Publications by authors named "Chan Eng Chong"

Claim this Profile
C
Characterisation of protein-truncating and missense variants in in 15 768 women from Malaysia and Singapore.
Pei Sze Ng, Rick Acm Boonen, Eldarina Wijaya, Chan Eng Chong, Milan Sharma

J Med Genet· May 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Epidemiological and ES cell-based functional evaluation of BRCA2 variants identified in families with breast cancer.
Teresa Sullivan, Eswary Thirthagiri, Chan-Eng Chong, Stacey Stauffer, Susan Reid

Hum Mutat· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.
Anna L Brown, Peer Arts, Catherine L Carmichael, Milena Babic, Julia Dobbins, Chan-Eng Chong

Blood Adv· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
miR-3099 promotes neurogenesis and inhibits astrogliogenesis during murine neural development.
Shahidee Zainal Abidin, Sze-Zheng Fam, Chan-Eng Chong, Syahril Abdullah, Pike-See Cheah

Gene· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome.
Sunita M C De Sousa, Karin S Kassahn, Liam C McIntyre, Chan-Eng Chong, Hamish S Scott

BMC Endocr Disord· November 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing.
Christopher P Barnett, Nathalie J Nataren, Manuela Klingler-Hoffmann, Quenten Schwarz, Chan-Eng Chong

Hum Mutat· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.
Maya Lewinsohn, Anna L Brown, Luke M Weinel, Connie Phung, George Rafidi, Chan-Eng Chong

Blood· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GATA2 is required for lymphatic vessel valve development and maintenance.
Jan Kazenwadel, Kelly L Betterman, Chan-Eng Chong, Philippa H Stokes, Young K Lee

J Clin Invest· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel MDM2 splice variants identified from oral squamous cell carcinoma.
Kin Kit Sam, Chai Phei Gan, Pei San Yee, Chan Eng Chong, Kue Peng Lim

Oral Oncol· November 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Over-expression of MAGED4B increases cell migration and growth in oral squamous cell carcinoma and is associated with poor disease outcome.
Chan Eng Chong, Kue Peng Lim, Chai Phei Gan, Christina A Marsh, Rosnah Binti Zain

Cancer Lett· August 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature.
Jan Kazenwadel, Genevieve A Secker, Yajuan J Liu, Jill A Rosenfeld, Robert S Wildin, Chan-Eng Chong

Blood· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.
Christopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, Ella J Wilkins, Peter J Brautigan

Nat Genet· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide prediction and annotation of Burkholderia pseudomallei AraC/XylS family transcription regulator.
Boon-San Lim, Chan-Eng Chong, Zulkeflie Zamrod, Sheila Nathan, Rahmah Mohamed

In Silico Biol· April 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Burkholderia pseudomallei animal and human isolates from Malaysia exhibit different phenotypic characteristics.
Song-Hua Lee, Chan-Eng Chong, Boon-San Lim, San-Jiun Chai, Kin-Kit Sam

Diagn Microbiol Infect Dis· July 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
In silico analysis of Burkholderia pseudomallei genome sequence for potential drug targets.
Chan-Eng Chong, Boon-San Lim, Sheila Nathan, Rahmah Mohamed

In Silico Biol· February 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis