Dong-Jay Lee

Changhua Christian Hospital — Taiwan

Agricultural and Biological Sciences · Life Sciences

7h-index148citations19works2.02yr avg
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Research Topics

Chromosomal and Genetic Variations(5), Genetic diversity and population structure(4), Prenatal Screening and Diagnostics(4), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(3), Genomic variations and chromosomal abnormalities(3)

Publications17 total

Genetic investigations of autosomal recessive inherited ichthyosis impressed by fetal ultrasound: Exome sequencing and haplotype linkage analysis
Taiwanese Journal of Obstetrics and Gynecology·2025· 3 citedOpen Access
De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study
International Journal of Molecular Sciences·2024· 1 citedOpen Access
Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients
Diagnostics·2022· 7 citedOpen Access
Proposal for Practical Approach in Prenatal Diagnosis of Beckwith–Wiedemann Syndrome and Review of the Literature
Diagnostics·2022· 5 citedOpen Access
Genome-Wide Microarray Analysis Suggests Transcriptomic Response May Not Play a Major Role in High- to Low-Altitude Acclimation in Harvest Mouse (Micromys minutus)
Animals·2019Open Access
Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification
Journal of the Formosan Medical Association·2018· 5 citedOpen Access
Noninvasive prenatal diagnosis of fetal aneuploidy by circulating fetal nucleated red blood cells and extravillous trophoblasts using silicon-based nanostructured microfluidics
Molecular Cytogenetics·2017· 40 citedOpen Access
Genomic analyses of the Formosan harvest mouse (Micromys minutus) and comparisons to the brown Norway rat (Rattus norvegicus) and the house mouse (Mus musculus)
Zoology·2013· 4 cited
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2
Taiwanese Journal of Obstetrics and Gynecology·2012· 9 citedOpen Access
Use of a cytogenetic whole-genome comparison to resolve phylogenetic relationships among three species: Implications for mammalian systematics and conservation biology
Theriogenology·2011· 6 cited
A compound heterozygous GNPTAB mutation causes mucolipidosis II with marked hair color change in a Han Chinese baby
American Journal of Medical Genetics Part A·2011· 9 citedOpen Access
Molecular delineation of the Y-borne Sry gene in the Formosan pangolin (Manis pentadactyla pentadactyla) and its phylogenetic implications for Pholidota in extant mammals
Theriogenology·2010· 21 cited
Comparison of Immunohistochemical and Fluorescence In Situ Hybridization Assessment for HER-2/neu Status in Taiwanese Breast Cancer Patients
Taiwanese Journal of Obstetrics and Gynecology·2007· 21 citedOpen Access
Interstitial Deletion 13q31 Associated with Normal Phenotype: Cytogenetic Study of a Family with Concomitant Segregation of Reciprocal Translocation and Interstitial Deletion
Journal of the Formosan Medical Association·2007· 3 citedOpen Access
Cytogenetic analysis of the formosan pangolin, Manis pentadactyla pentadactyla (Mammalia: Pholidota)
Zoological studies·2007· 13 cited
B Group Vitamin and Methylenetetrahydrofolate Reductase C677T Related Alteration of Plasma Homocysteine
Zānghuà yīxué·2005
Huge duplication cyst of small intestine: ultrasonographic features and prenatal aspiration
Prenatal Diagnosis·2005· 1 cited

Frequent Co-authors

Ming Chen(15), Gwo‐Chin Ma(12), Wen‐Hsiang Lin(8), Shun‐Ping Chang(6), Sheng-Hai Wu(5), Tze-Ho Chen(4), Hon‐Tsen Yu(3), Shih‐Chien Chin(3), Hsien‐Shao Tsao(2), Yu‐Yuan Ke(2), Ming‐Ching Shen(2), Wan‐Ju Wu(2), Liang‐Kong Lin(2), Chung-Er Huang(1), Hei‐Jen Jou(1), Yi-Shing Lin(1), Norman Ginsberg(1), Hsin‐Fu Chen(1), Frank Mau-Chung Chang(1), Ming Chen(1)