Publications and communications of François BOEMER

Meiouet, F., & Boemer, F. (03 June 2026). Rapid LC-MS/MS Method for Targeted Assay of Creatine Deficiency Syndromes in Morocco. Metabolites, 16 (6), 388. doi:10.3390/metabo16060388

Francisca, I. N., Ghislain, B. B., Gaylord, A. N., Boemer, F., Vincent, B., Oreste, B., & Richard, M. K. (2026). Neonate screening for glucose-6-phosphate dehydrogenase deficiency in South Kivu, eastern Democratic Republic of Congo. BMC Pediatrics. doi:10.1186/s12887-026-07093-x

Hovhannesyan, K., Helou, L., Charloteaux, B., JACQUEMIN, V., Piazzon, F., Mni, M., Flohimont, C., Fasquelle, C., Mashhadizadeh, D., Dangouloff, T., Bours, V., Servais, L., Palmeira, L., & Boemer, F. (13 November 2025). Analytical Validation of a Genomic Newborn Screening Workflow. International Journal of Neonatal Screening, 11 (4), 91. doi:10.3390/ijns11040091

Downie, L., Yeo, J., Minten, T., Heald, R., Ansel, D., Baker, M., Balciuniene, J., Berg, J., Boemer, F., Chung, W., Cope, H., Eckstein, D., Encina, N., Faivre, L., Ferlini, A., García-Villoria, J., Gelb, M., Gonz´ Alez De Aledo-Castillo, M., Golden-Grant, K., ... Gold, N. (24 October 2025). Operationalizing the Wilson-Jungner principles for the genomics era: Consensus recommendations from the International Consortium on Newborn Sequencing. Genetics in Medicine, 28 (1), 101618. doi:10.1016/j.gim.2025.101618

Boemer, F., & Servais, L. (2025). Genomic Newborn Screening-A Long Road From Pilot to Public Policy. JAMA Pediatrics. doi:10.1001/jamapediatrics.2025.3639

Bartoszek, P., Boemer, F., Hovhannesyan, K., JACQUEMIN, V., Piazzon, F., Mashhadizadeh, D., Bours, V., HELOU, L., Rigo, V., HENNUY, N., Dangouloff, T., & Servais, L. (01 October 2025). Genetic Newborn Screening for Retinoblastoma: A Belgian Initiative Baby Detect. International Ophthalmology Clinics, 65 (4), 47 - 50. doi:10.1097/IIO.0000000000000593

Boemer, F., Hovhannesyan, K., JACQUEMIN, V., Mni, M., Flohimont, C., Mashhadizadeh, D., HELOU, L., Palmeira, L., Dangouloff, T., & Servais, L. (October 2025). Population-based 1st-tier Genomic Newborn Screening : Results of BabyDetect Study [Poster presentation]. ICoNS 2025, Londres, United Kingdom.

Simon, G., Boemer, F., LUIS, G., Gothot, A., Tassin, F., & Keutgens, A. (26 August 2025). Diagnostic performance of morphological analysis and red blood cell parameter-based algorithms in the routine laboratory screening of heterozygous haemoglobinopathies. Clinical Chemistry and Laboratory Medicine, 63 (9), 1855 - 1863. doi:10.1515/cclm-2025-0210

Donge, M., Marie, S., Pochet, A., Marcelis, L., LUIS, G., Boemer, F., Prouteau, C., Mesli, S., Cuykx, M., Nguyen-Khoa, T., Guénet, D., Empain, A., Barth, M., Dauriat, B., Laroche-Raynaud, C., De Laet, C., Verloo, P., Jonckheere, A. I., Schiff, M., ... Dewulf, J. P. (30 July 2025). Advancing Neonatal Screening for Pyridoxine-Dependent Epilepsy-ALDH7A1 Through Combined Analysis of 2-OPP, 6-Oxo-Pipecolate and Pipecolate in a Butylated FIA-MS/MS Workflow. International Journal of Neonatal Screening, 11 (3), 59. doi:10.3390/ijns11030059

Dangouloff, T., Hovhannesyan, K., JACQUEMIN, V., Mashhadizadeh, D., Mni, M., Flohimont, C., HELOU, L., PALMEIRA, L., Pieltain, C., Grandfils, S., Rigo, V., HENNUY, N., Boemer, F., & Servais, L. (June 2025). Dépistage néonatal génomique : vers une identification précoce et ciblée des maladies rares. Percentile, 30 (3), 15-18.

