Search Results - Van, Allison Alicia

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    Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848 by Koczkowska, Magdalena, Chen, Yunjia, Callens, Tom, Gomes, Alicia, Sharp, Angela, Johnson, Sherrell, Hsiao, Meng-Chang, Chen, Zhenbin, Balasubramanian, Meena, Barnett, Christopher P., Becker, Troy A., Ben-Shachar, Shay, Bertola, Debora R., Blakeley, Jaishri O., Burkitt-Wright, Emma M.M., Callaway, Alison, Crenshaw, Melissa, Cunha, Karin S., Cunningham, Mitch, D’Agostino, Maria D., Dahan, Karin, De Luca, Alessandro, Destrée, Anne, Dhamija, Radhika, Eoli, Marica, Evans, D. Gareth R., Galvin-Parton, Patricia, George-Abraham, Jaya K., Gripp, Karen W., Guevara-Campos, Jose, Hanchard, Neil A., Hernández-Chico, Concepcion, Immken, LaDonna, Janssens, Sandra, Jones, Kristi J., Keena, Beth A., Kochhar, Aaina, Liebelt, Jan, Martir-Negron, Arelis, Mahoney, Maurice J., Maystadt, Isabelle, McDougall, Carey, McEntagart, Meriel, Mendelsohn, Nancy, Miller, David T., Mortier, Geert, Morton, Jenny, Pappas, John, Plotkin, Scott R., Pond, Dinel, Rosenbaum, Kenneth, Rubin, Karol, Russell, Laura, Rutledge, Lane S., Saletti, Veronica, Schonberg, Rhonda, Schreiber, Allison, Seidel, Meredith, Siqveland, Elizabeth, Stockton, David W., Trevisson, Eva, Ullrich, Nicole J., Upadhyaya, Meena, van Minkelen, Rick, Verhelst, Helene, Wallace, Margaret R., Yap, Yoon-Sim, Zackai, Elaine, Zonana, Jonathan, Zurcher, Vickie, Claes, Kathleen, Martin, Yolanda, Korf, Bruce R., Legius, Eric, Messiaen, Ludwine M.

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    Epigenome-wide association studies identify novel DNA methylation sites associated with PTSD: a meta-analysis of 23 military and civilian cohorts by Katrinli, Seyma, Wani, Agaz H, Maihofer, Adam X, Ratanatharathorn, Andrew, Daskalakis, Nikolaos P, Montalvo-Ortiz, Janitza, Núñez-Ríos, Diana L, Zannas, Anthony S, Zhao, Xiang, Aiello, Allison E, Ashley-Koch, Allison E, Avetyan, Diana, Baker, Dewleen G, Beckham, Jean C, Boks, Marco P, Brick, Leslie A, Bromet, Evelyn, Champagne, Frances A, Chen, Chia-Yen, Dalvie, Shareefa, Dennis, Michelle F, Fatumo, Segun, Fortier, Catherine, Galea, Sandro, Garrett, Melanie E, Geuze, Elbert, Grant, Gerald, Hauser, Michael A, Hayes, Jasmeet P, Hemmings, Sian M J, Huber, Bertrand Russel, Jajoo, Aarti, Jansen, Stefan, Kessler, Ronald C, Kimbrel, Nathan A, King, Anthony P, Kleinman, Joel E, Koen, Nastassja, Koenen, Karestan C, Kuan, Pei-Fen, Liberzon, Israel, Linnstaedt, Sarah D, Lori, Adriana, Luft, Benjamin J, Luykx, Jurjen J, Marx, Christine E, McLean, Samuel A, Mehta, Divya, Milberg, William, Miller, Mark W, Mufford, Mary S, Musanabaganwa, Clarisse, Mutabaruka, Jean, Mutesa, Leon, Nemeroff, Charles B, Nugent, Nicole R, Orcutt, Holly K, Qin, Xue-Jun, Rauch, Sheila A M, Ressler, Kerry J, Risbrough, Victoria B, Rutembesa, Eugène, Rutten, Bart P F, Seedat, Soraya, Stein, Dan J, Stein, Murray B, Toikumo, Sylvanus, Ursano, Robert J, Uwineza, Annette, Verfaellie, Mieke H, Vermetten, Eric, Vinkers, Christiaan H, Ware, Erin B, Wildman, Derek E, Wolf, Erika J, Young, Ross McD, Zhao, Ying, van den Heuvel, Leigh L, Uddin, Monica, Nievergelt, Caroline M, Smith, Alicia K, Logue, Mark W

    Published in Genome medicine
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