Search Results - "Ratner, Samantha"

O35: Feasibility of expanded newborn screening using genome sequencing for early actionable conditions in a diverse city by Chung, Wendy, Ziegler, Alban, Koval-Burt, Carrie, Kay, Denise, Suchy, Sharon, Bergtrup, Amber, Langley, Katherine, Amendola, Laura, Boyd, Brenna, Bradley, Jennifer, Brandt, Tracy, Cohen, Lilian, Coffey, Alison, Devaney, Joseph, Dygulska, Beata, Friedman, Bethany, Fuleihan, Ramsey, Gyimah, Awura, Hernan, Rebecca, Hofherr, Sean, Hruska, Kathleen, Hu, Zhanzhi, Jeanne, Mederic, Jin, Guanjun, Johnson, Aaron, Kavus, Haluk, Leibel, Rudolph, McWalter, Kirsty, Monaghan, Kristin, Soler, Nicole Pimentel, Quevedo, Yeyson, Ratner, Samantha, Retterer, Kyle, Shapiro, Natasha, Sicko, Robert, Storm, Samuel, Torene, Rebecca, Williams, Olatundun, Wynn, Julia, Taft, Ryan, Kruszka, Paul, Caggana, Michele

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The Outer Surface Protease, SepM, Is Required for blp Locus Activation in Three of the Four Most Common Pherotypes of Streptococcus pneumoniae by Ratner, Samantha, Bollinger, Kevin, Richardson, John, Dawid, Suzanne

“…Streptococcus pneumoniae (pneumococcus) is an important human pathogen that primarily resides in the nasopharynx. To persist in this polymicrobial environment,…”
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Socio-ecological model of barriers to cascade testing for hereditary cancer syndromes: Systematic review of the literature (057) by Li, Xuan, Ahsan, Muhammad Danyal, Feit, Julia, Ratner, Samantha, Holcomb, Kevin, Chapman-Davis, Eloise, Cantillo, Evelyn, Frey, Melissa

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Cascade genetic testing for hereditary cancer syndromes: a review of barriers and breakthroughs by Levine, Rachel, Kahn, Ryan M., Perez, Luiza, Brewer, Jesse, Ratner, Samantha, Li, Xuan, Yeoshoua, Effi, Frey, Melissa K.

“…Germline genetic sequencing is now at the forefront of cancer treatment and preventative medicine. Cascade genetic testing, or the testing of at-risk…”
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Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions by Ziegler, Alban, Koval-Burt, Carrie, Kay, Denise M, Suchy, Sharon F, Begtrup, Amber, Langley, Katherine G, Hernan, Rebecca, Amendola, Laura M, Boyd, Brenna M, Bradley, Jennifer, Brandt, Tracy, Cohen, Lilian L, Coffey, Alison J, Devaney, Joseph M, Dygulska, Beata, Friedman, Bethany, Fuleihan, Ramsay L, Gyimah, Awura, Hahn, Sihoun, Hofherr, Sean, Hruska, Kathleen S, Hu, Zhanzhi, Jeanne, Médéric, Jin, Guanjun, Johnson, D. Aaron, Kavus, Haluk, Leibel, Rudolph L, Lobritto, Steven J, McGee, Stephen, Milner, Joshua D, McWalter, Kirsty, Monaghan, Kristin G, Orange, Jordan S, Pimentel Soler, Nicole, Quevedo, Yeyson, Ratner, Samantha, Retterer, Kyle, Shah, Ankur, Shapiro, Natasha, Sicko, Robert J, Silver, Eric S, Strom, Samuel, Torene, Rebecca I, Williams, Olatundun, Ustach, Vincent D, Wynn, Julia, Taft, Ryan J, Kruszka, Paul, Caggana, Michele, Chung, Wendy K

“…IMPORTANCE: The feasibility of implementing genome sequencing as an adjunct to traditional newborn screening (NBS) in newborns of different racial and ethnic…”
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