Minten, T., Bick, S., Adelson, S., Gehlenborg, N., Amendola, L. M., Boemer, F., Coffey, A. J., Encina, N., Ferlini, A., Kirschner, J., Russell, B. E., Servais, L., Sund, K. L., Taft, R. J., Tsipouras, P., Zouk, H., ICoNS Gene List Contributors, Green, R. C., Gold, N. B., ... Nusair, A. (2025). Data-driven consideration of genetic disorders for global genomic newborn screening programs. Genetics in Medicine, 101443. doi:10.1016/j.gim.2025.101443

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., Alkan, S. (Other coll.), ... VAESSEN, S. (Other coll.). (28 January 2025). Population-based, first-tier genomic newborn screening in the maternity ward. Nature Medicine, 31 (4), 1339-1350. doi:10.1038/s41591-024-03465-x

François, A.-C.* , Cesarini Latorre, C.* , Taminiau, B., Renaud, B., Kruse, C., Boemer, F., van Loon, G., Palmers, K., Daube, G., Wouters, C., Lecoq, L., Gustin, P., & Votion, D. (26 January 2025). Unravelling Faecal Microbiota Variations in Equine Atypical Myopathy: Correlation with Blood Markers and Contribution of Microbiome. Animals, 15 (3), 354. doi:10.3390/ani15030354

Gold, N., Yeo, J., Ansel, D., Baker, M., Balciuniene, J., Berg, J., Boemer, F., Chung, W., Cope, H., Eckstein, D., Encina, N., Faivre, L., Ferlini, A., Garcia-Villoria, J., Gelb, M., Gonzalez De Aledo Castillo, J. M., Golden-Grant, K., Minten, T., Parad, R., ... Downie, L. (2025). O48: International Consortium on Newborn Sequencing (ICoNS) consensus guidelines for gene selection in genomic newborn screening programs. Genetics in Medicine Open, 3, 102421. doi:10.1016/j.gimo.2025.102421

Rousseau, A.-F., Farnir, F., Cavalier, E., LUIS, G., Kellens, I., Lambermont, B., & Boemer, F. (2025). Serum acylcarnitines profile at ICU discharge to predict mid-term muscle outcomes: an exploratory study. Frontiers in Medicine, 12, 1622116. doi:10.3389/fmed.2025.1622116

Kuypers, A. M., Bouva, M. J., Loeber, J. G., Boelen, A., Dekkers, E., Petritis, K., Pickens, C. A., Boemer, F., van Spronsen, F. J., & Heiner-Fokkema, M. R. (16 December 2024). Evaluation of Neonatal Screening Programs for Tyrosinemia Type 1 Worldwide. International Journal of Neonatal Screening, 10 (4), 82. doi:10.3390/ijns10040082

Wouters, C., Klein, B., Price, N., Boemer, F., Voz, M., & Votion, D. (19 October 2024). A Zebrafish Embryo Model to Screen Potential Therapeutic Compounds in Sapindaceae Poisoning. Molecules, 29, 1-17. doi:10.3390/molecules29204954

Thimmesch, M., Boemer, F., LUIS, G., LIBIOULLE, C., Dideberg, V., & Boboli, H. (October 2024). Dépistage néonatal de la mucoviscidose en région liégeoise : première évaluation après 4 ans. Revue Médicale de Liège, 79 (10), 664-669.

Minten, T., Gold, N. B., Bick, S., Adelson, S., Gehlenborg, N., Amendola, L. M., Boemer, F., Coffey, A. J., Encina, N., Ferlini, A., Kirschner, J., Russell, B. E., Servais, L., Sund, K. L., Taft, R. J., Tsipouras, P., Zouk, H., ICoNS Gene List Contributors, Bick, D., ... International Consortium on Newborn Sequencing (ICoNS). (2024). Data-driven prioritization of genetic disorders for global genomic newborn screening programs. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/325175. doi:10.1101/2024.03.24.24304797

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

Renaud, B., Kruse, C.-J., François, A.-C., Cesarini, C., van Loon, G., Palmers, K., Boemer, F., LUIS, G., Gustin, P., & Votion, D. (2024). Large-Scale Study of Blood Markers in Equine Atypical Myopathy Reveals Subclinical Poisoning and Advances in Diagnostic and Prognostic Criteria. Environmental Toxicology and Pharmacology, 104515. doi:10.1016/j.etap.2024.104515

