Gen Nishimura
Impact in
- Genetics top 0.2%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Developmental Biology top 2%
Papers in
- Genetics 210
- Connective tissue disorders research 127
- Dermatological and Skeletal Disorders 39
- Genomic variations and chromosomal abnormalities 19
-
- Bone Metabolism and Diseases 27
- RNA modifications and cancer 21
- Co-authors
- Shiro Ikegawa (75 shared papers)Andrea Superti‐Furga (39 shared papers)Sheila Unger (37 shared papers)Hirofumi Ohashi (37 shared papers)Tsutomu Ogata (24 shared papers)Geert Mortier (10 shared papers)Ravi Savarirayan (7 shared papers)Valérie Cormier‐Daire (8 shared papers)
- Journals
- Skeletal Radiology (12 papers)American Journal of Medical Genetics Part A (83 papers)Journal of Medical Genetics (8 papers)European Journal of Medical Genetics (8 papers)Human Mutation (8 papers)
- Partner nations
- JapanUnited StatesGermany
In The Last Decade
Gen Nishimura
348 papers receiving 7.3k citations
Gen Nishimura's Hit Papers
Peers
Comparison fields: 5 of 134
- Genetics 3.7k
- Developmental Biology 200
- Rheumatology 1.1k
- Immunology and Allergy 363
- Sensory Systems 232
Countries citing papers authored by Gen Nishimura
This map shows the geographic impact of Gen Nishimura'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 Gen Nishimura with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gen Nishimura more than expected).
Fields of papers citing papers by Gen Nishimura
This network shows the impact of papers produced by Gen Nishimura. 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 Gen Nishimura. The network helps show where Gen Nishimura may publish in the future.
Co-authors
The 25 scholars most cited alongside Gen Nishimura, 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 365 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nosology and classification of genetic skeletal disorders: 2010 revision Hit paper breakdown → | 2011 | 501 |
| 2 | Nosology and classification of genetic skeletal disorders: 2019 revision Hit paper breakdown → | 2019 | 393 |
| 3 | Nosology and classification of genetic skeletal disorders: 2015 revision Hit paper breakdown → | 2015 | 390 |
| 4 | 2000 | 188 | |
| 5 | 1999 | 139 | |
| 6 | 2005 | 132 | |
| 7 | 2005 | 130 | |
| 8 | 2001 | 104 | |
| 9 | 2007 | 95 | |
| 10 | 2011 | 92 | |
| 11 | 2001 | 88 | |
| 12 | 2007 | 87 | |
| 13 | 2005 | 86 | |
| 14 | 2006 | 79 | |
| 15 | 2017 | 75 | |
| 16 | 2019 | 71 | |
| 17 | 2001 | 70 | |
| 18 | 2010 | 70 | |
| 19 | 2012 | 70 | |
| 20 | 2010 | 69 |
About Gen Nishimura
Gen Nishimura is a scholar working on Genetics, Molecular Biology, Rheumatology, Oncology and Surgery, having authored 365 papers that have together received 7.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (127 papers), Bone health and treatments (45 papers), Dermatological and Skeletal Disorders (39 papers), Bone Metabolism and Diseases (27 papers), RNA modifications and cancer (21 papers), Cell Adhesion Molecules Research (20 papers), Genomic variations and chromosomal abnormalities (19 papers) and Osteoarthritis Treatment and Mechanisms (17 papers). The work is most often cited by research in Genetics (3.7k citations), Developmental Biology (200 citations), Rheumatology (1.1k citations), Immunology and Allergy (363 citations) and Sensory Systems (232 citations). Gen Nishimura has collaborated with scholars based in Japan, United States and Germany. Frequent co-authors include Shiro Ikegawa, Andrea Superti‐Furga, Sheila Unger, Hirofumi Ohashi, Tsutomu Ogata, Geert Mortier, Ravi Savarirayan, Valérie Cormier‐Daire, Christine M Hall and Matthew L. Warman. Their work appears in journals such as Skeletal Radiology, American Journal of Medical Genetics Part A, Journal of Medical Genetics, European Journal of Medical Genetics and Human Mutation.
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.