Understanding Performance and Learning in Consistent Memory Search: An Age-Related Perspective von Fisk, Arthur D, Cooper, Brian P, Hertzog, Christopher, Anderson-Garlach, Marjo M, Lee, Mark D

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Age-Related Effects in Consistent Memory Search: Performance is the Same but What about Learning? von Cooper, Brian P., Lee, Mark D., Goska, Robert E., Anderson, Marjo M., Gay, Paul E., Fickes, Lynne Ann, Fisk, Arthur D.

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Evidence of direction loss in elderly movement preparation is not due to spatial orienting effects von Amrhein, Paul C., Dras, Dean Von, Anderson, Marjo

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Long-Term Retention of Skilled Visual Search: Do Young Adults Retain More Than Old Adults? von Fisk, Arthur D, Hertzog, Christopher, Lee, Mark D, Rogers, Wendy A, Anderson-Garlach, Marjo

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The American census - a social history von Anderson, Marjo J, Melnick, Daniel

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The Politics of Numbers von Melnick, Daniel

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High throughput screening of technological and biopreservation traits of a large set of wild lactic acid bacteria from Brazilian artisanal cheeses von Margalho, Larissa P., Kamimura, Bruna A., Brexó, Ramon P., Alvarenga, Verônica O., Cebeci, Alp Sabri, Janssen, Patrick W.M., Dijkstra, Annereinou, Starrenburg, Marjo J.C., Sheombarsing, Reshtrie S., Cruz, Adriano G., Alkema, Wynand, Bachmann, Herwig, Sant’Ana, Anderson S.

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Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age von Merid, Simon Kebede, Novoloaca, Alexei, Sharp, Gemma C, Küpers, Leanne K, Kho, Alvin T, Roy, Ritu, Gao, Lu, Annesi-Maesano, Isabella, Jain, Pooja, Plusquin, Michelle, Kogevinas, Manolis, Allard, Catherine, Vehmeijer, Florianne O, Kazmi, Nabila, Salas, Lucas A, Rezwan, Faisal I, Zhang, Hongmei, Sebert, Sylvain, Czamara, Darina, Rifas-Shiman, Sheryl L, Melton, Phillip E, Lawlor, Debbie A, Pershagen, Göran, Breton, Carrie V, Huen, Karen, Baiz, Nour, Gagliardi, Luigi, Nawrot, Tim S, Corpeleijn, Eva, Perron, Patrice, Duijts, Liesbeth, Nohr, Ellen Aagaard, Bustamante, Mariona, Ewart, Susan L, Karmaus, Wilfried, Zhao, Shanshan, Page, Christian M, Herceg, Zdenko, Jarvelin, Marjo-Riitta, Lahti, Jari, Baccarelli, Andrea A, Anderson, Denise, Kachroo, Priyadarshini, Relton, Caroline L, Bergström, Anna, Eskenazi, Brenda, Soomro, Munawar Hussain, Vineis, Paolo, Snieder, Harold, Bouchard, Luigi, Jaddoe, Vincent W, Sørensen, Thorkild I A, Vrijheid, Martine, Arshad, S Hasan, Holloway, John W, Håberg, Siri E, Magnus, Per, Dwyer, Terence, Binder, Elisabeth B, DeMeo, Dawn L, Vonk, Judith M, Newnham, John, Tantisira, Kelan G, Kull, Inger, Wiemels, Joseph L, Heude, Barbara, Sunyer, Jordi, Nystad, Wenche, Munthe-Kaas, Monica C, Räikkönen, Katri, Oken, Emily, Huang, Rae-Chi, Weiss, Scott T, Antó, Josep Maria, Bousquet, Jean, Kumar, Ashish, Söderhäll, Cilla, Almqvist, Catarina, Cardenas, Andres, Gruzieva, Olena, Xu, Cheng-Jian, Reese, Sarah E, Kere, Juha, Brodin, Petter, Solomon, Olivia, Wielscher, Matthias, Holland, Nina, Ghantous, Akram, Hivert, Marie-France, Felix, Janine F, Koppelman, Gerard H, London, Stephanie J, Melén, Erik

