Elizabeth M. Sharp

2.2k citations

19 papers · 1.5k indexed · h-index 15

Cellular and Molecular Neuroscience top 2%
- Neuroscience and Neuropharmacology Research 4
- Photoreceptor and optogenetics research 3
- Neuroscience and Neural Engineering 3
Ophthalmology top 2%
- Retinal Diseases and Treatments 3
Molecular Biology top 5%
- Retinal Development and Disorders 12
- Ion channel regulation and function 6
- Retinoids in leukemia and cellular processes 5
Cell Biology top 10%
Cardiology and Cardiovascular Medicine top 10%
Radiology, Nuclear Medicine and Imaging
- Retinopathy of Prematurity Studies 4

Co-authors: William A. Catterall Todd Scheuer Marian M. Humphries Paul F. Kenna Denise M. Sheils Rajendra Kumar‐Singh Siobhán A. Jordan Vladimir Yarov‐Yarovoy
Cited by: Cellular and Molecular Neuroscience Ophthalmology Molecular Biology
Journals: Genomics (7 papers)Proceedings of the National Academy of Sciences (3 papers)Molecular and Cellular Neuroscience (2 papers)
Partner nations: Ireland United States Netherlands

In The Last Decade

Elizabeth M. Sharp

19 papers receiving 1.5k citations

Peers

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

The 25 scholars most cited alongside Elizabeth M. Sharp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Elizabeth M. Sharp Line = papers co-authored together Elizabeth M. Sharp links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Sequential formation of ion pairs during activation of a sodium channel voltage sensor Proceedings of the National Academy of Sciences ·Paul G. DeCaen,Vladimir Yarov‐Yarovoy,Elizabeth M. Sharp,Todd Scheuer,William A. Catterall	2009	115
2	Functional properties and differential neuromodulation of Nav1.6 channels Molecular and Cellular Neuroscience ·Yuan Chen,Frank H. Yu,Elizabeth M. Sharp,Daniel Beacham,Todd Scheuer,William A. Catterall	2008	103
3	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 ·Angela R. Cantrell,Verònica Vèlez Ruìz,Frank H. Yu,Brian J. Murphy,Elizabeth M. Sharp,Yusheng Qu,William A. Catterall,Todd Scheuer	2002	82
4	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 ·Vladimir Yarov‐Yarovoy,Jacob L. Brown,Elizabeth M. Sharp,Jeff J. Clare,Todd Scheuer,William A. Catterall	2001	203
5	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 ·Damian McHugh,Elizabeth M. Sharp,Todd Scheuer,William A. Catterall	2000	106
6	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 ·Gregory H. Hockerman,Blaise Z. Peterson,Elizabeth M. Sharp,M Auerbach,Todd Scheuer,William A. Catterall	1997	63
7	Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC) Cytogenetic and Genome Research ·S. van Soest,B. Henderson Sellers,L. Ingeborgh van den Born,E. M. Bleeker‐Wagemakers,Elizabeth M. Sharp,L. Sandkuijl,A. Westerveld,Arthur A. Bergen	1996	10
8	Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree Genomics ·G. Jane Farrar,Paul F. Kenna,Siobhán A. Jordan,Rajendra Kumar‐Singh,Marian M. Humphries,Elizabeth M. Sharp,Denise M. Sheils,Peter Humphries	1992	45
9	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 ·Siobhán A. Jordan,G. Jane Farrar,Rajendra Kumar‐Singh,Paul F. Kenna,Marian M. Humphries,S.M. Abazari,Elizabeth M. Sharp,Peter Humphries	1992	27
10	Autosomal dominant retinitis pigmentosa: Localization of a disease gene (RP6) to the short arm of chromosome 6 Genomics ·G. Jane Farrar,Siobhán A. Jordan,Paul F. Kenna,Marian M. Humphries,Rajendra Kumar‐Singh,Peter McWilliam,S.M. Abazari,Elizabeth M. Sharp,Peter Humphries	1991	55
11	A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa Nature ·G. Jane Farrar,Paul F. Kenna,Siobhán A. Jordan,Rajendra Kumar‐Singh,Marian M. Humphries,Elizabeth M. Sharp,Denise M. Sheils,Peter Humphries	1991	313
