Ikuko E. Teshima
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
- Genetic Associations and Epidemiology
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Developmental Biology top 5%
Papers in
- Genetics 41
- Genomic variations and chromosomal abnormalities 32
- Genetic Syndromes and Imprinting 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Fetal and Pediatric Neurological Disorders 2
- Co-authors
- Diane Wilson Cox (3 shared papers)Vera D. Markovic (2 shared papers)Teresa Costa (4 shared papers)Jackie Siegel-Bartelt (5 shared papers)David A. Chitayat (10 shared papers)Stephen W. Scherer (4 shared papers)Małgorzata J.M. Nowaczyk (3 shared papers)Rosanna Weksberg (7 shared papers)
- Journals
- Genomics (4 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (3 papers)The American Journal of Surgical Pathology (3 papers)Science (2 papers)
- Partner nations
- CanadaUnited StatesJapan
In The Last Decade
Ikuko E. Teshima
57 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 80
- Genetics 1.1k
- Developmental Biology 45
- Pediatrics, Perinatology and Child Health 214
- Genetics 61
- Developmental Neuroscience 14
Countries citing papers authored by Ikuko E. Teshima
This map shows the geographic impact of Ikuko E. Teshima'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 Ikuko E. Teshima with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ikuko E. Teshima more than expected).
Fields of papers citing papers by Ikuko E. Teshima
This network shows the impact of papers produced by Ikuko E. Teshima. 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 Ikuko E. Teshima. The network helps show where Ikuko E. Teshima may publish in the future.
Co-authors
The 25 scholars most cited alongside Ikuko E. Teshima, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 166 | |
| 2 | 1986 | 127 | |
| 3 | 1982 | 124 | |
| 4 | 2006 | 104 | |
| 5 | 2001 | 84 | |
| 6 | 1993 | 81 | |
| 7 | 1990 | 75 | |
| 8 | 2002 | 69 | |
| 9 | 2002 | 68 | |
| 10 | 1998 | 57 | |
| 11 | 1999 | 43 | |
| 12 | 1992 | 42 | |
| 13 | 1999 | 40 | |
| 14 | 1993 | 36 | |
| 15 | 2009 | 35 | |
| 16 | 1991 | 32 | |
| 17 | 2003 | 32 | |
| 18 | 1997 | 31 | |
| 19 | 1998 | 31 | |
| 20 | 1995 | 30 |
About Ikuko E. Teshima
Ikuko E. Teshima is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Pulmonary and Respiratory Medicine and Genetics, having authored 57 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Sarcoma Diagnosis and Treatment (5 papers), Genetic Syndromes and Imprinting (5 papers), Acute Myeloid Leukemia Research (4 papers), Congenital Anomalies and Fetal Surgery (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Genomics and Chromatin Dynamics (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (1.1k citations), Developmental Biology (45 citations), Pediatrics, Perinatology and Child Health (214 citations), Genetics (61 citations) and Developmental Neuroscience (14 citations). Ikuko E. Teshima has collaborated with scholars based in Canada, United States and Japan. Frequent co-authors include Diane Wilson Cox, Vera D. Markovic, Teresa Costa, Jackie Siegel-Bartelt, David A. Chitayat, Stephen W. Scherer, Małgorzata J.M. Nowaczyk, Rosanna Weksberg, Shelley J. Kennedy and Ahmad Said Teebi. Their work appears in journals such as Genomics, Clinical Genetics, Journal of Medical Genetics, The American Journal of Surgical Pathology and Science.
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.