David Ng

3.6k total citations
45 papers, 1.9k citations indexed

About

David Ng is a scholar working on Molecular Biology, Genetics and Electrical and Electronic Engineering. According to data from OpenAlex, David Ng has authored 45 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Genetics and 9 papers in Electrical and Electronic Engineering. Recurrent topics in David Ng's work include Wireless Communication Security Techniques (9 papers), Genomics and Rare Diseases (7 papers) and Energy Harvesting in Wireless Networks (5 papers). David Ng is often cited by papers focused on Wireless Communication Security Techniques (9 papers), Genomics and Rare Diseases (7 papers) and Energy Harvesting in Wireless Networks (5 papers). David Ng collaborates with scholars based in United States, Hong Kong and United Kingdom. David Ng's co-authors include Leslie G. Biesecker, James C. Mullikin, Jennifer J. Johnston, Jamie K. Teer, Alisa M. Goldstein, Michael J. Kelley, Larry N. Singh, David A. Alcorta, Sufeng Li and Shing Fai Chan and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

David Ng

43 papers receiving 1.8k citations

Author Peers

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

Author Last Decade Papers Cites
David Ng 924 550 340 275 233 45 1.9k
Andrew J. Wallace 1.1k 1.2× 636 1.2× 485 1.4× 481 1.7× 581 2.5× 129 3.6k
Eul‐Ju Seo 796 0.9× 417 0.8× 106 0.3× 285 1.0× 197 0.8× 116 1.9k
Syed M. Jalal 1.3k 1.4× 1.0k 1.8× 163 0.5× 310 1.1× 317 1.4× 71 2.6k
Janet M. Cowan 1.1k 1.2× 553 1.0× 305 0.9× 508 1.8× 169 0.7× 56 2.0k
Kyle C. Kurek 594 0.6× 281 0.5× 228 0.7× 296 1.1× 174 0.7× 46 1.4k
Andreas Zankl 881 1.0× 1.1k 2.0× 216 0.6× 167 0.6× 64 0.3× 82 1.9k
Karen E. Heath 1.3k 1.4× 1.1k 1.9× 273 0.8× 95 0.3× 131 0.6× 106 2.6k
J. S. Lanchbury 723 0.8× 345 0.6× 308 0.9× 647 2.4× 309 1.3× 41 2.4k
Anne O’Meara 665 0.7× 176 0.3× 338 1.0× 228 0.8× 138 0.6× 62 1.6k
Bogdan Dumitriu 726 0.8× 391 0.7× 215 0.6× 284 1.0× 94 0.4× 48 2.5k

Countries citing papers authored by David Ng

Since Specialization
Citations

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

Fields of papers citing papers by David Ng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Ng

This figure shows the co-authorship network connecting the top 25 collaborators of David Ng. A scholar is included among the top collaborators of David Ng 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 David Ng. David Ng 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.
Costa, Max H. M., Chandra Nair, & David Ng. (2024). Critical Points in the Noiseberg Achievable Region of the Gaussian Z-Interference Channel. Entropy. 26(11). 898–898.
2.
Costa, Max H. M., et al.. (2020). On the structure of certain non-convex functionals and the Gaussian Z-interference channel. 1522–1527. 6 indexed citations
3.
Lawal, Tokunbor A., Katie L. Lewis, Jennifer J. Johnston, et al.. (2018). Disclosure of cardiac variants of uncertain significance results in an exome cohort. Clinical Genetics. 93(5). 1022–1029. 14 indexed citations
4.
Lewis, Katie L., Paul K. J. Han, Kristen Fishler, et al.. (2018). Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort. Genetics in Medicine. 21(6). 1355–1362. 21 indexed citations
5.
Lewis, Katie L., Tokunbor A. Lawal, David Ng, et al.. (2018). Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes. Genetics in Medicine. 21(3). 748–752. 4 indexed citations
6.
Ng, David, Celine Hong, Larry N. Singh, et al.. (2016). Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screening. Genetics in Medicine. 19(3). 357–361. 16 indexed citations
7.
Johnston, Jennifer J., Katie L. Lewis, David Ng, et al.. (2015). Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations. The American Journal of Human Genetics. 96(6). 913–925. 43 indexed citations
8.
Ng, David. (2014). Lenz Microphthalmia Syndrome. 3 indexed citations
9.
Posokhova, Ekaterina, David Ng, Ikuo Masuho, et al.. (2013). Essential Role of the m2R-RGS6-IKACh Pathway in Controlling Intrinsic Heart Rate Variability. PLoS ONE. 8(10). e76973–e76973. 35 indexed citations
10.
Johnston, Jennifer J., Wendy S. Rubinstein, Flavia M. Facio, et al.. (2012). Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes. The American Journal of Human Genetics. 91(1). 97–108. 155 indexed citations
11.
Rees, Matthew G., David Ng, Clesson Turner, et al.. (2011). Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes. Journal of Clinical Investigation. 122(1). 205–217. 36 indexed citations
12.
Hu, Nan, Chaoyu Wang, David Ng, et al.. (2009). Genomic Characterization of Esophageal Squamous Cell Carcinoma from a High-Risk Population in China. Cancer Research. 69(14). 5908–5917. 45 indexed citations
13.
Liang, Xueying, Neil E. Caporaso, Mary L. McMaster, et al.. (2009). Common genetic variants in candidate genes and risk of familial lymphoid malignancies. British Journal of Haematology. 146(4). 418–423. 34 indexed citations
14.
Lung, Raymond Wai Ming, Joanna Hung‐Man Tong, David Ng, et al.. (2009). Modulation of LMP2A Expression by a Newly Identified Epstein-Barr Virus-Encoded MicroRNA miR-BART22. Neoplasia. 11(11). 1174–IN17. 177 indexed citations
15.
Yang, Xiaohong R., David Ng, David A. Alcorta, et al.. (2009). T (brachyury) gene duplication confers major susceptibility to familial chordoma. Nature Genetics. 41(11). 1176–1178. 209 indexed citations
16.
Ng, David, Xiaohong R. Yang, Margaret A. Tucker, & Alisa M. Goldstein. (2008). Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes. BMC Research Notes. 1(1). 86–86. 10 indexed citations
17.
Tse, Gary M., Philip C.W. Lui, Joaquim S. L. Vong, et al.. (2008). Increased epidermal growth factor receptor (EGFR) expression in malignant mammary phyllodes tumors. Breast Cancer Research and Treatment. 114(3). 441–448. 50 indexed citations
18.
Caporaso, Neil E., Lynn R. Goldin, Christoph Plass, et al.. (2007). Chronic lymphocytic leukaemia genetics overview. British Journal of Haematology. 139(5). 630–634. 27 indexed citations
19.
Ng, David, Nalin Thakker, Connie M. Corcoran, et al.. (2004). Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Nature Genetics. 36(4). 411–416. 237 indexed citations
20.
Ng, David, Donald W. Hadley, Cynthia J. Tifft, & Leslie G. Biesecker. (2002). Genetic heterogeneity of syndromic X‐linked recessive microphthalmia‐anophthalmia: Is Lenz microphthalmia a single disorder?. American Journal of Medical Genetics. 110(4). 308–314. 19 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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