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List of works by Sarah J. Lindsay

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

scientific article

Absence of heterozygosity due to template switching during replicative rearrangements

scientific article

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

scientific journal article

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

scientific article published on 4 April 2010

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

scientific article published on 3 March 2016

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

scientific article published in July 2014

Rare variants in NR2F2 cause congenital heart defects in humans

scientific article published on April 2014

Shotgun haplotyping: a novel method for surveying allelic sequence variation

scientific article

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

scientific article published on 06 September 2019

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

scientific article

The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age

scientific article published on 06 March 2014

Timing, rates and spectra of human germline mutation

scientific article published on 14 December 2015

Ultra-high resolution array painting facilitates breakpoint sequencing

scientific article published on 13 September 2006

Variation in genome-wide mutation rates within and between human families

scientific article

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