Amanda J. Gladwin

The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.

Sara J. Edwards, Amanda J. Gladwin, Michael J. Dixon · PubMed · 1997 · 158 citations

Life Sciences, Genetics, Molecular Genetics +13

Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene

Amanda J. Gladwin · Human Molecular Genetics · 1996 · 77 citations

Life Sciences, Genetics, Molecular Genetics +17

Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24

Amanda J. Gladwin · Human Molecular Genetics · 1997 · 71 citations

Life Sciences, Genetics, Molecular Genetics +13

A retrospective analysis of RET translocation, gene copy number gain and expression in NSCLC patients treated with vandetanib in four randomized Phase III studies

Adam Platt, John Morten, Qunsheng Ji et al. · BMC Cancer · 2015 · 59 citations · Full text

Medicine, Genetics, Oncology +17

Angiotensin-converting enzyme gene insertion/deletion polymorphism in migraine patients

Erling Tronvik, Lars Jacob Stovner, Gunnar Bovim et al. · BMC Neurology · 2008 · 47 citations · Full text

Medicine, Genetics, Pharmacology +16