Jiansheng Xie

发表

A novel splicing mutation in the SEDL gene causes spondyloepiphyseal dysplasia tarda in a large Chinese pedigree.

Weiqin Wu, Hui Wang, Zhi-yong Xu, 2013, Clinica chimica acta; international journal of clinical chemistry.

Circular RNA hsa_circ_0081343 promotes trophoblast cell migration and invasion and inhibits trophoblast apoptosis by regulating miR-210-5p/DLX3 axis

Zhi-yong Xu, Jiansheng Xie, Hui Wang, 2021, Reproductive Biology and Endocrinology.

Non-Invasive Prenatal Diagnosis: A Comparison of Cell Free Fetal DNA (cffDNA) Based Screening and Fetal Nucleated Red Blood Cell (fnRBC) Initiated Testing

Xinghua Pan, Qinghua Zhou, Peining Li, 2013 .

A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report

Yang Liu, Xingping Li, Jiansheng Xie, 2018, BMC Medical Genetics.

De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome

Qinghua Zhou, Peining Li, Jiansheng Xie, 2017, Molecular Cytogenetics.

De novo nonsense variant in ASXL3 in a Chinese girl causing Bainbridge–Ropers syndrome: A case report and review of literature

Xiaoshan Zhao, Jiansheng Xie, Nan Jiang, 2021, Molecular genetics & genomic medicine.

The significance of polymorphism and expression of oestrogen metabolism-related genes in Chinese women with premature ovarian insufficiency.

Weiqin Wu, Jiansheng Xie, Ji-long Yao, 2017, Reproductive biomedicine online.

A melting curve analysis--based PCR assay for one-step genotyping of β-thalassemia mutations a multicenter validation.

Qingge Li, Xiaoyun Chen, Xiangmin Xu, 2011, The Journal of molecular diagnostics : JMD.

AMH and AMHR2 genetic variants in Chinese women with primary ovarian insufficiency and normal age at natural menopause.

Wenjie Zhu, Weiqin Wu, Jiansheng Xie, 2014, Reproductive biomedicine online.

Primer-Introduced Restriction Analysis Polymerase Chain Reaction Method for Non-Invasive Prenatal Testing of β-Thalassemia

Hui Jiang, Fengping Xu, Wei Wang, 2015, Hemoglobin.

Influence of post-annealing time on properties of ZnO: (Li, N) thin films prepared by ion beam enhanced deposition method

Qiang Chen, Jiansheng Xie, J. Xie, 2015, Journal of Materials Science: Materials in Electronics.

Annealing characteristics of the vanadium oxide films prepared by modified ion beam enhanced deposition

Jinhua Li, N. Yuan, Jiansheng Xie, 2005 .

Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature

Weiqin Wu, Qinghua Zhou, Peining Li, 2015, Molecular Cytogenetics.

Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities

Fang Xu, Peining Li, Zhi-yong Xu, 2014, Molecular Cytogenetics.

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization

Fang Xu, M. Mahoney, Peining Li, 2011, American journal of medical genetics. Part A.

There is a Strong Association between Early Preeclampsia and Congenital Heart Defects: A Large Population-Based, Retrospective Study

Jie Liu, Jiansheng Xie, Ji-long Yao, 2020, Gynecologic and Obstetric Investigation.

Noninvasive Fetal Trisomy ( NIFTY ) test : an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

Wei-Mou Zheng, Songgang Li, Xiuqing Zhang, 2013 .

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

Wei-Mou Zheng, Songgang Li, Hui Jiang, 2012, BMC Medical Genomics.

Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity Syndrome

Weiqin Wu, Peining Li, Zhi-yong Xu, 2017, Fetal and pediatric pathology.

Compound heterozygous variants in MYH11 underlie autosomal recessive megacystis-microcolon-intestinal hypoperistalsis syndrome in a Chinese family

Hui Wang, Jiansheng Xie, Jianming Zhang, 2019, Journal of Human Genetics.

Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature

Weiqin Wu, Qinghua Zhou, Peining Li, 2015, Molecular Cytogenetics.

Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities

Fang Xu, Peining Li, Zhi-yong Xu, 2014, Molecular Cytogenetics.

Biobanking of Residual Specimens from Diagnostic Genetic Laboratories: Standard Operating Procedures, Ethical and Legal Considerations, and Research Applications

Xinghua Pan, Brittany Grommisch, Peining Li, 2013 .

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

Jun Zhang, Wei Wang, Hui Jiang, 2016, Genetics in Medicine.

Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissue

Jianguo Chen, Wenyong Zhang, Zhi-yong Xu, 2019, Journal of Assisted Reproduction and Genetics.

A case of prenatal diagnosis of 16q24.3 microdeletion KBG syndrome and review of the literature

Jiansheng Xie, B. Yao, Tianqin Deng, 2021, Clinical case reports.

Circular RNA hsa_circ_0081343 promotes trophoblast cell migration and invasion and inhibits trophoblast apoptosis by regulating miR-210-5p/DLX3 axis

Zhi-yong Xu, Jiansheng Xie, Hui Wang, 2021, Reproductive Biology and Endocrinology.

Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B.

X. Yi, N. Qu, Yu Liang, 2012, Clinica chimica acta; international journal of clinical chemistry.

A novel missense mutation of FGFR3 in a Chinese female and her fetus with Hypochondroplasia by next-generation sequencing.

