Hypertensive Encephalopathy Presenting as Status Epilepticus in a Three Year Old von Sanford, Erica F., BS, Stein, John C., MD

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Better and faster is cheaper von Sanford Kobayashi, Erica F., Dimmock, David P.

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Penile foreskin avulsion from parrot fish bite von Kobayashi, Sow A, Sanford, Erica F, Witucki, Peter

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Effect of Ventral vs Dorsal Spinal Surgery on Patient-Reported Physical Functioning in Patients With Cervical Spondylotic Myelopathy: A Randomized Clinical Trial von Ghogawala, Zoher, Terrin, Norma, Dunbar, Melissa R, Breeze, Janis L, Freund, Karen M, Kanter, Adam S, Mummaneni, Praveen V, Bisson, Erica F, Barker, Fred G, Schwartz, J. Sanford, Harrop, James S, Magge, Subu N, Heary, Robert F, Fehlings, Michael G, Albert, Todd J, Arnold, Paul M, Riew, K. Daniel, Steinmetz, Michael P, Wang, Marjorie C, Whitmore, Robert G, Heller, John G, Benzel, Edward C

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The Genomic landscape of short tandem repeats across multiple ancestries von Vijayaraghavan, Prashanth, Batalov, Sergey, Ding, Yan, Sanford, Erica, Kingsmore, Stephen F, Dimmock, David, Hobbs, Charlotte, Bainbridge, Matthew

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An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm von Dimmock, David P, Clark, Michelle M, Gaughran, Mary, Cakici, Julie A, Caylor, Sara A, Clarke, Christina, Feddock, Michele, Chowdhury, Shimul, Salz, Lisa, Cheung, Cynthia, Bird, Lynne M, Hobbs, Charlotte, Wigby, Kristen, Farnaes, Lauge, Bloss, Cinnamon S, Kingsmore, Stephen F

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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases von Kingsmore, Stephen F., Smith, Laurie D., Kunard, Chris M., Bainbridge, Matthew, Batalov, Sergey, Benson, Wendy, Blincow, Eric, Caylor, Sara, Chambers, Christina, Del Angel, Guillermo, Dimmock, David P., Ding, Yan, Ellsworth, Katarzyna, Feigenbaum, Annette, Frise, Erwin, Green, Robert C., Guidugli, Lucia, Hall, Kevin P., Hansen, Christian, Hobbs, Charlotte A., Kahn, Scott D., Kiel, Mark, Van Der Kraan, Lucita, Krilow, Chad, Kwon, Yong H., Madhavrao, Lakshminarasimha, Le, Jennie, Lefebvre, Sebastien, Mardach, Rebecca, Mowrey, William R., Oh, Danny, Owen, Mallory J., Powley, George, Scharer, Gunter, Shelnutt, Seth, Tokita, Mari, Mehtalia, Shyamal S., Oriol, Albert, Papadopoulos, Stavros, Perry, James, Rosales, Edwin, Sanford, Erica, Schwartz, Steve, Tran, Duke, Reese, Martin G., Wright, Meredith, Veeraraghavan, Narayanan, Wigby, Kristen, Willis, Mary J., Wolen, Aaron R., Defay, Thomas

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Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning von Peterson, Bennet, Hernandez, Edgar Javier, Hobbs, Charlotte, Malone Jenkins, Sabrina, Moore, Barry, Rosales, Edwin, Zoucha, Samuel, Sanford, Erica, Bainbridge, Matthew N, Frise, Erwin, Oriol, Albert, Brunelli, Luca, Kingsmore, Stephen F, Yandell, Mark

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High-volume hemofiltration in adult burn patients with septic shock and acute kidney injury: a multicenter randomized controlled trial von Chung, Kevin K, Coates, Elsa C, Smith, Jr, David J, Karlnoski, Rachel A, Hickerson, William L, Arnold-Ross, Angela L, Mosier, Michael J, Halerz, Marcia, Sprague, Amy M, Mullins, Robert F, Caruso, Daniel M, Albrecht, Marlene, Arnoldo, Brett D, Burris, Agnes M, Taylor, Sandra L, Wolf, Steven E

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Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care Unit von Sanford Kobayashi, Erica, Waldman, Bryce, Engorn, Branden M, Perofsky, Katherine, Allred, Erika, Briggs, Benjamin, Gatcliffe, Chelsea, Ramchandar, Nanda, Gold, Jeffrey J, Doshi, Ami, Ingulli, Elizabeth G, Thornburg, Courtney D, Benson, Wendy, Farnaes, Lauge, Chowdhury, Shimul, Rego, Seema, Hobbs, Charlotte, Kingsmore, Stephen F, Dimmock, David P, Coufal, Nicole G

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Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system von Allred, Erika T, Perens, Elliot A, Coufal, Nicole G, Sanford Kobayashi, Erica, Kingsmore, Stephen F, Dimmock, David P

