Publications — Radcliffe Department of Medicine

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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome.

Liu D. et al, (2024), Journal of the American Heart Association, 13

Measurable residual disease in patients undergoing allogeneic transplant for acute myeloid leukemia

Wong ZC. et al, (2023), Best Practice & Research Clinical Haematology, 36, 101468 - 101468

DNA Sequencing to Detect Residual Disease in Adults With Acute Myeloid Leukemia Prior to Hematopoietic Cell Transplant.

Dillon LW. et al, (2023), JAMA, 329, 745 - 755

Identifying environmental risk factors and gene-environment interactions in holoprosencephaly.

Addissie YA. et al, (2021), Birth Defects Res, 113, 63 - 76

Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study.

Addissie YA. et al, (2020), Environ Health, 19

Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome.

Lugo M. et al, (2020), Am J Med Genet A, 182, 1008 - 1020

The bacterial virulence factor CagA induces microbial dysbiosis that contributes to excessive epithelial cell proliferation in the Drosophila gut.

Jones TA. et al, (2017), PLoS pathogens, 13

Factor XII promotes blood coagulation independent of factor XI in the presence of long-chain polyphosphates.

Puy C. et al, (2013), Journal of thrombosis and haemostasis : JTH, 11, 1341 - 1352

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