M.C. Sparkes

860 total citations
29 papers, 724 citations indexed

About

M.C. Sparkes is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, M.C. Sparkes has authored 29 papers receiving a total of 724 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Surgery. Recurrent topics in M.C. Sparkes's work include Retinal Development and Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Advanced biosensing and bioanalysis techniques (4 papers). M.C. Sparkes is often cited by papers focused on Retinal Development and Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Advanced biosensing and bioanalysis techniques (4 papers). M.C. Sparkes collaborates with scholars based in United States, United Kingdom and Germany. M.C. Sparkes's co-authors include R S Sparkes, T. Mohandas, L J Shapiro, Michol Crist, M. Anne Spence, T. Mohandas, Aldons J. Lusis, James Scott, Timothy J. Knott and Steve J. Funderburk and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Blood.

In The Last Decade

M.C. Sparkes

29 papers receiving 648 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.C. Sparkes United States	16	379	295	90	73	63	29	724
M.Q. Islam Sweden	16	538 1.4×	273 0.9×	64 0.7×	57 0.8×	73 1.2×	46	805
Sarah Ball United Kingdom	14	518 1.4×	141 0.5×	75 0.8×	40 0.5×	27 0.4×	26	814
L.L. Haley United States	14	442 1.2×	177 0.6×	34 0.4×	31 0.4×	124 2.0×	24	734
JT den Dunnen Netherlands	3	402 1.1×	244 0.8×	73 0.8×	17 0.2×	65 1.0×	6	825
Alison J. Coffey United Kingdom	17	699 1.8×	242 0.8×	42 0.5×	53 0.7×	35 0.6×	27	1.0k
Godfrey T. Gillett United Kingdom	13	286 0.8×	138 0.5×	50 0.6×	50 0.7×	31 0.5×	20	677
R Misra United States	9	544 1.4×	79 0.3×	44 0.5×	65 0.9×	89 1.4×	17	829
Ilenia Simeoni United Kingdom	12	391 1.0×	125 0.4×	39 0.4×	15 0.2×	33 0.5×	16	608
Alan Bruzel United States	11	802 2.1×	150 0.5×	62 0.7×	51 0.7×	31 0.5×	17	973
Wanda E. Filipiak United States	8	407 1.1×	234 0.8×	85 0.9×	12 0.2×	77 1.2×	11	906

Countries citing papers authored by M.C. Sparkes

Since Specialization

Citations

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

Fields of papers citing papers by M.C. Sparkes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M.C. Sparkes

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lusis, Aldons J., Camilla Heinzmann, R S Sparkes, et al.. (1986). Regional mapping of human chromosome 19: organization of genes for plasma lipid transport (APOC1, -C2, and -E and LDLR) and the genes C3, PEPD, and GPI.. Proceedings of the National Academy of Sciences. 83(11). 3929–3933. 93 indexed citations

Crist, Michol, et al.. (1985). Glutamate Pyruvate Transaminase Null Allele (GPT°) in the Navajo. Human Heredity. 35(1). 59–61. 2 indexed citations

Sparkes, R S, M. Anne Spence, Robert G. Gray, et al.. (1985). Genetic Linkage Analysis of the Carpal Tunnel Syndrome. Human Heredity. 35(5). 288–291. 9 indexed citations

Sparkes, R S, L. Leigh Field, M.C. Sparkes, et al.. (1984). Genetic Linkage Studies of Transf errin, Pseudocholinesterase, and Chromosome 1 Loci. Human Heredity. 34(2). 96–100. 23 indexed citations

Bateman, J. Bronwyn, M.C. Sparkes, & R S Sparkes. (1984). Aniridia: enzyme studies in an 11p--chromosomal deletion.. PubMed. 25(5). 612–6. 3 indexed citations

Sparkes, R S, T. Mohandas, & M.C. Sparkes. (1983). The human phosphoserine phosphatase gene (PSP) is mapped to chromosome 7 by somatic cell genetic analysis. Cytogenetic and Genome Research. 35(1). 70–71. 1 indexed citations

Hodge, Susan E., Carol E. Anderson, Katherine Neiswanger, et al.. (1983). Association studies between type 1 (insulin-dependent) diabetes and 27 genetic markers: Lack of association between type 1 diabetes and kidd blood group. Diabetologia. 25(4). 343–7. 14 indexed citations

Field, L. Leigh, J. R. Heckenlively, R.S. Sparkes, et al.. (1982). Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.. Journal of Medical Genetics. 19(4). 266–270. 25 indexed citations

Rs, Sparkes, et al.. (1982). Possible Assignment of a Dominant Retinitis pigmentosa Gene to Chromosome. Ophthalmic Research. 14(1). 46–53. 15 indexed citations

10.

Neiswanger, Katherine, M. Anne Spence, M.C. Sparkes, et al.. (1981). CLOSE GENETIC LINKAGE BETWEEN DIABETES MELLITUS AND KIDD BLOOD GROUP. The Lancet. 318(8252). 893–895. 53 indexed citations

11.

Oriol, Rafaël, Jacques Le Pendu, R.S. Sparkes, et al.. (1981). Insights into the expression of ABH and Lewis antigens through human bone marrow transplantation.. PubMed. 33(4). 551–60. 27 indexed citations

12.

Field, L. Leigh, J. R. Heckenlively, R.S. Sparkes, et al.. (1980). Linkage analysis of several families with dominant form retinitis pigmentosa. The American Journal of Human Genetics. 32(6). 105. 1 indexed citations

13.

Mohandas, T., R S Sparkes, Merry Passage, et al.. (1980). Regional mapping of ADA and ITP on human chromosome 20: cytogenetic and somatic cell studies in an X/20 translocation. Cytogenetic and Genome Research. 26(1). 28–35. 32 indexed citations

14.

Mohandas, T., et al.. (1980). Assignment of PGM3 to the long arm of human chromosome 6. Cytogenetic and Genome Research. 28(1-2). 116–120. 16 indexed citations

15.

Sparkes, R S, et al.. (1980). Assignment of the human gene for phosphoglycolate phosphatase to chromosome 16. Human Genetics. 54(2). 159–161. 3 indexed citations

16.

Sparkes, R S, et al.. (1980). Expression of GALT in 9p chromosome alterations: assignment of GALT locus to 9cen→9p22. Annals of Human Genetics. 43(4). 343–348. 9 indexed citations

17.

Mohandas, T., et al.. (1979). Regional localization of human gene loci on chromosome 9: studies of somatic cell hybrids containing human translocations.. PubMed. 31(5). 586–600. 52 indexed citations

18.

Sparkes, R S, et al.. (1978). Aconitase (E.C. 4.2.1.3) mitochondrial locus (ACONM) mapped to human chromosome 22. Cytogenetic and Genome Research. 22(1-6). 226–227. 6 indexed citations

19.

Sparkes, R S, et al.. (1978). Regional localization of human phosphoglucomutase-2 locus on chromosome 4. Experimental Cell Research. 111(2). 492–495. 4 indexed citations

20.

Sparkes, M.C., et al.. (1977). Improved technique for electrophoresis of human galactose-1-P uridyl transferase (EC 2.7.7.12). Human Genetics. 40(1). 93–7. 31 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