Ikuko Teshima
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 34
- Genomic variations and chromosomal abnormalities 23
- Genetics and Neurodevelopmental Disorders 9
- Genetic Syndromes and Imprinting 7
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- Epigenetics and DNA Methylation 6
- Renal and related cancers 4
- Co-authors
- Diane W. Cox (3 shared papers)V. D. Marković (3 shared papers)J. Siegel‐Bartelt (6 shared papers)Stephen W. Scherer (4 shared papers)David Chitayat (13 shared papers)Małgorzata J.M. Nowaczyk (5 shared papers)Jacqueline Siegel‐Bartelt (1 shared paper)Rosanna Weksberg (7 shared papers)
- Journals
- Genomics (4 papers)The American Journal of Surgical Pathology (3 papers)Clinical Genetics (3 papers)American Journal of Medical Genetics (21 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- CanadaUnited StatesJapan
In The Last Decade
Ikuko Teshima
59 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 78
- Genetics 797
- Pediatrics, Perinatology and Child Health 292
- Developmental Biology 30
- Molecular Biology 731
- Genetics 112
Countries citing papers authored by Ikuko Teshima
This map shows the geographic impact of Ikuko 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 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 Teshima more than expected).
Fields of papers citing papers by Ikuko Teshima
This network shows the impact of papers produced by Ikuko 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 Teshima. The network helps show where Ikuko Teshima may publish in the future.
Co-authors
The 25 scholars most cited alongside Ikuko 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1986 | 119 | |
| 2 | 1982 | 119 | |
| 3 | 2006 | 97 | |
| 4 | 1993 | 76 | |
| 5 | 2001 | 75 | |
| 6 | 1990 | 64 | |
| 7 | 2002 | 54 | |
| 8 | 2002 | 46 | |
| 9 | 1992 | 43 | |
| 10 | 1999 | 39 | |
| 11 | 1998 | 35 | |
| 12 | 1999 | 34 | |
| 13 | 1991 | 31 | |
| 14 | 1991 | 29 | |
| 15 | 1995 | 28 | |
| 16 | 1996 | 27 | |
| 17 | 1997 | 26 | |
| 18 | 2002 | 25 | |
| 19 | 1993 | 25 | |
| 20 | 2005 | 24 |
About Ikuko Teshima
Ikuko Teshima is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 61 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (12 papers), Genetics and Neurodevelopmental Disorders (9 papers), Chromosomal and Genetic Variations (8 papers), Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (6 papers), Acute Myeloid Leukemia Research (5 papers) and Renal and related cancers (4 papers). The work is most often cited by research in Genetics (797 citations), Pediatrics, Perinatology and Child Health (292 citations), Developmental Biology (30 citations), Molecular Biology (731 citations) and Genetics (112 citations). Ikuko Teshima has collaborated with scholars based in Canada, United States and Japan. Frequent co-authors include Diane W. Cox, V. D. Marković, J. Siegel‐Bartelt, Stephen W. Scherer, David Chitayat, Małgorzata J.M. Nowaczyk, Jacqueline Siegel‐Bartelt, Rosanna Weksberg, Cheryl Cytrynbaum and Russell Schachar. Their work appears in journals such as Genomics, The American Journal of Surgical Pathology, Clinical Genetics, American Journal of Medical Genetics and Journal of Medical 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.