Edward D. Bird

15.1k total citations · 3 hit papers
117 papers, 11.8k citations indexed

About

Edward D. Bird is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Edward D. Bird has authored 117 papers receiving a total of 11.8k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Cellular and Molecular Neuroscience, 50 papers in Molecular Biology and 33 papers in Neurology. Recurrent topics in Edward D. Bird's work include Genetic Neurodegenerative Diseases (47 papers), Neuroscience and Neuropharmacology Research (28 papers) and Neurological disorders and treatments (25 papers). Edward D. Bird is often cited by papers focused on Genetic Neurodegenerative Diseases (47 papers), Neuroscience and Neuropharmacology Research (28 papers) and Neurological disorders and treatments (25 papers). Edward D. Bird collaborates with scholars based in United States, United Kingdom and Canada. Edward D. Bird's co-authors include Edward P. Richardson, Richard H. Myers, Robert J. Ferrante, Thomas J. Stevens, Jean‐Paul Vonsattel, Joseph B. Martin, L L Iversen, M. Flint Beal, Leslie L. Iversen and M. Flint Beal and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Edward D. Bird

117 papers receiving 11.4k citations

Hit Papers

Neuropathological Classif... 1974 2026 1991 2008 1985 1997 1974 500 1000 1.5k 2.0k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Edward D. Bird 7.3k 5.4k 3.4k 2.0k 1.2k 117 11.8k
PierFranco Spano 7.0k 1.0× 5.7k 1.0× 2.5k 0.7× 2.4k 1.2× 1.1k 0.9× 386 14.7k
B. Scatton 10.4k 1.4× 6.0k 1.1× 2.6k 0.7× 2.2k 1.1× 1.7k 1.4× 290 16.5k
Giuseppe Battaglia 7.8k 1.1× 4.9k 0.9× 1.9k 0.5× 1.8k 0.9× 807 0.7× 325 13.3k
Stephen J. Kish 9.5k 1.3× 5.6k 1.0× 6.3k 1.8× 2.2k 1.1× 1.5k 1.3× 284 17.9k
C. Anthony Altar 7.8k 1.1× 3.6k 0.7× 1.2k 0.4× 1.2k 0.6× 1.7k 1.5× 116 12.5k
B. Costall 8.5k 1.2× 5.2k 1.0× 1.4k 0.4× 1.5k 0.7× 1.3k 1.1× 307 13.3k
Maurizio Raiteri 8.7k 1.2× 6.1k 1.1× 844 0.2× 1.2k 0.6× 685 0.6× 273 11.3k
Norman G. Bowery 9.0k 1.2× 5.6k 1.0× 1.1k 0.3× 2.6k 1.3× 1.0k 0.9× 179 12.0k
Ian Creese 10.7k 1.5× 7.8k 1.4× 1.5k 0.4× 1.3k 0.6× 2.2k 1.9× 158 14.7k
Sami S. Zoghbi 6.1k 0.8× 3.6k 0.7× 2.5k 0.7× 1.4k 0.7× 2.3k 2.0× 271 14.2k

