DeBaun, Michael R.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Taliun, D., Harris, D. N., Kessler, M. D., Carlson, J., Szpiech, Z. A., Torres, R., Taliun, S. A. G., Corvelo, A., Gogarten, S. M., Kang, H. M., et al. (2021) · Nature

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 2,213

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Bick, A. G., Weinstock, J. S., Nandakumar, S. K., Fulco, C. P., Bao, E. L., Zekavat, S. M., Szeto, M. D., Liao, X., Leventhal, M. J., Nasser, J., et al. (2020) · Nature

Acute Myeloid Leukemia ResearchGenetic Associations and Epidemiology

Cited by 733

Controlled Trial of Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia

DeBaun, M. R., Gordon, M., McKinstry, R. C., Noetzel, M. J., White, D. A., Sarnaik, S. A., Meier, E. R., Howard, T. H., Majumdar, S., Inusa, B. P. D., et al. (2014) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersBlood transfusion and management

Cited by 545

Silent cerebral infarcts in sickle cell anemia: a risk factor analysis

Kinney, T. R., Sleeper, L. A., Wang, W. C., Zimmerman, R. A., Pegelow, C. H., Ohene-Frempong, K., Wethers, D. L., Bello, J. A., Vichinsky, E. P., Moser, F. G., et al. (1999) · PEDIATRICS

Hemoglobinopathies and Related DisordersAcute Ischemic Stroke Management

Cited by 309

Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: A report from the Cooperative Study of Sickle Cell Disease

Miller, S. T., Macklin, E. A., Pegelow, C. H., Kinney, T. R., Sleeper, L. A., Bello, J. A., DeWitt, L. D., Gallagher, D. M., Guarini, L., Moser, F. G., et al. (2001) · The Journal of Pediatrics

Hemoglobinopathies and Related DisordersAcute Ischemic Stroke Management

Cited by 287

The intersection between asthma and acute chest syndrome in children with sickle-cell anaemia

DeBaun, M. R., & Strunk, R. C. (2016) · The Lancet

Hemoglobinopathies and Related DisordersAsthma and respiratory diseases

Cited by 82

Rapidly progressive acute chest syndrome in individuals with sickle cell anemia: a distinct acute chest syndrome phenotype

Chaturvedi, S., Ghafuri, D. L., Glassberg, J., Kassim, A. A., Rodeghier, M., & DeBaun, M. R. (2016) · American Journal of Hematology

Hemoglobinopathies and Related DisordersMethemoglobinemia and Tumor Lysis Syndrome

Cited by 60

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Cade, B. E., Lee, J., Sofer, T., Wang, H., Zhang, M., Chen, H., Gharib, S. A., Gottlieb, D. J., Guo, X., Lane, J. M., et al. (2021) · Genome Medicine

Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology

Cited by 33

The Role of Fibrocytes in Sickle Cell Lung Disease

Field, J. J., Burdick, M. D., DeBaun, M. R., Strieter, B. A., Liu, L., Mehrad, B., Rose, C. E., Linden, J., & Strieter, R. M. (2012) · PLoS ONE

Hemoglobinopathies and Related DisordersInterstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

Cited by 23

Aeroallergen sensitization predicts acute chest syndrome in children with sickle cell anaemia

Willen, S. M., Rodeghier, M., Strunk, R. C., Bacharier, L. B., Rosen, C. L., Kirkham, F. J., DeBaun, M. R., & Cohen, R. T. (2018) · British Journal of Haematology

Hemoglobinopathies and Related DisordersAsthma and respiratory diseases

Cited by 20