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, Sufeng Li, David A. Alcorta and Dong‐Yan Jin 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

Peers

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

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

20 of 20 papers shown

#	Work	Indexed citations
1	Critical Points in the Noiseberg Achievable Region of the Gaussian Z-Interference Channel 2024 ·Entropy ·Max H. M. Costa, Chandra Nair, David Ng	0
2	On the structure of certain non-convex functionals and the Gaussian Z-interference channel 2020 ·Max H. M. Costa, Chandra Nair, David Ng, (unknown)	6
3	Disclosure of cardiac variants of uncertain significance results in an exome cohort 2018 ·Clinical Genetics ·Tokunbor A. Lawal, Katie L. Lewis, Jennifer J. Johnston, (unknown), David Ng, F. Gaston‐Johansson, William M. P. Klein, Barbara B. Biesecker, Leslie G. Biesecker	14
4	Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes 2018 ·Genetics in Medicine ·(unknown), Katie L. Lewis, Tokunbor A. Lawal, David Ng, Jennifer J. Johnston, Barbara B. Biesecker, Leslie G. Biesecker	4
5	Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screening 2016 ·Genetics in Medicine ·David Ng, Celine Hong, Larry N. Singh, Jennifer J. Johnston, James C. Mullikin, Leslie G. Biesecker	16
6	Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations 2015 ·The American Journal of Human Genetics ·Jennifer J. Johnston, Katie L. Lewis, David Ng, Larry N. Singh, (unknown), Carmen C. Brewer, Brian P. Brooks, Isaac Brownell, Fabio Candotti, Stephen G. Gonsalves, (unknown), Heidi H. Kong, Kristina I. Rother, Robert Sokolic, Benjamin D. Solomon, Wadih M. Zein, D.N. Cooper, Peter D. Stenson, James C. Mullikin, Leslie G. Biesecker	43
7	Lenz Microphthalmia Syndrome 2014 ·David Ng	3
8	Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes 2012 ·The American Journal of Human Genetics ·Jennifer J. Johnston, Wendy S. Rubinstein, Flavia M. Facio, David Ng, Larry N. Singh, Jamie K. Teer, James C. Mullikin, Leslie G. Biesecker	155
9	Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes 2011 ·Journal of Clinical Investigation ·Matthew G. Rees, David Ng, (unknown), Clesson Turner, Nicola L. Beer, Amy J. Swift, Mario A. Morken, Jennifer E. Below, Ilana Blech, James C. Mullikin, Mark I. McCarthy, Leslie G. Biesecker, Anna L. Gloyn, Francis S. Collins	36
10	Putative tumour-suppressor gene DAB2is frequently down regulated by promoter hypermethylation in nasopharyngeal carcinoma 2010 ·BMC Cancer ·Joanna H. Tong, David Ng, Shuk L. Chau, (unknown), Patrick P.S. Leung, TL Lee, Raymond Wai Ming Lung, Michael W.Y. Chan, Anthony W.H. Chan, Kwok Wai Lo, Ka‐Fai To	54
11	Genomic Characterization of Esophageal Squamous Cell Carcinoma from a High-Risk Population in China 2009 ·Cancer Research ·Nan Hu, Chaoyu Wang, David Ng, Robert Clifford, Howard H. Yang, Ze‐Zhong Tang, Quanhong Wang, (unknown), Carol Giffen, Alisa M. Goldstein, Philip R. Taylor, Maxwell P. Lee	45
12	Association of a de novo16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes 2009 ·BMC Medical Genetics ·Tanya Bardakjian, Adele Schneider, David Ng, Jennifer J. Johnston, Leslie G. Biesecker	18
13	Common genetic variants in candidate genes and risk of familial lymphoid malignancies 2009 ·British Journal of Haematology ·Xueying Liang, Neil E. Caporaso, Mary L. McMaster, David Ng, Ola Landgren, Meredith Yeager, Stephen J. Chanock, Lynn R. Goldin	34
14	High‐density mapping and follow‐up studies on chromosomal regions 1, 3, 6, 12, 13 and 17 in 28 families with chronic lymphocytic leukaemia 2006 ·British Journal of Haematology ·David Ng, Gerald E. Marti, Laura Fontaine, Jorge R. Toro, Neil E. Caporaso, Lynn R. Goldin	12
15	Mitochondrial targeting of growth suppressor protein DLC2 through the START domain 2005 ·FEBS Letters ·David Ng, Shing Fai Chan, Kin Hang Kok, Judy Wai Ping Yam, Ching C. Lau, Irene Oi‐Lin Ng, Dong‐Yan Jin	24
16	Retrospective family study of childhood medulloblastoma 2005 ·American Journal of Medical Genetics Part A ·David Ng, Theodora Stavrou, Ling Liu, Michael D. Taylor, Bert Gold, Michael Dean, Michael J. Kelley, (unknown), Gilbert Vézina, H. Stacy Nicholson, Julianne Byrne, James T. Rutka, David Hogg, Gregory H. Reaman, Alisa M. Goldstein	22
17	Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR 2004 ·Nature Genetics ·David Ng, Nalin Thakker, Connie M. Corcoran, Dian Donnai, Rahat Perveen, Adele Schneider, Donald W. Hadley, Cynthia J. Tifft, Liqun Zhang, Andrew O.M. Wilkie, Jasper J. van der Smagt, Robert J. Gorlin, Shawn M. Burgess, Vivian J. Bardwell, Graeme C. Black, Leslie G. Biesecker	237
18	Gonadal mosaicism in severe Pallister–Hall syndrome 2003 ·American Journal of Medical Genetics Part A ·David Ng, Jennifer J. Johnston, Joyce Turner, Eilis Boudreau, Edythe Wiggs, William H. Theodore, Leslie G. Biesecker	17
19	Deleted in Liver Cancer (DLC) 2 Encodes a RhoGAP Protein with Growth Suppressor Function and Is Underexpressed in Hepatocellular Carcinoma 2003 ·Journal of Biological Chemistry ·Ching C. Lau, Chun‐Ming Wong, Shing Fai Chan, Thomas Leung, David Ng, Dong‐Yan Jin, Irene Oi‐Lin Ng	157
20	Genetic heterogeneity of syndromic X‐linked recessive microphthalmia‐anophthalmia: Is Lenz microphthalmia a single disorder? 2002 ·American Journal of Medical Genetics ·David Ng, Donald W. Hadley, Cynthia J. Tifft, Leslie G. Biesecker	19

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