Hui Jiang

Xiuqing Zhang, Hui Jiang, T. Lau, 2012, 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.

Identification of MFRP Mutations in Chinese Families with High Hyperopia

Hui Jiang, Jianguo Zhang, Ye Yin, 2015, Optometry and vision science : official publication of the American Academy of Optometry.

A whole-genome sequencing–based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations

Hui Jiang, Fang Chen, T. Du, 2020, Journal of Assisted Reproduction and Genetics.

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma

Ping Liu, Hui Jiang, Wen-ting Jiang, 2015, Genetics in Medicine.

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

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

Massively targeted evaluation of therapeutic CRISPR off-targets in cells

George M. Church, Ping Liu, Huanming Yang, 2022, Nature Communications.

Detection and characterization of copy number variants based on whole-genome sequencing by MGI platforms

Hui Jiang, Junhua Rao, F. Mu, 2019 .

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies

Hui Jiang, Yuan Wei, Yangyu Zhao, 2014, Prenatal diagnosis.

CoolMPS: evaluation of antibody labeling based massively parallel non-coding RNA sequencing

R. Drmanac, M. Callow, Hui Jiang, 2020, Nucleic acids research.

The Setup and Application of Reference Material in Sequencing-Based Noninvasive Prenatal Testing

Yanyan Zhang, Hui Jiang, F. Mu, 2021, Gynecologic and Obstetric Investigation.

POPDC1(S201F) causes muscular dystrophy and arrhythmia by affecting protein trafficking.

E. Bertini, Hui Jiang, E. Arbustini, 2016, The Journal of clinical investigation.

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness

Yanyan Zhang, Xun Xu, Hui Jiang, 2014, Genetics in Medicine.

Rapid diagnosis of Propionibacterium acnes infection in patient with hyperpyrexia after hematopoietic stem cell transplantation by next-generation sequencing: a case report

Hui Jiang, M. Ye, Zhikai Yang, 2015, BMC Infectious Diseases.

Erratum to: Comparative performance of the BGISEQ-500 vs Illumina HiSeq2500 sequencing platforms for palaeogenomic sequencing

T. Sicheritz-Pontén, Wenwei Zhang, T. Marquès-Bonet, 2018, GigaScience.

Retinoic acid combined with spermatogonial stem cell conditions facilitate the generation of mouse germ-like cells

Huanming Yang, Hui Jiang, Xin Liu, 2017, Bioscience reports.

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

Asan, Huanming Yang, Jian Wang, 2017, EBioMedicine.

Ratio-based quantitative multiomics profiling using universal reference materials empowers data integration

Ruiqiang Li, Leming Shi, W. Tong, 2022, bioRxiv.

Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA

Hui Jiang, Wei Wang, Xuyang Yin, 2016, PloS one.

Analysis of the genotype-phenotype correlation in patients with phenylketonuria in mainland China

Hui Jiang, Yan-ping Wang, Jun Zhu, 2018, Scientific Reports.

Quartet RNA reference materials and ratio-based reference datasets for reliable transcriptomic profiling

W. Xiao, Leming Shi, W. Tong, 2022, bioRxiv.

ALMS1 null mutations: a common cause of Leber congenital amaurosis and early‐onset severe cone–rod dystrophy

Qi Zhang, Hui Jiang, Xinxing Guo, 2016, Clinical genetics.

The mitochondrial DNA content can not predict the embryo viability

Huanming Yang, Jian Wang, Hui Jiang, 2018, bioRxiv.

ADH4 is a TP53-associated immunometabolic signature for prediction of prognosis in hepatocellular carcinoma

Yuan Zhang, Hui Jiang, B. Zhai, 2022 .

Noninvasive prenatal diagnosis for X-linked disease by maternal plasma sequencing in a family of Hemophilia B.

Hui Jiang, R. Sun, Zhengfeng Xu, 2017, Taiwanese journal of obstetrics & gynecology.

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 prenatal genetic testing for fetal aneuploidy detects maternal trisomy X

Hui Jiang, Wei Wang, Zhiqing Liang, 2012, Prenatal diagnosis.

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.

Comprehensive preimplantation genetic testing by massively parallel sequencing.

Hui Jiang, Xinming Liang, Xuyang Yin, 2020, Human reproduction.

A reference human genome dataset of the BGISEQ-500 sequencer

Hui Jiang, Wenwei Zhang, Xinming Liang, 2017, GigaScience.

Noninvasive prenatal detection for Pathogenic CNVs

Hui Jiang, Wei Wang, Shengpei Chen, 2015 .

