Ingrid Simonic

5.0k citations
23 papers · 758 · h-index 14

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Cancer Genomics and Diagnostics

Papers in

    • Genetics and Neurodevelopmental Disorders 8
    • Genomic variations and chromosomal abnormalities 8
    • Genomics and Rare Diseases 2
    • Congenital heart defects research 4

Ingrid Simonic

22 papers receiving 722 citations

Peers

Ingrid Simonic
Comparison fields: 5 of 78
  • Genetics 331
  • Cancer Research 110
  • Pediatrics, Perinatology and Child Health 111
  • Molecular Biology 371
  • Cognitive Neuroscience 98
Replace Kyle Retterer with:
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Bradford Coffee United States
Zhuozhi Wang Canada
Charles H. Hensel United States
Alina T. Midro Poland
Megan T. Cho United States
Davut Pehli̇van United States
Yotam Kaufman Israel
Fabienne Giuliano France
Samantha A. Schrier Vergano United States
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Citations per field
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Citations per year

Countries citing papers authored by Ingrid Simonic

Since Specialization
Citations

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

Fields of papers citing papers by Ingrid Simonic

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ingrid Simonic, 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 Ingrid Simonic Line = papers co-authored together Ingrid Simonic links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2014208
2 200993
3 199857
4 201353
5 200151
6 200042
7 201241
8 201835
9 199633
10 201025
11 201220
12 199716
13 201816
14 199515
15 202013
16 200612
17 199610
18 20175
19 20134
20 19964

About Ingrid Simonic

Ingrid Simonic is a scholar working on Genetics, Molecular Biology, Clinical Psychology, Cognitive Neuroscience and Genetics, having authored 23 papers that have together received 758 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Autism Spectrum Disorder Research (5 papers), Obsessive-Compulsive Spectrum Disorders (4 papers), Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (3 papers), Chromosomal and Genetic Variations (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (331 citations), Cancer Research (110 citations), Pediatrics, Perinatology and Child Health (111 citations), Molecular Biology (371 citations) and Cognitive Neuroscience (98 citations). Ingrid Simonic has collaborated with scholars based in United Kingdom, South Africa and United States. Frequent co-authors include George S. Gericke, Jürg Ott, James L. Weber, Derek Gordon, Lionel Willatt, Kristin M. Abbott, C. Lees, John C. Whittaker, Sancha Martin and Chris Tyler‐Smith. Their work appears in journals such as Human Genetics, Nature Genetics, Gene, European Journal of Human Genetics and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

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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