Tracey Flint

2.0k total citations
44 papers, 1.4k citations indexed

About

Tracey Flint is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Tracey Flint has authored 44 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 22 papers in Molecular Biology and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Tracey Flint's work include Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (9 papers) and Muscle Physiology and Disorders (8 papers). Tracey Flint is often cited by papers focused on Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (9 papers) and Muscle Physiology and Disorders (8 papers). Tracey Flint collaborates with scholars based in Denmark, United Kingdom and United States. Tracey Flint's co-authors include Ole Mors, H. Ewald, Kay E. Davies, Andreas Speer, K. E. Davies, Torben A. Kruse, S. M. Forrest, Yutaka Nakahori, Mark C. Hirst and Gareth Cross and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Tracey Flint

43 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tracey Flint Denmark 20 900 768 245 188 139 44 1.4k
Leland Allen United States 12 659 0.7× 739 1.0× 95 0.4× 297 1.6× 45 0.3× 13 1.4k
Paolo Alfieri Italy 20 648 0.7× 327 0.4× 187 0.8× 144 0.8× 57 0.4× 69 1.1k
Barbara Weiffenbach United States 24 1.3k 1.4× 314 0.4× 90 0.4× 312 1.7× 237 1.7× 37 1.7k
Harold G. Marks United States 24 840 0.9× 292 0.4× 127 0.5× 685 3.6× 147 1.1× 48 1.6k
Toshiyuki Kumagai Japan 23 852 0.9× 286 0.4× 121 0.5× 345 1.8× 103 0.7× 60 1.5k
Keiko Shimojima Japan 25 1.0k 1.2× 1.2k 1.5× 99 0.4× 190 1.0× 38 0.3× 125 1.9k
Dawna D. Armstrong United States 21 730 0.8× 754 1.0× 510 2.1× 231 1.2× 41 0.3× 33 1.6k
Zohreh Talebizadeh United States 17 973 1.1× 1.0k 1.3× 422 1.7× 75 0.4× 32 0.2× 31 1.7k
Atle Melberg Sweden 25 1.4k 1.5× 239 0.3× 323 1.3× 432 2.3× 181 1.3× 44 2.1k
Ági K. Gedeon Australia 30 2.5k 2.7× 2.0k 2.6× 512 2.1× 404 2.1× 351 2.5× 53 3.5k

Countries citing papers authored by Tracey Flint

Since Specialization
Citations

This map shows the geographic impact of Tracey Flint'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 Tracey Flint with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tracey Flint more than expected).

Fields of papers citing papers by Tracey Flint

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tracey Flint. 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 Tracey Flint. The network helps show where Tracey Flint may publish in the future.

Co-authorship network of co-authors of Tracey Flint

This figure shows the co-authorship network connecting the top 25 collaborators of Tracey Flint. A scholar is included among the top collaborators of Tracey Flint 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 Tracey Flint. Tracey Flint is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Buttenschøn, Henriette N., Tracey Flint, Leslie Foldager, et al.. (2013). An association study of suicide and candidate genes in the serotonergic system. Journal of Affective Disorders. 148(2-3). 291–298. 28 indexed citations
2.
Demontis, Ditte, Mette Nyegaard, Henriette N. Buttenschøn, et al.. (2011). Association of GRIN1 and GRIN2A‐D With schizophrenia and genetic interaction with maternal herpes simplex virus‐2 infection affecting disease risk. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(8). 913–922. 39 indexed citations
3.
Teruel, Beatríz Marcheco, Tracey Flint, Friedrik P. Wikman, et al.. (2006). A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(8). 833–843. 21 indexed citations
4.
Als, Thomas D., Hans A. Dahl, Tracey Flint, et al.. (2003). Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands. Molecular Psychiatry. 9(1). 93–98. 28 indexed citations
5.
Børglum, Anders D., Tracey Flint, Niels Tommerup, et al.. (1996). Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2→q32.32. Cytogenetic and Genome Research. 73(1-2). 99–103. 7 indexed citations
6.
Børglum, Anders D., Tracey Flint, Lise Lotte Hansen, & Thomas Kruse. (1996). Refined localization of the pyruvate dehydrogenase E1α gene (PDHA1) by linkage analysis. Human Genetics. 99(1). 80–82. 5 indexed citations
7.
Ewald, H., Hans Eiberg, Ole Mors, Tracey Flint, & Torben A. Kruse. (1996). Linkage study between manic-depressive illness and chromosome 21. American Journal of Medical Genetics. 67(2). 218–224. 9 indexed citations
8.
Ewald, H., et al.. (1995). A possible locus for manic depressive illness on chromosome 16p13. Psychiatric Genetics. 5(2). 71–82. 41 indexed citations
9.
Ewald, H., Ole Mors, Tracey Flint, et al.. (1995). Linkage analysis between manic‐depressive illness and markers on the long arm of chromosome 11. American Journal of Medical Genetics. 60(5). 386–392. 3 indexed citations
10.
Ewald, H., Ole Mors, Hans Eiberg, Tracey Flint, & Thomas Kruse. (1995). No evidence of linkage between manic depressive illness and the dopa decarboxylase gene or nearby region on chromosome 7p. Psychiatric Genetics. 5(4). 161–170. 3 indexed citations
11.
Madsen, Peder, Hanne H. Rasmussen, Tracey Flint, et al.. (1995). Cloning, Expression, and Chromosome Mapping of Human Galectin-7. Journal of Biological Chemistry. 270(11). 5823–5829. 126 indexed citations
12.
13.
Ewald, H., Ole Mors, Tracey Flint, & Thomas Kruse. (1994). Linkage analysis between manic depressive illness and the region on chromosome 12q involved in Darierʼs disease. Psychiatric Genetics. 4(4). 195–200. 3 indexed citations
14.
Ewald, H., Ole Mors, Tracey Flint, Hans Eiberg, & Torben A. Kruse. (1994). Linkage analysis between manic depressive illness and the dopamine beta-hydroxylase gene. Psychiatric Genetics. 4(3). 177–184. 4 indexed citations
15.
Bell, M.V., Mark C. Hirst, Yutaka Nakahori, et al.. (1991). Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome. Cell. 64(4). 861–866. 287 indexed citations
16.
DeLisi, Lynn E., Timothy J. Crow, Joseph D. Terwilliger, et al.. (1991). No Genetic Linkage Detected for Schizophrenia to Xq27–q28. The British Journal of Psychiatry. 158(5). 630–634. 15 indexed citations
17.
Hirst, Mark C., Yutaka Nakahori, Samantha J.L. Knight, et al.. (1991). Genotype prediction in the fragile X syndrome.. Journal of Medical Genetics. 28(12). 824–829. 34 indexed citations
18.
Thakker, Rajesh V., K.E. Davies, Andrew Read, et al.. (1990). Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics. 8(2). 189–193. 18 indexed citations
19.
Forrest, S. M., Terry Smith, Gareth Cross, et al.. (1988). Molecular Analysis and Diagnosis of Duchenne Muscular Dystrophy. Journal of the Royal College of Physicians of London. 22(2). 65–67.
20.
Forrest, S. M., Gareth Cross, Tracey Flint, et al.. (1988). Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies. Genomics. 2(2). 109–114. 147 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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