Wendy N. Cooper

Enhanced detection of circulating tumor DNA by fragment size analysis

Florent Moulière, Dineika Chandrananda, Anna Piskorz et al. · Science Translational Medicine · 2018 · 1K citations · Full text

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome

Paul Gissen, Colin A. Johnson, Neil V. Morgan et al. · Nature Genetics · 2004 · 339 citations · Full text

Arthrogryposis–renal Dysfunction–cholestasis, Renal Pathology, Pathology +6

Residual ctDNA after treatment predicts early relapse in patients with early-stage non-small cell lung cancer

Davina Gale, Katrin Heider, Andrea Ruiz-Valdepeñas et al. · Annals of Oncology · 2022 · 319 citations · Full text

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

Wendy N. Cooper, Anita Luharia, Gail A Evans et al. · European Journal of Human Genetics · 2005 · 302 citations

Genetic Disorder, Genetics, Pathogenesis +5

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

Dewi Astuti, Mark R. Morris, Wendy N. Cooper et al. · Nature Genetics · 2012 · 247 citations

Perlman Syndrome, Somatic Variant, Genetic Disorder +10