S. White

520 total citations
5 papers, 374 citations indexed

About

S. White is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, S. White has authored 5 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cardiology and Cardiovascular Medicine, 2 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in S. White's work include Cardiomyopathy and Myosin Studies (2 papers), Muscle Physiology and Disorders (2 papers) and Genetic Neurodegenerative Diseases (2 papers). S. White is often cited by papers focused on Cardiomyopathy and Myosin Studies (2 papers), Muscle Physiology and Disorders (2 papers) and Genetic Neurodegenerative Diseases (2 papers). S. White collaborates with scholars based in Australia, United States and New Zealand. S. White's co-authors include Eric Haan, Nigel G. Laing, P. Anthony Akkari, Karyn Boundy, Donald R. Love, S.M. Dorosz, Steve D. Wilton, Peter Blumbergs, Hugh Watkins and Bernadette T. Majda and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

S. White

5 papers receiving 364 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. White Australia	5	311	289	108	93	73	5	374
Hayley J. Durling Australia	8	465 1.5×	419 1.4×	133 1.2×	108 1.2×	83 1.1×	10	535
Jenni Laitila Finland	9	226 0.7×	225 0.8×	92 0.9×	88 0.9×	36 0.5×	18	313
E. Hammouda France	4	1.1k 3.4×	260 0.9×	99 0.9×	148 1.6×	62 0.8×	4	1.1k
J.A. Urtizberea France	4	1.1k 3.4×	224 0.8×	80 0.7×	171 1.8×	100 1.4×	5	1.1k
L. Demay France	13	596 1.9×	301 1.0×	42 0.4×	78 0.8×	58 0.8×	18	661
Satu Sandell Finland	10	232 0.7×	114 0.4×	56 0.5×	41 0.4×	89 1.2×	21	313
S.M. Dorosz Australia	4	342 1.1×	324 1.1×	107 1.0×	102 1.1×	95 1.3×	6	421
S. Lillis United Kingdom	6	173 0.6×	102 0.4×	74 0.7×	56 0.6×	57 0.8×	6	237
William Wallefeld Australia	6	266 0.9×	258 0.9×	91 0.8×	78 0.8×	44 0.6×	11	333
H. Luque Finland	6	231 0.7×	129 0.4×	55 0.5×	39 0.4×	50 0.7×	11	265

Countries citing papers authored by S. White

Since Specialization

Citations

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

Fields of papers citing papers by S. White

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. White

This figure shows the co-authorship network connecting the top 25 collaborators of S. White. A scholar is included among the top collaborators of S. White 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 S. White. S. White 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:

5 of 5 papers shown

1.

Eyre, Stephen, Anne Myerscough, Anne Barton, et al.. (2002). Whole-genome linkage analysis of rheumatoid arthritis susceptibility loci in 252 affected sibling pairs in the United Kingdom (vol 46,pg 632, 2002). Queensland's institutional digital repository (The University of Queensland). 46(5). 1406–1406. 15 indexed citations

2.

Benson, Kathleen F., Marshall S. Horwitz, John Wolff, et al.. (1998). CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients. Human Molecular Genetics. 7(11). 1779–1786. 20 indexed citations

3.

Laing, Nigel G., Steve D. Wilton, P. Anthony Akkari, et al.. (1995). A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy. Nature Genetics. 9(1). 75–79. 274 indexed citations

4.

Laing, Nigel G., Bernadette T. Majda, P. Anthony Akkari, et al.. (1992). Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.. PubMed. 50(3). 576–83. 52 indexed citations

5.

Mulley, John C., Ági K. Gedeon, S. White, Eric Haan, & Robert I. Richards. (1991). Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.. Journal of Medical Genetics. 28(7). 448–452. 13 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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