R.E. Hurd

2.4k citations

27 papers · 1.9k indexed · 1 hit paper · h-index 12

Impact in

Ophthalmology top 1%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
Cellular and Molecular Neuroscience top 5%
- Photoreceptor and optogenetics research
- Neuroscience and Neuropharmacology Research
- Neuroscience and Neural Engineering

Papers in ⓘ

Ophthalmology 8
- Retinal Diseases and Treatments 5
- Glaucoma and retinal disorders 4
Endocrine and Autonomic Systems 3
- Circadian rhythm and melatonin 3

Co-authors: Bo Chang (25 shared papers)John R. Heckenlively (10 shared papers)Norman L. Hawes (11 shared papers)Steven Nusinowitz (14 shared papers)Muriel T. Davisson (9 shared papers)Patsy M. Nishina (7 shared papers)Jieping Wang (3 shared papers)M. Phillips (1 shared paper)
Journals: Investigative Ophthalmology & Visual Science (12 papers)Vision Research (2 papers)Human Molecular Genetics (1 paper)Journal of Clinical Investigation (1 paper)Mammalian Genome (1 paper)
Partner nations: United States Germany United Kingdom

In The Last Decade

R.E. Hurd

27 papers receiving 1.9k citations

Hit Papers

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Retinal degeneration mutants in the mouse 2002 · 690 citations