Everard, E., Laeremans, H., Boemer, F., Marie, S., Vincent, M.-F., Dewulf, J. P., Debray, F.-G., De Laet, C., & Nassogne, M.-C. (March 2024). Impact of newborn screening for fatty acid oxidation disorders on neurological outcome: A Belgian retrospective and multicentric study. European Journal of Paediatric Neurology, 49, 60 - 65. doi:10.1016/j.ejpn.2024.02.003

Kruse, C., Dieu, M., Renaud, B., François, A.-C., Stern, D., Demazy, C., Burteau, S., Boemer, F., Art, T., Renard, P., & Votion, D. (2024). New Pathophysiological Insights from Serum Proteome Profiling in Equine Atypical Myopathy. ACS Omega. doi:10.1021/acsomega.3c06647

Abiusi, E., Costa-Roger, M., Bertini, E. S., Tiziano, F. D., Tizzano, E. F., SMN2 Study group, Abiusi, E., Baranello, G., Bertini, E., Boemer, F., Burghes, A., Codina-Solà, M., Costa-Roger, M., Dangouloff, T., Groen, E., Gos, M., Jędrzejowska, M., Kirschner, J., Lemmink, H. H., ... Wirth, B. (January 2024). 270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands. Neuromuscular Disorders, 34, 114-122. doi:10.1016/j.nmd.2023.12.008

Delrez, S., Boemer, F., COLSON, C., MINGUET, P., NEIS GILSON, S., Lambermont, B., & Rousseau, A.-F. (2024). Association between serum acylcarnitine profile after ICU discharge and mid‐term muscle outcomes: an observational study. Intensive Care Medicine Experimental, 12 (Suppl 1), 000753.

Minten, T., Adelson, S., Amendola, L., Bick, D., Boemer, F., Coffey, A., Encina, N., Russell, B., Servais, L., Sund, K., Taft, R., Green, R., & Gold, N. (2024). P213: Exploring heterogeneity among gene lists proposed for newborn sequencing. Genetics in Medicine Open, 2, 101110. doi:10.1016/j.gimo.2024.101110

Wouters, C., Klein, B., Price, N., Boemer, F., Joris, M., Voz, M., & Votion, D. (21 December 2023). Zebrafish embryos as alternative model to study intoxication by Acer pseudoplatanus toxins: Hypoglycin A, Methylenecyclopropylglycine and Methylenecyclopropylacetate [Paper presentation]. FarahDay 2023, Liège, Belgium.

Bonhomme, M., Patarin, F., Kruse, C., François, A.-C., Renaud, B., Couroucé, A., Leleu, C., Boemer, F., Toquet, M.-P., Richard, E. A., Seignot, J., Wouters, C., & Votion, D. (2023). Untargeted Metabolomics Profiling Reveals Exercise Intensity-Dependent Alterations in Thoroughbred Racehorses’ Plasma after Routine Conditioning Sessions. ACS Omega. doi:10.1021/acsomega.3c08583

Rousseau, A.-F., Ngongan, A., COLSON, C., MINGUET, P., NEIS GILSON, S., Cavalier, E., MINGUET, G., Misset, B., & Boemer, F. (16 August 2023). Mid-Term Evolution of the Serum Acylcarnitine Profile in Critically Ill Survivors: A Metabolic Insight into Survivorship. Nutrients, 15 (16), 3595. doi:10.3390/nu15163595

Sander, J., Terhardt, M., Janzen, N., Renaud, B., Kruse, C., François, A.-C., Wouters, C., Boemer, F., & Votion, D. (26 July 2023). Tissue Specific Distribution and Activation of Sapindaceae Toxins in Horses Suffering from Atypical Myopathy. Animals, 13 (15), 2410. doi:10.3390/ani13152410

ISIA NANCI, F., Battisti, O., & Boemer, F. (17 June 2023). DEPISTAGE NEONATAL DE LA DREPANOCYTOSE ET DU DEFICIT EN GLUCOSE-6-PHOSPHATE DESHYDROGENASE AU SEIN DE TROIS MATERNITES DU SUD KIVU [Paper presentation]. conférence facultaire, bukavu, Congo - Kinshasa.

