Chris Neff

2.9k total citations
18 papers, 940 citations indexed

About

Chris Neff is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Chris Neff has authored 18 papers receiving a total of 940 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Oncology. Recurrent topics in Chris Neff's work include DNA Repair Mechanisms (9 papers), PARP inhibition in cancer therapy (9 papers) and BRCA gene mutations in cancer (7 papers). Chris Neff is often cited by papers focused on DNA Repair Mechanisms (9 papers), PARP inhibition in cancer therapy (9 papers) and BRCA gene mutations in cancer (7 papers). Chris Neff collaborates with scholars based in United States, Germany and Denmark. Chris Neff's co-authors include Donna Shattuck, Jerry S. Lanchbury, Alexander Gutin, Victor Abkevich, Kirsten M. Timms, Max T. Dufford, Thanh V. Tran, Jennifer Potter, Diana Iliev and Zaina Sangale and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Cancer Research.

In The Last Decade

Chris Neff

18 papers receiving 927 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chris Neff United States	12	546	351	257	160	79	18	940
Syed Hamid Ali United States	11	433 0.8×	279 0.8×	149 0.6×	79 0.5×	65 0.8×	13	859
Florence Cammas France	23	1.4k 2.5×	196 0.6×	337 1.3×	127 0.8×	111 1.4×	35	1.9k
Yuichi Kumaki Japan	10	1.1k 2.1×	117 0.3×	306 1.2×	96 0.6×	49 0.6×	31	1.4k
Peter I. Duncan Switzerland	16	1.5k 2.7×	167 0.5×	197 0.8×	67 0.4×	82 1.0×	19	1.8k
Marita Büscher Germany	11	657 1.2×	123 0.4×	210 0.8×	108 0.7×	397 5.0×	11	1.3k
Dean Clift United Kingdom	17	1.1k 2.1×	175 0.5×	202 0.8×	43 0.3×	97 1.2×	21	1.7k
Nathalie Bédard Canada	25	799 1.5×	170 0.5×	133 0.5×	80 0.5×	446 5.6×	44	1.6k
Samantha Cooper United States	14	515 0.9×	201 0.6×	233 0.9×	152 0.9×	75 0.9×	20	940
Christine S. Cheng United States	12	1.5k 2.8×	123 0.4×	227 0.9×	279 1.7×	54 0.7×	18	1.9k
David Schuermann Switzerland	13	839 1.5×	116 0.3×	109 0.4×	80 0.5×	29 0.4×	15	1.1k

Countries citing papers authored by Chris Neff

Since Specialization

Citations

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

Fields of papers citing papers by Chris Neff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chris Neff

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

All Works

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18 of 18 papers shown

Siedel, Jean, Kari L. Ring, Wei Hu, et al.. (2021). Clinical significance of homologous recombination deficiency score testing in endometrial Cancer. Gynecologic Oncology. 160(3). 777–785. 26 indexed citations

Telli, Melinda L., Charles C. Chu, Sunil Badve, et al.. (2019). Association of Tumor-Infiltrating Lymphocytes with Homologous Recombination Deficiency and BRCA1/2 Status in Patients with Early Triple-Negative Breast Cancer: A Pooled Analysis. Clinical Cancer Research. 26(11). 2704–2710. 23 indexed citations

Telli, Melinda L., Jessica A. Hellyer, William Audeh, et al.. (2017). Homologous recombination deficiency (HRD) status predicts response to standard neoadjuvant chemotherapy in patients with triple-negative or BRCA1/2 mutation-associated breast cancer. Breast Cancer Research and Treatment. 168(3). 625–630. 78 indexed citations

Timms, Kirsten M., Anees B. Chagpar, Vikram B. Wali, et al.. (2016). Intratumor Heterogeneity of Homologous Recombination Deficiency in Primary Breast Cancer. Clinical Cancer Research. 23(5). 1193–1199. 26 indexed citations

