Qixi Wu

发表

MosaicBase: A Knowledgebase of Postzygotic Mosaic Variants in Noncancer Diseases and Asymptomatic Human Individuals

Changhong Yang, A. Y. Ye, Meng Wang, 2020, bioRxiv.

Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations

M. Wang, A. Y. Ye, Liping Wei, 2019, Human mutation.

Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients

Su-xia Wang, Zhaoxia Wang, Yun Yuan, 2020, Journal of Medical Genetics.

A novel NGS-based microsatellite instability (MSI) status classifier with 9 loci for colorectal cancer patients

Chunze Zhang, Guangyu Shan, Qixi Wu, 2020, Journal of Translational Medicine.

Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations

A. Y. Ye, Liping Wei, X. Yang, 2017, Human mutation.

Genetic and Clinicopathologic Characteristics of Papillary Thyroid Carcinoma in the Chinese Population: High BRAF Mutation Allele Frequency, Multiple Driver Gene Mutations, and RET Fusion May Indicate More Advanced TN Stage

Qixi Wu, Ge Chen, Jia-xin Zhang, 2022, OncoTargets and therapy.

Mosaicism and incomplete penetrance of PCDH19 mutations

Liping Wei, Jing Zhang, Zhixian Yang, 2018, Journal of Medical Genetics.

Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening

Yongtao Guan, Qixi Wu, Ling Bai, 2019, Genetics in Medicine.

RJAfinder: An automated tool for quantification of responding to joint attention behaviors in autism spectrum disorder using eye tracking data

A. Y. Ye, Liping Wei, Yige Wu, 2022, Frontiers in Neuroscience.

ATP1A3 mosaicism in families with alternating hemiplegia of childhood

A. Y. Ye, Liping Wei, Zhe Yu, 2019, Clinical genetics.

AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder

Meng Wang, Jie Zhang, Dechang Yang, 2018, Database J. Biol. Databases Curation.

Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome

A. Y. Ye, Meng Wang, Liping Wei, 2015, Human mutation.

Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs

Liping Wei, Adam Yongxin Ye, Xiaoxu Yang, 2018, bioRxiv.

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

A. Y. Ye, Liping Wei, Zhe Yu, 2017, Scientific Reports.

Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Liping Wei, Qixi Wu, X. Bao, 2018, Genetics in Medicine.

Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals

Meng Wang, Liping Wei, Linlin Yan, 2014, Cell Research.

Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals

A. Y. Ye, Qing-Rong Liu, Liping Wei, 2019, PLoS genetics.

Title Somatic LINE-1 retrotransposition in cortical neurons of Rett patients and healthy individuals

A. Y. Ye, Qing-Rong Liu, Liping Wei, 2018, bioRxiv.

Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Liping Wei, Xiaoxu Yang, Qixi Wu, 2018, Genetics in Medicine.

Concordance of Genomic Alterations between Circulating Tumor DNA and Matched Tumor Tissue in Chinese Patients with Breast Cancer

Guangyu Shan, Qixi Wu, Yaping Yang, 2020, Journal of oncology.

Adaptive parameter of standard deviation enhances the power of noninvasive prenatal screens

Guangyu Shan, Qixi Wu, Jingbo Zhang, 2021, 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 new and improved method of library preparation for non-invasive prenatal testing: plasma to library express technology

Qixi Wu, H. Rao, X. Kong, 2023, Clinical chemistry and laboratory medicine.

A novel NGS-based microsatellite instability (MSI) status classifier with 9 loci for colorectal cancer patients

Chunze Zhang, J Zhang, Guangyu Shan, 2020, Journal of Translational Medicine.

Establishment and validation of a multigene model to predict the risk of relapse in hormone receptor-positive early-stage Chinese breast cancer patients

Guangyu Shan, J. Ying, Yueping Liu, 2022, Chinese medical journal.

Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening

Yongtao Guan, Qixi Wu, Ling Bai, 2019, Genetics in Medicine.

MosaicBase: A Knowledgebase of Postzygotic Mosaic Variants in Noncancer Disease-related and Healthy Human Individuals

Junyu Luo, Meng Wang, Changhong Yang, 2020, Genom. Proteom. Bioinform..

A robust microsatellite instability detection model for unpaired colorectal cancer tissue samples

Guangyu Shan, Qixi Wu, Zili Zhang, 2023, Chinese Medical Journal.

The concomitant EGFR T790M/C797S in trans and cis in three osimertinib-resistant lung adenocarcinoma patients.

Hailong Liu, Qixi Wu, Wang Jianwei, 2019, Journal of Clinical Oncology.

Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals

A. Y. Ye, Qing-Rong Liu, Liping Wei, 2019, PLoS genetics.

High-resolution dissection of human cell type-specific enhancers in cis and trans activities

Qixi Wu, Xiaoxu Yang, Meng Wang, 2023, bioRxiv.

Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations

M. Wang, A. Y. Ye, Liping Wei, 2019, Human Mutation.