R.E. Hurd

2.4k total citations · 1 hit paper
27 papers, 1.9k citations indexed

About

R.E. Hurd is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, R.E. Hurd has authored 27 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 8 papers in Ophthalmology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in R.E. Hurd's work include Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (5 papers) and Retinoids in leukemia and cellular processes (4 papers). R.E. Hurd is often cited by papers focused on Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (5 papers) and Retinoids in leukemia and cellular processes (4 papers). R.E. Hurd collaborates with scholars based in United States, Germany and United Kingdom. R.E. Hurd's co-authors include Bo Chang, John R. Heckenlively, Norman L. Hawes, Steven Nusinowitz, Muriel T. Davisson, Patsy M. Nishina, Jieping Wang, Machelle T. Pardue, K Rengarajan and J M Nickerson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Physiology.

In The Last Decade

R.E. Hurd

27 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Retinal degeneration mutants in the mouse

2002 690 citations Bo Chang, Norman L. Hawes et al. Vision Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R.E. Hurd United States	12	1.6k	651	584	345	238	27	1.9k
Pete Humphries Ireland	26	1.3k 0.8×	553 0.8×	428 0.7×	249 0.7×	126 0.5×	55	1.7k
Naheed W. Khan United States	23	1.4k 0.8×	706 1.1×	483 0.8×	183 0.5×	181 0.8×	43	1.6k
Neena B. Haider United States	23	1.4k 0.9×	584 0.9×	383 0.7×	439 1.3×	199 0.8×	46	2.0k
Eckart Apfelstedt-Sylla Germany	18	1.8k 1.1×	740 1.1×	696 1.2×	209 0.6×	266 1.1×	30	2.1k
Steven J. Pittler United States	25	2.8k 1.7×	999 1.5×	1.1k 1.9×	399 1.2×	369 1.6×	66	3.1k
Claudio Punzo United States	22	1.6k 1.0×	588 0.9×	473 0.8×	246 0.7×	199 0.8×	41	1.8k
Christian P. Hamel France	26	2.0k 1.2×	933 1.4×	366 0.6×	273 0.8×	216 0.9×	71	2.4k
Naoyuki Tanimoto Germany	31	2.4k 1.5×	1.1k 1.6×	935 1.6×	292 0.8×	329 1.4×	92	3.1k
Leah C. Byrne United States	20	1.8k 1.1×	462 0.7×	498 0.9×	612 1.8×	77 0.3×	42	2.0k
Fulton Wong United States	28	2.5k 1.5×	810 1.2×	1.4k 2.5×	296 0.9×	270 1.1×	65	3.1k

Countries citing papers authored by R.E. Hurd

Since Specialization

Citations

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

Fields of papers citing papers by R.E. Hurd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R.E. Hurd. 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 R.E. Hurd. The network helps show where R.E. Hurd may publish in the future.

Co-authorship network of co-authors of R.E. Hurd

This figure shows the co-authorship network connecting the top 25 collaborators of R.E. Hurd. A scholar is included among the top collaborators of R.E. Hurd 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 R.E. Hurd. R.E. Hurd 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

Maddox, Dennis M., Gayle B. Collin, Akihiro Ikeda, et al.. (2015). A Mutation inSyne2Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia. Investigative Ophthalmology & Visual Science. 56(6). 3776–3776. 17 indexed citations

Chang, Bo, R.E. Hurd, Jieping Wang, & Patsy M. Nishina. (2013). Survey of Common Genetic Eye Diseases in Mouse Strains. Investigative Ophthalmology & Visual Science. 54(15). 265–265. 1 indexed citations

Chang, Bo, R.E. Hurd, Jieping Wang, & Patsy M. Nishina. (2013). Survey of Common Eye Diseases in Laboratory Mouse Strains. Investigative Ophthalmology & Visual Science. 54(7). 4974–4974. 75 indexed citations

Boldt, Karsten, Dorus A. Mans, Jungyeon Won, et al.. (2011). Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. Journal of Clinical Investigation. 121(6). 2169–2180. 81 indexed citations

