Dagmar K. Kalousek

University of British Columbia — Canada

Medicine · Health Sciences

47h-index7.0kcitations165works0.02yr avg
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Research Topics

Prenatal Screening and Diagnostics(88), Genetic Syndromes and Imprinting(39), Genomic variations and chromosomal abnormalities(33), Acute Myeloid Leukemia Research(20), Congenital Anomalies and Fetal Surgery(19)

Publications165 total

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss
Human Reproduction·2010· 112 citedOpen Access
Genomic changes detected by array CGH in human embryos with developmental defects
Molecular Human Reproduction·2009· 117 cited
Placental Weight in Pregnancies With Trisomy Confined to the Placenta
Journal of Obstetrics and Gynaecology Canada·2009· 16 cited
Autologous bone marrow transplantation for children with AML in first remission
Bone Marrow Transplantation·2007· 7 cited
Postnatal follow‐up of prenatally diagnosed trisomy 16 mosaicism
Prenatal Diagnosis·2006· 130 cited
Frequency of chromosomal abnormalities in spontaneous abortions derived from intracytoplasmic sperm injection compared with those from in vitro fertilization
Fertility and Sterility·2006· 31 citedOpen Access
Prenatally detected trisomy 20 mosaicism
Prenatal Diagnosis·2005· 78 cited
Abnormal embryonic development diagnosed embryoscopically in early intrauterine deaths after in vitro fertilization: A preliminary report of 23 cases
Fertility and Sterility·2004· 19 cited
Effects of triploidy on early human development
Prenatal Diagnosis·2004· 34 cited
Molecular Cytogenetics in Reproductive Pathology
Molecular Cytogenetics·2003· 3 cited
Transcervical fetoscopic diagnosis of structural defects in four first‐trimester monochorionic twin intrauterine deaths
Prenatal Diagnosis·2003· 5 cited
Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization
Cancer Genetics and Cytogenetics·2003· 29 cited
Morphology of the 45,X embryo: An embryoscopic study
American Journal of Medical Genetics Part A·2003· 6 cited
Skewed X-Chromosome Inactivation Is Associated with Trisomy in Women Ascertained on the Basis of Recurrent Spontaneous Abortion or Chromosomally Abnormal Pregnancies
The American Journal of Human Genetics·2003· 77 citedOpen Access
Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism
Prenatal Diagnosis·2002· 92 cited
Evidence for imprinting on chromosome 16: The effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies
American Journal of Medical Genetics·2002· 114 cited
Generalized abnormal embryonic development in missed abortion: Embryoscopic and cytogenetic findings
American Journal of Medical Genetics·2002· 48 cited
Cytogenetics of Placenta—A Workshop Report
Placenta·2002· 2 cited
Interphase fluorescence in situ hybridization and DNA flow cytometry analysis of medulloblastomas with a normal karyotype
Cancer Genetics and Cytogenetics·2002· 4 cited
Neural tube defects in missed abortions: embryoscopic and cytogenetic findings
American Journal of Medical Genetics·2001· 20 cited
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Frequent Co-authors

Irene Barrett(16), Wendy P. Robinson(10), Sylvie Langlois(8), R. Douglas Wilson(5), Connie J. Eaves(4), P. N. Howard‐Peebles(4), AC Eaves(4), Barbara McGillivray(4), F. J. Dill(4), L.E. Bernard(3), Adèle Telenius(3), Siu Li Yong(3), Maria S. Peñaherrera(3), Mary D. Stephenson(3), Tom Philipp(3), Brian D. Kuchinka(3), Brenda Lomax(3), Nathan L. Kobrinsky(2), Jonathan D. Buckley(2), JE Sanders(2)