Shotgun haplotyping: a novel method for surveying allelic sequence variation

por Lindsay, Sarah J., Bonfield, James K., Hurles, Matthew E.
Publicado 2005

The genome-wide effects of ionizing radiation on mutation induction in the mammalian germline

por Adewoye, Adeolu B., Lindsay, Sarah J., Dubrova, Yuri E., Hurles, Matthew E.
Publicado 2015

Similarities and differences in patterns of germline mutation between mice and humans

por Lindsay, Sarah J., Rahbari, Raheleh, Kaplanis, Joanna, Keane, Thomas, Hurles, Matthew E.
Publicado 2019

The Rate of Nonallelic Homologous Recombination in Males Is Highly Variable, Correlated between Monozygotic Twins and Independent of Age

por MacArthur, Jacqueline A. L., Spector, Timothy D., Lindsay, Sarah J., Mangino, Massimo, Gill, Raj, Small, Kerrin S., Hurles, Matthew E.
Publicado 2014

Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspring

por Beal, Marc A., Meier, Matthew J., Williams, Andrew, Rowan-Carroll, Andrea, Gagné, Rémi, Lindsay, Sarah J., Fitzgerald, Tomas, Hurles, Matthew E., Marchetti, Francesco, Yauk, Carole L.
Publicado 2019

Timing, rates and spectra of human germline mutation

por Rahbari, Raheleh, Wuster, Arthur, Lindsay, Sarah J., Hardwick, Robert J., Alexandrov, Ludmil B., Turki, Saeed Al, Dominiczak, Anna, Morris, Andrew, Porteous, David, Smith, Blair, Stratton, Michael R., Hurles, Matthew E.
Publicado 2015

Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders

por Gardner, Eugene J., Sifrim, Alejandro, Lindsay, Sarah J., Prigmore, Elena, Rajan, Diana, Danecek, Petr, Gallone, Giuseppe, Eberhardt, Ruth Y., Martin, Hilary C., Wright, Caroline F., FitzPatrick, David R., Firth, Helen V., Hurles, Matthew E.
Publicado 2021