Andrew Read
University of Queensland(AU)University of Minnesota System(US)University of Oxford(GB)
Publications by Year
Research Areas
Nutrition, Genetics, and Disease, Prenatal Screening and Diagnostics, RNA regulation and disease, melanin and skin pigmentation, Muscle Physiology and Disorders
Most-Cited Works
- → A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets(1995)1,110 cited
- → SOX10 mutations in patients with Waardenburg-Hirschsprung disease(1998)818 cited
- → Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene(1992)694 cited
- → Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene(1994)668 cited
- → POSSIBLE PREVENTION OF NEURAL-TUBE DEFECTS BY PERICONCEPTIONAL VITAMIN SUPPLEMENTATION(1980)659 cited
- → Human Molecular Genetics(2018)510 cited