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BMJ Paediatrics Open|December 26, 2024
Impact of maternal antenatal nutrition and infection treatment interventions on Longitudinal Infant Development and Growth in rural Ethiopia: protocol of the LIDG child follow-up studyFirehiwot Workneh, Theresa I Chin, Kalkidan Yibeltal, et al.
Neuroimage|July 5, 2024
Identifying novel data-driven subgroups in congenital heart disease using multi-modal measures of brain structureMarlee M Vandewouw, Ami Norris-Brilliant, Anum Rahman, et al.
JAMA Network Open|January 26, 2023
Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart DiseaseSarah U Morton, Ami Norris-Brilliant, Sean Cunningham, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Nature Medicine|April 14, 2026
Antisense oligonucleotide-mediated knockdown therapy in two infants with severe KCNT1 epileptic encephalopathyTojo Nakayama, Christelle M El Achkar, Lisseth E Burbano, et al.
World Journal of Pediatrics : WJP|May 29, 2025
Advances in magnetic resonance imaging of the developing brain and its applications in pediatricsRui-Ke Chen, Ming-Yang Li, Zhi-Yong Zhao, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 10, 2024
Early and extended erythropoietin monotherapy after hypoxic ischaemic encephalopathy: a multicentre double-blind pilot randomised controlled trialReema Garegrat, Atul Londhe, Swati Manerkar, et al.
The New England Journal of Medicine|October 10, 2019
Patient-Customized Oligonucleotide Therapy for a Rare Genetic DiseaseJinkuk Kim, Chunguang Hu, Christelle Moufawad El Achkar, et al.
JAMA Psychiatry|December 3, 2015
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical ComorbiditiesDebra D'Angelo, Sébastien Lebon, Qixuan Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2012
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humansTrygve E Bakken, J Cooper Roddey, Srdjan Djurovic, et al.
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