Francesco Vallania

3.5k total citations
32 papers, 1.9k citations indexed

About

Francesco Vallania is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Francesco Vallania has authored 32 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Immunology. Recurrent topics in Francesco Vallania's work include Genomics and Rare Diseases (7 papers), Single-cell and spatial transcriptomics (5 papers) and Cancer Genomics and Diagnostics (5 papers). Francesco Vallania is often cited by papers focused on Genomics and Rare Diseases (7 papers), Single-cell and spatial transcriptomics (5 papers) and Cancer Genomics and Diagnostics (5 papers). Francesco Vallania collaborates with scholars based in United States, China and France. Francesco Vallania's co-authors include Purvesh Khatri, Robi D. Mitra, Winston Haynes, Mark M. Davis, Paul J. Utz, Steven Schaffert, Todd E. Druley, Timothy E. Sweeney, Michele Donato and Erika Bongen and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Francesco Vallania

32 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francesco Vallania United States 21 1.0k 428 427 286 244 32 1.9k
Vincenzo Calvanese Spain 23 1.5k 1.4× 260 0.6× 389 0.9× 339 1.2× 247 1.0× 36 2.4k
Matthew F. Starost United States 28 1.3k 1.3× 335 0.8× 392 0.9× 186 0.7× 205 0.8× 97 2.4k
Søren Germer United States 21 1.0k 1.0× 510 1.2× 276 0.6× 423 1.5× 282 1.2× 36 2.4k
Puping Liang China 19 2.0k 2.0× 428 1.0× 355 0.8× 204 0.7× 239 1.0× 38 2.5k
Vincent Ollendorff France 27 1.5k 1.4× 341 0.8× 458 1.1× 303 1.1× 174 0.7× 44 2.4k
Sandro Orrù Italy 23 725 0.7× 310 0.7× 515 1.2× 135 0.5× 127 0.5× 84 1.8k
Kevin S. Smith United States 27 1.8k 1.8× 543 1.3× 415 1.0× 153 0.5× 203 0.8× 61 3.1k
André F. Rendeiro Austria 20 2.3k 2.3× 264 0.6× 696 1.6× 173 0.6× 234 1.0× 32 3.3k
Christelle Borel Switzerland 27 1.6k 1.6× 858 2.0× 353 0.8× 144 0.5× 329 1.3× 50 2.8k
Katherine J. Martin United States 30 1.4k 1.4× 399 0.9× 235 0.6× 130 0.5× 235 1.0× 66 2.7k

Countries citing papers authored by Francesco Vallania

Since Specialization
Citations

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

Fields of papers citing papers by Francesco Vallania

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesco Vallania

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

All Works

20 of 20 papers shown
1.
Vallania, Francesco, Claudia Macaubas, Shu-Chen Hung, et al.. (2021). Multicohort Analysis Identifies Monocyte Gene Signatures to Accurately Monitor Subset-Specific Changes in Human Diseases. Frontiers in Immunology. 12. 659255–659255. 8 indexed citations
2.
Feen, Diederik E. van der, Guido P. L. Bossers, Quint A. J. Hagdorn, et al.. (2020). Cellular senescence impairs the reversibility of pulmonary arterial hypertension. Science Translational Medicine. 12(554). 85 indexed citations
3.
Tomczak, Aurelie, Jonathan Mortensen, Rainer Winnenburg, et al.. (2018). Interpretation of biological experiments changes with evolution of the Gene Ontology and its annotations. Scientific Reports. 8(1). 5115–5115. 98 indexed citations
4.
Vallania, Francesco, Andrew Tam, Shane Lofgren, et al.. (2018). Leveraging heterogeneity across multiple datasets increases cell-mixture deconvolution accuracy and reduces biological and technical biases. Nature Communications. 9(1). 4735–4735. 100 indexed citations
5.
Cheung, Peggie, Francesco Vallania, Mai Dvorak, et al.. (2018). Single-cell epigenetics – Chromatin modification atlas unveiled by mass cytometry. Clinical Immunology. 196. 40–48. 24 indexed citations
6.
Bongen, Erika, Francesco Vallania, Paul J. Utz, & Purvesh Khatri. (2018). KLRD1-expressing natural killer cells predict influenza susceptibility. Genome Medicine. 10(1). 45–45. 42 indexed citations
7.
Chowdhury, Roshni Roy, Francesco Vallania, Qianting Yang, et al.. (2018). A multi-cohort study of the immune factors associated with M. tuberculosis infection outcomes. Nature. 560(7720). 644–648. 156 indexed citations
8.
Gaujoux, Renaud, Elina Starosvetsky, Francesco Vallania, et al.. (2018). Cell-centred meta-analysis reveals baseline predictors of anti-TNFα non-response in biopsy and blood of patients with IBD. Gut. 68(4). 604–614. 141 indexed citations
9.
Jain, Sanjay, Michiel J. Noordam, Masato Hoshi, Francesco Vallania, & Donald F. Conrad. (2014). Validating single-cell genomics for the study of renal development. Kidney International. 86(5). 1049–1055. 2 indexed citations
10.
Spencer, David H., Manoj Tyagi, Francesco Vallania, et al.. (2013). Performance of Common Analysis Methods for Detecting Low-Frequency Single Nucleotide Variants in Targeted Next-Generation Sequence Data. Journal of Molecular Diagnostics. 16(1). 75–88. 84 indexed citations
11.
Cruchaga, Carlos, Sumitra Chakraverty, Kevin H. Mayo, et al.. (2012). Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families. PLoS ONE. 7(2). e31039–e31039. 206 indexed citations
12.
Ramos, Enrique, Sara E. Chasnoff, Andrew Hughes, et al.. (2012). Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing. BMC Genomics. 13(1). 683–683. 18 indexed citations
13.
Cruchaga, Carlos, Sumitra Chakraverty, Kevin H. Mayo, et al.. (2012). Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families. PLoS ONE. 7(5). 30 indexed citations
14.
Vallania, Francesco, et al.. (2012). Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER. Journal of Visualized Experiments. 2 indexed citations
15.
Vallania, Francesco, Enrique Ramos, Sharon Cresci, Robi D. Mitra, & Todd E. Druley. (2012). Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER. Journal of Visualized Experiments. 7 indexed citations
16.
Haller, Gabe, Todd E. Druley, Francesco Vallania, et al.. (2011). Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence. Human Molecular Genetics. 21(3). 647–655. 43 indexed citations
17.
Mogno, Ilaria, Francesco Vallania, Robi D. Mitra, & Barak A. Cohen. (2010). TATA is a modular component of synthetic promoters. Genome Research. 20(10). 1391–1397. 77 indexed citations
18.
Vallania, Francesco, et al.. (2010). High-throughput discovery of rare insertions and deletions in large cohorts. Genome Research. 20(12). 1711–1718. 43 indexed citations
19.
Matkovich, Scot J., Derek J. Van Booven, Anna Hindes, et al.. (2009). Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease. Journal of Clinical Investigation. 120(1). 280–289. 44 indexed citations
20.
Druley, Todd E., Francesco Vallania, Daniel Wegner, et al.. (2009). Quantification of rare allelic variants from pooled genomic DNA. Nature Methods. 6(4). 263–265. 125 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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