Dianna K. Hughbanks-Wheaton

1.4k total citations
20 papers, 908 citations indexed

About

Dianna K. Hughbanks-Wheaton is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Dianna K. Hughbanks-Wheaton has authored 20 papers receiving a total of 908 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Ophthalmology and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Dianna K. Hughbanks-Wheaton's work include Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (7 papers) and Retinoids in leukemia and cellular processes (4 papers). Dianna K. Hughbanks-Wheaton is often cited by papers focused on Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (7 papers) and Retinoids in leukemia and cellular processes (4 papers). Dianna K. Hughbanks-Wheaton collaborates with scholars based in United States, Sweden and Chile. Dianna K. Hughbanks-Wheaton's co-authors include David G. Birch, Sara J. Bowne, Stephen P. Daiger, Lori S. Sullivan, Dennis R. Hoffman, John R. Heckenlively, Anisa Gire, Eileen E. Birch, Sharon Garfield and Yolanda S. Castañeda and has published in prestigious journals such as Journal of Biological Chemistry, American Journal of Ophthalmology and Investigative Ophthalmology & Visual Science.

In The Last Decade

Dianna K. Hughbanks-Wheaton

20 papers receiving 877 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dianna K. Hughbanks-Wheaton United States	13	681	330	159	117	103	20	908
Dianna K. Wheaton United States	12	475 0.7×	291 0.9×	156 1.0×	59 0.5×	123 1.2×	31	679
Sharee Kuny Canada	14	281 0.4×	102 0.3×	32 0.2×	93 0.8×	105 1.0×	21	471
Alina German Israel	11	366 0.5×	115 0.3×	24 0.2×	125 1.1×	38 0.4×	26	532
Claudia Yahalom Israel	14	123 0.2×	185 0.6×	23 0.1×	18 0.2×	53 0.5×	43	467
Sallyanne Davies United Kingdom	6	637 0.9×	539 1.6×	16 0.1×	99 0.8×	8 0.1×	7	930
Hans‐Jürgen Fülle United States	13	433 0.6×	76 0.2×	221 1.4×	404 3.5×	33 0.3×	15	979
Krzysztof Mazuruk United States	9	257 0.4×	63 0.2×	7 0.0×	73 0.6×	62 0.6×	13	521
T. C. Chu United States	11	469 0.7×	62 0.2×	26 0.2×	67 0.6×	36 0.3×	17	591
Catherine J. Spellicy United States	13	484 0.7×	149 0.5×	3 0.0×	128 1.1×	88 0.9×	20	587
Davide Martini Italy	15	352 0.5×	163 0.5×	3 0.0×	120 1.0×	43 0.4×	29	749

Countries citing papers authored by Dianna K. Hughbanks-Wheaton

Since Specialization

Citations

This map shows the geographic impact of Dianna K. Hughbanks-Wheaton'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 Dianna K. Hughbanks-Wheaton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dianna K. Hughbanks-Wheaton more than expected).

Fields of papers citing papers by Dianna K. Hughbanks-Wheaton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dianna K. Hughbanks-Wheaton. 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 Dianna K. Hughbanks-Wheaton. The network helps show where Dianna K. Hughbanks-Wheaton may publish in the future.

Co-authorship network of co-authors of Dianna K. Hughbanks-Wheaton

This figure shows the co-authorship network connecting the top 25 collaborators of Dianna K. Hughbanks-Wheaton. A scholar is included among the top collaborators of Dianna K. Hughbanks-Wheaton 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 Dianna K. Hughbanks-Wheaton. Dianna K. Hughbanks-Wheaton 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

Shankar, Suma P., Dianna K. Hughbanks-Wheaton, David G. Birch, et al.. (2016). Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, inPRPH2and Protein Haplotypes intransas Modifiers. Investigative Ophthalmology & Visual Science. 57(2). 349–349. 24 indexed citations

Shankar, Suma P., David G. Birch, Robert R. German, et al.. (2015). Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies. JAMA Ophthalmology. 133(5). 511–511. 16 indexed citations

Hoffman, Dennis R., Dianna K. Hughbanks-Wheaton, Rand Spencer, et al.. (2015). Docosahexaenoic Acid Slows Visual Field Progression in X-Linked Retinitis Pigmentosa: Ancillary Outcomes of the DHAX Trial. Investigative Ophthalmology & Visual Science. 56(11). 6646–6646. 50 indexed citations

