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Sarah J Lindsay

Showing results (1-10 of 17) with videos related to

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Nucleic Acids Research|October 14, 2005
Shotgun haplotyping: a novel method for surveying allelic sequence variationSarah J Lindsay, James K Bonfield, Matthew E Hurles
American Journal of Human Genetics|October 13, 2006
A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombinationSarah J Lindsay, Mehrdad Khajavi, James R Lupski, et al.
Nature Communications|September 8, 2019
Similarities and differences in patterns of germline mutation between mice and humansSarah J Lindsay, Raheleh Rahbari, Joanna Kaplanis, et al.
Nature Communications|March 27, 2015
The genome-wide effects of ionizing radiation on mutation induction in the mammalian germlineAdeolu B Adewoye, Sarah J Lindsay, Yuri E Dubrova, et al.
Gigascience|June 9, 2026
Improved discovery of de novo mutations using TrioDNM and VRFSPetr Danecek, Eugene J Gardner, Joanna Kaplanis, et al.
Plos Genetics|March 8, 2014
The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of ageJacqueline A L MacArthur, Timothy D Spector, Sarah J Lindsay, et al.
Communications Biology|June 27, 2019
Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspringMarc A Beal, Matthew J Meier, Andrew Williams, et al.
Nature Genetics|December 15, 2015
Timing, rates and spectra of human germline mutationRaheleh Rahbari, Arthur Wuster, Sarah J Lindsay, et al.
American Journal of Human Genetics|October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disordersEugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
Genome Medicine|October 31, 2025
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disordersOlivia Wootton, Patrick Campbell, Sarah Richardson, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|October 14, 2005
Shotgun haplotyping: a novel method for surveying allelic sequence variationSarah J Lindsay, James K Bonfield, Matthew E Hurles
American Journal of Human Genetics|October 13, 2006
A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombinationSarah J Lindsay, Mehrdad Khajavi, James R Lupski, et al.
Nature Communications|September 8, 2019
Similarities and differences in patterns of germline mutation between mice and humansSarah J Lindsay, Raheleh Rahbari, Joanna Kaplanis, et al.
Nature Communications|March 27, 2015
The genome-wide effects of ionizing radiation on mutation induction in the mammalian germlineAdeolu B Adewoye, Sarah J Lindsay, Yuri E Dubrova, et al.
Gigascience|June 9, 2026
Improved discovery of de novo mutations using TrioDNM and VRFSPetr Danecek, Eugene J Gardner, Joanna Kaplanis, et al.
Plos Genetics|March 8, 2014
The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of ageJacqueline A L MacArthur, Timothy D Spector, Sarah J Lindsay, et al.
Communications Biology|June 27, 2019
Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspringMarc A Beal, Matthew J Meier, Andrew Williams, et al.
Nature Genetics|December 15, 2015
Timing, rates and spectra of human germline mutationRaheleh Rahbari, Arthur Wuster, Sarah J Lindsay, et al.
American Journal of Human Genetics|October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disordersEugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
Genome Medicine|October 31, 2025
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disordersOlivia Wootton, Patrick Campbell, Sarah Richardson, et al.
Pageof 2