Glenn, Orit A.

Growth trajectories of the human fetal brain tissues estimated from 3D reconstructed in utero MRI

Scott, J. A., Habas, P. A., Kim, K., Rajagopalan, V., Hamzelou, K. S., Corbett‐Detig, J. M., Barkovich, A. J., Glenn, O. A., & Studholme, C. (2011) · International Journal of Developmental Neuroscience

Fetal and Pediatric Neurological DisordersMedical Image Segmentation Techniques

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Vanishing MS T2-bright lesions before puberty: A distinct MRI phenotype?

Chabas, D., Castillo-Trivino, T., Mowry, E. M., Strober, J. B., Glenn, O. A., & Waubant, E. (2008) · Neurology

Multiple Sclerosis Research StudiesPolyomavirus and related diseases

Cited by 105

Quantifying the effects of 16p11.2 copy number variants on brain structure: a multisite genetic-first study

Martin-Brevet, S., Rodríguez-Herreros, B., Nielsen, J. A., Moreau, C., Modenato, C., Maillard, A. M., Pain, A., Richetin, S., Jønch, A. E., Qureshi, A. Y., et al. (2018) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 75

3D Morphometric Analysis of Human Fetal Cerebellar Development

Scott, J. A., Hamzelou, K. S., Rajagopalan, V., Habas, P. A., Kim, K., Barkovich, A. J., Glenn, O. A., & Studholme, C. (2012) · The Cerebellum

Fetal and Pediatric Neurological DisordersSpinal Dysraphism and Malformations

Cited by 59

Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2

Owen, J. P., Bukshpun, P., Pojman, N., Thieu, T., Chen, Q., Lee, J., D’Angelo, D., Glenn, O. A., Hunter, J. V., Berman, J. I., et al. (2018) · Radiology

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 40