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A new Finnish flavor of feline coat coloration, “salmiak,” is associated with a 95‐kb deletion downstream of the KIT gene von Anderson, Heidi, Salonen, Milla, Toivola, Sari, Blades, Matthew, Lyons, Leslie A., Forman, Oliver P., Hytönen, Marjo K., Lohi, Hannes

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Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders von Donner, Jonas, Kaukonen, Maria, Anderson, Heidi, Möller, Fredrik, Kyöstilä, Kaisa, Sankari, Satu, Hytönen, Marjo, Giger, Urs, Lohi, Hannes

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A novel complex neurological phenotype due to a homozygous mutation in FDX2 von Gurgel-Giannetti, Juliana, Lynch, David S, Paiva, Anderson Rodrigues Brandão de, Lucato, Leandro Tavares, Yamamoto, Guilherme, Thomsen, Christer, Basu, Somsuvro, Freua, Fernando, Giannetti, Alexandre Varella, de Assis, Bruno Della Ripa, Ribeiro, Mara Dell Ospedale, Barcelos, Isabella, Sayão Souza, Katiane, Monti, Fernanda, Melo, Uirá Souto, Amorim, Simone, Silva, Leonardo G L, Macedo-Souza, Lúcia Inês, Vianna-Morgante, Angela M, Hirano, Michio, Van der Knaap, Marjo S, Lill, Roland, Vainzof, Mariz, Oldfors, Anders, Houlden, Henry, Kok, Fernando

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Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations von Sakornsakolpat, Phuwanat, Prokopenko, Dmitry, Lamontagne, Maxime, Reeve, Nicola F., Guyatt, Anna L., Jackson, Victoria E., Shrine, Nick, Qiao, Dandi, Bartz, Traci M., Kim, Deog Kyeom, Lee, Mi Kyeong, Latourelle, Jeanne C., Li, Xingnan, Morrow, Jarrett D., Obeidat, Ma’en, Wyss, Annah B., Bakke, Per, Barr, R. Graham, Beaty, Terri H., Belinsky, Steven A., Brusselle, Guy G., Crapo, James D., de Jong, Kim, DeMeo, Dawn L., Fingerlin, Tasha E., Gharib, Sina A., Gulsvik, Amund, Hall, Ian P., Hokanson, John E., Kim, Woo Jin, Lomas, David A., London, Stephanie J., Meyers, Deborah A., O’Connor, George T., Rennard, Stephen I., Schwartz, David A., Sliwinski, Pawel, Sparrow, David, Strachan, David P., Tal-Singer, Ruth, Tesfaigzi, Yohannes, Vestbo, Jørgen, Vonk, Judith M., Yim, Jae-Joon, Zhou, Xiaobo, Bossé, Yohan, Manichaikul, Ani, Lahousse, Lies, Silverman, Edwin K., Boezen, H. Marike, Wain, Louise V., Tobin, Martin D., Hobbs, Brian D., Cho, Michael H.

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Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin von Bolton, Jennifer L, Hayward, Caroline, Direk, Nese, Lewis, John G, Hammond, Geoffrey L, Hill, Lesley A, Anderson, Anna, Huffman, Jennifer, Wilson, James F, Campbell, Harry, Rudan, Igor, Wright, Alan, Hastie, Nicholas, Wild, Sarah H, Velders, Fleur P, Hofman, Albert, Uitterlinden, Andre G, Lahti, Jari, Räikkönen, Katri, Kajantie, Eero, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G, Kaakinen, Marika, Järvelin, Marjo-Riitta, Timpson, Nicholas J, Davey Smith, George, Ring, Susan M, Evans, David M, St Pourcain, Beate, Tanaka, Toshiko, Milaneschi, Yuri, Bandinelli, Stefania, Ferrucci, Luigi, van der Harst, Pim, Rosmalen, Judith G M, Bakker, Stephen J L, Verweij, Niek, Dullaart, Robin P F, Mahajan, Anubha, Lindgren, Cecilia M, Morris, Andrew, Lind, Lars, Ingelsson, Erik, Anderson, Laura N, Pennell, Craig E, Lye, Stephen J, Matthews, Stephen G, Eriksson, Joel, Mellstrom, Dan, Ohlsson, Claes, Price, Jackie F, Strachan, Mark W J, Reynolds, Rebecca M, Tiemeier, Henning, Walker, Brian R

