Lynette G. Sadleir

9.2k total citations
66 papers, 2.3k citations indexed

About

Lynette G. Sadleir is a scholar working on Psychiatry and Mental health, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lynette G. Sadleir has authored 66 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Psychiatry and Mental health, 33 papers in Genetics and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lynette G. Sadleir's work include Epilepsy research and treatment (47 papers), Genetics and Neurodevelopmental Disorders (26 papers) and Genomics and Rare Diseases (16 papers). Lynette G. Sadleir is often cited by papers focused on Epilepsy research and treatment (47 papers), Genetics and Neurodevelopmental Disorders (26 papers) and Genomics and Rare Diseases (16 papers). Lynette G. Sadleir collaborates with scholars based in New Zealand, Australia and United States. Lynette G. Sadleir's co-authors include Ingrid E. Scheffer, Samuel F. Berkovic, K Farrell, Mary Connolly, Jacinta M. McMahon, Sara Kivity, Douglas E. Crompton, Leanne M. Dibbens, Deepak Gill and Scott C. Smith and has published in prestigious journals such as Neurology, PEDIATRICS and Annals of Neurology.

In The Last Decade

Lynette G. Sadleir

64 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lynette G. Sadleir New Zealand 24 1.4k 813 576 570 538 66 2.3k
Sara Kivity Israel 24 1.5k 1.0× 549 0.7× 449 0.8× 615 1.1× 795 1.5× 61 2.2k
Sarah Weckhuysen Belgium 26 961 0.7× 860 1.1× 1.0k 1.8× 584 1.0× 339 0.6× 71 2.3k
Ingo Helbig United States 30 1.1k 0.8× 1.3k 1.6× 1.0k 1.8× 648 1.1× 332 0.6× 124 2.8k
Lucia Fusco Italy 28 1.5k 1.0× 454 0.6× 449 0.8× 587 1.0× 740 1.4× 87 2.2k
Andreas Brunklaus United Kingdom 22 1.0k 0.7× 622 0.8× 560 1.0× 358 0.6× 458 0.9× 47 1.8k
Giuseppe Gobbi Italy 28 1.2k 0.8× 551 0.7× 435 0.8× 433 0.8× 649 1.2× 85 2.1k
Elena Freri Italy 25 908 0.6× 358 0.4× 434 0.8× 555 1.0× 476 0.9× 67 1.7k
Dinesh Talwar United States 17 978 0.7× 414 0.5× 390 0.7× 494 0.9× 524 1.0× 33 1.7k
Tilman Polster Germany 22 1.2k 0.8× 370 0.5× 348 0.6× 447 0.8× 672 1.2× 54 2.1k
Norimichi Higurashi Japan 15 2.6k 1.8× 488 0.6× 437 0.8× 1.0k 1.8× 1.4k 2.6× 40 3.4k

Countries citing papers authored by Lynette G. Sadleir

Since Specialization
Citations

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

Fields of papers citing papers by Lynette G. Sadleir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lynette G. Sadleir. 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 Lynette G. Sadleir. The network helps show where Lynette G. Sadleir may publish in the future.

