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Huang, Mengmeng, Feria A Ladha, Yunxia Wang, Michael A Trembley, Hui-Min Yin, Rongbin Zheng, Maksymilian Prondzynski, et al. 2025. “Dosage-Sensitive RBFOX2 Autoregulation Promotes Cardiomyocyte Differentiation by Maturing the Transcriptome.”. BioRxiv : The Preprint Server for Biology.

Ladha, Feria A, Christina VanderPluym, Enrique Mondragon-Estrada, Paul Avillach, Martina Brueckner, Wendy K Chung, James F Cnota, et al. 2026. “Prothrombin G20210A and Factor V Leiden Variants Are Not Associated With Thrombotic Events in Congenital Heart Disease: An Observational Trial.”. Journal of the American Heart Association, e046959.

Penner, Yvette, Sabah Sabir, Kathleen Quirk, Julia Foster, Kristen Earley Lindamood, Jaclyn Mello, Jimena Gayol Ortega, et al. 2025. “Increasing Length Board Use in a Neonatal Intensive Care Unit: A Quality Improvement Initiative.”. Journal of Perinatology : Official Journal of the California Perinatal Association.

Suresh, Abhilash, Sarah U Morton, Daniel Quiat, Steven R DePalma, Joshua M Gorham, Martina Brueckner, Martin Tristani-Firouzi, et al. 2025. “Enrichment of Tandem Repeat Element Variants Near CHD Genes Identified by Short- and Long-Read Genome Sequencing.”. BMC Medical Genomics 18 (1): 120.

Field, Thalia S, Sarah U Morton, Marie Brossard-Racine, Scott Cohen, Howard H Feldman, Ai Wern Chung, Jane W Newburger, Rick Puder, Michelle Gurvitz, and Adam R Cassidy. 2026. “Genetics and Brain Health in Adults With Congenital Heart Disease: A Consensus Statement From the ACHD/Neuro 2024 Conference.”. Journal of the American Heart Association, e042617.

Lee, Jodi, Jingshing Wu, Maureen Pittman, Zoe L Grant, Shuzhen Kuang, Daniel Quiat, Sarah U Morton, et al. 2026. “Structural Variants in Human Congenital Heart Disease Disrupt Distal Genomic Regulatory Contacts of Developmental Genes.”. BioRxiv : The Preprint Server for Biology.

Cohen, Jennifer L, Michael Duyzend, Sophia M Adelson, Julie Yeo, Mark Fleming, Rebecca Ganetzky, Rebecca Hale, et al. 2025. “Advancing Precision Care in Pregnancy through a Treatable Fetal Findings List.”. American Journal of Human Genetics.

Movassagh, Mercedeh, Lucinda Newbury, Christine Hehnly, Andrew J Whalen, Mallory Peterson, Enrique Mondragon-Estrada, Jessica E Ericson, et al. 2026. “Genome Admixture Analysis of 1,030 Ugandan Infants With Neonatal Sepsis and Hydrocephalus Demonstrates Geographical Stratification of Population Disease Risk.”. MedRxiv : The Preprint Server for Health Sciences.

Mondragon-Estrada, Enrique, Xingyan Wang, Michael D Uhler, Afifah Farooque, Kelly Liu, Sudipta Kumer Mukherjee, Sheikh Muhammad Ekramullah, et al. 2025. “Folate Interaction With Genetic Risk for Neural Tube Defects Among Infants in Bangladesh.”. Birth Defects Research 117 (12): e70007.

Lima, Giulia P, Alyssa R Thomas, Victoria R Bradford, Sarah U Morton, Francesca Sperotto, and Philip T Levy. 2026. “Advances in Interdisciplinary Care for Term and Preterm Neonates With Congenital Heart Disease: A Narrative Review.”. European Journal of Pediatrics 185 (2): 66.