Deborah Packham

730 total citations
14 papers, 490 citations indexed

About

Deborah Packham is a scholar working on Pathology and Forensic Medicine, Cancer Research and Molecular Biology. According to data from OpenAlex, Deborah Packham has authored 14 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pathology and Forensic Medicine, 8 papers in Cancer Research and 7 papers in Molecular Biology. Recurrent topics in Deborah Packham's work include Genetic factors in colorectal cancer (11 papers), Cancer Genomics and Diagnostics (8 papers) and Colorectal Cancer Screening and Detection (4 papers). Deborah Packham is often cited by papers focused on Genetic factors in colorectal cancer (11 papers), Cancer Genomics and Diagnostics (8 papers) and Colorectal Cancer Screening and Detection (4 papers). Deborah Packham collaborates with scholars based in Australia, United States and Hong Kong. Deborah Packham's co-authors include Robyn L. Ward, Nicholas J. Hawkins, Megan P. Hitchins, Rachel Williams, Luke B. Hesson, Chau‐To Kwok, Mathew A. Sloane, Catherine M. Suter, Andrew Buckle and Graeme Suthers and has published in prestigious journals such as Gastroenterology, Cancer Research and Clinical Cancer Research.

In The Last Decade

Deborah Packham

14 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Deborah Packham Australia	11	288	245	202	195	89	14	490
Joan Shaw United Kingdom	6	275 1.0×	218 0.9×	109 0.5×	178 0.9×	83 0.9×	9	476
Slavomir Dzieciatkowski United States	10	281 1.0×	420 1.7×	188 0.9×	298 1.5×	53 0.6×	12	651
Kelle Steenblock United States	7	347 1.2×	96 0.4×	158 0.8×	221 1.1×	99 1.1×	8	407
Isabella Gazzoli Netherlands	8	235 0.8×	247 1.0×	164 0.8×	162 0.8×	71 0.8×	13	444
Mohammad Daremipouran United States	8	123 0.4×	176 0.7×	114 0.6×	108 0.6×	37 0.4×	16	341
Mario A. Hermsen Netherlands	2	145 0.5×	112 0.5×	105 0.5×	98 0.5×	116 1.3×	2	301
Patrícia Rocha Portugal	12	116 0.4×	179 0.7×	139 0.7×	141 0.7×	121 1.4×	21	369
RA Walker United Kingdom	5	117 0.4×	141 0.6×	204 1.0×	238 1.2×	114 1.3×	6	410
Masaaki Nagatake Japan	7	119 0.4×	438 1.8×	85 0.4×	282 1.4×	94 1.1×	7	560
Corinne Serruya Canada	5	94 0.3×	218 0.9×	172 0.9×	93 0.5×	310 3.5×	6	520

Countries citing papers authored by Deborah Packham

Since Specialization

Citations

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

Fields of papers citing papers by Deborah Packham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deborah Packham

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

All Works

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14 of 14 papers shown

Poulos, Rebecca C., D. S. Perera, Deborah Packham, et al.. (2019). Scarcity of Recurrent Regulatory Driver Mutations in Colorectal Cancer Revealed by Targeted Deep Sequencing. JNCI Cancer Spectrum. 3(2). pkz012–pkz012. 2 indexed citations

Liu, Qing, Julie A.I. Thoms, Andrea C. Nunez, et al.. (2018). Disruption of a −35 kb Enhancer Impairs CTCF Binding and MLH1 Expression in Colorectal Cells. Clinical Cancer Research. 24(18). 4602–4611. 10 indexed citations

Hesson, Luke B., Sameer Srivastava, Deborah Packham, et al.. (2016). Integrated Genetic, Epigenetic, and Transcriptional Profiling Identifies Molecular Pathways in the Development of Laterally Spreading Tumors. Molecular Cancer Research. 14(12). 1217–1228. 15 indexed citations

Liu, Qing, Luke B. Hesson, Andrea C. Nunez, et al.. (2016). Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients. Cancer Genetics. 209(11). 497–500. 7 indexed citations

Hesson, Luke B., Deborah Packham, Chau‐To Kwok, et al.. (2015). Lynch Syndrome Associated with Two MLH1 Promoter Variants and Allelic Imbalance of MLH1 Expression. Human Mutation. 36(6). 622–630. 24 indexed citations

Liu, Qing, Luke B. Hesson, Andrea C. Nunez, et al.. (2015). A cryptic paracentric inversion ofMSH2exons 2–6 causes Lynch syndrome. Carcinogenesis. 37(1). 10–17. 32 indexed citations

Sloane, Mathew A., Andrea C. Nunez, Deborah Packham, et al.. (2015). Mosaic Epigenetic Inheritance as a Cause of Early-Onset Colorectal Cancer. JAMA Oncology. 1(7). 953–953. 22 indexed citations

Hesson, Luke B., et al.. (2012). A reinvestigation of somatic hypermethylation at the PTEN CpG island in cancer cell lines. Biological Procedures Online. 14(1). 5–5. 24 indexed citations

Goel, Ajay, Thuy‐Phuong Nguyen, Hon‐Chiu Eastwood Leung, et al.. (2010). De novo constitutional MLH1 epimutations confer early‐onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one. International Journal of Cancer. 128(4). 869–878. 69 indexed citations

10.

Packham, Deborah, et al.. (2009). Implementation of Novel Pyrosequencing Assays to Screen for Common Mutations of BRAF and KRAS in a Cohort of Sporadic Colorectal Cancers. Diagnostic Molecular Pathology. 18(2). 62–71. 43 indexed citations

11.

Hitchins, Megan P., Andrew Buckle, Chau‐To Kwok, et al.. (2007). Epigenetic Inactivation of a Cluster of Genes Flanking MLH1 in Microsatellite-Unstable Colorectal Cancer. Cancer Research. 67(19). 9107–9116. 56 indexed citations

12.

Hitchins, Megan P., Rachel Williams, Deborah Packham, et al.. (2005). MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer. Gastroenterology. 129(5). 1392–1399. 134 indexed citations

13.

Ward, Robyn L., Jennifer Turner, Rachel Williams, et al.. (2005). Routine testing for mismatch repair deficiency in sporadic colorectal cancer is justified. The Journal of Pathology. 207(4). 377–384. 46 indexed citations

14.

Ward, Robyn L., Deborah Packham, Jayne Murray, et al.. (2000). Phase I clinical trial of the chimeric monoclonal antibody (c30.6) in patients with metastatic colorectal cancer.. PubMed. 6(12). 4674–83. 6 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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