N.S.F. Ma
Impact in
- Genetics top 5%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Connective tissue disorders research
- Developmental Biology top 10%
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
-
- Chromosomal and Genetic Variations 6
- Co-authors
- William A. Paznekas (1 shared paper)Timothy D. Howard (1 shared paper)Ethylin Wang Jabs (1 shared paper)Eric D. Green (1 shared paper)Rosa Isela Ortiz De Luna (1 shared paper)Richard W. Thorington (1 shared paper)Robert W. Cooper (1 shared paper)T. C. Jones (1 shared paper)
- Journals
- Genomics (2 papers)Journal of Medical Primatology (1 paper)Nature Genetics (1 paper)Chromosoma (1 paper)Cytogenetics and Cell Genetics (7 papers)
- Partner nations
- United StatesMexicoJapan
In The Last Decade
N.S.F. Ma
7 papers receiving 565 citations
N.S.F. Ma's Hit Papers
Peers
Comparison fields: 5 of 60
- Genetics 378
- Developmental Biology 17
- Molecular Biology 371
- Aging 7
- Genetics 33
Countries citing papers authored by N.S.F. Ma
This map shows the geographic impact of N.S.F. Ma'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 N.S.F. Ma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N.S.F. Ma more than expected).
Fields of papers citing papers by N.S.F. Ma
This network shows the impact of papers produced by N.S.F. Ma. 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 N.S.F. Ma. The network helps show where N.S.F. Ma may publish in the future.
Co-authors
The 25 scholars most cited alongside N.S.F. Ma, 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 | Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome Hit paper breakdown → | 1997 | 532 |
| 2 | 1992 | 29 | |
| 3 | 1974 | 23 | |
| 4 | 1994 | 3 | |
| 5 | 1987 | 2 | |
| 6 | 2008 | 2 | |
| 7 | 2008 | 1 | |
| 8 | 2008 | 0 | |
| 9 | 2008 | 0 | |
| 10 | 2008 | 0 | |
| 11 | 2008 | 0 | |
| 12 | 2008 | 0 |
About N.S.F. Ma
N.S.F. Ma is a scholar working on Genetics, Plant Science, Molecular Biology, Social Psychology and Cardiology and Cardiovascular Medicine, having authored 12 papers that have together received 592 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Muscle Physiology and Disorders (1 paper), Animal Ecology and Behavior Studies (1 paper), Microtubule and mitosis dynamics (1 paper) and Pluripotent Stem Cells Research (1 paper). The work is most often cited by research in Genetics (378 citations), Developmental Biology (17 citations), Molecular Biology (371 citations), Aging (7 citations) and Genetics (33 citations). N.S.F. Ma has collaborated with scholars based in United States, Mexico and Japan. Frequent co-authors include William A. Paznekas, Timothy D. Howard, Ethylin Wang Jabs, Eric D. Green, Rosa Isela Ortiz De Luna, Richard W. Thorington, Robert W. Cooper, T. C. Jones, Jun Wu and Daniela S. Gerhard. Their work appears in journals such as Genomics, Journal of Medical Primatology, Nature Genetics, Chromosoma and Cytogenetics and Cell Genetics.
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.