F Murton

685 total citations
12 papers, 551 citations indexed

About

F Murton is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Sociology and Political Science. According to data from OpenAlex, F Murton has authored 12 papers receiving a total of 551 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 2 papers in Sociology and Political Science. Recurrent topics in F Murton's work include BRCA gene mutations in cancer (10 papers), Nutrition, Genetics, and Disease (4 papers) and Prenatal Screening and Diagnostics (2 papers). F Murton is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Nutrition, Genetics, and Disease (4 papers) and Prenatal Screening and Diagnostics (2 papers). F Murton collaborates with scholars based in United Kingdom and Portugal. F Murton's co-authors include Nina Hallowell, Helen Statham, Martin Richards, Josephine Green, Matt Richards, Jonathan Green and MA Richards and has published in prestigious journals such as Journal of Medical Genetics, Patient Education and Counseling and Child Care Health and Development.

In The Last Decade

F Murton

12 papers receiving 526 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F Murton United Kingdom	10	417	204	159	68	66	12	551
Vivienne Schnieden Australia	10	303 0.7×	229 1.1×	118 0.7×	80 1.2×	54 0.8×	20	528
Samuel Lloyd United Kingdom	6	391 0.9×	251 1.2×	152 1.0×	145 2.1×	47 0.7×	8	522
Erna Claes Belgium	9	507 1.2×	207 1.0×	160 1.0×	116 1.7×	38 0.6×	14	635
Lori d’Agincourt-Canning Canada	8	307 0.7×	112 0.5×	117 0.7×	41 0.6×	61 0.9×	15	441
Lindsey Hoskins United States	12	367 0.9×	225 1.1×	113 0.7×	81 1.2×	62 0.9×	17	506
Joanna Dundon United Kingdom	5	295 0.7×	97 0.5×	75 0.5×	60 0.9×	88 1.3×	5	462
Lieve Denayer Belgium	18	592 1.4×	244 1.2×	285 1.8×	117 1.7×	55 0.8×	25	923
Danielle Hanna Canada	7	374 0.9×	119 0.6×	87 0.5×	69 1.0×	26 0.4×	9	435
Alison Fry United Kingdom	14	444 1.1×	193 0.9×	116 0.7×	193 2.8×	128 1.9×	18	752
Robin E. Grubs United States	15	381 0.9×	87 0.4×	169 1.1×	37 0.5×	74 1.1×	26	624

Countries citing papers authored by F Murton

Since Specialization

Citations

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

Fields of papers citing papers by F Murton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Murton

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

All Works

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12 of 12 papers shown

Hallowell, Nina, Helen Statham, & F Murton. (1998). Women's Understanding of Their Risk of Developing Breast/Ovarian Cancer Before and After Genetic Counseling. Journal of Genetic Counseling. 7(4). 345–364. 39 indexed citations

Murton, F, et al.. (1998). Genetic Counseling, Reproductive Behavior and Future Reproductive Intentions of People with Neurofibromatosis Type 1 (NF1). Journal of Genetic Counseling. 7(4). 331–344. 9 indexed citations

Hallowell, Nina & F Murton. (1998). The value of written summaries of genetic consultations. Patient Education and Counseling. 35(1). 27–34. 47 indexed citations

Statham, Helen, et al.. (1997). Genetic counselling for breast and ovarian cancer: Why do women attend?. 8. 179–180. 3 indexed citations

Murton, F, et al.. (1997). Family communication following genetic counselling for breast/ovarian cancer. 8. 178–179. 2 indexed citations

Hallowell, Nina, et al.. (1997). Women's need for information before attending genetic counselling for familial breast or ovarian cancer: a questionnaire, interview, and observational study. BMJ. 314(7076). 281–281. 87 indexed citations

Green, Josephine, Martin Richards, F Murton, Helen Statham, & Nina Hallowell. (1997). Family Communication and Genetic Counseling: The Case of Hereditary Breast and Ovarian Cancer. Journal of Genetic Counseling. 6(1). 45–60. 158 indexed citations

Hallowell, Nina, et al.. (1997). Recall of numerical risk estimates and counsellees' perceptions of the importance of risk information following genetic counselling for breast and ovarian cancer. Psychology Health & Medicine. 2(2). 149–159. 32 indexed citations

Hallowell, Nina, et al.. (1997). “Talking About Chance”: The Presentation of Risk Information During Genetic Counseling for Breast and Ovarian Cancer. Journal of Genetic Counseling. 6(3). 269–286. 69 indexed citations

10.

Murton, F, et al.. (1996). Diagnosis of Duchenne muscular dystrophy: parents’experiences and satisfaction. Child Care Health and Development. 22(2). 113–128. 27 indexed citations

11.

Hallowell, Nina, et al.. (1995). Counseling families with hereditary breast and ovarian cancer: A psychosocial perspective. Journal of Genetic Counseling. 4(3). 219–233. 44 indexed citations

12.

Murton, F, et al.. (1993). Psychosocial issues raised by a familial ovarian cancer register.. Journal of Medical Genetics. 30(7). 575–579. 34 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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