Dalyir Pretto

1.0k total citations
19 papers, 771 citations indexed

About

Dalyir Pretto is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Dalyir Pretto has authored 19 papers receiving a total of 771 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Cognitive Neuroscience. Recurrent topics in Dalyir Pretto's work include Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (6 papers) and Tissue Engineering and Regenerative Medicine (3 papers). Dalyir Pretto is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (6 papers) and Tissue Engineering and Regenerative Medicine (3 papers). Dalyir Pretto collaborates with scholars based in United States, Netherlands and Belgium. Dalyir Pretto's co-authors include Flora Tassone, Randi J. Hagerman, Blythe Durbin‐Johnson, Carolyn M. Yrigollen, Walter Chazin, Leszek Kaczmarek, Mary Jacena Leigh, Aleksandra Janusz, Magdalena Dziembowska and Robert F. Berman and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

Dalyir Pretto

19 papers receiving 761 citations

Peers

Dalyir Pretto
Lies‐Anne Severijnen Netherlands
Daniela Orteschi Italy
Matthew Pastore United States
Katrien Storm Belgium
Lars Riff Jensen Germany
Rosangela Artuso Italy
Moritz Meins Germany
A. Moncla France
R. Curtis Rogers United States
Audrey Labalme France
Lies‐Anne Severijnen Netherlands
Dalyir Pretto
Citations per year, relative to Dalyir Pretto Dalyir Pretto (= 1×) peers Lies‐Anne Severijnen

Countries citing papers authored by Dalyir Pretto

Since Specialization
Citations

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

Fields of papers citing papers by Dalyir Pretto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dalyir Pretto

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

All Works

19 of 19 papers shown
1.
Sun, Yaohui, Phung N. Thai, Che‐Wei Chang, et al.. (2023). The sinoatrial node extracellular matrix promotes pacemaker phenotype and protects automaticity in engineered heart tissues from cyclic strain. Cell Reports. 42(12). 113505–113505. 4 indexed citations
2.
Chang, Che‐Wei, Dalyir Pretto, Xiao-Dong Zhang, et al.. (2020). NODAL inhibition promotes differentiation of pacemaker-like cardiomyocytes from human induced pluripotent stem cells. Stem Cell Research. 49. 102043–102043. 27 indexed citations
3.
Sun, Yaohui, Che-Wei Chang, Alexander A. Merleev, et al.. (2019). Human induced pluripotent stem cell line with genetically encoded fluorescent voltage indicator generated via CRISPR for action potential assessment post-cardiogenesis. Stem Cells. 38(1). 90–101. 18 indexed citations
4.
Sweha, Stefan R., Blythe Durbin‐Johnson, Carolyn M. Yrigollen, et al.. (2017). Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome. Brain and Development. 39(6). 483–492. 29 indexed citations
5.
Schneider, Andrea, Louise W. Gane, Bryan K. Woodruff, et al.. (2015). High functioning male with fragile X syndrome and fragile X‐associated tremor/ataxia syndrome. American Journal of Medical Genetics Part A. 167(9). 2154–2161. 22 indexed citations
6.
Ludwig, A. L., Dalyir Pretto, Glòria Arqué, et al.. (2014). CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size. Human Molecular Genetics. 23(12). 3228–3238. 57 indexed citations
7.
Pretto, Dalyir, John Eid, Carolyn M. Yrigollen, et al.. (2014). Differential increases of specific FMR1 mRNA isoforms in premutation carriers. Journal of Medical Genetics. 52(1). 42–52. 27 indexed citations
8.
Pretto, Dalyir, Joyce Lo, Ru Cao, et al.. (2014). CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles. Journal of Medical Genetics. 51(5). 309–318. 66 indexed citations
9.
Berman, Robert F., Ronald A.M. Buijsen, Karen Usdin, et al.. (2014). Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome. Journal of Neurodevelopmental Disorders. 6(1). 25–25. 55 indexed citations
10.
Pretto, Dalyir, Carolyn M. Yrigollen, John B. Williamson, et al.. (2014). Clinical and molecular implications of mosaicism in FMR1 full mutations. Frontiers in Genetics. 5. 318–318. 78 indexed citations
11.
Pretto, Dalyir, et al.. (2014). Screening Newborn Blood Spots for 22q11.2 Deletion Syndrome Using Multiplex Droplet Digital PCR. Clinical Chemistry. 61(1). 182–190. 22 indexed citations
12.
Dziembowska, Magdalena, Dalyir Pretto, Aleksandra Janusz, et al.. (2013). High MMP‐9 activity levels in fragile X syndrome are lowered by minocycline. American Journal of Medical Genetics Part A. 161(8). 1897–1903. 136 indexed citations
13.
Pretto, Dalyir, Michael R. Hunsaker, Christopher L. Cunningham, et al.. (2013). Intranuclear inclusions in a fragile X mosaic male. Translational Neurodegeneration. 2(1). 10–10. 27 indexed citations
14.
15.
Pretto, Dalyir, Susan E. Tsutakawa, Chris A. Brosey, et al.. (2010). Structural Dynamics and Single-Stranded DNA Binding Activity of the Three N-Terminal Domains of the Large Subunit of Replication Protein A from Small Angle X-ray Scattering. Biochemistry. 49(13). 2880–2889. 38 indexed citations
16.
Sowd, Gregory A., Hong Wang, Dalyir Pretto, Walter Chazin, & Patricia L. Opresko. (2009). Replication Protein A Stimulates the Werner Syndrome Protein Branch Migration Activity. Journal of Biological Chemistry. 284(50). 34682–34691. 20 indexed citations
17.
Brosey, Chris A., et al.. (2009). NMR Analysis of the Architecture and Functional Remodeling of a Modular Multidomain Protein, RPA. Journal of the American Chemical Society. 131(18). 6346–6347. 43 indexed citations
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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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