Ying Chen

Preterm birth and single nucleotide polymorphisms in cytokine genes.

Qin Zhu, Jian Sun, Ying Chen, 2014, Translational pediatrics.

Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.

Hong Li, Ben-jing Wang, Minjuan Liu, 2015, Translational pediatrics.

Associations between Maternal AFP and β-HCG and Preterm Birth

Daozhen Chen, Ailing Chen, Rui Yang, 2019, American Journal of Perinatology.

A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.

K. Choy, D. Cram, Hong Li, 2014, Clinica chimica acta; international journal of clinical chemistry.

[Application of next-generation sequencing technology for genetic diagnosis of Duchenne muscular dystrophy].

Hong Li, J. Mao, Minjuan Liu, 2012, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

D. Cram, Hong Li, Ting Wang, 2014, Clinica chimica acta; international journal of clinical chemistry.

BACs-on-beads: a new robust and rapid detection method for prenatal diagnosis

T. Leung, Xiao-fang Sun, Y. K. Kwok, 2014, Expert review of molecular diagnostics.

Identification of novel rare mutations of DACT1 in human neural tube defects

Bai-Lin Wu, Hong Li, Xueyan Yang, 2012, Human mutation.

A novel mutation (C1425Y) in the FBN2 gene in a father and son with congenital contractural arachnodactyly.

Wei Wang, Hong Li, Jing Zhang, 2009, Genetic testing and molecular biomarkers.

Association of UGT1A1 Variants and Hyperbilirubinemia in Breast-Fed Full-Term Chinese Infants

Li Jin, Q. Peng, Shilin Li, 2014, PloS one.

Quantitative trait analysis of polymorphisms in two bilirubin metabolism enzymes to physiologic bilirubin levels in Chinese newborns.

Li Jin, Q. Peng, Shilin Li, 2014, The Journal of pediatrics.

Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss

D. Cram, Hong Li, Ting Wang, 2016, Prenatal diagnosis.

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease

Hong Li, Ben-jing Wang, J. Mao, 2013, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

[A literature review of epidemiological studies on mutation hot spots of Chinese population with non-syndromic hearing loss].

Hong Li, Haibo Li, Ying Chen, 2012, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

A novel mutation of GATA4 in a familial atrial septal defect.

Ying Sun, K. Choy, Hong Li, 2010, Clinica chimica acta; international journal of clinical chemistry.

Quantitative trait analysis of polymorphisms in two bilirubin metabolism enzymes to physiologic bilirubin levels in Chinese newborns.

Li Jin, Q. Peng, Shilin Li, 2014, The Journal of pediatrics.