Kerry Phillips

1.6k total citations
9 papers, 272 citations indexed

About

Kerry Phillips is a scholar working on Pathology and Forensic Medicine, Genetics and Surgery. According to data from OpenAlex, Kerry Phillips has authored 9 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pathology and Forensic Medicine, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Kerry Phillips's work include Genetic factors in colorectal cancer (4 papers), Acute Myeloid Leukemia Research (3 papers) and Colorectal Cancer Screening and Detection (2 papers). Kerry Phillips is often cited by papers focused on Genetic factors in colorectal cancer (4 papers), Acute Myeloid Leukemia Research (3 papers) and Colorectal Cancer Screening and Detection (2 papers). Kerry Phillips collaborates with scholars based in Australia, United States and Canada. Kerry Phillips's co-authors include Graeme Suthers, Daniel L. Worthley, Noralane M. Lindor, Andrew D. Clouston, Digby J Cullen, Sue Healey, Florian Grimpen, Fátima Carneiro, David G. Huntsman and Xingqiao Wen and has published in prestigious journals such as Blood, Gastroenterology and Gut.

In The Last Decade

Kerry Phillips

9 papers receiving 261 citations

Peers

Kerry Phillips

PFM

SURGE

PRM

ONCOL

GENET

S Whitelaw United Kingdom

Helen More New Zealand

Lauren A. Gamble United States

L. A. A. Brosens Netherlands

Masakazu Maruyama Japan

Federica Domati Italy

Lizhen Zhu China

Satoshi Okada Japan

Seiichi YAMAGATA Japan

Emanuele Urso Italy

S Whitelaw United Kingdom

Kerry Phillips

258 ×1.3

PFM

64 ×0.5

SURGE

41 ×0.4

PRM

182 ×1.9

ONCOL

74 ×1.4

GENET

Citations per year, relative to Kerry Phillips Kerry Phillips (= 1×) peers S Whitelaw

Countries citing papers authored by Kerry Phillips

Since Specialization

Citations

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

Fields of papers citing papers by Kerry Phillips

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kerry Phillips

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

All Works

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9 of 9 papers shown

1.

Venugopal, Parvathy, Lucia Gagliardi, Cecily Forsyth, et al.. (2020). Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss. BMC Medical Genetics. 21(1). 35–35. 2 indexed citations

2.

Hahn, Christopher N, Milena Babic, Peter J Brautigan, et al.. (2019). Australian Familial Haematological Cancer Study - Findings from 15 Years of Aggregated Clinical, Genomic and Transcriptomic Data. Blood. 134(Supplement_1). 1439–1439. 1 indexed citations

3.

Venugopal, Parvathy, Leila Eshraghi, Nur Hezrin Shahrin, et al.. (2019). An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated with Hematological Malignancy Development in DDX41 Mutated Families. Blood. 134(Supplement_1). 2686–2686. 2 indexed citations

4.

Brown, Anna, Milena Babic, Andreas Schreiber, et al.. (2019). Familial Clustering of Hematological Malignancies: Harbingers of Wider Germline Cancer Susceptibility. Blood. 134(Supplement_1). 3794–3794. 1 indexed citations

5.

Phillips, Kerry. (2014). Is the evidence on waterbirth watertight?. British Journal of Midwifery. 22(11). 776–780. 1 indexed citations

6.

Worthley, Daniel L., Kerry Phillips, Kasmintan A. Schrader, et al.. (2011). Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome. Gut. 61(5). 774–779. 171 indexed citations

7.

Madlensky, Lisa, Darshana Daftary, Terrilea Burnett, et al.. (2007). Accuracy of Colorectal Polyp Self-Reports: Findings from the Colon Cancer Family Registry. Cancer Epidemiology Biomarkers & Prevention. 16(9). 1898–1901. 16 indexed citations

8.

Chen, Celia S., Kerry Phillips, Scott Grist, et al.. (2006). Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer. Familial Cancer. 5(4). 397–404. 22 indexed citations

9.

Worthley, Daniel L., Michael D. Walsh, Melissa Barker, et al.. (2005). Familial Mutations in PMS2 Can Cause Autosomal Dominant Hereditary Nonpolyposis Colorectal Cancer. Gastroenterology. 128(5). 1431–1436. 56 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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