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Search results (265)

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Preventing premature deaths through polygenic risk scores.

Chuong M. et al, (2026), Nat Commun, 17

Polygenic risk score adds to a clinical risk score in the prediction of cardiovascular disease in a clinical setting.

Samani NJ. et al, (2024), Eur Heart J, 45, 3152 - 3160

polygenic risk score added to a QRISK®2 cardiovascular disease risk calculator demonstrated robust clinical acceptance and clinical utility in the primary care setting.

Fuat A. et al, (2024), Eur J Prev Cardiol, 31, 716 - 722

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

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

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

Hinch R. et al, (2023), Science, 382

2022 William Allan Award.

Donnelly P., (2023), Am J Hum Genet, 110, 404 - 408

Altering the binding properties of PRDM9 partially restores fertility across the species boundary

DAVIES B., (2021), Molecular Biology and Evolution

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

Weale ME. et al, (2021), Am J Cardiol, 148, 157 - 164

Platypus and echidna genomes reveal mammalian biology and evolution.

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

An Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction.

Riveros-Mckay F. et al, (2021), Circulation. Genomic and precision medicine

A polygenic resilience score moderates the genetic risk for schizophrenia.

Hess JL. et al, (2021), Mol Psychiatry, 26, 800 - 815

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

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

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

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

Sequencing of human genomes with nanopore technology.

Bowden R. et al, (2019), Nature communications, 10, 1869 - 1869

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

Harold D. et al, (2019), Am J Med Genet B Neuropsychiatr Genet, 180, 223 - 231

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