Rousseau, A.-F., Dongier, A., COLSON, C., MINGUET, P., Defraigne, J.-O., MINGUET, G., Misset, B., & Boemer, F. (19 May 2023). Serum Acylcarnitines Profile in Critically Ill Survivors According to Illness Severity and ICU Length of Stay: An Observational Study. Nutrients, 15 (10), 2392. doi:10.3390/nu15102392

Meiouet, F., El Kabbaj, S., Abilkassem, R., & Boemer, F. (10 March 2023). Moroccan Experience of Targeted Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry. Pediatric Reports, 15 (1), 227 - 236. doi:10.3390/pediatric15010018

Lumaka Zola, A., Fasquelle, C., Debray, F.-G., Alkan, S., Jacquinet, A., Harvengt, J., Boemer, F., Mulder, A., VAESSEN, S., Viellevoye, R., Palmeira, L., CHARLOTEAUX, B., Brysse, A., BULK, S., Rigo, V., & Bours, V. (16 February 2023). Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours. International Journal of Molecular Sciences, 24 (4), 4003. doi:10.3390/ijms24044003

Kasai, E. T., Gulbis, B., Ntukamunda, J. K., Bours, V., Batina Agasa, S., Marini Djang'Eing'A, R., Boemer, F., Katenga Bosunga, G., Ngbonda Dauly, N., Sokoni Vutseme, L. J., Boso Mokili, B., & Alworong’a Opara, J. P. (2023). Newborn screening for sickle cell disease in Kisangani, Democratic Republic of the Congo: an update. Hematology, 28 (1). doi:10.1080/16078454.2023.2213043

Ngongan, A., Boemer, F., COLSON, C., Misset, B., MINGUET, G., & Rousseau, A.-F. (2023). Mid-term acylcarnitine profile evolution in survivors of a prolonged ICU stay. European Journal of Anaesthesiology, 40 (eSuppl 61), 280.

Rousseau, A.-F., Dongier, A., COLSON, C., Misset, B., MINGUET, G., & Boemer, F. (2023). Acylcarnitine profile in survivors of a prolonged versus a short stay in ICU. European Journal of Anaesthesiology, 40 (e-Suppl 61), 279.

Kruse, C., Dieu Marc, Renaud, B., François, A.-C., Boemer, F., Art, T., Demazy, C., Renard, P., & Votion, D. (15 December 2022). Proteomic profiling in equine atypical myopathy: new metabolic insights [Paper presentation]. FARAH-Day 2022, Liège, Belgium.

Renaud, B., Kruse, C., François, A.-C., Brisson, L., Boemer, F., Gustin, P., & Votion, D. (15 December 2022). Confirmed hypoglycin A toxicosis in two gnus [Paper presentation]. FARAH-Day, Liege, Belgium.

Kasai, E. T., Kadima, J. N., Alworong'a Opara, J. P., Boemer, F., Dresse, M. F., Makani, J., Bours, V., Marini Djang'Eing'A, R., Paul, K.-K., & Batina Agasa, S. (08 August 2022). Pairing parents and offspring's HemoTypeSC Test to validate results and confirm sickle cell pedigree:  a case study in Kisangani, the Democratic Republic of the Congo. Hematology (Amsterdam, Netherlands), 27 (1), 853-859. doi:10.1080/16078454.2022.2107351

Renaud, B., Kruse, C., François, A.-C., Grund, L., Bunert, C., Brisson, L., Boemer, F., Gault, G., Ghislain, B., Petitjean, T., Gustin, P., & Votion, D. (26 July 2022). Acer pseudoplatanus: A Potential Risk of Poisoning for Several Herbivore Species. Toxins, 14 (8). doi:10.3390/toxins14080512

Tosi, I., Kruse, C., Boemer, F., & Votion, D. (28 June 2022). Serum acylcarnitine profiles in horses affected by type-1 PSSM before and after submaximal exercise. Comparative Exercise Physiology, 18.

Dangouloff, T., Hiligsmann, M., Deconinck, N., D'Amico, A., Seferian, A. M., Boemer, F., & Servais, L. (2022). Financial cost and quality of life of patients with spinal muscular atrophy identified by symptoms or newborn screening. Developmental Medicine and Child Neurology. doi:10.1111/dmcn.15286

Bonhomme, M., Patarin, F., Kruse, C., François, A.-C., Tosi, I., Boemer, F., CHERAMY-BIEN, J.-P., Leleu, C., Couroucé, A., Renaud, B., Pincemail, J., Wouters, C., & Votion, D. (03 June 2022). Importance du métabolisme lipidique chez le galopeur [Poster presentation]. Journées Sciences & Innovations Équines, Saumur, France.

