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American Journal of Medical Genetics. Part A|February 6, 2021
A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum diseaseAlanna Strong, Dong Li, Frank Mentch, et al.Clinical Liver Disease|November 8, 2021
Hepatic Manifestations of Urea Cycle DisordersAlanna Strong, Jessica Gold, Nina B Gold, et al.American Journal of Medical Genetics. Part A|April 1, 2025
A New EP300-Related Syndrome With Prominent Developmental and Immune PhenotypesDevi Priyanka Maripuri, Jessica Gold, Nina Gold, et al.American Journal of Medical Genetics. Part A|February 5, 2026
Novel Features of RASopathies: Liver Disease as an Emerging PhenotypeAlyssa L Rippert, Alanna Strong, Rebecca C Ahrens-NicklasJournal of Inherited Metabolic Disease|September 30, 2025
Are Inherited Metabolic Disorders More Common and Less Predictable Than We Thought?Nina B Gold, Alanna Strong, Harini Somanchi, et al.Pediatric Transplantation|June 11, 2010
Two decades of pediatric kidney transplantation in a multi-ethnic cohortSamina Muneeruddin, Jayanthi Chandar, Carolyn L Abitbol, et al.Ophthalmic Genetics|January 4, 2021
Ocular manifestations and surgical interventions in pediatric patients with Koolen-de-Vries syndromeDaphna Prat, William R Katowitz, Alanna Strong, et al.Orphanet Journal of Rare Diseases|May 2, 2021
Ocular manifestations of ectodermal dysplasiaDaphna Landau Prat, William R Katowitz, Alanna Strong, et al.Pharmacy (Basel, Switzerland)|October 5, 2017
Creating a Distinct Medication-Use System for Children at the Point of Care: The Time is NowRichard Parrish Ii, Ibolja CernakCureus|February 22, 2024
An Adolescent Boy With Hypoxia, Microscopic Hematuria, and HypertensionMelissa S Zhou, Clement D Lee, Benjamin J Lerman, et al.Pageof 8