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Anna Murray

14PUBLICATIONS

190CO-AUTHORS

Foetal development and medicineGene expression (incl. microarray and other genome-wide approaches)Gene mappingDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)

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Publications (14)

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|Apr 19, 2026

Large-scale analysis of FMR1 CGG repeat length and risk of premature ovarian insufficiency in over 92 000 women.

|Feb 06, 2026

Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations.

Gareth Hawkes, Harrison I W Wright, Robin N Beaumont

|Feb 24, 2025

Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels.

Gareth Hawkes, Kartik Chundru, Leigh Jackson

|Oct 03, 2024

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height.

Gareth Hawkes, Robin N Beaumont, Zilin Li

|Sep 11, 2024

Genetic links between ovarian ageing, cancer risk and de novo mutation rates.

Stasa Stankovic, Saleh Shekari, Qin Qin Huang

|Jul 29, 2024

Guidance for estimating penetrance of monogenic disease-causing variants in population cohorts.

Caroline F Wright, Luke N Sharp, Leigh Jackson

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Frequent Collaborators

6 joint publications

Caroline F Wright

6 joint publications

Robin N Beaumont

6 joint publications

John R B Perry

5 joint publications

Gareth Hawkes

5 joint publications

Andrew R Wood

5 joint publications

Timothy M Frayling

5 joint publications

Michael N Weedon

5 joint publications

Felix R Day

4 joint publications

Katherine S Ruth

4 joint publications

Eugene J Gardner

Frequent Collaborators

6 joint publications

Caroline F Wright

6 joint publications

Robin N Beaumont

6 joint publications

John R B Perry

5 joint publications

Gareth Hawkes

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