Linda C. Walker

692 total citations
14 papers, 517 citations indexed

About

Linda C. Walker is a scholar working on Genetics, Molecular Biology and Urology. According to data from OpenAlex, Linda C. Walker has authored 14 papers receiving a total of 517 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Urology. Recurrent topics in Linda C. Walker's work include Connective tissue disorders research (11 papers), Microbial metabolism and enzyme function (4 papers) and Dermatological and Skeletal Disorders (3 papers). Linda C. Walker is often cited by papers focused on Connective tissue disorders research (11 papers), Microbial metabolism and enzyme function (4 papers) and Dermatological and Skeletal Disorders (3 papers). Linda C. Walker collaborates with scholars based in United States, Netherlands and Finland. Linda C. Walker's co-authors include Heather N. Yeowell, Sheldon R. Pinnell, Mark Levine, Nancy A. Monteiro‐Riviere, Saood Murad, Raili Myllylä, Jari Heikkinen, Luitgard M. Neumann, Dorothy K. Grange and Joan C. Marini and has published in prestigious journals such as Archives of Biochemistry and Biophysics, Journal of Investigative Dermatology and Human Mutation.

In The Last Decade

Linda C. Walker

14 papers receiving 467 citations

Peers

Linda C. Walker
Shingo Tajima Japan
Philipp M. Amann Germany
Megumi Tobiishi Japan
Michelle L. Kerns United States
Alix Gazel United States
Amandine Scandolera France
J. M. Tixier France
Takako Baba Japan
C. Pain France
Richard I. Schwarz United States
Shingo Tajima Japan
Linda C. Walker
Citations per year, relative to Linda C. Walker Linda C. Walker (= 1×) peers Shingo Tajima

Countries citing papers authored by Linda C. Walker

Since Specialization
Citations

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

Fields of papers citing papers by Linda C. Walker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Linda C. Walker. 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 Linda C. Walker. The network helps show where Linda C. Walker may publish in the future.

Co-authorship network of co-authors of Linda C. Walker

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

All Works

14 of 14 papers shown
1.
Yeowell, Heather N., Linda C. Walker, David Mauger, Puneet Seth, & Mariano A. García-Blanco. (2008). TIA Nuclear Proteins Regulate the Alternate Splicing of Lysyl Hydroxylase 2. Journal of Investigative Dermatology. 129(6). 1402–1411. 12 indexed citations
2.
Yeowell, Heather N., Linda C. Walker, & Luitgard M. Neumann. (2006). An Ehlers-Danlos syndrome type VIA patient with cystic malformations of the meninges.. PubMed. 15(5). 353–8. 11 indexed citations
3.
Walker, Linda C., Adnan H. Siddiqui, Anne De Paepe, et al.. (2005). A Novel Mutation in the Lysyl Hydroxylase 1 Gene Causes Decreased Lysyl Hydroxylase Activity in an Ehlers–Danlos VIA Patient. Journal of Investigative Dermatology. 124(5). 914–918. 17 indexed citations
4.
Pinnell, Sheldon R., et al.. (2001). Topical L-Ascorbic Acid: Percutaneous Absorption Studies. Dermatologic Surgery. 27(2). 137–142. 159 indexed citations
5.
Pinnell, Sheldon R., et al.. (2001). Topical L-Ascorbic Acid. Dermatologic Surgery. 27(2). 137–142. 5 indexed citations
6.
7.
Yeowell, Heather N., et al.. (2000). Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activity and causes Ehlers–Danlos syndrome type VI. Matrix Biology. 19(1). 37–46. 18 indexed citations
8.
Yeowell, Heather N. & Linda C. Walker. (2000). Mutations in the Lysyl Hydroxylase 1 Gene That Result in Enzyme Deficiency and the Clinical Phenotype of Ehlers–Danlos Syndrome Type VI. Molecular Genetics and Metabolism. 71(1-2). 212–224. 117 indexed citations
9.
Yeowell, Heather N. & Linda C. Walker. (1999). Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene. Matrix Biology. 18(2). 179–187. 73 indexed citations
10.
Yeowell, Heather N. & Linda C. Walker. (1999). Prenatal Exclusion of Ehlers‐Danlos Syndrome Type VI by Mutational Analysis. PubMed. 111(1). 57–62. 7 indexed citations
11.
Walker, Linda C., Joan C. Marini, Dorothy K. Grange, Jane D. Filie, & Heather N. Yeowell. (1999). A Patient with Ehlers-Danlos Syndrome Type VI Is Homozygous for a Premature Termination Codon in Exon 14 of the Lysyl Hydroxylase 1 Gene. Molecular Genetics and Metabolism. 67(1). 74–82. 15 indexed citations
12.
Yeowell, Heather N., Linda C. Walker, Saood Murad, & Sheldon R. Pinnell. (1997). A Common Duplication in the Lysyl Hydroxylase Gene of Patients with Ehlers Danlos Syndrome Type VI Results in Preferential Stimulation of Lysyl Hydroxylase Activity and mRNA by Hydralazine. Archives of Biochemistry and Biophysics. 347(1). 126–131. 6 indexed citations
13.
Murad, Saood, et al.. (1996). The Expression of a Functional, Secreted Human Lysyl Hydroxylase in a Baculovirus System. Journal of Investigative Dermatology. 106(1). 11–16. 16 indexed citations
14.

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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