Adeline Ngoh

1.4k total citations
15 papers, 367 citations indexed

About

Adeline Ngoh is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Adeline Ngoh has authored 15 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Psychiatry and Mental health, 7 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Adeline Ngoh's work include Epilepsy research and treatment (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Adeline Ngoh is often cited by papers focused on Epilepsy research and treatment (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Adeline Ngoh collaborates with scholars based in United Kingdom, Singapore and India. Adeline Ngoh's co-authors include Esther Meyer, Amy McTague, Manju A. Kurian, Apostolos Papandreou, Richard H. Scott, Natalie Trump, Rodger Palmer, Jane A. Hurst, Lucy Jenkins and C. R. Boustred and has published in prestigious journals such as SHILAP Revista de lepidopterología, Nature Neuroscience and Annals of Neurology.

In The Last Decade

Adeline Ngoh

14 papers receiving 363 citations

Peers

Adeline Ngoh

GENET

PMH

CMN

NEURO

Théo Ribierre France

Shino Shimada Japan

Manuela Pendziwiat Germany

Francisca Millan United States

Takuya Hiraide Japan

Delphine Héron France

Holger Trucks Germany

Christopher M. LaCoursiere United States

Tomoko Toyota Japan

Amanda Lindy United States

Théo Ribierre France

Adeline Ngoh

216 ×1.2

GENET

245 ×1.8

146 ×1.1

PMH

90 ×1.3

CMN

10 ×0.2

NEURO

Citations per year, relative to Adeline Ngoh Adeline Ngoh (= 1×) peers Théo Ribierre

Countries citing papers authored by Adeline Ngoh

Since Specialization

Citations

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

Fields of papers citing papers by Adeline Ngoh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adeline Ngoh

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

All Works

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15 of 15 papers shown

Ngoh, Adeline, Xiumin Chen, Kimberley M. Reid, et al.. (2025). Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study. Annals of Neurology. 98(5). 951–966.

Huang, Hua, Rui Dong, Derrick Chan, et al.. (2024). Targeting heterozygous dominant negative variant of KCNA2 using Gapmer ASO for the treatment of drug-resistant epilepsy. Molecular Therapy — Nucleic Acids. 35(4). 102316–102316. 1 indexed citations

Yoon, Sungwon, Hendra Goh, Sze Ling Chan, et al.. (2022). Parents’ priorities for decision-making of pediatric epilepsy treatments and perceived needs for decision support in multi-ethnic Asian clinical setting: A qualitative analysis. Epilepsy & Behavior. 135. 108880–108880. 3 indexed citations

Kumar, Pavanish, Sharifah Nur Hazirah, Camillus Chua, et al.. (2022). Single-cell transcriptomics and surface epitope detection in human brain epileptic lesions identifies pro-inflammatory signaling. Nature Neuroscience. 25(7). 956–966. 68 indexed citations

Tan, Siqi, Adeline Ngoh, Wai Hoe Ng, et al.. (2021). Evaluation and outcomes of paediatric epilepsy surgery in Singapore: A single-centre audit. Neurology Asia. 26(3). 509–520. 1 indexed citations

Ngoh, Adeline, et al.. (2021). Overview of Landau–Kleffner syndrome: early treatment, tailored education and therapy improve outcome. Paediatrics and Child Health. 31(5). 207–219. 3 indexed citations

Ngoh, Adeline, et al.. (2021). Unique Severe HyperEkplexia-Like Apneic Events (SHELAE) Improved by High-Dose Piracetam. SHILAP Revista de lepidopterología. 8. 2329048X211046447–2329048X211046447. 1 indexed citations

Kumar, Pavanish, Derrick Chan, Bhairav Paleja, et al.. (2019). Proinflammatory IL-17 pathways dominate the architecture of the immunome in pediatric refractory epilepsy. JCI Insight. 4(8). 36 indexed citations

Ngoh, Adeline, José Brás, Rita Guerreiro, et al.. (2017). <i>TBC1D24</i> Mutations in a Sibship with Multifocal Polymyoclonus. Tremor and Other Hyperkinetic Movements. 7(0). 452–452. 11 indexed citations

10.

Ngoh, Adeline & Alasdair Parker. (2017). New developments in epilepsy management. Paediatrics and Child Health. 27(6). 281–286. 1 indexed citations

11.

Ngoh, Adeline, José Brás, Rita Guerreiro, et al.. (2017). TBC1D24 Mutations in a Sibship with Multifocal Polymyoclonus. SHILAP Revista de lepidopterología. 7. 452–452. 8 indexed citations

12.

Trump, Natalie, Amy McTague, Helen Brittain, et al.. (2016). Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. Journal of Medical Genetics. 53(5). 310–317. 147 indexed citations

13.

Ngoh, Adeline, José Brás, Rita Guerreiro, et al.. (2016). RARS2 mutations in a sibship with infantile spasms. Epilepsia. 57(5). e97–e102. 22 indexed citations

14.

Papandreou, Apostolos, Amy McTague, Natalie Trump, et al.. (2015). GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy. Developmental Medicine & Child Neurology. 58(4). 416–420. 48 indexed citations

15.

Ngoh, Adeline, Amy McTague, Ingrid M. Wentzensen, et al.. (2014). Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum. Developmental Medicine & Child Neurology. 56(11). 1124–1128. 17 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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