Noninvasive Prenatal Detection for Pathogenic CNVs: The Application in α-Thalassemia

N. Chen, Hui Jiang, Fang Chen, 2013, PloS one.

Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts1

Xiuqing Zhang, Y. Liang, Hui Jiang, 2013, Biology of reproduction.

Haplotype-assisted accurate non-invasive fetal whole genome recovery through maternal plasma sequencing

Jian Wang, Wei Wang, Hui Jiang, 2013, Genome Medicine.

Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation Sequencing

Hui Jiang, Xin Yi, Qian Zhu, 2011, PloS one.

Genomic and oncogenic preference of HBV integration in hepatocellular carcinoma

Xiuqing Zhang, L. Tang, Hui Jiang, 2016, Nature Communications.

An integrated map of genetic variation from 1,092 human genomes

Kenny Q. Ye, Mauricio O. Carneiro, Francisco M. De La Vega, 2012, Nature.

Promoter targeted bisulfite sequencing reveals DNA methylation profiles associated with low sperm motility in asthenozoospermia.

Z. Cai, Hui Jiang, Yaoting Gui, 2016, Human reproduction.

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing

Ping Liu, Songgang Li, Xiuqing Zhang, 2013, Prenatal diagnosis.

Sequencing of the MHC region defines HLA-DQA1 as the major independent risk for anti-citrullinated protein antibodies (ACPA)-positive rheumatoid arthritis in Han population

Huijue Jia, Huanming Yang, Jian Wang, 2018, bioRxiv.

Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencing

Hui Jiang, Jun Wang, Jianguo Zhang, 2015, Molecular vision.

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

Hui Jiang, Wenwei Zhang, Xinming Liang, 2018, PloS one.

An Integrated Tool to Study MHC Region: Accurate SNV Detection and HLA Genes Typing in Human MHC Region Using Targeted High-Throughput Sequencing

Xun Xu, Hui Jiang, H. Cao, 2013, PloS one.

Extensive X-linked adaptive evolution in central chimpanzees

Jun Wang, A. Hobolth, Ruiqiang Li, 2012, Proceedings of the National Academy of Sciences.

Comprehensive analysis of serum tumor markers and BRCA1/2 germline mutations in Chinese ovarian cancer patients

Hui Jiang, Jun Wang, B. Liu, 2019, Molecular genetics & genomic medicine.

Prevalence and spectrum of AKT1, PIK3CA, PTEN and TP53 somatic mutations in Chinese breast cancer patients

Hui Jiang, Jun Wang, Ming Chen, 2018, PloS one.

Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease

Huanming Yang, Jian Wang, Qibin Li, 2016, Nature Genetics.

A Zebrafish Loss‐of‐Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function

Hui Jiang, Z. Bhuiyan, T. Momenah, 2016, Human mutation.

Balanced Chromosomal Rearrangement Detection by Low‐Pass Whole‐Genome Sequencing

Hui Jiang, Fang Chen, Jun Wang, 2018, Current protocols in human genetics.

Identification of Balanced Chromosomal Rearrangements Previously Unknown Among Participants in the 1000 Genomes Project: Implications for Interpretation of Structural Variation in Genomes and the Future of Clinical Cytogenetics

Hui Jiang, Zhenjun Yang, Jianying Yuan, 2017, Genetics in Medicine.

Copy‐Number Variants Detection by Low‐Pass Whole‐Genome Sequencing

Hui Jiang, K. Choy, Z. Dong, 2017, Current protocols in human genetics.

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

S. Cheung, Yuan Jiang, Huanming Yang, 2019, American journal of human genetics.

A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole‐Genome Low‐Coverage Sequencing

Xun Xu, Hui Jiang, Wen-Jing Wang, 2014, Human mutation.

A large-scale screen for coding variants predisposing to psoriasis

Renhua Wu, Lin Yang, Hui Jiang, 2013, Nature Genetics.

Clustering of Cancer Cell Lines Using A Promoter- Targeted Liquid Hybridization Capture-Based Bisulfite Sequencing Approach

Huanming Yang, Xiuqing Zhang, Hui Jiang, 2015, Technology in cancer research & treatment.

A high-resolution cell atlas of the domestic pig lung and an online platform for exploring lung single-cell data.

Ping Liu, Hui Jiang, Lihua Luo, 2021, Journal of genetics and genomics = Yi chuan xue bao.

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Xin Liu, Hui Jiang, Fang Chen, 2020, BMC Bioinform..

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

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

Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing

Huanming Yang, L. Bolund, Xiuqing Zhang, 2014, GigaScience.

A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing

Xun Xu, Fang Chen, Ping Hu, 2013, PloS one.

