David F. Bishop

5.5k total citations
86 papers, 4.2k citations indexed

About

David F. Bishop is a scholar working on Molecular Biology, Rheumatology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David F. Bishop has authored 86 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 33 papers in Rheumatology and 29 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David F. Bishop's work include Porphyrin Metabolism and Disorders (55 papers), Folate and B Vitamins Research (33 papers) and Neonatal Health and Biochemistry (29 papers). David F. Bishop is often cited by papers focused on Porphyrin Metabolism and Disorders (55 papers), Folate and B Vitamins Research (33 papers) and Neonatal Health and Biochemistry (29 papers). David F. Bishop collaborates with scholars based in United States, United Kingdom and Germany. David F. Bishop's co-authors include Robert J. Desnick, Ruth Kornreich, Kenneth H. Astrin, Philip D. Cotter, Alison May, Christine M. Eng, Harold S. Bernstein, Edward J. Fitzsimons, A.S. Henderson and Hitoshi Sakuraba and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

David F. Bishop

85 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David F. Bishop United States 40 2.6k 1.5k 1.0k 682 585 86 4.2k
Nobuyuki Shimozawa Japan 38 4.2k 1.6× 1.2k 0.8× 262 0.3× 515 0.8× 107 0.2× 217 5.3k
Michael Cantz Germany 29 1.9k 0.7× 1.3k 0.9× 214 0.2× 291 0.4× 155 0.3× 79 3.2k
Mitsuo Nishikawa Japan 24 1.4k 0.5× 346 0.2× 211 0.2× 171 0.3× 74 0.1× 83 2.6k
Richard Possemato United States 26 4.1k 1.5× 656 0.4× 112 0.1× 319 0.5× 71 0.1× 40 5.5k
Akihiko Muto Japan 35 2.9k 1.1× 235 0.2× 119 0.1× 189 0.3× 177 0.3× 80 4.5k
Jessica E. Bolden Australia 14 3.7k 1.4× 806 0.5× 50 0.0× 373 0.5× 56 0.1× 17 4.9k
Raffaella Di Micco Italy 18 3.3k 1.3× 1.6k 1.1× 85 0.1× 328 0.5× 50 0.1× 31 4.9k
Olga Chernova United States 27 2.2k 0.8× 635 0.4× 85 0.1× 257 0.4× 43 0.1× 42 3.7k
Shigeki Sugii Singapore 26 1.4k 0.5× 944 0.6× 67 0.1× 491 0.7× 49 0.1× 50 2.6k
Juping Yuan Germany 38 2.6k 1.0× 184 0.1× 49 0.0× 258 0.4× 270 0.5× 88 4.9k

Countries citing papers authored by David F. Bishop

Since Specialization
Citations

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

Fields of papers citing papers by David F. Bishop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David F. Bishop. 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 David F. Bishop. The network helps show where David F. Bishop may publish in the future.

