Marcelle Jay

4.3k total citations
70 papers, 2.9k citations indexed

About

Marcelle Jay is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Marcelle Jay has authored 70 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 23 papers in Ophthalmology and 19 papers in Genetics. Recurrent topics in Marcelle Jay's work include Retinal Development and Disorders (36 papers), Ocular Oncology and Treatments (16 papers) and Retinoids in leukemia and cellular processes (14 papers). Marcelle Jay is often cited by papers focused on Retinal Development and Disorders (36 papers), Ocular Oncology and Treatments (16 papers) and Retinoids in leukemia and cellular processes (14 papers). Marcelle Jay collaborates with scholars based in United Kingdom, Mexico and Australia. Marcelle Jay's co-authors include Alan C. Bird, Shomi S. Bhattacharya, Alan F. Wright, C.F. Inglehearn, Fred W. Fitzke, G. B. Arden, Chris F. Inglehearn, Siladitya Bhattacharya, Anja Eckstein and John A. Wells and has published in prestigious journals such as Nature, Nature Genetics and American Journal of Psychiatry.

In The Last Decade

Marcelle Jay

69 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marcelle Jay United Kingdom 26 2.3k 978 562 467 458 70 2.9k
Terri L. McGee United States 28 3.8k 1.7× 1.5k 1.5× 608 1.1× 1.4k 3.0× 552 1.2× 40 4.4k
A. Pinckers Netherlands 24 1.7k 0.8× 990 1.0× 357 0.6× 286 0.6× 480 1.0× 133 2.6k
Jean‐Michel Rozet France 34 3.8k 1.6× 1.8k 1.8× 1.2k 2.1× 654 1.4× 500 1.1× 120 4.5k
Valeria Marigo Italy 35 4.3k 1.9× 658 0.7× 1.1k 1.9× 791 1.7× 638 1.4× 88 5.0k
Isabelle Perrault France 30 2.7k 1.2× 1.5k 1.6× 628 1.1× 452 1.0× 357 0.8× 71 3.0k
Arnold Munnich France 25 1.9k 0.8× 860 0.9× 724 1.3× 254 0.5× 310 0.7× 54 3.2k
G. Jane Farrar Ireland 35 3.5k 1.5× 1.1k 1.2× 709 1.3× 1.1k 2.3× 434 0.9× 93 4.1k
Marian M. Humphries Ireland 32 2.8k 1.2× 1.1k 1.1× 386 0.7× 930 2.0× 463 1.0× 68 3.5k
August F. Deutman Netherlands 36 2.7k 1.2× 2.9k 3.0× 403 0.7× 301 0.6× 555 1.2× 120 4.5k
Paul F. Kenna Ireland 38 3.9k 1.7× 1.4k 1.5× 666 1.2× 1.3k 2.7× 595 1.3× 121 4.8k

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-authorship network of co-authors of Marcelle Jay