Countries citing papers authored by Edward D. Bird

Since Specialization
Citations

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

Fields of papers citing papers by Edward D. Bird

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edward D. Bird

This figure shows the co-authorship network connecting the top 25 collaborators of Edward D. Bird. A scholar is included among the top collaborators of Edward D. Bird 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 Edward D. Bird. Edward D. Bird 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.
MacDonald, Marcy E., Jean Paul Vonsattel, L. Adrienne Cupples, et al.. (1999). Evidence for the GluR6 gene associated with younger onset age of Huntington’s disease. Neurology. 53(6). 1330–1330. 98 indexed citations
2.
Browne, Susan, et al.. (1997). Oxidative damage and metabolic dysfunction in Huntington's disease: Selective vulnerability of the basal ganglia. Annals of Neurology. 41(5). 646–653. 691 indexed citations breakdown →
3.
4.
Urbańska, Ewa M., Paolo Guidetti, Edward D. Bird, et al.. (1995). Dysfunction of brain kynurenic acid metabolism in Huntington's disease: focus on kynurenine aminotransferases. Journal of the Neurological Sciences. 130(1). 39–47. 102 indexed citations
5.
Dure, Leon, G. Bernhard Landwehrmeyer, Jeffrey A. Golden, et al.. (1994). IT15 gene expression in fetal human brain. Brain Research. 659(1-2). 33–41. 19 indexed citations
6.
Persichetti, Francesca, Jayalakshmi Srinidhi, Pei Ge, et al.. (1994). Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains. Neurobiology of Disease. 1(3). 159–166. 67 indexed citations
7.
Lexow, Nedra, Jeffrey N. Joyce, Soo Jin Kim, et al.. (1994). Alterations in TRH receptors in temporal lobe of schizophrenics: A quantitative autoradiographic study. Synapse. 18(4). 315–327. 6 indexed citations
8.
Beneš, Francine M., et al.. (1992). Increased Density of Glutamate-immunoreactive Vertical Processes in Superficial Laminae in Cingulate Cortex of Schizophrenic Brain. Cerebral Cortex. 2(6). 503–512. 103 indexed citations
9.
Myers, Richard H., Jean Paul Vonsattel, Peter A. Paskevich, et al.. (1991). Decreased Neuronal and Increased Oligodendroglial Densities in Huntington's Disease Caudate Nucleus. Journal of Neuropathology & Experimental Neurology. 50(6). 729–742. 179 indexed citations
10.
Beneš, Francine M., et al.. (1991). Evidence for axonal loss in regions occupied by senile plaques in Alzheimer cortex. Neuroscience. 42(3). 651–660. 35 indexed citations
11.
Vogt, Brent A., et al.. (1990). Laminar distributions of muscarinic acetylcholine, serotonin, GABA and opioid receptors in human posterior cingulate cortex. Neuroscience. 36(1). 165–174. 18 indexed citations
12.
Stopa, Edward G., Ana-Maria González, Robert J. Corona, et al.. (1990). Basic fibroblast growth factor in Alzheimer's disease. Biochemical and Biophysical Research Communications. 171(2). 690–696. 147 indexed citations
13.
Crino, Peter B., et al.. (1989). Brain Gangliosides in Dementia of the Alzheimer Type. Archives of Neurology. 46(4). 398–401. 64 indexed citations
15.
Svendsen, Clive N., Mark Froimowitz, Alexander Campbell, et al.. (1988). Receptor affinity, neurochemistry and behavioral characteristics of the enantiomers of thioridazine: Evidence for different stereoselectivities at D1 and D2 receptors in rat brain. Neuropharmacology. 27(11). 1117–1124. 34 indexed citations
16.
Meissen, Gregory J., Richard H. Myers, Carol A. Mastromauro, et al.. (1988). Predictive Testing for Huntingtons Disease with Use of a Linked DNA Marker. New England Journal of Medicine. 318(9). 535–542. 130 indexed citations
17.
Beal, M. Flint, et al.. (1988). Amino acid and neuropeptide neurotransmitters in Huntington's disease cerebellum. Brain Research. 454(1-2). 393–396. 12 indexed citations
18.
Seeman, Philip, Natalie Bzowej, H C Guan, et al.. (1987). Human brain dopamine receptors in children and aging adults. Synapse. 1(5). 399–404. 337 indexed citations
19.
Beal, M. Flint, Michael F. Mazurek, Clive N. Svendsen, Edward D. Bird, & Joseph B. Martin. (1986). Widespread reduction of somatostatin‐like immunoreactivity in the cerebral cortex in Alzheimer's disease. Annals of Neurology. 20(4). 489–495. 84 indexed citations
20.
Langlais, Philip J., et al.. (1985). Cerebrospinal Fluid Neurotransmitter Metabolites in Neurologically Normal Infants and Children. PEDIATRICS. 75(3). 580–586. 59 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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