D.L. Browne

1.8k citations

31 papers · 1.3k indexed · 1 hit paper · h-index 16

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Molecular Biology top 10%
- Ion channel regulation and function
- Mitochondrial Function and Pathology
- Viral Infectious Diseases and Gene Expression in Insects
- Insect Resistance and Genetics

Papers in ⓘ

Molecular Biology 21
- RNA and protein synthesis mechanisms 6
- DNA Repair Mechanisms 5
- RNA modifications and cancer 5
- Ion channel regulation and function 3
- Cancer-related gene regulation 3
- DNA and Nucleic Acid Chemistry 3
- Insect Resistance and Genetics 3
Cellular and Molecular Neuroscience 8
- Genetic Neurodegenerative Diseases 6

Co-authors: M. Litt (16 shared papers)E. R. Brunt (5 shared papers)John G. Nutt (4 shared papers)Eric A. Smith (4 shared papers)Stephen T. Gancher (3 shared papers)Patricia Kramer (1 shared paper)Lois K. Miller (3 shared papers)J. Zonana (5 shared papers)
Journals: Human Molecular Genetics (7 papers)Nucleic Acids Research (6 papers)Gene (2 papers)Journal of Virology (2 papers)Nature Genetics (1 paper)
Partner nations: United States South Africa United Kingdom

In The Last Decade

D.L. Browne

29 papers receiving 1.3k citations

Hit Papers

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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 1994 · 561 citations

Peers

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-authors

The 25 scholars most cited alongside D.L. Browne, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with D.L. Browne Line = papers co-authored together D.L. Browne links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 Nature Genetics ·D.L. Browne, Stephen T. Gancher, John G. Nutt, E. R. Brunt, Eric A. Smith, Patricia Kramer, M. Litt Hit paper breakdown →	1994	561
2	Investigation of the organization of mammalian chromosomes at the DNA sequence level. PubMed ·Winston Salser, S. L. Bowen, D.L. Browne, F el-Adli, Nina V. Fedoroff, Fry K, Howard C. Heindell, G V Paddock, Raymond Poon, B Wallace, Philip Whitcome	1976	104
3	Identification of two new KCNA1 mutations in episodic ataxia/myokymia families Human Molecular Genetics ·D.L. Browne, E. R. Brunt, Robert C. Griggs, John G. Nutt, Stephen T. Gancher, Eric A. Smith, M. Litt	1995	74
4	A gene for episodic ataxia/myokymia maps to chromosome 12p13. PubMed ·M. Litt, P. L. Kramer, D.L. Browne, S. Gancher, E. R. Brunt, David E. Root, T. Phromchotikul, Christopher Dubay, John G. Nutt	1994	69
5	Nongenomic vasodilator action of progesterone on primate coronary arteries Journal of Applied Physiology ·Richard D. Minshall, Dušan Pavčnik, D.L. Browne, Kent Hermsmeyer	2002	57
6	Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide. Journal of Neurology Neurosurgery & Psychiatry ·W J Lubbers, E. R. Brunt, Hans Scheffer, M. Litt, Rein P. Stulp, D.L. Browne, Tiemen W. van Weerden	1995	54
7	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 ·Megumi Adachi, D.L. Browne, Elaine J. Lewis	2000	46
8	Baculovirus induction of a DNA polymerase Journal of Virology ·Lois K. Miller, Jean E. Jewell, D.L. Browne	1981	43
9	A temperature-sensitive mutant of the baculovirus Autographa californica Nuclear polyhedrosis virus defective in an early function required for further gene expression Virology ·Lois K. Miller, Ruth E. Trimarchi, D.L. Browne, Gregory D. Pennock	1983	41
10	Characterization of (CA)_nmicrosatellites with degenerate sequencing primers Nucleic Acids Research ·D.L. Browne, M. Litt	1992	31
11	High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus. PubMed ·J. Zonana, Melanie A. Jones, D.L. Browne, M. Litt, P. L. Kramer, Heiko Becker, Neil Brockdorff, Sohaila Rastan, K P Davies, Angus Clarke	1992	27
12	Protein Kinase Activity Associated with the Extracellular and Occluded Forms of the Baculovirus Autographa californica Nuclear Polyhedrosis Virus Journal of Virology ·Lois K. Miller, Michael J. Adang, D.L. Browne	1983	24
13	Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. PubMed ·J. Zonana, Judith Gault, K. J. P. Davies, Melanie A. Jones, D.L. Browne, M. Litt, Neil Brockdorff, Sohaila Rastan, Angus Clarke, N S Thomas	1993	22
14	Dinucleotide repeat polymorphism at the DXYS1X locus Nucleic Acids Research ·D.L. Browne, J. Zonana, M. Litt	1991	20
15	Chicken chromosomal protein HMG-14 and HMG-17 cDNA clones: isolation, characterization and sequence comparison Gene ·Jerry B. Dodgson, D.L. Browne, Andrew J. Black	1988	18
16	Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci Human Molecular Genetics ·D.L. Browne, David Barker, M. Litt	1992	16
17	Dinucleotide repeat polymorphism at the D11S527 locus Nucleic Acids Research ·D.L. Browne, Judith Gault, Monica Thompson, X.Y. Hauge, Gerald A. Evans, M. Litt	1991	15
18	Tetranucleotide repeat polymorphism at the D11S488 locus Human Molecular Genetics ·D.L. Browne, Michael W. Gen, Glen A. Evans, Stephen P. Clark, M. Litt	1993	14
19	Dinucleotide repeat polymorphism at the DXS538 locus Nucleic Acids Research ·D.L. Browne, J.A. Luty, M. Litt	1991	13
20	Microsatellite polymorphisms at the D11S554 and D11S569 loci Human Molecular Genetics ·T. Phromchotikul, D.L. Browne, M. Litt	1992	13

About D.L. Browne

D.L. Browne is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Plant Science and Neurology, having authored 31 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), RNA and protein synthesis mechanisms (6 papers), DNA Repair Mechanisms (5 papers), RNA modifications and cancer (5 papers), Ion channel regulation and function (3 papers), Cancer-related gene regulation (3 papers), DNA and Nucleic Acid Chemistry (3 papers) and Insect Resistance and Genetics (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (575 citations), Molecular Biology (977 citations), Neurology (200 citations), Cardiology and Cardiovascular Medicine (261 citations) and Genetics (250 citations). D.L. Browne has collaborated with scholars based in United States, South Africa and United Kingdom. Frequent co-authors include M. Litt, E. R. Brunt, John G. Nutt, Eric A. Smith, Stephen T. Gancher, Patricia Kramer, Lois K. Miller, J. Zonana, Elaine J. Lewis and Megumi Adachi. Their work appears in journals such as Human Molecular Genetics, Nucleic Acids Research, Gene, Journal of Virology and Nature 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.

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