This figure shows the co-authorship network connecting the top 25 collaborators of Marcelle Jay. A scholar is included among the top collaborators of Marcelle Jay 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 Marcelle Jay. Marcelle Jay 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.
Fletcher, Olivia, Douglas F. Easton, Kristin Anderson, et al.. (2004). Lifetime Risks of Common Cancers Among Retinoblastoma Survivors. JNCI Journal of the National Cancer Institute. 96(5). 357–363. 172 indexed citations
2.
Thiselton, Dawn L., Ilaria Zito, Catherine Plant, et al.. (2000). Novel frameshift mutations in theRP2 gene and polymorphic variants. Human Mutation. 15(6). 580–580. 21 indexed citations
3.
Hardcastle, Alison J., et al.. (1999). Mutations in the RP2 gene cause disease in 10% of familial XLRP assessed in this study. UCL Discovery (University College London). 9 indexed citations
4.
Gregory-Evans, Kevin, Marcelle Jay, Claire Davison, et al.. (1996). Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes.. Genome Research. 6(2). 92–101. 32 indexed citations
5.
Meindl, A, Katherine L. Dry, Karin A. Herrmann, et al.. (1996). A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3). Nature Genetics. 13(1). 35–42. 391 indexed citations
6.
Jay, Marcelle, Catherine Plant, Kevin Gregory-Evans, & Cheryl Y. Gregory. (1996). Doyne revisited. Eye. 10(4). 469–472. 2 indexed citations
7.
Dry, Katherine L., Micheala A. Aldred, Forbes Manson, et al.. (1995). Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3). Human Molecular Genetics. 4(12). 2347–2353. 23 indexed citations
8.
Breimer, Lars H., et al.. (1995). A trinucleotide deletion together with a base duplication event at codon 439 in the human tyrosinase gene identifies a mutational hotspot. Clinica Chimica Acta. 243(1). 35–42. 2 indexed citations
9.
Al-Maghtheh, Mai, Chris F. Inglehearn, Peter Lunt, et al.. (1994). Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosa. Human Mutation. 3(4). 409–410. 19 indexed citations
10.
Breimer, Lars H., A F Winder, Barrie Jay, & Marcelle Jay. (1994). Initiation codon mutation of the tyrosinase gene as a cause of human albinism. Clinica Chimica Acta. 227(1-2). 17–22. 13 indexed citations
11.
Bokhoven, Hans van, Marianne Schwartz, Sten Andréasson, et al.. (1994). Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients. Human Molecular Genetics. 3(7). 1047–1051. 60 indexed citations
12.
Carter, Dee, Dominique Campion, Thierry d’Amato, et al.. (1993). No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients. Human Molecular Genetics. 2(3). 321–321. 3 indexed citations
13.
Inglehearn, Chris F., Simon Carter, Janet C. Lindsey, et al.. (1993). A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nature Genetics. 4(1). 51–53. 69 indexed citations
14.
Jay, Marcelle, et al.. (1993). Familial malignant melanoma of the uvea and p53: A victorian detective story. Survey of Ophthalmology. 37(6). 457–462. 34 indexed citations
15.
Bashir, R., C.F. Inglehearn, T J Keen, et al.. (1992). Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP. Genomics. 14(1). 191–193. 4 indexed citations
16.
Fitzke, FW, et al.. (1991). COMPARISON OF FUNCTIONAL-CHARACTERISTICS OF AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA WITH DIFFERENT AMINO-ACID CHANGES IN THE RHODOPSIN MOLECULE. Investigative Ophthalmology & Visual Science. 4 indexed citations
17.
Jay, Marcelle. (1991). The use of diagnostic registers. Ophthalmic Paediatrics and Genetics. 12(2). 65–71. 1 indexed citations
18.
Cowell, John K., John L. Hungerford, Paul Rutland, & Marcelle Jay. (1989). Genetic and Cytogenetic Analysis of Patients Showing Reduced Esterase-D Levels and Mental Retardation from a Survey of 500 Individuals with Retinoblastoma. Ophthalmic Paediatrics and Genetics. 10(2). 117–127. 25 indexed citations
19.
Cowell, John K., Paul Rutland, John L. Hungerford, & Marcelle Jay. (1988). Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma. Human Genetics. 80(1). 43–45. 12 indexed citations
20.
Jay, Marcelle. (1977). THE EYE IN CHROMOSOME DUPLICATIONS AND DEFICIENCIES. Optometry and Vision Science. 54(9). 648–648. 5 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Terri L. McGee Breakdown of academic impact, for papers by A. Pinckers Breakdown of academic impact, for papers by Jean‐Michel Rozet Breakdown of academic impact, for papers by Valeria Marigo Breakdown of academic impact, for papers by Isabelle Perrault Breakdown of academic impact, for papers by Arnold Munnich Breakdown of academic impact, for papers by G. Jane Farrar Breakdown of academic impact, for papers by Marian M. Humphries Breakdown of academic impact, for papers by August F. Deutman Breakdown of academic impact, for papers by Paul F. Kenna
Rankless by CCL
2026