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Biomolecules|August 26, 2022
HOXA Amplification Defines a Genetically Distinct Subset of AngiosarcomasHongbo M Xie, Kathrin M Bernt
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2014
Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesionsPeter S White, Hongbo M Xie, Petra Werner, et al.
Congenital Heart Disease|May 21, 2013
The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesionsLisa C A D'Alessandro, Petra Werner, Hongbo M Xie, et al.
Birth Defects Research|April 12, 2017
Rare copy number variants in patients with congenital conotruncal heart defectsHongbo M Xie, Petra Werner, Dwight Stambolian, et al.
BMC Bioinformatics|February 26, 2014
Efficient digest of high-throughput sequencing data in a reproducible reportZhe Zhang, Jeremy Leipzig, Ariella Sasson, et al.
American Journal of Hematology|December 1, 2015
Disrupted lymphocyte homeostasis in hepatitis-associated acquired aplastic anemia is associated with short telomeresDaria V Babushok, Anne-Laure Grignon, Yimei Li, et al.
Blood Advances|October 9, 2021
Inducible Sbds deletion impairs bone marrow niche capacity to engraft donor bone marrow after transplantationJi Zha, Lori K Kunselman, Hongbo M Xie, et al.
BMC Bioinformatics|February 6, 2010
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnosticsXiaowu Gai, Juan C Perin, Kevin Murphy, et al.
Leukemia|February 5, 2021
Menin is necessary for long term maintenance of meningioma-1 driven leukemiaClara Libbrecht, Hongbo M Xie, Molly C Kingsley, et al.
Birth Defects Research|June 22, 2019
Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion statusHongbo M Xie, Deanne M Taylor, Zhe Zhang, et al.
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