Ikuko Teshima

2.5k total citations
61 papers, 1.5k citations indexed

About

Ikuko Teshima is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ikuko Teshima has authored 61 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 26 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ikuko Teshima's work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Ikuko Teshima is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Ikuko Teshima collaborates with scholars based in Canada, United States and Japan. Ikuko Teshima's co-authors include Diane W. Cox, V. D. Marković, J. Siegel‐Bartelt, Stephen W. Scherer, David Chitayat, Małgorzata J.M. Nowaczyk, Cheryl Cytrynbaum, Rosanna Weksberg, Russell Schachar and Jacqueline Siegel‐Bartelt and has published in prestigious journals such as Nature, Science and Blood.

In The Last Decade

Ikuko Teshima

59 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ikuko Teshima Canada 23 797 731 292 171 170 61 1.5k
Alan Shanske United States 26 931 1.2× 976 1.3× 310 1.1× 193 1.1× 141 0.8× 84 1.9k
Shivanand R. Patil United States 24 1.2k 1.5× 1.2k 1.6× 418 1.4× 269 1.6× 113 0.7× 77 2.2k
Frank Majewski Germany 16 755 0.9× 579 0.8× 271 0.9× 86 0.5× 81 0.5× 26 1.3k
G. Shashidhar Pai United States 25 981 1.2× 796 1.1× 450 1.5× 257 1.5× 180 1.1× 55 1.9k
Keiko Wakui Japan 28 1.4k 1.7× 1.3k 1.8× 283 1.0× 353 2.1× 153 0.9× 89 2.3k
J P Fryns Belgium 25 1.2k 1.6× 1.1k 1.5× 430 1.5× 190 1.1× 259 1.5× 90 2.2k
Ursula G. Froster Germany 23 886 1.1× 900 1.2× 371 1.3× 74 0.4× 106 0.6× 79 2.0k
Jay W. Ellison United States 23 1.2k 1.6× 1.2k 1.7× 438 1.5× 210 1.2× 249 1.5× 52 2.6k
Mitsuo Masuno Japan 21 1.1k 1.4× 1.4k 1.9× 180 0.6× 138 0.8× 90 0.5× 86 2.3k
Trijnie Dijkhuizen Netherlands 24 677 0.8× 801 1.1× 201 0.7× 84 0.5× 382 2.2× 62 1.6k

Countries citing papers authored by Ikuko Teshima

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Ikuko Teshima

This figure shows the co-authorship network connecting the top 25 collaborators of Ikuko Teshima. A scholar is included among the top collaborators of Ikuko Teshima based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ikuko Teshima. Ikuko Teshima is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Wang, Jia‐Chi, et al.. (2009). 4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generations. American Journal of Medical Genetics Part A. 149A(10). 2274–2279. 18 indexed citations
2.
Maegawa, Gustavo, et al.. (2008). Interstitial deletion of 1p22.2p31.1 and medium‐chain acyl‐CoA dehydrogenase deficiency in a patient with global developmental delay. American Journal of Medical Genetics Part A. 146A(12). 1581–1586. 10 indexed citations
3.
Somers, Gino R., Sandra Viero, Paul C. Nathan, et al.. (2005). Association of the t(12;22)(q13;q12) EWS/ATF1 Rearrangement With Polyphenotypic Round Cell Sarcoma of Bone. The American Journal of Surgical Pathology. 29(12). 1673–1679. 24 indexed citations
4.
Teshima, Ikuko, et al.. (2005). A der(19)t(12;19)(q12;p13.3) in a case of pediatric acute leukemia with unusual immunophenotype. Cancer Genetics and Cytogenetics. 157(2). 164–168. 1 indexed citations
5.
Sharathkumar, Anjali, Melanie Kirby, Melvin H. Freedman, et al.. (2003). Malignant hematological disorders in children with Wolf–Hirschhorn syndrome. American Journal of Medical Genetics Part A. 119A(2). 194–199. 18 indexed citations
6.
Pavenski, Katerina, Lucie Dupuis, Shelley Kennedy, et al.. (2002). Detecting rearrangements in children using subtelomeric FISH and SKY. American Journal of Medical Genetics. 107(4). 267–274. 46 indexed citations
7.
Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations
8.
Hodaie, Mojgan, L. E. Becker, Ikuko Teshima, & Jim Rutka. (2001). Total Resection of an Intracerebral Hemangioendothelioma in an Infant. Pediatric Neurosurgery. 34(2). 104–112. 17 indexed citations
9.
Arnold, Paul, Jacqueline Siegel‐Bartelt, Cheryl Cytrynbaum, Ikuko Teshima, & Russell Schachar. (2001). Velo‐cardio‐facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders. American Journal of Medical Genetics. 105(4). 354–362. 75 indexed citations
10.
Teshima, Ikuko, Erawati V. Bawle, Rosanna Weksberg, et al.. (2000). Analphoid 3qter markers. American Journal of Medical Genetics. 94(2). 113–119. 14 indexed citations
11.
Teshima, Ikuko, et al.. (1999). Analysis of Chromosome 22q as an Aid to the Diagnosis of Rhabdoid Tumor. The American Journal of Surgical Pathology. 23(8). 982–982. 15 indexed citations
12.
Chitayat, David, Ants Toi, Riyana Babul, et al.. (1997). Omphalocele in Miller-Dieker syndrome: Expanding the phenotype. American Journal of Medical Genetics. 69(3). 293–298. 21 indexed citations
13.
Chitayat, David, Riyana Babul, Meredith M. Silver, et al.. (1996). Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27→qter)]. American Journal of Medical Genetics. 61(1). 45–48. 23 indexed citations
14.
Chitayat, David, Rogelio H.A. Ruvalcaba, Riyana Babul, et al.. (1995). Syndrome of proximal interstitial deletion 4p15: Report of three cases and review of the literature. American Journal of Medical Genetics. 55(2). 147–154. 28 indexed citations
15.
Tomkins, Darrell J., Michel Vekemans, Ikuko Teshima, et al.. (1992). Annex 5: List of all cytogenetic abnormalities detected. Prenatal Diagnosis. 12(5). 439–441.
16.
Teshima, Ikuko, E.J.T. Winsor, & Margot I. Van Allen. (1992). Trisomy 18 and a constitutional maternal translocation (2;18). American Journal of Medical Genetics. 43(4). 759–761. 13 indexed citations
17.
18.
Musewe, Norman N., et al.. (1990). Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18. Journal of the American College of Cardiology. 15(3). 673–677. 64 indexed citations
19.
Hofker, Marten H., et al.. (1990). Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency. Genomics. 6(1). 33–38. 18 indexed citations
20.
Høgdall, Claus, T.A. Doran, J. Shime, Stephanie R. Wilson, & Ikuko Teshima. (1988). Transabdominal chorionic villus sampling in the second trimester. American Journal of Obstetrics and Gynecology. 158(2). 345–349. 15 indexed citations

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.

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