Keng Wee Teik

899 total citations
11 papers, 131 citations indexed

About

Keng Wee Teik is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Keng Wee Teik has authored 11 papers receiving a total of 131 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Keng Wee Teik's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Genetic factors in colorectal cancer (2 papers). Keng Wee Teik is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Genetic factors in colorectal cancer (2 papers). Keng Wee Teik collaborates with scholars based in Malaysia, Japan and Kuwait. Keng Wee Teik's co-authors include Noriko Miyake, Naomichi Matsumoto, Gaik-Siew Ch’ng, Takeshi Mizuguchi, Mitsuhiro Kato, Rohani Md Yasin, Satoko Miyatake, Hirotomo Saitsu, Jamalia Rahmat and Mitsuko Nakashima and has published in prestigious journals such as International Journal of Environmental Research and Public Health, Human Mutation and Clinical Genetics.

In The Last Decade

Keng Wee Teik

11 papers receiving 129 citations

Peers

Keng Wee Teik

GENET

MB

ONCOL

CMN

CB

Theresa Brunet Germany

Sylvia Redon France

Tova Hershkovitz Israel

K. Kubzdela

Monika Weisz Hubshman Israel

Salima El Chehadeh-Djebbar France

Alka V. Ekbote India

Laurence Faivre France

Anne‐Marie Guerrot France

Haley Streff United States

Theresa Brunet Germany

Keng Wee Teik

47 ×0.7

GENET

54 ×0.8

MB

15 ×0.6

ONCOL

8 ×0.6

CMN

12 ×0.9

CB

Citations per year, relative to Keng Wee Teik Keng Wee Teik (= 1×) peers Theresa Brunet

Countries citing papers authored by Keng Wee Teik

Since Specialization

Citations

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

Fields of papers citing papers by Keng Wee Teik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Keng Wee Teik. 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 Keng Wee Teik. The network helps show where Keng Wee Teik may publish in the future.

Co-authorship network of co-authors of Keng Wee Teik

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

All Works

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11 of 11 papers shown

1.

Teik, Keng Wee, et al.. (2021). NOVEL MUTATIONS OF THE G6PC GENE IN MALAYSIANS WITH GLYCOGEN STORAGE DISEASE 1a (GSD1a). 40(1). 34–45. 2 indexed citations

2.

Aizuddin, Azimatun Noor, Zuria Mahmud, Zarina Abdul Latiff, et al.. (2021). Genetic Testing for Cancer Risk: Is the Community Willing to Pay for It?. International Journal of Environmental Research and Public Health. 18(16). 8752–8752. 7 indexed citations

3.

Manaf, Mohd Rizal Abdul, Azimatun Noor Aizuddin, Zarina Abdul Latiff, et al.. (2021). Cost-Effectiveness of Colorectal Cancer Genetic Testing. International Journal of Environmental Research and Public Health. 18(16). 8330–8330. 5 indexed citations

4.

Lautrup, Charlotte Kvist, Keng Wee Teik, Shuji Mizumoto, et al.. (2020). Delineation of musculocontractural Ehlers–Danlos Syndrome caused by dermatan sulfate epimerase deficiency. Molecular Genetics & Genomic Medicine. 8(5). e1197–e1197. 18 indexed citations

5.

Beaman, Glenda M., Keng Wee Teik, John A. Sayer, et al.. (2020). Early B-cell Factor 3–Related Genetic Disease Can Mimic Urofacial Syndrome. Kidney International Reports. 5(10). 1823–1827. 7 indexed citations

6.

Beaman, Glenda M., Keng Wee Teik, Jill Urquhart, et al.. (2019). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical Genetics. 96(6). 515–520. 9 indexed citations

7.

Tsuchida, Naomi, Keisuke Hamada, Masaaki Shiina, et al.. (2018). GRIN2D variants in three cases of developmental and epileptic encephalopathy. Clinical Genetics. 94(6). 538–547. 16 indexed citations

8.

Tsuchida, Naomi, Mitsuko Nakashima, Akihiko Miyauchi, et al.. (2017). Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy. Clinical Genetics. 93(2). 266–274. 23 indexed citations

9.

Khalid, Mohd Khairul Nizam Mohd, et al.. (2015). Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.. PubMed. 21. 1185–90. 17 indexed citations

10.

Demuth, Ilja, Ulrich Baumann, Detlev Schindler, et al.. (2010). Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype. Human Mutation. 31(9). 1059–1068. 22 indexed citations

11.

Berg, Jonathan, et al.. (2000). Bullous ichthyosiform erythroderma, developmental delay, aortic and pulmonary stenosis in association with a FRA12A. Clinical Dysmorphology. 9(3). 213–219. 5 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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