Timms, Kirsten M., Jack Cuzick, Chris Neff, et al.. (2016). The molecular landscape of genome instability in prostate cancer (PC). Annals of Oncology. 27. vi35–vi35. 2 indexed citations

Telli, Melinda L., William Audeh, Shikha Bose, et al.. (2015). Abstract P5-06-01: Homologous recombination deficiency (HRD) score predicts response to standard neoadjuvant chemotherapy in patients with triple negative or BRCA1/2 mutation-associated breast cancer. Cancer Research. 75(9_Supplement). P5–6. 1 indexed citations

Richardson, Andrea L., Daniel P. Silver, Zoltán Szállási, et al.. (2015). Abstract P3-06-11: Homologous recombination deficiency (HRD) assay predicts response to cisplatin neoadjuvant chemotherapy in patients with triple negative breast cancer. Cancer Research. 75(9_Supplement). P3–6. 5 indexed citations

Timms, Kirsten M., Victor Abkevich, Elisha Hughes, et al.. (2014). Association of BRCA1/2defects with genomic scores predictive of DNA damage repair deficiency among breast cancer subtypes. Breast Cancer Research. 16(6). 475–475. 273 indexed citations

Yates, Melinda S., Kirsten M. Timms, Molly S. Daniels, et al.. (2014). Next Generation Sequencing of Brca1/2 in High Grade Ovarian Tumors Expands Brca Defects Beyond Germline Mutations. Annals of Oncology. 25. iv308–iv308. 4 indexed citations

10.

Timms, Kirsten M., Victor Abkevich, Chris Neff, et al.. (2013). Abstract 1763: Frequency of homologous recombination repair defects across breast cancer subtypes.. Cancer Research. 73(8_Supplement). 1763–1763. 1 indexed citations

11.

Dyer, Matthew D., Chris Neff, Max T. Dufford, et al.. (2010). The Human-Bacterial Pathogen Protein Interaction Networks of Bacillus anthracis, Francisella tularensis, and Yersinia pestis. PLoS ONE. 5(8). e12089–e12089. 108 indexed citations

12.

Neff, Chris, et al.. (2009). Evidence for epistasis between SLC6A4 and a chromosome 4 gene as risk factors in major depression. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 321–322. 8 indexed citations

13.

Mohamed, Mohamed R., Masmudur M. Rahman, Jerry S. Lanchbury, et al.. (2009). Proteomic screening of variola virus reveals a unique NF-κB inhibitor that is highly conserved among pathogenic orthopoxviruses. Proceedings of the National Academy of Sciences. 106(22). 9045–9050. 57 indexed citations

14.

Werden, Steven J., Jerry S. Lanchbury, Donna Shattuck, et al.. (2009). The Myxoma Virus M-T5 Ankyrin Repeat Host Range Protein Is a Novel Adaptor That Coordinately Links the Cellular Signaling Pathways Mediated by Akt and Skp1 in Virus-Infected Cells. Journal of Virology. 83(23). 12068–12083. 35 indexed citations

15.

Zhang, Leiliang, Nancy Villa, Masmudur M. Rahman, et al.. (2009). Analysis of Vaccinia Virus−Host Protein−Protein Interactions: Validations of Yeast Two-Hybrid Screenings. Journal of Proteome Research. 8(9). 4311–4318. 49 indexed citations

16.

Neff, Chris, Victor Abkevich, Jeremy C.L. Packer, et al.. (2008). Evidence for HTR1A and LHPP as interacting genetic risk factors in major depression. Molecular Psychiatry. 14(6). 621–630. 83 indexed citations

17.

Stone, Steven, Victor Abkevich, Deanna L. Russell, et al.. (2006). TBC1D1 is a candidate for a severe obesity gene and evidence for a gene/gene interaction in obesity predisposition. Human Molecular Genetics. 15(18). 2709–2720. 119 indexed citations

18.

Hunt, Steven C., Victor Abkevich, Charles H. Hensel, et al.. (2001). Linkage of body mass index to chromosome 20 in Utah pedigrees. Human Genetics. 109(3). 279–285. 42 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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