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Finding latent groups in observed data: A primer on latent profile analysis in Mplus for applied researchers

International journal of behavioral development, 2020-09, Vol.44 (5), p.458-468

2020

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On the Joys of Missing Data

Journal of pediatric psychology, 2014-03, Vol.39 (2), p.151-162

2014

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A retrospective comparison of the biceps femoris long head muscle structure in athletes with and without hamstring strain injury history

PloS one, 2024-02, Vol.19 (2), p.e0298146-e0298146

2024

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Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy

Gut, 2009-04, Vol.58 (4), p.537-544

2009

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Effects of a large-scale, natural sediment deposition event on plant cover in a Massachusetts salt marsh

PloS one, 2021-01, Vol.16 (1), p.e0245564-e0245564

2021

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Dinuclear triple stranded phenyl-spaced 1,3-bis-β-diketonato lanthanide() complexes: synthesis, structures and spectroscopy

Dalton transactions : an international journal of inorganic chemistry, 2021-04, Vol.5 (14), p.4874-4879

2021

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Limited Evolutionary Conservation of Imprinting in the Human Placenta

Proceedings of the National Academy of Sciences - PNAS, 2006-04, Vol.103 (17), p.6623-6628

2006

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Factor Structure of the Barriers to Physical Activity Scale for Youth With Visual Impairments

Adapted physical activity quarterly, 2021-10, Vol.38 (4), p.585

2021

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2010 ACVIM Small Animal Consensus Statement on Leptospirosis: Diagnosis, Epidemiology, Treatment, and Prevention

Journal of veterinary internal medicine, 2011-01, Vol.25 (1), p.1-13

2011

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The genetic aetiology of Silver–Russell syndrome

Journal of medical genetics, 2008-04, Vol.45 (4), p.193-199

2008

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Exploring classroom teachers’ efficacy towards implementing physical activity breaks in the classroom

Health education journal, 2022-08, Vol.81 (5), p.585-596

2022

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Epigenotype–phenotype correlations in Silver–Russell syndrome

Journal of medical genetics, 2010-11, Vol.47 (11), p.760-768

2010

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Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations

Journal of dental research, 2011-04, Vol.90 (4), p.450-455

2011

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Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem-cell phenotype

British journal of dermatology (1951), 2013-08, Vol.169 (2), p.374-383

2013

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Genome-wide methylation analysis in Silver–Russell syndrome patients

Human genetics, 2015-03, Vol.134 (3), p.317-332

2015

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Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family

Journal of dental research, 2019-06, Vol.98 (6), p.659-665

2019

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Environmental Exposures and Airway Inflammation in Young Thoroughbred Horses

Journal of veterinary internal medicine, 2014-05, Vol.28 (3), p.918-924

2014

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Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human

Human molecular genetics, 2006-04, Vol.15 (8), p.1259-1269

2006

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A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly

Clinical genetics, 2018-04, Vol.93 (4), p.870-879

2018

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Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

Journal of molecular medicine (Berlin, Germany), 2007-04, Vol.85 (4), p.379-387

2007

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The Association Between Sexual Initiation and Membership in Dyadic Profiles of Perceived Shared Power

Archives of sexual behavior, 2024-03, Vol.53 (3), p.1091-1105

2024

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A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia

Journal of medical genetics, 2009-08, Vol.46 (8), p.555-561

2009

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A novel item-allocation procedure for the three-form planned missing data design

MethodsX, 2020-01, Vol.7, p.100941-100941, Article 100941

2020

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Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss‐of‐function vs missense variants

Clinical genetics, 2017-05, Vol.91 (5), p.683-689

2017

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Physical education students' ownership, empowerment, and satisfaction with PE and physical activity

Research quarterly for exercise and sport, 2017-10, Vol.88 (4), p.468-478

2017

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Finding latent groups in observed data: A primer on latent profile analysis in Mplus for applied researchers

On the Joys of Missing Data

A retrospective comparison of the biceps femoris long head muscle structure in athletes with and without hamstring strain injury history

Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy

Effects of a large-scale, natural sediment deposition event on plant cover in a Massachusetts salt marsh

Dinuclear triple stranded phenyl-spaced 1,3-bis-β-diketonato lanthanide() complexes: synthesis, structures and spectroscopy

Limited Evolutionary Conservation of Imprinting in the Human Placenta

Factor Structure of the Barriers to Physical Activity Scale for Youth With Visual Impairments

2010 ACVIM Small Animal Consensus Statement on Leptospirosis: Diagnosis, Epidemiology, Treatment, and Prevention

The genetic aetiology of Silver–Russell syndrome

Exploring classroom teachers’ efficacy towards implementing physical activity breaks in the classroom

Epigenotype–phenotype correlations in Silver–Russell syndrome

Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations

Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem-cell phenotype

Genome-wide methylation analysis in Silver–Russell syndrome patients

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family

Environmental Exposures and Airway Inflammation in Young Thoroughbred Horses

Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

The Association Between Sexual Initiation and Membership in Dyadic Profiles of Perceived Shared Power

A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia

A novel item-allocation procedure for the three-form planned missing data design

Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss‐of‐function vs missense variants

Physical education students' ownership, empowerment, and satisfaction with PE and physical activity

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