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Ellen A. van der Plas, Ph.D. - Publications

Affiliations: 
2011 Neuroscience University of Iowa, Iowa City, IA 
Area:
Neuroscience Biology, Human Development, Developmental Psychology
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25 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Koscik TR, van der Plas E, Long JD, Cross S, Gutmann L, Cumming SA, Monckton DG, Shields RK, Magnotta V, Nopoulos PC. Longitudinal changes in white matter as measured with diffusion tensor imaging in adult-onset myotonic dystrophy type 1. Neuromuscular Disorders : Nmd. PMID 37419717 DOI: 10.1016/j.nmd.2023.05.010  0.583
2023 Zhang L, Guo Z, Zhang H, van der Plas E, Koscik TR, Nopoulos PC, Sonka M. Assisted annotation in Deep LOGISMOS: Simultaneous multi-compartment 3D MRI segmentation of calf muscles. Medical Physics. PMID 36750977 DOI: 10.1002/mp.16284  0.563
2022 Schultz JL, Langbehn DR, Al-Kaylani HM, van der Plas E, Koscik TR, Epping EA, Espe-Pfeifer PB, Martin EP, Moser DJ, Magnotta VA, Nopoulos PC. Longitudinal Clinical and Biological Characteristics in Juvenile-Onset Huntington's Disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36318082 DOI: 10.1002/mds.29251  0.587
2022 Schultz JL, Epping EA, van der Plas E, Magnotta VA, Nopoulos PC. Striatal Development in Early-Onset Huntington's Disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36177602 DOI: 10.1002/mds.29227  0.573
2022 Reasoner EE, van der Plas E, Al-Kaylani HM, Langbehn DR, Conrad AL, Schultz JL, Epping EA, Magnotta VA, Nopoulos PC. Behavioral features in child and adolescent huntingtin gene-mutation carriers. Brain and Behavior. e2630. PMID 35604958 DOI: 10.1002/brb3.2630  0.553
2022 Byrne LM, Schultz JL, Rodrigues FB, van der Plas E, Langbehn D, Nopoulos PC, Wild EJ. Neurofilament Light Protein as a Potential Blood Biomarker for Huntington's Disease in Children. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 35437792 DOI: 10.1002/mds.29027  0.58
2022 Hamilton MJ, Atalaia A, McLean J, Cumming SA, Evans JJ, Ballantyne B, Jampana R, Longman C, Livingston E, van der Plas E, Koscik T, Nopoulos P, Farrugia ME, Monckton DG. Clinical and neuroradiological correlates of sleep in myotonic dystrophy type 1. Neuromuscular Disorders : Nmd. PMID 35361525 DOI: 10.1016/j.nmd.2022.02.003  0.543
2022 Reasoner EE, van der Plas E, Langbehn DR, Conrad AL, Koscik TR, Epping EA, Magnotta VA, Nopoulos PC. Cortical Features in Child and Adolescent Carriers of Mutant Huntingtin (mHTT). Journal of Huntington's Disease. PMID 35275555 DOI: 10.3233/JHD-210512  0.541
2022 van der Plas E, Long JD, Koscik TR, Magnotta V, Monckton DG, Cumming SA, Gottschalk AC, Hefti M, Gutmann L, Nopoulos PC. Blood-Based Markers of Neuronal Injury in Adult-Onset Myotonic Dystrophy Type 1. Frontiers in Neurology. 12: 791065. PMID 35126292 DOI: 10.3389/fneur.2021.791065  0.566
2021 van der Plas E, Solomon MA, Hopkins L, Koscik T, Schultz J, Brophy PD, Nopoulos PC, Harshman LA. Global and Regional White Matter Fractional Anisotropy in Children with Chronic Kidney Disease. The Journal of Pediatrics. 242: 166-173.e3. PMID 34758354 DOI: 10.1016/j.jpeds.2021.11.006  0.569
2021 Miller JN, Kruger A, Moser DJ, Gutmann L, van der Plas E, Koscik TR, Cumming SA, Monckton DG, Nopoulos PC. Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1. Frontiers in Neurology. 12: 700796. PMID 34276551 DOI: 10.3389/fneur.2021.700796  0.693
2021 van der Plas E, Lullmann O, Hopkins L, Schultz JL, Nopoulos PC, Harshman LA. Associations between neurofilament light-chain protein, brain structure, and chronic kidney disease. Pediatric Research. PMID 34274959 DOI: 10.1038/s41390-021-01649-6  0.579
