Gregory B. Willer

548 total citations
12 papers, 438 citations indexed

About

Gregory B. Willer is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gregory B. Willer has authored 12 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Cell Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gregory B. Willer's work include Connexins and lens biology (3 papers), Retinal Development and Disorders (3 papers) and Developmental Biology and Gene Regulation (2 papers). Gregory B. Willer is often cited by papers focused on Connexins and lens biology (3 papers), Retinal Development and Disorders (3 papers) and Developmental Biology and Gene Regulation (2 papers). Gregory B. Willer collaborates with scholars based in United States, Italy and Canada. Gregory B. Willer's co-authors include Ronald G. Gregg, Brian A. Link, Jason R. Willer, James M. Fadool, John E. Dowling, Thomas S. Vihtelic, David R. Hyde, V M Lee, Jiwoon Lee and Jeffrey M. Gross and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Gregory B. Willer

12 papers receiving 436 citations

Peers

Gregory B. Willer

GENET

RNMI

CMN

Fabrice Richard France

Gaël Manès France

Charles E. Hawkins United States

Meredith O. Sweeney United States

Mingchu Xu United States

Dhani Tracey‐White United Kingdom

Larry Fromm United States

Peter Humphries Ireland

Béatrice Bocquet France

Takuya Tomemori Japan

Fabrice Richard France

Gregory B. Willer

430 ×1.2

236 ×1.3

121 ×2.3

GENET

40 ×0.9

RNMI

57 ×1.3

CMN

Citations per year, relative to Gregory B. Willer Gregory B. Willer (= 1×) peers Fabrice Richard

Countries citing papers authored by Gregory B. Willer

Since Specialization

Citations

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

Fields of papers citing papers by Gregory B. Willer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory B. Willer. 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 Gregory B. Willer. The network helps show where Gregory B. Willer may publish in the future.

Co-authorship network of co-authors of Gregory B. Willer

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

All Works

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12 of 12 papers shown

Willer, Jason R., Gregory B. Willer, Ronald G. Gregg, et al.. (2015). pigkMutation underliesmachobehavior and affects Rohon-Beard cell excitability. Journal of Neurophysiology. 114(2). 1146–1157. 7 indexed citations

Vihtelic, Thomas S., Kristina E. Ile, Corey T. Watson, et al.. (2011). Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye. Experimental Eye Research. 93(4). 460–474. 14 indexed citations

Willer, Jason R., Ross F. Collery, Matthew P. Gray, et al.. (2011). Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma. PLoS Genetics. 7(2). e1001310–e1001310. 79 indexed citations

Thomas, Jennifer L., Thomas S. Vihtelic, Aaron D. denDekker, et al.. (2011). The Loss of Vacuolar Protein Sorting 11 (vps11) Causes Retinal Pathogenesis in a Vertebrate Model of Syndromic Albinism. Investigative Ophthalmology & Visual Science. 52(6). 3119–3119. 25 indexed citations

Song, Yuanquan, Jason R. Willer, Paul Scherer, et al.. (2010). Neural and Synaptic Defects in slytherin, a Zebrafish Model for Human Congenital Disorders of Glycosylation. PLoS ONE. 5(10). e13743–e13743. 28 indexed citations

Willer, Gregory B., et al.. (2009). Muscle Contractions Guide Rohon–Beard Peripheral Sensory Axons. Journal of Neuroscience. 29(42). 13190–13201. 16 indexed citations

Song, Yuanquan, Mary Selak, Corey T. Watson, et al.. (2009). Mechanisms Underlying Metabolic and Neural Defects in Zebrafish and Human Multiple Acyl-CoA Dehydrogenase Deficiency (MADD). PLoS ONE. 4(12). e8329–e8329. 50 indexed citations

Lee, Jiwoon, et al.. (2008). Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye. Developmental Biology. 319(1). 10–22. 49 indexed citations

Vihtelic, Thomas S., et al.. (2007). Zebrafish lens opaque (lop) Mutation Mapping and Gene Identification. Investigative Ophthalmology & Visual Science. 48(13). 2447–2447. 2 indexed citations

10.

Semina, Elena V., D.V. Bosenko, Kelly Soules, et al.. (2006). Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish. Developmental Biology. 299(1). 63–77. 58 indexed citations

11.

Willer, Gregory B., et al.. (2005). Analysis of the Zebrafish perplexed Mutation Reveals Tissue-Specific Roles for de Novo Pyrimidine Synthesis During Development. Genetics. 170(4). 1827–1837. 35 indexed citations

12.

Gregg, Ronald G., Gregory B. Willer, James M. Fadool, John E. Dowling, & Brian A. Link. (2003). Positional cloning of the young mutation identifies an essential role for the Brahma chromatin remodeling complex in mediating retinal cell differentiation. Proceedings of the National Academy of Sciences. 100(11). 6535–6540. 75 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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