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 |
0.636 |
|
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 |
0.614 |
|
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 |
0.64 |
|
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 |
0.625 |
|
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 |
0.605 |
|
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 |
0.631 |
|
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 |
0.6 |
|
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 |
0.596 |
|
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 |
0.619 |
|
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 |
0.623 |
|
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 |
0.657 |
|
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 |
0.657 |
|
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 |
0.631 |
|
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 |
0.639 |
|
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 |
0.638 |
|
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 |
0.612 |
|
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 |
0.632 |
|
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 |
0.669 |
|
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 |
0.61 |
|
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 |
0.659 |
|
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 |
0.599 |
|
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 |
0.633 |
|
2020 |
Lee JC, Nopoulos PC, Tomblin JB. Procedural and declarative memory brain systems in developmental language disorder (DLD). Brain and Language. 205: 104789. PMID 32240854 DOI: 10.1016/J.Bandl.2020.104789 |
0.303 |
|
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 |
0.637 |
|
2019 |
Benavides A, Conrad AL, Brumbaugh JE, Magnotta V, Bell EF, Nopoulos P. Long-term outcome of brain structure in female preterm infants: possible associations of liberal versus restrictive red blood cell transfusions. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 1-8. PMID 31722594 DOI: 10.1080/14767058.2019.1683157 |
0.318 |
|
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 |
0.671 |
|
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 |
0.665 |
|
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 |
0.638 |
|
2019 |
Horton MC, Nopoulos P, Nance M, Landwehrmyer GB, Barker RA, Squitieri F, Burgunder JM, Quarrell O. Assessment of the Performance of a Modified Motor Scale as Applied to Juvenile Onset Huntington's Disease. Journal of Huntington's Disease. PMID 30856116 DOI: 10.3233/Jhd-180306 |
0.357 |
|
2019 |
Al-Huniti A, Harshman LA, Novak M, Nopoulos P, Staber JM. Brain Anomalies in Children with Severe Factor VIII Deficiency- a Pilot Study Blood. 134: 1121-1121. DOI: 10.1182/Blood-2019-131804 |
0.31 |
|
2016 |
Brumbaugh JE, Conrad AL, Lee JK, DeVolder IJ, Zimmerman MB, Magnotta VA, Axelson ED, Nopoulos PC. Altered Brain Function, Structure, and Developmental Trajectory in Children Born Late Preterm. Pediatric Research. PMID 27064239 DOI: 10.1038/Pr.2016.82 |
0.334 |
|
2016 |
Nopoulos P, Lee J, Epping E, Martin E, Mathews K, Espe-Pfeiffer P, Magnotta V. I12 The role of the cerebellum in juvenile huntington’s disease (JHD) Journal of Neurology, Neurosurgery & Psychiatry. 87: A63.2-A63. DOI: 10.1136/Jnnp-2016-314597.177 |
0.318 |
|
2016 |
Nopoulos P, Lee J, Epping E, Mathews K, Magnotta V, Dawson J. D17 Effects of the huntingtin gene (HTT) on brain development Journal of Neurology, Neurosurgery & Psychiatry. 87: A40.1-A40. DOI: 10.1136/Jnnp-2016-314597.116 |
0.304 |
|
2014 |
McCoy TE, Conrad AL, Richman LC, Brumbaugh JE, Magnotta VA, Bell EF, Nopoulos PC. The relationship between brain structure and cognition in transfused preterm children at school age. Developmental Neuropsychology. 39: 226-32. PMID 24742312 DOI: 10.1080/87565641.2013.874428 |
0.346 |
|
2014 |
