Argiropoulos, Bob

Hox genes in hematopoiesis and leukemogenesis

Argiropoulos, B., & Humphries, R. K. (2007) · Oncogene

Hematopoietic Stem Cell TransplantationAcute Myeloid Leukemia Research

Cited by 492

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

Lionel, A. C., Tammimies, K., Vaags, A. K., Rosenfeld, J. A., Ahn, J. W., Merico, D., Noor, A., Runke, C. K., Pillalamarri, V. K., Carter, M. T., et al. (2014) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 163

DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies

Ji, J., Lee, H., Argiropoulos, B., Dorrani, N., Mann, J., Martinez-Agosto, J. A., Gomez-Ospina, N., Gallant, N., Bernstein, J. A., Hudgins, L., et al. (2015) · European Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 145

Unraveling the crucial roles of Meis1 in leukemogenesis and normal hematopoiesis

Argiropoulos, B., Yung, E., & Humphries, R. K. (2007) · Genes & Development

Acute Myeloid Leukemia ResearchHematopoietic Stem Cell Transplantation

Cited by 101