Soul, Janet S.
for the Polymicrogyria Genetics Research Network
6 papers on CoChatORCID 0000-0001-6998-7753
Most cited papers
- Verified
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
Miller, D. T., Shen, Y., Weiss, L. A., Korn, J., Anselm, I., Bridgemohan, C., Cox, G. F., Dickinson, H., Gentile, J., Harris, D. J., et al. (2009) · Journal of Medical Genetics
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 427
- Verified · note
Profile of neonatal epilepsies: Characteristics of a prospective US cohort
Shellhaas, R. A., Wusthoff, C. J., Tsuchida, T. N., Glass, H. C., Chu, C. J., Massey, S. L., Soul, J. S., Wiwattanadittakun, N., Abend, N. S., Cilio, M. R., et al. (2017) · Neurology
Epilepsy research and treatmentNeonatal and fetal brain pathology
Cited by 208
- Verified
Fetal Brain Volume Predicts Neurodevelopment in Congenital Heart Disease
Sadhwani, A., Wypij, D., Rofeberg, V., Gholipour, A., Mittleman, M., Rohde, J., Velasco-Annis, C., Calderon, J., Friedman, K. G., Tworetzky, W., et al. (2022) · Circulation
Congenital Heart Disease StudiesFetal and Pediatric Neurological Disorders
Cited by 169
- Verified
White Matter Volume Predicts Language Development in Congenital Heart Disease
Rollins, C. K., Asaro, L. A., Akhondi-Asl, A., Kussman, B. D., Rivkin, M. J., Bellinger, D. C., Warfield, S. K., Wypij, D., Newburger, J. W., & Soul, J. S. (2017) · The Journal of Pediatrics
Congenital Heart Disease StudiesCongenital heart defects research
Cited by 70
- Verified
Advanced diffusion imaging for assessing normal white matter development in neonates and characterizing aberrant development in congenital heart disease
Karmacharya, S., Gagoski, B., Ning, L., Vyas, R., Cheng, H. H., Soul, J., Newberger, J. W., Shenton, M. E., Rathi, Y., & Grant, P. E. (2018) · NeuroImage: Clinical
Advanced Neuroimaging Techniques and ApplicationsAdvanced MRI Techniques and Applications
Cited by 46
- Verified
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria
Akula, S. K., Chen, A. Y., Neil, J. E., Shao, D. D., Mo, A., Hylton, N. K., DiTroia, S., Ganesh, V. S., Smith, R. S., O’Kane, K., et al. (2023) · JAMA Neurology
Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases
Cited by 37
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