2021 van der Plas E, Koscik TR, Magnotta V, Cumming SA, Monckton D, Gutmann L, Nopoulos P. Neurocognitive Features of Motor Premanifest Individuals With Myotonic Dystrophy Type 1. Neurology. Genetics. 7: e577. PMID 33912661 DOI: 10.1212/NXG.0000000000000577  0.593
2021 Koscik TR, van der Plas E, Gutmann L, Cumming SA, Monckton DG, Magnotta V, Shields RK, Nopoulos PC. White matter microstructure relates to motor outcomes in myotonic dystrophy type 1 independently of disease duration and genetic burden. Scientific Reports. 11: 4886. PMID 33649422 DOI: 10.1038/s41598-021-84520-2  0.585
2021 Langbehn KE, Carlson-Stadler Z, van der Plas E, Hefti MM, Dawson JD, Moser DJ, Nopoulos PC. DMPK mRNA Expression in Human Brain Tissue Throughout the Lifespan. Neurology. Genetics. 7: e537. PMID 33575482 DOI: 10.1212/NXG.0000000000000537  0.55
2021 van der Plas E, Gutmann L, Thedens D, Shields RK, Langbehn K, Guo Z, Sonka M, Nopoulos P. Quantitative muscle MRI as a sensitive marker of early muscle pathology in myotonic dystrophy type 1. Muscle & Nerve. PMID 33462896 DOI: 10.1002/mus.27174  0.587
2020 Koscik TR, Sloat L, van der Plas E, Joers JM, Deelchand DK, Lenglet C, Öz G, Nopoulos PC. Brainstem and striatal volume changes are detectable in under 1 year and predict motor decline in spinocerebellar ataxia type 1. Brain Communications. 2: fcaa184. PMID 33409488 DOI: 10.1093/braincomms/fcaa184  0.617
2020 Guo Z, Zhang H, Chen Z, van der Plas E, Gutmann L, Thedens D, Nopoulos P, Sonka M. Fully automated 3D segmentation of MR-imaged calf muscle compartments: Neighborhood relationship enhanced fully convolutional network. Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society. 87: 101835. PMID 33373972 DOI: 10.1016/j.compmedimag.2020.101835  0.559
2020 Solomon M, van der Plas E, Langbehn KE, Novak M, Schultz JL, Koscik TR, Conrad AL, Brophy PD, Furth SL, Nopoulos PC, Harshman LA. Early pediatric chronic kidney disease is associated with brain volumetric gray matter abnormalities. Pediatric Research. PMID 33069166 DOI: 10.1038/s41390-020-01203-w  0.607
2020 Johnson C, Langbehn KE, Long JD, Moser D, Cross S, Gutmann L, Nopoulos PC, van der Plas E. Encoding of facial expressions in individuals with adult-onset myotonic dystrophy type 1. Journal of Clinical and Experimental Neuropsychology. 1-9. PMID 33028165 DOI: 10.1080/13803395.2020.1826410  0.543
2020 Miller JN, van der Plas E, Hamilton M, Koscik TR, Gutmann L, Cumming SA, Monckton DG, Nopoulos PC. Variant repeats within the CTG expansion protect function in myotonic dystrophy type 1. Neurology. Genetics. 6: e504. PMID 32851192 DOI: 10.1212/Nxg.0000000000000504  0.556
2020 Langbehn KE, van der Plas E, Moser DJ, Long JD, Gutmann L, Nopoulos PC. Cognitive function and its relationship with brain structure in myotonic dystrophy type 1. Journal of Neuroscience Research. PMID 32056295 DOI: 10.1002/Jnr.24595  0.583
2019 van der Plas E, Langbehn DR, Conrad AL, Koscik TR, Tereshchenko A, Epping EA, Magnotta VA, Nopoulos PC. Abnormal brain development in child and adolescent carriers of mutant huntingtin. Neurology. PMID 31371571 DOI: 10.1212/Wnl.0000000000008066  0.598
2019 van der Plas E, Hamilton MJ, Miller JN, Koscik TR, Long JD, Cumming S, Povilaikaite J, Farrugia ME, McLean J, Jampana R, Magnotta VA, Gutmann L, Monckton DG, Nopoulos PC. Brain Structural Features of Myotonic Dystrophy Type 1 and their Relationship with Ctg Repeats. Journal of Neuromuscular Diseases. PMID 31306140 DOI: 10.3233/Jnd-190397  0.594
2019 van der Plas E, Schubert R, Reilmann R, Nopoulos PC. A Feasibility Study of Quantitative Motor Assessments in Children Using the Q-Motor Suite. Journal of Huntington's Disease. PMID 31256146 DOI: 10.3233/Jhd-190353  0.556
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