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The age and position of the southern boundary of prehistoric Polynesian dispersal von Anderson, Atholl, Becerra‐Valdivia, Lorena, Cadd, Haidee, Marjo, Christopher E., Palmer, Jonathan, Turney, Chris, Wilmshurst, Janet M.

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Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus von Anderson, Beverley H, Kasher, Paul R, Mayer, Josephine, Szynkiewicz, Marcin, Jenkinson, Emma M, Bhaskar, Sanjeev S, Urquhart, Jill E, Daly, Sarah B, Dickerson, Jonathan E, O'Sullivan, James, Leibundgut, Elisabeth Oppliger, Muter, Joanne, Abdel-Salem, Ghada M H, Babul-Hirji, Riyana, Baxter, Peter, Berger, Andrea, Bonafé, Luisa, Brunstom-Hernandez, Janice E, Buckard, Johannes A, Chitayat, David, Chong, Wui K, Cordelli, Duccio M, Ferreira, Patrick, Fluss, Joel, Forrest, Ewan H, Franzoni, Emilio, Garone, Caterina, Hammans, Simon R, Houge, Gunnar, Hughes, Imelda, Jacquemont, Sebastien, Jeannet, Pierre-Yves, Jefferson, Rosalind J, Kumar, Ram, Kutschke, Georg, Lundberg, Staffan, Lourenço, Charles M, Mehta, Ramesh, Naidu, Sakkubai, Nischal, Ken K, Nunes, Luís, Õunap, Katrin, Philippart, Michel, Prabhakar, Prab, Risen, Sarah R, Schiffmann, Raphael, Soh, Calvin, Stephenson, John B P, Stewart, Helen, Stone, Jon, Tolmie, John L, van der Knaap, Marjo S, Vieira, Jose P, Vilain, Catheline N, Wakeling, Emma L, Wermenbol, Vanessa, Whitney, Andrea, Lovell, Simon C, Meyer, Stefan, Livingston, John H, Baerlocher, Gabriela M, Black, Graeme C M, Rice, Gillian I, Crow, Yanick J

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A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies von Joo, Yoonjung Yoonie, Actkins, Ky’Era, Pacheco, Jennifer A, Basile, Anna O, Carroll, Robert, Crosslin, David R, Day, Felix, Denny, Joshua C, Velez Edwards, Digna R, Hakonarson, Hakon, Harley, John B, Hebbring, Scott J, Ho, Kevin, Jarvik, Gail P, Jones, Michelle, Karaderi, Tugce, Mentch, Frank D, Meun, Cindy, Namjou, Bahram, Pendergrass, Sarah, Ritchie, Marylyn D, Stanaway, Ian B, Urbanek, Margrit, Walunas, Theresa L, Smith, Maureen, Chisholm, Rex L, Kho, Abel N, Davis, Lea, Hayes, M Geoffrey

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Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes von Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste, Witt, Stephanie H., Binz, Tina M., McGrath, John, Hickie, Ian B., Hansell, Narelle K., Wright, Margaret J., Gillespie, Nathan A., Forstner, Andreas J., Schulze, Thomas G, Wüst, Stefan, Nöthen, Markus M., Baumgartner, Markus R., Walker, Brian R., Crawford, Andrew A., Colodro-Conde, Lucía, Medland, Sarah E., Martin, Nicholas G., Rietschel, Marcella

