Kristine Hovhannesyan
Publications by Year
Research Areas
Genomics and Rare Diseases, Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Neurogenetic and Muscular Disorders Research, Metabolism and Genetic Disorders
Most-Cited Works
- → Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go(2021)167 cited
- → Measuring European Population Stratification with Microarray Genotype Data(2007)166 cited
- → An X-Linked Haplotype of Neandertal Origin Is Present Among All Non-African Populations(2011)68 cited
- → Population-based, first-tier genomic newborn screening in the maternity ward(2025)31 cited
- → Feasibility and Acceptability of a Newborn Screening Program Using Targeted Next-Generation Sequencing in One Maternity Hospital in Southern Belgium(2024)12 cited
- → Population-Based, First-Tier Genomic Newborn Screening in a Single Maternity Ward in Belgium: Results of Babydetect Project(2024)2 cited
- → Baby detect: Universal genomic newborn screening for early, treatable, and severe conditions(2023)2 cited
- → Analytical Validation of a Genomic Newborn Screening Workflow(2025)1 cited
- → A combined genomic and functional approach to One-Carbon Metabolism disorders in a population-based newborn screening(2026)
- → Genetic Newborn Screening for Retinoblastoma: A Belgian Initiative Baby Detect(2025)