Single-cell sequencing analysis characterizes common and cell-lineage-specific mutations in a muscle-invasive bladder cancer

Huanming Yang, K. Kristiansen, Z. Cai, 2012, GigaScience.

Generation and quality control of maternal plasma lipidomics data associated with preterm birth

Hui Jiang, Lingfei Ye, Zhanlong Mei, 2019, bioRxiv.

Toward the massive genome of Proteus anguinus—illuminating longevity, regeneration, convergent evolution, and metabolic disorders

L. Bolund, Hui Jiang, Guangyi Fan, 2021, Annals of the New York Academy of Sciences.

Rapid detection of aneuploidies on a benchtop sequencing platform

Xiuqing Zhang, Hui Jiang, Wei Wang, 2013, Prenatal diagnosis.

Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non‐invasive prenatal testing

Lars Bolund, Wei Wang, Hui Jiang, 2017, Prenatal diagnosis.

Pregnancy-induced metabolic phenotype variations in maternal plasma.

Ping Liu, Jun Wang, Xun Xu, 2014, Journal of proteome research.

Genomic and oncogenic preference of HBV integration in hepatocellular carcinoma

Xiuqing Zhang, L. Tang, Hui Jiang, 2016, Nature Communications.

Integration of targeted sequencing and NIPT into clinical practice in a Chinese family with maple syrup urine disease

X. Yi, Hui Jiang, Wei Wang, 2014, Genetics in Medicine.

Adaptation to High Altitude Sequencing of 50 Human Exomes Reveals

Huanming Yang, K. Kristiansen, J. Qin, 2010 .

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.

Dynamic PB2-E627K substitution of influenza H7N9 virus indicates the in vivo genetic tuning and rapid host adaptation

Hui Jiang, K. Yuen, G. Gao, 2020, Proceedings of the National Academy of Sciences.

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Weiwei Guo, Ping Chen, Hui Jiang, 2014, Cell Research.

The effect of cell isolation methods on the human transcriptome profiling and microbial transcripts of peripheral blood

Hui Jiang, Mark R. Johnson, Fang Chen, 2021, Molecular Biology Reports.

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing

Hui Jiang, Jun Wang, Jianguo Zhang, 2014, Human Genetics.

Advanced Whole Genome Sequencing Using an Entirely PCR-free Massively Parallel Sequencing Workflow

Zhe Lin, Jing Zhao, Yinlong Xie, 2019, bioRxiv.

Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing

Chung Wen Yu, H. Hakonarson, Yiran Guo, 2016, BMC Medical Genetics.

CoolMPS™: Advanced massively parallel sequencing using antibodies specific to each natural nucleobase

Linsu Chen, R. Drmanac, Jian Wang, 2020, bioRxiv.

Complete mitochondrial genome of the Saker falcon, Falco cherrug (Falco, Falconidae)

Hui Jiang, Jiang Lu, Xiangfeng Li, 2016, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.

Clinical experience from Thailand: noninvasive prenatal testing as screening tests for trisomies 21, 18 and 13 in 4736 pregnancies

Hui Jiang, B. Uerpairojkit, Y. Gao, 2016, Prenatal diagnosis.

Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β‐thalassemia by a novel method of noninvasive prenatal testing

Yanyan Zhang, Hui Jiang, Fang Chen, 2020, Prenatal diagnosis.

Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women

Hui Jiang, H. Yang, Huixin Xu, 2018, Science China Life Sciences.

Peptidomics combined with cDNA library unravel the diversity of centipede venom.

Jun Wang, Hui Jiang, R. Lai, 2015, Journal of proteomics.

HIVID: an efficient method to detect HBV integration using low coverage sequencing.

Xun Xu, Guan Wang, Hui Jiang, 2013, Genomics.

Non-invasive fetal sex determination by maternal plasma sequencing and application in X-linked disorder counseling

Yanyan Zhang, Xiuqing Zhang, Hui Jiang, 2014, 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.

Effective Noninvasive Zygosity Determination by Maternal Plasma Target Region Sequencing

Xun Xu, Hui Jiang, Yuan Wei, 2013, PloS one.

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.

Xiuqing Zhang, Hui Jiang, Xun Xu, 2015, Clinical chemistry.

Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.

Hui Jiang, Jun Wang, Jianguo Zhang, 2015, Investigative ophthalmology & visual science.

Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa.

Hui Jiang, Jun Wang, Jianguo Zhang, 2014, International journal of molecular medicine.

Effect of storage conditions on peripheral leukocytes transcriptome

Hui Jiang, Fang Chen, Mark R. Johnson, 2020, bioRxiv.

