Christopher Arnell

2.0k citations
14 papers · 1.4k · 1 hit paper · h-index 7

Impact in

Papers in

    • BRCA gene mutations in cancer 9
    • Nutrition, Genetics, and Disease 4
    • Genomics and Rare Diseases 1
    • Chronic Lymphocytic Leukemia Research 1
    • Genetic factors in colorectal cancer 3

Christopher Arnell

14 papers receiving 1.4k citations

Christopher Arnell's Hit Papers

Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories 2015 · 1.0k citations
1.0k0+3+7Years since publication2505007501000

Peers

Christopher Arnell
Comparison fields: 5 of 55
  • Pathology and Forensic Medicine 759
  • Cancer Research 369
  • Oncology 466
  • Genetics 486
  • Reproductive Medicine 84
Replace Ingrid Marino with:
Ingrid Marino United States
Astrid Stormorken Norway
H. T. Lynch United States
Rachel Pearlman United States
Michelle Landon United States
Tadashi Nomizu Japan
Laura Renkonen‐Sinisalo Finland
Jill S. Dolinsky United States
PM Khan Netherlands
Peggy Conrad United States
Christopher Arnell relative to Ingrid Marino United States Ingrid Marino's profile →
Citations per field
00.5×1.5×2.4×
Ingrid Marino · 1×
Citations per year

Countries citing papers authored by Christopher Arnell

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Arnell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Christopher Arnell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Christopher Arnell Line = papers co-authored together Christopher Arnell links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1
Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories
Hit paper breakdown →
20151045
2 2013152
3 2012105
4 201444
5 201742
6 201411
7 20148
8 20145
9 20214
10 20173
11 20123
12 20132
13 20141
14 20141

About Christopher Arnell

Christopher Arnell is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Molecular Biology and Surgery, having authored 14 papers that have together received 1.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (9 papers), Nutrition, Genetics, and Disease (4 papers), Cancer Genomics and Diagnostics (3 papers), Genetic factors in colorectal cancer (3 papers), Genomics and Rare Diseases (1 paper), Chronic Lymphocytic Leukemia Research (1 paper), DNA Repair Mechanisms (1 paper) and Genetically Modified Organisms Research (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (759 citations), Cancer Research (369 citations), Oncology (466 citations), Genetics (486 citations) and Reproductive Medicine (84 citations). Christopher Arnell has collaborated with scholars based in United States, Switzerland and Germany. Frequent co-authors include Richard Wenstrup, Jennifer Saam, Aaron Theisen, Kelsey Moyes, Ingrid Marino, Kirstin M. Roundy, Eric T. Rosenthal, Lynn Anne Burbidge, Jeffrey T. Trost and Thaddeus Judkins. Their work appears in journals such as Journal of Experimental & Clinical Cancer Research, Oncology, Clinical Genetics, Journal of Clinical Oncology and Journal of Managed Care & Specialty Pharmacy.

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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