Marcelle Jay

4.3k citations

70 papers · 2.9k indexed · h-index 26

Impact in

Ophthalmology top 0.5%
- Retinal Diseases and Treatments
- Ocular Oncology and Treatments
Molecular Biology top 5%
- Retinal Development and Disorders
- RNA regulation and disease
- Retinoids in leukemia and cellular processes
- Advanced biosensing and bioanalysis techniques

Papers in ⓘ

Ophthalmology 23
- Ocular Oncology and Treatments 16
Molecular Biology 52
- Retinal Development and Disorders 36
- Retinoids in leukemia and cellular processes 14
- RNA regulation and disease 10
- Advanced biosensing and bioanalysis techniques 10

Co-authors: Alan C. Bird (23 shared papers)Alan F. Wright (11 shared papers)Shomi S. Bhattacharya (7 shared papers)C.F. Inglehearn (8 shared papers)Fred W. Fitzke (4 shared papers)G. B. Arden (5 shared papers)Chris F. Inglehearn (8 shared papers)Siladitya Bhattacharya (8 shared papers)
Journals: Journal of Medical Genetics (7 papers)Human Molecular Genetics (5 papers)Eye (5 papers)British Journal of Ophthalmology (5 papers)Human Genetics (4 papers)
Partner nations: United Kingdom Mexico Australia

In The Last Decade

Marcelle Jay

69 papers receiving 2.8k citations

Peers

Countries citing papers authored by Marcelle Jay

Since Specialization

Citations

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

Fields of papers citing papers by Marcelle Jay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marcelle Jay. 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 Marcelle Jay. The network helps show where Marcelle Jay may publish in the future.

