Elizabeth M. Sharp

2.2k total citations
19 papers, 1.5k citations indexed

About

Elizabeth M. Sharp is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Elizabeth M. Sharp has authored 19 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Elizabeth M. Sharp's work include Retinal Development and Disorders (12 papers), Ion channel regulation and function (6 papers) and Retinoids in leukemia and cellular processes (5 papers). Elizabeth M. Sharp is often cited by papers focused on Retinal Development and Disorders (12 papers), Ion channel regulation and function (6 papers) and Retinoids in leukemia and cellular processes (5 papers). Elizabeth M. Sharp collaborates with scholars based in Ireland, United States and Netherlands. Elizabeth M. Sharp's co-authors include Todd Scheuer, William A. Catterall, Paul F. Kenna, Marian M. Humphries, Denise M. Sheils, Rajendra Kumar‐Singh, Siobhán A. Jordan, Vladimir Yarov‐Yarovoy, Peter Humphries and G. Jane Farrar and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Elizabeth M. Sharp

19 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elizabeth M. Sharp Ireland	15	1.4k	657	231	222	201	19	1.5k
Maxim Sokolov Russia	19	1.0k 0.8×	617 0.9×	58 0.3×	110 0.5×	178 0.9×	38	1.4k
Norbert Tinel France	11	1.1k 0.8×	661 1.0×	369 1.6×	16 0.1×	65 0.3×	11	1.4k
Günter Niemeyer Switzerland	20	928 0.7×	551 0.8×	25 0.1×	405 1.8×	78 0.4×	66	1.2k
M.B.A. Djamgoz United Kingdom	14	763 0.6×	315 0.5×	71 0.3×	107 0.5×	67 0.3×	24	1.2k
Nikolai O. Artemyev United States	34	3.0k 2.2×	1.1k 1.7×	45 0.2×	288 1.3×	383 1.9×	118	3.2k
Neil J. Cook Germany	18	1.4k 1.0×	1.1k 1.7×	116 0.5×	53 0.2×	127 0.6×	28	1.7k
Lisa Ebihara United States	29	2.7k 2.0×	398 0.6×	579 2.5×	176 0.8×	84 0.4×	45	3.1k
Irina Surgucheva United States	26	1.1k 0.8×	658 1.0×	35 0.2×	347 1.6×	315 1.6×	35	1.7k
Artur Llobet Spain	19	651 0.5×	472 0.7×	21 0.1×	126 0.6×	257 1.3×	42	1.1k
T L Deckwerth United States	10	1.2k 0.9×	895 1.4×	20 0.1×	60 0.3×	226 1.1×	10	1.7k

Countries citing papers authored by Elizabeth M. Sharp

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth M. Sharp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth M. Sharp. 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 Elizabeth M. Sharp. The network helps show where Elizabeth M. Sharp may publish in the future.

Co-authorship network of co-authors of Elizabeth M. Sharp

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

All Works

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19 of 19 papers shown

DeCaen, Paul G., Vladimir Yarov‐Yarovoy, Elizabeth M. Sharp, Todd Scheuer, & William A. Catterall. (2009). Sequential formation of ion pairs during activation of a sodium channel voltage sensor. Proceedings of the National Academy of Sciences. 106(52). 22498–22503. 115 indexed citations

Chen, Yuan, Frank H. Yu, Elizabeth M. Sharp, et al.. (2008). Functional properties and differential neuromodulation of Nav1.6 channels. Molecular and Cellular Neuroscience. 38(4). 607–615. 103 indexed citations

Cantrell, Angela R., Frank H. Yu, Brian J. Murphy, et al.. (2002). Molecular Mechanism of Convergent Regulation of Brain Na+ Channels by Protein Kinase C and Protein Kinase A Anchored to AKAP-15. Molecular and Cellular Neuroscience. 21(1). 63–80. 82 indexed citations

Yarov‐Yarovoy, Vladimir, Jacob L. Brown, Elizabeth M. Sharp, et al.. (2001). Molecular Determinants of Voltage-dependent Gating and Binding of Pore-blocking Drugs in Transmembrane Segment IIIS6 of the Na+ Channel α Subunit. Journal of Biological Chemistry. 276(1). 20–27. 203 indexed citations

McHugh, Damian, Elizabeth M. Sharp, Todd Scheuer, & William A. Catterall. (2000). Inhibition of cardiac L-type calcium channels by protein kinase C phosphorylation of two sites in the N-terminal domain. Proceedings of the National Academy of Sciences. 97(22). 12334–12338. 106 indexed citations

Hockerman, Gregory H., et al.. (1997). Construction of a high-affinity receptor site for dihydropyridine agonists and antagonists by single amino acid substitutions in a non- l -type Ca ²⁺ channel. Proceedings of the National Academy of Sciences. 94(26). 14906–14911. 63 indexed citations

Soest, S. van, L. Ingeborgh van den Born, E. M. Bleeker‐Wagemakers, et al.. (1996). Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC). Cytogenetic and Genome Research. 73(1-2). 81–85. 10 indexed citations

Farrar, G. Jane, Paul F. Kenna, Siobhán A. Jordan, et al.. (1992). Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree. Genomics. 14(3). 805–807. 45 indexed citations

Jordan, Siobhán A., G. Jane Farrar, Rajendra Kumar‐Singh, et al.. (1992). Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.. The American Journal of Human Genetics. 50(3). 634–9. 27 indexed citations

10.

Farrar, G. Jane, Siobhán A. Jordan, Paul F. Kenna, et al.. (1991). Autosomal dominant retinitis pigmentosa: Localization of a disease gene (RP6) to the short arm of chromosome 6. Genomics. 11(4). 870–874. 55 indexed citations

11.

Farrar, G. Jane, Paul F. Kenna, Siobhán A. Jordan, et al.. (1991). A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa. Nature. 354(6353). 478–480. 313 indexed citations

12.

Farrar, G. Jane, Paul F. Kenna, R M Redmond, et al.. (1991). Autosomal dominant retinitis pigmentosa: A mutation in codon 178 of the rhodopsin gene in two families of celtic origin. Genomics. 11(4). 1170–1171. 42 indexed citations

13.

Humphries, Marian M., Denise M. Sheils, Mark Lawler, et al.. (1990). Epidermolysis bullosa: Evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex form. Genomics. 7(3). 377–381. 17 indexed citations

14.

Farrar, G. Jane, Paul F. Kenna, R M Redmond, et al.. (1990). Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline->histidine substitution (codon 23) in pedigrees from Europe. PubMed. 47(6). 941–5. 55 indexed citations

15.

McWilliam, Peter, Daniel G. Bradley, Paul F. Kenna, et al.. (1990). Autosomal dominant retinitis pigmentosa: Linkage to rhodopsin and evidence for genetic heterogeneity. Genomics. 8(1). 35–40. 88 indexed citations

16.

Bradley, Daniel G., G. Jane Farrar, Elizabeth M. Sharp, et al.. (1989). Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus.. PubMed. 44(4). 570–6. 11 indexed citations

17.

Humphries, Marian M., Elizabeth M. Sharp, Peter McWilliam, et al.. (1989). Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups. Cytogenetic and Genome Research. 50(4). 181–187. 10 indexed citations

18.

Farrar, G. Jane, Peter McWilliam, Elizabeth M. Sharp, et al.. (1989). Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21. Genomics. 5(3). 612–618. 8 indexed citations

19.

McWilliam, Peter, G. Jane Farrar, Paul F. Kenna, et al.. (1989). Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3. Genomics. 5(3). 619–622. 160 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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