Astrid M. Manuel

537 total citations
19 papers, 255 citations indexed

About

Astrid M. Manuel is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Astrid M. Manuel has authored 19 papers receiving a total of 255 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Physiology. Recurrent topics in Astrid M. Manuel's work include Bioinformatics and Genomic Networks (9 papers), Genetic Associations and Epidemiology (6 papers) and RNA Research and Splicing (4 papers). Astrid M. Manuel is often cited by papers focused on Bioinformatics and Genomic Networks (9 papers), Genetic Associations and Epidemiology (6 papers) and RNA Research and Splicing (4 papers). Astrid M. Manuel collaborates with scholars based in United States and France. Astrid M. Manuel's co-authors include Zhongming Zhao, Yulin Dai, Peilin Jia, Ruifeng Hu, Andi Liu, Xiaoyang Li, Xianjun Dong, Guangsheng Pei, Léorah Freeman and Gleb Kichaev and has published in prestigious journals such as Nucleic Acids Research, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Astrid M. Manuel

16 papers receiving 252 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Astrid M. Manuel United States 10 131 111 30 25 25 19 255
Rungnapa Ittiwut Thailand 10 85 0.6× 83 0.7× 17 0.6× 17 0.7× 18 0.7× 26 213
Katalin Szakszon Hungary 10 178 1.4× 103 0.9× 26 0.9× 17 0.7× 9 0.4× 29 276
Zhanye Zheng China 6 159 1.2× 107 1.0× 20 0.7× 15 0.6× 19 0.8× 7 255
Shruti Marwaha United States 6 131 1.0× 123 1.1× 12 0.4× 23 0.9× 15 0.6× 19 283
Jorge Oscanoa United Kingdom 3 111 0.8× 91 0.8× 22 0.7× 19 0.8× 18 0.7× 4 241
Vlad Makarov United States 4 207 1.6× 293 2.6× 22 0.7× 15 0.6× 17 0.7× 5 420
Julie Choi United States 7 105 0.8× 93 0.8× 10 0.3× 27 1.1× 25 1.0× 11 242
Tabish Hussain United States 11 125 1.0× 86 0.8× 11 0.4× 19 0.8× 36 1.4× 25 287
Gundula Povysil United States 9 131 1.0× 141 1.3× 11 0.4× 16 0.6× 17 0.7× 18 314
Ke Zhao China 7 176 1.3× 95 0.9× 17 0.6× 8 0.3× 16 0.6× 17 263

Countries citing papers authored by Astrid M. Manuel

Since Specialization
Citations

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

Fields of papers citing papers by Astrid M. Manuel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Astrid M. Manuel. 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 Astrid M. Manuel. The network helps show where Astrid M. Manuel may publish in the future.

