S. Tsang

发表

Molecular analysis of urothelial cancer cell lines for modeling tumor biology and drug response

J. Costello, D. Theodorescu, M. Nickerson, 2016, Oncogene.

Single-Cell Exome Sequencing Reveals Single-Nucleotide Mutation Characteristics of a Kidney Tumor

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

Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation

Huanming Yang, Jian Wang, Yingrui Li, 2013, Nature Genetics.

Identification of Gene Signatures Used to Recognize Biological Characteristics of Gastric Cancer Upon Gene Expression Data

B. Luke, R. Xing, Yuan-ming Pan, 2014, Biomarker insights.

Proteogenomic Characterization Reveals Therapeutic Vulnerabilities in Lung Adenocarcinoma

Jeffrey R. Whiteaker, Dana R. Valley, Karna L. Robinson, 2020, Cell.

Evaluation of the multicenter variations of urinary metabolomics

Xiaohang Zhao, Yajie Wang, S. Tsang, 2019, URINE.

Vitamins B2, B6, and B12 and Risk of New Colorectal Adenomas in a Randomized Trial of Aspirin Use and Folic Acid Supplementation

Elizabeth L. Barry, J. Baron, R. Sandler, 2008, Cancer Epidemiology Biomarkers & Prevention.

Association of MC1R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN2A Mutations

M. Tucker, A. Goldstein, M. Landi, 2005, Cancer Epidemiology Biomarkers & Prevention.

Genetic Polymorphisms and Spontaneous Preterm Birth

J. Dambrosia, K. Nelson, A. Maclennan, 2007, Obstetrics and gynecology.

Candidate Genes and Cerebral Palsy: A Population-Based Study

K. Nelson, A. Maclennan, G. Dekker, 2008, Pediatrics.

Comparison of variations detection between whole-genome amplification methods used in single-cell resequencing

Ting Wang, Xun Xu, Yong Hou, 2015, GigaScience.

Association of MC 1 R Variants and Risk of Melanoma in Melanoma-Prone Families with CDKN 2 A Mutations

M. Tucker, A. Goldstein, M. Landi, 2005 .

A prognostic risk model for glioma patients by systematic evaluation of genomic variations

Shengjie Gao, K. Rodland, Youyong Lu, 2022, iScience.

Concurrent Alterations in TERT, KDM6A, and the BRCA Pathway in Bladder Cancer

Zhiming Cai, Garrett M. Dancik, Dan Theodorescu, 2014, Clinical Cancer Research.

MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population.

Maria Teresa Landi, Mohammad Hedayati, Ruth M Pfeiffer, 2005, Journal of the National Cancer Institute.

Real-time PCR analysis of candidate imprinted genes on mouse chromosome 11 shows balanced expression from the maternal and paternal chromosomes and strain-specific variation in expression levels

Karlyne M. Reilly, K. Reilly, E. Rozenblum, 2008, Epigenetics.

An imprinted locus epistatically influences Nstr1 and Nstr2 to control resistance to nerve sheath tumors in a neurofibromatosis type 1 mouse model.

Karlyne M. Reilly, K. Broman, K. Reilly, 2006, Cancer research.

Susceptibility to astrocytoma in mice mutant for Nf1 and Trp53 is linked to chromosome 11 and subject to epigenetic effects.

Karlyne M. Reilly, T. Jacks, K. Reilly, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Biology of Human Tumors Concurrent Alterations in TERT , KDM 6 A , and the BRCA Pathway in Bladder Cancer

Garrett M. Dancik, Z. Cai, M. Lucia, 2014 .

A proteogenomic portrait of lung squamous cell carcinoma

Dana R. Valley, Matthew A. Wyczalkowski, Ratna R. Thangudu, 2021, Cell.

A comprehensive SNP-based genetic analysis of inbred mouse strains

N. Copeland, N. Jenkins, B. Luke, 2005, Mammalian Genome.

Histopathologic and proteogenomic heterogeneity reveals features of clear cell renal cell carcinoma aggressiveness.

Guo Ci Teo, Matthew A. Wyczalkowski, Ratna R. Thangudu, 2022, Cancer cell.

Genetic susceptibility in familial melanoma from northeastern Italy

A. Goldstein, W. Modi, R. Steighner, 2004, Journal of Medical Genetics.

Evolution of multiple cell clones over a 29-year period of a CLL patient

Huanming Yang, G. Marti, Kui Wu, 2016, Nature Communications.

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.

Investigation of Plasma Metabolic and Lipidomic Characteristics of a Chinese Cohort and a Pilot Study of Renal Cell Carcinoma Biomarker

X. Liu, Yajie Wang, S. Tsang, 2020, Frontiers in Oncology.

Cyclooxygenase-2 Polymorphisms, Aspirin Treatment, and Risk for Colorectal Adenoma Recurrence—Data from a Randomized Clinical Trial

J. Baron, R. Sandler, J. Gui, 2009, Cancer Epidemiology, Biomarkers & Prevention.

Proteogenomic characterization of pancreatic ductal adenocarcinoma

Dana R. Valley, Matthew A. Wyczalkowski, Ratna R. Thangudu, 2021, Cell.

Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations.

M. Tucker, A. Goldstein, M. Landi, 2005, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Sequence Variant in the TRIM39-RPP21 Gene Readthrough is Shared Across a Cohort of Arabian Foals Diagnosed with Juvenile Idiopathic Epilepsy.

X. Fang, Yinfu Feng, S. Tsang, 2022, Journal of genetic mutation disorders.

MC1R variants increase risk of melanomas harboring BRAF mutations.

D. Elder, P. Carli, E. Rozenblum, 2008, The Journal of investigative dermatology.

Protective effect of Cox-2 allelic variants on risk of colorectal adenoma development in African Americans.

B. Luke, H. Ashktorab, D. Smoot, 2008, Anticancer research.

MTHFR Genotype and Colorectal Adenoma Recurrence: Data from a Double-blind Placebo-controlled Clinical Trial

Elizabeth L. Barry, J. Baron, D. Ahnen, 2008, Cancer Epidemiology Biomarkers & Prevention.

Gene Expression Browser: large-scale and cross-experiment microarray data integration, management, search & visualization

Li Liu, Yudong Zhang, Ming Zhang, 2010, BMC Bioinformatics.

Development of multiplex DNA electronic microarrays using a universal adaptor system for detection of single nucleotide polymorphisms.

S. Tsang, D. Munroe, C. Frankenberger, 2004, BioTechniques.

Cyclooxygenase-2 Polymorphisms, Aspirin Treatment, and Risk for Colorectal Adenoma Recurrence—Data from a Randomized Clinical Trial

Elizabeth L. Barry, J. Baron, R. Sandler, 2009, Cancer Epidemiology, Biomarkers & Prevention.

Genetic susceptibility in familial melanoma from northeastern Italy

A. Goldstein, W. Modi, R. Steighner, 2004, Journal of Medical Genetics.

Evolution of multiple cell clones over a 29-year period of a CLL patient

Huanming Yang, G. Marti, Kui Wu, 2016, Nature Communications.