S. E. A. Leigh

6.2k total citations
19 papers, 722 citations indexed

About

S. E. A. Leigh is a scholar working on Surgery, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, S. E. A. Leigh has authored 19 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Surgery, 9 papers in Pathology and Forensic Medicine and 7 papers in Genetics. Recurrent topics in S. E. A. Leigh's work include Lipoproteins and Cardiovascular Health (10 papers), Genetic factors in colorectal cancer (9 papers) and Genomics and Rare Diseases (3 papers). S. E. A. Leigh is often cited by papers focused on Lipoproteins and Cardiovascular Health (10 papers), Genetic factors in colorectal cancer (9 papers) and Genomics and Rare Diseases (3 papers). S. E. A. Leigh collaborates with scholars based in United Kingdom, Netherlands and United States. S. E. A. Leigh's co-authors include Steve E. Humphries, Christina Hubbart, Ros Whittall, Marta Futema, Nicholas Lench, Alison Taylor, Christine Orengo, Corin Yeats, Jacopo Celli and Andrew C.R. Martin and has published in prestigious journals such as British Journal of Cancer, Atherosclerosis and Journal of Endocrinology.

In The Last Decade

S. E. A. Leigh

19 papers receiving 706 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S. E. A. Leigh United Kingdom 10 504 175 146 142 140 19 722
E. Langenhoven South Africa 14 526 1.0× 166 0.9× 68 0.5× 165 1.2× 152 1.1× 27 631
Claudio Rabacchi Italy 13 266 0.5× 118 0.7× 44 0.3× 105 0.7× 170 1.2× 27 539
Gertraud Erhart Austria 11 187 0.4× 108 0.6× 13 0.1× 143 1.0× 64 0.5× 13 430
A. Dhyani Italy 6 205 0.4× 57 0.3× 19 0.1× 192 1.4× 53 0.4× 11 479
Matthew Peach United States 5 174 0.3× 72 0.4× 14 0.1× 112 0.8× 75 0.5× 7 366
Melanie P. Derman United States 6 124 0.2× 39 0.2× 19 0.1× 184 1.3× 92 0.7× 7 420
Alexandra Coomans de Brachène Belgium 9 240 0.5× 101 0.6× 30 0.2× 292 2.1× 149 1.1× 14 688
Makoto Naito Japan 7 151 0.3× 150 0.9× 75 0.5× 388 2.7× 131 0.9× 16 774
Ye Jin Ha South Korea 13 96 0.2× 89 0.5× 93 0.6× 160 1.1× 113 0.8× 27 615
Haitao Zheng China 17 208 0.4× 232 1.3× 49 0.3× 316 2.2× 189 1.4× 58 724

Countries citing papers authored by S. E. A. Leigh

Since Specialization
Citations

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

Fields of papers citing papers by S. E. A. Leigh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. E. A. Leigh