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Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2 von Neilson, Derek E., Adams, Mark D., Orr, Caitlin M.D., Schelling, Deborah K., Eiben, Robert M., Kerr, Douglas S., Anderson, Jane, Bassuk, Alexander G., Bye, Ann M., Childs, Anne-Marie, Clarke, Antonia, Crow, Yanick J., Di Rocco, Maja, Dohna-Schwake, Christian, Dueckers, Gregor, Fasano, Alfonso E., Gika, Artemis D., Gionnis, Dimitris, Gorman, Mark P., Grattan-Smith, Padraic J., Hackenberg, Annette, Kuster, Alice, Lentschig, Markus G., Lopez-Laso, Eduardo, Marco, Elysa J., Mastroyianni, Sotiria, Perrier, Julie, Schmitt-Mechelke, Thomas, Servidei, Serenella, Skardoutsou, Angeliki, Uldall, Peter, van der Knaap, Marjo S., Goglin, Karrie C., Tefft, David L., Aubin, Cristin, de Jager, Philip, Hafler, David, Warman, Matthew L.

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Poly( β-amino ester)–DNA complexes: Time-resolved fluorescence and cellular transfection studies von Vuorimaa, Elina, Ketola, Tiia-Maaria, Green, Jordan J., Hanzlíková, Martina, Lemmetyinen, Helge, Langer, Robert, Anderson, Daniel G., Urtti, Arto, Yliperttula, Marjo

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Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight von Kupers, Leanne K, Monnereau, Claire, Sharp, Gemma C, Yousefi, Paul, Salas, Lucas A, Ghantous, Akram, Page, Christian M, Reese, Sarah E, Wilcox, Allen J, Czamara, Darina, Starling, Anne P, Novoloaca, Alexei, Lent, Samantha, Roy, Ritu, Hoyo, Cathrine, Breton, Carrie, Allard, Catherine, Just, Allan C, Bakulski, Kelly M, Holloway, John W, Everson, Todd M, Xu, Cheng-Jian, Huang, Rae-Chi, van der Plaat, Diana A, Wielscher, Matthias, Merid, Simon Kebede, Ullemar, Vilhelmina, Rezwan, Faisal, Lahti, Jari, van Dongen, Jenny, Langie, Sabine A.S, Richardson, Tom G, Magnus, Maria C, Nohr, Ellen A, Xu, Zongli, Duijts, Liesbeth, Zhao, Shanshan, Zhang, Weiming, Plusquin, Michelle, DeMeo, Dawn L, Solomon, Olivia, Heimovaara, Joosje H, Jima, Dereje D, Gao, Lu, Bustamante, Mariona, Perron, Patrice, Wright, Robert O, Hertz-Picciotto, Irva, Zhang, Hongmei, Karagas, Margaret R, Gehring, Ulrike, Marsit, Carmen J, Beilin, Lawrence J, Vonk, Judith M, Jarvelin, Marjo-Riitta, Bergstrom, Anna, Ortqvist, Anne K, Ewart, Susan, Villa, Pia M, Moore, Sophie E, Willemsen, Gonneke, Standaert, Arnout R.L, Haberg, Siri E, Sorensen, Thorkild I.A, Taylor, Jack A, Raikkonen, Katri, Yang, Ivana, Kechris, Katerina, Nawrot, Tim S, Silver, Matt J, Gong, Yun Yun, Richiardi, Lorenzo, Kogevinas, Manolis, Litonjua, Augusto A, Eskenazi, Brenda, Huen, Karen, Mbarek, Hamdi, Maguire, Rachel L, Dwyer, Terence, Vrijheid, Martine, Bouchard, Luigi, Baccarelli, Andrea A, Croen, Lisa A, Karmaus, Wilfried, Anderson, Denise, de Vries, Maaike, Sebert, Sylvain, Kere, Juha, Karlsson, Robert, Arshad, Syed Hasan, Hamalainen, Esa, Routledge, Michael N, Boomsma, Dorret, Feinberg, Andrew P, Newschaffer, Craig J, Govarts, Eva, Moisse, Matthieu, Fallin, M. Daniele, Melen, Erik, Prentice, Andrew M

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