L Kerzin-Storrar

1.1k total citations
23 papers, 728 citations indexed

About

L Kerzin-Storrar is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Clinical Psychology. According to data from OpenAlex, L Kerzin-Storrar has authored 23 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 4 papers in Clinical Psychology. Recurrent topics in L Kerzin-Storrar's work include BRCA gene mutations in cancer (7 papers), Ethics and Legal Issues in Pediatric Healthcare (5 papers) and Prenatal Screening and Diagnostics (3 papers). L Kerzin-Storrar is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Ethics and Legal Issues in Pediatric Healthcare (5 papers) and Prenatal Screening and Diagnostics (3 papers). L Kerzin-Storrar collaborates with scholars based in United Kingdom, Australia and Canada. L Kerzin-Storrar's co-authors include David Craufurd, R. Harris, R Harris, Dian Donnai, Andrew Colley, Caroline Benjamin, Helen Kingston, M.J.W. Faed, Peter G. Smith and Jenny MacGillivray and has published in prestigious journals such as The Lancet, Neurology and British Journal of Cancer.

In The Last Decade

L Kerzin-Storrar

23 papers receiving 704 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L Kerzin-Storrar United Kingdom 16 374 211 108 104 100 23 728
Joanna H. Fanos United States 18 301 0.8× 257 1.2× 107 1.0× 86 0.8× 53 0.5× 30 762
Andrea Boogaerts Belgium 15 587 1.6× 183 0.9× 181 1.7× 106 1.0× 289 2.9× 19 929
Susan Holloway United Kingdom 15 356 1.0× 149 0.7× 276 2.6× 135 1.3× 63 0.6× 29 818
Mercy Laurino United States 13 245 0.7× 138 0.7× 99 0.9× 87 0.8× 102 1.0× 31 548
Marlene J. Huggins Canada 15 553 1.5× 147 0.7× 313 2.9× 164 1.6× 422 4.2× 20 1.1k
Sheila A Simpson United Kingdom 16 301 0.8× 113 0.5× 200 1.9× 219 2.1× 363 3.6× 24 776
Kathryn F. Peters United States 12 343 0.9× 198 0.9× 108 1.0× 26 0.3× 18 0.2× 27 636
Jonathon Gray United Kingdom 18 439 1.2× 116 0.5× 75 0.7× 17 0.2× 33 0.3× 41 897
Juan Clinton Llerena Brazil 23 601 1.6× 346 1.6× 400 3.7× 37 0.4× 31 0.3× 112 1.6k
Tracy L. Trotter United States 13 400 1.1× 141 0.7× 137 1.3× 105 1.0× 16 0.2× 19 821

Countries citing papers authored by L Kerzin-Storrar

Since Specialization
Citations

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

Fields of papers citing papers by L Kerzin-Storrar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L Kerzin-Storrar. 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 L Kerzin-Storrar. The network helps show where L Kerzin-Storrar may publish in the future.

Co-authorship network of co-authors of L Kerzin-Storrar

This figure shows the co-authorship network connecting the top 25 collaborators of L Kerzin-Storrar. A scholar is included among the top collaborators of L Kerzin-Storrar 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 L Kerzin-Storrar. L Kerzin-Storrar 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.
Alexander, Elizabeth, Susan Kelly, & L Kerzin-Storrar. (2014). Non‐Invasive Prenatal Testing: UK Genetic Counselors’ Experiences and Perspectives. Journal of Genetic Counseling. 24(2). 300–311. 21 indexed citations
2.
MacLeod, Rhona, et al.. (2013). Experiences of predictive testing in young people at risk of Huntington’s disease, familial cardiomyopathy or hereditary breast and ovarian cancer. European Journal of Human Genetics. 22(3). 396–401. 36 indexed citations
3.
Skirton, Heather, L Kerzin-Storrar, Chris Barnes, et al.. (2013). Building the Genetic Counsellor Profession in the United Kingdom: Two Decades of Growth and Development. Journal of Genetic Counseling. 22(6). 902–906. 24 indexed citations
4.
Barnes, Chris, et al.. (2012). The Department of Health-supported genetic counsellor training post scheme in England: a unique initiative?. Journal of Community Genetics. 3(4). 297–302. 5 indexed citations
5.
Caldwell, Jane C., Naz Khan, L Kerzin-Storrar, et al.. (2012). The clinical management of relatives of young sudden unexplained death victims; implantable defibrillators are rarely indicated. Heart. 98(8). 631–636. 22 indexed citations
6.
Lehmann, Anna, et al.. (2011). Extended Family Impact of Genetic Testing: The Experiences of X‐linked Carrier Grandmothers. Journal of Genetic Counseling. 20(4). 365–373. 16 indexed citations
7.
Gale, Theodora, et al.. (2010). Explaining Mendelian Inheritance in Genetic Consultations: An IPR Study of Counselor and Counselee Experiences. Journal of Genetic Counseling. 19(1). 55–67. 3 indexed citations
8.
Kerzin-Storrar, L. (2007). Genetic Counselling: A Psychological Approach. Journal of Genetic Counseling. 16(3). 383–384. 14 indexed citations
9.
Clarke, Angus, Martin Richards, L Kerzin-Storrar, et al.. (2005). Genetic professionals' reports of nondisclosure of genetic risk information within families. European Journal of Human Genetics. 13(5). 556–562. 92 indexed citations
10.
11.
Liede, Alexander, L Kerzin-Storrar, & David Craufurd. (2000). A Method for Analyzing Videotaped Genetic Counseling Sessions. Journal of Genetic Counseling. 9(2). 117–136. 7 indexed citations
12.
Kerzin-Storrar, L. (1995). Prenatal Diagnosis: The Human Side. Journal of Medical Genetics. 32(12). 998.2–998. 20 indexed citations
13.
Kerzin-Storrar, L. (1993). Psychosocial Aspects of Genetic Counselling. Journal of Medical Genetics. 30(5). 448.1–448. 5 indexed citations
14.
Kerzin-Storrar, L, et al.. (1990). Adult polycystic kidney disease: knowledge, experience, and attitudes to prenatal diagnosis.. Journal of Medical Genetics. 27(9). 552–558. 32 indexed citations
15.
Craufurd, David, et al.. (1989). UPTAKE OF PRESYMPTOMATIC PREDICTIVE TESTING FOR HUNTINGTON'S DISEASE. The Lancet. 334(8663). 603–605. 170 indexed citations
16.
Kerzin-Storrar, L. (1988). Genetic Risk, Risk Perception, and Decision Making. Journal of Medical Genetics. 25(9). 647–648. 19 indexed citations
17.
Donnai, Dian, L Kerzin-Storrar, & R Harris. (1987). Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease.. Journal of Medical Genetics. 24(2). 84–87. 37 indexed citations
18.
Read, Andrew, L Kerzin-Storrar, R. Mountford, R Elles, & R Harris. (1986). A register based system for gene tracking in Duchenne muscular dystrophy.. Journal of Medical Genetics. 23(6). 581–586. 15 indexed citations
19.
Kerzin-Storrar, L. (1986). Family Studies in Genetic Disorders. Journal of Medical Genetics. 23(3). 286.2–287. 1 indexed citations
20.
Kerzin-Storrar, L, M.J.W. Faed, Jenny MacGillivray, & Peter G. Smith. (1983). Incidence of familial Hodgkin's disease. British Journal of Cancer. 47(5). 707–712. 37 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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