Winnie Ong

656 total citations
5 papers, 115 citations indexed

About

Winnie Ong is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Winnie Ong has authored 5 papers receiving a total of 115 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Clinical Biochemistry. Recurrent topics in Winnie Ong's work include Metabolism and Genetic Disorders (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genetic Syndromes and Imprinting (1 paper). Winnie Ong is often cited by papers focused on Metabolism and Genetic Disorders (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genetic Syndromes and Imprinting (1 paper). Winnie Ong collaborates with scholars based in Malaysia, Australia and Austria. Winnie Ong's co-authors include Kenji Sugai, Atsuo Fukuda, Shinji Saitoh, Chihiro Ohba, Mitsuhiro Kato, Satoko Miyatake, Hirotomo Saitsu, Tenpei Akita, Naomichi Matsumoto and Miho Watanabe and has published in prestigious journals such as Scientific Reports, Epilepsy & Behavior and Clinical Genetics.

In The Last Decade

Winnie Ong

5 papers receiving 114 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Winnie Ong Malaysia	3	87	53	47	17	9	5	115
Dana Marafi United States	8	88 1.0×	22 0.4×	70 1.5×	13 0.8×	6 0.7×	24	171
Natalia Juliá‐Palacios Spain	7	86 1.0×	39 0.7×	51 1.1×	17 1.0×	6 0.7×	16	138
Kirill Shkura United Kingdom	5	127 1.5×	39 0.7×	58 1.2×	39 2.3×	11 1.2×	5	212
Patrícia B. S. Celestino-Soper United States	5	97 1.1×	26 0.5×	76 1.6×	6 0.4×	8 0.9×	8	166
Marie‐Aude Spitz France	7	99 1.1×	21 0.4×	53 1.1×	16 0.9×	6 0.7×	11	136
Tara Skelly United States	7	123 1.4×	31 0.6×	57 1.2×	51 3.0×	11 1.2×	9	231
Thibaud Jouan France	5	66 0.8×	26 0.5×	57 1.2×	11 0.6×	9 1.0×	7	111
Steffi Patzer Germany	3	48 0.6×	42 0.8×	48 1.0×	41 2.4×	7 0.8×	3	97
Matthew Zemel United States	5	89 1.0×	32 0.6×	63 1.3×	35 2.1×	15 1.7×	6	160
Nicoletta Zanotta Italy	8	70 0.8×	59 1.1×	53 1.1×	69 4.1×	32 3.6×	16	169

Countries citing papers authored by Winnie Ong

Since Specialization

Citations

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

Fields of papers citing papers by Winnie Ong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Winnie Ong

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

All Works

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5 of 5 papers shown

1.

Liang, Jao‐Shwann, Kun‐Long Hung, Li‐Ju Lin, et al.. (2023). Novel PEX1 mutations in fibroblasts from children with Zellweger spectrum disorders exhibit temperature sensitive characteristics. Epilepsy & Behavior. 145. 109266–109266. 1 indexed citations

2.

Saitsu, Hirotomo, Miho Watanabe, Tenpei Akita, et al.. (2016). Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay. Scientific Reports. 6(1). 30072–30072. 65 indexed citations

3.

Ong, Winnie, Lock Hock Ngu, Nisha Patel, et al.. (2015). AB168. Novel DYM compound heterozygous mutations in a Malaysian boy with Dyggve-Melchior-Clausen syndrome. Annals of Translational Medicine. 3(2). 169–169. 1 indexed citations

4.

McInerney‐Leo, Aideen, Jennifer Harris, Paul Leo, et al.. (2014). Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short‐rib thoracic dystrophies. Clinical Genetics. 88(6). 550–557. 42 indexed citations

5.

Ch’ng, Gaik-Siew, et al.. (2013). Hyperexcretion of homocitrulline in a Malaysian patient with lysinuric protein intolerance. European Journal of Pediatrics. 172(9). 1277–1281. 6 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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