ROUSSEAU, A.-F., schmitz, S., CAVALIER, E., Misset, B., & BOEMER, F. (07 March 2022). Altered Serum Acylcarnitines Profile after a Prolonged Stay in Intensive Care. Nutrients, 14 (5), 1122. doi:10.3390/nu14051122

Koracin, V., Loeber, J. G., Mlinaric, M., Battelino, T., Bonham, J. R., Groselj, U., COVID-NBS ISNS global, N., Greaves, R. (Other coll.), Junek, R. (Other coll.), Zeyda, M. (Other coll.), BOEMER, F. (Other coll.), Liu, Z. (Other coll.), Sosova, I. (Other coll.), Skaricic, A. (Other coll.), Zigman, T. (Other coll.), Nicolau, A. (Other coll.), Vogazianos, M. (Other coll.), Chrastina, P. (Other coll.), Blankenstein, O. (Other coll.), ... Mai, T. (Other coll.). (March 2022). Global impact of COVID-19 on newborn screening programmes. BMJ Global Health, 7 (3). doi:10.1136/bmjgh-2021-007780

BOEMER, F., JOSSE, C., LUIS, G., Di Valentin, E., Thiry, J., CELLO, C., CABERG, J.-H., DADOUMONT, C., HARVENGT, J., Lumaka, A., BOURS, V., & DEBRAY, F.-G. (18 February 2022). Novel Loss of Function Variant in BCKDK Causes a Treatable Developmental and Epileptic Encephalopathy. International Journal of Molecular Sciences, 23 (4), 2253. doi:10.3390/ijms23042253

Kasai, E. T., Alworong'a Opara, J. P., Ntokamunda Kadima, J., Kalenga, M., Batina Agasa, S., Marini Djang'Eing'A, R., & Boemer, F. (24 January 2022). Overview of current progress and challenges in diagnosis, and management of pediatric sickle cell disease in Democratic Republic of the Congo. Hematology (Amsterdam, Netherlands), 27 (1), 132-140. doi:10.1080/16078454.2021.2023399

schmitz, S., BOEMER, F., FARRAUTO, L., CAVALIER, E., Misset, B., & ROUSSEAU, A.-F. (December 2021). Acylcarnitines profile in survivors of a prolonged ICU stay. European Journal of Anaesthesiology, 38 (e-Suppl 39), 169.

Beckers, P., Boemer, F., Servais, L., & Bours, V. (21 September 2021). METHODS AND TOOLS FOR ANALYSING THE DUCHENNE MUSCULAR DYSTROPHY (DMD) GENE.

Lopez Granados, L., BOEMER, F., Pereira, T., Servais, L., & Morales, I. (April 2021). Cribado neonatal de la atrofia muscular espinal: el momento es ahora. Pediatria de Atencion Primaria, 23.

Vandevelde, N. M., Vermeersch, P., Devreese, K. M. J., Vincent, M.-F., Gulbis, B., Eyskens, F., BOEMER, F., GOTHOT, A., Van Hoof, V. O., Bonroy, C., Stepman, H., Martens, G. A., Bossuyt, X., Roosens, L., Smet, J., Laeremans, H., Weets, I., Minon, J.-M., Vernelen, K., & Coucke, W. (17 February 2021). Belgian rare diseases plan in clinical pathology: identification of key biochemical diagnostic tests and establishment of reference laboratories and financing conditions. Orphanet Journal of Rare Diseases, 16 (1), 89. doi:10.1186/s13023-021-01728-1

BECKERS, P., CABERG, J.-H., DIDEBERG, V., Dangouloff, T., den Dunnen, J. T., BOURS, V., Servais, L., & BOEMER, F. (04 February 2021). Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon‑skipping therapy. Scientific Reports, 11, 3011. doi:10.1038/s41598-021-82725-z

BOEMER, F., Caberg, J.-H., Beckers, P., Dideberg, V., di Fiore, S., Bours, V., Marie, S., Dewulf, J., Marcelis, L., Deconinck, N., Daron, A., Blasco-Perez, L., Tizzano, E., Hiligsmann, M., Lombet, J., Pereira, T., Lopez-Granados, L., Shalchian-Tehran, S., van Assche, V., ... Servais, L. (2021). Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium. Scientific Reports, 11 (1), 19922. doi:10.1038/s41598-021-99496-2

