Sheila Goff

476 total citations
5 papers, 219 citations indexed

About

Sheila Goff is a scholar working on Genetics, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Sheila Goff has authored 5 papers receiving a total of 219 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Pathology and Forensic Medicine and 2 papers in Oncology. Recurrent topics in Sheila Goff's work include BRCA gene mutations in cancer (3 papers), Genomics and Rare Diseases (2 papers) and Genetic factors in colorectal cancer (2 papers). Sheila Goff is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Genomics and Rare Diseases (2 papers) and Genetic factors in colorectal cancer (2 papers). Sheila Goff collaborates with scholars based in United Kingdom, Qatar and Netherlands. Sheila Goff's co-authors include Hans F. A. Vasen, R Carpenter, Isis Dove‐Edwin, Gemma G. Kenter, Huw Thomas, S V Hodgson, Fergus J. Couch, Sue Healey, Bryony A. Thompson and Sunil R. Lakhani and has published in prestigious journals such as Cancer, Human Mutation and Clinical Genetics.

In The Last Decade

Sheila Goff

5 papers receiving 210 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sheila Goff United Kingdom	5	149	110	73	44	38	5	219
Marieke G. M. Braem Netherlands	4	48 0.3×	55 0.5×	30 0.4×	20 0.5×	27 0.7×	4	135
Bartłomiej Gliniewicz Poland	4	49 0.3×	37 0.3×	94 1.3×	41 0.9×	69 1.8×	9	168
Mónica Salinas Spain	8	51 0.3×	37 0.3×	87 1.2×	41 0.9×	85 2.2×	15	163
Thuy M. Vu United States	5	72 0.5×	46 0.4×	82 1.1×	35 0.8×	22 0.6×	8	138
James G. Dowty Australia	8	33 0.2×	40 0.4×	74 1.0×	48 1.1×	59 1.6×	18	161
Lydia Ioannidou-Mouzaka Greece	5	49 0.3×	26 0.2×	36 0.5×	38 0.9×	31 0.8×	10	126
Yael Laitman Israel	9	39 0.3×	30 0.3×	136 1.9×	72 1.6×	77 2.0×	18	176
Daliah Tsoref Israel	6	25 0.2×	59 0.5×	41 0.6×	33 0.8×	66 1.7×	15	166
Christina Rybak United States	6	66 0.4×	37 0.3×	119 1.6×	34 0.8×	36 0.9×	11	164
Beata Kozak‐Klonowska Poland	5	41 0.3×	48 0.4×	90 1.2×	34 0.8×	42 1.1×	5	153

Countries citing papers authored by Sheila Goff

Since Specialization

Citations

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

Fields of papers citing papers by Sheila Goff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sheila Goff

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

All Works

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5 of 5 papers shown

1.

Walker, Logan C., Phillip J Whiley, Fergus J. Couch, et al.. (2010). Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity. Human Mutation. 31(6). E1484–E1505. 40 indexed citations

2.

Rafi, Imran, Nadeem Qureshi, Anneke Lucassen, et al.. (2009). ‘Over-the-counter’ genetic testing: what does it really mean for primary care?. British Journal of General Practice. 59(561). 283–287. 12 indexed citations

3.

Goff, Sheila, et al.. (2007). Nurse-led cancer genetics clinics in primary and secondary care in varied ethnic population areas: interaction with primary care to improve ascertainment of individuals from ethnic minorities. Familial Cancer. 6(2). 205–212. 6 indexed citations

4.

Sutton, Stephen, et al.. (2004). Anticipated reactions to genetic testing for hereditary non‐polyposis colorectal cancer susceptibility*. Clinical Genetics. 66(5). 437–444. 14 indexed citations

5.

Dove‐Edwin, Isis, Sheila Goff, Gemma G. Kenter, et al.. (2002). The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma. Cancer. 94(6). 1708–1712. 147 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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