Rosemary E. Kelsell

4.1k citations

20 papers · 2.4k indexed · 1 hit paper · h-index 17

Molecular Biology top 10%
Sensory Systems top 0.2%
Cellular and Molecular Neuroscience top 2%
Nutrition and Dietetics top 2%
Ophthalmology top 2%

Co-authors: Andrew D. Randall Christopher D. Benham Andrew D. Medhurst Menelas N. Pangalos Paul R. Murdock Shaun McNulty David M. Hunt Fiona S. Cusdin
Topics: Retinal Development and Disorders (7 papers)Retinal Diseases and Treatments (7 papers)Ion channel regulation and function (5 papers)
Cited by: Sensory Systems Cellular and Molecular Neuroscience Ophthalmology
Journals: Nature Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: United Kingdom United States Germany

In The Last Decade

Rosemary E. Kelsell

19 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

TRPV3 is a temperature-sensitive vanilloid receptor-like protein

2002 633 citations George Davey Smith, Martin J. Gunthorpe et al. Nature profile →

Peers

Countries citing papers authored by Rosemary E. Kelsell

Since Specialization

Citations

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

Fields of papers citing papers by Rosemary E. Kelsell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosemary E. Kelsell. 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 Rosemary E. Kelsell. The network helps show where Rosemary E. Kelsell may publish in the future.

