Christopher K. Edlund

5.8k total citations
17 papers, 482 citations indexed

About

Christopher K. Edlund is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Christopher K. Edlund has authored 17 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Christopher K. Edlund's work include Genetic Associations and Epidemiology (5 papers), Genetic factors in colorectal cancer (5 papers) and Genomics and Rare Diseases (3 papers). Christopher K. Edlund is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genetic factors in colorectal cancer (5 papers) and Genomics and Rare Diseases (3 papers). Christopher K. Edlund collaborates with scholars based in United States, Australia and Canada. Christopher K. Edlund's co-authors include David V. Conti, Andrew W. Bergen, James W. Baurley, David Van Den Berg, Neal L. Benowitz, Gary E. Swan, Harold S. Javitz, Ruth E. Krasnow, Dalin Li and Maria P. Intermaggio and has published in prestigious journals such as PLoS ONE, Cancer Research and The Lancet Oncology.

In The Last Decade

Christopher K. Edlund

17 papers receiving 477 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher K. Edlund United States 14 227 174 89 89 70 17 482
В. Н. Максимов Russia 10 145 0.6× 71 0.4× 58 0.7× 42 0.5× 58 0.8× 158 461
Adri N. Mul Netherlands 12 362 1.6× 99 0.6× 98 1.1× 35 0.4× 27 0.4× 16 563
Theresa Swift‐Scanlan United States 14 493 2.2× 124 0.7× 112 1.3× 49 0.6× 32 0.5× 32 693
Valerie Pestinger United Kingdom 10 211 0.9× 73 0.4× 59 0.7× 23 0.3× 55 0.8× 13 578
Robert C. Elston United States 11 191 0.8× 554 3.2× 42 0.5× 57 0.6× 63 0.9× 15 781
Mireia Vilardell Spain 12 243 1.1× 170 1.0× 65 0.7× 30 0.3× 56 0.8× 27 553
Xiangwei Li China 13 169 0.7× 209 1.2× 45 0.5× 57 0.6× 17 0.2× 31 508
James E. Browning United States 13 237 1.0× 36 0.2× 64 0.7× 61 0.7× 34 0.5× 22 492
Dor Mohammad Kordi-Tamandani Iran 17 481 2.1× 147 0.8× 120 1.3× 49 0.6× 30 0.4× 63 895
Lydia Choi United States 10 146 0.6× 36 0.2× 132 1.5× 53 0.6× 43 0.6× 21 430

Countries citing papers authored by Christopher K. Edlund

Since Specialization
Citations

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

Fields of papers citing papers by Christopher K. Edlund

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher K. Edlund

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

All Works

17 of 17 papers shown
1.
Matejcic, Marco, Melanie Quintana, Fredrick R. Schumacher, et al.. (2021). Rare Variants in the DNA Repair Pathway and the Risk of Colorectal Cancer. Cancer Epidemiology Biomarkers & Prevention. 30(5). 895–903. 4 indexed citations
2.
Edlund, Christopher K., et al.. (2019). Impacts of Climate Change and Anthropogenic Activity on Permafrost Soils at Eielson Air Force Base, Alaska. Journal of Cold Regions Engineering. 33(3). 3 indexed citations
3.
Salomon, Matthew P., Christopher K. Edlund, John L. Morrison, et al.. (2016). GWASeq: targeted re-sequencing follow up to GWAS. BMC Genomics. 17(1). 176–176. 17 indexed citations
4.
Baurley, James W., et al.. (2016). Smokescreen: a targeted genotyping array for addiction research. BMC Genomics. 17(1). 145–145. 74 indexed citations
5.
Baurley, James W., Christopher K. Edlund, David V. Conti, et al.. (2016). Genome-Wide Association of the Laboratory-Based Nicotine Metabolite Ratio in Three Ancestries. Nicotine & Tobacco Research. 18(9). 1837–1844. 31 indexed citations
6.
Bergen, Andrew W., Harold S. Javitz, Ruth E. Krasnow, et al.. (2014). Organic Cation Transporter Variation and Response to Smoking Cessation Therapies. Nicotine & Tobacco Research. 16(12). 1638–1646. 16 indexed citations
7.
Schmit, Stephanie L., Fredrick R. Schumacher, Christopher K. Edlund, et al.. (2014). A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study. Carcinogenesis. 35(11). 2512–2519. 17 indexed citations
8.
Fortini, Barbara K., Sarah J. Plummer, Christopher K. Edlund, et al.. (2014). Multiple Functional Risk Variants in a SMAD7 Enhancer Implicate a Colorectal Cancer Risk Haplotype. PLoS ONE. 9(11). e111914–e111914. 27 indexed citations
9.
Corral, Román, Juan Pablo Lewinger, David Van Den Berg, et al.. (2014). Comprehensive analyses of DNA repair pathways, smoking and bladder cancer risk in Los Angeles and Shanghai. International Journal of Cancer. 135(2). 335–347. 20 indexed citations
10.
Figueiredo, Jane C., James W. Baurley, Pedro A. Sanchez‐Lara, et al.. (2014). Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians. American Journal of Medical Genetics Part A. 164(10). 2572–2580. 24 indexed citations
11.
Biancolella, Michela, Barbara K. Fortini, Sarah J. Plummer, et al.. (2013). Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1. Human Molecular Genetics. 23(8). 2198–2209. 31 indexed citations
12.
Widschwendter, Martin, Adam N. Rosenthal, Sue Philpott, et al.. (2013). The sex hormone system in carriers of BRCA1/2 mutations: a case-control study. The Lancet Oncology. 14(12). 1226–1232. 84 indexed citations
13.
Bergen, Andrew W., Harold S. Javitz, Ruth E. Krasnow, et al.. (2012). Nicotinic acetylcholine receptor variation and response to smoking cessation therapies. Pharmacogenetics and Genomics. 23(2). 94–103. 61 indexed citations
14.
Levine, A. Joan, Won Lee, Jane C. Figueiredo, et al.. (2012). Genetic variation in insulin pathway genes and distal colorectal adenoma risk. International Journal of Colorectal Disease. 27(12). 1587–1595. 5 indexed citations
15.
Leng, Shuguang, Christine A. Stidley, Yushi Liu, et al.. (2011). Genetic Determinants for Promoter Hypermethylation in the Lungs of Smokers: A Candidate Gene-Based Study. Cancer Research. 72(3). 707–715. 21 indexed citations
16.
Levine, A. Joan, Jane C. Figueiredo, David V. Conti, et al.. (2011). Variation in folate pathway genes and distal colorectal adenoma risk: a sigmoidoscopy-based case–control study. Cancer Causes & Control. 22(4). 541–552. 14 indexed citations
17.
Edlund, Christopher K., et al.. (2008). Snagger: A user-friendly program for incorporating additional information for tagSNP selection. BMC Bioinformatics. 9(1). 174–174. 33 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by В. Н. Максимов Breakdown of academic impact, for papers by Adri N. Mul Breakdown of academic impact, for papers by Theresa Swift‐Scanlan Breakdown of academic impact, for papers by Valerie Pestinger Breakdown of academic impact, for papers by Robert C. Elston Breakdown of academic impact, for papers by Mireia Vilardell Breakdown of academic impact, for papers by Xiangwei Li Breakdown of academic impact, for papers by James E. Browning Breakdown of academic impact, for papers by Dor Mohammad Kordi-Tamandani Breakdown of academic impact, for papers by Lydia Choi
Rankless by CCL
2026