Htoo A. Wai

626 total citations
13 papers, 221 citations indexed

About

Htoo A. Wai is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Htoo A. Wai has authored 13 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Htoo A. Wai's work include RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers) and Genomics and Rare Diseases (3 papers). Htoo A. Wai is often cited by papers focused on RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers) and Genomics and Rare Diseases (3 papers). Htoo A. Wai collaborates with scholars based in United Kingdom, United States and Czechia. Htoo A. Wai's co-authors include Andrew G. L. Douglas, Diana Baralle, David J. Bunyan, Jenny Lord, Sian Ellard, N. Simon Thomas, Matthew Lyon, Adam C. Gunning, Diana Baralle and Eleanor G. Seaby and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and The International Journal of Biochemistry & Cell Biology.

In The Last Decade

Htoo A. Wai

11 papers receiving 221 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Htoo A. Wai 149 86 26 17 14 13 221
Pekka Ihalmo 148 1.0× 37 0.4× 19 0.7× 21 1.2× 9 0.6× 8 243
Lynn Pais 96 0.6× 52 0.6× 26 1.0× 8 0.5× 6 0.4× 19 168
Anthony P. Popkie 244 1.6× 78 0.9× 42 1.6× 25 1.5× 14 1.0× 10 345
Stephanie L. Battle 200 1.3× 34 0.4× 41 1.6× 5 0.3× 13 0.9× 12 326
Peter Seranski 149 1.0× 85 1.0× 23 0.9× 19 1.1× 17 1.2× 8 208
Xiangfan Zhang 308 2.1× 253 2.9× 26 1.0× 6 0.4× 10 0.7× 19 664
Jarrod A. Marto 121 0.8× 40 0.5× 27 1.0× 53 3.1× 7 0.5× 3 214
Mariko Yamane 308 2.1× 86 1.0× 21 0.8× 6 0.4× 15 1.1× 17 388
Mafei Xu 177 1.2× 34 0.4× 61 2.3× 9 0.5× 29 2.1× 12 241
Gregory Papagregoriou 135 0.9× 60 0.7× 64 2.5× 16 0.9× 14 1.0× 22 263

Countries citing papers authored by Htoo A. Wai

Since Specialization
Citations

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

Fields of papers citing papers by Htoo A. Wai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Htoo A. Wai. 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 Htoo A. Wai. The network helps show where Htoo A. Wai may publish in the future.

Co-authorship network of co-authors of Htoo A. Wai

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

All Works

13 of 13 papers shown
1.
2.
Wheway, Gabrielle, Htoo A. Wai, Woolf T. Walker, et al.. (2024). Uplift of genetic diagnosis of rare respiratory disease using airway epithelium transcriptome analysis. Human Molecular Genetics. 34(2). 148–160.
3.
Wai, Htoo A., David J. Bunyan, N. Simon Thomas, et al.. (2024). Identification of diagnostic candidates in Mendelian disorders using an RNA sequencing-centric approach. Genome Medicine. 16(1). 110–110. 3 indexed citations
4.
Lord, Jenny, Htoo A. Wai, Elena Arciero, et al.. (2024). Noncoding variants are a rare cause of recessive developmental disorders in trans with coding variants. Genetics in Medicine. 26(12). 101249–101249. 3 indexed citations
5.
Wai, Htoo A., Andrew G. L. Douglas, John W. Holloway, et al.. (2024). Tailored antisense oligonucleotides designed to correct aberrant splicing reveal actionable groups of mutations for rare genetic disorders. Experimental & Molecular Medicine. 56(8). 1816–1825. 4 indexed citations
6.
Wai, Htoo A., Tessy Thomas, David J. Bunyan, et al.. (2022). A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project. Genome Medicine. 14(1). 79–79. 20 indexed citations
7.
Jackson, Claire, Janice Coles, Amanda Harris, et al.. (2022). Temporal Whole-Transcriptomic Analysis of Characterized In Vitro and Ex Vivo Primary Nasal Epithelia. Frontiers in Cell and Developmental Biology. 10. 907511–907511. 4 indexed citations
8.
9.
Macken, William L., Gabrielle Wheway, Karen Stals, et al.. (2021). Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly. Genome Medicine. 13(1). 34–34. 23 indexed citations
10.
Wai, Htoo A., Jenny Lord, Matthew Lyon, et al.. (2020). Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance. Genetics in Medicine. 22(6). 1005–1014. 103 indexed citations
11.
Wai, Htoo A., Andrew G. L. Douglas, & Diana Baralle. (2018). RNA splicing analysis in genomic medicine. The International Journal of Biochemistry & Cell Biology. 108. 61–71. 20 indexed citations
12.
Lange, Anke, Aaron Scott, Maciej Trznadel, et al.. (2018). Early life exposure to ethinylestradiol enhances subsequent responses to environmental estrogens measured in a novel transgenic zebrafish. Scientific Reports. 8(1). 2699–2699. 16 indexed citations
13.

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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