Beth A. Kozel

3.3k total citations
64 papers, 1.6k citations indexed

About

Beth A. Kozel is a scholar working on Genetics, Developmental Neuroscience and Molecular Biology. According to data from OpenAlex, Beth A. Kozel has authored 64 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 29 papers in Developmental Neuroscience and 16 papers in Molecular Biology. Recurrent topics in Beth A. Kozel's work include Williams Syndrome Research (29 papers), Connective tissue disorders research (21 papers) and Cardiomyopathy and Myosin Studies (8 papers). Beth A. Kozel is often cited by papers focused on Williams Syndrome Research (29 papers), Connective tissue disorders research (21 papers) and Cardiomyopathy and Myosin Studies (8 papers). Beth A. Kozel collaborates with scholars based in United States, Canada and Hungary. Beth A. Kozel's co-authors include Robert P. Mecham, Elaine C. Davis, Russell H. Knutsen, Thomas J. Broekelmann, Barbara R. Pober, Hiroshi Wachi, Christopher Ciliberto, András Czirók, Brenda J. Rongish and Jessica E. Wagenseil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Beth A. Kozel

63 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beth A. Kozel United States 22 792 515 295 212 185 64 1.6k
Makoto Migita Japan 19 269 0.3× 640 1.2× 113 0.4× 57 0.3× 103 0.6× 70 1.8k
Christina A. Pacak United States 21 651 0.8× 1.6k 3.2× 69 0.2× 405 1.9× 53 0.3× 68 2.4k
Koichi Miyake Japan 26 379 0.5× 1.2k 2.4× 53 0.2× 69 0.3× 53 0.3× 73 2.1k
Thomas D. Arnold United States 20 110 0.1× 661 1.3× 89 0.3× 76 0.4× 287 1.6× 30 2.0k
M. L. Chu United States 27 449 0.6× 965 1.9× 29 0.1× 159 0.8× 101 0.5× 53 2.1k
T. Grimm Germany 28 618 0.8× 1.6k 3.0× 77 0.3× 317 1.5× 34 0.2× 100 2.3k
Michael J. Workman United States 19 173 0.2× 808 1.6× 62 0.2× 86 0.4× 180 1.0× 31 2.0k
Guibin Chen United States 17 264 0.3× 1.6k 3.2× 69 0.2× 55 0.3× 62 0.3× 30 2.3k
Andrew S. Lee United States 21 257 0.3× 1.8k 3.6× 77 0.3× 112 0.5× 71 0.4× 28 2.5k
Mirella Meregalli Italy 23 154 0.2× 1.3k 2.5× 73 0.2× 113 0.5× 43 0.2× 64 1.8k

Countries citing papers authored by Beth A. Kozel

Since Specialization
Citations

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

Fields of papers citing papers by Beth A. Kozel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beth A. Kozel. 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 Beth A. Kozel. The network helps show where Beth A. Kozel may publish in the future.

