Resultados da busca - Powell, Bradford C

Similarity-based gene detection: using COGs to find evolutionarily-conserved ORFs por Powell, Bradford C, Hutchison, Clyde A

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A Millennial Myosin Census por Berg, Jonathan S., Powell, Bradford C., Cheney, Richard E.

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Transcriptional Analysis of the Conserved ftsZ Gene Cluster in Mycoplasma genitalium and Mycoplasma pneumoniae por Benders, Gwynedd A., Powell, Bradford C., Hutchison, Clyde A.

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Tracking the evolution of alternatively spliced exons within the Dscam family por Crayton, Mack E, Powell, Bradford C, Vision, Todd J, Giddings, Morgan C

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Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty por Waltz, Margaret, Prince, Anya E. R., O’Daniel, Julianne M., Foreman, Ann Katherine M., Powell, Bradford C., Berg, Jonathan S.

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Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert Panels por Kanavy, Dona M., McNulty, Shannon M., Jairath, Meera K., Brnich, Sarah E., Bizon, Chris, Powell, Bradford C., Berg, Jonathan S.

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Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction por Filer, Dayne L., Mieczkowski, Piotr A., Brandt, Alicia, Gilmore, Kelly L., Powell, Bradford C., Berg, Jonathan S., Wilhelmsen, Kirk C., Vora, Neeta L.

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Testing and Extending Strategies for Identifying Genetic Disease-Related Encounters in Pediatric Patients por Spees, Lisa P., Hicklin, Karen, Adams, Michael C., Farnan, Laura, Bensen, Jeannette T., Gilleskie, Donna B., Berg, Jonathan S., Powell, Bradford C., Lich, Kristen Hassmiller

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Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making por DeCristo, Daniela M., Milko, Laura V., O’Daniel, Julianne M., Foreman, Ann Katherine M., Mollison, Lonna F., Powell, Bradford C., Powell, Cynthia M., Berg, Jonathan S.

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Identification of TP53 as an Acute Lymphocytic Leukemia Susceptibility Gene Through Exome Sequencing por Powell, Bradford C., Jiang, Lichun, Muzny, Donna M., Treviño, Lisa R., Dreyer, ZoAnn E., Strong, Louise C., Wheeler, David A., Gibbs, Richard A., Plon, Sharon E.

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Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogs por Saliba, Jason, Zabriskie, Ryan, Ghosh, Rajarshi, Powell, Bradford C, Hicks, Stephanie, Kimmel, Marek, Meng, Qingchang, Ritter, Deborah I, Wheeler, David A, Gibbs, Richard A, Tsai, Francis T F, Plon, Sharon E

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Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized... por Milko, Laura V., Rini, Christine, Lewis, Megan A., Butterfield, Rita M., Lin, Feng-Chang, Paquin, Ryan S., Powell, Bradford C., Roche, Myra I., Souris, Katherine J., Bailey, Donald B., Berg, Jonathan S., Powell, Cynthia M.

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An approach to integrating exome sequencing for fetal structural anomalies into clinical practice por Vora, Neeta L., Gilmore, Kelly, Brandt, Alicia, Gustafson, Chelsea, Strande, Natasha, Ramkissoon, Lori, Hardisty, Emily, Foreman, Ann Katherine M., Wilhelmsen, Kirk, Owen, Phillips, Weck, Karen E., Berg, Jonathan S., Powell, Cynthia M., Powell, Bradford C.

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The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study por Rini, Christine, Khan, Cynthia M., Moore, Elizabeth, Roche, Myra I., Evans, James P., Berg, Jonathan S., Powell, Bradford C., Corbie-Smith, Giselle, Foreman, Ann Katherine M., Griesemer, Ida, Lee, Kristy, O’Daniel, Julianne M., Henderson, Gail E.

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Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings por Roche, Myra I., Griesemer, Ida, Khan, Cynthia M., Moore, Elizabeth, Lin, Feng-Chang, O’Daniel, Julianne M., Foreman, Ann Katherine M., Lee, Kristy, Powell, Bradford C., Berg, Jonathan S., Evans, James P., Henderson, Gail E., Rini, Christine

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Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing por Filer, Dayne L., Kuo, Fengshen, Brandt, Alicia T., Tilley, Christian R., Mieczkowski, Piotr A., Berg, Jonathan S., Robasky, Kimberly, Li, Yun, Bizon, Chris, Tilson, Jeffery L., Powell, Bradford C., Bost, Darius M., Jeffries, Clark D., Wilhelmsen, Kirk C.

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Anticipated Responses of Early Adopter Genetic Specialists and Non-Genetic Specialists to Unsolicited Genomic Secondary Findings por Christensen, Kurt D., Bernhardt, Barbara A., Jarvik, Gail P., Hindorff, Lucia A., Ou, Jeffrey, Biswas, Sawona, Powell, Bradford C., Grundmeier, Robert W., Machini, Kalotina, Karavite, Dean J., Pennington, Jeffrey W., Krantz, Ian D., Berg, Jonathan S., Goddard, Katrina A. B.

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Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Seq... por Staley, Brooke S., Milko, Laura V., Waltz, Margaret, Griesemer, Ida, Mollison, Lonna, Grant, Tracey L., Farnan, Laura, Roche, Myra, Navas, Angelo, Lightfoot, Alexandra, Foreman, Ann Katherine M., O’Daniel, Julianne M., O’Neill, Suzanne C., Lin, Feng-Chang, Roman, Tamara S., Brandt, Alicia, Powell, Bradford C., Rini, Christine, Berg, Jonathan S., Bensen, Jeannette T.

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An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening por Milko, Laura V., O’Daniel, Julianne M., DeCristo, Daniela M., Crowley, Stephanie B., Foreman, Ann Katherine M., Wallace, Kathleen E., Mollison, Lonna F., Strande, Natasha T., Girnary, Zahra S., Boshe, Lacey J., Aylsworth, Arthur S., Gucsavas-Calikoglu, Muge, Frazier, Dianne M., Vora, Neeta L., Roche, Myra I., Powell, Bradford C., Powell, Cynthia M., Berg, Jonathan S.

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Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience por Muenzen, Kathleen D., Amendola, Laura M., Kauffman, Tia L., Mittendorf, Kathleen F., Bensen, Jeannette T., Chen, Flavia, Green, Richard, Powell, Bradford C., Kvale, Mark, Angelo, Frank, Farnan, Laura, Fullerton, Stephanie M., Robinson, Jill O., Li, Tianran, Murali, Priyanka, Lawlor, James M.J., Ou, Jeffrey, Hindorff, Lucia A., Jarvik, Gail P., Crosslin, David R.

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