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Perfluorinated compounds in umbilical cord blood and adverse birth outcomes

PloS one, 2012-08, Vol.7 (8), p.e42474-e42474

2012

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TP53 alterations in relapsed childhood acute lymphoblastic leukemia

Cancer science, 2020-01, Vol.111 (1), p.229-238

2020

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The effects of a Journey of the Brave Counseling Program on anxiety, well-being, and life adjustment in Taiwanese children

BMC psychiatry, 2023-09, Vol.23 (1), p.1-17, Article 657

2023

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Newborn genetic screening for hearing impairment: a population-based longitudinal study

Genetics in medicine, 2017-01, Vol.19 (1), p.6-12

2017

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Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan

The Journal of pediatrics, 2018-08, Vol.199, p.144-150.e1

2018

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Perfluorinated Compound Levels in Cord Blood and Neurodevelopment at 2 Years of Age

Epidemiology (Cambridge, Mass.), 2013-11, Vol.24 (6), p.800-808

2013

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Clinical outcomes of fetuses with chromosome 16 short arm copy number variants

Molecular genetics & genomic medicine, 2023-07, Vol.11 (7), p.e2174-n/a

2023

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Investigation of the Associations Between Low-Dose Serum Perfluorinated Chemicals and Liver Enzymes in US Adults

The American journal of gastroenterology, 2010-06, Vol.105 (6), p.1354-1363

2010

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Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study

PloS one, 2011-02, Vol.6 (2), p.e17067-e17067

2011

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Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan

PloS one, 2017-02, Vol.12 (2), p.e0170517-e0170517

2017

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Fragile X syndrome carrier screening in pregnant women in Chinese Han population

Scientific reports, 2019-10, Vol.9 (1), p.15456-7, Article 15456

2019

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MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia

Scientific reports, 2020-07, Vol.10 (1), p.11501-11501, Article 11501

2020

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Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta

Orphanet journal of rare diseases, 2015-12, Vol.10 (1), p.152-152, Article 152

2015

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Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum

American journal of medical genetics. Part A, 2019-09, Vol.179 (9), p.1878-1883

2019

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Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center

PloS one, 2011-07, Vol.6 (7), p.e22314-e22314

2011

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The sFlt-1/PlGF Ratio as a Predictor for Poor Pregnancy and Neonatal Outcomes

Pediatrics and neonatology, 2017-12, Vol.58 (6), p.529-533

2017

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IKZF1 deletions predict a poor prognosis in children with B‐cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan

Cancer science, 2011-10, Vol.102 (10), p.1874-1881

2011

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Mesothelin inhibits paclitaxel-induced apoptosis through the PI3K pathway

Biochemical journal, 2009-12, Vol.424 (3), p.449-458

2009

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First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2022-01, Vol.61 (1), p.174-179

2022

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Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan

PloS one, 2017-08, Vol.12 (8), p.e0183406-e0183406

2017

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Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome (PAPA syndrome): Report of a sporadic case without an identifiable mutation in the CD2BP1 gene

Journal of the American Academy of Dermatology, 2009-09, Vol.61 (3), p.533-535

2009

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Factors affecting pregnant women's decisions regarding prenatal pertussis vaccination: A decision-making study in the nationwide Prenatal Pertussis Immunization Program in Taiwan

Taiwanese journal of obstetrics & gynecology, 2020-03, Vol.59 (2), p.200-206

2020

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Maternal-reported behavioral and emotional problems in Taiwanese preschool children

Research in developmental disabilities, 2012-05, Vol.33 (3), p.866-873

2012

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Targeted disruption in mice of a neural stem cell-maintaining, KRAB-Zn finger-encoding gene that has rapidly evolved in the human lineage

PloS one, 2012-10, Vol.7 (10), p.e47481-e47481

2012

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Mutation screening of the EYA1, SIX1, and SIX5 genes in an east asian cohort with branchio-oto-renal syndrome

The Laryngoscope, 2012-05, Vol.122 (5), p.1130-1136

2012

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Perfluorinated compounds in umbilical cord blood and adverse birth outcomes

TP53 alterations in relapsed childhood acute lymphoblastic leukemia

The effects of a Journey of the Brave Counseling Program on anxiety, well-being, and life adjustment in Taiwanese children

Newborn genetic screening for hearing impairment: a population-based longitudinal study

Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan

Perfluorinated Compound Levels in Cord Blood and Neurodevelopment at 2 Years of Age

Clinical outcomes of fetuses with chromosome 16 short arm copy number variants

Investigation of the Associations Between Low-Dose Serum Perfluorinated Chemicals and Liver Enzymes in US Adults

Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study

Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan

Fragile X syndrome carrier screening in pregnant women in Chinese Han population

MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia

Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta

Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum

Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center

The sFlt-1/PlGF Ratio as a Predictor for Poor Pregnancy and Neonatal Outcomes

IKZF1 deletions predict a poor prognosis in children with B‐cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan

Mesothelin inhibits paclitaxel-induced apoptosis through the PI3K pathway

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan

Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome (PAPA syndrome): Report of a sporadic case without an identifiable mutation in the CD2BP1 gene

Factors affecting pregnant women's decisions regarding prenatal pertussis vaccination: A decision-making study in the nationwide Prenatal Pertussis Immunization Program in Taiwan

Maternal-reported behavioral and emotional problems in Taiwanese preschool children

Targeted disruption in mice of a neural stem cell-maintaining, KRAB-Zn finger-encoding gene that has rapidly evolved in the human lineage

Mutation screening of the EYA1, SIX1, and SIX5 genes in an east asian cohort with branchio-oto-renal syndrome

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