Search Results - "MOORE, G. E"

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

“…The present guide provides a practical guide to conducting latent profile analysis (LPA) in the Mplus software system. This guide is intended for researchers…”
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On the Joys of Missing Data by LITTLE, Todd D, JORGENSEN, Terrence D, LANG, Kyle M, MOORE, E. Whitney G

“…We provide conceptual introductions to missingness mechanisms--missing completely at random, missing at random, and missing not at random--and state-of-the-art…”
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A retrospective comparison of the biceps femoris long head muscle structure in athletes with and without hamstring strain injury history by Yagiz, Gokhan, Fredianto, Meiky, Ulfa, Maria, Ariani, Indira, Agustin, Avika Dwi, Shida, Nami, Moore, E Whitney G, Kubis, Hans-Peter

“…Hamstring strain injuries (HSI) and re-injuries are endemic in high-speed running sports. The biceps femoris long head (BFlh) is the most frequently injured…”
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Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy by 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-A, Marschall, H-U, Molokhia, M, Moore, G E, Linton, K J, Williamson, C

“…Intrahepatic cholestasis of pregnancy (ICP) has a complex aetiology with a significant genetic component. ABCB11 encodes the bile salt export pump (BSEP);…”
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Effects of a large-scale, natural sediment deposition event on plant cover in a Massachusetts salt marsh by Moore, G E, Burdick, D M, Routhier, M R, Novak, A B, Payne, A R

“…In mid-winter 2018, an unprecedented sediment deposition event occurred throughout portions of the Great Marsh in Massachusetts. Evaluation of this event in…”
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Factor Structure of the Barriers to Physical Activity Scale for Youth With Visual Impairments by Martin, Jeffrey J, Snapp, Erin E, G Moore, E Whitney, Lieberman, Lauren J, Armstrong, Ellen, Mannella, Staci

“…Youth with visual impairments (VIs) often experience unique barriers to physical activity compared with their sighted peers. A psychometrically sound scale for…”
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Limited Evolutionary Conservation of Imprinting in the Human Placenta by Monk, D., Arnaud, P., Apostolidou, S., Hills, F. A., Kelsey, G., Stanier, P., Feil, R., Moore, G. E.

“…The epigenetic phenomenon of genomic imprinting provides an additional level of gene regulation that is confined to a limited number of genes, frequently, but…”
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The genetic aetiology of Silver-Russell syndrome by Abu-Amero, S, Monk, D, Frost, J, Preece, M, Stanier, P, Moore, G E

“…Silver-Russell syndrome (SRS MIM180860) is a disorder characterised by intrauterine and/or postnatal growth restriction and typical facies. However, the…”
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Exploring classroom teachers’ efficacy towards implementing physical activity breaks in the classroom by McKown, Hayley B, Centeio, Erin E, Barcelona, Jeanne M, Pedder, Christine, Whitney G Moore, E, Erwin, Heather E

“…Objective: The purpose of this study was to determine classroom teachers’ self-efficacy towards, and perceptions of, physical activity in the classroom…”
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Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations by Kantaputra, P.N., Paramee, M., Kaewkhampa, A., Hoshino, A., Lees, M., McEntagart, M., Masrour, N., Moore, G.E., Pauws, E., Stanier, P.

“…X-linked cleft palate and ankyloglossia (CPX) are caused by mutations in the TBX22 transcription factor. To investigate whether patients with ankyloglossia…”
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2010 ACVIM Small Animal Consensus Statement on Leptospirosis: Diagnosis, Epidemiology, Treatment, and Prevention by Sykes, J.E, Hartmann, K, Lunn, K.F, Moore, G.E, Stoddard, R.A, Goldstein, R.E

“…This report offers a consensus opinion on the diagnosis, epidemiology, treatment, and prevention of leptospirosis in dogs, an important zoonosis. Clinical…”
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Genome-wide methylation analysis in Silver–Russell syndrome patients by 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.

“…Silver–Russell syndrome (SRS) is a clinically heterogeneous disorder characterised by severe in utero growth restriction and poor postnatal growth, body…”
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Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem-cell phenotype by Kinsler, V.A., Anderson, G., Latimer, B., Natarajan, D., Healy, E., Moore, G.E., Sebire, N.J.

“…Summary Background Multiple congenital melanocytic naevi (CMN) in one individual are caused by somatic mosaicism for NRAS mutations; however, the lineage of…”
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Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight by 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

“…The identification of genes that regulate fetal growth will help establish the reasons for intrauterine growth restriction. Most autosomal genes are expressed…”
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Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human by 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.

“…Genomic imprinting is limited to a subset of genes that play critical roles in fetal growth, development and behaviour. One of the most studied imprinted genes…”
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A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly by 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.

“…Neural tube defects (NTDs) affecting the brain (anencephaly) are lethal before or at birth, whereas lower spinal defects (spina bifida) may lead to lifelong…”
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Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family by 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.

“…This study investigated the genetic basis of an unusual autosomal dominant phenotype characterized by familial absent uvula, with a short posterior border of…”
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A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia by Pauws, E, Moore, G E, Stanier, P

“…Mutations in the T-box transcription factor gene TBX22 are found in patients with X-linked cleft palate and ankyloglossia (CPX), and are reported in…”
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A novel item-allocation procedure for the three-form planned missing data design by Lang, Kyle M., Moore, E. Whitney G., Grandfield, Elizabeth M.

“…We propose a new method of constructing questionnaire forms in the three-form planned missing data design (PMDD). The random item allocation (RIA) procedure…”
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The Association Between Sexual Initiation and Membership in Dyadic Profiles of Perceived Shared Power by Hanna-Walker, Veronica, Busby, Dean M., Moore, E. Whitney G., Holmes, Erin K.

“…There is scarce empirical evidence examining whether sexual initiation and power are associated with each other. Utilizing latent profile analyses, we examined…”
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