Countries citing papers authored by Richard G. Weleber
Since
Specialization
Citations
This map shows the geographic impact of Richard G. Weleber'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 Richard G. Weleber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard G. Weleber more than expected).
Fields of papers citing papers by Richard G. Weleber
This network shows the impact of papers produced by Richard G. Weleber. 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 Richard G. Weleber. The network helps show where Richard G. Weleber may publish in the future.
Co-authorship network of co-authors of Richard G. Weleber
This figure shows the co-authorship network connecting the top 25 collaborators of Richard G. Weleber.
A scholar is included among the top collaborators of Richard G. Weleber 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 Richard G. Weleber. Richard G. Weleber 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.
Yang, Paul, Aaron S. Coyner, Robert M. Duvoisin, et al.. (2018). Early Treatment with Mycophenolate Mofetil Reduces Retinal Degeneration and cGMP Dysregulation in rd10 and rd1 mice. Investigative Ophthalmology & Visual Science. 59(9). 2503–2503.1 indexed citations
Wilson, David J., José‐Alain Sahel, Richard G. Weleber, et al.. (2017). One Year Results of a Phase I/IIa Study of SAR422459 in Patients with Stargardt Macular Degeneration (SMD). Investigative Ophthalmology & Visual Science. 58(8). 3385–3385.8 indexed citations
4.
Smith, Travis, Ning Smith, & Richard G. Weleber. (2015). Comparison of interpolation algorithms for static visual field data. Investigative Ophthalmology & Visual Science. 56(7). 3907–3907.2 indexed citations
5.
Weleber, Richard G., Andreas Lauer, Mark E. Pennesi, et al.. (2015). Early findings in a Phase I/IIa clinical program for Usher syndrome 1B (USH1B; MIM #276900). Investigative Ophthalmology & Visual Science. 56(7). 2286–2286.4 indexed citations
6.
Weleber, Richard G., David J. Wilson, Dawn Peters, et al.. (2013). Treatment of Patients with Leber Congenital Amaurosis Type 2 with an AAV Vector Expressing RPE65. Investigative Ophthalmology & Visual Science. 54(15). 5964–5964.1 indexed citations
Bech‐Hansen, N. Torben, Catrina M. Loucks, Chandree L. Beaulieu, et al.. (2010). Mutation Analysis in a Cohort of CSNB Patients: Novel Mutations in TRPM1 Gene. Investigative Ophthalmology & Visual Science. 51(13). 4129–4129.1 indexed citations
9.
Chan-Kai, Brian T., et al.. (2010). Electroretinographic findings in transplant chorioretinopathy. SHILAP Revista de lepidopterología.1 indexed citations
10.
Branham, Kari, Mohammad Othman, Richard G. Weleber, et al.. (2010). X-Linked Recessive Mutations in Simplex Males With Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 51(13). 1399–1399.1 indexed citations
11.
Weleber, Richard G., Peter J. Francis, Stuart K. Gardiner, et al.. (2009). Modeling and Analysis of the Hill of Vision of Full-Field Static Perimetry. Investigative Ophthalmology & Visual Science. 50(13). 3813–3813.1 indexed citations
12.
Adamus, Grazyna, et al.. (2008). Prediction of Retinal Phenotype and Progression Based on Autoantibody Profile in Paraneoplastic and Autoimmune Retinopathy. Investigative Ophthalmology & Visual Science. 49(13). 4748–4748.1 indexed citations
Neuringer, Martha, et al.. (2003). Incidence of Drusen-like Changes in a Rhesus Monkey Colony: Effects of Age, Gender and Dietary Carotenoids. Investigative Ophthalmology & Visual Science. 44(13). 4949–4949.4 indexed citations
15.
Lotery, Andrew, Samuel G. Jacobson, Richard G. Weleber, et al.. (2003). Prevalence of Mutations in the RPE65, CRX, AIPL1, TULP1, GUCY2D and CRB1 Genes in Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 44(13). 2301–2301.4 indexed citations
16.
Weleber, Richard G., Jacek Majewski, David Schultz, et al.. (2003). Age-related Macular Degeneration: A Genome-wide Scan in Extended Families. Investigative Ophthalmology & Visual Science. 44(13). 1503–1503.2 indexed citations
17.
Schultz, David, et al.. (2003). Evidence that FIBL-6 is the ARMD1 Gene. Investigative Ophthalmology & Visual Science. 44(13). 2017–2017.4 indexed citations
18.
Lotery, Andrew, F.L. Munier, Gerald A. Fishman, et al.. (2000). Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.. PubMed. 41(6). 1291–6.126 indexed citations
Weleber, Richard G., et al.. (1994). Electroretinographic genotype-phenotype correlations for mouse and man at the dmd/DMD locus. The American Journal of Human Genetics. 55.1 indexed citations
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