Susan Creighton

1.2k total citations
18 papers, 754 citations indexed

About

Susan Creighton is a scholar working on Cellular and Molecular Neuroscience, Genetics and Neurology. According to data from OpenAlex, Susan Creighton has authored 18 papers receiving a total of 754 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 7 papers in Genetics and 5 papers in Neurology. Recurrent topics in Susan Creighton's work include Genetic Neurodegenerative Diseases (11 papers), BRCA gene mutations in cancer (4 papers) and Neurological disorders and treatments (4 papers). Susan Creighton is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), BRCA gene mutations in cancer (4 papers) and Neurological disorders and treatments (4 papers). Susan Creighton collaborates with scholars based in Canada, United States and United Kingdom. Susan Creighton's co-authors include Michael R. Hayden, Yvonne Bombard, Joan L. Bottorff, Jan M. Friedman, M. E. Suzanne Lewis, Gerry Veenstra, Jane S. Paulsen, Jeanette J. A. Holden, Louise Mercer and Alicia Semaka and has published in prestigious journals such as Neurology, The Lancet Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Susan Creighton

18 papers receiving 717 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susan Creighton Canada 14 292 234 179 159 127 18 754
Rhona MacLeod United Kingdom 20 182 0.6× 183 0.8× 257 1.4× 486 3.1× 73 0.6× 43 1.3k
Beena Koshy India 15 351 1.2× 384 1.6× 94 0.5× 52 0.3× 132 1.0× 48 1.1k
Sandi Wiggins Canada 8 216 0.7× 119 0.5× 89 0.5× 301 1.9× 25 0.2× 10 660
Marlene J. Huggins Canada 15 422 1.4× 313 1.3× 164 0.9× 553 3.5× 44 0.3× 20 1.1k
J Artigas-Pallarés Spain 18 95 0.3× 200 0.9× 101 0.6× 170 1.1× 315 2.5× 77 1.1k
A J Holland United Kingdom 8 120 0.4× 147 0.6× 84 0.5× 181 1.1× 36 0.3× 9 462
Nancy J. Butcher Canada 23 175 0.6× 759 3.2× 58 0.3× 439 2.8× 164 1.3× 69 1.5k
Milena Paneque Portugal 16 266 0.9× 272 1.2× 134 0.7× 474 3.0× 32 0.3× 65 827
Jeff L. Waugh United States 17 182 0.6× 92 0.4× 279 1.6× 48 0.3× 72 0.6× 51 819
Erick Sell Canada 13 65 0.2× 179 0.8× 64 0.4× 78 0.5× 91 0.7× 34 627

Countries citing papers authored by Susan Creighton

Since Specialization
Citations

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

Fields of papers citing papers by Susan Creighton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Creighton

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

All Works

18 of 18 papers shown
1.
Sturrock, Aaron, Katy Wyper, Ruth Milner, et al.. (2015). A longitudinal study of magnetic resonance spectroscopy Huntington's disease biomarkers. Movement Disorders. 30(3). 393–401. 38 indexed citations
2.
Potter, Kathryn J., Susan Creighton, Linlea Armstrong, et al.. (2013). The c.7409G>A (p.Cys2470Tyr) Variant of <b><i>FBN1</i></b>: Phenotypic Variability across Three Generations. Molecular Syndromology. 4(3). 125–135. 6 indexed citations
3.
Bombard, Yvonne, Jan M. Friedman, Gerry Veenstra, et al.. (2012). Beyond the patient: The broader impact of genetic discrimination among individuals at risk of Huntington disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(2). 217–226. 35 indexed citations
4.
Hawkins, Alice K., Susan Creighton, & Michael R. Hayden. (2012). When access is an issue: exploring barriers to predictive testing for Huntington disease in British Columbia, Canada. European Journal of Human Genetics. 21(2). 148–153. 22 indexed citations
5.
Virani, Alice, Susan Creighton, & Michael R. Hayden. (2012). Developing a comprehensive, effective patient-friendly website to enhance decision making in predictive testing for Huntington disease. Genetics in Medicine. 15(6). 466–472. 10 indexed citations
6.
Creighton, Susan, et al.. (2012). Providing predictive testing for Huntington disease via telehealth: results of a pilot study in British Columbia, Canada. Clinical Genetics. 84(1). 60–64. 26 indexed citations
7.
Bombard, Yvonne, Jan M. Friedman, Gerry Veenstra, et al.. (2010). Factors associated with experiences of genetic discrimination among individuals at risk for huntington disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(1). 19–27. 14 indexed citations
8.
Sturrock, Aaron, Joji Decolongon, Susan Creighton, et al.. (2010). H06 Cross sectional and longitudinal 3T magnetic resonance spectroscopy in a TRACK-HD cohort of individuals with premanifest and early Huntington's disease. Journal of Neurology Neurosurgery & Psychiatry. 81(Suppl 1). A35.2–A35. 2 indexed citations
9.
Sturrock, Aaron, Joji Decolongon, R. Dar Santos, et al.. (2010). Magnetic resonance spectroscopy biomarkers in premanifest and early Huntington disease. Neurology. 75(19). 1702–1710. 73 indexed citations
10.
Bombard, Yvonne, Gerry Veenstra, Jan M. Friedman, et al.. (2009). Perceptions of genetic discrimination among people at risk for Huntington's disease: a cross sectional survey. BMJ. 338(jun08 3). b2175–b2175. 169 indexed citations
11.
Bombard, Yvonne, Elizabeth Penziner, Joji Decolongon, et al.. (2007). Managing genetic discrimination: Strategies used by individuals found to have the Huntington disease mutation. Clinical Genetics. 71(3). 220–231. 29 indexed citations
12.
Semaka, Alicia, Susan Creighton, Simon C. Warby, & Michael R. Hayden. (2006). Predictive testing for Huntington disease: interpretation and significance of intermediate alleles. Clinical Genetics. 70(4). 283–294. 96 indexed citations
13.
Mercer, Louise, Susan Creighton, Jeanette J. A. Holden, & M. E. Suzanne Lewis. (2006). Parental Perspectives on the Causes of an Autism Spectrum Disorder in their Children. Journal of Genetic Counseling. 15(1). 41–50. 98 indexed citations
15.
Harper, Peter S., Sjef Gevers, Guido de Wert, et al.. (2004). Genetic testing and Huntington's disease: issues of employment. The Lancet Neurology. 3(4). 249–252. 19 indexed citations
16.
Newcomb, William W., et al.. (1981). A reinvestigation of the origin of the peribacteroid membrane in root nodules of Vicia faba. Canadian Journal of Botany. 59(9). 1547–1552. 3 indexed citations
17.
Hayes, M. Anthony, et al.. (1978). Acute Necrotizing Myelopathy from Nucleus Pulposus Embolism in Dogs with Intervertebral Disk Degeneration. Journal of the American Veterinary Medical Association. 173(3). 289–295. 44 indexed citations
18.
Turkewitz, Gerald & Susan Creighton. (1975). Changes in lateral differentiation of head posture in the human neonate. Developmental Psychobiology. 8(1). 85–89. 45 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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