Friedman, James S., Bo Chang, R.E. Hurd, et al.. (2010). Loss of Lysophosphatidylcholine Acyltransferase 1 (LPCAT1) Leads to Photoreceptor Degeneration in rd11 Mice. Investigative Ophthalmology & Visual Science. 51(13). 2943–2943. 1 indexed citations

Chang, Bo, R.E. Hurd, Bernhard Jurklies, et al.. (2009). A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Proceedings of the National Academy of Sciences. 106(46). 19581–19586. 154 indexed citations

Chang, Bo, et al.. (2008). A New Mouse Model of a Retinal Detachment With Secondary Angle Closure Glaucoma. Investigative Ophthalmology & Visual Science. 49(13). 5225–5225. 1 indexed citations

Maddox, Dennis M., Kirstan A. Vessey, Gary L. Yarbrough, et al.. (2008). Allelic variance between GRM6 mutants, Grm6^nob3 and Grm6^nob4 results in differences in retinal ganglion cell visual responses. The Journal of Physiology. 586(18). 4409–4424. 61 indexed citations

Haider, Neena B., Weidong Zhang, R.E. Hurd, et al.. (2008). Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity. Mammalian Genome. 19(3). 145–154. 33 indexed citations

10.

Chang, Bo, Norman L. Hawes, Machelle T. Pardue, et al.. (2007). Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene. Vision Research. 47(5). 624–633. 300 indexed citations

11.

Chang, Bo, Hemant Khanna, Norman L. Hawes, et al.. (2006). In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse. Human Molecular Genetics. 15(11). 1847–1857. 303 indexed citations

12.

Lyons, Bonnie, Richard S. Smith, R.E. Hurd, et al.. (2006). Deficiency of SHP-1 Protein-Tyrosine Phosphatase in “Viable Motheaten” Mice Results in Retinal Degeneration. Investigative Ophthalmology & Visual Science. 47(3). 1201–1201. 19 indexed citations

13.

Heckenlively, John R., Norman L. Hawes, R.E. Hurd, et al.. (2005). Cone Photoreceptor Function Loss–3 (Cpfl3), a New Mouse Model of Achromatopsia Due to Missense Mutation in GNAT2. Investigative Ophthalmology & Visual Science. 46(13). 3190–3190. 1 indexed citations

14.

Hawes, Norman L., R.E. Hurd, Muriel T. Davisson, et al.. (2005). A New Mouse Model of Retinal Degeneration (rd15) With Retinal Outer Plexiform Dystrophy. 46(13). 3175–3175. 3 indexed citations

15.

Chang, Bo, N. L. Hawes, R.E. Hurd, et al.. (2005). Mouse models of ocular diseases. Visual Neuroscience. 22(5). 587–593. 62 indexed citations

16.

Zhang, J., Norman L. Hawes, Belinda S. Harris, et al.. (2005). A New Mouse Model of Retinal Degeneration (RD14) Associated With Neurological Defects. 46(13). 3170–3170. 1 indexed citations

17.

Chang, Bo, Norman L. Hawes, R.E. Hurd, et al.. (2004). Selective Loss Of ERG b–Wave Caused By An Autosomal Recessive Mutation In Mice.. Investigative Ophthalmology & Visual Science. 45(13). 1019–1019. 2 indexed citations

18.

Chang, Bo, et al.. (2003). Comparison of Electroretinographic Responses across Eleven Normal Inbred Mouse Strains. Investigative Ophthalmology & Visual Science. 44(13). 1896–1896. 2 indexed citations

19.

Chang, Bo, N. L. Hawes, R.E. Hurd, et al.. (2003). A Gene Responsible for Light-induced Visual Impairment (lvi) in Mice. Investigative Ophthalmology & Visual Science. 44(13). 4532–4532. 1 indexed citations

20.

Chang, Bo, Norman L. Hawes, R.E. Hurd, et al.. (2002). Retinal degeneration mutants in the mouse. Vision Research. 42(4). 517–525. 690 indexed citations breakdown →

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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