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Publications

Meiotic DNA breaks drive multifaceted mutagenesis in the human germ line.

Hinch R. et al, (2023), Science (New York, N.Y.), 382

Characterization of meiotic recombination intermediates through gene knockouts in founder hybrid mice

Davies B. et al, (2023), Genome Research, 33, 2018 - 2027

2022 William Allan Award.

Donnelly P., (2023), American journal of human genetics, 110, 404 - 408

Altering the Binding Properties of PRDM9 Partially Restores Fertility across the Species Boundary

Davies B. et al, (2021), Molecular Biology and Evolution, 38, 5555 - 5562

Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries.

Weale ME. et al, (2021), The American journal of cardiology, 148, 157 - 164

Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction

Riveros-Mckay F. et al, (2021), Circulation: Genomic and Precision Medicine, 14

Platypus and echidna genomes reveal mammalian biology and evolution.

Zhou Y. et al, (2021), Nature, 592, 756 - 762

ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair

Wells D. et al, (2020), eLife, 9

The Configuration of RPA, RAD51, and DMC1 Binding in Meiosis Reveals the Nature of Critical Recombination Intermediates

Hinch AG. et al, (2020), Molecular Cell, 79, 689 - 701.e10

Sequencing of human genomes with nanopore technology

Bowden R. et al, (2019), Nature Communications, 10

ZCWPW1 is recruited to recombination hotspots by PRDM9, and is essential for meiotic double strand break repair

Wells D. et al, (2019)

A polygenic resilience score moderates the genetic risk for schizophrenia.

Hess JL. et al, (2019), Molecular psychiatry

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.

Harold D. et al, (2019), American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 180, 223 - 231

Factors influencing meiotic recombination revealed by whole-genome sequencing of single sperm

Hinch AG. et al, (2019), Science, 363

Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula.

Bycroft C. et al, (2019), Nat Commun, 10

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Flannick J. et al, (2018), Scientific Data, 5

Identifying loci affecting trait variability and detecting interactions in genome-wide association studies.

Young AI. et al, (2018), Nat Genet, 50, 1608 - 1614

Phenome-wide association studies across large population cohorts support drug target validation.

Diogo D. et al, (2018), Nat Commun, 9

The UK Biobank resource with deep phenotyping and genomic data

Bycroft C. et al, (2018), Nature, 562, 203 - 209

Long-read whole genome sequencing and comparative analysis of six strains of the human pathogen Orientia tsutsugamushi

Batty EM. et al, (2018), PLOS Neglected Tropical Diseases, 12, e0006566 - e0006566

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