Validation of a liquid biopsy assay with molecular and clinical profiling of circulating tumor DNA by Finkle, Justin D., Boulos, Hala, Driessen, Terri M., Lo, Christine, Blidner, Richard A., Hafez, Ashraf, Khan, Aly A., Lozac’hmeur, Ariane, McKinnon, Kelly E., Perera, Jason, Zhu, Wei, Dowlati, Afshin, White, Kevin P., Tell, Robert, Beaubier, Nike

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Tissue- and strain-specific effects of a genotoxic carcinogen 1,3-butadiene on chromatin and transcription by Israel, Jennifer W., Chappell, Grace A., Simon, Jeremy M., Pott, Sebastian, Safi, Alexias, Lewis, Lauren, Cotney, Paul, Boulos, Hala S., Bodnar, Wanda, Lieb, Jason D., Crawford, Gregory E., Furey, Terrence S., Rusyn, Ivan

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Abstract 3106: Accurate estimation of circulating tumor DNA fraction from ultra low-pass whole-genome sequencing by Finkle, Justin, Lo, Christine, Boulos, Hala, Driessen, Terri, Zhu, Wei, Tell, Robert

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A tumor-naive ctDNA assay detects minimal residual disease in resected stage II or III colorectal cancer and predicts recurrence: subset analysis from the GALAXY study in CIRCULATE... by Nakamura, Yoshiaki, Kaneva, Kristiyana, Lo, Christine, Neems, Daniel, Freaney, Jonathan E, Boulos, Hala, Hyun, Seung Won, Islam, Farahnaz, Yamada-Hanff, Jason, Driessen, Terri M, Sonnenschein, Anne, DeSantis, Dana F, Kotani, Daisuke, Watanabe, Jun, Kotaka, Masahito, Mishima, Saori, Bando, Hideaki, Yamazaki, Kentaro, Taniguchi, Hiroya, Takemasa, Ichiro, Kato, Takeshi, Sangli, Chithra, Tell, Robert, Blidner, Richard, Yoshino, Takayuki, Sasser, Kate, Oki, Eiji, Nimeiri, Halla

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Functional constraints on the constitutive androstane receptor inferred from human sequence variation and cross-species comparisons by Thompson, Emma E, Kuttab-Boulos, Hala, Krasowski, Matthew D, Di Rienzo, Anna

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Tissue- and strain-specific effects of a genotoxic carcinogen1,3-butadiene on chromatin and transcription by Israel, Jennifer W., Chappell, Grace A., Simon, Jeremy M., Pott, Sebastian, Safi, Alexias, Lewis, Lauren, Cotney, Paul, Boulos, Hala S., Bodnar, Wanda, Lieb, Jason D., Crawford, Gregory E., Furey, Terrence S., Rusyn, Ivan

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Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome by Kambouris, Marios, Maroun, Rachid C, Ben-Omran, Tawfeg, Al-Sarraj, Yasser, Errafii, Khaoula, Ali, Rehab, Boulos, Hala, Curmi, Patrick A, El-Shanti, Hatem

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Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy by Kambouris, Marios, Thevenon, Julien, Soldatos, Ariane, Cox, Allison, Stephen, Joshi, Ben‐Omran, Tawfeg, Al‐Sarraj, Yasser, Boulos, Hala, Bone, William, Mullikin, James C., Masurel‐Paulet, Alice, St‐Onge, Judith, Dufford, Yannis, Chantegret, Corrine, Thauvin‐Robinet, Christel, Al‐Alami, Jamil, Faivre, Laurence, Riviere, Jean Baptiste, Gahl, William A., Bassuk, Alexander G., Malicdan, May Christine V., El‐Shanti, Hatem

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Biallelic SCN 10A mutations in neuromuscular disease and epileptic encephalopathy by Kambouris, Marios, Thevenon, Julien, Soldatos, Ariane, Cox, Allison, Stephen, Joshi, Ben‐Omran, Tawfeg, Al‐Sarraj, Yasser, Boulos, Hala, Bone, William, Mullikin, James C., Masurel‐Paulet, Alice, St‐Onge, Judith, Dufford, Yannis, Chantegret, Corrine, Thauvin‐Robinet, Christel, Al‐Alami, Jamil, Faivre, Laurence, Riviere, Jean Baptiste, Gahl, William A., Bassuk, Alexander G., Malicdan, May Christine V., El‐Shanti, Hatem

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Systemic mastocytosis with renal light chain amyloidosis: associated non-mast cell disorder or concurrent disease by Damlaj, Moussab, Ashi, Hanadi, Boulos, Fouad, Kfoury, Hala, Chakhachiro, Zaher

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XQueryViz: A Visual Dataflow XQuery Tool by Karam, M., Boulos, J., Ollaic, H., Koteiche, Z.

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