Christopher E. Pearson

11.3k citations
110 papers · 7.7k · 2 hit papers · h-index 44

Impact in

    • Genetic Neurodegenerative Diseases
    • DNA Repair Mechanisms
    • Mitochondrial Function and Pathology
    • RNA Research and Splicing
    • RNA and protein synthesis mechanisms
    • DNA and Nucleic Acid Chemistry
    • Genomics and Chromatin Dynamics

Papers in

Christopher E. Pearson

110 papers receiving 7.6k citations

Christopher E. Pearson's Hit Papers

Repeat instability: mechanisms of dynamic mutations 2005 · 690 citations
6900+7+14Years since publication200400600

Peers

Christopher E. Pearson
Comparison fields: 5 of 126
  • Cellular and Molecular Neuroscience 3.7k
  • Molecular Biology 6.2k
  • Genetics 1.7k
  • Neurology 783
  • Genetics 432
Replace Thomas A. Cooper with:
Thomas A. Cooper United States
Maria Teresa Bassi Italy
Włodzimierz J. Krzyżosiak Poland
Laurent Schaeffer France
Shomi S. Bhattacharya United Kingdom
Roland Heilig France
Leeju C. Wu United States
Stephen H. Tsang United States
Harald Jockusch Germany
Jon W. Gordon United States
Christopher E. Pearson relative to Thomas A. Cooper United States Thomas A. Cooper's profile →
Citations per field
00.5×1.5×1.8×
Thomas A. Cooper · 1×
Citations per year

Countries citing papers authored by Christopher E. Pearson

Since Specialization
Citations

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

Fields of papers citing papers by Christopher E. Pearson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Christopher E. Pearson, 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 E. Pearson Line = papers co-authored together Christopher E. Pearson links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 110 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Repeat instability: mechanisms of dynamic mutations
Hit paper breakdown →
2005690
2
Repeat instability : mechanisms of dynamic mutations
Hit paper breakdown →
2005637
3 2010347
4 2003304
5 2013258
6 1996224
7 2013179
8 1998172
9 2002169
10 2013165
11 2000163
12 2015163
13 1996141
14 1997133
15 1998132
16 2002130
17 2012126
18 2010125
19 1998123
20 2005122

About Christopher E. Pearson

Christopher E. Pearson is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Pathology and Forensic Medicine, having authored 110 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (64 papers), DNA Repair Mechanisms (50 papers), Mitochondrial Function and Pathology (31 papers), Genetics and Neurodevelopmental Disorders (19 papers), RNA Research and Splicing (10 papers), Genetic factors in colorectal cancer (8 papers), RNA and protein synthesis mechanisms (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.7k citations), Molecular Biology (6.2k citations), Genetics (1.7k citations), Neurology (783 citations) and Genetics (432 citations). Christopher E. Pearson has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include John D. Cleary, Kerrie Nichol Edamura, Richard R. Sinden, Arturo López Castel, Kaalak Reddy, Bita Zamiri, Robert B. Macgregor, Gagan B. Panigrahi, Maria Zannis‐Hadjopoulos and Yuh‐Hwa Wang. Their work appears in journals such as Journal of Biological Chemistry, PLoS Genetics, Nucleic Acids Research, Human Molecular Genetics and Biochemistry.

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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