Anna Murray

17.6k citations

88 papers · 4.4k · 1 hit paper · h-index 37

Impact in

Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Reproductive Medicine top 1%
- Ovarian function and disorders
- Hypothalamic control of reproductive hormones

Papers in

Genetics 52
- Genetics and Neurodevelopmental Disorders 26
- Genetic Associations and Epidemiology 17
- Genomic variations and chromosomal abnormalities 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genomics and Rare Diseases 4
Cognitive Neuroscience 11
- Autism Spectrum Disorder Research 11

Co-authors: Timothy Mark Frayling (30 shared papers)M. Weedon (27 shared papers)John R. B. Perry (8 shared papers)Sarah A. Ennis (12 shared papers)Ken K. Ong (5 shared papers)Felix R. Day (4 shared papers)James L. Webb (6 shared papers)Katherine S. Ruth (20 shared papers)
Journals: Human Reproduction (8 papers)Human Molecular Genetics (7 papers)Genetics in Medicine (4 papers)Annals of Human Genetics (4 papers)European Journal of Human Genetics (4 papers)
Partner nations: United Kingdom United States Italy

In The Last Decade

Anna Murray

87 papers receiving 4.2k citations

Anna Murray's Hit Papers

align trajectories log scale

Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study 2015 · 397 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2015 Scientific Reports

