Suzanne Lillis

1.7k total citations
21 papers, 829 citations indexed

About

Suzanne Lillis is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Suzanne Lillis has authored 21 papers receiving a total of 829 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 6 papers in Genetics. Recurrent topics in Suzanne Lillis's work include Cardiomyopathy and Myosin Studies (7 papers), Muscle Physiology and Disorders (5 papers) and Ion channel regulation and function (5 papers). Suzanne Lillis is often cited by papers focused on Cardiomyopathy and Myosin Studies (7 papers), Muscle Physiology and Disorders (5 papers) and Ion channel regulation and function (5 papers). Suzanne Lillis collaborates with scholars based in United Kingdom, United States and Australia. Suzanne Lillis's co-authors include Heinz Jungbluth, Stephen Abbs, Caroline A. Sewry, Francesco Muntoni, Nicole Monnier, Haiyan Zhou, Andrea Klein, Volker Straub, Thomas Winder and Kristen L. Nowak and has published in prestigious journals such as The Journal of Pediatrics, Neurobiology of Aging and Frontiers in Physiology.

In The Last Decade

Suzanne Lillis

20 papers receiving 806 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suzanne Lillis United Kingdom 13 609 388 198 143 138 21 829
Marco Savarese Finland 20 983 1.6× 477 1.2× 271 1.4× 166 1.2× 224 1.6× 72 1.3k
Edoardo Malfatti France 19 867 1.4× 370 1.0× 185 0.9× 94 0.7× 164 1.2× 89 1.1k
Emmanuelle Lacène France 17 1.3k 2.1× 415 1.1× 356 1.8× 370 2.6× 212 1.5× 32 1.5k
Gianina Ravenscroft Australia 25 1.1k 1.8× 628 1.6× 367 1.9× 239 1.7× 313 2.3× 94 1.5k
Angela Belsito Italy 10 586 1.0× 142 0.4× 77 0.4× 133 0.9× 168 1.2× 12 730
Fabiana Lubieniecki Argentina 14 362 0.6× 97 0.3× 149 0.8× 77 0.5× 126 0.9× 53 651
Jaclyn P. Kerr United States 15 615 1.0× 132 0.3× 55 0.3× 211 1.5× 103 0.7× 19 783
Nasim Vasli France 10 353 0.6× 203 0.5× 109 0.6× 87 0.6× 78 0.6× 16 466
Fédérica Piccolo United States 10 897 1.5× 238 0.6× 126 0.6× 259 1.8× 409 3.0× 21 969
Nuria Muelas Spain 18 422 0.7× 148 0.4× 160 0.8× 106 0.7× 370 2.7× 50 922

Countries citing papers authored by Suzanne Lillis

Since Specialization
Citations

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

Fields of papers citing papers by Suzanne Lillis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Lillis

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

All Works

20 of 20 papers shown
1.
Lillis, Suzanne, et al.. (2023). Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype. Clinical Dysmorphology. 32(3). 116–123. 2 indexed citations
2.
Sabir, Ataf, Jameela Sheikh, Alistair Calder, et al.. (2021). Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era. BMC Medical Genomics. 14(1). 148–148. 11 indexed citations
3.
Sambrotta, Melissa, Sandra Strautnieks, Pierre Foskett, et al.. (2021). Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology. The Journal of Pediatrics. 236. 124–130. 14 indexed citations
4.
5.
Vontell, Regina, Veena G. Supramaniam, Alice Davidson, et al.. (2019). Post-mortem Characterisation of a Case With an ACTG1 Variant, Agenesis of the Corpus Callosum and Neuronal Heterotopia. Frontiers in Physiology. 10. 623–623. 13 indexed citations
6.
Tomlinson, Andrew, Suzanne Lillis, Alexander J. German, & Robert A. Burrow. (2016). Pyloric localisation in 57 dogs of breeds susceptible to gastric dilatation‐volvulus using computed tomography. Veterinary Record. 179(24). 626–626. 4 indexed citations
7.
Astrea, Guja, Iulia Munteanu, Denise Cassandrini, et al.. (2015). A Diagnostic Dilemma in a Family With Cystinuria Type B Resolved by Muscle Magnetic Resonance. Pediatric Neurology. 52(5). 548–551. 4 indexed citations
8.
Piccirillo, Sara, Sue Colman, Nicola Potter, et al.. (2014). Genetic and Functional Diversity of Propagating Cells in Glioblastoma. Stem Cell Reports. 4(1). 7–15. 57 indexed citations
9.
Maggi, Lorenzo, Mariacristina Scoto, Sebahattin Çirak, et al.. (2013). Congenital myopathies – Clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom. Neuromuscular Disorders. 23(3). 195–205. 96 indexed citations
10.
Lillis, Suzanne, Stephen Abbs, Ana Ferreiro, Francesco Muntoni, & Heinz Jungbluth. (2011). Clinical utility gene card for: Multi-minicore disease. European Journal of Human Genetics. 20(2). 5–5. 3 indexed citations
11.
Lillis, Suzanne, et al.. (2011). Clinical utility gene card for: Central core disease. European Journal of Human Genetics. 20(2). 5–5. 6 indexed citations
12.
Dowling, James J., Suzanne Lillis, Haiyan Zhou, et al.. (2011). King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders. 21(6). 420–427. 72 indexed citations
13.
Klein, Andrea, Heinz Jungbluth, Emma Clement, et al.. (2011). Muscle Magnetic Resonance Imaging in Congenital Myopathies Due to Ryanodine Receptor Type 1 Gene Mutations. Archives of Neurology. 68(9). 1171–1171. 65 indexed citations
14.
Maggi, Lorenzo, Suzanne Lillis, Thomas Cullup, et al.. (2011). P3.31 Congenital myopathies – clinical features and frequency of individual subtypes diagnosed in a five-year period: the UK experience. Neuromuscular Disorders. 21(9-10). 691–691. 3 indexed citations
15.
Clarke, Nigel F., Leigh B. Waddell, Sandra T. Cooper, et al.. (2010). Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion. Human Mutation. 31(7). E1544–E1550. 126 indexed citations
16.
Zhou, Haiyan, Suzanne Lillis, Ryan E. Loy, et al.. (2010). Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders. 20(3). 166–173. 64 indexed citations
17.
Church, Alistair, et al.. (2010). A novel presenilin 1 mutation, I202F occurring at a previously predicted pathogenic site causing autosomal dominant Alzheimer's disease. Neurobiology of Aging. 32(3). 556.e1–556.e2. 13 indexed citations
18.
Jungbluth, Heinz, Tom Cullup, Suzanne Lillis, et al.. (2009). Centronuclear myopathy with cataracts due to a novel dynamin 2 (DNM2) mutation. Neuromuscular Disorders. 20(1). 49–52. 28 indexed citations
19.
Laing, Nigel G., Danielle E. Dye, Carina Wallgren‐Pettersson, et al.. (2009). Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1). Human Mutation. 30(9). 1267–1277. 173 indexed citations
20.
Jungbluth, Heinz, Suzanne Lillis, Haiyan Zhou, et al.. (2009). Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders. 19(5). 344–347. 39 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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