Integrating factor analysis and a transgenic mouse model to reveal a peripheral blood predictor of breast tumors von LaBreche, Heather G, Nevins, Joseph R, Huang, Erich

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Curation and reporting of pathogenic genome-wide copy-number variants in a prenatal cell-free DNA screen von Cox, Samuel G, Acevedo, Ashley, Ahuja, Anand, LaBreche, Heather G, Alfaro, Maria P, Pierson, Summer, Westover, Thomas, Ratzel, Sarah, Hancock, Susan, Moyer, Krista, Muzzey, Dale

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Fetal fraction amplification within prenatal cfDNA screening enables detection of genome-wide copy-number variants at enhanced resolution von Acevedo, Ashley, Teng, Oyang, LaBreche, Heather G, Nguyen, Alison, Jazo, Luis, Hong, Sun Hae, Suk, John, Pierson, Summer, Westover, Thomas, Ratzel, Sarah, Haas, Kevin R, Muzzey, Dale

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Peripheral blood signatures of lead exposure von LaBreche, Heather G, Meadows, Sarah K, Nevins, Joseph R, Chute, John P

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A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis: Can We Put It to Work? von LaBreche, Heather G., Sebastian, Siby

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A Proof-of-Concept Case Study for Personalized Noninvasive Prenatal Diagnosis von LaBreche, Heather G, Sebastian, Siby

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Induction of Wilms' Tumor Protein (WT1)–Specific Antitumor Immunity Using a Truncated WT1-Expressing Adenovirus Vaccine von OSADA, Takuya, WOO, Christopher Y, MORSE, Michael A, KIM LYERLY, H, CLAY, Timothy M, MCKINNEY, Matthew, XIAO YI YANG, GANGJUN LEI, LABRECHE, Heather G, HARTMAN, Zachary C, NIEDZWIECKI, Donna, CHAO, Nelson, AMALFITANO, Andrea

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Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly von Griffin, Nicole G, Cronin, Kenneth D, Walley, Nicole M, Hulette, Christine M, Grant, Gerald A, Mikati, Mohamad A, LaBreche, Heather G, Rehder, Catherine W, Allen, Andrew S, Crino, Peter B, Heinzen, Erin L

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