Helen Cox

5.5k total citations
76 papers, 2.1k citations indexed

About

Helen Cox is a scholar working on Molecular Biology, Food Science and Genetics. According to data from OpenAlex, Helen Cox has authored 76 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 19 papers in Food Science and 15 papers in Genetics. Recurrent topics in Helen Cox's work include Proteins in Food Systems (12 papers), Pickering emulsions and particle stabilization (10 papers) and Genomic variations and chromosomal abnormalities (8 papers). Helen Cox is often cited by papers focused on Proteins in Food Systems (12 papers), Pickering emulsions and particle stabilization (10 papers) and Genomic variations and chromosomal abnormalities (8 papers). Helen Cox collaborates with scholars based in United Kingdom, United States and Canada. Helen Cox's co-authors include Ian T. Norton, C. R. Thomas, P.J. Fryer, Fotis Spyropoulos, Paul Hooley, Fideline Tchuenbou‐Magaia, Taghi Miri, Reza Mousavi, Gopal Chandra Paul and Antonio Guerrero and has published in prestigious journals such as Brain, The Journal of Clinical Endocrinology & Metabolism and Annals of Neurology.

In The Last Decade

Helen Cox

72 papers receiving 2.1k citations

Peers

Helen Cox

GENET

Lokesh Kumar India

Salvatore Foti Italy

Chunsheng Zhang China

Yuanyuan Wu China

Jolon M. Dyer New Zealand

Bal Ram Singh United States

Kun Yao China

Xueqin Gao China

Lokesh Kumar India

Helen Cox

624 ×0.8

933 ×1.4

216 ×0.7

128 ×0.5

115 ×0.5

GENET

Citations per year, relative to Helen Cox Helen Cox (= 1×) peers Lokesh Kumar

Countries citing papers authored by Helen Cox

Since Specialization

Citations

This map shows the geographic impact of Helen Cox'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 Helen Cox with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Helen Cox more than expected).

Fields of papers citing papers by Helen Cox

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helen Cox. 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 Helen Cox. The network helps show where Helen Cox may publish in the future.

Co-authorship network of co-authors of Helen Cox

This figure shows the co-authorship network connecting the top 25 collaborators of Helen Cox. A scholar is included among the top collaborators of Helen Cox 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 Helen Cox. Helen Cox is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Steeds, Richard P., Jennifer H. Pinney, Shanat Baig, et al.. (2024). Extending the reach of expert amyloidosis care: A feasibility study exploring the staged implementation of a UK amyloidosis network. Clinical Medicine. 24(1). 100004–100004. 1 indexed citations

Pagnamenta, Alistair T., Jing Yu, Tracey Willis, et al.. (2023). A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and SRRM2 Haploinsufficiency. Human Mutation. 2023. 1–9. 2 indexed citations

Gillmore, Julian D., Mary M. Reilly, Caroline Coats, et al.. (2022). Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UK. Advances in Therapy. 39(6). 2292–2301. 19 indexed citations

Brasch‐Andersen, Charlotte, Helen Cox, Michael Parker, et al.. (2020). A new 1p36.13‐1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis. Clinical Genetics. 97(6). 927–932. 2 indexed citations

Zepeda‐Mendoza, Cinthya, Tammy Kammin, David J. Harris, et al.. (2018). Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin. European Journal of Human Genetics. 26(3). 374–381. 4 indexed citations

Cox, Helen, et al.. (2013). The Busy General Practitioner’s Reference Guide to Increasing Physical Activity Levels in the British population and Associated Benefits/Risks: A Review of the Literature. Journal of General Practice. 1(1). 1 indexed citations

Brown, Ian, Timothy R. Dafforn, P.J. Fryer, & Helen Cox. (2013). Kinetic study of the thermal denaturation of a hyperthermostable extracellular α-amylase from Pyrococcus furiosus. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1834(12). 2600–2605. 23 indexed citations

Patel, Chirag, Lee Silcock, Dominic McMullan, Louise Brueton, & Helen Cox. (2012). TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype. European Journal of Human Genetics. 20(8). 863–869. 39 indexed citations

Cox, Helen, et al.. (2011). Refining the Mungaroo Formation and Lower Barrow Group depositional models, Exmouth Plateau, North Carnarvon Basin: WA-390-P phase II exploration*. The APPEA Journal. 51(2). 713–713.

10.

Norton, Ian T., Fotis Spyropoulos, & Helen Cox. (2010). Practical Food Rheology. University of Birmingham Research Portal (University of Birmingham). 74 indexed citations

11.

Cox, Helen, et al.. (2010). Food grade duplex emulsions designed and stabilised with different osmotic pressures. Journal of Colloid and Interface Science. 352(1). 59–67. 83 indexed citations

12.

Cox, Helen, Anneke Lucassen, Marlène Rio, et al.. (2009). Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings. Clinical Dysmorphology. 18(2). 98–102. 3 indexed citations

13.

Salo, Antti M., Helen Cox, Peter Farndon, et al.. (2008). A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene. The American Journal of Human Genetics. 83(4). 495–503. 99 indexed citations

14.

Cox, Helen & David I. Wilson. (2007). GENETICS OF HYPOPLASTIC LEFT HEART SYNDROME. Fetal and Maternal Medicine Review. 18(2). 103–119. 3 indexed citations

15.

Masabanda, Julio, David W. Burt, Patricia C. O’Brien, et al.. (2004). Molecular cytogenetic definition of the chicken genome. Genetics. 166(3). 1 indexed citations

16.

Cox, Helen, H. Bullman, & I. Karen Temple. (2003). Maternal UPD(14) in the patient with a normal karyotype: Clinical report and a systematic search for cases in samples sent for testing for Prader–Willi syndrome. American Journal of Medical Genetics Part A. 127A(1). 21–25. 24 indexed citations

17.

Cox, Helen, et al.. (2002). Phenotypic spectrum of interstitial 7p duplication in mosaic and non‐mosaic forms. American Journal of Medical Genetics. 109(4). 306–310. 8 indexed citations

18.

McIntyre, Mhairi, Helen Cox, C. R. Thomas, et al.. (2001). Quantification of autolysis inPenicillium chrysogenumby semiautomated image analysis. Canadian Journal of Microbiology. 47(4). 315–321. 5 indexed citations

19.

Robinson, S., et al.. (1994). Participatory Health Development in Rural Nepal: Clarifying the Process of Community Empowerment. Health Education Quarterly. 21(3). 329–343. 44 indexed citations

20.

Cox, Helen, et al.. (1961). The reliability of an experimental transistorized data handling system. Journal of the British Institution of Radio Engineers. 22(1). 17–29. 1 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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