Allan Bayat

2.4k total citations
61 papers, 557 citations indexed

About

Allan Bayat is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Allan Bayat has authored 61 papers receiving a total of 557 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 28 papers in Molecular Biology and 9 papers in Epidemiology. Recurrent topics in Allan Bayat's work include Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (18 papers) and Metabolism and Genetic Disorders (9 papers). Allan Bayat is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Genomics and Rare Diseases (18 papers) and Metabolism and Genetic Disorders (9 papers). Allan Bayat collaborates with scholars based in Denmark, United Kingdom and United States. Allan Bayat's co-authors include Rikke S. Møller, Helle Hjalgrim, Guido Rubboli, Marie-Laure Bouchy Jacobsson, Christina Fenger, Konstantinos Kamperis, Troels Herlin, Bronwyn Kerr, Laura Roos and Sofia Douzgou and has published in prestigious journals such as Bioinformatics, The American Journal of Human Genetics and Molecules.

In The Last Decade

Allan Bayat

54 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Allan Bayat Denmark 13 233 205 167 111 59 61 557
Radhika Dhamija United States 16 193 0.8× 222 1.1× 144 0.9× 76 0.7× 92 1.6× 64 721
Shin Okazaki Japan 12 160 0.7× 243 1.2× 148 0.9× 66 0.6× 112 1.9× 79 620
Ichiro Kuki Japan 13 143 0.6× 203 1.0× 192 1.1× 106 1.0× 107 1.8× 87 675
Pilar Póo Spain 17 201 0.9× 187 0.9× 155 0.9× 206 1.9× 44 0.7× 34 688
Haiqing Xu China 8 284 1.2× 217 1.1× 243 1.5× 84 0.8× 111 1.9× 16 588
Takehiko Inui Japan 13 116 0.5× 194 0.9× 126 0.8× 103 0.9× 46 0.8× 48 459
Hisashi Kawawaki Japan 12 116 0.5× 173 0.8× 177 1.1× 78 0.7× 96 1.6× 63 541
Robertino Dilena Italy 13 106 0.5× 170 0.8× 319 1.9× 155 1.4× 162 2.7× 39 716
Shin Nabatame Japan 12 99 0.4× 155 0.8× 87 0.5× 57 0.5× 74 1.3× 39 408
Rosario Berardi Italy 14 189 0.8× 146 0.7× 84 0.5× 108 1.0× 47 0.8× 29 422

Countries citing papers authored by Allan Bayat

Since Specialization
Citations

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

Fields of papers citing papers by Allan Bayat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Allan Bayat

This figure shows the co-authorship network connecting the top 25 collaborators of Allan Bayat. A scholar is included among the top collaborators of Allan Bayat 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 Allan Bayat. Allan Bayat 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.
Low, Karen, Julia Foreman, Berta Almoguera, et al.. (2025). The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disorders. European Journal of Human Genetics. 34(3). 348–356.
2.
Nicolai, Joost, Elisabeth A. Cats, Gerhard Kluger, et al.. (2025). Amitriptyline use in individuals with KCNQ2/3 gain‐of‐function variants: A retrospective cohort study. Epilepsia. 66(5). 1628–1640. 2 indexed citations
3.
Vriendt, Els De, An‐Sofie Schoonjans, Allan Bayat, et al.. (2025). Fibroblast transcriptomics uncovers pathogenic genomic variants in individuals with exome‐negative childhood onset epilepsy. Epilepsia. 66(5). 1613–1627.
4.
Stödberg, Tommy, Malin Kvarnung, Katrina Tatton‐Brown, et al.. (2024). Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variant. Clinical Genetics. 106(4). 427–436. 1 indexed citations
5.
Lefebvre, Mathilde, Caterina Zanus, Irene Bruno, et al.. (2024). In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder. Biomolecules. 14(12). 1626–1626. 1 indexed citations
6.
Sjöström, Elisabeth Stoltz, Ange‐Line Bruel, Christophe Philippe, et al.. (2024). Exploring the Cognitive and Behavioral Aspects of Shprintzen‐Goldberg Syndrome; a Novel Cohort and Literature Review. Clinical Genetics. 107(3). 328–334.
7.
Ali, Quratulain Zulfiqar, Ángel Aledo‐Serrano, Allan Bayat, et al.. (2024). Adult Phenotype of CHD2 -Associated Disorders. Neurology Genetics. 10(6). e200194–e200194.
8.
Lewis, Sara A., Somayeh Bakhtiari, Allan Bayat, et al.. (2023). AGAP1-associated endolysosomal trafficking abnormalities link gene–environment interactions in neurodevelopmental disorders. Disease Models & Mechanisms. 16(9). 5 indexed citations
9.
Fenger, Christina, Trine Bjørg Hammer, Veronica M. Pravatà, et al.. (2023). An O-GlcNAc transferase pathogenic variant linked to intellectual disability affects pluripotent stem cell self-renewal. Disease Models & Mechanisms. 16(6). 10 indexed citations
10.
Jansen, Floor E., Charlotte W. Ockeloen, Marjan J. A. van Kempen, et al.. (2023). Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome. Epilepsia Open. 8(4). 1300–1313. 7 indexed citations
11.
Pérez‐Palma, Eduardo, Tobias Brünger, Konrad Platzer, et al.. (2023). CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online. Bioinformatics. 39(5). 8 indexed citations
12.
13.
Johannesen, Katrine M., Zeynep Tümer, Sarah Weckhuysen, Tahsin Stefan Barakat, & Allan Bayat. (2023). Solving the unsolved genetic epilepsies: Current and future perspectives. Epilepsia. 64(12). 3143–3154. 8 indexed citations
14.
Grimmel, Mona, Darius Ebrahimi‐Fakhari, Angelika Rieß, et al.. (2022). Expansion of the phenotypic and molecular spectrum of CWF19L1 ‐related disorder. Clinical Genetics. 103(5). 566–573. 2 indexed citations
15.
Bayat, Allan, et al.. (2022). Neurological manifestation of 22q11.2 deletion syndrome. Neurological Sciences. 43(3). 1695–1700. 16 indexed citations
16.
Bayat, Allan, et al.. (2022). Atypical painful stroke presentations: A review. Acta Neurologica Scandinavica. 146(5). 465–474. 1 indexed citations
17.
Ellard, Sian, Karen Stals, Emma L. Baple, et al.. (2022). Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome. The American Journal of Human Genetics. 109(7). 1217–1241. 22 indexed citations
18.
Ivanovski, Ivan, Stefano Giuseppe Caraffi, Maria Elisabeth Street, et al.. (2018). Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11. American Journal of Medical Genetics Part A. 176(9). 1991–1995. 4 indexed citations
19.
Bayat, Allan, Lisbeth Birk Møller, & Allan M. Lund. (2015). [Diagnostics and treatment of phenylketonuria].. PubMed. 177(8). 2 indexed citations
20.
Bayat, Allan, et al.. (2013). Nitrous oxide provides safe and effective analgesia for minor paediatric procedures--a systematic review.. PubMed. 60(6). A4627–A4627. 45 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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