D.L. Browne

1.8k total citations · 1 hit paper
31 papers, 1.3k citations indexed

About

D.L. Browne is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, D.L. Browne has authored 31 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in D.L. Browne's work include Genetic Neurodegenerative Diseases (6 papers), RNA and protein synthesis mechanisms (6 papers) and DNA Repair Mechanisms (5 papers). D.L. Browne is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), RNA and protein synthesis mechanisms (6 papers) and DNA Repair Mechanisms (5 papers). D.L. Browne collaborates with scholars based in United States, South Africa and United Kingdom. D.L. Browne's co-authors include M. Litt, E. R. Brunt, John G. Nutt, Eric A. Smith, Stephen T. Gancher, Patricia Kramer, Lois K. Miller, J. Zonana, Megumi Adachi and Elaine J. Lewis and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Virology.

In The Last Decade

D.L. Browne

29 papers receiving 1.3k citations

Hit Papers

Episodic ataxia/myokymia syndrome is associated with poin... 1994 2026 2004 2015 1994 100 200 300 400 500
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.

  1. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
    1994 561 citations D.L. Browne, Stephen T. Gancher et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D.L. Browne United States 16 977 575 261 250 200 31 1.3k
J. Michael Andresen United States 17 1.2k 1.2× 552 1.0× 55 0.2× 170 0.7× 164 0.8× 21 1.6k
R. E. Madrid United States 16 414 0.4× 605 1.1× 52 0.2× 109 0.4× 268 1.3× 38 1.2k
Kenzo Hamano Japan 11 720 0.7× 261 0.5× 71 0.3× 141 0.6× 30 0.1× 23 1.0k
Patrick W. Dunne United States 11 1.4k 1.4× 1.3k 2.2× 183 0.7× 247 1.0× 450 2.3× 20 1.7k
Gabriele Dekomien Germany 21 586 0.6× 186 0.3× 96 0.4× 301 1.2× 119 0.6× 65 1.1k
Allyson Cole-Strauss United States 20 920 0.9× 319 0.6× 17 0.1× 280 1.1× 346 1.7× 32 1.5k
Stanka Romac Serbia 17 522 0.5× 375 0.7× 29 0.1× 157 0.6× 279 1.4× 73 842
Margaret J. Kovach United States 14 895 0.9× 308 0.5× 32 0.1× 188 0.8× 720 3.6× 17 1.8k
Heather Kulaga United States 14 655 0.7× 172 0.3× 70 0.3× 355 1.4× 50 0.3× 19 1.3k
Hideji Hashida Japan 19 672 0.7× 520 0.9× 42 0.2× 81 0.3× 434 2.2× 49 1.2k

Countries citing papers authored by D.L. Browne

Since Specialization
Citations

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

Fields of papers citing papers by D.L. Browne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D.L. Browne. 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 D.L. Browne. The network helps show where D.L. Browne may publish in the future.

Co-authorship network of co-authors of D.L. Browne

This figure shows the co-authorship network connecting the top 25 collaborators of D.L. Browne. A scholar is included among the top collaborators of D.L. Browne 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 D.L. Browne. D.L. Browne 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.
Adachi, Megumi, D.L. Browne, & Elaine J. Lewis. (2000). Paired-Like Homeodomain Proteins Phox2a/Arix and Phox2b/NBPhox Have Similar Genetic Organization and Independently Regulate Dopamine β-Hydroxylase Gene Transcription. DNA and Cell Biology. 19(9). 539–554. 46 indexed citations
2.
Browne, D.L., et al.. (1995). Dinucleotide repeat polymorphism at the human chromosome 11p telomere (D11S2071). Genomics. 25(2). 600–601. 6 indexed citations
3.
Browne, D.L., E. R. Brunt, Robert C. Griggs, et al.. (1995). Identification of two new KCNA1 mutations in episodic ataxia/myokymia families. Human Molecular Genetics. 4(9). 1671–1672. 74 indexed citations
4.
Aerssens, Jeroen, Changhong Guo, Joris Vermeesch, et al.. (1995). A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13). Cytogenetic and Genome Research. 71(3). 268–275. 7 indexed citations
5.
Litt, M., et al.. (1994). EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE KCNA1 (KV1.1). The Journal of General Physiology. 104(6). 3 indexed citations
6.
Browne, D.L., Stephen T. Gancher, & John G. Nutt. (1994). Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene-KCNA1 (Kv1.1). The American Journal of Human Genetics. 55.
7.
Browne, D.L., Stephen T. Gancher, John G. Nutt, et al.. (1994). Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genetics. 8(2). 136–140. 561 indexed citations breakdown →
8.
Browne, D.L., Veronica van Heyningen, Wendy A. Bickmore, & M. Litt. (1993). Dinucleotide repeat polymorphism at the D11S995 locus. Human Molecular Genetics. 2(8). 1332–1332.
9.
Browne, D.L., et al.. (1993). Tetranucleotide repeat polymorphism at the D11S488 locus. Human Molecular Genetics. 2(1). 89–89. 14 indexed citations
10.
Browne, D.L., Kenneth D. McMilin, & M. Litt. (1993). Dinucleotide repeat polymorphism at the DXS1111 locus. Human Molecular Genetics. 2(5). 611–611. 3 indexed citations
11.
Browne, D.L., et al.. (1993). Dinucleotide repeat polymorphism at the KCNA5 locus. Human Molecular Genetics. 2(9). 1512–1512. 8 indexed citations
12.
Browne, D.L. & Jerry B. Dodgson. (1993). The gene encoding chicken chromosomal protein HMG-14a is transcribed into multiple mRNAs. Gene. 124(2). 199–206. 4 indexed citations
13.
Browne, D.L., J. Zonana, & M. Litt. (1992). Dinucleotide repeat polymorphism at the PGK1P1 locus. Nucleic Acids Research. 20(5). 1169–1169. 12 indexed citations
14.
Browne, D.L., et al.. (1992). Microsatellite polymorphisms at the D11S554 and D11S569 loci. Human Molecular Genetics. 1(3). 214–214. 13 indexed citations
15.
Browne, D.L. & M. Litt. (1992). Characterization of (CA)nmicrosatellites with degenerate sequencing primers. Nucleic Acids Research. 20(1). 141–141. 31 indexed citations
16.
Browne, D.L., David Barker, & M. Litt. (1992). Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci. Human Molecular Genetics. 1(3). 213–213. 16 indexed citations
17.
Browne, D.L., J.A. Luty, & M. Litt. (1991). Dinucleotide repeat polymorphism at the DXS538 locus. Nucleic Acids Research. 19(5). 1161–1161. 13 indexed citations
18.
Browne, D.L., J. Zonana, & M. Litt. (1991). Dinucleotide repeat polymorphism at the PGK1 locus. Nucleic Acids Research. 19(7). 1721–1721. 10 indexed citations
19.
Dodgson, Jerry B., D.L. Browne, & Andrew J. Black. (1988). Chicken chromosomal protein HMG-14 and HMG-17 cDNA clones: isolation, characterization and sequence comparison. Gene. 63(2). 287–295. 18 indexed citations
20.

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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