Paul R. Billings

6.8k total citations
98 papers, 2.1k citations indexed

About

Paul R. Billings is a scholar working on Cancer Research, Oncology and Molecular Biology. According to data from OpenAlex, Paul R. Billings has authored 98 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Cancer Research, 29 papers in Oncology and 25 papers in Molecular Biology. Recurrent topics in Paul R. Billings's work include Cancer Genomics and Diagnostics (33 papers), Renal Transplantation Outcomes and Treatments (13 papers) and Genetic factors in colorectal cancer (11 papers). Paul R. Billings is often cited by papers focused on Cancer Genomics and Diagnostics (33 papers), Renal Transplantation Outcomes and Treatments (13 papers) and Genetic factors in colorectal cancer (11 papers). Paul R. Billings collaborates with scholars based in United States, New Zealand and United Kingdom. Paul R. Billings's co-authors include Joseph S. Alper, Marvin R. Natowicz, Jon Beckwith, Melvin A. Kohn, Margaret de Cuevas, Zachary Demko, Baruj Benacerraf, Jonathan Beckwith, Carol Isaacson Barash and Lisa N. Geller and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature Medicine.

In The Last Decade

Paul R. Billings

89 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paul R. Billings United States	29	532	522	382	357	304	98	2.1k
Kouji Banno Japan	33	230 0.4×	1.2k 2.3×	564 1.5×	934 2.6×	314 1.0×	211	3.5k
Vijayakrishna K. Gadi United States	24	371 0.7×	476 0.9×	572 1.5×	288 0.8×	127 0.4×	87	1.6k
Keyvan Keyvanfar United States	35	521 1.0×	1.3k 2.5×	786 2.1×	413 1.2×	1.6k 5.4×	110	4.1k
Georgia M. Dunston United States	24	715 1.3×	433 0.8×	273 0.7×	177 0.5×	202 0.7×	72	1.8k
Sun Lee United States	29	157 0.3×	467 0.9×	643 1.7×	149 0.4×	208 0.7×	160	3.2k
Tracey O’Brien Australia	27	204 0.4×	522 1.0×	360 0.9×	100 0.3×	295 1.0×	124	1.9k
Kathryn M. Verbanac United States	22	127 0.2×	327 0.6×	346 0.9×	638 1.8×	366 1.2×	42	1.7k
Pablo Rubinstein United States	26	384 0.7×	739 1.4×	608 1.6×	41 0.1×	1.2k 3.8×	86	4.4k
Sebastian Mayer United States	24	86 0.2×	836 1.6×	643 1.7×	281 0.8×	213 0.7×	111	2.0k

Countries citing papers authored by Paul R. Billings

Since Specialization

Citations

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

Fields of papers citing papers by Paul R. Billings

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul R. Billings

This figure shows the co-authorship network connecting the top 25 collaborators of Paul R. Billings. A scholar is included among the top collaborators of Paul R. Billings 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 Paul R. Billings. Paul R. Billings 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

Hinestrosa, Juan Pablo, Rosalie C. Sears, Jean M. Lewis, et al.. (2023). Development of a blood-based extracellular vesicle classifier for detection of early-stage pancreatic ductal adenocarcinoma. SHILAP Revista de lepidopterología. 3(1). 146–146. 13 indexed citations

Kasi, Pashtoon Murtaza, Sakti Chakrabarti, Sarah Sawyer, et al.. (2022). BESPOKE IO protocol: a multicentre, prospective observational study evaluating the utility of ctDNA in guiding immunotherapy in patients with advanced solid tumours. BMJ Open. 12(5). e060342–e060342. 9 indexed citations

Kim, Paul, Michael Olymbios, Omar Wever‐Pinzon, et al.. (2022). A novel donor-derived cell-free DNA assay for the detection of acute rejection in heart transplantation. The Journal of Heart and Lung Transplantation. 41(7). 919–927. 38 indexed citations

Bleyer, Anthony J., Jing Xie, Michelle S. Bloom, et al.. (2022). Genetic Etiologies for Chronic Kidney Disease Revealed through Next-Generation Renal Gene Panel. American Journal of Nephrology. 53(4). 297–306. 28 indexed citations

