H. Lindsay

Genomic Subtypes of Non-invasive Bladder Cancer with Distinct Metabolic Profile and Female Gender Bias in KDM6A Mutation Frequency.

Olivia Alder, Alastair Droop, Lucy F. Stead, 2017, Cancer cell.

Genetic diagnosis of familial breast cancer using clonal sequencing

Eamonn Sheridan, Graham R Taylor, D. Bonthron, 2010, Human mutation.

Genomic Subtypes of Non-Invasive Bladder Cancer with Distinct Metabolic Profile, Clinical Outcome and Female Gender Bias in KDM6A Mutation Frequency

Lucy F. Stead, D. Gordenin, L. Klimczak, 2017 .

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.

W. Foulkes, G. Capellá, I. Tomlinson, 2019, Cancer cell.

Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant-Filtering Interface

Laura A. Crinnion, D. Bonthron, G. Taylor, 2013, Human mutation.

Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertions

Laura A. Crinnion, D. Bonthron, H. Lindsay, 2020, Laboratory Investigation.

Pili annulati in a case of Rothmund–Thomson syndrome with a novel frameshift mutation in RECQL4

H. Lindsay, B. Bhoyrul, S. Clark, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants

P. Tarpey, D. Baralle, J. Tolmie, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies

Colin A. Johnson, C. Logan, H. Lindsay, 2012, Cilia.

Genomic Subtypes of Non-invasive Bladder Cancer with Distinct Metabolic Profile and Female Gender Bias in KDM6A Mutation Frequency.

Lucy F. Stead, D. Gordenin, L. Klimczak, 2017, Cancer cell.