Sue Shackleton

2.8k citations

24 papers · 2.0k indexed · 1 hit paper · h-index 16

Impact in

Cell Biology top 2%
- Cellular Mechanics and Interactions
- Microtubule and mitosis dynamics
Molecular Biology top 5%
- Nuclear Structure and Function
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
- RNA regulation and disease
- DNA Repair Mechanisms
- Muscle Physiology and Disorders

Papers in ⓘ

Genetics 3
- Congenital Ear and Nasal Anomalies 2
Molecular Biology 17
- Nuclear Structure and Function 14
- RNA Research and Splicing 13
- Genomics and Chromatin Dynamics 6
- RNA regulation and disease 4

Co-authors: David J. Lloyd (3 shared papers)Richard C. Trembath (3 shared papers)Farhana Haque (3 shared papers)Dawn T. Smallwood (4 shared papers)Catherine M. Shanahan (3 shared papers)Andrew M. Fry (2 shared papers)Carolyn L. Dent (1 shared paper)Hartmut Schmidt (1 shared paper)
Journals: Human Molecular Genetics (6 papers)Journal of Biological Chemistry (2 papers)Biochemical Society Transactions (2 papers)Nature Genetics (1 paper)Current Biology (1 paper)
Partner nations: United Kingdom India Germany

In The Last Decade

Sue Shackleton

24 papers receiving 2.0k citations

Hit Papers

align trajectories log scale

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy 2000 · 546 citations

Peers

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-authors

The 25 scholars most cited alongside Sue Shackleton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sue Shackleton Line = papers co-authored together Sue Shackleton links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	LMNA, encoding lamin A/C, is mutated in partial lipodystrophy Nature Genetics ·Sue Shackleton, David J. Lloyd, Stephen N.J. Jackson, Richard S. Evans, Martinus F. Niermeijer, Baldev Singh, Hartmut Schmidt, Georg Brabant, Sudhesh Kumar, Paul N. Durrington, Simon G. Gregory, Stephen O’Rahilly, Richard C. Trembath Hit paper breakdown →	2000	546
2	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 ·Farhana Haque, David J. Lloyd, Dawn T. Smallwood, Carolyn L. Dent, Catherine M. Shanahan, Andrew M. Fry, Richard C. Trembath, Sue Shackleton	2006	413
3	Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes Journal of Biological Chemistry ·Farhana Haque, Daniela Mazzeo, Jennifer T. Patel, Dawn T. Smallwood, Juliet A. Ellis, Catherine M. Shanahan, Sue Shackleton	2009	226
4	Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy. Diabetes ·Corinne Vigouroux, Jocelyne Magré, Marie‐Christine Vantyghem, Charlotte Bourut, Olivier Lascols, Sue Shackleton, David J. Lloyd, Bruno Guerci, Giuseppa Padova, P. Valensi, André Grimaldi, R. Piquemal, Philippe Touraine, Richard C. Trembath, Jacqueline Capeau	2000	137
5	Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization PLoS Genetics ·Peter Meinke, Elisabetta Mattioli, Farhana Haque, Susumu Antoku, Marta Columbaro, Kees R. Straatman, Howard J. Worman, Gregg G. Gundersen, Giovanna Lattanzi, Manfred Wehnert, Sue Shackleton	2014	134
6	Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells Current Biology ·Petra Gimpel, Yin Loon Lee, Radoslaw M. Sobota, Alessandra Calvi, Victoria Koullourou, Rutti Patel, Kamel Mamchaoui, François Nédélec, Sue Shackleton, Jan Schmoranzer, Brian Burke, Bruno Cadot, Edgar R. Gomes	2017	104
7	Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis Human Molecular Genetics ·Can Zhou, Chen Li, Bin Zhou, Huaqin Sun, Victoria Koullourou, Ian Holt, Megan J. Puckelwartz, Derek Warren, Robert Hayward, Ziyuan Lin, Lin Zhang, Glenn E. Morris, Elizabeth M. McNally, Sue Shackleton, Li Rao, Catherine M. Shanahan, Qiuping Zhang	2017	77
