Journal Article (116)
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Journal Article
20 (3), pp. 159 - 160 (2016)
Affect and motivation are critical in constructive meditation. Trends in Cognitive Sciences 82.
Journal Article
170 (3), pp. 615 - 621 (2016)
A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. American Journal of Medical Genetics Part A 83.
Journal Article
24 (3), pp. 392 - 399 (2016)
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration. European journal of human genetics 84.
Journal Article
16 (2), pp. 549 - 561 (2016)
Characterization of the genome and transcriptome of the blue tit Cyanistes caeruleus: polymorphisms, sex-biased expression and selection signals. Molecular Ecology Resources 85.
Journal Article
67 (1), pp. 78 - 83 (2016)
Identification of a molecular defect in a stillborn fetus with perinatal lethal hypophosphatasia using a disease-associated genome sequencing approach. Polish Journal of Pathology 86.
Journal Article
17 (3), pp. 139 - 154 (2016)
Molecular features of cellular reprogramming and development. Nature Reviews Molecular Cell Biology 87.
Journal Article
127, pp. 203 - 214 (2016)
Thinking about thinking: Neural mechanisms and effects on memory. NeuroImage 88.
Journal Article
36 (6), pp. 1794 - 1796 (2016)
Studying Mesodiencephalic Dopaminergic Neuron Development In Vivo to Improve Stem Cell Therapy in Parkinson’s Disease. The Journal of Neuroscience 89.
Journal Article
14 (5), pp. 1246 - 1257 (2016)
Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs. Cell Reports 90.
Journal Article
530 (7588), pp. 57 - 62 (2016)
Active medulloblastoma enhancers reveal subgroup-specific cellular origins. Nature 91.
Journal Article
2016, 15030 (2016)
The metabolic background is a global player in Saccharomyces gene expression epistasis. Nature Microbiology 92.
Journal Article
46 (2), pp. 637 - 648 (2016)
Preserved self-other distinction during empathy in autism is linked to network integrity of right supramarginal gyrus. Journal of Autism and Developmental Disorders 93.
Journal Article
37 (2), pp. 515 - 524 (2016)
Gray matter structural compromise is equally distributed in left and right temporal lobe epilepsy. Human Brain Mapping 94.
Journal Article
26 (2), pp. 183 - 191 (2016)
Exome Sequencing and CRISPR/Cas Genome Editing Identify Mutations of ZAK as a Cause of Limb Defects in Humans and Mice. Genome Research 95.
Journal Article
371 (1688), 20150547 (2016)
The role of self–other distinction in understanding others' mental and emotional states: Neurocognitive mechanisms in children and adults. Philosophical Transactions of the Royal Society of London, Series B: Biological Sciences 96.
Journal Article
2016, pp. 1 - 8 (2016)
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Famillial Cancer 97.
Journal Article
8, 8:85 (2016)
Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. Frontiers in Molecular Neuroscience 98.
Journal Article
575 (2 Pt 2), pp. 438 - 451 (2016)
Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 99.
Journal Article
80, pp. 71 - 78 (2016)
Understanding the influence of personality on dynamic social gesture processing: An fMRI study. Neuropsychologia 100.
Journal Article
13 (6), pp. 1183 - 1193 (2016)
Time-Dependent Gene Network Modelling by Sequential Monte Carlo. IEEE ACM Transactions on Computational Biology and Bioinformatics