Annette Payne

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok et al. · Nature Genetics · 1999 · 470 citations

Biology, Developmental Biology, Genetics +6

Machine Learning with Applications in Breast Cancer Diagnosis and Prognosis

Wenbin Yue, Zidong Wang, Hongwei Chen et al. · Designs · 2018 · 299 citations · Full text

Engineering, Machine Learning, Intelligent Diagnostics +21

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Melanie M. Sohocki, Sara J. Bowne, Lori S. Sullivan et al. · Nature Genetics · 2000 · 287 citations · Full text

Biology, Photoreceptor Cell, Genetic Disorder +6

Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy

Rosemary E. Kelsell, Kevin Gregory-Evans, Annette Payne et al. · Human Molecular Genetics · 1998 · 232 citations

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1

Annette Payne · Human Molecular Genetics · 1998 · 232 citations