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 (247)
Journal Article
59 (1), pp. 68 - 81 (2011)
Prospectively isolated CD133/CD24-positive ependymal cells from the adult spinal cord and lateral ventricle wall differ in their long-term in vitro self-renewal and in vivo gene expression. GLIA
Journal Article
6 (11), p. e27352 (2011)
Mitochondrial-associated cell death mechanisms are reset to an embryonic-like state in aged donor-derived iPS cells harboring chromosomal aberrations. PLoS ONE
Journal Article
29 (9), pp. 1338 - 48 (2011)
Human induced pluripotent stem cells harbor homoplasmic and heteroplasmic mitochondrial DNA mutations while maintaining human embryonic stem cell-like metabolic reprogramming. Stem Cells
Journal Article
475 (7354), pp. 101 - 5 (2011)
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature
Journal Article
12 (2), pp. 165 - 7 (2011)
Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features. Neurogenetics
Journal Article
89 (1), pp. 176 - 82 (2011)
Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability. Am J Hum Genet
Journal Article
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol Psychiatry (2011)
Journal Article
48 (2), pp. 136 - 40 (2011)
Cohen syndrome diagnosis using whole genome arrays. J Med Genet
Journal Article
80 (2), pp. 127 - 32 (2011)
Strategies for exome and genome sequence data analysis in disease-gene discovery projects. Clin Genet
Journal Article
39 (7), pp. 2492 - 502 (2011)
Integrative analysis of genomic, functional and protein interaction data predicts long-range enhancer-target gene interactions. Nucleic Acids Res
Journal Article
27 (6), pp. 829 - 36 (2011)
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics
Journal Article
27 (6), pp. 829 - 36 (2011)
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics
Journal Article
12, p. 624 (2011)
A tandem sequence motif acts as a distance-dependent enhancer in a set of genes involved in translation by binding the proteins NonO and SFPQ. BMC Genomics
Journal Article
20 (13), pp. 2585 - 90 (2011)
Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP. Hum Mol Genet
Journal Article
155A (10), pp. 2566 - 70 (2011)
Madelung deformity in a girl with a novel and de novo mutation in the GNAS gene. Am J Med Genet A
Journal Article
107 (2), pp. 268 - 74 (2011)
Predictors of outcome of mitral valve prolapse in patients with the Marfan syndrome. Am J Cardiol
Journal Article
6 (8), p. e23882 (2011)
Matrin 3 binds and stabilizes mRNA. PLoS ONE
Journal Article
498 (1), pp. 67 - 71 (2011)
A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay. Neurosci Lett
Journal Article
31 (11), pp. 2326 - 40 (2011)
Cysteine 27 variant of the delta-opioid receptor affects amyloid precursor protein processing through altered endocytic trafficking. Molecular and Cellular Biology
Journal Article
745, pp. 537 - 48 (2011)
Live cell imaging of meiotic chromosome dynamics in yeast. Methods Mol Biol