Andrew Orr
San Francisco VA Medical Center(US)University of California, San Francisco(US)
Publications by Year
Research Areas
Glaucoma and retinal disorders, Genomics and Rare Diseases, Folate and B Vitamins Research, Corneal surgery and disorders, Ethics in Clinical Research
Most-Cited Works
- → Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia(2009)246 cited
- → Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4(2010)195 cited
- → Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome(2011)171 cited
- → Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy(2007)164 cited
- → Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci(2017)156 cited
- → A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome(2015)128 cited
- → Attitudes of parents toward the return of targeted and incidental genomic research findings in children(2014)95 cited
- → Human monogenic disorders — a source of novel drug targets(2006)93 cited
- → Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2(2009)92 cited
- → Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease(2010)70 cited