Hughbanks-Wheaton, Dianna K., David G. Birch, Gary E. Fish, et al.. (2014). Safety Assessment of Docosahexaenoic Acid in X-Linked Retinitis Pigmentosa: The 4-Year DHAX Trial. Investigative Ophthalmology & Visual Science. 55(8). 4958–4958. 19 indexed citations

Hoffman, Dennis R., Dianna K. Hughbanks-Wheaton, N. Shirlene Pearson, et al.. (2014). Four-Year Placebo-Controlled Trial of Docosahexaenoic Acid in X-Linked Retinitis Pigmentosa (DHAX Trial). JAMA Ophthalmology. 132(7). 866–866. 54 indexed citations

Morale, Sarah E., et al.. (2012). Visual Acuity Assessment of Children with Special Needs. American Orthoptic Journal. 62(1). 90–98. 11 indexed citations

Bowne, Sara J., Lori S. Sullivan, Anisa Gire, et al.. (2008). Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa.. PubMed. 14. 922–7. 33 indexed citations

Birch, Eileen E., Sharon Garfield, Yolanda S. Castañeda, et al.. (2007). Visual acuity and cognitive outcomes at 4 years of age in a double-blind, randomized trial of long-chain polyunsaturated fatty acid-supplemented infant formula. Early Human Development. 83(5). 279–284. 183 indexed citations

Hughbanks-Wheaton, Dianna K., et al.. (2007). Parental refusal or delay of childhood immunization: Implications for nursing and health education. Teaching and learning in nursing. 2(4). 126–132. 3 indexed citations

10.

Gire, Anisa, Lori S. Sullivan, Sara J. Bowne, et al.. (2007). The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.. PubMed. 13. 1970–5. 49 indexed citations

11.

Sullivan, Lori S., Sara J. Bowne, David G. Birch, et al.. (2006). Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families. Investigative Ophthalmology & Visual Science. 47(7). 3052–3052. 220 indexed citations

12.

Sullivan, Lori S., Sara J. Bowne, Susan H. Blanton, et al.. (2006). Genomic Rearrangements of thePRPF31Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 47(10). 4579–4579. 64 indexed citations

13.

Kozma, Petra, Dianna K. Hughbanks-Wheaton, Kirsten G. Locke, et al.. (2005). Phenotypic Characterization of a Large Family With RP10 Autosomal-Dominant Retinitis Pigmentosa: An Asp226Asn Mutation in the IMPDH1 Gene. American Journal of Ophthalmology. 140(5). 858–867.e1. 16 indexed citations

14.

Bowne, Sara J., Lori S. Sullivan, Sarah Mortimer, et al.. (2005). Spectrum and Frequency of Mutations in IMPDH1 Associated with Autosomal Dominant Retinitis Pigmentosa and Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 47(1). 34–34. 117 indexed citations

15.

Sullivan, L.S., Sara J. Bowne, Suma P. Shankar, et al.. (2004). Autosomal dominant retinitis pigmentosa: exclusion of known and mapped genes in three families.. Investigative Ophthalmology & Visual Science. 45(13). 4747–4747. 1 indexed citations

16.

Kozma, Petra, David G. Birch, Dianna K. Hughbanks-Wheaton, et al.. (2004). Analysis of protein haplotypes in trans as factors modifying phenotypic variation of retinal dystrophies caused by a splice site mutation in the peripherin/RDS gene. Investigative Ophthalmology & Visual Science. 45(13). 3719–3719. 1 indexed citations

17.

Bowne, Sara J., Anisa Gire, Lori S. Sullivan, et al.. (2003). Frequency and Spectrum of IMPDH1 Mutations Associated with Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 44(13). 2307–2307. 1 indexed citations

18.

Kennan, Avril, Pete Humphries, Dianna K. Hughbanks-Wheaton, et al.. (2003). Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.. PubMed. 9. 129–37. 36 indexed citations

19.

Wimalasena, Kandatege, et al.. (1996). Reduction of Dopamine β-Monooxygenase. Journal of Biological Chemistry. 271(42). 26032–26043. 9 indexed citations

20.

Wimalasena, Kandatege, et al.. (1996). Reduction of dopamine beta-monooxygenase. A unified model for apparent negative cooperativity and fumarate activation.. PubMed. 271(42). 26032–43. 1 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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