Peers

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-authors

The 25 scholars most cited alongside R.E. Hurd, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with R.E. Hurd Line = papers co-authored together R.E. Hurd links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Retinal degeneration mutants in the mouse Vision Research ·Bo Chang, Norman L. Hawes, R.E. Hurd, Muriel T. Davisson, Steven Nusinowitz, John R. Heckenlively Hit paper breakdown →	2002	690
2	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 ·Bo Chang, Hemant Khanna, Norman L. Hawes, David Jimeno, Shirley He, Concepción Lillo, Sunil K. Parapuram, Hong Cheng, Alison Scott, R.E. Hurd, John A. Sayer, Edgar A. Otto, Massimo Attanasio, John F. O’Toole, Genglin Jin, Chengchao Shou, Friedhelm Hildebrandt, David S. Williams, John R. Heckenlively, Anand Swaroop	2006	303
3	Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene Vision Research ·Bo Chang, Norman L. Hawes, Machelle T. Pardue, Alina German, R.E. Hurd, Muriel T. Davisson, Steven Nusinowitz, K Rengarajan, Amber P. Boyd, S.S. Sidney, M. Phillips, R. E. Stewart, R. Chaudhury, J M Nickerson, John R. Heckenlively, Jeffrey H. Boatright	2007	300
4	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 ·Bo Chang, Tanja Grau, Susann Dangel, R.E. Hurd, Bernhard Jurklies, Emin Cumhur Şener, Sten Andréasson, Hélène Dollfus, Britta Baumann, Sylvia Bolz, Nikolai O. Artemyev, Susanne Kohl, John R. Heckenlively, Bernd Wissinger	2009	154
5	Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice Journal of Clinical Investigation ·Karsten Boldt, Dorus A. Mans, Jungyeon Won, Jeroen van Reeuwijk, Andreas Vogt, Norbert Kinkl, Stef J.F. Letteboer, Wanda L. Hicks, R.E. Hurd, Jürgen Κ. Naggert, Yves Texier, Anneke I. den Hollander, Robert K. Koenekoop, Jean Bennett, Frans P.M. Cremers, Christian Johannes Gloeckner, Patsy M. Nishina, Ronald Roepman, Marius Ueffing	2011	81
6	Survey of Common Eye Diseases in Laboratory Mouse Strains Investigative Ophthalmology & Visual Science ·Bo Chang, R.E. Hurd, Jieping Wang, Patsy M. Nishina	2013	75
7	Mouse models of ocular diseases Visual Neuroscience ·Bo Chang, N. L. Hawes, R.E. Hurd, J. Wang, Douglas Howell, Muriel T. Davisson, Thomas H. Roderick, Steven Nusinowitz, John R. Heckenlively	2005	62
8	Allelic variance between GRM6 mutants, Grm6^nob3 and Grm6^nob4 results in differences in retinal ganglion cell visual responses The Journal of Physiology ·Dennis M. Maddox, Kirstan A. Vessey, Gary L. Yarbrough, Brandon M. Invergo, Donald R. Cantrell, Samsoon Inayat, Victoria Balannik, Wanda L. Hicks, Norman L. Hawes, Shannon L. Byers, Richard S. Smith, R.E. Hurd, Douglas Howell, Ronald G. Gregg, Bo Chang, Jürgen Κ. Naggert, John B. Troy, Lawrence H. Pinto, Patsy M. Nishina, Maureen A. McCall	2008	61
9	Spontaneous CNV in a Novel Mutant Mouse Is Associated With Early VEGF-A–Driven Angiogenesis and Late-Stage Focal Edema, Neural Cell Loss, and Dysfunction Investigative Ophthalmology & Visual Science ·Norihiro Nagai, Pete Lundh von Leithner, Kanako Izumi‐Nagai, Brett Hosking, Bo Chang, R.E. Hurd, Peter Adamson, Anthony P. Adamis, Richard Foxton, Yin‐Shan Ng, David T. Shima	2014	40
10	Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity Mammalian Genome ·Neena B. Haider, Weidong Zhang, R.E. Hurd, Akihiro Ikeda, Arne Nystuen, Jürgen Κ. Naggert, Patsy M. Nishina	2008	33
11	Deficiency of SHP-1 Protein-Tyrosine Phosphatase in “Viable Motheaten” Mice Results in Retinal Degeneration Investigative Ophthalmology & Visual Science ·Bonnie Lyons, Richard S. Smith, R.E. Hurd, Norman L. Hawes, Lisa Burzenski, Steven Nusinowitz, Muneer G. Hasham, Bo Chang, Leonard D. Shultz	2006	19
12	A Mutation inSyne2Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia Investigative Ophthalmology & Visual Science ·Dennis M. Maddox, Gayle B. Collin, Akihiro Ikeda, C. Herbert Pratt, Sakae Ikeda, Britt Johnson, R.E. Hurd, Lindsay S. Shopland, Jürgen Κ. Naggert, Bo Chang, Mark P. Krebs, Patsy M. Nishina	2015	17
13	A Point Mutation in the Cnga3 Gene Causes Cone Photoreceptor Function Loss (cpfl5) in Mice Norman L. Hawes, X. Wang, R.E. Hurd, J. Wang, Muriel T. Davisson, Steven Nusinowitz, J. R. Heckenlively, Bo Chang	2006	8
14	Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ Investigative Ophthalmology & Visual Science ·Xiaojie Ji, Ye Liu, R.E. Hurd, Jieping Wang, Bernie Fitzmaurice, Patsy M. Nishina, Bo Chang	2016	7
15	Comparative Study of Cultured Limbal Epithelial Cells on a 3T3 Feeder Layer or in Defined Medium N. L. Hawes, Belinda S. Harris, R.E. Hurd, Penhryn Bailey, J. Wang, M.T. Davisson, Steven Nusinowitz, J. R. Heckenlively, Bo Chang	2003	6
16	A New Mouse Model of Retinal Degeneration (rd15) With Retinal Outer Plexiform Dystrophy Norman L. Hawes, R.E. Hurd, J. Wang, Muriel T. Davisson, Steven Nusinowitz, J. R. Heckenlively, Bo Chang	2005	3
17	Cone Phosphodiesterase Defects in the Murine cpfl1 Mutant and Human Achromatopsia Patients Bernd Wissinger, Bo Chang, Susann Dangel, N. L. Hawes, R.E. Hurd, Bernhard Jurklies, Emin Cumhur Şener, Sten Andréasson, Susanne Kohl, J. R. Heckenlively	2007	3
18	A New Mouse Model of Retinal Degeneration (rd13) Bo Chang, N. L. Hawes, R.E. Hurd, J. Wang, Muriel T. Davisson, Steven Nusinowitz, John R. Heckenlively	2005	3
19	Selective Loss Of ERG b–Wave Caused By An Autosomal Recessive Mutation In Mice. Investigative Ophthalmology & Visual Science ·Bo Chang, Norman L. Hawes, R.E. Hurd, J. Wang, Muriel T. Davisson, Steven Nusinowitz, John R. Heckenlively	2004	2
20	Comparison of Electroretinographic Responses across Eleven Normal Inbred Mouse Strains Investigative Ophthalmology & Visual Science ·Zahra Kashani, Bo Chang, N. L. Hawes, R.E. Hurd, J. R. Heckenlively, Steven Nusinowitz	2003	2

About R.E. Hurd

R.E. Hurd is a scholar working on Ophthalmology, Endocrine and Autonomic Systems, Molecular Biology, Cell Biology and Biochemistry, having authored 27 papers that have together received 1.9k indexed citations. Recurring topics across this work include Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (5 papers), Glaucoma and retinal disorders (4 papers), Retinoids in leukemia and cellular processes (4 papers), Connexins and lens biology (3 papers), Circadian rhythm and melatonin (3 papers), Genetic and Kidney Cyst Diseases (2 papers) and Phosphodiesterase function and regulation (2 papers). The work is most often cited by research in Ophthalmology (651 citations), Cellular and Molecular Neuroscience (584 citations), Molecular Biology (1.6k citations), Neurology (145 citations) and Cell Biology (238 citations). R.E. Hurd has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Bo Chang, John R. Heckenlively, Norman L. Hawes, Steven Nusinowitz, Muriel T. Davisson, Patsy M. Nishina, Jieping Wang, M. Phillips, R. Chaudhury and Alina German. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Vision Research, Human Molecular Genetics, Journal of Clinical Investigation and Mammalian Genome.

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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