Dalyir Pretto

1.0k citations
19 papers · 784 · h-index 17

Impact in

  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Autism Spectrum Disorder Research

Papers in

    • DNA Repair Mechanisms 2
    • Ubiquitin and proteasome pathways 2
    • Pluripotent Stem Cells Research 2
    • Congenital heart defects research 2
    • Genetics and Neurodevelopmental Disorders 9
    • Genomic variations and chromosomal abnormalities 2

Dalyir Pretto

19 papers receiving 774 citations

Peers

Dalyir Pretto
Comparison fields: 5 of 63
  • Genetics 486
  • Cognitive Neuroscience 254
  • Molecular Biology 477
  • Cellular and Molecular Neuroscience 84
  • Developmental Neuroscience 17
Replace Lies‐Anne Severijnen with:
Lies‐Anne Severijnen Netherlands
Rosangela Artuso Italy
Daniela Orteschi Italy
Showming Kwok United States
A. Moncla France
Zhou Xp China
Jamie M. Aye United States
Kristen M. West United States
Moritz Meins Germany
Dalyir Pretto relative to Lies‐Anne Severijnen Netherlands Lies‐Anne Severijnen's profile →
Citations per field
00.5×1.5×2.5×
Lies‐Anne Severijnen · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Dalyir Pretto, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dalyir Pretto Line = papers co-authored together Dalyir Pretto links everyone, so they are left out of the graph.

All Works

19 of 19 papers shown
#Work
1 2013136
2 201479
3 201467
4 200660
5 201457
6 201456
7 200943
8 201038
9 202031
10 201730
11 201328
12 201427
13 201326
14 201422
15 201522
16 200921
17 201919
18 200216
19 20236

About Dalyir Pretto

Dalyir Pretto is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Surgery and Cell Biology, having authored 19 papers that have together received 784 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (4 papers), DNA Repair Mechanisms (2 papers), Ubiquitin and proteasome pathways (2 papers), Pluripotent Stem Cells Research (2 papers), Endoplasmic Reticulum Stress and Disease (2 papers), Congenital heart defects research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (486 citations), Cognitive Neuroscience (254 citations), Molecular Biology (477 citations), Cellular and Molecular Neuroscience (84 citations) and Developmental Neuroscience (17 citations). Dalyir Pretto has collaborated with scholars based in United States, Netherlands and Belgium. Frequent co-authors include Flora Tassone, Randi J. Hagerman, Blythe Durbin‐Johnson, Carolyn M. Yrigollen, Walter Chazin, Magdalena Dziembowska, Leszek Kaczmarek, Mary Jacena Leigh, Aleksandra Janusz and Paul J. Hagerman. Their work appears in journals such as Journal of Medical Genetics, Cell Reports, Clinical Chemistry, Neurobiology of Aging and Biochemistry.

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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