The challenge of response shift for quality-of-life-based clinical oncology research von Sprangers, M. A. G., Schwartz, C. E.

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A missense mutation, p.V132G, in the X-linked spermine synthase gene (SMS) causes Snyder-Robinson syndrome von Becerra-Solano, L.E., Butler, J., Castañeda-Cisneros, G., McCloskey, D.E., Wang, X., Pegg, A.E., Schwartz, C.E., Sánchez-Corona, J., García-Ortiz, J.E.

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Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system von Cristino, A S, Williams, S M, Hawi, Z, An, J-Y, Bellgrove, M A, Schwartz, C E, Costa, L da F, Claudianos, C

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A phenotype of early infancy predicts reactivity of the amygdala in male adults von Schwartz, C E, Kunwar, P S, Greve, D N, Kagan, J, Snidman, N C, Bloch, R B

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Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies von Bhat, S.S., Schmidt, K.R., Ladd, S., Kim, K.C., Schwartz, C.E., Simensen, R.J., DuPont, B.R., Stevenson, R.E., Srivastava, A.K.

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The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome von Shashi, V., Xie, P., Schoch, K., Goldstein, D.B., Howard, T.D., Berry, M.N., Schwartz, C.E., Cronin, K., Sliwa, S., Allen, A., Need, A.C.

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Total synthesis of Resolvin E1 von Allard, Melissa, Barnes, Keith, Chen, Xuemei, Cheung, Yiu-Yin, Duffy, Bryan, Heap, Charles, Inthavongsay, John, Johnson, Matthew, Krishnamoorthy, Ravi, Manley, Chris, Steffke, Stephan, Varughese, Deepu, Wang, Ruifang, Wang, Yi, Schwartz, C.E.

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Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X) von Basehore, M.J., Michaelson-Cohen, R., Levy-Lahad, E., Sismani, C., Bird, L.M., Friez, M.J., Walsh, T., Abidi, F., Holloway, L., Skinner, C., McGee, S., Alexandrou, A., Syrrou, M., Patsalis, P.C., Raymond, G., Wang, T., Schwartz, C.E., King, M.-C., Stevenson, R.E.

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Alpha‐thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation – c. 109C >T (p. R37X ) von Basehore, M.J., Michaelson‐Cohen, R., Levy‐Lahad, E., Sismani, C., Bird, L.M., Friez, M.J., Walsh, T., Abidi, F., Holloway, L., Skinner, C., McGee, S., Alexandrou, A., Syrrou, M., Patsalis, P.C., Raymond, G., Wang, T., Schwartz, C.E., King, M.‐C., Stevenson, R.E.

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Renpenning syndrome comes into focus von Stevenson, Roger E., Bennett, C.W., Abidi, F., Kleefstra, T., Porteous, M., Simensen, R.J., Lubs, H.A., Hamel, B.C.J., Schwartz, C.E.

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Corrigendum to “Total synthesis of resolvin E1” [Tetrahedron Lett. 52 (2011) 2623–2626] von Allard, Melissa, Barnes, Keith, Chen, Xuemei, Cheung, Yiu-Yin, Duffy, Bryan, Heap, Charles, Inthavongsay, John, Johnson, Matthew, Krishnamoorthy, Ravi, Liu, Xuejin, Manley, Chris, Shan, Zhixing, Steffke, Stephan, Varughese, Deepu, Wang, Ruifang, Wang, Yi, Yang, Qiang, Schwartz, C.E.

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Phenotype and genotype in 101 males with X-linked creatine transporter deficiency von van de Kamp, J.M, Betsalel, O.T, Mercimek-Mahmutoglu, S, Abulhoul, L, Grünewald, S, Anselm, I, Azzouz, H, Bratkovic, D, de Brouwer, A, Hamel, B, Kleefstra, T, Yntema, H, Campistol, J, Vilaseca, M.A, Cheillan, D, D'Hooghe, M, Diogo, L, Garcia, P, Valongo, C, Fonseca, M, Frints, S, Wilcken, B, von der Haar, S, Meijers-Heijboer, H.E, Hofstede, F, Johnson, D, Kant, S.G, Lion-Francois, L, Pitelet, G, Longo, N, Maat-Kievit, J.A, Monteiro, J.P, Munnich, A, Muntau, A.C, Nassogne, M.C, Osaka, H, Ounap, K, Pinard, J.M, Quijano-Roy, S, Poggenburg, I, Poplawski, N, Abdul-Rahman, O, Ribes, A, Arias, A, Yaplito-Lee, J, Schulze, A, Schwartz, C.E, Schwenger, S, Soares, G, Sznajer, Y, Valayannopoulos, V, Van Esch, Hilde, Waltz, S, Wamelink, M.M.C, Pouwels, P.J.W, Errami, A, van der Knaap, M.S, Jakobs, C, Mancini, G.M, Salomons, G.S

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Factors associated with openness to research par&ticipation in an aging community:The importance of technophilia and social cohesion von Steinerman, J.R., Lipton, R.B., Rapkin, B.D., Quaranto, B.R., Schwartz, C.E.

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Personality Correlates of Amygdala Response to Masked Fear and Novelty von Reynolds, G.O., Saygin, Z.M., Sabhlok, S.R., Richey, T., Song, S.S., Shah, A.M., Hofmann, S.G., Pollack, M.T., Schwartz, C.E., Gabrieli, J.D., Polli, F.E.

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Mutation analysis of the tumor suppressor PTEN and the glypican 3 (GPC3) gene in patients diagnosed with Proteus syndrome von Thiffault, I., Schwartz, C.E., Der Kaloustian, V., Foulkes, W.D.

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Abnormal amygdala response to face and object novelty in social anxiety disorder von Saygin, Z.M., Sabhlok, S.R., Reynolds, G.O., Richey, J.A., Song, S.S., Shah, A.M., Hofmann, S.G., Pollack, M.T., Schwartz, C.E., DE Gabrieli, J., Polli, F.E.

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Clinical and molecular contributions to the understanding of X-linked mental retardation von Stevenson, R.E., Schwartz, C.E.

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A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58 von Abidi, F E, Holinski-Feder, E, Rittinger, O, Kooy, F, Lubs, H A, Stevenson, R E, Schwartz, C E

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SRPK3 Is essential for cognitive and ocular development in humans and zebrafish, explaining X-linked intellectual disability von Roychaudhury, A, Lee, Y, Choi, T, Thomas, M.G, Khan, T.N, Yousaf, H, Skinner, C, Maconachie, G, Crosier, M, Horak, H, Constantinescu, C.S, Kim, T, Lee, K, Kyung, J, Wang, T, Ku, B, Chodirker, B.N, Hammer, M.F, Gottlob, I, Norton, W.H.J, Gerlai, R, Kim, H, Graziano, C, Pippucci, T, Iovino, E, Montanari, F, Severi, G, Toro, C, Boerkoel, C.F, Cha, H.S, Choi, C.Y, Kim, S, Yoon, J, Gilmore, K, Vora, N.L, Davis, E.E, Chudley, A.E, Schwartz, C.E, Kim, C

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P63 mutations are not a major cause of non-syndromic split hand/foot malformation von de Mollerat, X J, Everman, D B, Morgan, C T, Clarkson, K B, Rogers, R C, Colby, R S, Aylsworth, A S, Graham, J M, Stevenson, R E, Schwartz, C E

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