M Jay

756 total citations
16 papers, 600 citations indexed

About

M Jay is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, M Jay has authored 16 papers receiving a total of 600 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in M Jay's work include Retinal Development and Disorders (10 papers), Photoreceptor and optogenetics research (4 papers) and Retinal Diseases and Treatments (3 papers). M Jay is often cited by papers focused on Retinal Development and Disorders (10 papers), Photoreceptor and optogenetics research (4 papers) and Retinal Diseases and Treatments (3 papers). M Jay collaborates with scholars based in United Kingdom, United States and Mexico. M Jay's co-authors include Mimi D. Johnson, Vaughn I. Rickert, Alan C. Bird, C.F. Inglehearn, Barrie Jay, Shoumo Bhattacharya, T J Keen, Douglas H. Lester, R. Bashir and Alan F. Wright and has published in prestigious journals such as British Journal of Ophthalmology, Genomics and Journal of Medical Genetics.

In The Last Decade

M Jay

16 papers receiving 573 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M Jay United Kingdom	9	387	145	143	108	100	16	600
Kanika Ghai United States	11	219 0.6×	71 0.5×	33 0.2×	22 0.2×	55 0.6×	12	401
D.F. Farrell United States	13	207 0.5×	77 0.5×	47 0.3×	31 0.3×	13 0.1×	23	463
Jue Ji China	12	177 0.5×	68 0.5×	148 1.0×	18 0.2×	10 0.1×	27	378
Margaret L. Entwistle United States	10	194 0.5×	99 0.7×	19 0.1×	435 4.0×	35 0.3×	11	1.1k
Mikhil Bamne United States	15	231 0.6×	87 0.6×	138 1.0×	12 0.1×	8 0.1×	22	579
Rolando Meloni France	15	346 0.9×	231 1.6×	152 1.1×	32 0.3×	23 0.2×	35	715
S. Christie United Kingdom	16	631 1.6×	95 0.7×	269 1.9×	44 0.4×	7 0.1×	23	874
Jean‐Bernard Dietrich France	12	434 1.1×	170 1.2×	166 1.2×	36 0.3×	22 0.2×	16	800
Karen Weissbecker United States	16	337 0.9×	162 1.1×	253 1.8×	260 2.4×	15 0.1×	31	957
Elisa De Grandis Italy	15	153 0.4×	69 0.5×	106 0.7×	19 0.2×	26 0.3×	46	578

Countries citing papers authored by M Jay

Since Specialization

Citations

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

Fields of papers citing papers by M Jay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Jay

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

All Works

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16 of 16 papers shown

Bruford, Elspeth A., Ruth Riise, Peter Teague, et al.. (1997). Linkage Mapping in 29 Bardet–Biedl Syndrome Families Confirms Loci in Chromosomal Regions 11q13, 15q22.3–q23, and 16q21. Genomics. 41(1). 93–99. 96 indexed citations

Jay, M, et al.. (1997). Tuboovarian Abscess in the Adolescent. Journal of Pediatric and Adolescent Gynecology. 10(2). 73–77. 2 indexed citations

Hardcastle, Alison J., Zoë K. David-Gray, M Jay, A.C. Bird, & Shoumo Bhattacharya. (1997). Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.. PubMed. 38(13). 2750–5. 13 indexed citations

Jay, M & Kathryn Evans. (1996). Retinal dystrophies and genetic counselling. Acta Ophthalmologica Scandinavica. 74(S219). 5–7. 4 indexed citations

Gregory-Evans, Kevin, Mai Al-Maghtheh, F.W. Fitzke, et al.. (1995). Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.. British Journal of Ophthalmology. 79(9). 841–846. 35 indexed citations

Gregory, Cheryl Y., et al.. (1995). Linkage refinement localises Sorsby fundus dystrophy between markers D22S275 and D22S278.. Journal of Medical Genetics. 32(3). 240–241. 5 indexed citations

Owens, Sarah L., Fred W. Fitzke, C.F. Inglehearn, et al.. (1994). Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.. British Journal of Ophthalmology. 78(5). 353–358. 7 indexed citations

Moore, Anthony T., F.W. Fitzke, M Jay, et al.. (1993). Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.. British Journal of Ophthalmology. 77(8). 473–479. 40 indexed citations

Keen, T J, C.F. Inglehearn, Douglas H. Lester, et al.. (1991). Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site. Genomics. 11(1). 199–205. 129 indexed citations

10.

Inglehearn, C.F., M Jay, Douglas H. Lester, et al.. (1990). no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneity. Genomics. 6(1). 168–173. 28 indexed citations

11.

Inglehearn, Chris F., S.S. Papiha, M Jay, et al.. (1990). Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.. Journal of Medical Genetics. 27(1). 14–16. 1 indexed citations

12.

Sankila, Eeva‐Marja, Frank Brunsmann, M Jay, et al.. (1990). Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.. PubMed. 47(4). 622–8. 56 indexed citations

13.

Jay, M, et al.. (1989). Microencapsulation of activable radiotherapeutic agents.. PubMed. 292. 293–300. 1 indexed citations

14.

Johnson, Mimi D., et al.. (1989). Anabolic steroid use by male adolescents.. PubMed. 83(6). 921–4. 121 indexed citations

15.

Venna, Nagagopal, et al.. (1988). Reversible depression in Binswanger's disease.. PubMed. 49(1). 23–6. 57 indexed citations

16.

Jay, M, Alan F. Wright, John Clayton, et al.. (1986). A genetic linkage study of choroideremia. Ophthalmic Paediatrics and Genetics. 7(3). 201–204. 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.

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