Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects von Pangilinan, F, Mitchell, A, VanderMeer, J, Molloy, A M, Troendle, J, Conley, M, Kirke, P N, Sutton, M, Sequeira, J M, Quadros, E V, Scott, J M, Mills, J L, Brody, L C

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Mammalian BUB1 protein kinases : Map positions and in vivo expression von PANGILINAN, F, LI, Q, WEAVER, T, LEWIS, B. C, DANG, C. V, SPENCER, F

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Abnormal kinetochore structure activates the spindle assembly checkpoint in budding yeast von Pangilinan, F, Spencer, F

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Reduced folate carrier polymorphisms and neural tube defect risk von O’Leary, Valerie B., Pangilinan, Faith, Cox, Christopher, Parle-McDermott, Anne, Conley, Mary, Molloy, Anne M., Kirke, Peadar N., Mills, James L., Brody, Lawrence C., Scott, John M.

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Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association von O’Leary, Valerie B., Mills, James L., Pangilinan, Faith, Kirke, Peadar N., Cox, Christopher, Conley, Mary, Weiler, Andrea, Peng, Kun, Shane, Barry, Scott, John M., Parle-McDermott, Anne, Molloy, Anne M., Brody, Lawrence C.

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A polymorphism in the MTHFD1 gene increases a mother’s risk of having an unexplained second trimester pregnancy loss von Parle-McDermott, Anne, Pangilinan, Faith, Mills, James L., Signore, Caroline C., Molloy, Anne M., Cotter, Amanda, Conley, Mary, Cox, Christopher, Kirke, Peadar N., Scott, John M., Brody, Lawrence C.

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Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects von Parle-McDermott, Anne, Mills, James L, Kirke, Peadar N, O'Leary, Valerie B, Swanson, Deborah A, Pangilinan, Faith, Conley, Mary, Molloy, Anne M, Cox, Christopher, Scott, John M, Brody, Lawrence C

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Saccharomyces cerevisiae BUB2 prevents mitotic exit in response to both spindle and kinetochore damage von Krishnan, R, Pangilinan, F, Lee, C, Spencer, F

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Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population von Swanson, Deborah A., Pangilinan, Faith, Mills, James L., Kirke, Peadar N., Conley, Mary, Weiler, Andrea, Frey, Tiffany, Parle-McDermott, Anne, O'Leary, Valerie B., Seltzer, Rebecca R., Moynihan, Kathryn A., Molloy, Anne M., Burke, Helen, Scott, John M., Brody, Lawrence C.

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Folate-related genes and omphalocele von Mills, James L., Druschel, Charlotte M., Pangilinan, Faith, Pass, Kenneth, Cox, Christopher, Seltzer, Rebecca R., Conley, Mary R., Brody, Lawrence C.

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Screening for new MTHFR polymorphisms and NTD risk von O'Leary, Valerie B., Mills, James L., Parle-McDermott, Anne, Pangilinan, Faith, Molloy, Anne M., Cox, Christopher, Weiler, Andrea, Conley, Mary, Kirke, Peadar N., Scott, John M., Brody, Lawrence C.

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MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae von Parle-McDermott, Anne, Mills, James L., Kirke, Peadar N., Cox, Christopher, Signore, Caroline C., Kirke, Sandra, Molloy, Anne M., O'Leary, Valerie B., Pangilinan, Faith J., O'Herlihy, Colm, Brody, Lawrence C., Scott, John M.

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Analysis of the human folate receptor β gene for an association with neural tube defects von O’Leary, Valerie B, Mills, James L, Kirke, Peadar N, Parle-McDermott, Anne, Swanson, Deborah A, Weiler, Andrea, Pangilinan, Faith, Conley, Mary, Molloy, Anne M, Lynch, Miriam, Cox, Christopher, Scott, John M, Brody, Lawrence C

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Polymorphisms within the vitamin B 12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects von Parle-McDermott, Anne, McManus, Edward J, Mills, James L, O’Leary, Valerie B, Pangilinan, Faith, Cox, Christopher, Weiler, Andrea, Molloy, Anne M, Conley, Mary, Watson, Deborah, Scott, John M, Brody, Lawrence C, Kirke, Peadar N

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Mitotic checkpoint locus MAD1L1 maps to human chromosome 7p22 and mouse chromosome 5 von JIN, D.-Y, KOZAK, C. A, PANGILINAN, F, SPENCER, F, GREEN, E. D, JEANG, K.-T

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QUICK CONNECT PIPE COUPLING von PANGILINAN F

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Application Design for a Virtual Reality Therapy Game for Patients with Behavioral and Psychological Symptoms of Dementia von Anlacan, Veeda Michelle M., Jamora, Roland Dominic G., Pangilinan, Angelo Cedric F., Salido, Isabel Teresa O., Jacinto, Maria Evelyn V., Tee, Michael L., Aguila, Maria Eliza R., Tee, Cherica A., Caro, Jaime D. L.

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Genomic Analysis Enlightens Agaricales Lifestyle Evolution and Increasing Peroxidase Diversity von Ruiz-Dueñas, Francisco J, Barrasa, José M, Sánchez-García, Marisol, Camarero, Susana, Miyauchi, Shingo, Serrano, Ana, Linde, Dolores, Babiker, Rashid, Drula, Elodie, Ayuso-Fernández, Iván, Pacheco, Remedios, Padilla, Guillermo, Ferreira, Patricia, Barriuso, Jorge, Kellner, Harald, Castanera, Raúl, Alfaro, Manuel, Ramírez, Lucía, Pisabarro, Antonio G, Riley, Robert, Kuo, Alan, Andreopoulos, William, LaButti, Kurt, Pangilinan, Jasmyn, Tritt, Andrew, Lipzen, Anna, He, Guifen, Yan, Mi, Ng, Vivian, Grigoriev, Igor V, Cullen, Daniel, Martin, Francis, Rosso, Marie-Noëlle, Henrissat, Bernard, Hibbett, David, Martínez, Angel T

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OC01.04: AI‐driven ultrasound detection of ovarian cancer that generalises: an international multicentre validation study von Christiansen, F., Konuk, E., Ganeshan, A., Welch, R., Huix, J. Palés, Czekierdowski, A., Leone, F., Haak, L.A., Fruscio, R., Gaurilcikas, A., Franchi, D., Fischerová, D., Mor, E., Savelli, L., Pascual, M., Kudla, M.J., Guerriero, S., Buonomo, F., Liuba, K., Montik, N., Alcazar, J., Domali, E., Pangilinan, N.P., Carella, C., Munaretto, M., Šašková, P., Verri, D., Visenzi, C., Herman, P., Smith, K., Epstein, E.

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Obstacles to compassion‐giving among nursing and midwifery managers: an international study von Papadopoulos, I., Lazzarino, R., Koulouglioti, C., Aagard, M., Akman, Ö., Alpers, L.‐M., Apostolara, P., Araneda Bernal, J., Biglete‐Pangilinan, S., Eldar‐Regev, O., González‐Gil, M.T., Kouta, C., Krepinska, R., Lesińska‐Sawicka, M., Liskova, M., Lopez‐Diaz, A. L., Malliarou, M., Martín‐García, Á., Muñoz‐Salinas, M., Nagórska, M., Ngunyulu, R.N., Nissim, S., Nortvedt, L., Oconer‐Rubiano, M.F., Oter‐Quintana, C., Öztürk, C., Papp, K., Piratoba‐Hernandez, B., Rousou, E., Tolentino‐Diaz, M. Y., Tothova, V., Zorba, A.

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