
Last Updated: 09/26/2026
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Found 119 publications
Village-level surveillance of neonatal disease with integrated real-time dashboards and quality-control in Uganda.
Journal: medRxiv : the preprint server for health sciences
Published: August 01, 2026
Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease.
Journal: Research square
Published: August 01, 2026
Genetic Testing in Congenital Heart Disease: From Microarray to Genome Sequencing.
Journal: Circulation. Genomic and precision medicine
Published: May 21, 2026
Risk Factors for Mortality and Age at Discharge in Infants with Congenital Heart Disease Born Preterm.
Journal: The Journal of pediatrics
Published: April 23, 2026
Rare KDR Variants Define a Distinct Genetic Contribution to Congenital Heart Disease.
Journal: Circulation. Genomic and precision medicine
Published: April 22, 2026
Cutaneous Mycobacterium haemophilum Infection in an Immunosuppressed Host: A Case Report of Diagnostic Considerations and Microbiologic Confirmation.
Journal: Clinical case reports
Published: April 12, 2026
Genome admixture analysis of 1,030 Ugandan infants with neonatal sepsis and hydrocephalus demonstrates geographical stratification of population disease risk.
Journal: medRxiv : the preprint server for health sciences
Published: April 03, 2026
Physiologic signatures during extubation readiness trials in neonates >35 weeks' postmenstrual age.
Journal: Journal of perinatology : official journal of the California Perinatal Association
Published: March 29, 2026
Structural variants in human congenital heart disease disrupt distal genomic regulatory contacts of developmental genes.
Journal: bioRxiv : the preprint server for biology
Published: March 23, 2026
Prothrombin G20210A and Factor V Leiden Variants Are Not Associated With Thrombotic Events in Congenital Heart Disease: An Observational Trial.
Journal: Journal of the American Heart Association
Published: March 04, 2026
Last Updated: 09/26/2026