Frances Flinter
Impact in
- Immunology and Allergy top 0.2%
- Cell Adhesion Molecules Research
- Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Chronic Lymphocytic Leukemia Research
- Genetic Syndromes and Imprinting
Papers in
- Genetics 42
- Connective tissue disorders research 14
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 7
- Coagulation, Bradykinin, Polyphosphates, and Angioedema 6
-
- Cell Adhesion Molecules Research 36
- Co-authors
- Philip L. Beales (3 shared papers)Adrian S. Woolf (5 shared papers)Martin Bobrow (13 shared papers)Nursel Elçioğlu (1 shared paper)D. S. Parker (1 shared paper)David Vetrie (9 shared papers)Angela Davies (5 shared papers)Caroline Mackie Ogilvie (11 shared papers)
- Journals
- Journal of Medical Genetics (13 papers)Pediatric Nephrology (9 papers)European Journal of Human Genetics (6 papers)Genomics (5 papers)Human Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Frances Flinter
91 papers receiving 5.0k citations
Frances Flinter's Hit Papers
Peers
Comparison fields: 5 of 118
- Immunology and Allergy 1.1k
- Genetics 834
- Genetics 2.1k
- Nephrology 420
- Hematology 603
Countries citing papers authored by Frances Flinter
This map shows the geographic impact of Frances 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 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 Flinter more than expected).
Fields of papers citing papers by Frances Flinter
This network shows the impact of papers produced by Frances 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 Flinter. The network helps show where Frances Flinter may publish in the future.
Co-authors
The 25 scholars most cited alongside Frances 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 95 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 | 1204 |
| 2 | New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey Hit paper breakdown → | 1999 | 692 |
| 3 | 2013 | 235 | |
| 4 | 2004 | 207 | |
| 5 | 1997 | 172 | |
| 6 | 2002 | 169 | |
| 7 | 2015 | 112 | |
| 8 | 2000 | 112 | |
| 9 | 2013 | 112 | |
| 10 | 1999 | 91 | |
| 11 | 2016 | 89 | |
| 12 | 2018 | 89 | |
| 13 | 2002 | 84 | |
| 14 | 2017 | 84 | |
| 15 | 1995 | 80 | |
| 16 | 2016 | 66 | |
| 17 | 2003 | 64 | |
| 18 | 2013 | 59 | |
| 19 | 2014 | 58 | |
| 20 | 1989 | 57 |
About Frances Flinter
Frances Flinter is a scholar working on Genetics, Immunology and Allergy, Molecular Biology, Pediatrics, Perinatology and Child Health and Hematology, having authored 95 papers that have together received 5.3k indexed citations. Recurring topics across this work include Cell Adhesion Molecules Research (36 papers), Renal and related cancers (14 papers), Connective tissue disorders research (14 papers), Platelet Disorders and Treatments (13 papers), Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (6 papers). The work is most often cited by research in Immunology and Allergy (1.1k citations), Genetics (834 citations), Genetics (2.1k citations), Nephrology (420 citations) and Hematology (603 citations). Frances 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, Nursel Elçioğlu, D. S. Parker, David Vetrie, Angela Davies, Caroline Mackie Ogilvie, Paschalis Sideras and Christine Kinnon. Their work appears in journals such as Journal of Medical Genetics, Pediatric Nephrology, European Journal of Human Genetics, Genomics and 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.