Dangouloff, T., Boemer, F., & Servais, L. (2021). Newborn screening of neuromuscular diseases. Neuromuscular Disorders. doi:10.1016/j.nmd.2021.07.008

Kambale-Kombi, P., Marini Djang'Eing'A, R., Alworong'a Opara, J.-P., Minon, J.-M., BOEMER, F., BOURS, V., Tonen-Wolyec, S., Kayembe Tshilumba, C., & Batina-Agasa, S. (January 2021). Management of sickle cell disease: current practices and challenges in a northeastern region of the Democratic Republic of the Congo. Hematology, 26 (1), 199-205. doi:10.1080/16078454.2021.1880752

Loeber, J. G., Platis, D., Zetterström, R. H., Almashanu, S., BOEMER, F., Bonham, J. R., Borde, P., Brincat, I., Cheillan, D., Dekkers, E., Dimitrov, D., Fingerhut, R., Franzson, L., Groselj, U., Hougaard, D., Knapkova, M., Kocova, M., Kotori, V., Kozich, V., ... Schielen, P. C. J. I. (2021). Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010. International Journal of Neonatal Screening, 7 (1). doi:10.3390/ijns7010015

Renaud, B., François, A.-C., Boemer, F., Kruse, C., Stern, D., PIOT, A., Petitjean, T., Gustin, P., & Votion, D. (2021). Grazing Mares on Pasture with Sycamore Maples: A Potential Threat to Suckling Foals and Food Safety through Milk Contamination. Animals, 11 (1). doi:10.3390/ani11010087

Tosi, I., Art, T., BOEMER, F., Votion, D., & Davis, M. S. (2021). Acylcarnitine profile in Alaskan sled dogs during submaximal multiday exercise points out metabolic flexibility and liver role in energy metabolism. PLoS ONE, 16 (8), 0256009. doi:10.1371/journal.pone.0256009

Van Den Bogaert, K., Lannoo, L., Brison, N., Gatinois, V., Baetens, M., Blaumeiser, B., BOEMER, F., Bourlard, L., Bours, V., De Leener, A., De Rademaeker, M., Désir, J., Dheedene, A., Duquenne, A., Fieremans, N., Fieuw, A., GATOT, J.-S., Grisart, B., Janssens, K., ... Vermeesch, J. R. (2021). Outcome of publicly funded nationwide first-tier noninvasive prenatal screening. Genetics in Medicine, 23 (6), 1137-1142. doi:10.1038/s41436-021-01101-4

van Riel, M., Brison, N., Baetens, M., Blaumeiser, B., BOEMER, F., Bourlard, L., BULK, S., De Leener, A., Désir, J., Devriendt, K., Dheedene, A., Duquenne, A., Fieremans, N., Fieuw, A., GATOT, J.-S., GRISART, B., Janssens, S., Khudashvili, N., Lannoo, L., ... Janssens, K. (2021). Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations. Obstetrics and Gynecology, 137 (6), 1102-1108. doi:10.1097/AOG.0000000000004385

van Wegberg, A. M. J., Trefz, F., Gizewska, M., Ahmed, S., Chabraoui, L., Zaki, M. S., Maillot, F., van Spronsen, F. J., Ahring, K., Al Mutairi, F., Arnoux, J. B., Ballhausen, D., Baruteau, J., Bernstein, L., Bijarnia-Mahay, S., Boemer, F., Bordugo, A., Brodosi, L., Brooks, S., ... Study Group on Missed PKU and Missed to Follow-Up. (2021). Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey. Journal of Pediatrics, 239, 231 - 234.e2. doi:10.1016/j.jpeds.2021.08.070

Renaud, B., François, A.-C., BOEMER, F., Kruse, C., Stern, D., Gustin, P., & Votion, D. (20 November 2020). Hypoglycin A and methylenecyclopropyl acetic acid-carnitine transfer to milk: a potential exposition of unweaned foals [Poster presentation]. 7th FARAH Day, Sart Tilman, Belgium.

