J. Bronwyn Bateman

906 total citations
34 papers, 680 citations indexed

About

J. Bronwyn Bateman is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, J. Bronwyn Bateman has authored 34 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Cell Biology and 6 papers in Genetics. Recurrent topics in J. Bronwyn Bateman's work include Connexins and lens biology (10 papers), Retinal Development and Disorders (7 papers) and RNA regulation and disease (5 papers). J. Bronwyn Bateman is often cited by papers focused on Connexins and lens biology (10 papers), Retinal Development and Disorders (7 papers) and RNA regulation and disease (5 papers). J. Bronwyn Bateman collaborates with scholars based in United States, Australia and Russia. J. Bronwyn Bateman's co-authors include Robert S. Sparkes, Irene H. Maumenee, M. Anne Spence, R S Sparkes, Manfred Spitznas, Camilla Heinzmann, Pamela Flodman, T. Mohandas, Ivana Klisak and Kevin Clancy and has published in prestigious journals such as Ophthalmology, American Journal of Ophthalmology and Genomics.

In The Last Decade

J. Bronwyn Bateman

34 papers receiving 654 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Bronwyn Bateman United States	16	460	257	206	78	75	34	680
Nisha Patel Saudi Arabia	17	428 0.9×	267 1.0×	72 0.3×	69 0.9×	40 0.5×	39	727
Salma Ben‐Salem United Arab Emirates	13	256 0.6×	209 0.8×	64 0.3×	37 0.5×	41 0.5×	26	470
Lisa McKie United Kingdom	13	433 0.9×	128 0.5×	85 0.4×	218 2.8×	37 0.5×	24	702
Gail Billingsley Canada	16	727 1.6×	383 1.5×	444 2.2×	94 1.2×	185 2.5×	19	1.0k
R. Vervoort Belgium	13	727 1.6×	233 0.9×	283 1.4×	147 1.9×	65 0.9×	19	910
Katherine L. Dry United Kingdom	10	528 1.1×	164 0.6×	143 0.7×	117 1.5×	39 0.5×	13	592
Annabel Christ Germany	14	321 0.7×	101 0.4×	50 0.2×	97 1.2×	43 0.6×	18	556
Roberta Tammaro Italy	11	515 1.1×	180 0.7×	87 0.4×	91 1.2×	23 0.3×	12	615
Kamron N. Khan United Kingdom	17	603 1.3×	119 0.5×	599 2.9×	87 1.1×	248 3.3×	36	884

Countries citing papers authored by J. Bronwyn Bateman

Since Specialization

Citations

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

Fields of papers citing papers by J. Bronwyn Bateman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. Bronwyn Bateman. 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 J. Bronwyn Bateman. The network helps show where J. Bronwyn Bateman may publish in the future.

Co-authorship network of co-authors of J. Bronwyn Bateman

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

All Works

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20 of 20 papers shown

Higginbotham, Eve J., et al.. (2022). Gender Diversity on Corporate Boards Associated with Ophthalmology. American Journal of Ophthalmology. 239. 154–158. 3 indexed citations

Bateman, J. Bronwyn, et al.. (2006). Autosomal Dominant Cataract: Intrafamilial Phenotypic Variability, Interocular Asymmetry, and Variable Progression in Four Chilean Families. American Journal of Ophthalmology. 141(4). 750–750.e8. 8 indexed citations

Spence, M. Anne, Pamela Flodman, Kevin Clancy, et al.. (2006). Novel Single-Base Deletional Mutation in Major Intrinsic Protein (MIP) in Autosomal Dominant Cataract. American Journal of Ophthalmology. 141(4). 761–761.e4. 55 indexed citations

Lee, Brian L., et al.. (1996). Autosomal-dominant Anomalies of the Iris Pigment Epithelium. Ophthalmology. 103(10). 1696–1699. 2 indexed citations

Lee, Brian L., J. Bronwyn Bateman, & Steven D. Schwartz. (1996). Posterior Segment Neovascularization Associated With Optic Nerve Aplasia. American Journal of Ophthalmology. 122(1). 131–133. 12 indexed citations

Heinzmann, Camilla, Pamela Flodman, R S Sparkes, et al.. (1996). Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.. PubMed. 58(2). 347–55. 18 indexed citations

Bateman, J. Bronwyn, Rita M. Cantor, Camilla Heinzmann, et al.. (1993). 2×0．30ST钢丝帘线的开发. PubMed Central. 30(7). 299–434. 3 indexed citations

Bateman, J. Bronwyn, Tracy Kojis, Camilla Heinzmann, et al.. (1993). Mapping of Aldose Reductase Gene Sequences to Human Chromosomes 1, 3, 7, 9, 11, and 13. Genomics. 17(3). 560–565. 8 indexed citations

Glasgow, Ben J., Camilla Heinzmann, Tracy Kojis, et al.. (1993). Assignment of tear lipocalin gene to human chromosome 9q34–9qter. Current Eye Research. 12(11). 1019–1023. 35 indexed citations

10.

Sparkes, Robert S., Rehwa H. Lee, Toshimichi Shinohara, et al.. (1993). Assignment of the Phosducin (PDC) Gene to Human Chromosome 1q25-1q32.1 by Somatic Cell Hybridization and in Situ Hybridization. Genomics. 18(2). 426–428. 7 indexed citations

11.

Heinz, Grant W., et al.. (1993). Ocular Manifestations of the Lacrimo-auriculo-dento-digital Syndrome. American Journal of Ophthalmology. 115(2). 243–248. 22 indexed citations

12.

Bateman, J. Bronwyn, I Klisak, T. Mohandas, et al.. (1992). Assignment of the ?-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse gene) to human chromosome 4p16. Genomics. 12(3). 601–603. 7 indexed citations

13.

King, Richard A., et al.. (1992). Oculocutaneous Albinism: Variable Expressivity of Nystagmus in a Sibship. Journal of Pediatric Ophthalmology & Strabismus. 29(3). 185–188. 15 indexed citations

14.

Farber, Debora B., John R. Heckenlively, R S Sparkes, & J. Bronwyn Bateman. (1991). Molecular genetics of retinitis pigmentosa.. PubMed. 155(4). 388–99. 13 indexed citations

15.

Bateman, J. Bronwyn, M. Anne Spence, Victoria K. Cortessis, et al.. (1990). Ornithine aminotransferase (OAT): Recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locus. Genomics. 6(1). 123–128. 10 indexed citations

16.

Bateman, J. Bronwyn, Victoria K. Cortessis, Robert S. Sparkes, et al.. (1989). Norrie disease: Linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe. Genomics. 4(4). 539–545. 9 indexed citations

17.

Klisak, Ivana, Robert Dubin, Joram Piatigorsky, et al.. (1989). Assignment of the αB-crystallin gene to human chromosome 11. Genomics. 5(4). 665–669. 29 indexed citations

18.

Bateman, J. Bronwyn. (1984). Microphthalmos. International Ophthalmology Clinics. 24(1). 87–107. 22 indexed citations

19.

Bateman, J. Bronwyn, M.C. Sparkes, & R S Sparkes. (1984). Aniridia: enzyme studies in an 11p--chromosomal deletion.. PubMed. 25(5). 612–6. 3 indexed citations

20.

Bateman, J. Bronwyn, et al.. (1980). Heterogeneity of Retinal Degeneration and Hearing Impairment Syndromes. American Journal of Ophthalmology. 90(6). 755–767. 19 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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