Oliver Brandau
Publications by Year
Research Areas
Cell Adhesion Molecules Research, Retinal Development and Disorders, Genomics and Rare Diseases, RNA regulation and disease, Cardiomyopathy and Myosin Studies
Most-Cited Works
- → Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene(1998)757 cited
- → Tenomodulin Is Necessary for Tenocyte Proliferation and Tendon Maturation(2005)439 cited
- → Clinical exome sequencing: results from 2819 samples reflecting 1000 families(2016)366 cited
- → The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein(2000)259 cited
- → ESAM supports neutrophil extravasation, activation of Rho, and VEGF-induced vascular permeability(2006)248 cited
- → A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation(2000)236 cited
- → Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets(1997)162 cited
- → Mutation Screening of the BTK Gene in 56 Families With X-Linked Agammaglobulinemia (XLA): 47 Unique Mutations Without Correlation to Clinical Course(1998)128 cited
- → X-linked Retinitis Pigmentosa:RPGRMutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15(2003)116 cited
- → A novel gene, tendin, is strongly expressed in tendons and ligaments and shows high homology with chondromodulin‐I(2001)113 cited