Xuyu Cai

发表

Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain

C. Walsh, P. Park, E. Lee, 2012, Cell.

Somatic Mutation, Genomic Variation, and Neurological Disease

C. Walsh, A. Poduri, G. Evrony, 2013, Science.

Cell Lineage Analysis in Human Brain Using Endogenous Retroelements

C. Walsh, Y. Benjamini, P. Park, 2015, Neuron.

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

Annapurna Poduri, Christopher A. Walsh, C. Walsh, 2014, Cell reports.

A novel cell‐free DNA methylation‐based model improves the early detection of colorectal cancer

Jian-Bing Fan, Xiaosheng He, Xiaojian Wu, 2021, Molecular oncology.

Somatic mutation in single human neurons tracks developmental and transcriptional history

Peter J. Park, Eunjung Lee, Thomas W. Chittenden, 2015, Science.

Applications of Single-Cell Omics to Dissect Tumor Microenvironment

Wei-min Li, Xuyu Cai, Tingting Guo, 2020, Frontiers in Genetics.

Development and validation of an ultra-deep next-generation sequencing assay for 1 testing of plasma cell-free DNA from patients with advanced cancer 2

G. Mills, S. Gnerre, Richard Shen, 2017 .

Accessing Genetic Information with Liquid Biopsies.

Jian-Bing Fan, Q. Zhan, F. Janku, 2015, Trends in genetics : TIG.

Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development

Xuyu Cai, 2013 .

A duplex real-time reverse transcriptase polymerase chain reaction assay for detecting western equine and eastern equine encephalitis viruses

X. Kang, Yu-chang Li, F. Lin, 2010, Virology Journal.

OUTLINE “ Obligatory ” Somatic Mosaic Disorders ? How Do Somatic Mutations Manifest as Neurological Disease ? “ Second Hit ”

C. Walsh, A. Poduri, G. Evrony, 2013 .

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.

Annapurna Poduri, Christopher A Walsh, C. Walsh, 2015, Cell reports.

Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations

Maria K. Lehtinen, C. Walsh, R. Beroukhim, 2012, Neuron.

Non-invasive diagnosis of early-stage lung cancer using high-throughput targeted DNA methylation sequencing of circulating tumor DNA (ctDNA)

W. Liang, P. Laird, Jian-Bing Fan, 2019, Theranostics.

A Proximal Centriole-Like Structure Is Present in Drosophila Spermatids and Can Serve as a Model to Study Centriole Duplication

T. Avidor-Reiss, Xuyu Cai, A. Polyanovsky, 2009, Genetics.

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].

C. Walsh, G. Gascon, F. Alkuraya, 2011, American journal of human genetics.

Development and Validation of an Ultradeep Next-Generation Sequencing Assay for Testing of Plasma Cell-Free DNA from Patients with Advanced Cancer

G. Mills, Han-Yu Chuang, Jian-Bing Fan, 2017, Clinical Cancer Research.

Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells

Gang Wang, George Church, Jonathan Seidman, 2014, Nature Communications.

Enrichment of short mutant cell-free DNA fragments enhanced detection of pancreatic cancer

Z. Qiu, Xiaoyu Liu, D. Jin, 2018, bioRxiv.

Local Hosts and Organizing Committee

Lovelace J. Luquette, C. Walsh, P. Park, 2015 .

Abstract 5383: Non-invasive diagnosis of early-stage lung cancer via targeted high-throughput DNA methylation sequencing of circulating tumor DNA (ctDNA)

W. Liang, P. Laird, Hui Shen, 2017 .

Enrichment of short mutant cell-free DNA fragments enhanced detection of pancreatic cancer

Z. Qiu, Xiaoyu Liu, D. Jin, 2018 .

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].

G. Gascon, F. Alkuraya, R. Hill, 2011, American journal of human genetics.

Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain

E. Lee, A. Poduri, G. Evrony, 2012, Cell.