Fong Ct

434 citations

186 papers · 296 indexed · h-index 6

Impact in

Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Neurology
- Neuroblastoma Research and Treatments

Papers in

Clinical Biochemistry 25
- Metabolism and Genetic Disorders 25
Genetics 15
- Neurogenetic and Muscular Disorders Research 9
- Genetic Syndromes and Imprinting 8

Co-authors: Adam Mp Pagon Ra Ardinger Hh Mefford Hc Bird Td Bean Ljh A Amemiya Smith Rjh
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

Replace A Amemiya with:

A Amemiya Japan

Bird Td United States

Mefford Hc

Adam Mp

Bean Ljh

Alina Kurolap Israel

Ardinger Hh United States

Peter J. Francis United States

Cristina Dias United Kingdom

Sietske H. Kevelam Netherlands

Fong Ct relative to A Amemiya Japan A Amemiya's profile →

Citations per field

00.5×1.5×2.0×

A Amemiya · 1×

×0.7 38/53

CB

×2.0 57/29

NEURO

×0.7 74/104

GENET

×0.8 141/173

MB

×1.3 30/23

CR

Citations per year

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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-authorship network

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.

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	ADAMTSL4-Related Eye Disorders -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	0
2	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia -- GeneReviews(®) ACTA THERIOLOGICA ·Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, Edgar Paúl Suntasig Masabanda	2016	1
3	Chorea-Acanthocytosis -- GeneReviews(®) Memory & Cognition ·Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, S. Fadrhonc	2016	2
4	Multiple Endocrine Neoplasia Type 2 -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, S.R. Nasyrov	2016	1
5	Neurofibromatosis 2 -- GeneReviews® PLoS ONE ·Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	0
6	Progressive Myoclonus Epilepsy, Lafora Type -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, Edgar Paúl Suntasig Masabanda	2016	0
7	Hypertrophic Cardiomyopathy Overview -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, S. V. Tsylyaev	2016	1
8	Alpha-Thalassemia -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, Edgar Paúl Suntasig Masabanda	2016	0
9	Gaucher Disease -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	4
10	Rothmund-Thomson Syndrome -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	1
11	MED12-Related Disorders -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Adam C. Smith, K Stephens	2016	0
12	Polymicrogyria Overview -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Adam C. Smith, K Stephens	2016	1
13	Spinal Muscular Atrophy, X-Linked Infantile -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	1
14	Primary Ciliary Dyskinesia -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K. Stephens	2016	0
15	TSEN54-Related Pontocerebellar Hypoplasia -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, John Firth Stansfield, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	1
16	Diamond-Blackfan Anemia -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, K Stephens	2016	3
17	Prader-Willi Syndrome -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Adam C. Smith, K Stephens	2016	4
18	Generalized Arterial Calcification of Infancy -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, S. V. Tsylyaev	2016	0
19	Smith-Magenis Syndrome -- GeneReviews(®) Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, S. V. Tsylyaev	2016	1
20	Leber Hereditary Optic Neuropathy -- GeneReviews® Pagon Ra, Adam Mp, Ardinger Hh, Zhu Mj, A Amemiya, Bean Ljh, Bird Td, Fong Ct, Mefford Hc, Smith Rjh, S. Fadrhonc	2016	2

About Fong Ct

Fong Ct is a scholar working on Clinical Biochemistry, Genetics, Genetics, Rheumatology and Biochemistry, 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), Amino Acid Enzymes and Metabolism (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, Pagon Ra, Ardinger Hh, 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.

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