Co-authorship network of co-authors of Astrid M. Manuel

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

All Works

19 of 19 papers shown
1.
Liu, Andi, Xian Chen, Astrid M. Manuel, et al.. (2025). Single-nucleus multiomics reveals the disrupted regulatory programs in three brain regions of sporadic early-onset Alzheimer’s disease. Science Advances. 11(51). eadw4917–eadw4917.
2.
Manuel, Astrid M., et al.. (2025). Genetic, Transcriptomic, and Epigenomic Insights into Sjögren’s Disease: An Integrative Network Investigation and Immune Diseases Comparison. International Journal of Molecular Sciences. 26(10). 4637–4637.
3.
Chang, Le, et al.. (2025). Identification and catalog of viral transcriptional regulators in human diseases. iScience. 28(3). 112081–112081. 1 indexed citations
4.
Manuel, Astrid M., Assaf Gottlieb, Léorah Freeman, & Zhongming Zhao. (2024). Montelukast as a repurposable additive drug for standard-efficacy multiple sclerosis treatment: Emulating clinical trials with retrospective administrative health claims data. Multiple Sclerosis Journal. 30(6). 696–706. 1 indexed citations
5.
Dai, Yulin, Brisa S. Fernandes, Kai Zhang, et al.. (2024). Disentangling Accelerated Cognitive Decline from the Normal Aging Process and Unraveling Its Genetic Components: A Neuroimaging-Based Deep Learning Approach. Journal of Alzheimer s Disease. 97(4). 1807–1827. 2 indexed citations
6.
7.
Fan, Huihui, Jinze Li, Astrid M. Manuel, & Zhongming Zhao. (2023). Enzalutamide-induced signatures revealed by epigenetic plasticity using single-cell multi-omics sequencing in prostate cancer. Molecular Therapy — Nucleic Acids. 31. 648–661. 7 indexed citations
8.
Liu, Andi, Astrid M. Manuel, Yulin Dai, & Zhongming Zhao. (2022). Prioritization of risk genes in multiple sclerosis by a refined Bayesian framework followed by tissue-specificity and cell type feature assessment. BMC Genomics. 23(S4). 362–362. 8 indexed citations
9.
Liu, Andi, Astrid M. Manuel, Yulin Dai, et al.. (2022). Identifying candidate genes and drug targets for Alzheimer’s disease by an integrative network approach using genetic and brain region-specific proteomic data. Human Molecular Genetics. 31(19). 3341–3354. 10 indexed citations
10.
Manuel, Astrid M., Yulin Dai, Peilin Jia, Léorah Freeman, & Zhongming Zhao. (2022). A gene regulatory network approach harmonizes genetic and epigenetic signals and reveals repurposable drug candidates for multiple sclerosis. Human Molecular Genetics. 32(6). 998–1009. 9 indexed citations
11.
Dai, Yulin, Ruifeng Hu, Andi Liu, et al.. (2022). WebCSEA: web-based cell-type-specific enrichment analysis of genes. Nucleic Acids Research. 50(W1). W782–W790. 64 indexed citations
12.
Manuel, Astrid M., Yulin Dai, Léorah Freeman, Peilin Jia, & Zhongming Zhao. (2021). An integrative study of genetic variants with brain tissue expression identifies viral etiology and potential drug targets of multiple sclerosis. Molecular and Cellular Neuroscience. 115. 103656–103656. 9 indexed citations
13.
Jia, Peilin, Astrid M. Manuel, Brisa S. Fernandes, Yulin Dai, & Zhongming Zhao. (2021). Distinct effect of prenatal and postnatal brain expression across 20 brain disorders and anthropometric social traits: a systematic study of spatiotemporal modularity. Briefings in Bioinformatics. 22(6). 10 indexed citations
14.
Manuel, Astrid M., Yulin Dai, Léorah Freeman, Peilin Jia, & Zhongming Zhao. (2020). Dense module searching for gene networks associated with multiple sclerosis. BMC Medical Genomics. 13(S5). 48–48. 13 indexed citations
15.
Shi, Huwenbo, Kathryn S. Burch, Ruth Johnson, et al.. (2020). Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data. The American Journal of Human Genetics. 106(6). 805–817. 46 indexed citations
16.
Dai, Yulin, Ruifeng Hu, Astrid M. Manuel, et al.. (2020). CSEA-DB: an omnibus for human complex trait and cell type associations. Nucleic Acids Research. 49(D1). D862–D870. 21 indexed citations
17.
Pei, Guangsheng, Ruifeng Hu, Yulin Dai, et al.. (2020). Predicting regulatory variants using a dense epigenomic mapped CNN model elucidated the molecular basis of trait-tissue associations. Nucleic Acids Research. 49(1). 53–66. 14 indexed citations
18.
Jia, Peilin, Yulin Dai, Ruifeng Hu, et al.. (2019). TSEA-DB: a trait–tissue association map for human complex traits and diseases. Nucleic Acids Research. 48(D1). D1022–D1030. 23 indexed citations
19.
Manuel, Astrid M., D Beaupain, Paul‐Henri Roméo, & Natacha Raich. (2000). Molecular Characterization of a Novel Gene Family (PHTF) Conserved from Drosophila To Mammals. Genomics. 64(2). 216–220. 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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