Ingrid Simonic
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 14
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 3
- Congenital Ear and Nasal Anomalies 2
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- Congenital heart defects research 3
- Co-authors
- George S. Gericke (7 shared papers)Jürg Ott (3 shared papers)James L. Weber (2 shared papers)Lionel Willatt (4 shared papers)Derek Gordon (2 shared papers)Kristin M. Abbott (2 shared papers)John C. Whittaker (1 shared paper)C. Lees (1 shared paper)
- Journals
- Human Genetics (2 papers)The American Journal of Human Genetics (1 paper)BJOG An International Journal of Obstetrics & Gynaecology (1 paper)Genomics (1 paper)Annals of Neurology (1 paper)
- Partner nations
- United KingdomSouth AfricaUnited States
In The Last Decade
Ingrid Simonic
23 papers receiving 750 citations
Peers
Comparison fields: 5 of 76
- Genetics 308
- Cancer Research 105
- Pediatrics, Perinatology and Child Health 114
- Virology 23
- Clinical Psychology 102
Countries citing papers authored by Ingrid Simonic
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
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.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 214 | |
| 2 | 2009 | 111 | |
| 3 | 1998 | 61 | |
| 4 | 2001 | 60 | |
| 5 | 2013 | 56 | |
| 6 | 2012 | 44 | |
| 7 | 2000 | 42 | |
| 8 | 2018 | 37 | |
| 9 | 1996 | 34 | |
| 10 | 2006 | 27 | |
| 11 | 2010 | 26 | |
| 12 | 2012 | 20 | |
| 13 | 1995 | 16 | |
| 14 | 2018 | 16 | |
| 15 | 1997 | 16 | |
| 16 | 2020 | 13 | |
| 17 | 1996 | 11 | |
| 18 | 2017 | 5 | |
| 19 | 2013 | 5 | |
| 20 | 1996 | 4 |
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 823 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Autism Spectrum Disorder Research (5 papers), Obsessive-Compulsive Spectrum Disorders (4 papers), Congenital heart defects research (3 papers), Genomics and Rare Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Genetics (308 citations), Cancer Research (105 citations), Pediatrics, Perinatology and Child Health (114 citations), Virology (23 citations) and Clinical Psychology (102 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, Lionel Willatt, Derek Gordon, Kristin M. Abbott, John C. Whittaker, C. Lees, Stian Knappskog and Manasa Ramakrishna. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, BJOG An International Journal of Obstetrics & Gynaecology, Genomics and Annals of Neurology.
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.