Hugues Sicotte

10.7k total citations
39 papers, 1.3k citations indexed

About

Hugues Sicotte is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Hugues Sicotte has authored 39 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Cancer Research and 10 papers in Genetics. Recurrent topics in Hugues Sicotte's work include Cancer Genomics and Diagnostics (8 papers), Prostate Cancer Treatment and Research (7 papers) and Genetic Associations and Epidemiology (6 papers). Hugues Sicotte is often cited by papers focused on Cancer Genomics and Diagnostics (8 papers), Prostate Cancer Treatment and Research (7 papers) and Genetic Associations and Epidemiology (6 papers). Hugues Sicotte collaborates with scholars based in United States, Mexico and Belarus. Hugues Sicotte's co-authors include Donna Maglott, Kim D. Pruitt, Kenneth Katz, Jean‐Pierre Kocher, Yan W. Asmann, Jinfu Nie, Gloria M. Petersen, Daniel R. O’Brien, Krishna R. Kalari and Asha Nair and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Oncology and Bioinformatics.

In The Last Decade

Hugues Sicotte

37 papers receiving 1.3k citations

Peers

Hugues Sicotte

GENET

ONCOL

PRM

Maria Grazia Cerrito Italy

Armand Valsesia Switzerland

Qianchuan He United States

Andreas Buneß Germany

Jian Bai China

Johann M. Kraus Germany

Denis Torre United States

Su Zhang China

Zhenyu Xu China

Charles E. Chapple France

Maria Grazia Cerrito Italy

Hugues Sicotte

526 ×0.7

137 ×0.5

208 ×0.8

GENET

251 ×1.3

ONCOL

116 ×1.0

PRM

Citations per year, relative to Hugues Sicotte Hugues Sicotte (= 1×) peers Maria Grazia Cerrito

Countries citing papers authored by Hugues Sicotte

Since Specialization

Citations

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

Fields of papers citing papers by Hugues Sicotte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hugues Sicotte

This figure shows the co-authorship network connecting the top 25 collaborators of Hugues Sicotte. A scholar is included among the top collaborators of Hugues Sicotte 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 Hugues Sicotte. Hugues Sicotte 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

Sicotte, Hugues, Krishna R. Kalari, Sisi Qin, et al.. (2022). Molecular Profile Changes in Patients with Castrate-Resistant Prostate Cancer Pre- and Post-Abiraterone/Prednisone Treatment. Molecular Cancer Research. 20(12). 1739–1750. 9 indexed citations

Marks, David L., Amanda Koenig, Luciana L. Almada, et al.. (2021). A rare germline CDKN2A variant (47T>G; p16-L16R) predisposes carriers to pancreatic cancer by reducing cell cycle inhibition. Journal of Biological Chemistry. 296. 100634–100634. 3 indexed citations

McElroy, Susan L., Stacey J. Winham, Alfredo B. Cuéllar‐Barboza, et al.. (2018). Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. Translational Psychiatry. 8(1). 40–40. 20 indexed citations

Ruan, Xiaoyang, Hugues Sicotte, Daniel R. O’Brien, et al.. (2017). Early genetic aberrations in patients with sporadic colorectal cancer. Molecular Carcinogenesis. 57(1). 114–124. 21 indexed citations

Armasu, Sebastian M., Bryan M. McCauley, Iftikhar Kullo, et al.. (2017). Identification of unique venous thromboembolism-susceptibility variants in African-Americans. Thrombosis and Haemostasis. 117(4). 758–768. 24 indexed citations

Hart, Steven N., Marissa S. Ellingson, Peter T. Vedell, et al.. (2016). Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer. BMJ Open. 6(4). e010332–e010332. 28 indexed citations

Wang, Liguo, Jinfu Nie, Hugues Sicotte, et al.. (2016). Measure transcript integrity using RNA-seq data. BMC Bioinformatics. 17(1). 58–58. 144 indexed citations

Bielinski, Suzette J., Cecilia Berardi, Paul A. Decker, et al.. (2015). P-selectin and subclinical and clinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA). Atherosclerosis. 240(1). 3–9. 55 indexed citations

Berardi, Cecilia, Nicholas B. Larson, Paul A. Decker, et al.. (2015). Multi-ethnic analysis reveals soluble l-selectin may be post-transcriptionally regulated by 3′UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA). Human Genetics. 134(4). 393–403. 9 indexed citations

10.

Bancks, Michael P., Suzette J. Bielinski, Paul A. Decker, et al.. (2015). Circulating level of hepatocyte growth factor predicts incidence of type 2 diabetes mellitus: The Multi-Ethnic Study of Atherosclerosis (MESA). Metabolism. 65(3). 64–72. 21 indexed citations

11.

Wu, Lang, Kari G. Chaffee, Alexander S. Parker, Hugues Sicotte, & Gloria M. Petersen. (2015). Zinc transporter genes and urological cancers: integrated analysis suggests a role for ZIP11 in bladder cancer. Tumor Biology. 36(10). 7431–7437. 22 indexed citations

12.

Kalari, Krishna R., Asha Nair, Jaysheel Bhavsar, et al.. (2014). MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing. BMC Bioinformatics. 15(1). 224–224. 239 indexed citations

13.

Berardi, Cecilia, Paul A. Decker, Mariza de Andrade, et al.. (2014). Plasma and serum L-selectin and clinical and subclinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA). Translational research. 163(6). 585–592. 11 indexed citations

14.

Smith, Stephen, et al.. (2012). IP-FCM Measures Physiologic Protein-Protein Interactions Modulated by Signal Transduction and Small-Molecule Drug Inhibition. PLoS ONE. 7(9). e45722–e45722. 13 indexed citations

15.

Bielinski, Suzette J., High Seng Chai, Jyotishman Pathak, et al.. (2011). Mayo Genome Consortia: A Genotype-Phenotype Resource for Genome-Wide Association Studies With an Application to the Analysis of Circulating Bilirubin Levels. Mayo Clinic Proceedings. 86(7). 606–614. 45 indexed citations

16.

McWilliams, Robert R., Eric D. Wieben, Kari G. Rabe, et al.. (2010). Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling. European Journal of Human Genetics. 19(4). 472–478. 97 indexed citations

17.

Chai, High-Seng, Hugues Sicotte, Kent R. Bailey, et al.. (2009). GLOSSI: a method to assess the association of genetic loci-sets with complex diseases. BMC Bioinformatics. 10(1). 102–102. 27 indexed citations

18.

Zhang, Mingrui, Wei Zhang, Hugues Sicotte, & Ping Yang. (2009). A new validity measure for a correlation-based fuzzy c-means clustering algorithm. PubMed. 2009. 3865–3868. 21 indexed citations

19.

Wang, Liang, Ann L. Oberg, Yan W. Asmann, et al.. (2009). Genome-Wide Transcriptional Profiling Reveals MicroRNA-Correlated Genes and Biological Processes in Human Lymphoblastoid Cell Lines. PLoS ONE. 4(6). e5878–e5878. 68 indexed citations

20.

Pruitt, Kim D., Kenneth Katz, Hugues Sicotte, & Donna Maglott. (2000). Introducing RefSeq and LocusLink: curated human genome resources at the NCBI. Trends in Genetics. 16(1). 44–47. 188 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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