Peers

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-authors

The 25 scholars most cited alongside Anna Murray, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Murray Line = papers co-authored together Anna Murray links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 88 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study Scientific Reports ·Felix R. Day, Cathy E. Elks, Anna Murray, Ken K. Ong, John R. B. Perry Hit paper breakdown →	2015	397
2	Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank BMJ ·Jess Tyrrell, Samuel E. Jones, Robin N. Beaumont, Christina M. Astley, Rebecca M. Lovell, Hanieh Yaghootkar, Marcus A. Tuke, Katherine S. Ruth, Rachel M. Freathy, Joel N. Hirschhorn, Andrew R. Wood, Anna Murray, M. Weedon, Timothy Mark Frayling	2016	253
3	Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing Aging Cell ·Lorna W. Harries, Dena Hernandez, William Henley, Andrew R. Wood, Alice C. Holly, Rachel Mary Bradley-Smith, Hanieh Yaghootkar, Ambarish Dutta, Anna Murray, Timothy Mark Frayling, Jack M. Guralnik, Stefania Bandinelli, Andrew B. Singleton, Luigi Ferrucci, David R. Melzer	2011	214
4	Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis Nature Genetics ·M. Weedon, Inês Cebola, Ann‐Marie Patch, Sarah Elizabeth Flanagan, Elisa De Franco, Richard C. Caswell, Santiago A. Rodríguez‐Seguí, Charles J Shaw-Smith, Candy H.-H. Cho, Hana Lango Allen, Jayne Houghton, Christian Ludwig Roth, Rongrong Chen, Khalid Hussain, Phil J. Marsh, Ludovic Vallier, Anna Murray, Sian Ellard, Jorge P. Ferrer, Andrew Tym Hattersley	2013	202
5	Fragile X premutation screening in women with premature ovarian failure Human Reproduction ·Gerard S. Conway, N. N. Payne, James L. Webb, Anna Murray, P.A. Jacobs	1998	168
6	Using genetics to understand the causal influence of higher BMI on depression International Journal of Epidemiology ·Jess Tyrrell, Anwar Mulugeta, Andrew R. Wood, Ang Zhou, Robin N. Beaumont, Marcus A. Tuke, Samuel E. Jones, Katherine S. Ruth, Hanieh Yaghootkar, Seth A. Sharp, William Thompson, Yingjie Ji, Jamie Harrison, Rachel M. Freathy, Anna Murray, M. Weedon, Cathryn M. Lewis, Timothy Mark Frayling, Elina Hyppönen	2018	164
7	Gene–obesogenic environment interactions in the UK Biobank study International Journal of Epidemiology ·Jess Tyrrell, Andrew R. Wood, Ryan M. Ames, Hanieh Yaghootkar, Robin N. Beaumont, Samuel E. Jones, Marcus A. Tuke, Katherine S. Ruth, Rachel M. Freathy, George Davey Smith, Stéphane Joost, Idris Guessous, Anna Murray, David Peter Strachan, Zoltán Kutalik, M. Weedon, Timothy Mark Frayling	2016	163
8	Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers Human Molecular Genetics ·Anna Murray	1996	146
9	Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers European Journal of Human Genetics ·Sarah A. Ennis, Daniel Ward, Anna Murray	2005	141
10	A Common Variation in Deiodinase 1 Gene DIO1 Is Associated with the Relative Levels of Free Thyroxine and Triiodothyronine The Journal of Clinical Endocrinology & Metabolism ·Vijay Panicker, Christie Cluett, Beverley M. Shields, Anna Murray, Kirstie S. Parnell, John R. B. Perry, M. Weedon, Andrew B. Singleton, Dena Hernandez, Jonathan Evans, Claire F. Durant, Luigi Ferrucci, David R. Melzer, Ponnusamy Saravanan, Theo J. Visser, Graziano Ceresini, Andrew Tym Hattersley, Bijay Vaidya, Colin Mark Dayan, Timothy Mark Frayling	2008	125
11	Studies of FRAXA and FRAXE in women with premature ovarian failure. Journal of Medical Genetics ·Anna Murray, James L. Webb, Sara Grimley, Gerard S. Conway, P.A. Jacobs	1998	121
12	A common variant of the interleukin 6 receptor (IL-6r) gene increases IL-6r and IL-6 levels, without other inflammatory effects Genes and Immunity ·Sajjad Rafiq, Timothy Mark Frayling, Anna Murray, Alison Jane Hurst, Kara Nicola Stevens, M. Weedon, William Henley, Luigi Ferrucci, Stefania Bandinelli, A-M Corsi, Jack M. Guralnik, David R. Melzer	2007	105
13	Fragile X premutations in familial premature ovarian failure The Lancet ·G. E. Conway, Shyamani Hettiarachchi, Anna Murray, PatriciaA. Jacobs	1995	102
14	Reproductive and menstrual history of females with fragile X expansions European Journal of Human Genetics ·Anna Murray, Sarah A. Ennis, Felicity M. Macswiney, James L. Webb, Newton E. Morton	2000	101
15	Mosaic Turner syndrome shows reduced penetrance in an adult population study Genetics in Medicine ·Marcus A. Tuke, Katherine S. Ruth, Andrew R. Wood, Robin N. Beaumont, Jess Tyrrell, Samuel E. Jones, Hanieh Yaghootkar, Claire Turner, Mollie E. Donohoe, Antonia M. Brooke, Morag N. Collinson, Rachel M. Freathy, M. Weedon, Timothy Mark Frayling, Anna Murray	2018	96
16	The 9p21 Myocardial Infarction Risk Allele Increases Risk of Peripheral Artery Disease in Older People Circulation Cardiovascular Genetics ·Christie Cluett, Mary McGrae McDermott, Jack M. Guralnik, Luigi Ferrucci, Stefania Bandinelli, IVA MILJKOVIC, Joseph M. Zmuda, Rongling Li, Greg J. Tranah, Tamara Harris, Neil E. Rice, William Henley, Timothy Mark Frayling, Anna Murray, David R. Melzer	2009	76
17	Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes European Journal of Human Genetics ·Katherine S. Ruth, Purdey J. Campbell, Shelby Chew, Ee Mun Lim, Narelle C. Hadlow, Bronwyn G. A. Stuckey, Suzanne J. Brown, Bjarke Feenstra, John Joseph, Gabriela L. Surdulescu, Hou Feng Zheng, John Brent Richards, Anna Murray, Tim D. Spector, Scott G. Wilson, John R.B. Perry	2015	75
18	Effects of the diabetes linked TCF7L2polymorphism in a representative older population BMC Medicine ·David R. Melzer, Anna Murray, Alison Jane Hurst, M. Weedon, Stefania Bandinelli, Anna Maria Corsi, Luigi Ferrucci, Giuseppe Paolisso, Jack M. Guralnik, Timothy Mark Frayling	2006	75
19	Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency Genetics in Medicine ·Anna Murray, Minouk J. Schoemaker, Claire E. Bennett, Sarah A. Ennis, James Macpherson, Michael Emlyn Jones, Danielle H. Morris, Nick Orr, Alan Ashworth, Patricia A. Jacobs, Anthony J. Swerdlow	2013	73
20	Common genetic variation in the gene encoding interleukin-1-receptor antagonist (IL-1RA) is associated with altered circulating IL-1RA levels Genes and Immunity ·Sajjad Rafiq, Kara Nicola Stevens, Alison Jane Hurst, Anna Murray, William Henley, M. Weedon, Stefania Bandinelli, Anna Maria Corsi, Jack M. Guralnik, Luigi Ferruci, David R. Melzer, Timothy Mark Frayling	2007	72

About Anna Murray

Anna Murray is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Reproductive Medicine and Endocrinology, Diabetes and Metabolism, having authored 88 papers that have together received 4.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (26 papers), Genetic Associations and Epidemiology (17 papers), Genomic variations and chromosomal abnormalities (13 papers), Autism Spectrum Disorder Research (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Congenital heart defects research (7 papers), Ovarian function and disorders (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (1.8k citations), Reproductive Medicine (498 citations), Aging (83 citations), Cognitive Neuroscience (471 citations) and Endocrinology, Diabetes and Metabolism (352 citations). Anna Murray has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Timothy Mark Frayling, M. Weedon, John R. B. Perry, Sarah A. Ennis, Ken K. Ong, Felix R. Day, James L. Webb, Katherine S. Ruth, David R. Melzer and Andrew R. Wood. Their work appears in journals such as Human Reproduction, Human Molecular Genetics, Genetics in Medicine, Annals of Human Genetics and European Journal of Human Genetics.

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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Anna Murray

Anna Murray's Hit Papers

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About Anna Murray

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