Kim, Paul, Michael Olymbios, Eric Adler, et al.. (2022). Absolute Quantification of Donor Derived Cell Free DNA in Heart Transplant Patients. The Journal of Heart and Lung Transplantation. 41(4). S116–S116. 1 indexed citations

Taniguchi, Hiroya, Yoshiaki Nakamura, Daisuke Kotani, et al.. (2021). CIRCULATE‐Japan: Circulating tumor DNA–guided adaptive platform trials to refine adjuvant therapy for colorectal cancer. Cancer Science. 112(7). 2915–2920. 92 indexed citations

Kasi, Pashtoon Murtaza, Sarah Sawyer, Michelle L. Munro, et al.. (2021). BESPOKE study protocol: a multicentre, prospective observational study to evaluate the impact of circulating tumour DNA guided therapy on patients with colorectal cancer. BMJ Open. 11(9). e047831–e047831. 33 indexed citations

Dhakal, Binod, Shruti Sharma, Svetlana Shchegrova, et al.. (2021). Personalized, ctDNA analysis to detect minimal residual disease and identify patients at high risk of relapse with multiple myeloma.. Journal of Clinical Oncology. 39(15_suppl). 8029–8029.

Martin, Kimberly, Carole Samango‐Sprouse, Danielle LaGrave, et al.. (2020). Detection of maternal X chromosome abnormalities using single nucleotide polymorphism–based noninvasive prenatal testing. American Journal of Obstetrics & Gynecology MFM. 2(3). 100152–100152. 10 indexed citations

10.

Kasi, Pashtoon Murtaza, Sarah Sawyer, Michelle L. Munro, et al.. (2020). 520TiP A multicenter study to evaluate the impact of circulating tumor DNA guided therapy (BESPOKE) in patients with stage II and III colorectal cancer. Annals of Oncology. 31. S459–S459. 2 indexed citations

11.

Saucier, Jennifer, Sarah A. Prins, Meenakshi Malhotra, et al.. (2020). Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach. Genetics in Medicine. 22(8). 1320–1328. 63 indexed citations

12.

Sigdel, Tara K., T Constantin, Sarah A. Prins, et al.. (2018). Optimizing Detection of Kidney Transplant Injury by Assessment of Donor-Derived Cell-Free DNA via Massively Multiplex PCR. Journal of Clinical Medicine. 8(1). 19–19. 142 indexed citations

13.

Semir, David de, Mehdi Nosrati, Vladimir Bezrookove, et al.. (2012). Pleckstrin homology domain-interacting protein (PHIP) as a marker and mediator of melanoma metastasis. Proceedings of the National Academy of Sciences. 109(18). 7067–7072. 30 indexed citations

14.

Barnes, Helen, et al.. (2009). Circulating Tumor Cells Are Transcriptionally Similar to the Primary Tumor in a Murine Prostate Model. Cancer Research. 69(19). 7860–7866. 45 indexed citations

15.

Billings, Paul R., et al.. (2005). Ready for Genomic Medicine? Perspectives of Health Care Decision Makers. Archives of Internal Medicine. 165(16). 1917–1917. 11 indexed citations

16.

Shibata, Atsuko, David T. Harris, & Paul R. Billings. (2002). Concentrations of Estrogens and IGFs in Umbilical Cord Blood Plasma: A Comparison among Caucasian, Hispanic, and Asian-American Females. The Journal of Clinical Endocrinology & Metabolism. 87(2). 810–815. 33 indexed citations

17.

Billings, Paul R., et al.. (1992). But is he genetically diseased?. PubMed. 22(4). S18–20. 1 indexed citations

18.

Billings, Paul R., Melvin A. Kohn, Margaret de Cuevas, et al.. (1992). Discrimination as a consequence of genetic testing.. PubMed. 50(3). 476–82. 330 indexed citations

19.

Billings, Paul R. & Jon Beckwith. (1992). Genetic testing in the workplace: a view from the USA. Trends in Genetics. 8(6). 198–202. 12 indexed citations

20.

Wilson, Stephen D., Paul R. Billings, Peter D’Eustachio, et al.. (1990). Clustering of cytokine genes on mouse chromosome 11.. The Journal of Experimental Medicine. 171(4). 1301–1314. 54 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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