Charlly Kao

1.7k total citations
20 papers, 233 citations indexed

About

Charlly Kao is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Charlly Kao has authored 20 papers receiving a total of 233 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Cognitive Neuroscience. Recurrent topics in Charlly Kao's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Autism Spectrum Disorder Research (4 papers). Charlly Kao is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Autism Spectrum Disorder Research (4 papers). Charlly Kao collaborates with scholars based in United States, Iceland and China. Charlly Kao's co-authors include Håkon Håkonarson, Joseph Glessner, Hui‐Qi Qu, Patrick Sleiman, Josephine Elia, John J. Connolly, Raquel E. Gur, Nadine Cohen, Dai Wang and Qingqin S. Li and has published in prestigious journals such as Nature Communications, Cancer Research and Scientific Reports.

In The Last Decade

Charlly Kao

16 papers receiving 230 citations

Peers

Charlly Kao

GENET

PMH

CMN

Aaron D. Besterman United States

Sorina Mihaela Papuc Romania

Matthew J. Gazzellone Canada

Guannan Li China

Amber Boys Australia

Heidi Mateus Colombia

Hirofumi Kashii Japan

Ping Yee Billie Au Canada

Dima El‐Khechen United States

Caroline Nava France

Aaron D. Besterman United States

Charlly Kao

110 ×1.0

130 ×1.2

GENET

52 ×1.3

45 ×1.1

PMH

30 ×1.2

CMN

Citations per year, relative to Charlly Kao Charlly Kao (= 1×) peers Aaron D. Besterman

Countries citing papers authored by Charlly Kao

Since Specialization

Citations

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

Fields of papers citing papers by Charlly Kao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charlly Kao

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Qu, Hui‐Qi, Joseph Glessner, Charlly Kao, & Håkon Håkonarson. (2025). Data-informed insights into sex differences in peripheral blood mononuclear cells from single-cell transcriptomics. Genes & Diseases. 12(5). 101525–101525.

Gutiérrez-Uzquiza, Álvaro, Paloma Bragado, Michael March, et al.. (2025). N-Acetylcysteine for Hereditary Cystatin C Amyloid Angiopathy. JAMA Neurology. 82(5). 486–486.

Qu, Hui‐Qi, Yichuan Liu, John J. Connolly, et al.. (2025). Risk of Alzheimer's disease in Down syndrome: Insights gained by multi‐omics. Alzheimer s & Dementia. 21(4). e14604–e14604. 1 indexed citations

Glessner, Joseph, Xiao Chang, Yichuan Liu, et al.. (2023). Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 15(1). 14–14. 5 indexed citations

Qu, Hui‐Qi, Charlly Kao, James Garifallou, et al.. (2023). Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples. Genes. 14(1). 142–142. 3 indexed citations

Martin, Kimberly, Mary E. Norton, Cora MacPherson, et al.. (2023). Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study. Prenatal Diagnosis. 43(13). 1574–1580.

Qu, Hui‐Qi, Charlly Kao, & Håkon Håkonarson. (2023). Single-Cell RNA Sequencing Technology Landscape in 2023. Stem Cells. 42(1). 1–12. 21 indexed citations

Qu, Hui‐Qi, James W. Snyder, Joseph Glessner, et al.. (2022). Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries. Biomedicines. 10(2). 264–264. 11 indexed citations

Qu, Hui‐Qi, Xiao Chang, Frank Mentch, et al.. (2022). Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap. Lara D. Veeken. 61(8). 3497–3501. 3 indexed citations

10.

March, Michael, Álvaro Gutiérrez-Uzquiza, Kenny Nguyen, et al.. (2021). NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients. Nature Communications. 12(1). 1827–1827. 10 indexed citations

11.

Martin, Kimberly, Carole Samango‐Sprouse, Danielle LaGrave, et al.. (2020). Detection of maternal X chromosome abnormalities using single nucleotide polymorphism–based noninvasive prenatal testing. American Journal of Obstetrics & Gynecology MFM. 2(3). 100152–100152. 10 indexed citations

12.

Li, Fang, Charlly Kao, Michael V. Gonzalez, et al.. (2019). LinkedSV for detection of mosaic structural variants from linked-read exome and genome sequencing data. Nature Communications. 10(1). 5585–5585. 27 indexed citations

13.

Poplawski, Shane G., Mathieu E. Wimmer, Charlly Kao, et al.. (2018). Learning-dependent chromatin remodeling highlights noncoding regulatory regions linked to autism. Science Signaling. 11(513). 14 indexed citations

14.

Glessner, Joseph, Jin Li, Dai Wang, et al.. (2017). Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders. Genome Medicine. 9(1). 106–106. 37 indexed citations

15.

Pellegrino, Renata, Andrew Price, Charlly Kao, et al.. (2017). Abstract 5353: High-throughput automation of the 10x Genomics® Chromium™ workflow for linked-read whole exome sequencing and a targeted lynch syndrome panel. Cancer Research. 77(13_Supplement). 5353–5353.

16.

Wenger, Tara, Charlly Kao, Donna M. McDonald‐McGinn, et al.. (2016). The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder. Scientific Reports. 6(1). 19372–19372. 24 indexed citations

17.

Kao, Charlly, et al.. (2016). Measurement of Adherence To Anti-Hypertensive Drugs in Asia. Value in Health. 19(7). A868–A868. 2 indexed citations

18.

Connolly, John J., Joseph Glessner, Charlly Kao, Josephine Elia, & Håkon Håkonarson. (2015). Attention-Deficit Hyperactivity Disorder and Pharmacotherapy—Past, Present, and Future: A Review of the Changing Landscape of Drug Therapy. Therapeutic Innovation & Regulatory Science. 49(5). 632–642. 28 indexed citations

19.

Hadley, Dexter, et al.. (2014). The impact of the metabotropic glutamate receptor and other gene family interaction networks on the autism spectrum disorders. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 1 indexed citations

20.

Sleiman, Patrick, Dai Wang, Joseph Glessner, et al.. (2013). GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus. Scientific Reports. 3(1). 3075–3075. 36 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.

Explore authors with similar magnitude of impact