1. Evolution of Brain Glucose Metabolic Abnormalities in Children With Epilepsy and SCN1A Gene Variants. (November 2018) Authors: Kumar, Ananyaa; Juhász, Csaba; Luat, Aimee; Govil-Dalela, Tuhina; Behen, Michael E.; Hicks, Melissa A.; Chugani, Harry T. Journal: Journal of child neurology Issue: Volume 33:Number 13(2018:Dec.) Page Start: 832 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Prenatal Lethal Diagnosis of 8p23.1 Duplication Syndrome Associated with Omphalocele and Encephalocele. (25th February 2023) Authors: Hicks, Melissa A.; Ebrahim, Salah; Gonik, Bernard Other Names: Mittal Balraj Academic Editor. Journal: Case reports in genetics Issue: Volume 2023(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The association of HBB-related significant hemoglobinopathies and low fetal fraction on noninvasive prenatal screening for fetal aneuploidy. (17th November 2021) Authors: Putra, Manesha; Idler, Jay; Patek, Kara; Contos, George; Walker, Christopher; Olson, Danielle; Hicks, Melissa A.; Chaperon, Jessica; Korzeniewski, Steven J.; Patwardhan, Sanjay C.; Sokol, Robert J. Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 34:Number 22(2021) Page Start: 3657 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The impact of HBB‐related hemoglobinopathies carrier status on fetal fraction in noninvasive prenatal screening. (23rd March 2022) Authors: Putra, Manesha; Kaseniit, Kristjan Eerik; Hicks, Melissa A.; Muzzey, Dale; Hackney, David Journal: Prenatal diagnosis Issue: Volume 42:Number 4(2022) Page Start: 524 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