Search Results - Lockwood, Christina M.
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Low fetal fraction in obese women at first trimester cell-free DNA based prenatal screening is not accompanied by differences in total cell-free DNA by SHREE, Raj, KOLAROVA, Teodora R., MACKINNON, Hayley J., HEDGE, Jaclynne M., VINOPAL, Elena, MA, Kimberly K., LOCKWOOD, Christina M., CHANDRASEKARAN, Suchitra
Published 2021Text -
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Microsatellite instability in prostate cancer by PCR or next-generation sequencing by Hempelmann, Jennifer A., Lockwood, Christina M., Konnick, Eric Q., Schweizer, Michael T., Antonarakis, Emmanuel S., Lotan, Tamara L., Montgomery, Bruce, Nelson, Peter S., Klemfuss, Nola, Salipante, Stephen J., Pritchard, Colin C.
Published 2018Text -
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Validation and implementation of a modular targeted capture assay for the detection of clinically significant molecular oncology alterations by Kuo, Ayako J., Paulson, Vera A., Hempelmann, Jennifer A., Beightol, Mallory, Todhunter, Sheena, Colbert, Brice G., Salipante, Stephen J., Konnick, Eric Q., Pritchard, Colin C., Lockwood, Christina M.
Published 2020Text -
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Development of an Immunoassay for the Kidney Specific Protein myo-Inositol Oxygenase, a Potential Biomarker of Acute Kidney Injury by Gaut, Joseph P., Crimmins, Dan L., Ohlendorf, Matt F., Lockwood, Christina M., Griest, Terry A., Brada, Nancy A., Hoshi, Masato, Sato, Bryan, Hotchkiss, Richard S., Jain, Sanjay, Ladenson, Jack H.
Published 2014Text -
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Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing by Abel, Haley J., Al-Kateb, Hussam, Cottrell, Catherine E., Bredemeyer, Andrew J., Pritchard, Colin C., Grossmann, Allie H., Wallander, Michelle L., Pfeifer, John D., Lockwood, Christina M., Duncavage, Eric J.
Published 2014Text -
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Histone deposition pathways determine the chromatin landscapes of H3.1 and H3.3 K27M oncohistones by Sarthy, Jay F, Meers, Michael P, Janssens, Derek H, Henikoff, Jorja G, Feldman, Heather, Paddison, Patrick J, Lockwood, Christina M, Vitanza, Nicholas A, Olson, James M, Ahmad, Kami, Henikoff, Steven
Published 2020Text -
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Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives by Byers, Heather M., Jacobson, Angela, McFaddin, Andrew S., Ussakli, Cigdem H., Newlin, Anna, Stanich, Peter P., More, Stephanie, Hamblett, Amanda, Tait, Jonathan F., Shirts, Brian, Pritchard, Colin C., Konnick, Eric Q., Lockwood, Christina M.
Published 2018Text -
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High-resolution profiling of human cytomegalovirus cell-free DNA in human plasma highlights its exceptionally fragmented nature by Peddu, Vikas, Bradley, Benjamin T., Casto, Amanda M., Shree, Raj, Colbert, Brice G., Xie, Hong, Santo, Tracy K., Huang, Meei-Li, Cheng, Edith Y., Konnick, Eric, Salipante, Stephen J., Jerome, Keith R., Lockwood, Christina M., Greninger, Alexander L.
Published 2020Text -
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Comparable specimen collection from both ends of at-home mid-turbinate swabs by Truong, Melissa, Pfau, Brian, McDermot, Evan, Han, Peter D., Brandstetter, Elisabeth, Richardson, Matthew, Kim, Ashley E., Rieder, Mark J., Chu, Helen Y., Englund, Janet A., Nickerson, Deborah A., Shendure, Jay, Lockwood, Christina M., Konnick, Eric Q., Starita, Lea M.
Published 2020Text -
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Comparable Specimen Collection from Both Ends of At-Home Midturbinate Swabs by Truong, Melissa, Pfau, Brian, McDermot, Evan, Han, Peter D., Brandstetter, Elisabeth, Richardson, Matthew, Kim, Ashley E., Rieder, Mark J., Chu, Helen Y., Englund, Janet A., Nickerson, Deborah A., Shendure, Jay, Lockwood, Christina M., Konnick, Eric Q., Starita, Lea M.
Published 2021Text -
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Mutations of the DNA repair gene PNKP in a patient with microcephaly, seizures, and developmental delay (MCSZ) presenting with a high-grade brain tumor by Jiang, Bingcheng, Murray, Cameron, Cole, Bonnie L., Glover, J. N. Mark, Chan, Gordon K., Deschenes, Jean, Mani, Rajam S., Subedi, Sudip, Nerva, John D., Wang, Anthony C., Lockwood, Christina M., Mefford, Heather C., Leary, Sarah E. S., Ojemann, Jeffery G., Weinfeld, Michael, Ene, Chibawanye I.
Published 2022Text -
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Desmoplastic Infantile Ganglioglioma/Astrocytoma (DIG/DIA) Are Distinct Entities with Frequent BRAFV600 Mutations by Wang, Anthony C., Jones, David T.W., Abecassis, Isaac Joshua, Cole, Bonnie L., Leary, Sarah E.S., Lockwood, Christina M., Chavez, Lukas, Capper, David, Korshunov, Andrey, Fallah, Aria, Wang, Shelly, Ene, Chibawanye, Olson, James M., Geyer, J. Russell, Holland, Eric C., Lee, Amy, Ellenbogen, Richard G., Ojemann, Jeffrey G.
Published 2018Text