Jack M. Fu
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Molecular Biology top 10%
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 12
- Genetics and Neurodevelopmental Disorders 5
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- Advanced Database Systems and Queries 6
- Co-authors
- Ernest Martinez (1 shared paper)Robert G. Roeder (1 shared paper)Tapas Kumar Kundu (1 shared paper)Michael E. Talkowski (6 shared papers)Michael R. Delannoy (1 shared paper)Kapil V. Ramachandran (1 shared paper)Chan Hyun Na (1 shared paper)Seth S. Margolis (1 shared paper)
- Journals
- Nature Genetics (4 papers)The American Journal of Human Genetics (3 papers)Bioinformatics (2 papers)Cell Genomics (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United StatesCanadaDenmark
In The Last Decade
Jack M. Fu
34 papers receiving 2.8k citations
Jack M. Fu's Hit Papers
Peers
Comparison fields: 5 of 120
- Genetics 1.3k
- Molecular Biology 1.3k
- Cancer Research 204
- Cognitive Neuroscience 272
- Aging 14
Countries citing papers authored by Jack M. Fu
This map shows the geographic impact of Jack M. Fu'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 Jack M. Fu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jack M. Fu more than expected).
Fields of papers citing papers by Jack M. Fu
This network shows the impact of papers produced by Jack M. Fu. 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 Jack M. Fu. The network helps show where Jack M. Fu may publish in the future.
Co-authors
The 25 scholars most cited alongside Jack M. Fu, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A genomic mutational constraint map using variation in 76,156 human genomes Hit paper breakdown → | 2023 | 736 |
| 2 | A structural variation reference for medical and population genetics Hit paper breakdown → | 2020 | 636 |
| 3 | Rare coding variation provides insight into the genetic architecture and phenotypic context of autism Hit paper breakdown → | 2022 | 335 |
| 4 | A cross-disorder dosage sensitivity map of the human genome Hit paper breakdown → | 2022 | 197 |
| 5 | 1998 | 158 | |
| 6 | Genome Sequencing for Diagnosing Rare Diseases Hit paper breakdown → | 2024 | 101 |
| 7 | 2021 | 84 | |
| 8 | 2022 | 61 | |
| 9 | 2018 | 61 | |
| 10 | 2023 | 60 | |
| 11 | 2022 | 54 | |
| 12 | 2023 | 52 | |
| 13 | 2020 | 52 | |
| 14 | 2023 | 34 | |
| 15 | 2024 | 30 | |
| 16 | 2022 | 29 | |
| 17 | 2021 | 28 | |
| 18 | 2022 | 26 | |
| 19 | 2004 | 17 | |
| 20 | 2024 | 14 |
About Jack M. Fu
Jack M. Fu is a scholar working on Genetics, Computer Networks and Communications, Molecular Biology, Artificial Intelligence and Cognitive Neuroscience, having authored 35 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (12 papers), Semantic Web and Ontologies (7 papers), Advanced Database Systems and Queries (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Biomedical Text Mining and Ontologies (4 papers), Autism Spectrum Disorder Research (4 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.3k citations), Cancer Research (204 citations), Cognitive Neuroscience (272 citations) and Aging (14 citations). Jack M. Fu has collaborated with scholars based in United States, Canada and Denmark. Frequent co-authors include Ernest Martinez, Robert G. Roeder, Tapas Kumar Kundu, Michael E. Talkowski, Michael R. Delannoy, Kapil V. Ramachandran, Chan Hyun Na, Seth S. Margolis, Thomas B. Schaffer and Ramez A. Elmasri. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Bioinformatics, Cell Genomics and Genetics in Medicine.
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.