Federico Santoni

6.6k total citations · 2 hit papers
65 papers, 2.6k citations indexed

About

Federico Santoni is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Federico Santoni has authored 65 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 27 papers in Genetics and 8 papers in Surgery. Recurrent topics in Federico Santoni's work include Genetics and Neurodevelopmental Disorders (9 papers), Congenital heart defects research (7 papers) and Genomics and Chromatin Dynamics (7 papers). Federico Santoni is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Congenital heart defects research (7 papers) and Genomics and Chromatin Dynamics (7 papers). Federico Santoni collaborates with scholars based in Switzerland, Italy and United States. Federico Santoni's co-authors include Jeremy Luban, Stylianos E. Antonarakis, Jessica Guerra, Michel Guipponi, Massimo Pizzato, Emilie Falconnet, Marco Garieri, Anne Vannier, Aurélie Bisiaux and Walther Mothes and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Federico Santoni

62 papers receiving 2.6k citations

Hit Papers

align trajectories

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.

TRIM5 is an innate immune sensor for the retrovirus capsid lattice

2011 513 citations Federico Santoni, Jeremy Luban et al. profile →
HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation

2015 325 citations Stylianos E. Antonarakis, Jeremy Luban et al. profile →

Peers

Federico Santoni

VIROL

GENET

IMMUN

EPIDE

Silvestro G. Conticello Italy

Jeremy Leipzig United States

Patrick Salmon Switzerland

R. Claudio Aguilar United States

Harald Petry Germany

Marcy E. MacDonald United States

Pratyush Kumar Das United States

David L. Ennist United States

Timothy S. Gomez United States

Darja Schmidt Germany

Silvestro G. Conticello Italy

Federico Santoni

2.3k ×1.7

776 ×1.2

VIROL

391 ×0.6

GENET

660 ×1.2

IMMUN

574 ×1.8

EPIDE

Citations per year, relative to Federico Santoni Federico Santoni (= 1×) peers Silvestro G. Conticello

Countries citing papers authored by Federico Santoni

Since Specialization

Citations

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

Fields of papers citing papers by Federico Santoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Federico Santoni

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

Irshad, Saba, Ambrin Fatima, Fernanda A. Correa, et al.. (2024). Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. BMC Genomics. 25(1). 787–787. 1 indexed citations

Rodríguez, David López, et al.. (2024). Fasting induces metabolic switches and spatial redistributions of lipid processing and neuronal interactions in tanycytes. Nature Communications. 15(1). 6604–6604. 6 indexed citations

Meylan, J, et al.. (2022). CoverageMaster: comprehensive CNV detection and visualization from NGS short reads for genetic medicine applications. Briefings in Bioinformatics. 23(2). 9 indexed citations

Porcu, Eleonora, Marie C. Sadler, Kaido Lepik, et al.. (2021). Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome. Nature Communications. 12(1). 5647–5647. 63 indexed citations

Antonarakis, Stylianos E., Aleš Holoubek, J Meylan, et al.. (2021). Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2. Human Molecular Genetics. 31(1). 1–9. 8 indexed citations

Caron, Émilie, et al.. (2021). Ablation of glucokinase-expressing tanycytes impacts energy balance and increases adiposity in mice. Molecular Metabolism. 53. 101311–101311. 21 indexed citations

Verkauskienė, Rasa, Jean‐Louis Blouin, Philippe Klee, et al.. (2020). Systematic Genetic Study of Youth With Diabetes in a Single Country Reveals the Prevalence of Diabetes Subtypes, Novel Candidate Genes, and Response to Precision Therapy. Diabetes. 69(5). 1065–1071. 19 indexed citations

Acierno, James S., Cheng Xu, Georgios Papadakis, et al.. (2020). Pathogenic mosaic variants in congenital hypogonadotropic hypogonadism. Genetics in Medicine. 22(11). 1759–1767. 8 indexed citations

Garieri, Marco, Georgios Stamoulis, Emilie Falconnet, et al.. (2018). Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts. Proceedings of the National Academy of Sciences. 115(51). 13015–13020. 56 indexed citations

10.

Garieri, Marco, Olivier Delaneau, Federico Santoni, et al.. (2017). The effect of genetic variation on promoter usage and enhancer activity. Nature Communications. 8(1). 40 indexed citations

11.

Letourneau, Audrey, Gilda Cobellis, Alexandre Fort, et al.. (2015). HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES Cells. PLoS ONE. 10(5). e0126475–e0126475. 9 indexed citations

12.

Sailani, M. Reza, Federico Santoni, Audrey Letourneau, et al.. (2015). DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins. PLoS ONE. 10(8). e0135555–e0135555. 41 indexed citations

13.

Santoni, Federico, Periklis Makrythanasis, & Stylianos E. Antonarakis. (2015). CATCHing putative causative variants in consanguineous families. BMC Bioinformatics. 16(1). 310–310. 5 indexed citations

14.

Klee, Philippe, et al.. (2015). Gene Variants Associated with Transient Neonatal Diabetes Mellitus in the Very Low Birth Weight Infant. Hormone Research in Paediatrics. 84(4). 283–288. 5 indexed citations

15.

Hibaoui, Youssef, Iwona Grad, Audrey Letourneau, et al.. (2014). Data in brief: Transcriptome analysis of induced pluripotent stem cells from monozygotic twins discordant for trisomy 21. Genomics Data. 2. 226–229. 9 indexed citations

16.

Santoni, Federico, Periklis Makrythanasis, Sergey I. Nikolaev, et al.. (2014). Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster. Genome Research. 24(2). 349–355. 26 indexed citations

17.

Nikolaev, Sergey I., Sotirios K. Sotiriou, Ioannis S. Pateras, et al.. (2012). A Single-Nucleotide Substitution Mutator Phenotype Revealed by Exome Sequencing of Human Colon Adenomas. Cancer Research. 72(23). 6279–6289. 49 indexed citations

18.

Bortolato, Marco, Roberto Frau, Marco Orrù, et al.. (2010). GABAB receptor activation exacerbates spontaneous spike-and-wave discharges in DBA/2J mice. Seizure. 19(4). 226–231. 16 indexed citations

19.

Santoni, Federico, Oliver Hartley, & Jeremy Luban. (2010). Deciphering the Code for Retroviral Integration Target Site Selection. PLoS Computational Biology. 6(11). e1001008–e1001008. 39 indexed citations

20.

Santoni, Federico, Monica Puligheddu, Luigi Barberini, et al.. (2005). Increase in 20–50 Hz (gamma frequencies) power spectrum and synchronization after chronic vagal nerve stimulation. Clinical Neurophysiology. 116(9). 2026–2036. 63 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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