Steven Wiltshire

6.3k total citations
39 papers, 1.8k citations indexed

About

Steven Wiltshire is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Steven Wiltshire has authored 39 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 8 papers in Physiology. Recurrent topics in Steven Wiltshire's work include Genetic Associations and Epidemiology (13 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Steven Wiltshire is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Steven Wiltshire collaborates with scholars based in United Kingdom, Australia and United States. Steven Wiltshire's co-authors include Mark I. McCarthy, Barry Schweitzer, Stephen F. Kingsmore, Jérémy Lambert, David C. Ward, Paul M. Lizardi, Zhengrong Zhu, Shawn O’Malley, Andrew T. Hattersley and Timothy M. Frayling and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Steven Wiltshire

39 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Steven Wiltshire United Kingdom	22	1.0k	551	319	258	254	39	1.8k
Jean‐François Denef Belgium	26	485 0.5×	182 0.3×	143 0.4×	742 2.9×	156 0.6×	69	1.8k
Waleed O. Twal United States	23	883 0.9×	355 0.6×	230 0.7×	105 0.4×	133 0.5×	43	1.9k
Chin Jia Lin Brazil	23	1.1k 1.1×	434 0.8×	113 0.4×	275 1.1×	203 0.8×	53	1.8k
H Sakura Japan	22	1.5k 1.4×	326 0.6×	594 1.9×	308 1.2×	65 0.3×	32	2.2k
Dan L. Crimmins United States	29	1.7k 1.7×	172 0.3×	318 1.0×	239 0.9×	59 0.2×	71	3.0k
Nicole L. Stone United States	20	727 0.7×	136 0.2×	381 1.2×	156 0.6×	140 0.6×	44	3.4k
Hsiao Chang Chan Hong Kong	26	761 0.7×	128 0.2×	125 0.4×	188 0.7×	46 0.2×	68	1.7k
M. Estela Rubio‐Gozalbo Netherlands	33	1.2k 1.2×	286 0.5×	155 0.5×	138 0.5×	20 0.1×	114	2.8k
Katrina M. Dipple United States	24	1.1k 1.1×	466 0.8×	172 0.5×	102 0.4×	31 0.1×	66	1.9k
Clinton H. Joiner United States	32	1.1k 1.1×	220 0.4×	344 1.1×	505 2.0×	243 1.0×	101	3.6k

Countries citing papers authored by Steven Wiltshire

Since Specialization

Citations

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

Fields of papers citing papers by Steven Wiltshire

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Wiltshire

This figure shows the co-authorship network connecting the top 25 collaborators of Steven Wiltshire. A scholar is included among the top collaborators of Steven Wiltshire 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 Steven Wiltshire. Steven Wiltshire is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Peters, Kirsten E., John Beilby, Gemma Cadby, et al.. (2013). A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome. BMC Medical Genetics. 14(1). 15–15. 68 indexed citations

Verbrugghe, Phebe, Steven Wiltshire, Kim W. Carter, et al.. (2012). Impact of the Reelin signaling cascade (Ligands–Receptors–Adaptor Complex) on cognition in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(4). 392–404. 27 indexed citations

Xiao, Jing, Fan Zhang, Steven Wiltshire, et al.. (2008). The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population. Atherosclerosis. 199(2). 333–339. 29 indexed citations

Wiltshire, Steven, Brenda L. Powell, Pamela A. McCaskie, et al.. (2008). Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease. Human Genetics. 123(3). 307–313. 14 indexed citations

Carter, Kim W., Joseph Hung, Brenda L. Powell, et al.. (2008). Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population. Human Genetics. 124(3). 199–206. 31 indexed citations

Gueorguiev, Maria, Steven Wiltshire, Edwin García, et al.. (2007). Examining the Candidacy of Ghrelin as a Gene Responsible for Variation in Adult Stature in a United Kingdom Population with Type 2 Diabetes. The Journal of Clinical Endocrinology & Metabolism. 92(6). 2201–2204. 8 indexed citations

