Bao Do

Publications

• Automatic Retrieval of Bone Fracture Knowledge Using Natural Language Processing. Do BH, Wu AS, Maley J, Biswal S. J Digit Imaging. 2012
• Evaluation of negation and uncertainty detection and its impact on precision and recall in search. Wu AS, Do BH, Kim J, Rubin DL. J Digit Imaging. 2011; 24 (2): 234-42
• Pattern of 18F-FDG uptake in the spinal cord in patients with non-central nervous system malignancy. Do BH, Mari C, Tseng JR, Quon A, Rosenberg J, Biswal S. Spine (Phila Pa 1976). 2011; 36 (21): E1395-401
• Informatics in radiology: RADTF: a semantic search-enabled, natural language processor-generated radiology teaching file. Do BH, Wu A, Biswal S, Kamaya A, Rubin DL. Radiographics. 2010; 30 (7): 2039-48
• Diagnosis of aseptic deep venous thrombosis of the upper extremity in a cancer patient using fluorine-18 fluorodeoxyglucose positron emission tomography/computerized tomography (FDG PET/CT). Do B, Mari C, Biswal S, Kalinyak J, Quon A, Gambhir SS. Ann Nucl Med. 2006; 20 (2): 151-5
• The role of selection in the evolution of human mitochondrial genomes. Kivisild T, Shen P, Wall DP, Do B, Sung R, Davis K, Passarino G, Underhill PA, Scharfe C, Torroni A, Scozzari R, Modiano D, Coppa A, de Knijff P, Feldman M, Cavalli-Sforza LL, Oefner PJ. Genetics. 2006; 172 (1): 373-87
• Conservation of the RB1 gene in human and primates. Sivakumaran TA, Shen P, Wall DP, Do BH, Kucheria K, Oefner PJ. Hum Mutat. 2005; 25 (4): 396-409
• A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. Horváth R, Lochmüller H, Scharfe C, Do BH, Oefner PJ, Müller-Höcker J, Schoser BG, Pongratz D, Auer DP, Jaksch M. J Med Genet. 2003; 40 (10): 752-7
• Analysis of FAS (CD95) gene mutations in higher-grade transformation of follicle center lymphoma. Do B, Lossos IS, Thorstenson Y, Oefner PJ, Levy R. Leuk Lymphoma. 2003; 44 (8): 1317-23
• Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Horváth R, Scharfe C, Hoeltzenbein M, Do BH, Schröder C, Warzok R, Vogelgesang S, Lochmüller H, Müller-Höcker J, Gerbitz KD, Oefner PJ, Jaksch M. J Med Genet. 2002; 39 (11): 812-6