Faye R. Harris

953 total citations
27 papers, 601 citations indexed

About

Faye R. Harris is a scholar working on Cancer Research, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Faye R. Harris has authored 27 papers receiving a total of 601 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cancer Research, 10 papers in Molecular Biology and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Faye R. Harris's work include Cancer Genomics and Diagnostics (16 papers), Genetic factors in colorectal cancer (5 papers) and Lung Cancer Treatments and Mutations (5 papers). Faye R. Harris is often cited by papers focused on Cancer Genomics and Diagnostics (16 papers), Genetic factors in colorectal cancer (5 papers) and Lung Cancer Treatments and Mutations (5 papers). Faye R. Harris collaborates with scholars based in United States, United Kingdom and Australia. Faye R. Harris's co-authors include George Vasmatzis, Stephen J. Murphy, Sarah H. Johnson, Geoffrey C. Halling, James B. Smadbeck, Dennis A. Wigle, Benjamin R. Kipp, Farhad Kosari, Marie-Christine Aubry and Eunhee S. Yi and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer Research.

In The Last Decade

Faye R. Harris

26 papers receiving 595 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Faye R. Harris United States	12	240	219	199	172	85	27	601
Osarenoma Olomu United States	6	183 0.8×	74 0.3×	257 1.3×	152 0.9×	51 0.6×	17	663
Eva Pros Spain	14	160 0.7×	84 0.4×	372 1.9×	159 0.9×	49 0.6×	19	619
Ilaria Alborelli Switzerland	13	167 0.7×	258 1.2×	309 1.6×	198 1.2×	34 0.4×	30	634
Domenico Trombetta Italy	12	209 0.9×	247 1.1×	358 1.8×	266 1.5×	75 0.9×	36	731
Sivasish Sindiri United States	13	154 0.6×	120 0.5×	230 1.2×	276 1.6×	32 0.4×	23	661
Gowtham Jayakumaran United States	11	275 1.1×	246 1.1×	562 2.8×	237 1.4×	65 0.8×	16	918
Alissa Minkovsky United States	6	112 0.5×	114 0.5×	258 1.3×	123 0.7×	128 1.5×	7	542
G. Danglot France	9	71 0.3×	167 0.8×	319 1.6×	102 0.6×	73 0.9×	12	577
David Eaves United States	8	166 0.7×	35 0.2×	191 1.0×	94 0.5×	55 0.6×	9	539
Jeff W. Martin Canada	6	185 0.8×	252 1.2×	388 1.9×	149 0.9×	51 0.6×	6	573

Countries citing papers authored by Faye R. Harris

Since Specialization

Citations

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

Fields of papers citing papers by Faye R. Harris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Faye R. Harris. 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 Faye R. Harris. The network helps show where Faye R. Harris may publish in the future.

Co-authorship network of co-authors of Faye R. Harris

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

All Works

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20 of 20 papers shown

Parikh, Kaushal, Faye R. Harris, Jay Mandrekar, et al.. (2024). Individualized Cell-Free DNA Monitoring With Chromosomal Junctions for Mesothelioma. JTO Clinical and Research Reports. 5(12). 100692–100692. 1 indexed citations

Barrett, Michael T., Faye R. Harris, Ryan W. Feathers, et al.. (2021). Combination targeted treatment may enhance antitumor activity in ERBB3 amplified high-grade serous endometrial cancer cells resistant to single agent targeted therapy. Gynecologic Oncology. 162. S114–S115.

Murphy, Stephen J., Faye R. Harris, James B. Smadbeck, et al.. (2020). Optimizing clinical cytology touch preparations for next generation sequencing. Genomics. 112(6). 5313–5323. 6 indexed citations

Murphy, Stephen J., James B. Smadbeck, Bruce W. Eckloff, et al.. (2020). Chromosomal Junction Detection from Whole-Genome Sequencing on Formalin-Fixed, Paraffin-Embedded Tumors. Journal of Molecular Diagnostics. 23(4). 375–388. 2 indexed citations

Vasmatzis, George, Farhad Kosari, Stephen J. Murphy, et al.. (2019). Large Chromosomal Rearrangements Yield Biomarkers to Distinguish Low-Risk From Intermediate- and High-Risk Prostate Cancer. Mayo Clinic Proceedings. 94(1). 27–36. 7 indexed citations

