Peter Broderick

14.9k citations
112 papers · 11.9k · 6 hit papers · h-index 50

Impact in

Papers in

    • Genetic factors in colorectal cancer 38
    • Lymphoma Diagnosis and Treatment 14
    • Genetic Associations and Epidemiology 22
    • Chronic Lymphocytic Leukemia Research 18
    • Genomic variations and chromosomal abnormalities 10

Peter Broderick

112 papers receiving 11.7k citations

Peter Broderick's Hit Papers

Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries 2022 · 146 citations
1460+6+12Years since publication2505007501000

Peers

Peter Broderick
Comparison fields: 5 of 150
  • Pathology and Forensic Medicine 3.6k
  • Cancer Research 2.1k
  • Genetics 3.3k
  • Genetics 948
  • Oncology 2.3k
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Citations per field
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Citations per year

Countries citing papers authored by Peter Broderick

Since Specialization
Citations

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

Fields of papers citing papers by Peter Broderick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 112 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1
Hit paper breakdown →
20081074
2
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Hit paper breakdown →
2012801
3
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
Hit paper breakdown →
2007696
4
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Hit paper breakdown →
2008499
5 2008482
6 2008474
7 2007439
8
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Hit paper breakdown →
2014363
9 2010336
10 2010315
11 2008301
12 2007261
13 2017256
14 2011204
15 2009201
16 2012197
17 2010195
18 2011189
19 2010171
20 2019171

About Peter Broderick

Peter Broderick is a scholar working on Pathology and Forensic Medicine, Genetics, Genetics, Cancer Research and Molecular Biology, having authored 112 papers that have together received 11.9k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (38 papers), Genetic Associations and Epidemiology (22 papers), Chronic Lymphocytic Leukemia Research (18 papers), Lymphoma Diagnosis and Treatment (14 papers), RNA modifications and cancer (12 papers), Genomic variations and chromosomal abnormalities (10 papers), Colorectal Cancer Screening and Detection (9 papers) and Multiple Myeloma Research and Treatments (8 papers). The work is most often cited by research in Pathology and Forensic Medicine (3.6k citations), Cancer Research (2.1k citations), Genetics (3.3k citations), Genetics (948 citations) and Oncology (2.3k citations). Peter Broderick has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Richard S. Houlston, Athena Matakidou, Jayaram Vijayakrishnan, Yufei Wang, Christopher Ian Amos, Margaret R. Spitz, Xifeng Wu, Xiangjun Gu, Qiong Dong and Timothy Eisen. Their work appears in journals such as Nature Genetics, Nature Communications, British Journal of Cancer, Human Molecular Genetics and Blood.

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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