Nicholas Sciascia

794 total citations
7 papers, 508 citations indexed

About

Nicholas Sciascia is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Nicholas Sciascia has authored 7 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Nicholas Sciascia's work include Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (3 papers) and CRISPR and Genetic Engineering (2 papers). Nicholas Sciascia is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (3 papers) and CRISPR and Genetic Engineering (2 papers). Nicholas Sciascia collaborates with scholars based in United States and Japan. Nicholas Sciascia's co-authors include André Nussenzweig, Anthony Tubbs, Paul S. Meltzer, Sriram Sridharan, Andrés Canela, Barry P. Sleckman, Sigal Shachar, Ty C. Voss, Gianluca Pegoraro and Tom Misteli and has published in prestigious journals such as Cell, Nature Communications and Molecular Cell.

In The Last Decade

Nicholas Sciascia

7 papers receiving 505 citations

Peers

Nicholas Sciascia
Advaitha Madireddy United States
Mary Gardiner United Kingdom
Petko Fiziev United States
Qiye He China
Lucas T. Gray United States
David Dickerson United States
Heejeong Yoon South Korea
Hien G. Hoang United States
Advaitha Madireddy United States
Nicholas Sciascia
Citations per year, relative to Nicholas Sciascia Nicholas Sciascia (= 1×) peers Advaitha Madireddy

Countries citing papers authored by Nicholas Sciascia

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas Sciascia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicholas Sciascia

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

All Works

7 of 7 papers shown
1.
Paiano, Jacob, Wei Wu, Shintaro Yamada, et al.. (2020). ATM and PRDM9 regulate SPO11-bound recombination intermediates during meiosis. Nature Communications. 11(1). 857–857. 80 indexed citations
2.
Kumari, Daman, Nicholas Sciascia, & Karen Usdin. (2020). Small Molecules Targeting H3K9 Methylation Prevent Silencing of Reactivated FMR1 Alleles in Fragile X Syndrome Patient Derived Cells. Genes. 11(4). 356–356. 19 indexed citations
3.
Sciascia, Nicholas, Wei Wu, Dali Zong, et al.. (2020). Suppressing proteasome mediated processing of topoisomerase II DNA-protein complexes preserves genome integrity. eLife. 9. 32 indexed citations
4.
Zhou, Yifan, Daman Kumari, Nicholas Sciascia, & Karen Usdin. (2016). CGG-repeat dynamics and FMR1 gene silencing in fragile X syndrome stem cells and stem cell-derived neurons. Molecular Autism. 7(1). 42–42. 36 indexed citations
5.
Canela, Andrés, Sriram Sridharan, Nicholas Sciascia, et al.. (2016). DNA Breaks and End Resection Measured Genome-wide by End Sequencing. Molecular Cell. 63(5). 898–911. 194 indexed citations
6.
Shachar, Sigal, Ty C. Voss, Gianluca Pegoraro, Nicholas Sciascia, & Tom Misteli. (2015). Identification of Gene Positioning Factors Using High-Throughput Imaging Mapping. Cell. 162(4). 911–923. 119 indexed citations
7.
Usdin, Karen, Bruce E. Hayward, Daman Kumari, et al.. (2014). Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders. Frontiers in Genetics. 5. 226–226. 28 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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