Anna Murray

17.4k citations

79 papers · 3.8k indexed · 1 hit paper · h-index 35

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

Papers in ⓘ

Genetics 53
- Genetics and Neurodevelopmental Disorders 25
- Genetic Associations and Epidemiology 17
- Genomic variations and chromosomal abnormalities 17
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Estrogen and related hormone effects 4
Reproductive Medicine 8
- Ovarian function and disorders 6

Co-authors: Timothy M. Frayling (27 shared papers)Michael N. Weedon (25 shared papers)John R. B. Perry (7 shared papers)Felix R. Day (4 shared papers)Ken K. Ong (4 shared papers)James L. Webb (6 shared papers)Katherine S. Ruth (19 shared papers)Sarah Ennis (9 shared papers)
Journals: Human Reproduction (8 papers)Human Molecular Genetics (7 papers)Annals of Human Genetics (4 papers)European Journal of Human Genetics (4 papers)Genetics in Medicine (3 papers)
Partner nations: United Kingdom United States Italy

In The Last Decade

Anna Murray

76 papers receiving 3.7k citations

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 · 367 citations

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

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

20 of 20 papers shown

Showing the 20 most-cited of 79 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	367
2	Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank BMJ ·Jessica Tyrrell, Samuel E. Jones, Robin N. Beaumont, Christina M. Astley, Rebecca Lovell, Hanieh Yaghootkar, Marcus A. Tuke, Katherine S. Ruth, Rachel M. Freathy, Joel N. Hirschhorn, Andrew R. Wood, Anna Murray, Michael N. Weedon, Timothy M. Frayling	2016	236
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 M. Frayling, Jack M. Guralnik, Stefania Bandinelli, Andrew Singleton, Luigi Ferrucci, David Melzer	2011	200
4	Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis Nature Genetics ·Michael N. Weedon, Inês Cebola, Ann‐Marie Patch, Sarah E. Flanagan, Elisa De Franco, Richard Caswell, Santiago A. Rodríguez‐Seguí, Charles Shaw‐Smith, Candy H.-H. Cho, Hana Lango Allen, Jayne Houghton, Christian L. Roth, Rongrong Chen, Khalid Hussain, Phil Marsh, Ludovic Vallier, Anna Murray, Sian Ellard, Jorge Ferrer, Andrew T. Hattersley	2013	191
5	Gene–obesogenic environment interactions in the UK Biobank study International Journal of Epidemiology ·Jessica 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 P. Strachan, Zoltán Kutalik, Michael N. Weedon, Timothy M. Frayling	2016	152
6	Using genetics to understand the causal influence of higher BMI on depression International Journal of Epidemiology ·Jessica 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, Michael N. Weedon, Cathryn M. Lewis, Timothy M. Frayling, Elina Hyppönen	2018	149
7	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	146
8	Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers European Journal of Human Genetics ·Sarah Ennis, Daniel Ward, Anna Murray	2005	130
9	Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers Human Molecular Genetics ·Anna Murray	1996	123
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 Parnell, John R. B. Perry, Michael N. Weedon, Andrew Singleton, Dena Hernandez, Jonathan Evans, Claire Durant, Luigi Ferrucci, David Melzer, Ponnusamy Saravanan, Theo J. Visser, Graziano Ceresini, Andrew T. Hattersley, Bijay Vaidya, Colin Dayan, Timothy M. Frayling	2008	110
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	105
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 M. Frayling, Anna Murray, Alison Hurst, Kara Stevens, Michael N. Weedon, William Henley, Luigi Ferrucci, Stefania Bandinelli, A-M Corsi, Jack M. Guralnik, David Melzer	2007	99
13	Reproductive and menstrual history of females with fragile X expansions European Journal of Human Genetics ·Anna Murray, Sarah Ennis, Felicity M. Macswiney, James L. Webb, Newton E. Morton	2000	93
14	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, Jessica Tyrrell, Samuel E. Jones, Hanieh Yaghootkar, Claire Turner, Mollie E. Donohoe, Antonia Brooke, Morag N. Collinson, Rachel M. Freathy, Michael N. Weedon, Timothy M. Frayling, Anna Murray	2018	86
15	Effects of the diabetes linked TCF7L2polymorphism in a representative older population BMC Medicine ·David Melzer, Anna Murray, Alison Hurst, Michael N. Weedon, Stefania Bandinelli, A. Corsi, Luigi Ferrucci, Giuseppe Paolisso, Jack M. Guralnik, Timothy M. Frayling	2006	75
16	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 Stevens, Alison Hurst, Anna Murray, William Henley, Michael N. Weedon, Stefania Bandinelli, A. Corsi, Jack M. Guralnik, Luigi Ferruci, David Melzer, Timothy M. Frayling	2007	73
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 Hadlow, Bronwyn Stuckey, Suzanne J. Brown, Bjarke Feenstra, John Joseph, Gabriela Surdulescu, Hou Feng Zheng, J. Brent Richards, Anna Murray, Tim D. Spector, Scott G. Wilson, John R.B. Perry	2015	72
18	The 9p21 Myocardial Infarction Risk Allele Increases Risk of Peripheral Artery Disease in Older People Circulation Cardiovascular Genetics ·Christie Cluett, Mary Mcdermott, Jack M. Guralnik, Luigi Ferrucci, Stefania Bandinelli, Iva Miljkovic, Joseph M. Zmuda, Rongling Li, Greg Tranah, Tamara Harris, Neil Rice, William Henley, Timothy M. Frayling, Anna Murray, David Melzer	2009	70
19	A common variant of the p16INK4a genetic region is associated with physical function in older people Mechanisms of Ageing and Development ·David Melzer, Timothy M. Frayling, Anna Murray, Alison Hurst, Lorna W. Harries, Honglin Song, Kay‐Tee Khaw, Robert Luben, Paul G. Surtees, Stefania Bandinelli, Anna-Maria Corsi, Luigi Ferrucci, Jack M. Guralnik, Robert B. Wallace, Andrew T. Hattersley, Paul D.P. Pharoah	2007	64
20	The Role of Size, Sequence and Haplotype in the Stability of FRAXA and FRAXE Alleles during Transmission Human Molecular Genetics ·Anna Murray, John MacPherson, M. C. Pound, Andrea Sharrock, Sheila Youings, N R Dennis, N. McKechnie, PAUL LINEHAN, Newton E. Morton, P.A. Jacobs	1997	62

About Anna Murray

Anna Murray is a scholar working on Genetics, Reproductive Medicine, Conservation, Cognitive Neuroscience and Pharmacy, having authored 79 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (25 papers), Genetic Associations and Epidemiology (17 papers), Genomic variations and chromosomal abnormalities (17 papers), Autism Spectrum Disorder Research (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Ovarian function and disorders (6 papers), Congenital heart defects research (5 papers) and Estrogen and related hormone effects (4 papers). The work is most often cited by research in Genetics (1.9k citations), Reproductive Medicine (470 citations), Aging (89 citations), Cognitive Neuroscience (540 citations) and Endocrinology, Diabetes and Metabolism (414 citations). Anna Murray has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Timothy M. Frayling, Michael N. Weedon, John R. B. Perry, Felix R. Day, Ken K. Ong, James L. Webb, Katherine S. Ruth, Sarah Ennis, Andrew R. Wood and David Melzer. Their work appears in journals such as Human Reproduction, Human Molecular Genetics, Annals of Human Genetics, European Journal of Human Genetics and Genetics in Medicine.

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.

Explore authors with similar magnitude of impact