Search results (18)
« Back to PublicationsDe novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Journal article
Chen Y. et al, (2024), Nature, 632, 832 - 840
Meiotic DNA breaks drive multifaceted mutagenesis in the human germ line.
Journal article
Hinch R. et al, (2023), Science (New York, N.Y.), 382
Characterization of meiotic recombination intermediates through gene knockouts in founder hybrid mice
Journal article
Davies B. et al, (2023), Genome Research, 33, 2018 - 2027
Altering the Binding Properties of PRDM9 Partially Restores Fertility across the Species Boundary
Journal article
Davies B. et al, (2021), Molecular Biology and Evolution, 38, 5555 - 5562
ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair
Journal article
Wells D. et al, (2020), eLife, 9
The Configuration of RPA, RAD51, and DMC1 Binding in Meiosis Reveals the Nature of Critical Recombination Intermediates
Journal article
Hinch AG. et al, (2020), Molecular Cell, 79, 689 - 701.e10
Molecular structures and mechanisms of DNA break processing in mouse meiosis.
Journal article
Yamada S. et al, (2020), Genes & development, 34, 806 - 818
ZCWPW1 is recruited to recombination hotspots by PRDM9, and is essential for meiotic double strand break repair
Journal article
Wells D. et al, (2019)
Factors influencing meiotic recombination revealed by whole-genome sequencing of single sperm
Journal article
Hinch AG. et al, (2019), Science, 363
Molecular structures and mechanisms of DNA break processing in mouse meiosis
Preprint
Yamada S. et al, (2019)
Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice
Journal article
Davies B. et al, (2016), Nature, 530, 171 - 176
A global reference for human genetic variation
Journal article
Auton A. et al, (2015), Nature, 526, 68 - 74
Recombination in the Human Pseudoautosomal Region PAR1
Journal article
Hinch AG. et al, (2014), PLoS Genetics, 10, e1004503 - e1004503
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Journal article
Delaneau O. et al, (2014), Nature Communications, 5