Kevin Iori

766 total citations
8 papers, 579 citations indexed

About

Kevin Iori is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kevin Iori has authored 8 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kevin Iori's work include Genomics and Rare Diseases (3 papers), Ubiquitin and proteasome pathways (3 papers) and Muscle Physiology and Disorders (3 papers). Kevin Iori is often cited by papers focused on Genomics and Rare Diseases (3 papers), Ubiquitin and proteasome pathways (3 papers) and Muscle Physiology and Disorders (3 papers). Kevin Iori collaborates with scholars based in United States. Kevin Iori's co-authors include Stéphane C. Boutet, Thomas A. Rando, Marie‐Hélène Disatnik, Imran S. Haque, Eric A. Evans, Jessica Jacobson, Pasquale Patrizio, J. R. Marshall, William Seltzer and Gabriel A. Lazarin and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Molecular Cell.

In The Last Decade

Kevin Iori

8 papers receiving 568 citations

Peers

Kevin Iori

MB

GENET

PRM

PPCH

CR

Natalia T. Leach United States

François Cartault France

Vanesa López‐González Spain

Jodi D. Hoffman United States

Erik L. Bao United States

Gökhan Yigit Germany

Marie‐Ange Delrue France

Diana M. Iglesias Canada

Jennifer Wright United States

Anthony Raizis New Zealand

Natalia T. Leach United States

Kevin Iori

199 ×0.6

MB

264 ×1.7

GENET

113 ×0.9

PRM

245 ×2.6

PPCH

62 ×0.9

CR

Citations per year, relative to Kevin Iori Kevin Iori (= 1×) peers Natalia T. Leach

Countries citing papers authored by Kevin Iori

Since Specialization

Citations

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

Fields of papers citing papers by Kevin Iori

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kevin Iori

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Hogan, Gregory J., Valentina Vysotskaia, Kyle A. Beauchamp, et al.. (2018). Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification. Clinical Chemistry. 64(7). 1063–1073. 46 indexed citations

2.

Vysotskaia, Valentina, Gregory J. Hogan, Xin Wang, et al.. (2017). Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment. PeerJ. 5. e3046–e3046. 15 indexed citations

3.

Lazarin, Gabriel A., Imran S. Haque, Shivani Nazareth, et al.. (2013). An Empirical Estimate of Carrier Frequencies for 400+ Causal Mendelian Variants. Obstetrical & Gynecological Survey. 68(8). 557–559. 3 indexed citations

4.

Boutet, Stéphane C., Tom H. Cheung, Ling Liu, et al.. (2012). Alternative Polyadenylation Mediates MicroRNA Regulation of Muscle Stem Cell Function. Cell stem cell. 10(3). 327–336. 124 indexed citations

5.

Lazarin, Gabriel A., Imran S. Haque, Shivani Nazareth, et al.. (2012). An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals. Genetics in Medicine. 15(3). 178–186. 188 indexed citations

6.

Andrejka, Laura, et al.. (2011). Animal-specific C-terminal domain links myeloblastosis oncoprotein (Myb) to an ancient repressor complex. Proceedings of the National Academy of Sciences. 108(42). 17438–17443. 17 indexed citations

7.

Boutet, Stéphane C., Stefano Biressi, Kevin Iori, Vanita Natu, & Thomas A. Rando. (2010). Taf1 Regulates Pax3 Protein by Monoubiquitination in Skeletal Muscle Progenitors. Molecular Cell. 40(5). 749–761. 34 indexed citations

8.

Boutet, Stéphane C., et al.. (2007). Regulation of Pax3 by Proteasomal Degradation of Monoubiquitinated Protein in Skeletal Muscle Progenitors. Cell. 130(2). 349–362. 152 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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