Peter Meinecke
Universität Hamburg(DE)University Medical Center Hamburg-Eppendorf(DE)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Connective tissue disorders research, Genomics and Rare Diseases, Congenital limb and hand anomalies, Craniofacial Disorders and Treatments
Most-Cited Works
- → A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis(2006)659 cited
- → Mutations in the Pericentrin ( PCNT ) Gene Cause Primordial Dwarfism(2008)393 cited
- → Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination(2000)392 cited
- → Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I(2000)372 cited
- → Mutations in STRA6 Cause a Broad Spectrum of Malformations Including Anophthalmia, Congenital Heart Defects, Diaphragmatic Hernia, Alveolar Capillary Dysplasia, Lung Hypoplasia, and Mental Retardation(2007)359 cited
- → Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome(2010)299 cited