Wiltshire, Steven, Andrew P. Morris, & Eleftheria Zeggini. (2007). Examining the statistical properties of fine‐scale mapping in large‐scale association studies. Genetic Epidemiology. 32(3). 204–214. 4 indexed citations

Groves, Christopher J., Eleftheria Zeggini, Jon Minton, et al.. (2006). Large scale case-control and family-based analyses of TCF7L2 variants in > 6000 UK subjects demonstrates an almost two-fold difference in relative risk between homozygote classes. Diabetologia. 49. 14–14. 1 indexed citations

Groves, Christopher J., Eleftheria Zeggini, Mark Walker, et al.. (2006). Significant Linkage of BMI to Chromosome 10p in the U.K. Population and Evaluation of GAD2 as a Positional Candidate. Diabetes. 55(6). 1884–1889. 21 indexed citations

10.

Wiltshire, Steven, Jordana T. Bell, Christopher J. Groves, et al.. (2006). Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21‐25 and 10q23‐26 in Northern Europeans. Annals of Human Genetics. 70(6). 726–737. 16 indexed citations

11.

Wiltshire, Steven, Andrew P. Morris, Mark I. McCarthy, & Lon R. Cardon. (2004). How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkage. Genetic Epidemiology. 28(1). 1–10. 11 indexed citations

12.

Groves, Christopher J., Steven Wiltshire, Eleftheria Zeggini, et al.. (2004). Analysis of the contribution to type 2 diabetes susceptibility of sequence variation in the gene encoding stearoyl-CoA desaturase, a key regulator of lipid and carbohydrate metabolism. Diabetologia. 47(12). 2168–2175. 26 indexed citations

13.

Démenais, Florence, Timo Kanninen, Cecilia M. Lindgren, et al.. (2003). A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes. Human Molecular Genetics. 12(15). 1865–1873. 48 indexed citations

14.

Wiltshire, Steven, Timothy M. Frayling, Andrew T. Hattersley, et al.. (2002). Evidence for Linkage of Stature to Chromosome 3p26 in a Large U.K. Family Data Set Ascertained for Type 2 Diabetes. The American Journal of Human Genetics. 70(2). 543–546. 48 indexed citations

15.

Haddad, Lema, Julie Evans, Neda Gharani, et al.. (2002). Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome. The Journal of Clinical Endocrinology & Metabolism. 87(6). 2606–2610. 60 indexed citations

16.

Leaves, N. I., Sumit Bhattacharyya, Steven Wiltshire, & William Cookson. (2002). A detailed genetic map of the chromosome 7 bronchial hyper-responsiveness locus. European Journal of Human Genetics. 10(3). 177–182. 11 indexed citations

17.

Gloyn, Anna L., Y Hashim, S. J. H. Ashcroft, et al.. (2001). Association studies of variants in promoter and coding regions of beta‐cell ATP‐sensitive K‐channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53). Diabetic Medicine. 18(3). 206–212. 135 indexed citations

18.

Bhattacharyya, Sumit, N. I. Leaves, Steven Wiltshire, Roger Cox, & William Cookson. (2000). A High-Density Genetic Map of the Chromosome 13q14 Atopy Locus. Genomics. 70(3). 286–291. 11 indexed citations

19.

Wiltshire, Steven, Sarmistha Sen Raychaudhuri, & S Eisenberg. (1997). An Abf1p C-terminal region lacking transcriptional activation potential stimulates a yeast origin of replication. Nucleic Acids Research. 25(21). 4250–4256. 16 indexed citations

20.

Wiltshire, Steven, et al.. (1995). ABF1 Ser-720 Is a Predominant Phosphorylation Site for Casein Kinase II of Saccharomyces cerevisiae. Journal of Biological Chemistry. 270(27). 16153–16159. 8 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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