S. Myint

发表

Exome sequencing of liver fluke–associated cholangiocarcinoma

Bin Tean Teh, Sopit Wongkham, Choon Kiat Ong, 2012, Nature Genetics.

Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma.

Bin Tean Teh, Hiromi Nakamura, Chern Han Yong, 2017, Cancer discovery.

Epigenomic signature of major congenital heart defects in newborns with Down syndrome

Swe Swe Myint, B. Laufer, J. LaSalle, 2023, Human Genomics.

VHL Deficiency Drives Enhancer Activation of Oncogenes in Clear Cell Renal Cell Carcinoma.

Swe Swe Myint, P. Tan, Qiang Yu, 2017, Cancer discovery.

1 VHL deficiency drives enhancer activation of oncogenes in clear cell renal cell carcinoma

Swe Swe Myint, P. Tan, Qiang Yu, 2017 .

The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis

Swe Swe Myint, P. Vyas, K. Siegmund, 2021, Nature Communications.

Mutational Signatures in Mandibular Ameloblastoma Correlate with Smoking

Swe Swe Myint, K. Soo, C. Ong, 2019, Journal of dental research.

SETD2 histone modifier loss in aggressive GI stromal tumours

Swe Swe Myint, K. Soo, H. Ong, 2015, Gut.

Exome sequencing identifies distinct mutational patterns in liver fluke–related and non-infection-related bile duct cancers

Swe Swe Myint, Dachuan Huang, C. Ong, 2013, Nature Genetics.

Randomized placebo-controlled clinical trial of immunoglobulin Y as adjunct to standard supportive therapy for rotavirus-associated diarrhea among pediatric patients.

Swe Swe Myint, S. S. Myint, Y. Kodama, 2012, Vaccine.

Loss of tumor suppressor KDM6A amplifies PRC2-regulated transcriptional repression in bladder cancer and can be targeted through inhibition of EZH2

Swe Swe Myint, P. Tan, Dachuan Huang, 2017, Science Translational Medicine.

Changes in specialized blood vessels in lymph nodes and their role in cancer metastasis

Swe Swe Myint, K. Soo, S. Lee, 2012, Journal of Translational Medicine.

Genomic and proteomic characterization of ARID1A chromatin remodeller in ampullary tumors.

Swe Swe Myint, C. Ong, B. Teh, 2017, American journal of cancer research.

DNA methylation at birth in monozygotic twins discordant for pediatric acute lymphoblastic leukemia

Swe Swe Myint, K. Siegmund, J. Wiemels, 2022, Nature Communications.

Genomic landscapes of breast fibroepithelial tumors

Swe Swe Myint, P. Tan, Dachuan Huang, 2015, Nature Genetics.

Comprehensive molecular characterization of collecting duct carcinoma for therapeutic vulnerability

C. Ong, Yiqing Du, Jianfeng Chen, 2024, EMBO molecular medicine.

Fumarate Hydratase-deficient Cell Line NCCFH1 as a New In Vitro Model of Hereditary Papillary Renal Cell Carcinoma Type 2.

Bernice Wong Huimin, Dachuan Huang, C. Ong, 2015, Anticancer research.

First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum

Bin Tean Teh, Khee Chee Soo, Choon Kiat Ong, 2011, Genome Biology.

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

Swe Swe Myint, P. Tan, C. Ong, 2014, Nature Genetics.