Anna Murray

17.4k total citations · 1 hit paper
79 papers, 3.8k citations indexed

About

Anna Murray is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Anna Murray has authored 79 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 24 papers in Molecular Biology and 10 papers in Cognitive Neuroscience. Recurrent topics in Anna Murray's work include Genetics and Neurodevelopmental Disorders (25 papers), Genetic Associations and Epidemiology (17 papers) and Genomic variations and chromosomal abnormalities (17 papers). Anna Murray is often cited by papers focused on Genetics and Neurodevelopmental Disorders (25 papers), Genetic Associations and Epidemiology (17 papers) and Genomic variations and chromosomal abnormalities (17 papers). Anna Murray collaborates with scholars based in United Kingdom, United States and Italy. Anna Murray's co-authors include Timothy M. Frayling, Michael N. Weedon, John R. B. Perry, Ken K. Ong, Felix R. Day, James L. Webb, Katherine S. Ruth, Andrew R. Wood, Sarah Ennis and Cathy E. Elks and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Anna Murray

76 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study

2015 367 citations Anna Murray, John R. B. Perry et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anna Murray United Kingdom	35	1.9k	1.2k	674	540	470	79	3.8k
Felix R. Day United Kingdom	27	2.3k 1.2×	1.1k 0.9×	633 0.9×	185 0.3×	457 1.0×	58	4.6k
John R. B. Perry United Kingdom	30	2.6k 1.4×	1.4k 1.1×	581 0.9×	187 0.3×	531 1.1×	75	5.2k
Manuela Uda Italy	32	984 0.5×	1.1k 0.9×	571 0.8×	156 0.3×	366 0.8×	43	3.6k
Andrew R. Wood United Kingdom	32	2.2k 1.2×	1.2k 1.0×	718 1.1×	195 0.4×	107 0.2×	79	4.8k
Michael P. Epstein United States	35	2.9k 1.5×	2.3k 1.9×	305 0.5×	617 1.1×	121 0.3×	125	5.7k
M. Tauber France	39	2.6k 1.4×	1.7k 1.3×	254 0.4×	189 0.3×	120 0.3×	174	4.6k
Markku Ryynänen Finland	38	953 0.5×	1.1k 0.9×	244 0.4×	399 0.7×	122 0.3×	132	4.4k
Margaret de Castro Brazil	37	1.0k 0.5×	1.5k 1.2×	462 0.7×	108 0.2×	620 1.3×	234	6.0k
Dietrich Klingmüller Germany	37	473 0.3×	892 0.7×	560 0.8×	147 0.3×	726 1.5×	113	3.9k
Göran Annerén Sweden	35	1.7k 0.9×	1.6k 1.3×	878 1.3×	210 0.4×	54 0.1×	167	4.8k

Countries citing papers authored by Anna Murray

Since Specialization

Citations

This map shows the geographic impact of Anna Murray's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Anna Murray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Murray more than expected).

Fields of papers citing papers by Anna Murray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Murray. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Anna Murray. The network helps show where Anna Murray may publish in the future.

Co-authorship network of co-authors of Anna Murray

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Murray. A scholar is included among the top collaborators of Anna Murray based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anna Murray. Anna Murray is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Murray, Anna, et al.. (2025). What Happens in Vegas: Enlisted Medical Providers Practice to Their Full Clinical Scope in a Civilian Hospital. Military Medicine. 190(5-6). 125–129.

Alshalalfa, Mohammed, Anna Murray, Gregory Azzam, et al.. (2024). Racial Disparities in Glioblastoma Genomic Alterations: A Comprehensive Analysis of a Multi-Institution Cohort of 2390 Patients. World Neurosurgery. 188. e625–e630.

Ruth, Katherine S., Robin N. Beaumont, Jonathan M. Locke, et al.. (2023). Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records. BMC Medical Genomics. 16(1). 231–231. 4 indexed citations

Murray, Anna, et al.. (2022). Working with local governments to increase access to WASH services: a case of WaterAid's participatory approaches in Nigeria. H2Open Journal. 5(3). 424–437. 1 indexed citations

Schouw, Yvonne T. van der, Carla H. van Gils, W. M. Monique Verschuren, et al.. (2022). Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women. Human Reproduction. 37(5). 1069–1082. 19 indexed citations

Robinson, Tim, Siddhartha Kar, Katherine S. Ruth, et al.. (2022). Do sex hormones confound or mediate the effect of chronotype on breast and prostate cancer? A Mendelian randomization study. PLoS Genetics. 18(1). e1009887–e1009887. 15 indexed citations

Su, Helen C., Michael Barnett, Anna Murray, et al.. (2022). Patient experience and satisfaction with symptomatic faecal immunochemical testing: an explanatory sequential mixed-methods evaluation. British Journal of General Practice. 73(727). e104–e114. 5 indexed citations

Ruth, Katherine S., Ana Gonçalves Soares, Maria Carolina Borges, et al.. (2019). Genome-wide association study of anti-Müllerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan. Human Molecular Genetics. 28(8). 1392–1401. 25 indexed citations

Pilling, Luke C., Janice L. Atkins, Michael O. Duff, et al.. (2017). Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. PLoS ONE. 12(9). e0185083–e0185083. 55 indexed citations

10.

Tyrrell, Jessica, Andrew R. Wood, Ryan M. Ames, et al.. (2016). Gene–obesogenic environment interactions in the UK Biobank study. International Journal of Epidemiology. 46(2). dyw337–dyw337. 152 indexed citations

11.

Ruth, Katherine S., Robin N. Beaumont, Jessica Tyrrell, et al.. (2016). Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health. Human Reproduction. 31(2). 473–481. 42 indexed citations

12.

Ruth, Katherine S., Purdey J. Campbell, Ee Mun Lim, et al.. (2015). Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes. European Journal of Human Genetics. 24(2). 284–290. 72 indexed citations

13.

Harries, Lorna W., Dena Hernandez, William Henley, et al.. (2011). Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing. Aging Cell. 10(5). 868–878. 200 indexed citations

14.

Bennett, C.E., Gerard Conway, John MacPherson, P. A. Jacobs, & Anna Murray. (2010). Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure. Human Reproduction. 25(5). 1335–1338. 60 indexed citations

15.

Murray, Anna, Claire E. Bennett, John R. B. Perry, et al.. (2010). Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study. Human Molecular Genetics. 20(1). 186–192. 52 indexed citations

16.

Ennis, Sarah, Anna Murray, Gale Brightwell, Newton E. Morton, & P. A. Jacobs. (2007). Closely linkedcis‐acting modifier of expansion of the CGG repeat in high riskFMR1haplotypes. Human Mutation. 28(12). 1216–1224. 18 indexed citations

17.

Frayling, Timothy M., Sajjad Rafiq, Anna Murray, et al.. (2007). An Interleukin-18 Polymorphism Is Associated With Reduced Serum Concentrations and Better Physical Functioning in Older People. The Journals of Gerontology Series A. 62(1). 73–78. 49 indexed citations

18.

Gunter, Chris, William Paradee, Dana C. Crawford, et al.. (1998). Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Human Molecular Genetics. 7(12). 1935–1946. 59 indexed citations

19.

Murray, Anna, et al.. (1996). Anxiety management “while you wait”: input from an assistant psychologist. Clinical Psychology Forum. 1(89). 33–36. 3 indexed citations

20.

Murray, Anna. (1996). Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers. Human Molecular Genetics. 5(6). 727–735. 123 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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