Lynda Ploder

2.2k total citations
15 papers, 1.8k citations indexed

About

Lynda Ploder is a scholar working on Molecular Biology, Materials Chemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lynda Ploder has authored 15 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Materials Chemistry and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lynda Ploder's work include Retinal Development and Disorders (10 papers), Photoreceptor and optogenetics research (3 papers) and Connexins and lens biology (3 papers). Lynda Ploder is often cited by papers focused on Retinal Development and Disorders (10 papers), Photoreceptor and optogenetics research (3 papers) and Connexins and lens biology (3 papers). Lynda Ploder collaborates with scholars based in Canada, United States and United Kingdom. Lynda Ploder's co-authors include Danka Vidgen, Roderick R. McInnes, Vitauts I. Kalnins, Roderick R. Mclnnes, Ivy S.C Liu, Derek van der Kooy, Carol L. Freund, Jens Looser, Jakub Novák and Margit Burmeister and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Lynda Ploder

15 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lynda Ploder Canada	12	1.6k	495	335	329	248	15	1.8k
Joseph A. Brzezinski United States	17	1.4k 0.9×	534 1.1×	288 0.9×	257 0.8×	131 0.5×	27	1.5k
Sabine Fuhrmann United States	20	1.5k 0.9×	485 1.0×	279 0.8×	263 0.8×	331 1.3×	35	1.7k
Nadean L. Brown United States	27	2.1k 1.3×	611 1.2×	489 1.5×	294 0.9×	253 1.0×	50	2.3k
Xiuqian Mu United States	22	1.4k 0.8×	452 0.9×	325 1.0×	251 0.8×	138 0.6×	39	1.5k
Deborah C. Otteson United States	21	1.2k 0.7×	395 0.8×	286 0.9×	194 0.6×	183 0.7×	41	1.4k
Juan Ramón Martínez‐Morales Spain	21	1.7k 1.0×	498 1.0×	458 1.4×	155 0.5×	409 1.6×	46	2.0k
Muriel Perron France	27	2.4k 1.5×	671 1.4×	600 1.8×	231 0.7×	317 1.3×	60	2.6k
Yuichiro Takada United States	13	1.5k 0.9×	491 1.0×	234 0.7×	509 1.5×	204 0.8×	16	1.6k
Thomas S. Vihtelic United States	22	1.5k 0.9×	389 0.8×	748 2.2×	195 0.6×	171 0.7×	34	1.8k
S. Sanyal Netherlands	22	1.3k 0.8×	602 1.2×	309 0.9×	327 1.0×	131 0.5×	53	1.6k

Countries citing papers authored by Lynda Ploder

Since Specialization

Citations

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

Fields of papers citing papers by Lynda Ploder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lynda Ploder. 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 Lynda Ploder. The network helps show where Lynda Ploder may publish in the future.

Co-authorship network of co-authors of Lynda Ploder

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

All Works

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15 of 15 papers shown

Singer, A.U., Levi L. Blazer, Lynda Ploder, et al.. (2024). Antigen‐binding fragments with improved crystal lattice packing and enhanced conformational flexibility at the elbow region as crystallization chaperones. Protein Science. 33(7). e5081–e5081. 1 indexed citations

Gallo, Eugenio, Peter Bayliss, Olga Egorova, et al.. (2020). In situ antibody phage display yields optimal inhibitors of integrin α11/β1. mAbs. 12(1). 1717265–1717265. 15 indexed citations

Pollock, Samuel B., Amy Hu, Yun Mou, et al.. (2018). Highly multiplexed and quantitative cell-surface protein profiling using genetically barcoded antibodies. Proceedings of the National Academy of Sciences. 115(11). 2836–2841. 40 indexed citations

Jung, Cynthia C., Denize Atan, David Ng, et al.. (2015). Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity. Proceedings of the National Academy of Sciences. 112(23). E3010–9. 23 indexed citations

Chow, Robert L., Brian J. Snow, Jens Looser, et al.. (2001). Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells. Mechanisms of Development. 109(2). 315–322. 83 indexed citations

Clarke, Geoff, Andrew F.X. Goldberg, Danka Vidgen, et al.. (2000). Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis. Nature Genetics. 25(1). 67–73. 133 indexed citations

Xu, Shunbin, Deborah A. Swanson, A Soltyk, et al.. (1999). PHR1 Encodes an Abundant, Pleckstrin Homology Domain-containing Integral Membrane Protein in the Photoreceptor Outer Segments. Journal of Biological Chemistry. 274(50). 35676–35685. 18 indexed citations

Howell, P. Lynne, Mary Ann Turner, John Christodoulou, et al.. (1998). Intragenic complementation at the argininosuccinate lyase locus: Reconstruction of the active site. Journal of Inherited Metabolic Disease. 21(S1). 72–85. 16 indexed citations

Swanson, Deborah A., Carol L. Freund, Shunbin Xu, et al.. (1997). A Differential Hybridization Scheme to Identify Photoreceptor-Specific Genes. Genome Research. 7(5). 513–521. 9 indexed citations

10.

Freund, Carol L., Cheryl Y. Gregory‐Evans, Takahisa Furukawa, et al.. (1997). Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene () Essential for Maintenance of the Photoreceptor. Cell. 91(4). 543–553. 448 indexed citations

11.

Walker, David C., John Christodoulou, Louise R. Simard, et al.. (1997). Intragenic Complementation at the Human Argininosuccinate Lyase Locus. Journal of Biological Chemistry. 272(10). 6777–6783. 24 indexed citations

12.

Belecky‐Adams, Teri L., Stanislav I. Tomarev, Lynda Ploder, et al.. (1997). Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cells.. PubMed. 38(7). 1293–303. 203 indexed citations

13.

Burmeister, Margit, Jakub Novák, Mei-Ying Liang, et al.. (1996). Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nature Genetics. 12(4). 376–384. 426 indexed citations

14.

McInnes, Roderick R., Jakub Novák, & Lynda Ploder. (1994). The ocular retardation (or{sup J}) mouse has an ochre mutation in the homeobox gene Chx10: Direct evidence for Chx10 as a major determinant of retinal development. The American Journal of Human Genetics. 55. 2 indexed citations

15.

Liu, Ivy S.C, Lynda Ploder, Danka Vidgen, et al.. (1994). Developmental expression of a novel murine homeobox gene (Chx10): Evidence for roles in determination of the neuroretina and inner nuclear layer. Neuron. 13(2). 377–393. 328 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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