Co-authorship network of co-authors of David F. Bishop

This figure shows the co-authorship network connecting the top 25 collaborators of David F. Bishop. A scholar is included among the top collaborators of David F. Bishop 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 David F. Bishop. David F. Bishop 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.
Bailey, H., G.A. Bezerra, Jason R. Marcero, et al.. (2020). Human aminolevulinate synthase structure reveals a eukaryotic-specific autoinhibitory loop regulating substrate binding and product release. Nature Communications. 11(1). 2813–2813. 28 indexed citations
2.
Backeris, Peter, Maria Suprun, Sunita L. D’Souza, et al.. (2018). Design and validation of an open-source modular Microplate Photoirradiation System for high-throughput photobiology experiments. PLoS ONE. 13(10). e0203597–e0203597. 5 indexed citations
3.
Bishop, David F., et al.. (2016). THE MEANING OF THE CHORAL METERS IN SENECAN TRAGEDY. 17(6). 485–90.
4.
Bonkovsky, Herbert L., Vinaya C. Maddukuri, Cemal Yazıcı, et al.. (2014). Acute Porphyrias in the USA: Features of 108 Subjects from Porphyrias Consortium. The American Journal of Medicine. 127(12). 1233–1241. 173 indexed citations
5.
6.
Clavero, Sonia, Yuri Ahuja, David F. Bishop, et al.. (2013). Diagnosis of feline acute intermittent porphyria presenting with erythrodontia requires molecular analyses. The Veterinary Journal. 198(3). 720–722. 3 indexed citations
7.
Camacho‐Vanegas, Olga, Sandra Catalina Camacho, Jacob E. Till, et al.. (2012). Primate Genome Gain and Loss: A Bone Dysplasia, Muscular Dystrophy, and Bone Cancer Syndrome Resulting from Mutated Retroviral-Derived MTAP Transcripts. The American Journal of Human Genetics. 90(4). 614–627. 23 indexed citations
8.
Zhang, Jinglan, Makiko Yasuda, Robert J. Desnick, et al.. (2011). A LC–MS/MS method for the specific, sensitive, and simultaneous quantification of 5-aminolevulinic acid and porphobilinogen. Journal of Chromatography B. 879(24). 2389–2396. 39 indexed citations
9.
Yasuda, Makiko, David F. Bishop, Mary Fowkes, et al.. (2009). AAV8-mediated Gene Therapy Prevents Induced Biochemical Attacks of Acute Intermittent Porphyria and Improves Neuromotor Function. Molecular Therapy. 18(1). 17–22. 41 indexed citations
10.
Martínez-Bermejo, A, Thomas P. Naidich, Walter E. Kaufmann, et al.. (2004). Acute Intermittent Porphyria. Archives of Neurology. 61(11). 1764–1764. 62 indexed citations
11.
Cunha, Luis F., et al.. (2002). Congenital erythropoietic porphyria: identification and expression of eight novel mutations in the uroporphyrinogen III synthase gene. British Journal of Haematology. 117(4). 980–987. 34 indexed citations
12.
Wallenstein, Sylvan, et al.. (2001). Nonoverlapping Clusters: Approximate Distribution and Application to Molecular Biology. Biometrics. 57(2). 420–426. 10 indexed citations
13.
Bishop, David F., et al.. (1996). The Entire Genomic Sequence and cDNA Expression of Mouse α-Galactosidase A. Biochemical and Molecular Medicine. 57(2). 139–148. 8 indexed citations
14.
15.
Cotter, Philip D., Huntington F. Willard, Jerome L. Gorski, & David F. Bishop. (1992). Assignment of human erythroid δ-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X;Autosome translocations. Genomics. 13(1). 211–212. 52 indexed citations
16.
Scheidt, Wolfgang von, Christine M. Eng, Thomas Fitzmaurice, et al.. (1991). An Atypical Variant of Fabry's Disease with Manifestations Confined to the Myocardium. New England Journal of Medicine. 324(6). 395–399. 297 indexed citations
17.
Bishop, David F., A.S. Henderson, & Kenneth H. Astrin. (1990). Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome. Genomics. 7(2). 207–214. 132 indexed citations
18.
Bishop, David F.. (1990). Two different genes encode δ-aminolevulinate synthase in humans: nucleotide sequences of cDNAs for the housekeeping and erythroid genes. Nucleic Acids Research. 18(23). 7187–7188. 50 indexed citations
19.
Tsai, Shih‐Feng, David F. Bishop, & Robert J. Desnick. (1987). Coupled-enzyme and direct assays for uroporphyrinogen III synthase activity in human erythrocytes and cultured lymphoblasts. Analytical Biochemistry. 166(1). 120–133. 42 indexed citations
20.
Bishop, David F.. (1981). Fabry disease: an asymptomatic hemizygote with significant residual α-galactosidase A activity.. The American Journal of Human Genetics. 33. 15 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Nobuyuki Shimozawa Breakdown of academic impact, for papers by Michael Cantz Breakdown of academic impact, for papers by Mitsuo Nishikawa Breakdown of academic impact, for papers by Richard Possemato Breakdown of academic impact, for papers by Akihiko Muto Breakdown of academic impact, for papers by Jessica E. Bolden Breakdown of academic impact, for papers by Raffaella Di Micco Breakdown of academic impact, for papers by Olga Chernova Breakdown of academic impact, for papers by Shigeki Sugii Breakdown of academic impact, for papers by Juping Yuan
Rankless by CCL
2026