TCF7L2 variants are associated with increased proinsulin/insulin ratios but not obesity traits in the Framingham Heart Study von Stolerman, E. S, Manning, A. K, McAteer, J. B, Fox, C. S, Dupuis, J, Meigs, J. B, Florez, J. C

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How can healthcare professionals assist in improving mothers’ health? von Bord, S, Inchi, L, Paldi, Y, Baruch, R, Stolerman, E, Schwartz Shpiro, M, Ronen, S, Eisenberg, L, Yaari, M

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Evaluation of the Beneficial Parenting Partnership Model Assimilation in Parent-Infant Centers von Bord, S, Paldi, Y, Baruch, R, Stolerman, E, Yeudai-Yadid, M, Zimmerman, D, Gens, I, Schuman Adatto, I, Yaari, M

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Increased degradation and altered tissue distribution of cartilage oligomeric matrix protein in human rheumatoid and osteoarthritic cartilage von Di Cesare, P E, Carlson, C S, Stolerman, E S, Hauser, N, Tulli, H, Paulsson, M

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Common Variants at 10 Genomic Loci Influence Hemoglobin A 1C Levels via Glycemic and Nonglycemic Pathways von Soranzo, N, Sanna, S, Wheeler, E, Gieger, C, Radke, D, Dupuis, J, Bouatia-Naji, N, Langenberg, C, Prokopenko, I, Stolerman, E

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Impaired performance of alpha7 nicotinic receptor knockout mice in the five-choice serial reaction time task von HOYLE, E, GENN, R. F, FERNANDES, C, STOLERMAN, I. P

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Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways von Soranzo, N, Sanna, S, Langenberg, C, Prokopenko, I, Stolerman, E, Sandhu, MS, Devaney, JM, Reilly, MP, Ricketts, SL, Stewart, AF, Arking, D, Balkau, B, Böhm, B, Bonnefond, A, Bonnycastle, LL, Bornstein, SR, Burnett-Miller, MS, Campbell, H, Cao, A, Chambers, J, Clark, R, Collins, FS, Deloukas, P, Egan, JM, Ferrucci, L, Forouhi, N, Fox, CS, Franzosi, MG, Goel, A, Grallert, H, Hadley, D, Hamsten, A, Hayward, C, Heath, S, Herder, C, Homuth, G, Hottenga, JJ, Hunter-Merrill, R, Illig, T, Jackson, AU, Kleber, M, Knouff, CW, Kooner, J, Köttgen, A, Kovacs, P, Kühnel, B, Lathrop, M, Loos, RJ, Mägi, R, Magnusson, PK, Mangino, M, McArdle, WL, McPherson, R, Meitinger, T, Melander, O, Mohlke, KL, Morken, MA, Nathan, DM, Oexle, K, Olla, N, Pankow, JS, Pedersen, NL, Peltonen, L, Perola, M, Polasek, O, Porcu, E, Rathmann, W, Rocheleau, G, Roden, M, Rudan, I, Salomaa, V, Schlessinger, D, Seedorf, U, Selvin, E, Serrano-Ríos, M, Shrader, P, Siscovick, D, Song, K, Spector, TD, Stefansson, K, Strawbridge, R, Stumvoll, M, Tanaka, T, Teumer, A, Thorsteinsdottir, U, Tönjes, A, Wallaschofski, H, Watkins, H, Wild, SH, Willemsen, G, Williams, GH, Wright, AF, Epstein, SE, Hakonarson, HH, Roberts, R, Fleming, MD, Sladek, R, Froguel, P, McCarthy, MI, Uda, M

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Molecular cloning, sequencing, and tissue and developmental expression of mouse cartilage oligomeric matrix protein (COMP) von Fang, Carrie, Carlson, Cathy S., Leslie, Michael P., Tulli, Hermina, Stolerman, Elliot, Perris, Roberto, Ni, Ligong, Di Cesare, Paul E.

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Non-benzodiazepine Hypnotics von Monti, Jaime M., Monti, Daniel