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Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial von Kingsmore, Stephen F., Wright, Meredith, Olsen, Lauren, Schultz, Brandan, Protopsaltis, Liana, Averbuj, Dan, Blincow, Eric, Carroll, Jeanne, Caylor, Sara, Defay, Thomas, Ellsworth, Katarzyna, Feigenbaum, Annette, Gover, Mia, Guidugli, Lucia, Hansen, Christian, Van Der Kraan, Lucita, Kunard, Chris M., Kwon, Hugh, Madhavrao, Lakshminarasimha, Leipzig, Jeremy, Liang, Yupu, Mardach, Rebecca, Mowrey, William R., Nguyen, Hung, Niemi, Anna-Kaisa, Oh, Danny, Saad, Muhammed, Scharer, Gunter, Schleit, Jennifer, Mehtalia, Shyamal S., Sanford, Erica, Smith, Laurie D., Willis, Mary J., Wigby, Kristen, Reimers, Rebecca

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Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection von Kingsmore, Stephen F., Wright, Meredith, Smith, Laurie D., Liang, Yupu, Mowrey, William R., Protopsaltis, Liana, Bainbridge, Matthew, Baker, Mei, Batalov, Sergey, Blincow, Eric, Cao, Bryant, Caylor, Sara, Chambers, Christina, Ellsworth, Katarzyna, Feigenbaum, Annette, Frise, Erwin, Guidugli, Lucia, Hall, Kevin P., Hansen, Christian, Kiel, Mark, Van Der Kraan, Lucita, Krilow, Chad, Kwon, Hugh, Madhavrao, Lakshminarasimha, Lefebvre, Sebastien, Leipzig, Jeremy, Mardach, Rebecca, Moore, Barry, Oh, Danny, Olsen, Lauren, Ontiveros, Eric, Owen, Mallory J., Reimers, Rebecca, Scharer, Gunter, Schleit, Jennifer, Shelnutt, Seth, Mehtalia, Shyamal S., Oriol, Albert, Sanford, Erica, Schwartz, Steve, Wigby, Kristen, Willis, Mary J., Yandell, Mark, Kunard, Chris M., Defay, Thomas

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The Pharmacogenomics Research Network Translational Pharmacogenetics Program: Overcoming Challenges of Real-World Implementation von Shuldiner, A R, Relling, M V, Peterson, J F, Hicks, K, Freimuth, R R, Sadee, W, Pereira, N L, Roden, D M, Johnson, J A, Klein, T E

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Abstract PD4-02: Safety and efficacy of a tucatinib-trastuzumab-capecitabine regimen for treatment of leptomeningeal metastasis (LM) in HER2-positive breast cancer: Results from TB... von Murthy, Rashmi K, O'Brien, Barbara, Berry, Donald A, Singareeka-Raghavendra, Akshara, Monroe, Maria Gule, Johnson, Jason, White, Jason, Childress, Jennifer, Sanford, Justin, Schwartz-Gomez, Jill, Melisko, Michelle, Morikawa, Aki, Ferguson, Sherise, de Groot, John F, Krop, Ian, Valero, Vicente, Rimawi, Mothaffar, Wolff, Antonio, Tripathy, Debu, Lin, Nancy U, Stringer-Reasor, Erica

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Response to Grosse et al von Kingsmore, Stephen F, Smith, Laurie D, Kunard, Chris M, Bainbridge, Matthew, Batalov, Sergey, Benson, Wendy, Blincow, Eric, Caylor, Sara, Chambers, Christina, Del Angel, Guillermo, Dimmock, David P, Ding, Yan, Ellsworth, Katarzyna, Feigenbaum, Annette, Frise, Erwin, Green, Robert C, Guidugli, Lucia, Hall, Kevin P, Hansen, Christian, Hobbs, Charlotte A, Kahn, Scott D, Kiel, Mark, Van Der Kraan, Lucita, Krilow, Chad, Kwon, Yong H, Madhavrao, Lakshminarasimha, Le, Jennie, Lefebvre, Sebastien, Mardach, Rebecca, Mowrey, William R, Oh, Danny, Owen, Mallory J, Powley, George, Scharer, Gunter, Shelnutt, Seth, Tokita, Mari, Mehtalia, Shyamal S, Oriol, Albert, Papadopoulos, Stavros, Perry, James, Rosales, Edwin, Sanford, Erica, Schwartz, Steve, Tran, Duke, Reese, Martin G, Wright, Meredith, Veeraraghavan, Narayanan, Wigby, Kristen, Willis, Mary J, Wolen, Aaron R, Defay, Thomas

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The Genomic landscape of short tandem repeats across multiple ancestries von Prashanth Vijayaraghavan, Sergey Batalov, Yan Ding, Erica Sanford, Stephen F. Kingsmore, David Dimmock, Charlotte Hobbs, Matthew Bainbridge

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Clinical utility of ultra-rapid whole-genome sequencing in an infant with atypical presentation of WT1 -associated nephrotic syndrome type 4 von Sanford, Erica, Wong, Terence, Ellsworth, Katarzyna A, Ingulli, Elizabeth, Kingsmore, Stephen F

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Postmortem diagnosis of PPA2-associated sudden cardiac death from dried blood spot in a neonate presenting with vocal cord paralysis von Sanford, Erica, Jones, Marilyn C, Brigger, Matthew, Hammer, Monia, Giudugli, Lucia, Kingsmore, Stephen F, Dimmock, David, Bainbridge, Matthew N

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Postmortem diagnosis of PPA2associated sudden cardiac death from dried blood spot in a neonate presenting with vocal cord paralysis von Sanford, Erica, Jones, Marilyn C, Brigger, Matthew, Hammer, Monia, Giudugli, Lucia, Kingsmore, Stephen F, Dimmock, David, Bainbridge, Matthew N

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