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
120 (2), pp. 151 - 7 (2011)
Rap1-independent telomere attachment and bouquet formation in mammalian meiosis. Chromosoma
Journal Article
68 (2), pp. 207 - 13 (2011)
The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels. Archives of General Psychiatry
Journal Article
88 (5), pp. 628 - 34 (2011)
Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. Am J Hum Genet
Journal Article
88 (5), pp. 628 - 34 (2011)
Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. Am J Hum Genet
Journal Article
12, p. 441 (2011)
Exact score distribution computation for ontological similarity searches. BMC Bioinformatics
Journal Article
152 (12), pp. 4641 - 51 (2011)
Role of medium- and short-chain L-3-hydroxyacyl-CoA dehydrogenase in the regulation of body weight and thermogenesis. Endocrinology
Journal Article
410 (1), pp. 155 - 157 (2011)
A streamlined protocol for emulsion polymerase chain reaction and subsequent purification. Analytical Biochemistry
Journal Article
6 (12), p. e29604 - e29604 (2011)
Probing the SELEX Process with Next-Generation Sequencing. PLoS ONE
Journal Article
30 (2), pp. 199 - 210 (2011)
The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations. Cancer Metastasis Reviews
Journal Article
6 (1), p. 18 (2011)
DeBi: Discovering Differentially Expressed Biclusters using a Frequent Itemset Approach. Algorithms Mol Biol
Journal Article
79 (6), pp. 568 - 74 (2011)
Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2. Clin Genet
Journal Article
155A (8), pp. 1848 - 56 (2011)
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Delta(1)-pyrroline-5-carboxylate synthase (P5CS). Am J Med Genet A
Journal Article
43 (10), pp. 977 - 83 (2011)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet
Journal Article
5 (2), pp. 63 - 77 (2011)
Mind-wandering while reading: Attentional decoupling, mindless reading and the cascade model of inattention. Language and Linguistics Compass
Journal Article
2 (2), pp. 122 - 123 (2011)
Stimulus independence, social cognition and consciousness. Cognitive Neuroscience
Journal Article
21 (3), pp. 364 - 76 (2011)
Interactome mapping suggests new mechanistic details underlying Alzheimer's disease. Genome Res
Journal Article
54 (4), pp. e441 - 5 (2011)
Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings. Eur J Med Genet
Journal Article
59 (3), pp. 549 - 55 (2011)
Chromosomal aberrations as detected by array comparative genomic hybridization in early low-grade intraepithelial neoplasias of the breast. Histopathology
Journal Article
48 (1), pp. 24 - 31 (2011)
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet
Journal Article
10, p. 54 (2011)
The structural impact of cancer-associated missense mutations in oncogenes and tumor suppressors. Molecular Cancer