Frances Flinter

13.5k total citations · 2 hit papers
89 papers, 4.9k citations indexed

About

Frances Flinter is a scholar working on Genetics, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Frances Flinter has authored 89 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 32 papers in Molecular Biology and 32 papers in Immunology and Allergy. Recurrent topics in Frances Flinter's work include Cell Adhesion Molecules Research (32 papers), Renal and related cancers (17 papers) and Platelet Disorders and Treatments (16 papers). Frances Flinter is often cited by papers focused on Cell Adhesion Molecules Research (32 papers), Renal and related cancers (17 papers) and Platelet Disorders and Treatments (16 papers). Frances Flinter collaborates with scholars based in United Kingdom, United States and Australia. Frances Flinter's co-authors include Philip L. Beales, Martin Bobrow, Adrian S. Woolf, David Vetrie, D. S. Parker, Nursel Elçioğlu, Angela Davies, Caroline Mackie Ogilvie, Lennart Hammarström and Paschalis Sideras and has published in prestigious journals such as Nature, Blood and Nature Biotechnology.

In The Last Decade

Frances Flinter

86 papers receiving 4.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

1993 1.1k citations David Vetrie, Igor Vořechovský et al. profile →
New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey

1999 628 citations Adrian S. Woolf, Frances Flinter et al. Journal of Medical Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Frances Flinter United Kingdom	34	2.1k	2.1k	1.1k	1.0k	897	89	4.9k
Ruth Gershoni‐Baruch Israel	39	1.7k 0.8×	3.1k 1.5×	436 0.4×	1.0k 1.0×	153 0.2×	145	6.1k
Anna Savoia Italy	38	778 0.4×	1.7k 0.8×	305 0.3×	406 0.4×	533 0.6×	121	4.1k
Toshio Mochizuki Japan	27	2.3k 1.1×	2.2k 1.0×	628 0.6×	87 0.1×	267 0.3×	109	4.1k
Lies H. Hoefsloot Netherlands	45	1.7k 0.8×	3.7k 1.8×	122 0.1×	532 0.5×	1.1k 1.3×	136	6.6k
Jean Michel Foidart Belgium	32	357 0.2×	1.2k 0.6×	523 0.5×	494 0.5×	352 0.4×	70	4.1k
Tero Kivelä Finland	47	430 0.2×	2.5k 1.2×	278 0.3×	823 0.8×	303 0.3×	254	8.0k
Sheila Unger Switzerland	36	2.3k 1.1×	2.2k 1.0×	248 0.2×	264 0.3×	273 0.3×	127	4.3k
John R.W. Yates United Kingdom	33	1.5k 0.7×	2.2k 1.1×	103 0.1×	427 0.4×	162 0.2×	82	5.4k
Mads Thomassen Denmark	33	559 0.3×	1.8k 0.9×	134 0.1×	279 0.3×	663 0.7×	179	3.3k
Jan P. Dumanski Sweden	43	2.0k 0.9×	3.6k 1.8×	130 0.1×	372 0.4×	690 0.8×	146	7.4k

Countries citing papers authored by Frances Flinter

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Frances Flinter

This figure shows the co-authorship network connecting the top 25 collaborators of Frances Flinter. A scholar is included among the top collaborators of Frances Flinter based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Frances Flinter. Frances Flinter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Deltas, Constantinos, Gregory Papagregoriou, Stavroula F. Louka, et al.. (2023). Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice. Genes. 14(9). 1686–1686. 8 indexed citations

Pearce, Caroline, et al.. (2019). Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis. Genetics in Medicine. 21(12). 2846–2846.

Eisler, Ivan, Frances Flinter, Louise Longworth, et al.. (2016). Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi‐Family Discussion Groups. Journal of Genetic Counseling. 26(2). 199–214. 16 indexed citations

Mencarelli, Maria Antonietta, Laurence Heidet, Helen Storey, et al.. (2015). Evidence of digenic inheritance in Alport syndrome. Journal of Medical Genetics. 52(3). 163–174. 107 indexed citations

Lennon, Rachel, Helen M. Stuart, Agnieszka Bierżyńska, et al.. (2015). Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease. Pediatric Nephrology. 30(9). 1459–1465. 33 indexed citations

Cafferkey, M, Joo Wook Ahn, Frances Flinter, & Caroline Mackie Ogilvie. (2014). Phenotypic features in patients with 15q11.2(BP1‐BP2) deletion: Further delineation of an emerging syndrome. American Journal of Medical Genetics Part A. 164(8). 1916–1922. 53 indexed citations

Savige, Judy, Martin C. Gregory, Oliver Groß, et al.. (2013). Expert Guidelines for the Management of Alport Syndrome and Thin Basement Membrane Nephropathy. Journal of the American Society of Nephrology. 24(3). 364–375. 222 indexed citations

Vetrie, David, Igor Vořechovský, Paschalis Sideras, et al.. (2012). Pillars Article: The Gene Involved in X-linked Agammaglobulinaemia Is a Member of the Src Family of Protein-Tyrosine Kinases. Nature. 1993. 361: 226–233. The Journal of Immunology. 188(7). 2948–2955. 2 indexed citations

Hanson, Helen, et al.. (2010). The Value of Clinical Criteria in Identifying Patients with X-Linked Alport Syndrome. Clinical Journal of the American Society of Nephrology. 6(1). 198–203. 31 indexed citations

10.

Kashtan, Clifford E., et al.. (2010). Aortic abnormalities in males with Alport syndrome. Nephrology Dialysis Transplantation. 25(11). 3554–3560. 46 indexed citations

11.

Crew, Vanja Karamatic, Nick Burton, Alexander Kagan, et al.. (2004). CD151, the first member of the tetraspanin (TM4) superfamily detected on erythrocytes, is essential for the correct assembly of human basement membranes in kidney and skin. Blood. 104(8). 2217–2223. 188 indexed citations

12.

Flinter, Frances, Eamonn R. Maher, & A K Saggar-Malik. (2003). The genetics of renal disease. Research Portal (King's College London). 4 indexed citations

13.

Pannett, A. A. J., Ann Kennedy, J Turner, et al.. (2003). Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. Clinical Endocrinology. 58(5). 639–646. 48 indexed citations

14.

McKee, Shane, et al.. (2001). Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome?. Clinical Dysmorphology. 10(3). 177–180. 4 indexed citations

15.

Plant, Kathryn E., Peter M. Green, David Vetrie, & Frances Flinter. (1999). Detection of mutations in COL4A5 in patients with Alport Syndrome. Human Mutation. 13(2). 124–132. 49 indexed citations

16.

Davies, Angela, Mark G. Olavesen, Richard Stephens, et al.. (1996). A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome. Human Genetics. 98(4). 454–459. 30 indexed citations

17.

Flinter, Frances, David Vetrie, & Martin Bobrow. (1993). The Implications of the Cloning of the XLA Gene. Journal of the Royal College of Physicians of London. 27(3). 233–235. 1 indexed citations

18.

Flinter, Frances & Martin Bobrow. (1992). The molecular genetics of Alport syndrome: report of two workshops.. Journal of Medical Genetics. 29(5). 352–353. 8 indexed citations

19.

Vetrie, David, Eileen Boye, Frances Flinter, Martin Bobrow, & Ann Harris. (1992). DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis. Genomics. 14(3). 624–633. 17 indexed citations

20.

Flinter, Frances, Martin Bobrow, & C Chantler. (1987). Alport's syndrome or hereditary nephritis?. Pediatric Nephrology. 1(3). 438–440. 14 indexed citations

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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