Anna Murray

17.6k citations
139 papers · 12.7k · 7 hit papers · h-index 60

Impact in

Papers in

    • Genetic Associations and Epidemiology 37
    • Genetics and Neurodevelopmental Disorders 30
    • Genomic variations and chromosomal abnormalities 16
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
    • Growth Hormone and Insulin-like Growth Factors 8

Anna Murray

137 papers receiving 12.3k citations

Anna Murray's Hit Papers

Using human genetics to understand the disease impacts of testosterone in men and women 2020 · 493 citations
4930+4+8Years since publication100200300400500

Peers

Anna Murray
Comparison fields: 5 of 171
  • Reproductive Medicine 1.6k
  • Aging 341
  • Genetics 4.5k
  • Endocrine and Autonomic Systems 548
  • Endocrinology, Diabetes and Metabolism 1.2k
Replace Lisette Stolk with:
Lisette Stolk Netherlands
Laura Crisponi Italy
David Schlessinger United States
Melissa E. Garcia United States
Liesbeth Vandenput Sweden
Linda Broer Netherlands
Lynda M. Rose United States
Eitan Friedman Israel
Anna‐Liisa Hartikainen Finland
Andrew C. Heath United States
Anna Murray relative to Lisette Stolk Netherlands Lisette Stolk's profile →
Citations per field
00.5×1.5×
Lisette Stolk · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 139 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The transcriptional landscape of age in human peripheral blood
Hit paper breakdown →
2015523
2
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms
Hit paper breakdown →
2019507
3
Using human genetics to understand the disease impacts of testosterone in men and women
Hit paper breakdown →
2020493
4
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Hit paper breakdown →
2014458
5 2010419
6
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Hit paper breakdown →
2017415
7 1999411
8
Puberty timing associated with diabetes, cardiovascular disease and also diverse health outcomes in men and women: the UK Biobank study
Hit paper breakdown →
2015405
9 2008393
10
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Hit paper breakdown →
2019385
11 2015314
12 2012306
13 2016295
14 2016264
15 2019242
16 2009235
17 2019220
18 2011218
19 2009213
20 2013212

About Anna Murray

Anna Murray is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Reproductive Medicine, Molecular Biology and Cognitive Neuroscience, having authored 139 papers that have together received 12.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (37 papers), Genetics and Neurodevelopmental Disorders (30 papers), Genomic variations and chromosomal abnormalities (16 papers), Autism Spectrum Disorder Research (12 papers), Growth Hormone and Insulin-like Growth Factors (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Congenital heart defects research (8 papers) and Epigenetics and DNA Methylation (7 papers). The work is most often cited by research in Reproductive Medicine (1.6k citations), Aging (341 citations), Genetics (4.5k citations), Endocrine and Autonomic Systems (548 citations) and Endocrinology, Diabetes and Metabolism (1.2k citations). Anna Murray has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Timothy Mark Frayling, Michael Weedon, John Richard Perry, Sarah A. Ennis, Felix R. Day, Ken K. Ong, James L. Webb, Katherine S. Ruth, David R. Melzer and Andrew R. Wood. Their work appears in journals such as Human Molecular Genetics, Nature Genetics, Nature Communications, Human Reproduction and PLoS 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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