Fong Ct
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
-
- Neuroblastoma Research and Treatments
Papers in
-
- Mitochondrial Function and Pathology 12
- RNA regulation and disease 8
- Genetics 34
- Neurogenetic and Muscular Disorders Research 9
- Genetic Syndromes and Imprinting 8
- Genetics and Neurodevelopmental Disorders 7
- Co-authors
- Adam Mp (185 shared papers)Ardinger Hh (185 shared papers)Pagon Ra (185 shared papers)Mefford Hc (181 shared papers)Bird Td (184 shared papers)Bean Ljh (184 shared papers)A Amemiya (175 shared papers)Smith Rjh (157 shared papers)
- Journals
- Memory & Cognition (1 paper)PLoS ONE (1 paper)PubMed (1 paper)Research Explorer (The University of Manchester) (1 paper)ACTA THERIOLOGICA (1 paper)
- Partner nations
- United States
In The Last Decade
Fong Ct
151 papers receiving 291 citations
Peers
Comparison fields: 5 of 63
- Clinical Biochemistry 38
- Neurology 57
- Genetics 74
- Molecular Biology 141
- Cancer Research 30
Countries citing papers authored by Fong Ct
This map shows the geographic impact of Fong Ct'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 Fong Ct with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fong Ct more than expected).
Fields of papers citing papers by Fong Ct
This network shows the impact of papers produced by Fong Ct. 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 Fong Ct. The network helps show where Fong Ct may publish in the future.
Co-authors
The 17 scholars most cited alongside Fong Ct, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 186 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular analysis and clinical significance of N-myc amplification and chromosome 1p monosomy in human neuroblastomas. | 1988 | 38 |
| 2 | Neurofibromatosis 1 -- GeneReviews(®) | 2016 | 6 |
| 3 | Fibrous Dysplasia/McCune-Albright Syndrome -- GeneReviews(®) | 2016 | 5 |
| 4 | Juvenile Polyposis Syndrome -- GeneReviews(®) | 2016 | 5 |
| 5 | Mitochondrial Disorders Overview -- GeneReviews(®) | 2016 | 5 |
| 6 | Barth Syndrome -- GeneReviews® | 2016 | 5 |
| 7 | Prader-Willi Syndrome -- GeneReviews® | 2016 | 4 |
| 8 | Gaucher Disease -- GeneReviews(®) | 2016 | 4 |
| 9 | Disorders of Intracellular Cobalamin Metabolism -- GeneReviews® | 2016 | 4 |
| 10 | Hereditary Paraganglioma-Pheochromocytoma Syndromes -- GeneReviews® | 2016 | 4 |
| 11 | PTEN Hamartoma Tumor Syndrome -- GeneReviews® | 2016 | 4 |
| 12 | Spinocerebellar Ataxia Type 8 -- GeneReviews(®) | 2016 | 4 |
| 13 | Niemann-Pick Disease Type C -- GeneReviews® | 2016 | 4 |
| 14 | Mitochondrial DNA Deletion Syndromes -- GeneReviews® | 2016 | 4 |
| 15 | Wilson Disease -- GeneReviews(®) | 2016 | 3 |
| 16 | Diamond-Blackfan Anemia -- GeneReviews® | 2016 | 3 |
| 17 | Hereditary Ataxia Overview -- GeneReviews® | 2016 | 3 |
| 18 | Beckwith-Wiedemann Syndrome -- GeneReviews® | 2016 | 3 |
| 19 | Familial Lipoprotein Lipase Deficiency -- GeneReviews® | 2016 | 3 |
| 20 | SUCLA2-Related Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria -- GeneReviews® | 2016 | 3 |
About Fong Ct
Fong Ct is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience and Rheumatology, having authored 186 papers that have together received 296 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (25 papers), Mitochondrial Function and Pathology (12 papers), Genetic Neurodegenerative Diseases (11 papers), Neurogenetic and Muscular Disorders Research (9 papers), Genetic Syndromes and Imprinting (8 papers), RNA regulation and disease (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Lysosomal Storage Disorders Research (7 papers). The work is most often cited by research in Clinical Biochemistry (38 citations), Neurology (57 citations), Genetics (74 citations), Molecular Biology (141 citations) and Cancer Research (30 citations). Fong Ct has collaborated with scholars based in United States. Frequent co-authors include Adam Mp, Ardinger Hh, Pagon Ra, Mefford Hc, Bird Td, Bean Ljh, A Amemiya, Smith Rjh, K Stephens and Seeger Rc. Their work appears in journals such as Memory & Cognition, PLoS ONE, PubMed, Research Explorer (The University of Manchester) and ACTA THERIOLOGICA.
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.