Victoria Harrison

2.1k total citations
22 papers, 302 citations indexed

About

Victoria Harrison is a scholar working on Molecular Biology, Genetics and Literature and Literary Theory. According to data from OpenAlex, Victoria Harrison has authored 22 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Literature and Literary Theory. Recurrent topics in Victoria Harrison's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Metabolism and Genetic Disorders (3 papers). Victoria Harrison is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Metabolism and Genetic Disorders (3 papers). Victoria Harrison collaborates with scholars based in United Kingdom, United States and Austria. Victoria Harrison's co-authors include A G Blakeley, D.P. Dearnaley, John R. Mathias, Edward Blair, Joanna McParland, Michael Pike, Kathy Rowan, Helen Stewart, Samantha J.L. Knight and Elham Sadighi Akha and has published in prestigious journals such as Annals of the New York Academy of Sciences, Fertility and Sterility and Journal of American History.

In The Last Decade

Victoria Harrison

20 papers receiving 268 citations

Peers

Victoria Harrison

GENET

CMN

C. Anthony Scott United States

Susan Zeesman Canada

A Mayerová Germany

Dimitris Avramopoulos Greece

Va Lip United States

Heidi Mateus Colombia

Bettina Lipkowitz Germany

Stetson Thacker United States

Leda Paganini Italy

Tiia Reimand Estonia

C. Anthony Scott United States

Victoria Harrison

322 ×2.5

146 ×1.3

GENET

17 ×0.3

17 ×0.5

CMN

10 ×0.3

Citations per year, relative to Victoria Harrison Victoria Harrison (= 1×) peers C. Anthony Scott

Countries citing papers authored by Victoria Harrison

Since Specialization

Citations

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

Fields of papers citing papers by Victoria Harrison

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Victoria Harrison

This figure shows the co-authorship network connecting the top 25 collaborators of Victoria Harrison. A scholar is included among the top collaborators of Victoria Harrison 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 Victoria Harrison. Victoria Harrison 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

Arrondel, Christelle, Giulia Barcia, Zahra Assouline, et al.. (2025). Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism. Pediatric Nephrology. 40(9). 2823–2828. 1 indexed citations

Harrison, Victoria, et al.. (2024). The biology of reactivity in human relationships: a conversation with Victoria Harrison. Australian and New Zealand Journal of Family Therapy. 45(2). 257–265.

Allen, Stephanie, Natalie Chandler, Esther Kinning, et al.. (2023). Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies. Prenatal Diagnosis. 44(4). 432–442. 3 indexed citations

Bourinaris, Thomas, Damian Smedley, Valentina Cipriani, et al.. (2020). Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project. European Journal of Human Genetics. 28(12). 1763–1768. 11 indexed citations

Harrison, Victoria, et al.. (2020). Genetic testing in Neurology. Medicine. 48(8). 545–549. 1 indexed citations

Harrison, Victoria. (2018). METÁFORAS CONCEITUAIS E O SENTIDO DO CONHECIMENTO: ORIENTE E OCIDENTE. 4(2). 41–56.

Bateman, Mark S., Morag N. Collinson, David J. Bunyan, et al.. (2017). Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities. American Journal of Medical Genetics Part A. 176(2). 319–329. 5 indexed citations

Harrison, Victoria. (2014). Emotional Reactivity, Fusion, and Differentiation of Self in Family Physiology: Clinical Case Research. 361–384. 1 indexed citations

Pagnamenta, Alistair T., Jennie Murray, Grace Yoon, et al.. (2012). A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss. American Journal of Medical Genetics Part A. 158A(10). 2577–2582. 33 indexed citations

10.

Harrison, Victoria, Jane A. Hurst, Tracy Lester, et al.. (2012). Segmental paternal uniparental disomy of chromosome 14 in a 4-year-old boy. Clinical Dysmorphology. 21(4). 208–211. 1 indexed citations

11.

Pagnamenta, Alistair T., Stefano Lise, Victoria Harrison, et al.. (2011). Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies. Journal of Human Genetics. 57(1). 70–72. 46 indexed citations

12.

Harrison, Victoria, et al.. (2011). Compound heterozygous deletion ofNRXN1causing severe developmental delay with early onset epilepsy in two sisters. American Journal of Medical Genetics Part A. 155(11). 2826–2831. 58 indexed citations

13.

Harrison, Victoria, et al.. (2010). Diagnosis of Pallister–Killian syndrome by array comparative genome hybridization from a spleen sample. Clinical Dysmorphology. 20(1). 58–60. 3 indexed citations

14.

Harrison, Victoria, Kathy Rowan, & John R. Mathias. (2005). Stress reactivity and family relationships in the development and treatment of endometriosis. Fertility and Sterility. 83(4). 857–864. 18 indexed citations

15.

Mathias, John R., et al.. (1998). Relation of endometriosis and neuromuscular disease of the gastrointestinal tract: new insights. Fertility and Sterility. 70(1). 81–88. 32 indexed citations

16.

Harrison, Victoria. (1997). Patterns of Ovulation, Reactivity, and Family Emotional Process. Annals of the New York Academy of Sciences. 807(1). 522–524. 4 indexed citations

17.

Harrison, Victoria, et al.. (1995). Elizabeth Bishop: Life and the Memory of it.. American Literature. 67(2). 406–406. 1 indexed citations

18.

Harrison, Victoria, et al.. (1994). Elizabeth Bishop's Poetics of Intimacy.. Journal of American History. 81(2). 773–773. 3 indexed citations

19.

Harrison, Victoria. (1993). Elizabeth Bishop's Poetics of Intimacy. Cambridge University Press eBooks. 17 indexed citations

20.

Blakeley, A G, D.P. Dearnaley, & Victoria Harrison. (1970). The noradrenaline content of the vas deferens of the guinea-pig. Proceedings of the Royal Society of London. Series B, Biological sciences. 174(1037). 491–502. 36 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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