Jennifer Webster

4.5k total citations · 1 hit paper
40 papers, 1.4k citations indexed

About

Jennifer Webster is a scholar working on Cancer Research, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jennifer Webster has authored 40 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cancer Research, 9 papers in Oncology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jennifer Webster's work include Cancer Genomics and Diagnostics (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and Colorectal Cancer Treatments and Studies (5 papers). Jennifer Webster is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and Colorectal Cancer Treatments and Studies (5 papers). Jennifer Webster collaborates with scholars based in United States, Australia and Iran. Jennifer Webster's co-authors include Derek R. Lovley, Barbara A. Methé, Kelly P. Nevin, Teena Mehta, Swades K. Chaudhuri, Trevor L. Woodard, Anna Liu, Dawn E. Holmes, Joy E. Ward and Vincent A. Miller and has published in prestigious journals such as Nature Medicine, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

Jennifer Webster

36 papers receiving 1.3k citations

Hit Papers

Molecular profiling of cancer patients enables personaliz... 2019 2026 2021 2023 2019 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Molecular profiling of cancer patients enables personalized combination therapy: the I-PREDICT study
    2019 429 citations Jason K. Sicklick, Shumei Kato et al. Nature Medicine profile →

Peers

Jennifer Webster
Aizhen Zhang China
Michael Walsh United States
Shengyu Yang United States
Linyu Li China
Jingcheng Zhou China
Charles E. Milliken United States
Yuting Yan China
Junlin Li China
Zhuo Wang China
Nancy Lan Guo United States
Aizhen Zhang China
Jennifer Webster
Citations per year, relative to Jennifer Webster Jennifer Webster (= 1×) peers Aizhen Zhang

Countries citing papers authored by Jennifer Webster

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Webster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Webster

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

All Works

20 of 20 papers shown
1.
Kan, Zhengyan, Ji Wen, Vinícius Bonato, et al.. (2025). Real-world clinical multi-omics analyses reveal bifurcation of ER-independent and ER-dependent drug resistance to CDK4/6 inhibitors. Nature Communications. 16(1). 932–932. 3 indexed citations
2.
Webster, Jennifer, et al.. (2024). Using Artificial Intelligence to Support Informed Decision-Making on BRAF Mutation Testing. JCO Precision Oncology. 8(8). e2300685–e2300685. 1 indexed citations
3.
4.
5.
Nyadjro, Ebenezer S., Jennifer Webster, Tim Boyer, et al.. (2023). The NOAA NCEI marine microplastics database. Scientific Data. 10(1). 726–726. 33 indexed citations
6.
Yakirevich, Evgeny, Russell W. Madison, Eddie Fridman, et al.. (2019). Comprehensive Genomic Profiling of Adult Renal Sarcomas Provides Insight into Disease Biology and Opportunities for Targeted Therapies. European Urology Oncology. 4(2). 282–288. 4 indexed citations
7.
Sicklick, Jason K., Shumei Kato, Ryosuke Okamura, et al.. (2019). Molecular profiling of cancer patients enables personalized combination therapy: the I-PREDICT study. Nature Medicine. 25(5). 744–750. 429 indexed citations breakdown →
8.
Aydin, Ebru, et al.. (2019). Real-world data analysis of ovarian cancer (OC) maintenance utilization among maintenance eligible patients.. Journal of Clinical Oncology. 37(15_suppl). 5579–5579. 6 indexed citations
9.
Goddard, Katrina A.B., Evelyn P Whitlock, Jonathan S. Berg, et al.. (2013). Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies. Genetics in Medicine. 15(9). 721–728. 31 indexed citations
10.
Goddard, Katrina A.B., Erin J. Aiello Bowles, Heather Spencer Feigelson, et al.. (2012). Utilization of HER2 genetic testing in a multi-institutional observational study.. PubMed. 18(11). 704–12. 12 indexed citations
11.
Webster, Jennifer. (2012). PS1-20: Hospice Use in Metastatic Colorectal Cancer Patients. Clinical Medicine & Research. 10(3). 149–149. 1 indexed citations
12.
Hildebrand, Michael S., Luke C. Gandolfo, A. Eliot Shearer, et al.. (2010). A novel mutation in COCH—implications for genotype‐phenotype correlations in DFNA9 hearing loss. The Laryngoscope. 120(12). 2489–2493. 17 indexed citations
13.
Grillet, Nicolas, Martin Schwander, Michael S. Hildebrand, et al.. (2009). Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans. The American Journal of Human Genetics. 85(3). 328–337. 110 indexed citations
14.
Shearer, A. Eliot, Michael S. Hildebrand, Catherine Bromhead, et al.. (2009). A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. American Journal of Medical Genetics Part A. 149A(3). 555–558. 15 indexed citations
15.
Shearer, A. Eliot, Michael S. Hildebrand, Jennifer Webster, et al.. (2009). Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss. The Laryngoscope. 119(4). 727–733. 41 indexed citations
16.
Lovley, Derek R., Dawn E. Holmes, Swades K. Chaudhuri, et al.. (2006). Microarray and Genetics Analysis of Electron Transfer Electrodes in Geobacter Sulfurreducens. Environmental Microbiology. 8.
17.
Holmes, Dawn E., Swades K. Chaudhuri, Kelly P. Nevin, et al.. (2006). Microarray and genetic analysis of electron transfer to electrodes in Geobacter sulfurreducens. Environmental Microbiology. 8(10). 1805–1815. 271 indexed citations
18.
Munroe, Patricia B., Chris Wallace, Charles A. Mein, et al.. (2005). Enhanced support for linkage to chromosome 5q13.1 and hypertension in the British Genetics of Hypertension (BRIGHT) study.. Hypertension. 46(4). 892–892. 1 indexed citations
19.
Padmanabhan, Sandosh, Chris Wallace, Patricia B. Munroe, et al.. (2005). Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study.. Hypertension. 46(5). 886–886. 3 indexed citations
20.
Knight, Jo, Patricia B. Munroe, J Pembroke, et al.. (2001). No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study.. The American Journal of Human Genetics. 69. 559–559. 1 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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