Dangouloff, T., Burghes, A., Bertini, E., BOEMER, F., Hiligsmann, M., Mueller-Felber, W., Tiziano, F. D., Young, P., Germanenko, O., De Lemus, M., Ouillade, L., Rucinski, K., Stephenson, K., Farwell, W., Gorni, K., Hjort, M., Kausar, I., Tizzano, E. F., & Servais, L. (January 2020). 244th ENMC International Workshop: Newborn screening in Spinal Muscular Atrophy May 10-12, 2019, Hoofdorp, The Netherlands. Neuromuscular Disorders, 30 (1), 93-103. doi:10.1016/j.nmd.2019.11.002

Debray, F.-G., WEEKERS, L., Dadoumont, C., Grandjean, C., DEBERG, M., Boemer, F., & Bours, V. (2020). Actualités thérapeutiques dans les erreurs innées du métabolisme. Revue Médicale de Liège, 75 (5-6), 420-425.

Dufour, P., PIRARD, C., SEGHAYE, M.-C., BOEMER, F., & CHARLIER, C. (January 2020). Associations entre exposition aux polluants organiques persistants durant la grossesse et fonction thyroïdienne durant la petite enfance : étude longitudinale pilote et revue de la littérature. Revue Médicale de Liège, 75 (1), 37-42.

Kambale-Kombi, P., Marini Djang'Eing'A, R., Alworong'a Opara, J.-P., Wa Inena, G. I., Falay Sadiki, D., BOEMER, F., BOURS, V., Tshilumba, C. K., & Batina-Agasa, S. (2020). Comorbidity of sickle cell trait and albinism: a cross-sectional survey in the Democratic Republic of the Congo. Pan African Medical Journal, 35, 127. doi:10.11604/pamj.2020.35.127.21113

Votion, D., François, A.-C., Renaud, B., Wouters, C., Farinelle, A., BOEMER, F., CELLO, C., Amory, H., Marcillaud-Pitel, C., Richard, E., & Gustin, P. (2019). La myopathie atypique : le top 10 des dernières nouvelles. In C. Mespoulhès, Proceeding Journée AVEF (Association des Vétérinaires Equins Français) (pp. 102-104). France: Association des Vétérinaires Equins Français.

Renaud, B., François, A.-C., BOEMER, F., Macillaud-Pitel, C., Gustin, P., & Votion, D. (2019). Diagnostic and prognostic value of hypoglycin A, methylenecyclopropyl acetic acidcarnitine and, acylcarnitines profile in horses with atypical myopathy. In C. Bayrou, C. Delguste, C. Douny, C. Gatez, Jauniaux, Ponthier, A. Sartelet, D. Thiry, ... D. Votion, Proceedings of the 6th FARAH-Day (pp. 25). Liège 1 (Sart Tilman), Belgium: Presses de la Faculté de Médecine vétérinaire de l’Université de Liège.

BOEMER, F., CABERG, J.-H., DIDEBERG, V., BECKERS, P., Marie, S., Marcelis, L., Bours, V., Dangouloff, T., & Servais, L. (September 2019). (S)un (M)ay (A)rise on SMA : l'espoir d'une region sans amyotrophie spinale. Revue Médicale de Liège, 74 (9), 461-464.

François, A.-C., Renaud, B., Weber, M., Marcillaud-Pitel, C., BOEMER, F., Jourdan, M., CELLO, C., Richard, E., Gustin, P., & Votion, D. (May 2019). Comment confirmer le diagnostic de myopathie atypique ? [Poster presentation]. Journées Sciences et Innovations équines, Saumur, France.

ONESTI, C. E., BOEMER, F., JOSSE, C., LEDUC, S., Poulet, C., BOURS, V., & JERUSALEM, G. (2019). Tryptophan catabolism differentiates breast cancer patients from healthy controls but does not predict outcome. Annals of Oncology.