Co-authorship network of co-authors of Rosemary E. Kelsell

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders 2018 ·Genetics in Medicine ·Caroline F. Wright,Jeremy F. McRae,Stephen Clayton,Giuseppe Gallone,Stuart Aitken,Tomas Fitzgerald,(unknown),Elena Prigmore,Diana Rajan,Jenny Lord,Alejandro Sifrim,Rosemary E. Kelsell,Michael Parker,Jeffrey C. Barrett,Matthew E. Hurles,David Fitzpatrick,Helen V. Firth	193
2	Identification of a novel 5-HT4 receptor splice variant (r5-HT4c1) and preliminary characterisation of specific 5-HT4a and 5-HT4b receptor antibodies 2008 ·European Journal of Pharmacology ·Alison M. Ray,Rosemary E. Kelsell,(unknown),F. M. Kelly,Andrew D. Medhurst,Helen M. Cox,Andrew R. Calver	16
3	Tissue Distribution Profiles of the Human TRPM Cation Channel Family 2006 ·Journal of Receptors and Signal Transduction ·Elena Fonfría,Paul R. Murdock,Fiona S. Cusdin,Christopher D. Benham,Rosemary E. Kelsell,Shaun McNulty	292
4	Characterisation of recombinant rat TRPM2 and a TRPM2-like conductance in cultured rat striatal neurones 2005 ·Neuropharmacology ·Kerstin Hill,Natalie J. Tigue,Rosemary E. Kelsell,Christopher D. Benham,Shaun McNulty,Michael Schaefer,Andrew D. Randall	51
5	Hybridization and Competition Hybridization of Southern Blots 2003 ·Humana Press eBooks ·Rosemary E. Kelsell	0
6	TRPV3 is a temperature-sensitive vanilloid receptor-like proteinbreakdown → 2002 ·Nature ·George Davey Smith,Martin J. Gunthorpe,Rosemary E. Kelsell,Philip D. Hayes,Peter J. Reilly,P. Facer,James E. Wright,Jeffrey C. Jerman,Jean‐Philippe Walhin,Lezanne Ooi,Julie Egerton,Charles Kornreich,D Smart,Andrew D. Randall,Praveen Anand,Janet L. Davis	633
7	Cloning and Functional Expression of Human Short TRP7, a Candidate Protein for Store-operated Ca2+ Influx 2002 ·Journal of Biological Chemistry ·Antonio Riccio,César Mattei,Rosemary E. Kelsell,Andrew D. Medhurst,Andrew R. Calver,Andrew D. Randall,John B. Davis,Christopher D. Benham,Menelas N. Pangalos	89
8	mRNA distribution analysis of human TRPC family in CNS and peripheral tissues 2002 ·Molecular Brain Research ·Antonio Riccio,Andrew D. Medhurst,César Mattei,Rosemary E. Kelsell,Andrew R. Calver,Andrew D. Randall,Christopher D. Benham,Menelas N. Pangalos	271
9	mRNA distribution analysis of TRPC family in human CNS and peripheral tissues 2002 ·University of Hertfordshire Research Archive (University of Hertfordshire) ·Andrea Riccio,Andrew D. Medhurst,César Mattei,Rosemary E. Kelsell,Andrew R. Calver,Andrew D. Randall,Christopher D. Benham,Menelas N. Pangalos	1
10	The neuroprotective agent sipatrigine (BW619C89) potently inhibits the human tandem pore-domain K+ channels TREK-1 and TRAAK 2001 ·Brain Research ·H.J. Meadows,C.G. Chapman,D. Malcolm Duckworth,Rosemary E. Kelsell,Paul R. Murdock,S. Nasir,(unknown),Andrew D. Randall	47
11	Distribution analysis of human two pore domain potassium channels in tissues of the central nervous system and periphery 2001 ·Molecular Brain Research ·Andrew D. Medhurst,(unknown),C.G. Chapman,H.J. Meadows,(unknown),Rosemary E. Kelsell,Israel Gloger,Menelas N. Pangalos	252
12	Cloning, localisation and functional expression of a novel human, cerebellum specific, two pore domain potassium channel 2000 ·Molecular Brain Research ·C.G. Chapman,H.J. Meadows,(unknown),David A. Campbell,Malcolm Duckworth,Rosemary E. Kelsell,Paul R. Murdock,Andrew D. Randall,(unknown),Israel Gloger	77
13	Autosomal dominant cone–rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D , which encodes retinal guanylate cyclase 1 1The authors have no proprietary interests in the materials mentioned in the study. 2000 ·Ophthalmology ·Kevin Gregory-Evans,Rosemary E. Kelsell,Cheryl Y. Gregory‐Evans,Susan M. Downes,Fred W. Fitzke,G.E. Holder,Matthew P. Simunovic,J. D. Mollon,Rachel M. Taylor,David M. Hunt,Alan C. Bird,Anthony T. Moore	77
14	North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis. 1999 ·PubMed ·Kent W. Small,Nitin Udar,(unknown),Robert R. Klein,Charles García,Guillermo Gallardo Madueño,Bernard Puech,Virginie Puech,David A. Saperstein,Jennifer I. Lim,József Haller,Christina J. Flaxel,Rosemary E. Kelsell,David M. Hunt,Kevin Gregory-Evans,Felicia Lennon,M. A. Pericak‐Vance	36
15	Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone–rod dystrophy 1999 ·Proceedings of the National Academy of Sciences ·Chandra L. Tucker,Sarah C. Woodcock,Rosemary E. Kelsell,Visvanathan Ramamurthy,David M. Hunt,James B. Hurley	87
16	Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy 1998 ·Human Molecular Genetics ·Rosemary E. Kelsell,Kevin Gregory-Evans,Annette Payne,Isabelle Perrault,Josseline Kaplan,Ruey‐Bing Yang,David L. Garbers,Alan C. Bird,Anthony T. Moore,David M. Hunt	187
17	Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1). 1998 ·Journal of Medical Genetics ·Andrea Gehrig,Ute Felbor,Rosemary E. Kelsell,David M. Hunt,Irene H. Maumenee,Bernhard H. F. Weber	14
18	Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p 1997 ·Human Molecular Genetics ·Rosemary E. Kelsell	40
19	Clinical Features of Progressive Bifocal Chonoretinal Atrophy 1996 ·Ophthalmology ·Bernard F. Godley,(unknown),Kevin Gregory-Evans,Rosemary E. Kelsell,David M. Hunt,A.C. Bird	25
20	Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q 1995 ·Human Molecular Genetics ·Rosemary E. Kelsell,Bernard F. Godley,Kevin Gregory-Evans,(unknown),Cheryl Y. Gregory,Catherine Plant,(unknown),Alan C. Bird,David M. Hunt	38

About Rosemary E. Kelsell

Rosemary E. Kelsell is a scholar working on Sensory Systems, Ophthalmology and Cellular and Molecular Neuroscience, having authored 20 papers that have together received 2.4k indexed citations. Recurring topics across this work include Retinal Development and Disorders (7 papers), Retinal Diseases and Treatments (7 papers) and Ion channel regulation and function (5 papers). The work is most often cited by research in Sensory Systems (1.2k citations), Cellular and Molecular Neuroscience (743 citations) and Ophthalmology (309 citations). Rosemary E. Kelsell has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Andrew D. Randall, Christopher D. Benham, Andrew D. Medhurst, Menelas N. Pangalos, Paul R. Murdock, Shaun McNulty, David M. Hunt, Fiona S. Cusdin, Elena Fonfría and Andrew R. Calver. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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