Murphy, Stephen J., Faye R. Harris, Farhad Kosari, et al.. (2019). Using Genomics to Differentiate Multiple Primaries From Metastatic Lung Cancer. Journal of Thoracic Oncology. 14(9). 1567–1582. 58 indexed citations

Vasmatzis, George, Minetta C. Liu, Ryan W. Feathers, et al.. (2019). Integration of Comprehensive Genomic Analysis and Functional Screening of Affected Molecular Pathways to Inform Cancer Therapy. Mayo Clinic Proceedings. 95(2). 306–318. 8 indexed citations

Bryce, Alan H., Jan B. Egan, James B. Smadbeck, et al.. (2019). Shared and unique genomic structural variants of different histological components within testicular germ cell tumours identified with mate pair sequencing. Scientific Reports. 9(1). 3586–3586. 5 indexed citations

Harris, Faye R., Lin Yang, Xiaonan Hou, et al.. (2018). Targeting HER2 in patient‐derived xenograft ovarian cancer models sensitizes tumors to chemotherapy. Molecular Oncology. 13(2). 132–152. 31 indexed citations

10.

Johnson, Sarah H., James B. Smadbeck, Stephanie A. Smoley, et al.. (2017). SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq). Cancer Genetics. 221. 1–18. 61 indexed citations

11.

Mansfield, Aaron S., Stephen J. Murphy, Faye R. Harris, et al.. (2016). Chromoplectic TPM3–ALK rearrangement in a patient with inflammatory myofibroblastic tumor who responded to ceritinib after progression on crizotinib. Annals of Oncology. 27(11). 2111–2117. 56 indexed citations

12.

Harris, Faye R., Irina V. Kovtun, Francesco Multinu, et al.. (2016). Abstract 440: Quantification of somatic chromosomal rearrangements in circulating cell-free DNA from ovarian cancers. Cancer Research. 76(14_Supplement). 440–440. 1 indexed citations

13.

Harris, Faye R., Irina V. Kovtun, Francesco Multinu, et al.. (2016). Quantification of Somatic Chromosomal Rearrangements in Circulating Cell-Free DNA from Ovarian Cancers. Scientific Reports. 6(1). 29831–29831. 47 indexed citations

14.

Murphy, Stephen J., Steven N. Hart, Geoffrey C. Halling, et al.. (2015). Integrated Genomic Analysis of Pancreatic Ductal Adenocarcinomas Reveals Genomic Rearrangement Events as Significant Drivers of Disease. Cancer Research. 76(3). 749–761. 25 indexed citations

15.

Murphy, Stephen J., R. Jeffrey Karnes, Farhad Kosari, et al.. (2015). Integrated analysis of the genomic instability of PTEN in clinically insignificant and significant prostate cancer. Modern Pathology. 29(2). 143–156. 32 indexed citations

16.

Budworth, Helen, Faye R. Harris, Paul D. Williams, et al.. (2015). Suppression of Somatic Expansion Delays the Onset of Pathophysiology in a Mouse Model of Huntington’s Disease. PLoS Genetics. 11(8). e1005267–e1005267. 66 indexed citations

17.

Aubry, Marie-Christine, Anja C. Roden, Stephen J. Murphy, et al.. (2014). Chromosomal rearrangements and copy number abnormalities of TP63 correlate with p63 protein expression in lung adenocarcinoma. Modern Pathology. 28(3). 359–366. 11 indexed citations

18.

Howard, P. J., Ian Lewis, Faye R. Harris, & Sally A. Walker. (1985). Centromeric instability of chromosomes 1 and 16 with variable immune deficiency: a new syndrome. Clinical Genetics. 27(5). 501–505. 26 indexed citations

19.

Owen, Leah A., Barbara A. Martin, C. E. Blank, & Faye R. Harris. (1974). Multiple congenital defects associated with trisomy for the short arm of chromosome 4. Journal of Medical Genetics. 11(3). 291–295. 14 indexed citations

20.

Dubowitz, Victor, et al.. (1971). Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases.. Journal of Medical Genetics. 8(2). 195–201. 5 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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