Cedrik Tekendo‐Ngongang
- Health Informatics top 10%
-
- Williams Syndrome Research 3
-
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 7
-
- Congenital heart defects research 5
- RNA modifications and cancer 3
- Protein Tyrosine Phosphatases 2
-
- Congenital Heart Disease Studies 2
-
- AI in cancer detection 2
- Co-authors
- Ambroise WonkamPaul KruszkaSophie DahounBenjamin D. SolomonMaximilian MuenkeDat DuongRebekah L. WaikelMichael A. Morris
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)European Journal of Medical Genetics (2 papers)Genes (2 papers)
- Partner nations
- United StatesSouth AfricaSwitzerland
In The Last Decade
Cedrik Tekendo‐Ngongang
22 papers receiving 210 citations
Peers
Comparison fields: 5 of 63
- Health Informatics 16
- Developmental Neuroscience 14
- Genetics 90
- Sensory Systems 7
- Cancer Research 18
Countries citing papers authored by Cedrik Tekendo‐Ngongang
This map shows the geographic impact of Cedrik Tekendo‐Ngongang'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 Cedrik Tekendo‐Ngongang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cedrik Tekendo‐Ngongang more than expected).
Fields of papers citing papers by Cedrik Tekendo‐Ngongang
This network shows the impact of papers produced by Cedrik Tekendo‐Ngongang. 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 Cedrik Tekendo‐Ngongang. The network helps show where Cedrik Tekendo‐Ngongang may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Cedrik Tekendo‐Ngongang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 2 | |
| 2 | 2024 | 10 | |
| 3 | 2024 | 0 | |
| 4 | 2024 | 9 | |
| 5 | 2022 | 2 | |
| 6 | 2022 | 12 | |
| 7 | 2022 | 16 | |
| 8 | 2021 | 10 | |
| 9 | 2021 | 11 | |
| 10 | 2021 | 4 | |
| 11 | 2020 | 5 | |
| 12 | 2020 | 7 | |
| 13 | 2020 | 3 | |
| 14 | 2019 | 12 | |
| 15 | 2019 | 8 | |
| 16 | 2019 | 14 | |
| 17 | 2017 | 8 | |
| 18 | 2014 | 14 | |
| 19 | 2011 | 36 | |
| 20 | 2011 | 1 |
About Cedrik Tekendo‐Ngongang
Cedrik Tekendo‐Ngongang is a scholar working on Health Informatics, Developmental Neuroscience, Genetics, Sensory Systems and Cancer Research, having authored 23 papers that have together received 214 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers), Williams Syndrome Research (3 papers), RNA modifications and cancer (3 papers), Congenital Heart Disease Studies (2 papers), AI in cancer detection (2 papers) and Protein Tyrosine Phosphatases (2 papers). The work is most often cited by research in Health Informatics (16 citations), Developmental Neuroscience (14 citations), Genetics (90 citations), Sensory Systems (7 citations) and Cancer Research (18 citations). Cedrik Tekendo‐Ngongang has collaborated with scholars based in United States, South Africa and Switzerland. Frequent co-authors include Ambroise Wonkam, Paul Kruszka, Sophie Dahoun, Benjamin D. Solomon, Maximilian Muenke, Dat Duong, Rebekah L. Waikel, Michael A. Morris, Ping Hu and Frédérique Béna. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, European Journal of Medical Genetics, Genes, Frontiers in Genetics and JAMA Network Open.
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.