Fong Ct

502 citations
202 papers · 375 · h-index 5

Impact in

Papers in

  • Clinical Biochemistry 36
    • Metabolism and Genetic Disorders 36
  • Genetics 66
    • Genomics and Rare Diseases 34
    • Connective tissue disorders research 17
    • Genetics and Neurodevelopmental Disorders 13
    • Genetic and rare skin diseases. 12
Co-authors
Ardinger Hh (200 shared papers)Margaret P Adam (200 shared papers)Heather C. Mefford (198 shared papers)Pagon Ra (200 shared papers)Thomas D. Bird (200 shared papers)Bean Ljh (194 shared papers)Smith Rjh (170 shared papers)A Amemiya (181 shared papers)
Journals
Yearbook of pediatric endocrinology (1 paper)PubMed (1 paper)Europe PMC (PubMed Central) (2 papers)Research Explorer (The University of Manchester) (1 paper)
Partner nations
United StatesUnited KingdomGermany

In The Last Decade

Fong Ct

175 papers receiving 364 citations

Peers

Fong Ct
Comparison fields: 5 of 57
  • Clinical Biochemistry 46
  • Neurology 63
  • Genetics 73
  • Cellular and Molecular Neuroscience 29
  • Aging 3
Replace Ardinger Hh with:
Ardinger Hh United States
Bean Ljh United States
A Amemiya Japan
Keiko Ishigaki Japan
Bita Bozorgmehr Iran
Juliette Dupont Portugal
Erin O’Ferrall Canada
Nada Abdelmagid Sweden
Fang Fang China
Susanne Gerit Kircher Austria
Fong Ct relative to Ardinger Hh United States Ardinger Hh's profile →
Citations per field
00.5×1.5×1.8×
Ardinger Hh · 1×
Citations per year

Countries citing papers authored by Fong Ct

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 16 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.

Border = papers with Fong Ct Line = papers co-authored together Fong Ct links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 202 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.
PubMed ·Brodeur Gm, Fong Ct, Rogers C. Griffith, Robert C. Seeger +2 others
198842
2
GTP Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia
Europe PMC (PubMed Central) ·Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
201519
3
Cleidocranial Dysplasia -- GeneReviews(®)
Europe PMC (PubMed Central) ·Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
201611
4
Neurofibromatosis 1 -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20166
5
Mitochondrial Disorders Overview -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20166
6
Barth Syndrome -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20165
7
Fibrous Dysplasia/McCune-Albright Syndrome -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20165
8
Juvenile Polyposis Syndrome -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20165
9
Maple Syrup Urine Disease -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, Anne R. Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
10
Niemann-Pick Disease Type C -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
11
Mitochondrial Neurogastrointestinal Encephalopathy Disease -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
12
SUCLA2-Related Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
13
PTEN Hamartoma Tumor Syndrome -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
14
Hereditary Ataxia Overview -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
15
Disorders of Intracellular Cobalamin Metabolism -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
16
Loeys-Dietz Syndrome -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
17
Mucopolysaccharidosis Type I -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
18
Prader-Willi Syndrome -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
19
Spinocerebellar Ataxia Type 8 -- GeneReviews(®)
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164
20
Hereditary Paraganglioma-Pheochromocytoma Syndromes -- GeneReviews®
Pagon Ra, Margaret P Adam, Ardinger Hh, Wallace Se, A Amemiya, Bean Ljh, Thomas D. Bird, Fong Ct
20164

About Fong Ct

Fong Ct is a scholar working on Clinical Biochemistry, Genetics, Cellular and Molecular Neuroscience, Molecular Biology and Genetics, having authored 202 papers that have together received 375 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (36 papers), Genomics and Rare Diseases (34 papers), Hereditary Neurological Disorders (19 papers), Connective tissue disorders research (17 papers), Genetics and Neurodevelopmental Disorders (13 papers), Genetic Neurodegenerative Diseases (12 papers), Genetic and rare skin diseases. (12 papers) and Lysosomal Storage Disorders Research (11 papers). The work is most often cited by research in Clinical Biochemistry (46 citations), Neurology (63 citations), Genetics (73 citations), Cellular and Molecular Neuroscience (29 citations) and Aging (3 citations). Fong Ct has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Ardinger Hh, Margaret P Adam, Heather C. Mefford, Pagon Ra, Thomas D. Bird, Bean Ljh, Smith Rjh, A Amemiya, Robert C. Seeger and Rogers C. Griffith. Their work appears in journals such as Yearbook of pediatric endocrinology, PubMed, Europe PMC (PubMed Central) and Research Explorer (The University of Manchester).

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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