Co-authorship network of co-authors of Beth A. Kozel

This figure shows the co-authorship network connecting the top 25 collaborators of Beth A. Kozel. A scholar is included among the top collaborators of Beth A. Kozel 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 Beth A. Kozel. Beth A. Kozel 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.
2.
Boechler, Michael, Yi‐Ping Fu, Sharon Osgood, et al.. (2024). Gastrointestinal manifestations in Williams syndrome: A prospective analysis of an adult and pediatric cohort. American Journal of Medical Genetics Part A. 194(12). e63827–e63827. 2 indexed citations
3.
Kozel, Beth A., et al.. (2024). A comparative evaluation of ChatGPT 3.5 and ChatGPT 4 in responses to selected genetics questions. Journal of the American Medical Informatics Association. 31(10). 2271–2283. 12 indexed citations
4.
Jacob, Benjamin, et al.. (2024). Genetic Testing for Supravalvar Aortic Stenosis: What to Do When It Is Not Williams Syndrome. Journal of the American Heart Association. 13(8). e034048–e034048. 2 indexed citations
5.
Huryn, Laryssa A., Lev Prasov, Wadih M. Zein, et al.. (2022). Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome. British Journal of Ophthalmology. 107(10). 1554–1559. 3 indexed citations
6.
Levin, Mark, et al.. (2022). Heart Rate Variability Analysis May Identify Individuals With Williams-Beuren Syndrome at Risk of Sudden Death. JACC. Clinical electrophysiology. 9(3). 359–370. 1 indexed citations
7.
Knutsen, Russell H., Danielle Donahue, Danielle Springer, et al.. (2022). Elastin Insufficiency Confers Proximal and Distal Pulmonary Vasculopathy in Mice, Partially Remedied by the KATP Channel Opener Minoxidil: Considerations and Cautions for the Treatment of People With Williams-Beuren Syndrome. Frontiers in Cardiovascular Medicine. 9. 886813–886813. 2 indexed citations
8.
Luperchio, Teresa Romeo & Beth A. Kozel. (2022). Extending the spectrum in aortopathy: stenosis to aneurysm. Current Opinion in Genetics & Development. 76. 101962–101962. 2 indexed citations
9.
10.
Park, Ki-Sun, Beenish Rahat, Hyung Chul Lee, et al.. (2021). Cardiac pathologies in mouse loss of imprinting models are due to misexpression of H19 long noncoding RNA. eLife. 10. 8 indexed citations
11.
Knutsen, Russell H., Carmen M. Halabi, Daniela Malide, et al.. (2021). Inhibition of NOX1 Mitigates Blood Pressure Increases in Elastin Insufficiency. Function. 2(3). zqab015–zqab015. 8 indexed citations
12.
Kozel, Beth A., Boaz Barak, Chong Ae Kim, et al.. (2021). Williams syndrome. Nature Reviews Disease Primers. 7(1). 42–42. 116 indexed citations
13.
Lin, Michelle, Robyn Roth, Beth A. Kozel, Robert P. Mecham, & Carmen M. Halabi. (2021). Loss of Angiotensin II Type 2 Receptor Improves Blood Pressure in Elastin Insufficiency. Frontiers in Cardiovascular Medicine. 8. 782138–782138. 5 indexed citations
14.
Levin, Mark, Simona Bianconi, Niamh X. Cawley, et al.. (2021). X-linked creatine transporter deficiency results in prolonged QTc and increased sudden death risk in humans and disease model. Genetics in Medicine. 23(10). 1864–1872. 12 indexed citations
15.
Addissie, Yonit A., Paul Kruszka, Zoë C. Wong, et al.. (2020). Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study. Environmental Health. 19(1). 65–65. 27 indexed citations
16.
Liu, Delong, Russell H. Knutsen, Charles J. Billington, et al.. (2020). Whole exome sequencing in patients with Williams–Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk. Human Molecular Genetics. 29(12). 2035–2050. 13 indexed citations
17.
Hirano, Eiichi, Russell H. Knutsen, Adrian Shifren, et al.. (2012). Alternative Splicing and Tissue-specific Elastin Misassembly Act as Biological Modifiers of Human Elastin Gene Frameshift Mutations Associated with Dominant Cutis Laxa. Journal of Biological Chemistry. 287(26). 22055–22067. 28 indexed citations
18.
Kozel, Beth A., Russell H. Knutsen, Ye Li, et al.. (2011). Genetic Modifiers of Cardiovascular Phenotype Caused by Elastin Haploinsufficiency Act by Extrinsic Noncomplementation. Journal of Biological Chemistry. 286(52). 44926–44936. 32 indexed citations
19.
Czirók, András, et al.. (2005). Elastic fiber macro‐assembly is a hierarchical, cell motion‐mediated process. Journal of Cellular Physiology. 207(1). 97–106. 73 indexed citations
20.
Kozel, Beth A., Christopher Ciliberto, & Robert P. Mecham. (2004). Deposition of tropoelastin into the extracellular matrix requires a competent elastic fiber scaffold but not live cells. Matrix Biology. 23(1). 23–34. 61 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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