Sarah Ball

1.2k total citations
26 papers, 814 citations indexed

About

Sarah Ball is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Sarah Ball has authored 26 papers receiving a total of 814 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Surgery and 5 papers in Genetics. Recurrent topics in Sarah Ball's work include Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Ubiquitin and proteasome pathways (3 papers). Sarah Ball is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Ubiquitin and proteasome pathways (3 papers). Sarah Ball collaborates with scholars based in United Kingdom, United States and Australia. Sarah Ball's co-authors include Keith Johnson, Paraskevi Briassouli, Spiros Linardopoulos, John P. de Koning, Maria Rosário Almeida, Bruce A.J. Ponder, John Burn, Hiroki Nagase, Amanda E. Toland and Florence Chan and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

Sarah Ball

26 papers receiving 782 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah Ball United Kingdom 14 518 181 154 141 134 26 814
Casey L. Moulson United States 12 770 1.5× 201 1.1× 81 0.5× 52 0.4× 67 0.5× 13 1.0k
Nicolas Gadot France 20 520 1.0× 126 0.7× 197 1.3× 87 0.6× 250 1.9× 46 990
Shun-Ai Li Japan 14 643 1.2× 188 1.0× 52 0.3× 238 1.7× 42 0.3× 17 1.0k
Brian Niland United States 13 467 0.9× 150 0.8× 141 0.9× 92 0.7× 283 2.1× 18 1.4k
Samuel Shao-Min Zhang United States 15 690 1.3× 86 0.5× 54 0.4× 133 0.9× 78 0.6× 22 1.3k
Ortal Barel Israel 15 450 0.9× 58 0.3× 73 0.5× 247 1.8× 78 0.6× 63 868
Consuelo González‐Manchón Spain 18 536 1.0× 76 0.4× 48 0.3× 165 1.2× 34 0.3× 61 1.2k
Angelo Notarangelo Italy 13 449 0.9× 151 0.8× 71 0.5× 148 1.0× 21 0.2× 29 806
D Flavell United Kingdom 11 451 0.9× 87 0.5× 245 1.6× 99 0.7× 85 0.6× 11 957
S.A. Whitmore Australia 18 536 1.0× 114 0.6× 167 1.1× 255 1.8× 58 0.4× 26 1.3k

Countries citing papers authored by Sarah Ball

Since Specialization
Citations

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

Fields of papers citing papers by Sarah Ball

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Ball

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Ball. A scholar is included among the top collaborators of Sarah Ball 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 Sarah Ball. Sarah Ball 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.
Barber, Thomas M., Patrick Elder, Sarah Ball, et al.. (2020). AMY1 Gene Copy Number Correlates With Glucose Absorption and Visceral Fat Volume, but Not with Insulin Resistance. The Journal of Clinical Endocrinology & Metabolism. 105(10). e3586–e3596. 10 indexed citations
2.
Kullar, Peter, Robert W. Taylor, Charlotte L. Alston, et al.. (2016). The frequency of the m.1555A > G (MTRNR1) variant in UK patients with suspected mitochondrial deafness. Hearing Balance and Communication. 14(2). 101–102. 3 indexed citations
3.
Angileri, Francesca, Anne Bergeron, Geneviève Morrow, et al.. (2014). Geographical and Ethnic Distribution of Mutations of the Fumarylacetoacetate Hydrolase Gene in Hereditary Tyrosinemia Type 1. JIMD Reports. 19. 43–58. 51 indexed citations
4.
Bruce, Christopher K, Fatima Rahman, Zhifeng Liu, et al.. (2010). Design and validation of a metabolic disorder resequencing microarray (BRUM1). Human Mutation. 31(7). 858–865. 13 indexed citations
5.
Pisciotta, Livia, Letizia Bocchi, Ilaria Zanotti, et al.. (2009). Severe HDL deficiency due to novel defects in the ABCA1 transporter. Journal of Internal Medicine. 265(3). 359–372. 21 indexed citations
6.
Toland, Amanda E., Paraskevi Briassouli, John P. de Koning, et al.. (2003). Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and human. Nature Genetics. 34(4). 403–412. 267 indexed citations
7.
Clark, Jeremy, Sarah Ball, Sandra Gill, et al.. (1995). The human SB1.8 gene (DXS423E) encodes a putative chromosome segregation protein conserved in lower eukaryotes and prokaryotes. Human Molecular Genetics. 4(2). 243–249. 24 indexed citations
8.
Ball, Sarah, Huw Dorkins, F.R. ELLIS, et al.. (1993). GENETIC LINKAGE ANALYSIS OF CHROMOSOME 19 MARKERS IN MALIGNANT HYPERTHERMIA. British Journal of Anaesthesia. 70(1). 70–75. 13 indexed citations
9.
Ball, Sarah, Anne Gibaud, Jacques Le Pendu, et al.. (1991). The human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9. Annals of Human Genetics. 55(3). 225–233. 21 indexed citations
10.
Humphry, R C, et al.. (1991). Lens epithelial cells adhere less to HEMA than to PMMA intraocular lenses. Eye. 5(1). 66–69. 7 indexed citations
11.
Davies, Kay E., S. M. Forrest, Terry Smith, et al.. (1987). Molecular analysis of human muscular dystrophies. Muscle & Nerve. 10(3). 191–199. 7 indexed citations
12.
Davies, Kay E., Sarah Ball, Huw Dorkins, et al.. (1986). Molecular analysis of X-linked diseases.. PubMed. 18(5-6). 231–3. 1 indexed citations
13.
Ball, Sarah, Susan Kenwrick, & Kay E. Davies. (1985). The Molecular Genetics of Human Monogenic Diseases. Biotechnology and Genetic Engineering Reviews. 3(1). 275–310. 2 indexed citations
14.
Ball, Sarah, Jennifer A. Donald, G. CORNEY, & Steve E. Humphries. (1985). Linkage between the loci for peptidase D and apolipoprotein CII on chromosome 19. Annals of Human Genetics. 49(2). 129–134. 4 indexed citations
15.
Donald, Jennifer A., S. Wallis, Anna M. Kessling, et al.. (1985). Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19. Human Genetics. 69(1). 39–43. 25 indexed citations
16.
Humphries, Steve E., Jennifer A. Donald, Johnjoe McFadden, et al.. (1984). The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia. Atherosclerosis. 52(3). 267–278. 20 indexed citations
17.
Donald, Jennifer A. & Sarah Ball. (1984). Approximate linkage equilibrium between two polymorphic sites within the gene for human complement component 3. Annals of Human Genetics. 48(3). 269–273. 11 indexed citations
18.
Davies, Kay E., R. Williamson, Peter S. Harper, et al.. (1983). Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.. Journal of Medical Genetics. 20(4). 259–263. 60 indexed citations
19.
O'Brien, T, Sarah Ball, M. Sarfarazi, P.S. Harper, & E.B. Robson. (1983). Genetic linkage between the loci for myotonic dystrophy and peptidase D. Annals of Human Genetics. 47(2). 117–121. 33 indexed citations
20.
Ball, Sarah, P.J.L. Cook, Maurice Mars, & K.E. Buckton. (1982). Linkage between dentinogenesis imperfecta and Gc. Annals of Human Genetics. 46(1). 35–40. 43 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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