Get started
Author

Ikuko E. Teshima

Observed names: I E Teshima, I TESHIMA, I Teshima, I. E. Teshima, I. Teshima, Ikuko E Teshima, Ikuko Teshima, IkukoE Teshima, IkukoE. Teshima
Observed institutions: Cleveland Clinic, University of Groningen, Baylor College of Medicine, University of Toronto, Wellington Hospital, Hospital for Sick Children, Toronto General Hospital, Scott & White Memorial Hospital, Sickkids Research Institute, Texas A&M University
OpenAlex ID: A5110161753
Human Chromosome 7: DNA Sequence and Biology
2003 · Stephen W. Scherer, Joseph Cheung, et al. · Science · 215
Characterization of the Supernumerary Chromosome in Cat Eye Syndrome
1986 · Heather E. McDermid, Alessandra M. V. Duncan, et al. · Science · 158
Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
1982 · Diane W. Cox, Vera D. Markovic, et al. · Nature · 136
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
2006 · Susan Zeesman, Małgorzata J.M. Nowaczyk, et al. · American Journal of Medical Genetics Part A · 120
Velo‐cardio‐facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders
2001 · Paul D. Arnold, Jacqueline Siegel‐Bartelt, et al. · American Journal of Medical Genetics · 113
Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted
1993 · R. Weksberg, I. Teshima, et al. · Human Molecular Genetics · 99
Detecting rearrangements in children using subtelomeric FISH and SKY
2002 · Blaise Clarkson, Katerina Pavenski, et al. · American Journal of Medical Genetics · 97
Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18
1990 · Norman N. Musewe, Diane J. Alexander, et al. · Journal of the American College of Cardiology · 95
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex
1998 · Teresa Costa, Marie Lambert, et al. · American Journal of Medical Genetics · 91
Genetic analysis of patients with the Saethre‐Chotzen phenotype
2002 · Kathy Chun, Ahmad S. Teebi, et al. · American Journal of Medical Genetics · 85
4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generations
2009 · Jia‐Chi Wang, Thomas Fisker, et al. · American Journal of Medical Genetics Part A · 76
Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma
2003 · Angela Punnett, Ikuko Teshima, et al. · American Journal of Medical Genetics Part A · 75
Trisomy 18 and a constitutional maternal translocation (2;18)
1992 · Ikuko E. Teshima, Elizabeth J. T. Winsor, et al. · American Journal of Medical Genetics · 70
Primary Ewing’s Sarcoma of the Skull in Children
1999 · Carlos G. Carlotti Jr., James M. Drake, et al. · Pediatric Neurosurgery · 52
Annex 6: Chromosome mosaicism in CVS and amniocentesis samples
1992 · I. E. Teshima, D. K. Kalousek, et al. · Prenatal Diagnosis · 52
Central neurocytoma: morphological, flow cytometric, polymerase chain reaction, fluorescence in situ hybridization, and karyotypic analyses
1999 · Venita Jay, Vern Edwards, et al. · Journal of neurosurgery · 44
Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome
2002 · Kazuhiko Nakabayashi, Bridget A. Fernandez, et al. · Genomics · 38
Omphalocele in Miller-Dieker syndrome: Expanding the phenotype
1997 · David Chitayat, Ants Toi, et al. · American Journal of Medical Genetics · 38
Mosaicism for duplication 12q (12q13-->q24.2) in a dysmorphic male infant.
1993 · J W Dixon, T Costa, et al. · Journal of Medical Genetics · 37
PDF
Ring chromosome 22 and autism: Report and review
2000 · Joanna E. MacLean, Ikuko E. Teshima, et al. · American Journal of Medical Genetics · 35
Syndrome of proximal interstitial deletion 4p15: Report of three cases and review of the literature
1995 · David Chitayat, Rogelio H. A. Ruvalcaba, et al. · American Journal of Medical Genetics · 35
Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies
1998 · Karen J. Harrison, Ikuko E. Teshima, et al. · American Journal of Medical Genetics · 34
Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and 4q13.2q23 deletions
1997 · M. J. M. Nowaczyk, I. E. Teshima, et al. · American Journal of Medical Genetics · 34
Holoprosencephaly and cleidocranial dysplasia in a patient due to two position‐effect mutations: case report and review of the literature
2005 · BA Fernandez, J Siegel‐Bartelt, et al. · Clinical Genetics · 32
Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review
1991 · S. A. Farrell, J. Siegel‐Bartelt, et al. · Clinical Genetics · 32
Works count: 66
Citation count: 2,454
H-index: 28
I10-index: 50
Year
Topic
Type