Sparkes Rs

475 citations
30 papers · 382 indexed · h-index 11

Impact in

  • Hematology top 10%
    • Chronic Myeloid Leukemia Treatments
    • Acute Myeloid Leukemia Research
    • Genomic variations and chromosomal abnormalities
    • Chronic Lymphocytic Leukemia Research
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Chronic Myeloid Leukemia Treatments 7
    • Acute Myeloid Leukemia Research 4
    • Genomic variations and chromosomal abnormalities 7
    • Chronic Lymphocytic Leukemia Research 4
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
Journals
Blood (8 papers)Ophthalmic Research (1 paper)Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) (2 papers)PubMed (19 papers)
Partner nations
United StatesJapan

In The Last Decade

Sparkes Rs

30 papers receiving 340 citations

Peers

Sparkes Rs
Comparison fields: 5 of 49
  • Hematology 122
  • Genetics 73
  • Genetics 132
  • Pediatrics, Perinatology and Child Health 72
  • Rheumatology 39
Replace Renée Bernstein with:
Renée Bernstein South Africa
Claudia Dellavecchia Italy
Lorna M. Webber Australia
Elena Gaber Israel
G.W. Dewald United States
B Kaiser-McCaw United States
Paolo Guanciali‐Franchi Italy
Birgitte Roland Canada
J. Ritterbach Germany
E. L. Prigogina United States
Sparkes Rs relative to Renée Bernstein South Africa Renée Bernstein's profile →
Citations per field
00.5×1.5×2.3×
Renée Bernstein · 1×
Citations per year

Countries citing papers authored by Sparkes Rs

Since Specialization
Citations

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

Fields of papers citing papers by Sparkes Rs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1
Regional mapping of the human MP70 (Cx50; connexin 50) gene by fluorescence in situ hybridization to 1q21.1.
199713
2 19892
3
The bcr gene is joined to c-abl in Ph1 chromosome negative chronic myelogenous leukemia.
19882
4
Trisomy 20p due to a paternal reciprocal translocation.
198311
5
Genetic linkage studies with cleft lip and palate: report of two family studies.
19832
6 198215
7
Familial Y-autosome translocation in two unrelated girls.
19825
8 198110
9
Balanced reciprocal (X;9) translocation in a girl with primary amenorrhea.
19818
10 19801
11
Two independent HLA-B-locus specificities expressed on a single haplotype.
19792
12
Control of red blood cell adenine nucleotide metabolism studies of adenosine deaminase.
19788
13
A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child.
19784
14
Extended evaluation of previously reported twins with a ring 14 chromosome.
19778
15
Duplication 11 (q21 to 23 leads to qter) syndrome.
197724
16
Pure gonadal dysgenesis with nonmosaic XY sex chromosomes.
19764
17
Partial trisomy of chromosome 11: a case report.
197312
18
Partial deletion syndromes of chromosome 18.
19715
19
Inherited 13/14 chromosome translocation as a cause of human fetal wastage.
19708
20
FAMILIAL INGUINAL HERNIA.
19656

About Sparkes Rs

Sparkes Rs is a scholar working on Hematology, Genetics, Genetics, Rheumatology and Physiology, having authored 30 papers that have together received 382 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chronic Myeloid Leukemia Treatments (7 papers), Acute Myeloid Leukemia Research (4 papers), Chronic Lymphocytic Leukemia Research (4 papers), Eosinophilic Disorders and Syndromes (4 papers), Prenatal Screening and Diagnostics (4 papers), Immune Cell Function and Interaction (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). The work is most often cited by research in Hematology (122 citations), Genetics (73 citations), Genetics (132 citations), Pediatrics, Perinatology and Child Health (72 citations) and Rheumatology (39 citations). Sparkes Rs has collaborated with scholars based in United States and Japan. Frequent co-authors include Townsend De, DW Golde, MJ Cline, HP Koeffler, M.C. Sparkes, AM Levine, Ivana Klisak, Uta Francke, J Mann and George Klein. Their work appears in journals such as Blood, Ophthalmic Research, Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) and PubMed.

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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