Sue Shackleton

2.8k total citations · 1 hit paper
24 papers, 2.0k citations indexed

About

Sue Shackleton is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Sue Shackleton has authored 24 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Sue Shackleton's work include Nuclear Structure and Function (14 papers), RNA Research and Splicing (13 papers) and Genomics and Chromatin Dynamics (6 papers). Sue Shackleton is often cited by papers focused on Nuclear Structure and Function (14 papers), RNA Research and Splicing (13 papers) and Genomics and Chromatin Dynamics (6 papers). Sue Shackleton collaborates with scholars based in United Kingdom, France and India. Sue Shackleton's co-authors include David J. Lloyd, Richard C. Trembath, Farhana Haque, Dawn T. Smallwood, Catherine M. Shanahan, Andrew M. Fry, Carolyn L. Dent, Hartmut Schmidt, Simon G. Gregory and Paul N. Durrington and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Nature Genetics.

In The Last Decade

Sue Shackleton

24 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

2000 546 citations Sue Shackleton, David J. Lloyd et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sue Shackleton United Kingdom	16	1.8k	471	132	128	122	24	2.0k
Elisabetta Mattioli Italy	26	1.8k 1.0×	333 0.7×	181 1.4×	88 0.7×	122 1.0×	52	2.0k
Zoe M. Goeckeler United States	12	733 0.4×	553 1.2×	131 1.0×	42 0.3×	149 1.2×	15	1.2k
Manfred Wehnert Germany	28	2.8k 1.6×	565 1.2×	116 0.9×	188 1.5×	272 2.2×	86	3.0k
Debora Rapaport Israel	19	805 0.5×	439 0.9×	235 1.8×	142 1.1×	140 1.1×	30	1.2k
Krishnakumar Kizhatil United States	16	591 0.3×	324 0.7×	326 2.5×	124 1.0×	78 0.6×	22	1.1k
Haruko Nakano United States	16	809 0.5×	205 0.4×	68 0.5×	107 0.8×	216 1.8×	34	1.1k
Steven G. Webster United States	4	995 0.6×	162 0.3×	129 1.0×	154 1.2×	155 1.3×	6	1.2k
Xiaozhong Shi United States	20	1.2k 0.7×	253 0.5×	122 0.9×	147 1.1×	78 0.6×	29	1.4k
Lily Shen Australia	9	887 0.5×	107 0.2×	93 0.7×	39 0.3×	63 0.5×	13	1.1k
Lauren M. Goddard United States	8	396 0.2×	163 0.3×	180 1.4×	50 0.4×	69 0.6×	9	868

Countries citing papers authored by Sue Shackleton

Since Specialization

Citations

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

Fields of papers citing papers by Sue Shackleton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sue Shackleton

This figure shows the co-authorship network connecting the top 25 collaborators of Sue Shackleton. A scholar is included among the top collaborators of Sue Shackleton 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 Sue Shackleton. Sue Shackleton 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

Shackleton, Sue, et al.. (2020). RAC1 induces nuclear alterations through the LINC complex to enhance melanoma invasiveness. Molecular Biology of the Cell. 31(25). 2768–2778. 11 indexed citations

Li, Chen, Bin Zhou, Ian Holt, et al.. (2017). Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis. Human Molecular Genetics. 26(12). 2258–2276. 77 indexed citations

Lee, Yin Loon, Radoslaw M. Sobota, Alessandra Calvi, et al.. (2017). Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells. Current Biology. 27(19). 2999–3009.e9. 104 indexed citations

Mikolčević, Petra, Michitaka Isoda, Hiroki Shibuya, et al.. (2016). Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelope. Nature Communications. 7(1). 11084–11084. 50 indexed citations

Bottrill, Andrew R., Suzanna L. Prosser, Sangeetha Jayaraman, et al.. (2014). Mitotic phosphorylation of SUN1 loosens its connection with the nuclear lamina while the LINC complex remains intact. Nucleus. 5(5). 462–473. 35 indexed citations

Meinke, Peter, Elisabetta Mattioli, Farhana Haque, et al.. (2014). Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization. PLoS Genetics. 10(9). e1004605–e1004605. 134 indexed citations

Watkins, Rachel, Rajkumar V. Patil, Benjamin T. Goult, et al.. (2013). A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus. Human Molecular Genetics. 22(10). 2105–2118. 47 indexed citations

Sylvius, Nicolas, et al.. (2011). MicroRNA expression profiling in patients with lamin A/C‐associated muscular dystrophy. The FASEB Journal. 25(11). 3966–3978. 43 indexed citations

Haque, Farhana, Daniela Mazzeo, Dawn T. Smallwood, et al.. (2009). Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes. Journal of Biological Chemistry. 285(5). 3487–3498. 226 indexed citations

10.

Mazereeuw‐Hautier, J., Louise C. Wilson, Shehla Mohammed, et al.. (2007). Hutchinson–Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature. British Journal of Dermatology. 156(6). 1308–1314. 29 indexed citations

11.

Haque, Farhana, David J. Lloyd, Dawn T. Smallwood, et al.. (2006). SUN1 Interacts with Nuclear Lamin A and Cytoplasmic Nesprins To Provide a Physical Connection between the Nuclear Lamina and the Cytoskeleton. Molecular and Cellular Biology. 26(10). 3738–3751. 413 indexed citations

12.

Shackleton, Sue, et al.. (2002). Role of Two Dileucine-like Motifs in Insulin Receptor Anchoring to Microvilli. Journal of Biological Chemistry. 277(46). 43631–43637. 7 indexed citations

13.

Shackleton, Sue, David J. Lloyd, Richard S. Evans, et al.. (2000). LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nature Genetics. 24(2). 153–156. 546 indexed citations breakdown →

14.

Shackleton, Sue, et al.. (1995). A cystic fibrosis patient who is homozygous for the A559T mutation.. PubMed. 57(3). 734–734. 3 indexed citations

15.

Hull, Jeremy, Sue Shackleton, & Ann Harris. (1994). The Stop Mutation R553X in the CFTR Gene Results in Exon Skipping. Genomics. 19(2). 362–364. 32 indexed citations

16.

Hull, Jeremy, Sue Shackleton, & Ann Harris. (1994). Analysis of mutations and alternative splicing patterns in the CFTR gene using mRNA derived from nasal epithelial cells. Human Molecular Genetics. 3(7). 1141–1146. 26 indexed citations

17.

Shackleton, Sue, Jeremy Hull, Simon Dear, et al.. (1994). Identification of rare and novel mutations in the CFTR genes of CF patients in Southern England. Human Mutation. 3(2). 141–151. 13 indexed citations

18.

Hull, Jeremy, Sue Shackleton, & Ann Harris. (1993). Abnormal mRNA splicing resulting from three different mutations in the CFTR gene. Human Molecular Genetics. 2(6). 689–692. 22 indexed citations

19.

Shackleton, Sue & A. Sidney Harris. (1992). G27X: a novel mutation in exon 2 of the CF gene. Human Molecular Genetics. 1(6). 445–445. 4 indexed citations

20.

Shackleton, Sue, Frances Beards, & Ann Harris. (1992). Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP. Human Molecular Genetics. 1(6). 439–440. 6 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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