Chloe Mighton

1.1k total citations
30 papers, 318 citations indexed

About

Chloe Mighton is a scholar working on Genetics, Pathology and Forensic Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Chloe Mighton has authored 30 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 10 papers in Pathology and Forensic Medicine and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Chloe Mighton's work include Genomics and Rare Diseases (20 papers), BRCA gene mutations in cancer (18 papers) and Genetic factors in colorectal cancer (10 papers). Chloe Mighton is often cited by papers focused on Genomics and Rare Diseases (20 papers), BRCA gene mutations in cancer (18 papers) and Genetic factors in colorectal cancer (10 papers). Chloe Mighton collaborates with scholars based in Canada, United States and United Kingdom. Chloe Mighton's co-authors include Yvonne Bombard, Salma Shickh, Elizabeth Uleryk, Petros Pechlivanoglou, Jordan Lerner‐Ellis, Marc Clausen, Nicholas A. Watkins, George S. Charames, Andrew Wong and Kasmintan A. Schrader and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Chloe Mighton

26 papers receiving 315 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chloe Mighton Canada 10 252 64 57 49 49 30 318
Salma Shickh Canada 9 201 0.8× 56 0.9× 46 0.8× 53 1.1× 31 0.6× 20 269
Vigdís Stefánsdóttir Iceland 9 210 0.8× 42 0.7× 29 0.5× 69 1.4× 57 1.2× 18 282
Elana Levinson United States 6 195 0.8× 49 0.8× 32 0.6× 62 1.3× 47 1.0× 9 282
Miranda L. G. Hallquist United States 10 201 0.8× 30 0.5× 33 0.6× 83 1.7× 29 0.6× 14 311
Lindsay Z. Feuerman United States 5 254 1.0× 25 0.4× 29 0.5× 101 2.1× 68 1.4× 6 333
Patrick Reineke United States 5 244 1.0× 64 1.0× 61 1.1× 132 2.7× 53 1.1× 10 355
Marian J. Gilmore United States 10 151 0.6× 14 0.2× 41 0.7× 65 1.3× 29 0.6× 25 267
Gabrielle Bertier France 6 75 0.3× 36 0.6× 16 0.3× 41 0.8× 37 0.8× 14 169
Parichoy Pal Choudhury United States 8 152 0.6× 38 0.6× 36 0.6× 10 0.2× 34 0.7× 17 304
Quinn Stein United States 9 133 0.5× 72 1.1× 16 0.3× 23 0.5× 12 0.2× 31 214

Countries citing papers authored by Chloe Mighton

Since Specialization
Citations

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

Fields of papers citing papers by Chloe Mighton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chloe Mighton

