Genetic Risk Factors for Folate-Responsive Neural Tube Defects von Molloy, Anne M, Pangilinan, Faith, Brody, Lawrence C

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Mice lacking the transcobalamin-vitamin B12 receptor, CD320, suffer from anemia and reproductive deficits when fed vitamin B12-deficient diet von Bernard, David J, Pangilinan, Faith J, Cheng, Jun, Molloy, Anne M, Brody, Lawrence C

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Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects von Pangilinan, Faith, Molloy, Anne M, Mills, James L, Troendle, James F, Parle-McDermott, Anne, Signore, Caroline, O'Leary, Valerie B, Chines, Peter, Seay, Jessica M, Geiler-Samerotte, Kerry, Mitchell, Adam, VanderMeer, Julia E, Krebs, Kristine M, Sanchez, Angelica, Cornman-Homonoff, Joshua, Stone, Nicole, Conley, Mary, Kirke, Peadar N, Shane, Barry, Scott, John M, Brody, Lawrence C

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Bioinformatic and genetic association analysis of microRNA target sites in one-carbon metabolism genes von Stone, Nicole, Pangilinan, Faith, Molloy, Anne M, Shane, Barry, Scott, John M, Ueland, Per Magne, Mills, James L, Kirke, Peader N, Sethupathy, Praveen, Brody, Lawrence C

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Mito-SiPE is a sequence-independent and PCR-free mtDNA enrichment method for accurate ultra-deep mitochondrial sequencing von Walsh, Darren J., Bernard, David J., Pangilinan, Faith, Esposito, Madison, Harold, Denise, Parle-McDermott, Anne, Brody, Lawrence C.

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Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome von Blue, Elizabeth E., White, Janson J., Dush, Michael K., Gordon, William W., Wyatt, Brent H., White, Peter, Marvin, Colby T., Helle, Emmi, Ojala, Tiina, Priest, James R., Jenkins, Mary M., Almli, Lynn M., Reefhuis, Jennita, Pangilinan, Faith, Brody, Lawrence C., McBride, Kim L., Garg, Vidu, Shaw, Gary M., Romitti, Paul A., Nembhard, Wendy N., Browne, Marilyn L., Werler, Martha M., Kay, Denise M., Mital, Seema, Chong, Jessica X., Nascone-Yoder, Nanette M., Bamshad, Michael J.

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Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy von Stevelink, Remi, Pangilinan, Faith, Jansen, Floor E., Braun, Kees P.J., Molloy, Anne M., Brody, Lawrence C., Koeleman, Bobby P.C.

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The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites von O'Reilly, Jessica, Pangilinan, Faith, Hokamp, Karsten, Ueland, Per M., Brosnan, John T., Brosnan, Margaret E., Brody, Lawrence C., Molloy, Anne M.

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Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population von Carter, Tonia C., Pangilinan, Faith, Troendle, James F., Molloy, Anne M., VanderMeer, Julia, Mitchell, Adam, Kirke, Peadar N., Conley, Mary R., Shane, Barry, Scott, John M., Brody, Lawrence C., Mills, James L.

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The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels von Parle-McDermott, Anne, Mills, James L., Molloy, Anne M., Carroll, Nicola, Kirke, Peadar N., Cox, Christopher, Conley, Mary R., Pangilinan, Faith J., Brody, Lawrence C., Scott, John M.

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The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population von Parle-McDermott, Anne, Pangilinan, Faith, Mills, James L., Kirke, Peadar N., Gibney, Eileen R., Troendle, James, O'Leary, Valerie B., Molloy, Anne M., Conley, Mary, Scott, John M., Brody, Lawrence C.

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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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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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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture von Stevelink, Remi, Campbell, Ciarán, Chen, Siwei, Abou-Khalil, Bassel, Adesoji, Oluyomi M., Afawi, Zaid, Amadori, Elisabetta, Anderson, Alison, Anderson, Joseph, Andrade, Danielle M., Annesi, Grazia, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bast, Thomas, Baum, Larry, Baumgartner, Tobias, Baykan, Betül, Bebek, Nerses, Becker, Albert J., Becker, Felicitas, Bennett, Caitlin A., Berghuis, Bianca, Berkovic, Samuel F., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blatt, Ilan, Bobbili, Dheeraj R., Borggraefe, Ingo, Bosselmann, Christian, Braatz, Vera, Bradfield, Jonathan P., Brockmann, Knut, Brody, Lawrence C., Buono, Russell J., Busch, Robyn M., Caglayan, Hande, Campbell, Ellen, Canafoglia, Laura, Canavati, Christina, Cascino, Gregory D., Castellotti, Barbara, Catarino, Claudia B., Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherny, Stacey S., Cheung, Ching-Lung, Chinthapalli, Krishna, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Clark, Peggy O., Cole, Andrew J., Compston, Alastair, Coppola, Antonietta, Cosico, Mahgenn, Cossette, Patrick, Craig, John J., Cusick, Caroline, Daly, Mark J., Davis, Lea K., de Haan, Gerrit-Jan, Delanty, Norman, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Di Vito, Lidia, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Elger, Christian E., Ellis, Colin A., Eriksson, Johan G., Faucon, Annika, Feng, Yen-Chen A., Ferguson, Lisa, Ferraro, Thomas N., Ferri, Lorenzo, Feucht, Martha, Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, Franke, Andre, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Geller, Eric B., Giangregorio, Tania, Gjerstad, Leif

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Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland von Minguzzi, Stefano, Molloy, Anne M, Peadar, Kirke, Mills, James, Scott, John M, Troendle, James, Pangilinan, Faith, Brody, Lawrence, Parle-McDermott, Anne

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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies von Anon

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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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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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A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 von Beaty, Terri H, Murray, Jeffrey C, Marazita, Mary L, Munger, Ronald G, Ruczinski, Ingo, Hetmanski, Jacqueline B, Liang, Kung Yee, Wu, Tao, Murray, Tanda, Fallin, M Daniele, Redett, Richard A, Raymond, Gerald, Schwender, Holger, Jin, Sheng-Chih, Cooper, Margaret E, Dunnwald, Martine, Mansilla, Maria A, Leslie, Elizabeth, Bullard, Stephen, Lidral, Andrew C, Moreno, Lina M, Menezes, Renato, Vieira, Alexandre R, Petrin, Aline, Wilcox, Allen J, Lie, Rolv T, Jabs, Ethylin W, Wu-Chou, Yah Huei, Chen, Philip K, Wang, Hong, Ye, Xiaoqian, Huang, Shangzhi, Yeow, Vincent, Chong, Samuel S, Jee, Sun Ha, Shi, Bing, Christensen, Kaare, Melbye, Mads, Doheny, Kimberly F, Pugh, Elizabeth W, Ling, Hua, Castilla, Eduardo E, Czeizel, Andrew E, Ma, Lian, Field, L Leigh, Brody, Lawrence, Pangilinan, Faith, Mills, James L, Molloy, Anne M, Kirke, Peadar N, Scott, John M, Arcos-Burgos, Mauricio, Scott, Alan F

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SLC25A48 influences plasma levels of choline and localizes to the inner mitochondrial membrane von Bernard, David J., Pangilinan, Faith, Mendina, Caitlin, Desporte, Tara, Wincovitch, Stephen M., Walsh, Darren J., Porter, Richard K., Molloy, Anne M., Shane, Barry, Brody, Lawrence C.

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