M.C. Sparkes

860 citations
29 papers · 724 · h-index 16

Impact in

  • Genetics top 10%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomic variations and chromosomal abnormalities
    • Diabetes and associated disorders
    • Genetics and Neurodevelopmental Disorders
    • Metabolism and Genetic Disorders

Papers in

    • Retinal Development and Disorders 5
    • Advanced biosensing and bioanalysis techniques 4
    • Glycosylation and Glycoproteins Research 3
    • Genomics and Chromatin Dynamics 2
    • Genomic variations and chromosomal abnormalities 4

M.C. Sparkes

29 papers receiving 648 citations

Peers

M.C. Sparkes
Comparison fields: 5 of 73
  • Genetics 295
  • Clinical Biochemistry 50
  • Biochemistry 40
  • Molecular Biology 379
  • Hematology 53
Replace JT den Dunnen with:
JT den Dunnen Netherlands
Yuan-Yuan Ho Hong Kong
M.Q. Islam Sweden
Alison J. Coffey United Kingdom
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Rosanna Gatti Italy
Andrew Orr Canada
L.L. Haley United States
Christina Rudduck Australia
Frédéric Esnard France
M.C. Sparkes relative to JT den Dunnen Netherlands JT den Dunnen's profile →
Citations per field
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Citations per year

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-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1979135
2 198693
3 198153
4
Regional localization of human gene loci on chromosome 9: studies of somatic cell hybrids containing human translocations.
197952
5 198449
6 197734
7 198032
8 197731
9 198030
10
Insights into the expression of ABH and Lewis antigens through human bone marrow transplantation.
198127
11 198225
12
Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1.
197725
13 198423
14 198120
15 198016
16 198215
17 198314
18 19859
19 19809
20 19787

About M.C. Sparkes

M.C. Sparkes is a scholar working on Molecular Biology, Genetics, Surgery, Endocrinology, Diabetes and Metabolism and Biochemistry, having authored 29 papers that have together received 724 indexed citations. Recurring topics across this work include Retinal Development and Disorders (5 papers), Advanced biosensing and bioanalysis techniques (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Glycosylation and Glycoproteins Research (3 papers), Amino Acid Enzymes and Metabolism (3 papers), Pancreatic function and diabetes (2 papers), Metabolism and Genetic Disorders (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (295 citations), Clinical Biochemistry (50 citations), Biochemistry (40 citations), Molecular Biology (379 citations) and Hematology (53 citations). M.C. Sparkes has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include R S Sparkes, T. Mohandas, L J Shapiro, Michol Crist, M. Anne Spence, T. Mohandas, Timothy J. Knott, Camilla Heinzmann, James Scott and Steve J. Funderburk. Their work appears in journals such as Cytogenetic and Genome Research, Proceedings of the National Academy of Sciences, Human Heredity, Journal of Medical Genetics 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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