Liesbeth Vossaert

机构：Baylor Genetics · ORCID：0000-0002-8888-8563

发表论文 69 篇 · 总被引 736 次 · h-index 14

代表论文

• Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic–ischemic encephalopathy: A retrospective analysis (2024 · Clinical Genetics · 被引 10)
• MED12 Loss‐of‐Function Variants as a Cause of Congenital Diaphragmatic Hernia in Females With Hardikar Syndrome and Nonspecific Intellectual Disability (2024 · American Journal of Medical Genetics Part A · 被引 7)
• Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage (2025 · Clinical Chemistry · 被引 4)
• Whole exome sequencing as a screening tool in dogs: A pilot study (2025 · Computational and Structural Biotechnology Journal · 被引 3)
• Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth (2025 · Prenatal Diagnosis · 被引 2)
• Untargeted metabolomics analysis as a potential screening tool for 3-methylglutaconic aciduria syndromes (2024 · Molecular Genetics and Metabolism · 被引 2)