Frances A. Flinter
Impact in
- Nephrology top 0.2%
- Renal Diseases and Glomerulopathies
- Genetics top 0.5%
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Nephrology 60
- Renal Diseases and Glomerulopathies 57
- Genetics 65
- Genomics and Rare Diseases 32
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 8
- Genetic and Kidney Cyst Diseases 7
- Co-authors
- Philip L. Beales (3 shared papers)Adrian S. Woolf (5 shared papers)Martin Bobrow (13 shared papers)David L.P. Vetrie (11 shared papers)Nursel H Elcioglu (1 shared paper)Angela F. Davies (5 shared papers)Caroline Mackie Ogilvie (10 shared papers)Paschalis Sideras (3 shared papers)
- Journals
- Journal of Medical Genetics (22 papers)The American Journal of Human Genetics (11 papers)Pediatric Nephrology (9 papers)Nephrology Dialysis Transplantation (7 papers)European Journal of Human Genetics (7 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Frances A. Flinter
152 papers receiving 10.5k citations
Frances A. Flinter's Hit Papers
Peers
Comparison fields: 5 of 127
- Nephrology 2.6k
- Genetics 3.7k
- Immunology 1k
- Pediatrics, Perinatology and Child Health 664
- Molecular Biology 1.9k
Countries citing papers authored by Frances A. Flinter
This map shows the geographic impact of Frances A. Flinter'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 Frances A. Flinter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frances A. Flinter more than expected).
Fields of papers citing papers by Frances A. Flinter
This network shows the impact of papers produced by Frances A. Flinter. 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 Frances A. Flinter. The network helps show where Frances A. Flinter may publish in the future.
Co-authors
The 25 scholars most cited alongside Frances A. Flinter, 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 157 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases Hit paper breakdown → | 1993 | 1246 |
| 2 | New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey Hit paper breakdown → | 1999 | 739 |
| 3 | 2000 | 447 | |
| 4 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 418 |
| 5 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 417 |
| 6 | 2016 | 382 | |
| 7 | 2003 | 363 | |
| 8 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. Hit paper breakdown → | 2021 | 290 |
| 9 | 2013 | 265 | |
| 10 | 2004 | 218 | |
| 11 | 2017 | 213 | |
| 12 | 2020 | 179 | |
| 13 | 2019 | 178 | |
| 14 | 1997 | 173 | |
| 15 | 2002 | 170 | |
| 16 | 2011 | 136 | |
| 17 | 2014 | 134 | |
| 18 | Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study Hit paper breakdown → | 2022 | 134 |
| 19 | 2013 | 127 | |
| 20 | 2015 | 127 |
About Frances A. Flinter
Frances A. Flinter is a scholar working on Nephrology, Genetics, Pediatrics, Perinatology and Child Health, Immunology and Cellular and Molecular Neuroscience, having authored 157 papers that have together received 10.9k indexed citations. Recurring topics across this work include Renal Diseases and Glomerulopathies (57 papers), Genomics and Rare Diseases (32 papers), Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (10 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic and Kidney Cyst Diseases (7 papers), Immunodeficiency and Autoimmune Disorders (7 papers) and Genetic Neurodegenerative Diseases (4 papers). The work is most often cited by research in Nephrology (2.6k citations), Genetics (3.7k citations), Immunology (1k citations), Pediatrics, Perinatology and Child Health (664 citations) and Molecular Biology (1.9k citations). Frances A. Flinter has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Philip L. Beales, Adrian S. Woolf, Martin Bobrow, David L.P. Vetrie, Nursel H Elcioglu, Angela F. Davies, Caroline Mackie Ogilvie, Paschalis Sideras, Igor Vořechovský and Lennart L G Hammarström. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Pediatric Nephrology, Nephrology Dialysis Transplantation and European Journal of Human Genetics.
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.