Weiqin Wu, Hui Wang, Jiansheng Xie, 2013, Clinica chimica acta; international journal of clinical chemistry.

Clinical application of massively parallel sequencing‐based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors

Jian Wang, Songgang Li, Xiuqing Zhang, 2012, Prenatal diagnosis.

De Novo Mutated TUBB2B Associated Pachygyria Diagnosed by Medical Exome Sequencing and Long-Range PCR

Wei Zhang, Hui Wang, Jiansheng Xie, 2018, Fetal and pediatric pathology.

Genotyping, generation and proteomic profiling of the first human autosomal dominant osteopetrosis type II-specific induced pluripotent stem cells

D. Tang, W. Sui, Jiansheng Xie, 2019, Stem Cell Research & Therapy.

Leading The Way in Genetic Fertility Screening FERTILITY GENETICS # 1 IN GENETIC FERTILITY SCREENING Volume 1 MAGAZINE IS THERE A SMALL RNA FINGERPRINT OF EMBRYO QUALITY AND HEALTH IN SPENT IVF MEDIA ?

Weiqing, Wenjie Zhu, L. Stalker, 2016 .

Performance characterization of PCR-free whole genome sequencing for clinical diagnosis

Zhiyu Peng, Xueqin Guo, Jiansheng Xie, 2020, bioRxiv.

Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families.

M. Qi, Jiansheng Xie, Yuchan Mao, 2013, Clinica chimica acta; international journal of clinical chemistry.

Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy.

Xiangmin Xu, Jiansheng Xie, X. Shang, 2010, Blood cells, molecules & diseases.

Identification of Two Missense Mutations of ERCC6 in Three Chinese Sisters with Cockayne Syndrome by Whole Exome Sequencing

X. Yi, Wei Tang, Shanshan Yu, 2014, PloS one.

Screening, prenatal diagnosis, and prenatal decision for sex chromosome aneuploidy

Yang Liu, Zhi-yong Xu, Jiansheng Xie, 2019, Expert review of molecular diagnostics.

Annealing behavior of vanadium oxide films prepared by modified ion-beam-enhanced deposition

Jinhua Li, Ningyi Yuan, Jiansheng Xie, 2004, SPIE Optics + Photonics.

Identification of novel missense mutations of the TGFBR3 gene in Chinese women with premature ovarian failure.

Weiqin Wu, Jian-sheng Xie, Shi-ling Chen, 2011, Reproductive biomedicine online.

Prenatal and postnatal diagnosis of Phelan–McDermid syndrome: A report of 21 cases from a medical center and review of the literature

Yang Liu, Peining Li, Jiansheng Xie, 2022, Frontiers in Genetics.

[Analysis of fetal chromosomal karyotype and etiology in 252 cases of early spontaneous abortion].

Jiansheng Xie, Juan Li, Hua-kun Zhang, 2011, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Clinical and genetic analysis for a Joubert syndrome family with CC2D2A gene mutations].

Weiqin Wu, Shanshan Yu, Zhi-yong Xu, 2015, Zhonghua er ke za zhi = Chinese journal of pediatrics.

UPD16 itself is not a cause of intrauterine growth restriction

Hui Wang, Jiansheng Xie, M. Zhong, 2018, Fetal and pediatric pathology.

Novel homozygous FANCL mutation and somatic heterozygous SETBP1 mutation in a Chinese girl with Fanconi Anemia.

Weiqin Wu, Qinghua Zhou, Peining Li, 2017, European journal of medical genetics.

[Gene mutation analysis and prenatal diagnosis of four pedigrees with methymalonic aciduria].

Weiqin Wu, Jiansheng Xie, Yang Liu, 2016, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome

Qinghua Zhou, Peining Li, Jiansheng Xie, 2017, Molecular Cytogenetics.

Circular RNA hsa_circ_0000848 Promotes Trophoblast Cell Migration and Invasion and Inhibits Cell Apoptosis by Sponging hsa-miR-6768-5p

Zhi-yong Xu, Jiansheng Xie, Hui Wang, 2020, Frontiers in Cell and Developmental Biology.

Single-Cell Sequencing Reveals the Relationship between Phenotypes and Genotypes of Klinefelter Syndrome

Hui Guo, Jian-sheng Xie, D. Tang, 2019, Cytogenetic and Genome Research.

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

Wei-Mou Zheng, Songgang Li, Xiuqing Zhang, 2012, BMC medical genomics.

FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure

Wenjie Zhu, Weiqin Wu, Jian-sheng Xie, 2011, Reproductive biology and endocrinology : RB&E.

FOXE 1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure

Wenjie Zhu, Weiqin Wu, Jian-sheng Xie, 2012 .

[Genetic and prenatal diagnosis for four families with Williams-Beuren syndrome].

Weiqin Wu, Zhi-yong Xu, Jiansheng Xie, 2015, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

FOXE1 polyalanine tract length screening by MLPA in idiopathic premature ovarian failure

Wenjie Zhu, Weiqin Wu, Jiansheng Xie, 2011, Reproductive biology and endocrinology : RB&E.

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization

Fang Xu, M. Mahoney, Peining Li, 2011, American journal of medical genetics. Part A.

℮-conome: an automated tissue counting platform of cone photoreceptors for rodent models of retinitis pigmentosa

Wei-Mou Zheng, Songgang Li, Xiuqing Zhang, 2011, BMC ophthalmology.