Heather N. Yeowell

1.8k total citations
42 papers, 1.3k citations indexed

About

Heather N. Yeowell is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Heather N. Yeowell has authored 42 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 20 papers in Molecular Biology and 7 papers in Rheumatology. Recurrent topics in Heather N. Yeowell's work include Connective tissue disorders research (28 papers), Dermatological and Skeletal Disorders (9 papers) and Microbial metabolism and enzyme function (6 papers). Heather N. Yeowell is often cited by papers focused on Connective tissue disorders research (28 papers), Dermatological and Skeletal Disorders (9 papers) and Microbial metabolism and enzyme function (6 papers). Heather N. Yeowell collaborates with scholars based in United States, Netherlands and Belgium. Heather N. Yeowell's co-authors include Linda C. Walker, James R. White, Melanie K. Marshall, Patricia Linko, Beat Steinmann, S.R. Pinnell, Lary C. Walker, Jorge Goldstein, Sheldon R. Pinnell and Saood Murad and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Biochemistry.

In The Last Decade

Heather N. Yeowell

42 papers receiving 1.2k citations

Peers

Heather N. Yeowell
M A Giambrone United States
Aaron E. Freeman United States
Y Niitsu Japan
E Abe Japan
Elizabeth M. Algar Australia
Ying Bao China
J Frei Canada
Nam‐ho Huh Japan
Miho Shiokawa Japan
B. Goldberg United States
M A Giambrone United States
Heather N. Yeowell
Citations per year, relative to Heather N. Yeowell Heather N. Yeowell (= 1×) peers M A Giambrone

Countries citing papers authored by Heather N. Yeowell

Since Specialization
Citations

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

Fields of papers citing papers by Heather N. Yeowell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heather N. Yeowell. 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 Heather N. Yeowell. The network helps show where Heather N. Yeowell may publish in the future.

Co-authorship network of co-authors of Heather N. Yeowell

This figure shows the co-authorship network connecting the top 25 collaborators of Heather N. Yeowell. A scholar is included among the top collaborators of Heather N. Yeowell 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 Heather N. Yeowell. Heather N. Yeowell 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.
Yeowell, Heather N. & S.R. Pinnell. (2020). The Ehlers-Danlos syndromes. Nature Reviews Disease Primers. 6(1). 229–40. 9 indexed citations
2.
Yeowell, Heather N. & Beat Steinmann. (2018). PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome. 13 indexed citations
3.
Seth, Puneet & Heather N. Yeowell. (2010). Fox‐2 protein regulates the alternative splicing of scleroderma‐associated lysyl hydroxylase 2 messenger RNA. Arthritis & Rheumatism. 62(4). 1167–1175. 12 indexed citations
4.
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
5.
Giunta, Cecilia, Nursel Elçioğlu, Beate Albrecht, et al.. (2008). Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13. The American Journal of Human Genetics. 82(6). 1290–1305. 149 indexed citations
6.
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
7.
Walker, Lary C., Marcia Willing, Joan C. Marini, et al.. (2004). Heterogeneous basis of the type VIB form of Ehlers–Danlos syndrome (EDS VIB) that is unrelated to decreased collagen lysyl hydroxylation. American Journal of Medical Genetics Part A. 131A(2). 155–162. 16 indexed citations
8.
Walker, Lary C., Ahmad S. Teebi, Joan C. Marini, et al.. (2004). Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene. Molecular Genetics and Metabolism. 83(4). 312–321. 10 indexed citations
9.
Uzawa, Katsuhiro, Heather N. Yeowell, Kazushi Yamamoto, et al.. (2003). Lysine hydroxylation of collagen in a fibroblast cell culture system. Biochemical and Biophysical Research Communications. 305(3). 484–487. 23 indexed citations
10.
11.
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
12.
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
13.
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
14.
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
15.
Yeowell, Heather N., et al.. (1994). Regulation of Lysyl Oxidase mRNA in Dermal Fibroblasts from Normal Donors and Patients with Inherited Connective Tissue Disorders. Archives of Biochemistry and Biophysics. 308(1). 299–305. 48 indexed citations
16.
Marshall, Melanie K., et al.. (1994). A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene.. Journal of Clinical Investigation. 93(4). 1716–1721. 47 indexed citations
17.
Yeowell, Heather N., et al.. (1994). Sequence Analysis of a cDNA for Lysyl Hydroxylase Isolated from Human Skin Fibroblasts from a Normal Donor: Differences from Human Placental Lysyl Hydroxylase cDNA. Journal of Investigative Dermatology. 102(3). 382–384. 22 indexed citations
18.
19.
Yeowell, Heather N., David J. Waxman, Gerald A. LeBlanc, Patricia Linko, & Joyce A. Goldstein. (1989). Suppression of male-specific cytochrome P450 2c and its mRNA by 3,4,5,3′,4′,5′-hexachlorobiphenyl in rat liver is not causally related to changes in serum testosterone. Archives of Biochemistry and Biophysics. 271(2). 508–514. 7 indexed citations
20.
Linko, Patricia, et al.. (1986). Induction of cytochrome P‐450 isozymes by hexachlorobenzene in rats and aromatic hydrocarbon (Ah)—Responsive mice. Journal of Biochemical Toxicology. 1(2). 95–107. 29 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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