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Clinical Endocrinology|July 15, 2024
Enzyme replacement therapy for hypophosphatasia-The current paradigmAaron Schindeler, Karissa Ludwig, Craig F MunnsJournal of Pediatric Endocrinology & Metabolism : JPEM|September 20, 2023
Genotyping in patients with congenital adrenal hyperplasia by sequencing of newborn bloodspot samplesKarissa Ludwig, Fei Lai, Veronica Wiley, et al.JBMR Plus|January 12, 2026
Denosumab as a treatment for pediatric hypercalcemia-a multicenter experienceAnnabelle Hobbs, Rishi Nair, Karissa Ludwig, et al.Pediatric Diabetes|August 23, 2023
Type 2 diabetes in children and adolescents across Australia and New Zealand: A 6-year audit from The Australasian Diabetes Data Network (ADDN)Karissa Ludwig, Maria E Craig, Kim C Donaghue, et al.The Journal of Clinical Endocrinology and Metabolism|November 8, 2024
RNA-First Approach Identifies Deep Intronic PHEX Variants in X-Linked Hypophosphatemic RicketsKarissa Ludwig, Zenghui Wu, Ghalib Bardai, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 9, 2023
RNA Sequencing of Urine-Derived Cells for the Characterization and Diagnosis of Osteogenesis ImperfectaKarissa Ludwig, Zenghui Wu, Ghalib Bardai, et al.International Journal of Molecular Sciences|April 14, 2026
Characterisation of Urine-Derived Cells for the Molecular Diagnosis of Rare DisordersKarissa Ludwig, Zenghui Wu, Ghalib Bardai, et al.Bone|August 15, 2022
Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAPJuliana Marulanda, Karissa Ludwig, Francis Glorieux, et al.Bone|July 16, 2023
X-linked hypophosphatemia caused by a deep intronic variant in PHEX identified by PCR-based RNA analysis of urine-derived cellsChelsey Grimbly, Karissa Ludwig, Zenghui Wu, et al.Bone|April 3, 2022
Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variantKarissa Ludwig, Leanne M Ward, Nasrin Khan, et al.Pageof 2