Nopoulos P, Lee J, Epping E, Mathews K, Magnotta V. J32 The Impact Of Cag Repeat Length In The Huntingtin Gene On Childhood Normal Brain Structure And Function Journal of Neurology, Neurosurgery, and Psychiatry. 85. DOI: 10.1136/Jnnp-2014-309032.215 |
0.398 |
|
2014 |
Nopoulos P, Tereskchenko A, McHugh M, Dawson J, Lockhart K, Gonzalez P. I07 Abnormalities In Weight And Bmi In Children With Juvenile Huntington's Disease Journal of Neurology, Neurosurgery & Psychiatry. 85: A60-A60. DOI: 10.1136/Jnnp-2014-309032.169 |
0.32 |
|
2014 |
Nopoulos P, Lee J, Magnotta V, Epping E, Mathews K. F04 Abnormal Motor Function in Children with the HD Gene Expansion Journal of Neurology, Neurosurgery & Psychiatry. 85: A49-A49. DOI: 10.1136/Jnnp-2014-309032.139 |
0.376 |
|
2013 |
Aylward EH, Harrington DL, Mills JA, Nopoulos PC, Ross CA, Long JD, Liu D, Westervelt HK, Paulsen JS. Regional atrophy associated with cognitive and motor function in prodromal Huntington disease. Journal of Huntington's Disease. 2: 477-89. PMID 25062732 DOI: 10.3233/Jhd-130076 |
0.396 |
|
2013 |
Quarrell OW, Nance MA, Nopoulos P, Paulsen JS, Smith JA, Squitieri F. Managing juvenile Huntington's disease. Neurodegenerative Disease Management. 3. PMID 24416077 DOI: 10.2217/Nmt.13.18 |
0.318 |
|
2013 |
Lee JC, Nopoulos PC, Bruce Tomblin J. Abnormal subcortical components of the corticostriatal system in young adults with DLI: a combined structural MRI and DTI study. Neuropsychologia. 51: 2154-61. PMID 23896446 DOI: 10.1016/J.Neuropsychologia.2013.07.011 |
0.374 |
|
2012 |
Beglinger LJ, Prest L, Mills JA, Paulsen JS, Smith MM, Gonzalez-Alegre P, Rowe KC, Nopoulos P, Uc EY. Clinical predictors of driving status in Huntington's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1146-52. PMID 22744778 DOI: 10.1002/Mds.25101 |
0.329 |
|
2012 |
Aylward EH, Liu D, Nopoulos PC, Ross CA, Pierson RK, Mills JA, Long JD, Paulsen JS. Striatal volume contributes to the prediction of onset of Huntington disease in incident cases. Biological Psychiatry. 71: 822-8. PMID 21907324 DOI: 10.1016/J.Biopsych.2011.07.030 |
0.397 |
|
2012 |
Nopoulos P, Epping E, Conrad A, Mathews K, Perlmutter J, Schlaggar B, Paulsen J, Byars J, Magnotta V. G04 Brain structure in children at risk for Huntington's disease Journal of Neurology, Neurosurgery & Psychiatry. 83: A27.2-A27. DOI: 10.1136/Jnnp-2012-303524.84 |
0.405 |
|
2012 |
Nopoulos P, Lee J, Mathews K, Epping E, Paulsen J, Conrad A. K01 Behaviour assessments in children at risk for huntington's disease Journal of Neurology, Neurosurgery & Psychiatry. 83: A41.2-A41. DOI: 10.1136/Jnnp-2012-303524.128 |
0.336 |
|
2012 |
Nopoulos P, Mathews K, Paulsen J, Epping E, Conrad A, Perlmutter J, Schlaggar B. I02 Effect of CAG length on motor scores of children at risk for huntington's disease Journal of Neurology, Neurosurgery & Psychiatry. 83: A33.1-A33. DOI: 10.1136/Jnnp-2012-303524.101 |
0.384 |
|
2011 |
Keppler-Noreuil KM, Blumhorst C, Sapp JC, Brinckman D, Johnston J, Nopoulos PC, Biesecker LG. Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS). Bmc Medical Genetics. 12: 101. PMID 21794117 DOI: 10.1186/1471-2350-12-101 |
0.361 |
|
2011 |
Aylward E, Mills J, Liu D, Nopoulos P, Ross CA, Pierson R, Paulsen JS. Association between Age and Striatal Volume Stratified by CAG Repeat Length in Prodromal Huntington Disease. Plos Currents. 3: RRN1235. PMID 21593963 DOI: 10.1371/Currents.Rrn1235 |
0.379 |
|
2011 |
Nopoulos PC, Aylward EH, Ross CA, Mills JA, Langbehn DR, Johnson HJ, Magnotta VA, Pierson RK, Beglinger LJ, Nance MA, Barker RA, Paulsen JS. Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment. Brain : a Journal of Neurology. 134: 137-42. PMID 20923788 DOI: 10.1093/Brain/Awq280 |
0.404 |
|
2011 |
Aylward EH, Nopoulos PC, Ross CA, Langbehn DR, Pierson RK, Mills JA, Johnson HJ, Magnotta VA, Juhl AR, Paulsen JS. Longitudinal change in regional brain volumes in prodromal Huntington disease. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 405-10. PMID 20884680 DOI: 10.1136/Jnnp.2010.208264 |
0.393 |
|
2010 |
