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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generations 2009 ·American Journal of Medical Genetics Part A ·Jia‐Chi Wang, (unknown), (unknown), Ikuko Teshima, Małgorzata J.M. Nowaczyk	18
2	Interstitial deletion of 1p22.2p31.1 and medium‐chain acyl‐CoA dehydrogenase deficiency in a patient with global developmental delay 2008 ·American Journal of Medical Genetics Part A ·Gustavo Maegawa, (unknown), Brage Storstein Andresen, S. E. Olpin, (unknown), Joe T.R. Clarke, Ikuko Teshima	10
3	Association of the t(12;22)(q13;q12) EWS/ATF1 Rearrangement With Polyphenotypic Round Cell Sarcoma of Bone 2005 ·The American Journal of Surgical Pathology ·Gino R. Somers, Sandra Viero, Paul C. Nathan, Ikuko Teshima, Carlos Alberto de Bragança Pereira, Maria Zieleńska	24
4	A der(19)t(12;19)(q12;p13.3) in a case of pediatric acute leukemia with unusual immunophenotype 2005 ·Cancer Genetics and Cytogenetics ·(unknown), Ikuko Teshima, (unknown), (unknown), Mohamed Abdelhaleem	1
5	Malignant hematological disorders in children with Wolf–Hirschhorn syndrome 2003 ·American Journal of Medical Genetics Part A ·Anjali Sharathkumar, Melanie Kirby, Melvin H. Freedman, Mohamed Abdelhaleem, David Chitayat, Ikuko Teshima, Yigal Dror	18
6	Detecting rearrangements in children using subtelomeric FISH and SKY 2002 ·American Journal of Medical Genetics ·(unknown), Katerina Pavenski, Lucie Dupuis, Shelley Kennedy, M. Stephen Meyn, Marjan M. Nezarati, (unknown), (unknown), (unknown), Nada Quercia, Ahmad S. Teebi, Ikuko Teshima	46
7	Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome 2002 ·Genomics ·Kazuhiko Nakabayashi, Bridget A. Fernandez, Ikuko Teshima, Cheryl Shuman, Virginia K. Proud, Cynthia J. Curry, David Chitayat, Theresa A. Grebe, Jeffrey E. Ming, Mitsuo Oshimura, Makiko Meguro, Kohzoh Mitsuya, Paromita Deb‐Rinker, Jo-Anne Herbrick, Rosanna Weksberg, Stephen W. Scherer	25
8	Total Resection of an Intracerebral Hemangioendothelioma in an Infant 2001 ·Pediatric Neurosurgery ·Mojgan Hodaie, L. E. Becker, Ikuko Teshima, Jim Rutka	17
9	Velo‐cardio‐facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders 2001 ·American Journal of Medical Genetics ·Paul Arnold, Jacqueline Siegel‐Bartelt, Cheryl Cytrynbaum, Ikuko Teshima, Russell Schachar	75
10	Analphoid 3qter markers 2000 ·American Journal of Medical Genetics ·Ikuko Teshima, Erawati V. Bawle, Rosanna Weksberg, Cheryl Shuman, Daniel L. Van Dyke, Stuart Schwartz	14
11	Analysis of Chromosome 22q as an Aid to the Diagnosis of Rhabdoid Tumor 1999 ·The American Journal of Surgical Pathology ·(unknown), Ikuko Teshima, Maria Zieleńska, Vern Edwards, (unknown), Jeremy A. Squire, Paul S. Thorner	15
12	Omphalocele in Miller-Dieker syndrome: Expanding the phenotype 1997 ·American Journal of Medical Genetics ·David Chitayat, Ants Toi, Riyana Babul, Susan Blaser, (unknown), (unknown), Mathew Sermer, (unknown), (unknown), Ikuko Teshima	21
13	Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27→qter)] 1996 ·American Journal of Medical Genetics ·David Chitayat, Riyana Babul, Meredith M. Silver, Venita Jay, Ikuko Teshima, Paul Babyn, Laurence E. Becker	23
14	Syndrome of proximal interstitial deletion 4p15: Report of three cases and review of the literature 1995 ·American Journal of Medical Genetics ·David Chitayat, Rogelio H.A. Ruvalcaba, Riyana Babul, Ikuko Teshima, Jeffrey C. Posnick, Michel Vekemans, (unknown), Horace C. Thuline	28
15	Annex 5: List of all cytogenetic abnormalities detected 1992 ·Prenatal Diagnosis ·Darrell J. Tomkins, Michel Vekemans, Ikuko Teshima, David M. Cox, Louis Dallaire, R. Gagné, Dagmar K. Kalousek, (unknown), V. D. Marković, (unknown), F. R. Sergovich, Irene A. Uchida, (unknown)	0
16	Trisomy 18 and a constitutional maternal translocation (2;18) 1992 ·American Journal of Medical Genetics ·Ikuko Teshima, E.J.T. Winsor, Margot I. Van Allen	13
17	Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: Identification of a hot spot for recombination 1991 ·Genomics ·(unknown), Ikuko Teshima, Michael A. Walter, (unknown), Ghaleb H. Daouk, Diane W. Cox	29
18	Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18 1990 ·Journal of the American College of Cardiology ·Norman N. Musewe, (unknown), Ikuko Teshima, Jeffrey F. Smallhorn, Robert M. Freedom	64
19	Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency 1990 ·Genomics ·Marten H. Hofker, (unknown), Yusuke Nakamura, Ikuko Teshima, R. White, Diane W. Cox	18
20	Transabdominal chorionic villus sampling in the second trimester 1988 ·American Journal of Obstetrics and Gynecology ·Claus Høgdall, T.A. Doran, J. Shime, Stephanie R. Wilson, Ikuko Teshima	15

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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