Co-authors

The 25 scholars most cited alongside Marcelle Jay, 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 Marcelle Jay Line = papers co-authored together Marcelle Jay links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 70 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) Nature Genetics ·A Meindl, Katherine L. Dry, Karin A. Herrmann, Forbes Manson, Alfredo Ciccodicola, Alexander J. Edgar, Maria Raquel Santos Carvalho, Helene Achatz, Heide Hellebrand, Alan Lennon, Carmela Migliaccio, Keith Porter, Eberhart Zrenner, Alan C. Bird, Marcelle Jay, Birgit Lorenz, B Wittwer, Michele D’Urso, Thomas Meitinger, Alan F. Wright	1996	391
2	Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy Nature Genetics ·John A. Wells, John J. Wroblewski, Jeffrey Keen, C.F. Inglehearn, C Jubb, Anja Eckstein, Marcelle Jay, G. B. Arden, Shomi S. Bhattacharya, Fred W. Fitzke, Alan C. Bird	1993	321
3	Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28 Nature ·Siladitya Bhattacharya, Alan F. Wright, John Clayton, W. H. Price, C I Phillips, C. McKeown, Marcelle Jay, Alan C. Bird, P. Pearson, E.M. Southern, H.J. Evans	1984	203
4	Lifetime Risks of Common Cancers Among Retinoblastoma Survivors JNCI Journal of the National Cancer Institute ·Olivia Fletcher, Douglas F. Easton, Kristin Anderson, Clare Gilham, Marcelle Jay, Julian Peto	2004	172
5	Localization of two genes for usher syndrome type I to chromosome 11 Genomics ·Richard J. Smith, E.C. Lee, William J. Kimberling, Stephen P. Daiger, Mary Z. Pelias, Bronya J.B. Keats, Marcelle Jay, Alan C. Bird, William Reardon, Mary Guest, Radha Ayyagari, J. Fielding Hejtmancik	1992	149
6	On the heredity of retinitis pigmentosa. British Journal of Ophthalmology ·Marcelle Jay	1982	134
7	A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosa Human Molecular Genetics ·Chris F. Inglehearn, T J Keen, Rumaisa Bashir, Marcelle Jay, Fred W. Fitzke, Alan C.Bird, A L Crombie, Shomi S. Bhattacharya	1992	101
8	A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa. PubMed ·C.F. Inglehearn, R. Bashir, Douglas H. Lester, Marcelle Jay, Alan C. Bird, Shoumo Bhattacharya	1991	94
9	Non-ocular cancer in relatives of retinoblastoma patients British Journal of Cancer ·B M Sanders, Marcelle Jay, G J Draper, E P Roberts	1989	87
10	Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19 Human Molecular Genetics ·Mai Al-Maghtheh, Chris F. Inglehearn, Tomkins Jeffrey, Kevin Gregory-Evans, Anthony T. Moore, Marcelle Jay, Alan C. Bird, Shomi S. Bhattacharya	1994	78
11	Gender and age at onset in schizophrenia: impact of family history American Journal of Psychiatry ·Philip Gorwood, Marion Leboyer, Marcelle Jay, Christopher Payan, J Feingold	1995	76
12	Macular Dystrophy Associated with Mutations at Codon 172 in the Human Retinal Degeneration Slow Gene Ophthalmology ·John J. Wroblewski, John A. Wells, Anja Eckstein, Fred W. Fitzke, Chris Jubb, T J Keen, Chris F. Inglehearn, Shomi S. Bhattacharya, G. B. Arden, Marcelle Jay, Alan C. Bird	1994	72
13	A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p Nature Genetics ·Chris F. Inglehearn, Simon Carter, TJeffrey Keen, Janet C. Lindsey, A. Stephenson, Rumaisa Bashir, May Al-Maghtheh, Anthony T. Moore, Marcelle Jay, Alan C. Bird, Shomi S. Bhattacharya	1993	69
14	Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients Human Molecular Genetics ·Hans van Bokhoven, Marianne Schwartz, Sten Andréasson, José A. J. M. van den Hurk, Liesbeth Bogerd, Marcelle Jay, Klaus Rüther, Barrie Jay, I. H. Pawlowitzki, Eeva‐Marja Sankila, Alan F. Wright, Hans‐Hilger Ropers, Thomas Rosenberg, Frans P.M. Cremers	1994	60
15	Heterogeneity analysis in 40 X-linked retinitis pigmentosa families. PubMed ·Peter Teague, Micheala A. Aldred, Marcelle Jay, Maureen Dempster, Christine J. Harrison, A D Carothers, L J Hardwick, H.J. Evans, Lisa Strain, D. J. H. Brock	1994	56
16	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
17	Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype. PubMed ·Mai Al-Maghtheh, Eranga N. Vithana, Emma E. Tarttelin, Marcelle Jay, Kevin Gregory-Evans, Tanya Moore, Siladitya Bhattacharya, Chris F. Inglehearn	1996	50
18	Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa British Journal of Ophthalmology ·Christina J. Flaxel, Marcelle Jay, Dawn L. Thiselton, M. V. Nayudu, Alison J. Hardcastle, Alan F. Wright, A.C. Bird	1999	47
19	Detection of the Carrier State of X-Linked Retinoschisis American Journal of Ophthalmology ·Michael B. Gorin, Philip J Polkinghorne, Marcelle Jay, G. B. Arden, Alan C. Bird	1988	41
20	Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14. PubMed ·Alan F. Wright, S.S. Bhattacharya, John Clayton, Maureen Dempster, P. Tippett, C. McKeown, Marcelle Jay, Barrie Jay, Alan C. Bird	1987	38

About Marcelle Jay

Marcelle Jay is a scholar working on Ophthalmology, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging, having authored 70 papers that have together received 2.9k indexed citations. Recurring topics across this work include Retinal Development and Disorders (36 papers), Ocular Oncology and Treatments (16 papers), Retinoids in leukemia and cellular processes (14 papers), RNA regulation and disease (10 papers), Advanced biosensing and bioanalysis techniques (10 papers), Photoreceptor and optogenetics research (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers) and Cancer-related Molecular Pathways (7 papers). The work is most often cited by research in Ophthalmology (978 citations), Molecular Biology (2.3k citations), Cell Biology (458 citations), Cellular and Molecular Neuroscience (467 citations) and Sensory Systems (124 citations). Marcelle Jay has collaborated with scholars based in United Kingdom, Mexico and Australia. Frequent co-authors include Alan C. Bird, Alan F. Wright, Shomi S. Bhattacharya, C.F. Inglehearn, Fred W. Fitzke, G. B. Arden, Chris F. Inglehearn, Siladitya Bhattacharya, John A. Wells and John J. Wroblewski. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Eye, British Journal of Ophthalmology and 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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