Gill Adams

Mutation in Rab3 GTPase-Activating Protein (RAB3GAP) Noncatalytic Subunit in a Kindred with Martsolf Syndrome

Irene A. Aligianis, Neil V. Morgan, Marina Mione et al. · The American Journal of Human Genetics · 2006 · 110 citations · Full text

Life Sciences, Genetics, Molecular Biology +7

Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study

Lucinda Teoh, Ameenat Lola Solebo, Jugnoo S. Rahi et al. · The Lancet Child & Adolescent Health · 2021 · 76 citations · Full text

Medicine, Ophthalmology, Pediatrics +16

Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA–protein interaction

Kathleen A. Williamson, Hildegard Nikki Hall, Liusaidh J. Owen et al. · Genetics in Medicine · 2019 · 63 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21

Cheryl Y. Gregory‐Evans, Helena Vieira, Rex Dalton et al. · American Journal of Medical Genetics Part A · 2004 · 60 citations

Medicine, Genetics, Ophthalmology +17

Monitoring ocular disease by impression cytology

Gill Adams, P. N. Dilly, C M Kirkness · Eye · 1988 · 47 citations

Medicine, Ophthalmology, Pathology +11