8	Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelope Nature Communications ·Petra Mikolčević, Michitaka Isoda, Hiroki Shibuya, Iván del Barco Barrantes, Ana Igea, José Á. Suja, Sue Shackleton, Yoshinori Watanabe, Ángel R. Nebreda	2016	50
9	A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus Human Molecular Genetics ·Rachel Watkins, Rajkumar V. Patil, Benjamin T. Goult, Mervyn G. Thomas, Irène Gottlob, Sue Shackleton	2013	47
10	MicroRNA expression profiling in patients with lamin A/C‐associated muscular dystrophy The FASEB Journal ·Nicolas Sylvius, Gisèle Bonne, Kees R. Straatman, T. Rama Reddy, Timothy W. Gant, Sue Shackleton	2011	43
11	The Role of FRMD7 in Idiopathic Infantile Nystagmus Journal of Ophthalmology ·Rachel Watkins, Mervyn G. Thomas, Chris J. Talbot, Irène Gottlob, Sue Shackleton	2011	37
12	Mitotic phosphorylation of SUN1 loosens its connection with the nuclear lamina while the LINC complex remains intact Nucleus ·Jennifer T. Patel, Andrew R. Bottrill, Suzanna L. Prosser, Sangeetha Jayaraman, Kees R. Straatman, Andrew M. Fry, Sue Shackleton	2014	35
13	The Stop Mutation R553X in the CFTR Gene Results in Exon Skipping Genomics ·Jeremy Hull, Sue Shackleton, Ann Harris	1994	32
14	Hutchinson–Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature British Journal of Dermatology ·J. Mazereeuw‐Hautier, Louise C. Wilson, Shehla Mohammed, Dawn T. Smallwood, Sue Shackleton, David J. Atherton, John Harper	2007	29
15	Analysis of mutations and alternative splicing patterns in the CFTR gene using mRNA derived from nasal epithelial cells Human Molecular Genetics ·Jeremy Hull, Sue Shackleton, Ann Harris	1994	26
16	Abnormal mRNA splicing resulting from three different mutations in the CFTR gene Human Molecular Genetics ·Jeremy Hull, Sue Shackleton, Ann Harris	1993	22
17	Identification of rare and novel mutations in the CFTR genes of CF patients in Southern England Human Mutation ·Sue Shackleton, Jeremy Hull, Simon Dear, A Seller, Anne Thomson, Ann Harris	1994	13
18	RAC1 induces nuclear alterations through the LINC complex to enhance melanoma invasiveness Molecular Biology of the Cell ·Paula Colón‐Bolea, Rocío García‐Gómez, Sue Shackleton, Piero Crespo, Xosé R. Bustelo, Berta Casar	2020	11
19	Role of Two Dileucine-like Motifs in Insulin Receptor Anchoring to Microvilli Journal of Biological Chemistry ·Sue Shackleton, Isabelle Hamer, Michelangelo Foti, Nicole Zumwald, Christine Maeder, Jean‐Louis Carpentier	2002	7
20	Lamin A-linked progerias: is farnesylation the be all and end all? Biochemical Society Transactions ·Dawn T. Smallwood, Sue Shackleton	2010	7

About Sue Shackleton

Sue Shackleton is a scholar working on Genetics, Molecular Biology, Neurology, Pulmonary and Respiratory Medicine and Ophthalmology, having authored 24 papers that have together received 2.0k indexed citations. Recurring topics across this work include Nuclear Structure and Function (14 papers), RNA Research and Splicing (13 papers), Genomics and Chromatin Dynamics (6 papers), Cystic Fibrosis Research Advances (5 papers), RNA regulation and disease (4 papers), Tracheal and airway disorders (4 papers), Neonatal Respiratory Health Research (3 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Cell Biology (471 citations), Molecular Biology (1.8k citations), Neurology (53 citations), Genetics (61 citations) and Developmental Biology (12 citations). Sue Shackleton has collaborated with scholars based in United Kingdom, India and Germany. Frequent 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 Georg Brabant. Their work appears in journals such as Human Molecular Genetics, Journal of Biological Chemistry, Biochemical Society Transactions, Nature Genetics and Current Biology.

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.

Explore authors with similar magnitude of impact