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Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways von Soranzo, Nicole, Sanna, Serena, Wheeler, Eleanor, Gieger, Christian, Radke, Dörte, Dupuis, Josée, Bouatia-Naji, Nabila, Langenberg, Claudia, Prokopenko, Inga, Stolerman, Elliot, Sandhu, Manjinder S, Heeney, Matthew M, Devaney, Joseph M, Reilly, Muredach P, Ricketts, Sally L, Stewart, Alexandre F R, Voight, Benjamin F, Willenborg, Christina, Wright, Benjamin, Altshuler, David, Arking, Dan, Balkau, Beverley, Barnes, Daniel, Boerwinkle, Eric, Böhm, Bernhard, Bonnefond, Amélie, Bonnycastle, Lori L, Boomsma, Dorret I, Bornstein, Stefan R, Böttcher, Yvonne, Bumpstead, Suzannah, Burnett-Miller, Mary Susan, Campbell, Harry, Cao, Antonio, Chambers, John, Clark, Robert, Collins, Francis S, Coresh, Josef, de Geus, Eco J C, Dei, Mariano, Deloukas, Panos, Döring, Angela, Egan, Josephine M, Elosua, Roberto, Ferrucci, Luigi, Forouhi, Nita, Fox, Caroline S, Franklin, Christopher, Franzosi, Maria Grazia, Gallina, Sophie, Goel, Anuj, Graessler, Jürgen, Grallert, Harald, Greinacher, Andreas, Hadley, David, Hall, Alistair, Hamsten, Anders, Hayward, Caroline, Heath, Simon, Herder, Christian, Homuth, Georg, Hottenga, Jouke-Jan, Hunter-Merrill, Rachel, Illig, Thomas, Jackson, Anne U, Jula, Antti, Kleber, Marcus, Knouff, Christopher W, Kong, Augustine, Kooner, Jaspal, Köttgen, Anna, Kovacs, Peter, Krohn, Knut, Kühnel, Brigitte, Kuusisto, Johanna, Laakso, Markku, Lathrop, Mark, Lecoeur, Cécile, Li, Man, Li, Mingyao, Loos, Ruth J F, Luan, Jian'an, Lyssenko, Valeriya, Mägi, Reedik, Magnusson, Patrik K E, Mälarstig, Anders, Mangino, Massimo, Martínez-Larrad, María Teresa, März, Winfried, McArdle, Wendy L, McPherson, Ruth, Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Mohlke, Karen L, Mooser, Vincent E, Morken, Mario A, Narisu, Narisu, Nathan, David M, Nauck, Matthias

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Pseudo-Hallucination

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Opiate

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Ultrasonic

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Developmental Toxicology

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Medial Prefrontal Cortex

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cAMP

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Egocentric

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Adenosine A1 Receptors

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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis von Mak, C.C.Y., Doherty, D., Lin, A.E., Vegas, N., Cho, M.T., Viot, G., Dimartino, C., Weisfeld-Adams, J.D., Lessel, D., Joss, S., Li, C.M., Gonzaga-Jauregui, C., Zarate, Y.A., Ehmke, N., Horn, D., Troyer, C., Kant, S.G., Lee, Y., Ishak, G.E., Leung, G., Pritchard, A.B., Yang, S., Bend, E.G., Filippini, F., Roadhouse, C., Lebrun, N., Mehaffey, M.G., Martin, P.M., Apple, B., Millan, F., Puk, O., Hoffer, M.J.V., Henderson, L.B., McGowan, R., Wentzensen, I.M., Pei, S., Zahir, F.R., Yu, M.L., Gibson, W.T., Seman, A., Steeves, M., Murrell, J.R., Luettgen, S., Francisco, E., Strom, T.M., Amlie-Wolf, L., Kaindl, A.M., Wilson, W.G., Halbach, S., Basel-Salmon, L., Lev-El, N., Denecke, J., Vissers, L.E.L.M., Radtke, K., Chelly, J., Zackai, E., Friedman, J.M., Bamshad, M.J., Nickerson, D.A., Reid, R.R., Devriendt, K., Chae, J.H., Stolerman, E., McDougall, C., Powis, Z., Bienvenu, T., Tan, T.Y., Orenstein, N., Dobyns, W.B., Shieh, J.T., Choi, M., Waggoner, D., Gripp, K.W., Parker, M.J., Stoler, J., Lyonnet, S., Cormier-Daire, V., Viskochil, D., Hoffman, T.L., Amiel, J., Chung, B.H.Y., Gordon, C.T.

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Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder von Kour, S, Rajan, DS, Fortuna, TR, Anderson, EN, Ward, C, Lee, Y, Lee, S, Shin, YB, Chae, J-H, Choi, M, Siquier, K, Cantagrel, V, Amiel, J, Stolerman, ES, Barnett, SS, Cousin, MA, Castro, D, McDonald, K, Kirmse, B, Nemeth, AH, Rajasundaram, D, Innes, AM, Lynch, D, Frosk, P, Collins, A, Gibbons, M, Yang, M, Desguerre, I, Boddaert, N, Gitiaux, C, Rydning, SL, Selmer, KK, Urreizti, R, Garcia-Oguiza, A, Osorio, AN, Verdura, E, Pujol, A, McCurry, HR, Landers, JE, Agnihotri, S, Andriescu, EC, Moody, SB, Phornphutkul, C, Sacoto, MJG, Begtrup, A, Houlden, H, Kirschner, J, Schorling, D, Rudnik-Schöneborn, S, Strom, TM, Leiz, S, Juliette, K, Richardson, R, Yang, Y, Zhang, Y, Wang, M, Wang, J, Wang, X, Platzer, K, Donkervoort, S, Bönnemann, CG, Wagner, M, Issa, MY, Elbendary, HM, Stanley, V, Maroofian, R, Gleeson, JG, Zaki, MS, Senderek, J, Pandey, UB

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