Mao Mao

发表

Single-Cell Exome Sequencing and Monoclonal Evolution of a JAK2-Negative Myeloproliferative Neoplasm

Huanming Yang, Jian Wang, K. Kristiansen, 2012, Cell.

Whole-genome sequencing and comprehensive molecular profiling identify new driver mutations in gastric cancer

Shibing Deng, Hans Clevers, Paul A Rejto, 2014, Nature Genetics.

Genome-wide survey of recurrent HBV integration in hepatocellular carcinoma

Angela M. Liu, Yingrui Li, Chunsheng Zhang, 2012, Nature Genetics.

Genome-wide identification of RNA editing in hepatocellular carcinoma.

Huanming Yang, Jun Wang, Yingrui Li, 2015, Genomics.

Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History

J. Shendure, A. Krogh, Huanming Yang, 2018, Cell.

Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer

Zhengyan Kan, Paul A Rejto, Suet Yi Leung, 2011, Nature Genetics.

Comprehensive analysis of RET and ROS1 rearrangement in lung adenocarcinoma

Boram Lee, Yoon-La Choi, Joungho Han, 2015, Modern Pathology.

Whole-genome sequencing of matched primary and metastatic hepatocellular carcinomas

Yujian Shi, Hancheng Zheng, Zhuolin Gong, 2014, BMC Medical Genomics.

Comprehensive Characterization of Oncogenic Drivers in Asian Lung Adenocarcinoma

Hancheng Zheng, Xiao Liu, Zhuolin Gong, 2016, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

A Novel Fusion of TPR and ALK in Lung Adenocarcinoma

H. Peckham, Zongli Zheng, Joungho Han, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Detecting ALK fusions in lung cancer: multiple choice testing?

Dong-Wan Kim, Mao Mao, 2013 .

Decoding complex patterns of genomic rearrangement in hepatocellular carcinoma.

W. Sung, Xiao Liu, P. Rejto, 2014, Genomics.

Copy number variation profile in noninvasive prenatal testing (NIPT) can identify co-existing maternal malignancies: Case reports and a literature review.

Huanming Yang, Jian Wang, Xin Jin, 2018, Taiwanese journal of obstetrics & gynecology.

Incidental identification of maternal malignancies in two Asian women underwent noninvasive prenatal test

Xin Jin, X. Ji, Mao Mao, 2016, bioRxiv.

Genomic portrait of resectable hepatocellular carcinomas: Implications of RB1 and FGF19 aberrations for patient stratification

W. Sung, Daehyun Baek, Seung‐Mo Hong, 2014, Hepatology.

Low pass genomes of 141,431 Chinese reveal patterns of viral infection, novel phenotypic associations, and the genetic history of China

J. Shendure, A. Krogh, Huanming Yang, 2019 .

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

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

Noninvasive saliva-based EGFR gene mutation detection in patients with lung cancer.

Chung-Liang Ho, D. Chia, Ziding Feng, 2014, American journal of respiratory and critical care medicine.

A single-tube multiplexed assay for detecting ALK, ROS1, and RET fusions in lung cancer.

Shibing Deng, M. Ahn, Joungho Han, 2014, The Journal of molecular diagnostics : JMD.

Longitudinal monitoring of EGFR mutations in plasma predicts outcomes of NSCLC patients treated with EGFR TKIs: Korean Lung Cancer Consortium (KLCC-12-02)

Sin-Ho Jung, Ho Yun Lee, J. Ahn, 2016, Oncotarget.

Patterns of somatic alterations between matched primary and metastatic colorectal tumors characterized by whole-genome sequencing.

Shibing Deng, Woo Yong Lee, Yong Beom Cho, 2014, Genomics.

A Comprehensive Characterization of Genome-Wide Copy Number Aberrations in Colorectal Cancer Reveals Novel Oncogenes and Patterns of Alterations

J. Lamb, J. Hodgson, M. Delorenzi, 2012, PloS one.

Comprehensive genomic profiling of lung cancer using a validated panel to explore therapeutic targets in East Asian patients

Karsten Kristiansen, Di Shao, Jianxing He, 2017, Cancer science.

Aberrant CDK4 Amplification in Refractory Rhabdomyosarcoma as Identified by Genomic Profiling

Kyoohyoung Rho, Jhingook Kim, Kyoung-Mee Kim, 2014, Scientific Reports.

Systematic identification of cancer-related long noncoding RNAs and aberrant alternative splicing of quintuple-negative lung adenocarcinoma through RNA-Seq.

Xuegong Zhang, Zhuolin Gong, Shiyong Li, 2017, Lung cancer.

HIP1–ALK, A Novel ALK Fusion Variant that Responds to Crizotinib

J. Christensen, Q. Gu, Bin Zhang, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Test of four colon cancer risk-scores in formalin fixed paraffin embedded microarray gene expression data.

Sabine Tejpar, Eva Budinska, Simona Rossi, 2014, Journal of the National Cancer Institute.

PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA

Joon-Oh Park, Shibing Deng, W. Kwon, 2015, Oncotarget.

A survey of c-MET expression and amplification in 287 patients with hepatocellular carcinoma.

Su Jin Lee, I. Sohn, C. Park, 2013, Anticancer research.

Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma

Lin Li, Shibing Deng, Hongyue Dai, 2013, Genome research.

Multiplexed deep sequencing analysis of ALK kinase domain identifies resistance mutations in relapsed patients following crizotinib treatment.

Shibing Deng, J. Christensen, J. Ahn, 2013, Genomics.

Genomic landscape of copy number aberrations enables the identification of oncogenic drivers in hepatocellular carcinoma

Zhou Zhu, Shibing Deng, P. Rejto, 2013, Hepatology.

ALK, ROS1 and RET rearrangements in lung squamous cell carcinoma are very rare.

Yoon-La Choi, Mao Mao, Ji-Young Song, 2016, Lung cancer.

HIP1–ALK, a Novel Fusion Protein Identified in Lung Adenocarcinoma

Joungho Han, Jhingook Kim, M. Hong, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Multiplexed gene expression and fusion transcript analysis to detect ALK fusions in lung cancer.

Shibing Deng, J. Ahn, M. Ahn, 2013, The Journal of molecular diagnostics : JMD.

Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples

Asan, Huanming Yang, Jian Wang, 2018, European Journal of Human Genetics.

Genetic Aberrations in Imatinib-Resistant Dermatofibrosarcoma Protuberans Revealed by Whole Genome Sequencing

Xiao Liu, Miao Li, Jeeyun Lee, 2013, PloS one.

Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR

Y. Shim, Xinyu Liu, Jhingook Kim, 2015, Oncotarget.

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

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

Next generation sequencing reveals genetic landscape of hepatocellular carcinomas.

Mao Mao, S. Li, 2013, Cancer letters.