Nopoulos P, Boes AD, Jabines A, Conrad AL, Canady J, Richman L, Dawson JD. Hyperactivity, impulsivity, and inattention in boys with cleft lip and palate: relationship to ventromedial prefrontal cortex morphology. Journal of Neurodevelopmental Disorders. 2: 235-42. PMID 22127933 DOI: 10.1007/S11689-010-9060-5 |
0.364 |
|
2010 |
Nopoulos PC, Aylward EH, Ross CA, Johnson HJ, Magnotta VA, Juhl AR, Pierson RK, Mills J, Langbehn DR, Paulsen JS. Cerebral cortex structure in prodromal Huntington disease. Neurobiology of Disease. 40: 544-54. PMID 20688164 DOI: 10.1016/J.Nbd.2010.07.014 |
0.341 |
|
2010 |
Paulsen JS, Nopoulos PC, Aylward E, Ross CA, Johnson H, Magnotta VA, Juhl A, Pierson RK, Mills J, Langbehn D, Nance M. Striatal and white matter predictors of estimated diagnosis for Huntington disease. Brain Research Bulletin. 82: 201-7. PMID 20385209 DOI: 10.1016/J.Brainresbull.2010.04.003 |
0.406 |
|
2010 |
Adams W, Byars J, O'Rourke J, Flynn A, Fiedorowicz J, Duff K, Leserman A, Nopoulos P, Beglinger L. Poster 26: Word Reading Compared to Demographics-Based Estimates of Premorbid IQ in Early Huntington Disease Neurotherapeutics. 7: 146-147. DOI: 10.1016/J.Nurt.2009.10.010 |
0.325 |
|
2010 |
Aylward E, Nopoulos P, Ross C, Pierson R, Mills J, Langbehn D, Magnotta V, Johnson H, Paulsen J. Poster 11: Striatal Volume Distinguishes Converters from Non-Converters: Findings from PREDICT-HD Neurotherapeutics. 7: 141-141. DOI: 10.1016/J.Nurt.2009.09.013 |
0.3 |
|
2009 |
Aylward E, Nopoulos P, Pierson R, Langbehn, Ross C, Paulsen J. Longitudinal Change in Striatal Volume in Pre-Clinical Huntington's Disease Neuroimage. 47. DOI: 10.1016/S1053-8119(09)70738-4 |
0.337 |
|
2009 |
AYLWARD E, NOPOULOS P, JOHNSON H, JUHL A, MAGNOTTA V, PIERSON R, LANGBEHN D, ROSS C, PAULSEN J. Platform Presentation—Longitudinal Structural MRI Data from PREDICT-HD: Striatal and Cortical Changes in Pre-Clinical HD Neurotherapeutics. 6: 202-203. DOI: 10.1016/J.Nurt.2008.09.006 |
0.337 |
|
2008 |
Davis LK, Hazlett HC, Librant AL, Nopoulos P, Sheffield VC, Piven J, Wassink TH. Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1145-51. PMID 18361446 DOI: 10.1002/Ajmg.B.30738 |
0.348 |
|
2008 |
NOPOULOS P, PAULSEN J, BEGLINGER L, JOHNSON H, MAGNOTTA V, PIERSON R, LANGBEHN D. Abnormal Structure of Cerebral White and Cortical Gray Matter in Preclinical Huntington’s Disease Neurotherapeutics. 5: 369-370. DOI: 10.1016/J.Nurt.2007.10.021 |
0.331 |
|
2006 |
McCormick LM, Ziebell S, Nopoulos P, Cassell M, Andreasen NC, Brumm M. Anterior cingulate cortex: an MRI-based parcellation method. Neuroimage. 32: 1167-75. PMID 16859929 DOI: 10.1016/J.Neuroimage.2006.04.227 |
0.344 |
|
2003 |
Milev P, Ho BC, Arndt S, Nopoulos P, Andreasen NC. Initial magnetic resonance imaging volumetric brain measurements and outcome in schizophrenia: a prospective longitudinal study with 5-year follow-up. Biological Psychiatry. 54: 608-15. PMID 13129655 DOI: 10.1016/S0006-3223(03)00293-2 |
0.34 |
|
2003 |
White T, Andreasen NC, Nopoulos P, Magnotta V. Gyrification abnormalities in childhood- and adolescent-onset schizophrenia. Biological Psychiatry. 54: 418-26. PMID 12915286 DOI: 10.1016/S0006-3223(03)00065-9 |
0.357 |
|
2003 |
Wassink TH, Nopoulos P, Pietila J, Crowe RR, Andreasen NC. NOTCH4 and the frontal lobe in schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 118: 1-7. PMID 12627456 DOI: 10.1002/Ajmg.B.10071 |
0.329 |
|
2002 |
Spinks R, Magnotta VA, Andreasen NC, Albright KC, Ziebell S, Nopoulos P, Cassell M. Manual and automated measurement of the whole thalamus and mediodorsal nucleus using magnetic resonance imaging. Neuroimage. 17: 631-42. PMID 12377139 DOI: 10.1006/Nimg.2002.1185 |
0.312 |
|
2002 |
White T, Andreasen NC, Nopoulos P. Brain volumes and surface morphology in monozygotic twins. Cerebral Cortex (New York, N.Y. : 1991). 12: 486-93. PMID 11950766 DOI: 10.1016/S1053-8119(01)92351-1 |
0.317 |
|
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