Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)
Journal Article (223)
41.
Journal Article
467 (7314), pp. 460 - 464 (2010)
A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk. Nature 42.
Journal Article
42A (4), pp. 267 - 282 (2010)
Molecular signatures and new candidates to target the pathogenesis of rheumatoid arthritis. Physiological Genomics 43.
Journal Article
A blueprint of ectoine metabolism from the genome of the industrial producer Halomonas elongata DSM 2581(T). Environmental Microbiology (2010)
44.
Journal Article
9, p. 9:99 - 9:99 (2010)
Genetic and diet effects on Ppar-α and Ppar-γ signaling pathways in the Berlin Fat Mouse Inbred line with genetic predisposition for obesity. Lipids in Health and Disease 45.
Journal Article
10 (3), pp. 207 - 219 (2010)
The 2nd Berlin BedRest Study: protocol and implementation. Journal of Musculoskeletal and Neuronal Interaction 46.
Journal Article
12 (9), pp. 2466 - 2478 (2010)
Cultivation-independent characterization of ‘Candidatus Magnetobacterium bavaricum’ via ultrastructural, geochemical, ecological and metagenomic methods. Environmental Microbiology 47.
Journal Article
74 (5), pp. 452 - 462 (2010)
Haplotype misclassification from genotype error and statistical reconstruction and its impact on association estimates. Annals of Human Genetics 48.
Journal Article
42 (10), pp. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 49.
Journal Article
42 (10), pp. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 50.
Journal Article
42 (10), pp. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 51.
Journal Article
Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1. Learning Disabilities, pp. 125 - 133 (2010)
52.
Journal Article
20, pp. 1441 - 1450 (2010)
Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage. Genome Research 53.
Journal Article
152A (10), pp. 2651 - 2655 (2010)
11q14.1-11q22.1 deletion in a 1-year-old male with minor dysmorphic features. American Journal of Medical Genetics. Part A. 54.
Journal Article
11, p. 11:476 - 11:476 (2010)
Gill transcriptome response to changes in environmental calcium in the green spotted puffer fish. BMC Genomics 55.
Journal Article
344 (2), pp. 1001 - 1010 (2010)
Severe developmental bone phenotype in ClC-7 deficient mice. Developmental Biology 56.
Journal Article
87 (2), pp. 265 - 273 (2010)
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. American Journal of Human Genetics 57.
Journal Article
2 (8), pp. 475 - 486 (2010)
A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging. Aging (Albany NY) 58.
Journal Article
19, pp. 115 - 117 (2010)
Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. European Journal of Human Genetics 59.
Journal Article
107 (32), pp. 14211 - 14216 (2010)
Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region. Proceedings of the National Academy of Sciences U S A 60.
Journal Article
2, p. 2:59 - 2:59 (2010)
The application of massively parallel sequencing technologies in diagnostics. F1000 Biology Reports