Deep functional analysis of synII, a 770-kilobase synthetic yeast chromosome

Jianhui Gong, Xun Xu, Yue Shen, 2017, Science.

Deep functional analysis of synII , a 770 kb synthetic yeast chromosome

Yun, Yue, Gong, 2017 .

Influence of sequencing depth on the fidelity and sensitivity of 1%-5% low-frequency mutation detection and recommendation for standardization of sequencing depth

Hui Jiang, Jun Xia, Xia Zhao, 2021, bioRxiv.

Enhancing CRISPR-Cas9 gRNA efficiency prediction by data integration and deep learning

G. Church, Huanming Yang, J. Gorodkin, 2021, Nature Communications.

Serum metabolomics reveals lipid metabolism variation between coronary artery disease and congestive heart failure: a pilot study

S. Zhong, Hui Jiang, Hemi Luan, 2013, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

Brian J. Stevenson, J. Rioux, Z. Kutalik, 2016, EMBO molecular medicine.

Prenatal Detection of Aneuploidy and Imbalanced Chromosomal Arrangements by Massively Parallel Sequencing

Hui Jiang, Fang Chen, Wei Wang, 2012, PloS one.

Non-targeted metabolomics and lipidomics LC–MS data from maternal plasma of 180 healthy pregnant women

Hui Jiang, Ping Liu, Jun Wang, 2015, GigaScience.

Erratum to: A reference human genome dataset of the BGISEQ-500 sequencer

Wenwei Zhang, Hui Jiang, Yuxiang Li, 2018, GigaScience.

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.

Yanyan Zhang, Hui Jiang, Xun Xu, 2014, Gene.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Yuan Jiang, J. Liu, R. Drmanac, 2018, bioRxiv.

Genome-Wide Transcriptome and Antioxidant Analyses on Gamma-Irradiated Phases of Deinococcus radiodurans R1

Jun Wang, Jun Li, Hui Jiang, 2014, PloS one.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Jian Wang, Xun Xu, Hui Jiang, 2018, BMC Genomics.

Dysfunction of Myosin Light‐Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically‐Engineered Rats

P. Sham, Hui Jiang, S. Nattel, 2017, Journal of the American Heart Association.

Analysis of the genotype-phenotype correlation in patients with phenylketonuria in mainland China

Hui Jiang, Yan-ping Wang, Jun Zhu, 2018, Scientific Reports.

Genome-wide annotation of protein-coding genes in pig

Huanming Yang, Jian Wang, C. Lindskog, 2022, BMC Biology.

Molecular genetic testing in clinical diagnostic assessments that demonstrate correlations in patients with autosomal recessive inherited retinal dystrophy.

Hui Jiang, Jianguo Zhang, Kanxing Zhao, 2015, JAMA ophthalmology.

Archaeology Augments Tibet's Genetic History--Response

Asan, Huanming Yang, Jian Wang, 2010 .

Erratum: Genomic and oncogenic preference of HBV integration in hepatocellular carcinoma

Xiuqing Zhang, L. Tang, Hui Jiang, 2016, Nature Communications.

Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women

Huanming Yang, Jian Wang, Hui Jiang, 2018, Science China Life Sciences.

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.

High-resolution Cell Atlas of Domestic Pig Lung and Online Platform Exploring for Lung Single Cell

Hui Jiang, Lihua Luo, Jiacheng Zhu, 2020, bioRxiv.

Impact of storage conditions on peripheral leukocytes transcriptome

Hui Jiang, Fang Chen, Mark R. Johnson, 2021, Molecular Biology Reports.

Integration of targeted sequencing and NIPT into clinical practice in a Chinese family with maple syrup urine disease

X. Yi, Hui Jiang, Wei Wang, 2014, Genetics in Medicine.

A Zebrafish Loss‐of‐Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function

Hui Jiang, Z. Bhuiyan, T. Momenah, 2016, Human mutation.

Genome-wide transcriptome and antioxidant analyses on Gamma-irradiated phases of Deinococcus radiodurans R 1

Jun Wang, Jun Li, Hui Jiang, 2014 .

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing

Hui Jiang, Jun Wang, Jianguo Zhang, 2014, Human Genetics.

Pregnancy-induced metabolic phenotype variations in maternal plasma.

Ping Liu, Jun Wang, Xun Xu, 2014, Journal of proteome research.

Application of Targeted Next-Generation Sequencing in Patients with Autosomal Recessive Inherited Retinal Dystrophies: Improvement of Genetic and Clinical Diagnosis

Jianguo, Hui Jiang, Kanxing Zhao, 2014 .

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.

Xiuqing Zhang, Hui Jiang, Xun Xu, 2015, Clinical chemistry.