Hannah C. Cox

1.8k total citations
36 papers, 741 citations indexed

About

Hannah C. Cox is a scholar working on Genetics, Psychiatry and Mental health and Endocrine and Autonomic Systems. According to data from OpenAlex, Hannah C. Cox has authored 36 papers receiving a total of 741 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Psychiatry and Mental health and 8 papers in Endocrine and Autonomic Systems. Recurrent topics in Hannah C. Cox's work include Migraine and Headache Studies (10 papers), Neuroscience of respiration and sleep (8 papers) and Genetic factors in colorectal cancer (7 papers). Hannah C. Cox is often cited by papers focused on Migraine and Headache Studies (10 papers), Neuroscience of respiration and sleep (8 papers) and Genetic factors in colorectal cancer (7 papers). Hannah C. Cox collaborates with scholars based in United States, Australia and New Zealand. Hannah C. Cox's co-authors include Krystal Brown, Lyn R. Griffiths, Rod A. Lea, Susan Manley, Gustavo Glusman, Jared C. Roach, Erin Mundt, Lisa E. Esterling, Sara Pirzadeh‐Miller and Jacqueline Mersch and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Hannah C. Cox

35 papers receiving 730 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hannah C. Cox United States 18 340 218 146 131 91 36 741
Miles C. Benton Australia 18 303 0.9× 693 3.2× 274 1.9× 96 0.7× 117 1.3× 48 1.2k
Jessica Moline United States 16 175 0.5× 279 1.3× 216 1.5× 260 2.0× 273 3.0× 28 1.1k
Aleš Maver Slovenia 20 340 1.0× 506 2.3× 74 0.5× 73 0.6× 53 0.6× 112 1.2k
Dalia Kasperavičiūtė United Kingdom 20 356 1.0× 274 1.3× 47 0.3× 81 0.6× 49 0.5× 27 942
Sarah M. Nikkel Canada 19 318 0.9× 358 1.6× 53 0.4× 35 0.3× 41 0.5× 41 1.0k
Janet Y. Lee United States 12 279 0.8× 250 1.1× 102 0.7× 38 0.3× 39 0.4× 21 948
Nana Matoba United States 12 514 1.5× 343 1.6× 65 0.4× 51 0.4× 57 0.6× 19 927
Elizabeth W. LaPensee United States 8 216 0.6× 244 1.1× 147 1.0× 29 0.2× 21 0.2× 13 881
Karin E. M. Diderich Netherlands 21 563 1.7× 822 3.8× 142 1.0× 49 0.4× 48 0.5× 60 1.6k

Countries citing papers authored by Hannah C. Cox

Since Specialization
Citations

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

Fields of papers citing papers by Hannah C. Cox

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hannah C. Cox

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

All Works

20 of 20 papers shown
1.
Pan, Shujuan, Hannah C. Cox, Erin Mundt, et al.. (2023). Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome. Frontiers in Oncology. 13. 1069467–1069467. 5 indexed citations
2.
Cox, Hannah C., et al.. (2021). Demographic and socioeconomic trends in DNA banking utilization in the USA. Journal of Community Genetics. 12(4). 593–602. 2 indexed citations
3.
Slavin, Thomas P., Bradford Coffee, Ryan Bernhisel, et al.. (2019). Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing. Cancer Genetics. 235-236. 31–38. 24 indexed citations
4.
Coffee, Bradford, Hannah C. Cox, John Kidd, et al.. (2017). Detection of somatic variants in peripheral blood lymphocytes using a next generation sequencing multigene pan cancer panel. Cancer Genetics. 211. 5–8. 39 indexed citations
5.
Qian, Yaping, Debora Mancini‐DiNardo, Thaddeus Judkins, et al.. (2017). Identification of pathogenic retrotransposon insertions in cancer predisposition genes. Cancer Genetics. 216-217. 159–169. 29 indexed citations
6.
Coffee, Bradford, et al.. (2016). Detection of somatic variants in peripheral blood lymphocytes using a 25-gene hereditary cancer panel.. Journal of Clinical Oncology. 34(15_suppl). 1580–1580. 1 indexed citations
7.
Glusman, Gustavo, Hannah C. Cox, & Jared C. Roach. (2014). Whole-genome haplotyping approaches and genomic medicine. Genome Medicine. 6(9). 73–73. 50 indexed citations
8.
Maher, Bridget H., Rod A. Lea, Jordan Follett, et al.. (2013). Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort. Research Bank (Australian Catholic University).
9.
Esposito, Teresa, Rod A. Lea, Bridget H. Maher, et al.. (2013). Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. Human Molecular Genetics. 22(18). 3654–3666. 1 indexed citations
10.
Cox, Hannah C., Rod A. Lea, Claire Bellis, et al.. (2012). A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility. Neurogenetics. 13(3). 261–266. 30 indexed citations
11.
Maher, Bridget H., Rod A. Lea, Miles C. Benton, et al.. (2012). An X Chromosome Association Scan of the Norfolk Island Genetic Isolate Provides Evidence for a Novel Migraine Susceptibility Locus at Xq12. PLoS ONE. 7(5). e37903–e37903. 34 indexed citations
12.
Mackey, David A., Justin C. Sherwin, Lisa S. Kearns, et al.. (2011). The Norfolk Island Study (NIES): Rationale, Methodology and Distribution of Ocular Biometry (Biometry of the Bounty). UWA Profiles and Research Repository (UWA). 11 indexed citations
13.
Mackey, David A., Justin C. Sherwin, Lisa S. Kearns, et al.. (2011). The Norfolk Island Eye Study (NIES): Rationale, Methodology and Distribution of Ocular Biometry (Biometry of the Bounty). Twin Research and Human Genetics. 14(1). 42–52. 1 indexed citations
14.
Cox, Hannah C., Rod A. Lea, Claire Bellis, et al.. (2011). Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island. Gene. 494(1). 119–123. 2 indexed citations
15.
Cox, Hannah C., Rod A. Lea, Claire Bellis, et al.. (2011). Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate. The Journal of Headache and Pain. 12(6). 603–608. 10 indexed citations
16.
Menon, Shruti, Hannah C. Cox, Masashi Kuwahata, et al.. (2010). Association of a Notch 3 gene polymorphism with migraine susceptibility. Cephalalgia. 31(3). 264–270. 20 indexed citations
17.
Liu, Annie, Natalie Colson, Sharon Quinlan, et al.. (2010). Analysis of the MTHFR C677T variant with migraine phenotypes. BMC Research Notes. 3(1). 213–213. 39 indexed citations
18.
Cox, Hannah C., Claire Bellis, Rod A. Lea, et al.. (2009). Principal Component and Linkage Analysis of Cardiovascular Risk Traits in the Norfolk Isolate. Human Heredity. 68(1). 55–64. 18 indexed citations
19.
MacGregor, Stuart, Claire Bellis, Rod A. Lea, et al.. (2009). Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island. European Journal of Human Genetics. 18(1). 67–72. 22 indexed citations
20.
Bellis, Claire, Hannah C. Cox, Rod A. Lea, et al.. (2007). Linkage disequilibrium analysis in the genetically isolated Norfolk Island population. Heredity. 100(4). 366–373. 21 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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