Felicity Collins
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 11
- Genetic and Kidney Cyst Diseases 3
- Genomics and Rare Diseases 3
- Connective tissue disorders research 2
- Genetic Syndromes and Imprinting 2
- Genetics and Neurodevelopmental Disorders 2
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- ATP Synthase and ATPases Research 2
- Co-authors
- David R. Thorburn (2 shared papers)Carolyn Ellaway (2 shared papers)Artur Darmanian (3 shared papers)Denise M. Kirby (1 shared paper)Joanne Dixon (1 shared paper)Michael T. Ryan (1 shared paper)Janice M. Fletcher (1 shared paper)Douglass M. Turnbull (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)Molecular Genetics and Metabolism (1 paper)The Journal of Experimental Medicine (1 paper)PEDIATRICS (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Felicity Collins
22 papers receiving 712 citations
Peers
Comparison fields: 5 of 70
- Clinical Biochemistry 140
- Genetics 326
- Rheumatology 127
- Nephrology 52
- Pediatrics, Perinatology and Child Health 133
Countries citing papers authored by Felicity Collins
This map shows the geographic impact of Felicity Collins'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 Felicity Collins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Felicity Collins more than expected).
Fields of papers citing papers by Felicity Collins
This network shows the impact of papers produced by Felicity Collins. 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 Felicity Collins. The network helps show where Felicity Collins may publish in the future.
Co-authors
The 25 scholars most cited alongside Felicity Collins, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 145 | |
| 2 | 2008 | 116 | |
| 3 | 2009 | 53 | |
| 4 | 2005 | 51 | |
| 5 | 2012 | 44 | |
| 6 | An amino acid substitution in the pyruvate dehydrogenase E1 alpha gene, affecting mitochondrial import of the precursor protein. | 1995 | 36 |
| 7 | 2013 | 35 | |
| 8 | 2010 | 34 | |
| 9 | 2007 | 34 | |
| 10 | 2013 | 33 | |
| 11 | 2003 | 32 | |
| 12 | 2017 | 30 | |
| 13 | 2022 | 27 | |
| 14 | 2015 | 23 | |
| 15 | 2020 | 19 | |
| 16 | 2014 | 15 | |
| 17 | 2020 | 14 | |
| 18 | 2000 | 6 | |
| 19 | 1990 | 5 | |
| 20 | 2012 | 4 |
About Felicity Collins
Felicity Collins is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Urology and Pulmonary and Respiratory Medicine, having authored 22 papers that have together received 760 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers), Urological Disorders and Treatments (3 papers), Genomics and Rare Diseases (3 papers), Connective tissue disorders research (2 papers), ATP Synthase and ATPases Research (2 papers), Genetic Syndromes and Imprinting (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Clinical Biochemistry (140 citations), Genetics (326 citations), Rheumatology (127 citations), Nephrology (52 citations) and Pediatrics, Perinatology and Child Health (133 citations). Felicity Collins has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include David R. Thorburn, Carolyn Ellaway, Artur Darmanian, Denise M. Kirby, Joanne Dixon, Michael T. Ryan, Janice M. Fletcher, Douglass M. Turnbull, Robert McFarland and Akira Ohtake. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Molecular Genetics and Metabolism, The Journal of Experimental Medicine and PEDIATRICS.
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.