Emergence and Apparent Transmission of Rimantadine-Resistant Influenza A Virus in Families von Hayden, Frederick G, Belshe, Robert B, Clover, Richard D, Hay, Alan J, Oakes, Marion G, Soo, Whaijen

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Sex-associated differences in frequencies and prognostic impact of recurrent genetic alterations in adult acute myeloid leukemia (Alliance, AMLCG) von Ozga, Michael, Nicolet, Deedra, Mrózek, Krzysztof, Yilmaz, Ayse S., Kohlschmidt, Jessica, Larkin, Karilyn T., Blachly, James S., Oakes, Christopher C., Buss, Jill, Walker, Christopher J., Orwick, Shelley, Jurinovic, Vindi, Rothenberg-Thurley, Maja, Dufour, Annika, Schneider, Stephanie, Sauerland, Maria Cristina, Görlich, Dennis, Krug, Utz, Berdel, Wolfgang E., Woermann, Bernhard J., Hiddemann, Wolfgang, Braess, Jan, Subklewe, Marion, Spiekermann, Karsten, Carroll, Andrew J., Blum, William G., Powell, Bayard L., Kolitz, Jonathan E., Moore, Joseph O., Mayer, Robert J., Larson, Richard A., Uy, Geoffrey L., Stock, Wendy, Metzeler, Klaus H., Grimes, H. Leighton, Byrd, John C., Salomonis, Nathan, Herold, Tobias, Mims, Alice S., Eisfeld, Ann-Kathrin

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Sex-Associated Differences in Frequencies and Outcome Prognostication of Recurrent Molecular Features in Adults with Acute Myeloid Leukemia (AML) (AMLCG, CALGB [Alliance]) von Ozga, Michael P., Nicolet, Deedra, Mrózek, Krzysztof, Yilmaz, Selen, Kohlschmidt, Jessica, Larkin, Karilyn T., Blachly, James S., Oakes, Christopher C., Buss, Jill, Walker, Christopher J., Orwick, Shelley, Jurinovic, Vindi, Rothenberg-Thurley, Maja, Dufour, Annika Maria, Schneider, Stephanie, Sauerland, Maria Cristina, Görlich, Dennis, Krug, Utz, Berdel, Wolfgang E., Woermann, Bernhard Josef, Hiddemann, Wolfgang, Braess, Jan, Subklewe, Marion, Spiekermann, Karsten, Carroll, Andrew J., Blum, William G., Powell, Bayard L., Kolitz, Jonathan E., Moore, Joseph O., Mayer, Robert James, Stone, Richard M., Uy, Geoffrey L., Stock, Wendy, Metzeler, Klaus H., Grimes, H. Leighton, Byrd, John C., Salomonis, Nathan, Herold, Tobias, Mims, Alice S., Eisfeld, Ann-Kathrin

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Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects von Deak, Kristen L., Siegel, Deborah G., George, Timothy M., Gregory, Simon, Ashley-Koch, Allison, Speer, Marcy C.

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Genetic Studies in Neural Tube Defects von Melvin, Elizabeth C., George, Timothy M., Worley, Gordon, Franklin, Amy, Mackey, Joanne, Viles, Kristi, Shah, Nishu, Drake, Courtney R., Enterline, David S., McLone, David, Nye, Jeffrey, Oakes, W. Jerry, McLaughlin, Colleen, Walker, Marion L., Peterson, Paula, Brei, Timothy, Buran, Connie, Aben, Joanna, Ohm, Bonnie, Bermans, Iskandar, Qumsiyeh, Mazin, Vance, Jeffrey, Pericak-Vance, Margaret A., Speer, Marcy C.

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Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2 von Deak, Kristen L., Dickerson, Margaret E., Linney, Elwood, Enterline, David S., George, Timothy M., Melvin, Elizabeth C., Graham, Felicia L., Siegel, Deborah G., Hammock, Preston, Mehltretter, Lorraine, Bassuk, Alexander G., Kessler, John A., Gilbert, John R., Speer, Marcy C.

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Refinement of 2q and 7p loci in a large multiplex NTD family von Stamm, Demetra S., Siegel, Deborah G., Mehltretter, Lorraine, Connelly, Jessica J., Trott, Alison, Ellis, Nathen, Zismann, Victoria, Stephan, Dietrich A., George, Timothy M., Vekemans, Michel, Ashley-Koch, Allison, Gilbert, John R., Gregory, Simon G., Speer, Marcy C.

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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects von DEAK, Kristen L, BOYLES, Abee L, MCCLAY, David, BASSUK, Alexander G, KESSLER, John A, LINNEY, Elwood, GILBERT, John R, SPEER, Marcy C, ETCHEVERS, Heather C, MELVIN, Elizabeth C, SIEGEL, Deborah G, GRAHAM, Felicia L, SLIFER, Susan H, ENTERLINE, David S, GEORGE, Timothy M, VEKEMANS, Michel

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High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35 von Stamm, Demetra S., Rampersaud, Evadnie, Slifer, Susan H., Mehltretter, Lorraine, Siegel, Deborah G., Xie, Jianzhen, Hu-Lince, Diane, Craig, David W., Stephan, Dietrich A., George, Timothy M., Gilbert, John R., Speer, Marcy C.

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Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects von Speer, MC, Nye, J, McLone, D, Worley, G, Melvin, EC, Viles, KD, Franklin, A, Drake, C, Mackey, J, George, TM

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TERC is not a major gene in human neural tube defects von Benz, Lisa P., Swift, Frances E., Graham, Felicia L., Enterline, David S., Melvin, Elizabeth C., Hammock, Preston, Gilbert, John R., Speer, Marcy C., Bassuk, Alexander G., Kessler, John A., George, Timothy M.

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T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families von Speer, Marcy C., Melvin, Elizabeth C., Viles, Kristi D., Bauer, Kim A., Rampersaud, Evadnie, Drake, Courtney, George, Timothy M., Enterline, David S., Mackey, Joanne F., Worley, Gordon, Gilbert, John R., Nye, Jeffery S.

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