R.S. Sparkes

1.3k total citations
32 papers, 978 citations indexed

About

R.S. Sparkes is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, R.S. Sparkes has authored 32 papers receiving a total of 978 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in R.S. Sparkes's work include Genomics and Rare Diseases (3 papers), RNA regulation and disease (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). R.S. Sparkes is often cited by papers focused on Genomics and Rare Diseases (3 papers), RNA regulation and disease (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). R.S. Sparkes collaborates with scholars based in United States, Germany and Spain. R.S. Sparkes's co-authors include C. Benjamin Graham, Elena Boder, Harry V. Vinters, Kurt Lange, R A Gatti, Amos Norman, Robert Peter Gale, Katherine Neiswanger, Carol E. Anderson and Susan E. Hodge and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and Neurology.

In The Last Decade

R.S. Sparkes

31 papers receiving 916 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R.S. Sparkes United States 16 484 373 135 133 113 32 978
J W Voss United States 8 575 1.2× 385 1.0× 126 0.9× 197 1.5× 109 1.0× 10 1.3k
Konrad Kölble Germany 15 388 0.8× 145 0.4× 197 1.5× 73 0.5× 131 1.2× 29 916
Leena Peltonen Finland 8 295 0.6× 311 0.8× 76 0.6× 78 0.6× 36 0.3× 9 935
George Steele-Perkins United States 10 912 1.9× 144 0.4× 123 0.9× 68 0.5× 145 1.3× 10 1.2k
Francis S. Collins United States 11 543 1.1× 182 0.5× 271 2.0× 96 0.7× 52 0.5× 14 1.4k
Monika Goś Poland 19 769 1.6× 331 0.9× 134 1.0× 114 0.9× 91 0.8× 49 1.2k
Beatrice B. Yaroslavskiy United States 15 681 1.4× 234 0.6× 365 2.7× 53 0.4× 75 0.7× 21 1.3k
Martin P. Powers United States 11 349 0.7× 292 0.8× 91 0.7× 59 0.4× 137 1.2× 18 805
Anas M. Alazami Saudi Arabia 22 857 1.8× 584 1.6× 79 0.6× 129 1.0× 95 0.8× 55 1.5k
Marjolein Kriek Netherlands 19 773 1.6× 607 1.6× 48 0.4× 59 0.4× 86 0.8× 31 1.4k

Countries citing papers authored by R.S. Sparkes

Since Specialization
Citations

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

Fields of papers citing papers by R.S. Sparkes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R.S. Sparkes

This figure shows the co-authorship network connecting the top 25 collaborators of R.S. Sparkes. A scholar is included among the top collaborators of R.S. 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 R.S. Sparkes. R.S. Sparkes 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.
Delgado‐Escueta, Antonio V., José M. Serratosa, Amy Liu, et al.. (1994). Progress in Mapping Human Epilepsy Genes. Epilepsia. 35(s1). S29–40. 78 indexed citations
2.
Sparkes, R.S., et al.. (1993). Ph1‐chromosome positive acute lymphoblastic leukemia: Is t(9;22) the initial abnormality?. American Journal of Hematology. 43(1). 61–62.
3.
Turk, Eric, et al.. (1993). Assignment of the Human Na+/Glucose Cotransporter Gene SGLT1 to Chromosome 22q13.1. Genomics. 17(3). 752–754. 16 indexed citations
4.
Millikan, Robert C., et al.. (1993). A linkage analysis of D17S74 (CMM86) in thirty-five families with premenopausal bilateral breast cancer.. PubMed. 53(2). 212–4. 4 indexed citations
5.
MacLaren, Duncan C., Clare M. O’Connor, Yu-Rong Xia, et al.. (1992). The l-isoaspartyl/d-aspartyl protein methyltransferase gene (PCMT1) maps to human chromosome 6q22.3–6q24 and the syntenic region of mouse chromosome 10. Genomics. 14(4). 852–856. 12 indexed citations
6.
Sparkes, R.S., Camilla Heinzmann, Tracy Kojis, et al.. (1992). Assignment of the gene (RLBP1) for cellular retinaldehyde-binding protein (CRALBP) to human chromosome 15q26 and mouse chromosome 7. Genomics. 12(1). 58–62. 27 indexed citations
7.
Fujimoto, Atsuko, et al.. (1991). Monozygotic twins of discordant sex both with 45, X/46, X, idic(Y) mosaicism. American Journal of Medical Genetics. 41(2). 239–245. 36 indexed citations
8.
Gatti, R A, Elena Boder, Harry V. Vinters, et al.. (1991). Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis.. PubMed. 70(2). 99–117. 185 indexed citations
9.
Diep, Anh, I Klisak, T. Mohandas, et al.. (1991). Assignment of the gene for cyclic AMP-response element binding protein 2 (CREB2) to human chromosome 2q24.1–q32. Genomics. 11(4). 1161–1163. 5 indexed citations
10.
Carlson, Harold E., Sandra L. H. Davenport, Alan M. Luger, et al.. (1986). Cowden disease: gene marker studies and measurements of epidermal growth factor.. PubMed. 38(6). 908–17. 21 indexed citations
11.
Petersen, Gloria M., JI Rotter, Maria I. New, et al.. (1984). EVIDENCE FOR INDEPENDENT MUTATION OF THE 21-HYDROXYLASE DEFICIENCY (210H DEF) GENE IN ALASKAN ESKIMOS WITH CONGENITAL ADRENAL HYPERPLASIA (CAH). Pediatric Research. 18. 173A–173A. 2 indexed citations
12.
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
13.
Hodge, Susan E., Carol E. Anderson, Katherine Neiswanger, R.S. Sparkes, & D L Rimoin. (1983). The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.. PubMed. 35(6). 1139–55. 100 indexed citations
14.
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
15.
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
16.
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
17.
Philippart, Michel, et al.. (1974). HETEROZYGOTE DETECTION IN FABRY'S DISEASE. Pediatric Research. 8(4). 393–393. 4 indexed citations
18.
Linde, Leonard M., et al.. (1973). Pulmonary valvular dysplasia. A cardiofacial syndrome.. Heart. 35(3). 301–304. 22 indexed citations
19.
Cederbaum, Stephen D., Gerald B. Holzman, & R.S. Sparkes. (1971). " SPONTANEOUS " ABORTION AND HÆMORRHAGE FOLLOWING ATTEMPTED AMNIOCENTESIS IN A CARRIER OF HÆMOPHILIA A. The Lancet. 298(7721). 429–430. 6 indexed citations
20.
Motulsky, Arno G., et al.. (1962). Marrow transplantation in newborn mice with hereditary spherocytosis: a model system.. PubMed. 75. 64–72. 4 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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