Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)
Journal Article (140)
61.
Journal Article
149 (7), pp. 1544 - 1549 (2009)
Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis. American Journal of Medical Genetics Part A 62.
Journal Article
24 (7), pp. 1247 - 1262 (2009)
Promiscuous and depolarization-induced immediate-early response genes are induced by mechanical strain of osteoblasts. Journal of Bone and Mineral Research 63.
Journal Article
94 (7), pp. 2658 - 2664 (2009)
Expanded clinical spectrum in hepatocyte nuclear factor 1B-maturity-onset diabetes of the young. Journal of Clinical Endocrinology & Metabolism 64.
Journal Article
27 (7), pp. 604 - 605 (2009)
Correspondence: Metabolic reconfiguration precedes transcriptional regulation in the antioxidant response. Nature biotechnology 65.
Journal Article
43 (10), pp. 941 - 945 (2009)
Exploring the genetic link between RLS and ADHD. Journal of Psychiatric Research 66.
Journal Article
10, p. 204 - 204 (2009)
Comparison of sequence-dependent tiling array normalization approaches. BMC Bioinformatics 67.
Journal Article
4 (6), p. e5967 - e5967 (2009)
Optimized null model for protein structure networks. PLoS ONE 68.
Journal Article
25 (21), pp. 2865 - 2871 (2009)
Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 69.
Journal Article
18 (12), pp. 2149 - 2165 (2009)
Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival. Human Molecular Genetics 70.
Journal Article
15, pp. 674 - 681 (2009)
Impaired gastric acidification negatively affects calcium homeostasis and bone mass. Nature Medicine 71.
Journal Article
10 (3), pp. 162 - 169 (2009)
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization. Amyotrophic Lateral Sclerosis 72.
Journal Article
21 (2), pp. 231 - 236 (2009)
Genetik der nichtsyndromalen geistigen Behinderung. Medizinische Genetik 73.
Journal Article
32 (3), pp. 226 - 230 (2009)
Hypergonadotropic hypogonadism in a patient with inv ins (2;4). International Journal of Andrology 74.
Journal Article
48 (6), pp. 510 - 520 (2009)
AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes. Genes, Chromosomes and Cancer 75.
Journal Article
24 (9), pp. 2225 - 2237 (2009)
Oct-4 regulates the expression of Stella and Foxj2 at the Nanog locus: implications for the developmental competence of mouse oocytes. Human Reproduction 76.
Journal Article
5, p. e1000487 - e1000487 (2009)
CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait. PLoS Genetics 77.
Journal Article
4 (5), p. e5548 - e5548 (2009)
Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. PLoS ONE 78.
Journal Article
106 (19), pp. 7810 - 7815 (2009)
Structure and function of primase RepB' encoded by broad-host-range plasmid RSF1010: that replicates exclusively in leading-strand mode. Proceedings of the National Academy of Sciences 79.
Journal Article
45 (5-6), pp. 252 - 263 (2009)
PBX1 is dispensable for neural commitment of RA-treated murine ES cells. In Vitro Cellular & Developmental Biology - Animal 80.
Journal Article
50 (5), pp. 816 - 828 (2009)
The Spt-Ada-Gcn5-acetyltransferase complex interaction motif of E2a is essential for a subset of transcriptional and oncogenic properties of E2a-Pbx1. Leukemia & Lymphoma