (2017)
Renal oncocytoma characterized by the defective complex I of the respiratory chain boosts the synthesis of the ROS scavenger glutathione. Oncotarget
Journal Article
261, pp. 157 - 168 (2017)
The SeqAn C++ template library for efficient sequence analysis: A resource for programmers. Journal of Biotechnology
Journal Article
372 (1733), pii: 20160366 (2017)
X-chromosome dosage as a modulator of pluripotency, signalling and differentiation? Philosophical Transactions of the Royal Society of London, Series B: Biological Sciences
Journal Article
101 (5), pp. 833 - 843 (2017)
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. The American Journal of Human Genetics
Journal Article
45 (19), pp. 11004 - 11018 (2017)
ssHMM: extracting intuitive sequence-structure motifs from high-throughput RNA-binding protein data. Nucleic Acids Research (London)
Journal Article
27 (11), pp. 1916 - 1929 (2017)
The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology. Genome Research
Journal Article
140 (11), pp. 2879 - 2894 (2017)
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features. Brain
Journal Article
54 (11), pp. 754 - 761 (2017)
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction. Journal of Medical Genetics
Journal Article
9, 349 (2017)
The influence of negative emotion on cognitive and emotional control remains intact in aging. Frontiers in Aging Neuroscience
Journal Article
8 (1), 1218 (2017)
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development. Nature Communications
Journal Article
14 (12), pp. 1213 - 1221 (2017)
Protein interaction perturbation profiling at amino-acid resolution. Nature methods
Journal Article
3 (10), e1700495 (2017)
Specific reduction in cortisol stress reactivity after social but not attention-based mental training. Science Advances
Journal Article
3 (10), e1700489 (2017)
Structural plasticity of the social brain: Differential change after socio-affective and cognitive mental training. Science Advances