Lie‐Jiau Hsieh
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics, Cholangiocarcinoma and Gallbladder Cancer Studies, RNA modifications and cancer
Most-Cited Works
- → Calreticulin expression in neuroblastoma—a novel independent prognostic factor(2005)93 cited
- → Prenatal diagnosis ofde novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertainedde novo apparently balanced complex and multiple chromosomal rearrangements(2006)84 cited
- → Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype(2006)78 cited
- → Prenatal diagnosis of low‐level mosaicism for a small XIST‐negative supernumerary ring X chromosome in a nondysmorphic male fetus(2006)71 cited
- → Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q(2006)48 cited
- → A paternally derived inverted duplication of distal 14q with a terminal 14q deletion(2005)31 cited
- → Karyotypic evolution of a novel cervid satellite DNA family isolated by microdissection from the Indian muntjac Y-chromosome(2005)21 cited
- → Perinatal findings and molecular cytogenetic analysis ofde novo partial trisomy 16q (16q22.1?qter) and partial monosomy 20q (20q13.3?qter)(2005)15 cited
- → Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)(2006)12 cited
- → Prenatal Diagnosis of a Fetus Affected with Down Syndrome and Deletion 1p36 Syndrome by Fluorescence in situ Hybridization and Spectral Karyotyping(2004)11 cited