Lorna Tinworth

Emberger syndrome—Primary lymphedema with myelodysplasia: Report of seven new cases

Sahar Mansour, Fiona Connell, Colin G. Steward et al. · American Journal of Medical Genetics Part A · 2010 · 82 citations

Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1–3 clinical trials: A Children’s Cancer and Leukaemia Group (CCLG) study

Boo Messahel, Richard D. Williams, Antonia Ridolfi et al. · European Journal of Cancer · 2009 · 53 citations

Hematological Malignancy, Oncology, Ukw1–3 Clinical Trials +7

Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulum

Bassam R. Ali, Steve Jeffery, Neha U. Patel et al. · Human Genetics · 2007 · 39 citations

Developmental Biology, Signal Transduction, Frizzled-like Domain +10

Tribal ethnicity and CYP2B6 genetics in Ugandan and Zimbabwean populations in the UK: implications for efavirenz dosing in HIV infection

Yalda Jamshidi, Michelle Moreton, Denise A. McKeown et al. · Journal of Antimicrobial Chemotherapy · 2010 · 38 citations

Developmentally acquired PKA localisation in mouse oocytes and embryos

Rachel J. Webb, Lorna Tinworth, Geraint Thomas et al. · Developmental Biology · 2008 · 27 citations

Oocyte, Developmental Biology, Cell Division +6