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Hovhannesyan Kristine

Département des sciences cliniques > Neuropédiatrie

See author's contact details
ORCID
0009-0001-4502-0502
Main Referenced Co-authors
Boemer, François  (3)
Dangouloff, Tamara  (3)
Helou, Laura  (3)
Mashhadizadeh, Davood (3)
Palmeira, Leonor  (3)
Main Referenced Keywords
genomic (1); newborn screening (1); Pediatrics, Perinatology and Child Health (1); targeted next-generation sequencing (1); treatable disease (1);
Main Referenced Disciplines
Neurology (1)
Pediatrics (1)
Genetics & genetic processes (1)

Publications (total 3)

The most downloaded
28 downloads
Boemer, F., Hovhannesyan, K., Piazzon, F., MINNER, F., Mni, M., Jacquemin, V., Mashhadizadeh, D., BENMHAMMED, N., Bours, V., Jacquinet, A., Harvengt, J., Bulk, S., Dideberg, V., Helou, L., Palmeira, L., Dangouloff, T., BabyDetect Expert Panel, & Servais, L. (2025). Population-based, first-tier genomic newborn screening in the maternity ward. Nature Medicine. doi:10.1038/s41591-024-03465-x https://hdl.handle.net/2268/329124

The most cited

4 citations (OpenAlex)

Dangouloff, T., Hovhannesyan, K., Mashhadizadeh, D., MINNER, F., Mni, M., Helou, L., Piazzon, F., Palmeira, L., Boemer, F., & Servais, L. (30 July 2024). Feasibility and Acceptability of a Newborn Screening Program Using Targeted Next-Generation Sequencing in One Maternity Hospital in Southern Belgium. Children, 11 (8), 926. doi:10.3390/children11080926 https://hdl.handle.net/2268/326120

Boemer, F., Hovhannesyan, K., Piazzon, F., MINNER, F., Mni, M., Jacquemin, V., Mashhadizadeh, D., BENMHAMMED, N., Bours, V., Jacquinet, A., Harvengt, J., Bulk, S., Dideberg, V., Helou, L., Palmeira, L., Dangouloff, T., BabyDetect Expert Panel, & Servais, L. (2025). Population-based, first-tier genomic newborn screening in the maternity ward. Nature Medicine. doi:10.1038/s41591-024-03465-x
Peer Reviewed verified by ORBi

Dangouloff, T., Hovhannesyan, K., Mashhadizadeh, D., MINNER, F., Mni, M., Helou, L., Piazzon, F., Palmeira, L., Boemer, F., & Servais, L. (30 July 2024). Feasibility and Acceptability of a Newborn Screening Program Using Targeted Next-Generation Sequencing in One Maternity Hospital in Southern Belgium. Children, 11 (8), 926. doi:10.3390/children11080926
Peer Reviewed verified by ORBi

Dangouloff, T., MOURAUX, C., Piazzon, F., Mashhadizadeh, D., Hovhannesyan, K., Helou, L., Palmeira, L., Boemer, F., & Servais, L. (2023). Dépistage génétique néonatal universel de 126 maladies précoces et traitables : premiers résultats du projet Babydetect [Poster presentation]. 33e Séminaire de Génétique Clinique, Angers, France.
Peer reviewed

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