Ka Man Wu

903 total citations
7 papers, 93 citations indexed

About

Ka Man Wu is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ka Man Wu has authored 7 papers receiving a total of 93 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ka Man Wu's work include CRISPR and Genetic Engineering (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Neuroscience and Neuropharmacology Research (2 papers). Ka Man Wu is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Neuroscience and Neuropharmacology Research (2 papers). Ka Man Wu collaborates with scholars based in Netherlands, Norway and Italy. Ka Man Wu's co-authors include Nael Nadif Kasri, Naoki Kogo, Hans van Bokhoven, Dirk Schubert, Elly Lewerissa, Ronald Roepman, Tjitske Kleefstra, Chantal Schoenmaker, Jon-Ruben van Rhijn and Ibrahim A. Akkouh and has published in prestigious journals such as Brain, Cell Reports and Stem Cell Research.

In The Last Decade

Ka Man Wu

7 papers receiving 92 citations

Peers

Ka Man Wu
Patrícia B. S. Celestino-Soper United States
Justin Truong United States
Danielle Nolan United States
Sohnee Ahmed Canada
Lea K. Davis United States
Chuan Tan Australia
Asraa Ahmed United States
Cailyn H. Spurrell United States
Kate V. Everett United Kingdom
Stephanie Karch Germany
Patrícia B. S. Celestino-Soper United States
Ka Man Wu
Citations per year, relative to Ka Man Wu Ka Man Wu (= 1×) peers Patrícia B. S. Celestino-Soper

Countries citing papers authored by Ka Man Wu

Since Specialization
Citations

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

Fields of papers citing papers by Ka Man Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ka Man Wu. 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 Ka Man Wu. The network helps show where Ka Man Wu may publish in the future.

Co-authorship network of co-authors of Ka Man Wu

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

All Works

7 of 7 papers shown
1.
Hugte, Eline van, Elly Lewerissa, Ka Man Wu, et al.. (2023). SCN1A -deficient excitatory neuronal networks display mutation-specific phenotypes. Brain. 146(12). 5153–5167. 22 indexed citations
2.
Schoenmaker, Chantal, et al.. (2023). Generation of induced pluripotent stem cell line carrying frameshift variants in NPHP1 (UCSFi001-A-68) using CRISPR/Cas9. Stem Cell Research. 68. 103053–103053. 2 indexed citations
3.
Wu, Ka Man, et al.. (2023). Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9. Stem Cell Research. 71. 103173–103173. 3 indexed citations
4.
Wu, Ka Man, et al.. (2023). Generation of an induced pluripotent stem cell line carrying a biallelic deletion (SCTCi019-A) in GCDH using CRISPR/Cas9. Stem Cell Research. 69. 103069–103069. 2 indexed citations
5.
Wang, Shan, Jon-Ruben van Rhijn, Ibrahim A. Akkouh, et al.. (2022). Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through the cAMP/PKA pathway. Cell Reports. 39(5). 110790–110790. 37 indexed citations
6.
Wang, Shan, Jon-Ruben van Rhijn, Ibrahim A. Akkouh, et al.. (2021). Loss-of-Function Variants in the Schizophrenia Risk Gene Setd1a Alter Neuronal Network Activity in Human Neurons Through Camp/Pka Pathway. SSRN Electronic Journal. 2 indexed citations
7.
Oud, Machteld M., Brooke Latour, Zeineb Bakey, et al.. (2018). Cellular ciliary phenotyping indicates pathogenicity of novel variants in IFT140 and confirms a Mainzer–Saldino syndrome diagnosis. PubMed. 7(1). 1–1. 25 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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2026