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

All Works

19 of 19 papers shown
1.
Iacocca, Michael A., Joana Rita Chora, Alain Carrié, et al.. (2018). Adaptation of ACMG/AMP Guidelines for Standardized Variant Interpretation in Familial Hypercholesterolemia. Atherosclerosis Supplements. 32. 51–51. 1 indexed citations
2.
Chora, Joana Rita, Michael A. Iacocca, Alain Carrié, et al.. (2018). Adaptation of ACMG/AMP guidelines for variant interpretation in familial hypercholesterolemia - A clingen fh expert panel pilot study. Atherosclerosis. 275. e98–e98. 3 indexed citations
3.
Leigh, S. E. A., Marta Futema, Ros Whittall, et al.. (2016). The UCL low-density lipoprotein receptor gene variant database: pathogenicity update. Journal of Medical Genetics. 54(4). 217–223. 69 indexed citations
4.
Khamis, Amna, Jutta Palmen, Nicholas Lench, et al.. (2014). Functional analysis of four LDLR 5′UTR and promoter variants in patients with familial hypercholesterolaemia. European Journal of Human Genetics. 23(6). 790–795. 22 indexed citations
5.
Futema, Marta, Ros Whittall, Jackie A. Cooper, et al.. (2013). Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic. Atherosclerosis. 229(1). 161–168. 77 indexed citations
6.
Leigh, S. E. A., Ros Whittall, Nicholas Lench, et al.. (2012). Low‐Density Lipoprotein Receptor Gene Familial Hypercholesterolemia Variant Database: Update and Pathological Assessment. Annals of Human Genetics. 76(5). 387–401. 152 indexed citations
7.
Pećin, Ivan, Ros Whittall, Marta Futema, et al.. (2012). Mutation detection in Croatian patients with Familial Hypercholesterolemia. Annals of Human Genetics. 77(1). 22–30. 9 indexed citations
8.
Humphries, Steve E., et al.. (2008). What is the clinical utility of DNA testing in patients with familial hypercholesterolaemia?. Current Opinion in Lipidology. 19(4). 362–368. 53 indexed citations
9.
Leigh, S. E. A., et al.. (2008). Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database. Annals of Human Genetics. 72(4). 485–498. 184 indexed citations
10.
Leigh, S. E. A., Ros Whittall, & Steve E. Humphries. (2007). Update and analysis of the UCL low density lipoprotein receptor gene familial hypercholesterolemia database. Atherosclerosis. 194(1). 283–283. 2 indexed citations
11.
Lloyd, Sarah E., J T Pang, Simon H. S. Pearce, S. E. A. Leigh, & Rajesh V. Thakker. (1997). Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1). Human Genetics. 99(5). 585–589. 4 indexed citations
12.
Pang, J T, Sarah E. Lloyd, C Wooding, et al.. (1996). Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene. Human Genetics. 97(6). 732–741. 29 indexed citations
13.
Rees, Mark I., S. E. A. Leigh, Joy D.A. Delhanty, L Bowles, & I C Talbot. (1993). Molecular genetic evidence for the delineation of more severe form of familial adenomatous polyposis which results from fresh mutation. Annals of Human Genetics. 57(2). 97–104. 4 indexed citations
14.
Sowden, Jane C., S. E. A. Leigh, Ian Talbot, Joy D.A. Delhanty, & Yvonne H. Edwards. (1993). Expression from the proximal promoter of the carbonic anhydrase 1 gene as a marker for differentiation in colon epithelia. Differentiation. 53(2). 67–74. 37 indexed citations
15.
Leigh, S. E. A. & F. Stewart. (1990). Partial cDNA sequence for the donkey chorionic gonadotrophin-β subunit suggests evolution from an ancestral LH-β gene. Journal of Molecular Endocrinology. 4(2). 143–150. 9 indexed citations
16.
Leigh, S. E. A., et al.. (1990). Use of fluorescent in situ hybridization to confirm trisomy of chromosome region 1q32‐qter as the sole karyotypic defect in a colon cancer cell line. Genes Chromosomes and Cancer. 1(4). 281–283. 3 indexed citations
17.
Rees, Mark I., S. E. A. Leigh, JDA Delhanty, & Jeremy R. Jass. (1989). Chromosome 5 allele loss in familial and sporadic colorectal adenomas. British Journal of Cancer. 59(3). 361–365. 33 indexed citations
18.
Rees, Mark I., S. E. A. Leigh, Jeremy R. Jass, A Gunn, & Joy D.A. Delhanty. (1989). 117 Chromosome 5 allele loss in familial and sporadic colorectal adenomas. Cancer Genetics and Cytogenetics. 38(2). 197–197. 1 indexed citations
19.
Stewart, F., J A Thomson, S. E. A. Leigh, & J Warwick. (1987). Nucleotide (cDNA) sequence encoding the horse gonadotrophin α-subunit. Journal of Endocrinology. 115(2). 341–346. 30 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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