Finding latent groups in observed data: A primer on latent profile analysis in Mplus for applied researchers von Ferguson, Sarah L., G. Moore, E. Whitney, Hull, Darrell M.

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On the Joys of Missing Data von LITTLE, Todd D, JORGENSEN, Terrence D, LANG, Kyle M, MOORE, E. Whitney G

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A retrospective comparison of the biceps femoris long head muscle structure in athletes with and without hamstring strain injury history von Yagiz, Gokhan, Fredianto, Meiky, Ulfa, Maria, Ariani, Indira, Agustin, Avika Dwi, Shida, Nami, Moore, E Whitney G, Kubis, Hans-Peter

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Effects of a large-scale, natural sediment deposition event on plant cover in a Massachusetts salt marsh von Moore, G E, Burdick, D M, Routhier, M R, Novak, A B, Payne, A R

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Dinuclear triple stranded phenyl-spaced 1,3-bis-β-diketonato lanthanide() complexes: synthesis, structures and spectroscopy von Brock, A. J, Etchells, I. M, Moore, E. G, Clegg, J. K

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Limited Evolutionary Conservation of Imprinting in the Human Placenta von Monk, D., Arnaud, P., Apostolidou, S., Hills, F. A., Kelsey, G., Stanier, P., Feil, R., Moore, G. E.

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Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy von Dixon, P H, van Mil, S W C, Chambers, J, Strautnieks, S, Thompson, R J, Lammert, F, Kubitz, R, Keitel, V, Glantz, A, Mattsson, L-Å, Marschall, H-U, Molokhia, M, Moore, G E, Linton, K J, Williamson, C

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2010 ACVIM Small Animal Consensus Statement on Leptospirosis: Diagnosis, Epidemiology, Treatment, and Prevention von Sykes, J.E, Hartmann, K, Lunn, K.F, Moore, G.E, Stoddard, R.A, Goldstein, R.E

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Exploring classroom teachers’ efficacy towards implementing physical activity breaks in the classroom von McKown, Hayley B, Centeio, Erin E, Barcelona, Jeanne M, Pedder, Christine, Whitney G Moore, E, Erwin, Heather E

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The genetic aetiology of Silver–Russell syndrome von Abu-Amero, S, Monk, D, Frost, J, Preece, M, Stanier, P, Moore, G E

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Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations von Kantaputra, P.N., Paramee, M., Kaewkhampa, A., Hoshino, A., Lees, M., McEntagart, M., Masrour, N., Moore, G.E., Pauws, E., Stanier, P.

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Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem-cell phenotype von Kinsler, V.A., Anderson, G., Latimer, B., Natarajan, D., Healy, E., Moore, G.E., Sebire, N.J.

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Genome-wide methylation analysis in Silver–Russell syndrome patients von Prickett, A. R., Ishida, M., Böhm, S., Frost, J. M., Puszyk, W., Abu-Amero, S., Stanier, P., Schulz, R., Moore, G. E., Oakey, R. J.

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Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family von Seselgyte, R., Bryant, D., Demetriou, C., Ishida, M., Peskett, E., Moreno, N., Morrogh, D., Sell, D., Lees, M., Farrall, M., Moore, G.E., Sommerlad, B., Pauws, E., Stanier, P.

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A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly von Ishida, M., Cullup, T., Boustred, C., James, C., Docker, J., English, C., Lench, N., Copp, A.J., Moore, G.E., Greene, N.D.E., Stanier, P.

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Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human von Monk, D., Sanches, R., Arnaud, P., Apostolidou, S., Hills, F.A., Abu-Amero, S., Murrell, A., Friess, H., Reik, W., Stanier, P., Constância, M., Moore, G.E.

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The Association Between Sexual Initiation and Membership in Dyadic Profiles of Perceived Shared Power von Hanna-Walker, Veronica, Busby, Dean M., Moore, E. Whitney G., Holmes, Erin K.

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Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight von APOSTOLIDOU, S, ABU-AMERO, S, O'DONOGHUE, K, FROST, J, OLAFSDOTTIR, O, CHAVELE, K. M, WHITTAKER, J. C, LOUGHNA, P, STANIER, P, MOORE, G. E

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A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia von Pauws, E, Moore, G E, Stanier, P

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Bertrand Russell’s Principles of Mathematics [introductory paragraph] von Moore, G. E

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