12	Autosomal dominant retinitis pigmentosa: A mutation in codon 178 of the rhodopsin gene in two families of celtic origin Genomics ·G. Jane Farrar,Paul F. Kenna,R M Redmond,TingJuan Wang,Peter McWilliam,Marian M. Humphries,Elizabeth M. Sharp,Siobhán A. Jordan,Rajendra Kumar‐Singh,Peter Humphries	1991	42
13	Epidermolysis bullosa: Evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex form Genomics ·Marian M. Humphries,Denise M. Sheils,Mark Lawler,G. Jane Farrar,Peter McWilliam,Paul F. Kenna,Daniel G. Bradley,Elizabeth M. Sharp,米盖尔·马丁,Martin A. Young,Jouni Uitto,Peter Humphries	1990	17
14	Autosomal dominant retinitis pigmentosa: Linkage to rhodopsin and evidence for genetic heterogeneity Genomics ·张嫣然,Peter McWilliam,Daniel G. Bradley,Paul F. Kenna,Mark Lawler,Elizabeth M. Sharp,Marian M. Humphries,Stephan Stilgenbauer,G. Claflin,James A. Trofatter,Peter Humphries	1990	88
15	Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline->histidine substitution (codon 23) in pedigrees from Europe PubMed ·G. Jane Farrar,Paul F. Kenna,R M Redmond,Peter McWilliam,Daniel G. Bradley,Marian M. Humphries,Elizabeth M. Sharp,C.F. Inglehearn,R. Bashir,Marcelle Jay,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	1990	55
16	Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3 Genomics ·Peter McWilliam,G. Jane Farrar,Paul F. Kenna,Daniel G. Bradley,Marian M. Humphries,Elizabeth M. Sharp,David J. McConnell,Mark Lawler,Denise M. Sheils,朱昱静,Karen Stevens,Stephen P. Daiger,Peter Humphries	1989	160
17	Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21 Genomics ·G. Jane Farrar,Peter McWilliam,Elizabeth M. Sharp,Paul F. Kenna,Daniel G. Bradley,Marian M. Humphries,David J. McConnell,Peter Humphries	1989	8
18	Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups Cytogenetic and Genome Research ·Xavier Bisaro,Marian M. Humphries,Bae-Geun Lee,Elizabeth M. Sharp,Peter McWilliam,Jorge A. Castelán-Pedraza,Daniel G. Bradley,Paul F. Kenna,David J. McConnell,R S Sparkes,M. Anne Spence,John R. Heckenlively,Peter Humphries	1989	10
19	Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus. PubMed ·Daniel G. Bradley,G. Jane Farrar,Elizabeth M. Sharp,Paul F. Kenna,Marian M. Humphries,David J. McConnell,Stephen P. Daiger,Peter McWilliam,Peter Humphries	1989	11

About Elizabeth M. Sharp

Elizabeth M. Sharp is a scholar working on Cellular and Molecular Neuroscience, Ophthalmology and Molecular Biology, having authored 19 papers that have together received 1.5k indexed citations. Recurring topics across this work include Retinal Development and Disorders (12 papers), Ion channel regulation and function (6 papers), Retinoids in leukemia and cellular processes (5 papers), Neuroscience and Neuropharmacology Research (4 papers), Retinopathy of Prematurity Studies (4 papers), Photoreceptor and optogenetics research (3 papers), Retinal Diseases and Treatments (3 papers) and Neuroscience and Neural Engineering (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (657 citations), Ophthalmology (222 citations) and Molecular Biology (1.4k citations). Elizabeth M. Sharp has collaborated with scholars based in Ireland, United States and Netherlands. Frequent co-authors include William A. Catterall, Todd Scheuer, Marian M. Humphries, Paul F. Kenna, Denise M. Sheils, Rajendra Kumar‐Singh, Siobhán A. Jordan, Vladimir Yarov‐Yarovoy, Peter Humphries and G. Jane Farrar. Their work appears in journals such as Genomics, Proceedings of the National Academy of Sciences, Molecular and Cellular Neuroscience, Cytogenetic and Genome Research and The American Journal of Human Genetics.

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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