This figure shows the co-authorship network connecting the top 25 collaborators of Chloe Mighton. A scholar is included among the top collaborators of Chloe Mighton 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 Chloe Mighton. Chloe Mighton 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.
Mighton, Chloe, et al.. (2026). Correspondence on “Parents’ perceptions of the utility of genetic testing in the NICU” by Callahan et al. Genetics in Medicine. 28(1). 101638–101638.
2.
Mighton, Chloe, Katrina Hueniken, Vivek M. Philip, et al.. (2025). Pathogenic germline variants in small cell lung cancer: A systematic review and meta-analysis. Human Genetics and Genomics Advances. 6(3). 100445–100445.
3.
Goh, Elaine, Lauren Chad, Julie Richer, et al.. (2024). Canadian College of Medical Geneticists: clinical practice advisory document – responsibility to recontact for reinterpretation of clinical genetic testing. Journal of Medical Genetics. 61(12). 1123–1131. 2 indexed citations
4.
Mighton, Chloe, Abdul Noor, Nicholas A. Watkins, et al.. (2024). Validation of low‐pass genome sequencing for prenatal diagnosis. Prenatal Diagnosis. 44(4). 443–453. 3 indexed citations
5.
Johnston, Christine, Saumeh Saeedi, Chloe Mighton, et al.. (2024). International policies guiding the selection, analysis, and clinical management of secondary findings from genomic sequencing: A systematic review. The American Journal of Human Genetics. 111(10). 2079–2093. 1 indexed citations
6.
Richardson, Marina, Beate Sander, Nick Daneman, Chloe Mighton, & Fiona A. Miller. (2023). Moving from intervention management to disease management: a qualitative study exploring a systems approach to health technology assessment in Canada. International Journal of Technology Assessment in Health Care. 39(1). e67–e67. 1 indexed citations
7.
Mighton, Chloe, Marc Clausen, Selina Casalino, et al.. (2023). Parents’ attitudes towards research involving genome sequencing of their healthy children: a qualitative study. European Journal of Human Genetics. 32(2). 171–175. 1 indexed citations
8.
Shickh, Salma, Chloe Mighton, Marc Clausen, et al.. (2023). P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review. SHILAP Revista de lepidopterología. 1(1). 100445–100445.
9.
10.
Shickh, Salma, Chloe Mighton, Marc Clausen, et al.. (2022). “Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing. Genetics in Medicine. 24(9). 1888–1898. 2 indexed citations
11.
Novembre, John, Catherine M. Stein, Samira Asgari, et al.. (2022). Addressing the challenges of polygenic scores in human genetic research. The American Journal of Human Genetics. 109(12). 2095–2100. 24 indexed citations
12.
Carroll, June, Leslie E. Oldfield, Chloe Mighton, et al.. (2021). Effect of genetics clinical decision support tools on health-care providers’ decision making: a mixed-methods systematic review. Genetics in Medicine. 23(4). 593–602. 11 indexed citations
13.
Carroll, June, Meredith Vanstone, Marc Clausen, et al.. (2021). Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings. European Journal of Human Genetics. 30(5). 595–603. 7 indexed citations
14.
Mighton, Chloe, Marc Clausen, Salma Shickh, et al.. (2021). Patient and public preferences for being recontacted with updated genomic results: a mixed methods study. Human Genetics. 140(12). 1695–1708. 7 indexed citations
15.
Shickh, Salma, Chloe Mighton, Elizabeth Uleryk, Petros Pechlivanoglou, & Yvonne Bombard. (2021). The clinical utility of exome and genome sequencing across clinical indications: a systematic review. Human Genetics. 140(10). 1403–1416. 54 indexed citations
16.
Mighton, Chloe, Salma Shickh, Elizabeth Uleryk, Petros Pechlivanoglou, & Yvonne Bombard. (2020). Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis. Genetics in Medicine. 23(1). 22–33. 39 indexed citations
17.
Clausen, Marc, Chloe Mighton, Wei Fang Dai, et al.. (2020). Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders’ perspectives. CMAJ Open. 8(4). E772–E778. 7 indexed citations
18.
Lerner‐Ellis, Jordan, Chloe Mighton, Conxi Lázaro, et al.. (2020). Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario. Journal of Cancer Research and Clinical Oncology. 147(3). 871–879. 12 indexed citations
19.
Mighton, Chloe, Lindsay Carlsson, Marc Clausen, et al.. (2020). Quality of life drives patients’ preferences for secondary findings from genomic sequencing. European Journal of Human Genetics. 28(9). 1178–1186. 17 indexed citations
20.
Mighton, Chloe, Marc Clausen, Selina Casalino, et al.. (2019). Primary care provider perspectives on using genomic sequencing in the care of healthy children. European Journal of Human Genetics. 28(5). 551–557. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Salma Shickh Breakdown of academic impact, for papers by Vigdís Stefánsdóttir Breakdown of academic impact, for papers by Elana Levinson Breakdown of academic impact, for papers by Miranda L. G. Hallquist Breakdown of academic impact, for papers by Lindsay Z. Feuerman Breakdown of academic impact, for papers by Patrick Reineke Breakdown of academic impact, for papers by Marian J. Gilmore Breakdown of academic impact, for papers by Gabrielle Bertier Breakdown of academic impact, for papers by Parichoy Pal Choudhury Breakdown of academic impact, for papers by Quinn Stein
Rankless by CCL
2026