Co-authorship network of co-authors of Lynette G. Sadleir

This figure shows the co-authorship network connecting the top 25 collaborators of Lynette G. Sadleir. A scholar is included among the top collaborators of Lynette G. Sadleir 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 Lynette G. Sadleir. Lynette G. Sadleir 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.
Schneider, Amy, Gaëtan Lesca, Joseph D. Symonds, et al.. (2025). SCN1A pathogenic variants do not have a distinctive blood‐derived DNA methylation signature. Epilepsia. 66(4). e66–e72.
2.
Jetté, Nathalie, Karen Parko, Pamela Roach, et al.. (2025). Epilepsy in the Indigenous peoples in Canada, Australia, New Zealand, and the USA: a systematic scoping review. The Lancet Global Health. 13(4). e656–e668. 1 indexed citations
3.
Valles‐Ibáñez, Guillem de, et al.. (2024). SCN8A self‐limited infantile epilepsy: Does epilepsy resolve?. Epilepsia. 65(8). e156–e162.
4.
Stanley, James, et al.. (2023). Indications and prescribing patterns of antiseizure medications in children in New Zealand. Developmental Medicine & Child Neurology. 65(9). 1247–1255. 2 indexed citations
5.
Hildebrand, Michael S., Guillem de Valles‐Ibáñez, Zimeng Ye, et al.. (2023). Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report. Epilepsia Open. 9(2). 758–764. 1 indexed citations
6.
Oliver, Karen, Colin A. Ellis, Ingrid E. Scheffer, et al.. (2022). Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery. EBioMedicine. 81. 104079–104079. 17 indexed citations
7.
Myers, Kenneth A., Mark F. Bennett, Bronwyn E. Grinton, et al.. (2021). Contribution of rare genetic variants to drug response in absence epilepsy. Epilepsy Research. 170. 106537–106537. 7 indexed citations
8.
Sadleir, Lynette G., Guillem de Valles‐Ibáñez, Chontelle King, et al.. (2020). Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsy. Epilepsia. 61(4). e23–e29. 16 indexed citations
9.
Scheffer, Ingrid E., Joseph Hulihan, John A. Messenheimer, et al.. (2020). Cannabidiol Transdermal Gel in Children and Adolescents with Developmental and Epileptic Encephalopathies: An Open-label Clinical Trial (1631). Neurology. 94(15_supplement). 1 indexed citations
10.
11.
Myers, Kenneth A., et al.. (2019). Fragile Females: Case Series of Epilepsy in Girls With FMR1 Disruption. PEDIATRICS. 144(3). 6 indexed citations
12.
Bergin, Peter S., Ettore Beghi, Lynette G. Sadleir, et al.. (2017). Do neurologists around the world agree when diagnosing epilepsy? – Results of an international EpiNet study. Epilepsy Research. 139. 43–50. 4 indexed citations
13.
Bergin, Peter S., Ettore Beghi, Wendyl D’Souza, et al.. (2015). The EpiNet Collaboration: Do Neurologists Around the World Agree when Diagnosing Epilepsy? - Results of a Multinational Study. (S14.004). Neurology. 84(14_supplement). 1 indexed citations
14.
Sadleir, Lynette G., E Chabrol, Eric Leguern, et al.. (2013). Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations. Epilepsy Research. 107(3). 311–317. 11 indexed citations
15.
Vears, Danya F., Meng‐Han Tsai, Lynette G. Sadleir, et al.. (2012). Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes. Epilepsia. 53(2). 319–324. 41 indexed citations
16.
Bergin, Peter S., Lynette G. Sadleir, Benjamin Legros, et al.. (2012). An international pilot study of an internet‐based platform to facilitate clinical research in epilepsy: The EpiNet project. Epilepsia. 53(10). 1829–1835. 10 indexed citations
17.
Sadleir, Lynette G. & Ingrid E. Scheffer. (2010). Optimizing Electroencephalographic Studies for Epilepsy Diagnosis in Children With New-Onset Seizures. Archives of Neurology. 67(11). 1345–9. 6 indexed citations
18.
Wiltshire, Esko, Guido Davidzon, Salvatore DiMauro, et al.. (2008). Juvenile Alpers Disease. Archives of Neurology. 65(1). 121–4. 30 indexed citations
19.
Sadleir, Lynette G. & Mary Connolly. (1998). Acquired brachial‐plexus neuropathy in the neonate: a rare presentation of late‐onset group‐B streptococcal osteomyelitis. Developmental Medicine & Child Neurology. 40(7). 496–499. 19 indexed citations
20.
Sadleir, Lynette G., et al.. (1990). Indoor cricket finger injuries.. PubMed. 103(882). 3–5. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Sara Kivity Breakdown of academic impact, for papers by Sarah Weckhuysen Breakdown of academic impact, for papers by Ingo Helbig Breakdown of academic impact, for papers by Lucia Fusco Breakdown of academic impact, for papers by Andreas Brunklaus Breakdown of academic impact, for papers by Giuseppe Gobbi Breakdown of academic impact, for papers by Elena Freri Breakdown of academic impact, for papers by Dinesh Talwar Breakdown of academic impact, for papers by Tilman Polster Breakdown of academic impact, for papers by Norimichi Higurashi
Rankless by CCL
2026