Dangouloff, T., BOEMER, F., CABERG, J.-H., DIFIORE, S., BECKERS, P., MARIE, S., MARCELIS, L., & Servais, L. (2019). Reducing the diagnosis time of neonatal screening by optimizing the screening process: the southern Belgian experience. Neuromuscular Disorders, 29, 132. doi:10.1016/j.nmd.2019.06.339

ONESTI, C. E., BOEMER, F., JOSSE, C., LEDUC, S., BOURS, V., & JERUSALEM, G. (2019). Tryptophan catabolism increases in breast cancer patients compared to healthy controls without affecting the cancer outcome or response to chemotherapy. Journal of Translational Medicine, 17, 239. doi:10.1186/s12967-019-1984-2

Gulbis, B., Lê, P.-Q., Ketelslegers, DRESSE, M.-F., Adam, A.-S., Cotton, F., BOEMER, F., BOURS, V., Minon, J.-M., & Ferster, A. (2018). Neonatal Screening for Sickle Cell Disease in Belgium for More than 20 Years: An Experience for Comprehensive Care Improvement. International Journal of Neonatal Screening. doi:10.3390/ijns4040037

BOBOLI, H., BOEMER, F., MASTOURI, M., & Seghaye, M.-C. (October 2018). Depistage neonatal de la mucoviscidose : vers une implementation nationale en Belgique en 2019. Revue Médicale de Liège, 73 (10), 497-501.

BOEMER, F. (2018). (S)un (M)ay (A)rise on SMA: The Newborn Screening Liege’s Experience. In Meeting Report - Reliability of Neonatal Screening Results.

Bonham, J., Carling, R., Lindner, M., Franzson, L., Zetterstrom, R., BOEMER, F., Cerone, R., Eyskens, F., Vilarinho, L., Hougaard, D., & Schielen, P. (2018). Raising Awareness of False Positive Newborn Screening Results Arising from Pivalate-Containing Creams and Antibiotics in Europe When Screening for Isovaleric Acidaemia. International Journal of Neonatal Screening. doi:10.3390/ijns4010008

Dangouloff, T., Hiligsmann, M., CABERG, J.-H., BOEMER, F., & Servais, L. (2018). Development of a decision-analytic model for the economic evaluation of newborn screening for spinal muscular atrophy. Neuromuscular Disorders, 28 (S29–S146), 59. doi:10.1016/j.nmd.2018.06.125

BOEMER, F. (12 May 2017). NGS for NBS : Are we ready for « Next Generation » Newborn Screening ? [Paper presentation]. Metabolics.be Annual Meeting.

BOEMER, F., Detilleux, J., CELLO, C., Amory, H., Marcillaud-Pitel, C., Richard, E., Van Galen, G., van Loon, G., Lefère, L., & Votion, D. (2017). Acylcarnitines profile best predicts survival in horses with atypical myopathy. PLoS ONE, 1-16. doi:10.1371/journal.pone.0182761

BOEMER, F., Fasquelle, C., D'OTREPPE DE BOUVETTE, S., JOSSE, C., DIDEBERG, V., SEGERS, K., GUISSARD, V., CAPRARO, V., Debray, F.-G., & Bours, V. (2017). A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases. Scientific Reports, 7 (1), 17641. doi:10.1038/s41598-017-18038-x

Detemmerman, L., Olivier, S., BOURS, V., & BOEMER, F. (2017). Innovative PCR without DNA extraction for African sickle cell disease diagnosis. Hematology, 1-6. doi:10.1080/10245332.2017.1371470

Winckert, A., VRANKEN, L., BOEMER, F., Courtois, J., & Cavalier, E. (2017). L'hypophosphatasie. Revue Médicale de Liège, 72 (12), 547-551.

Filee, R., Schoos, R., & BOEMER, F. (2013). Evaluation of Physiological Amino Acids Profiling by Tandem Mass Spectrometry. JIMD Reports.

Stephenne, X., DEBRAY, F.-G., Smets, F., Jazouli, N., Sana, G., Tondreau, T., Menten, R., Goffette, P., BOEMER, F., Schoos, R., Gersting, S. W., Najimi, M., Muntau, A. C., Goyens, P., & Sokal, E. M. (2012). Hepatocyte transplantation using the domino concept in a child with Tetrabiopterin non-responsive phenylketonuria. Cell Transplantation, 21 (12), 2765-70. doi:10.3727/096368912X653255

Vandevijvere, S., Coucke, W., Vanderpas, J., Trumpff, C., Fauvart, M., Meulemans, A., Marie, S., Vincent, M., SCHOOS, R., BOEMER, F., Vanwynsberghe, T., Philips, E., Eyskens, F., Wuyts, B., Selimaj, V., Van Overmeire, B., Kirkpatrick, C., Van Oyen, H., & Moreno-Reyes, R. (2012). Neonatal thyroid-stimulating hormone concentrations in Belgium: a useful indicator for detecting mild iodine deficiency? PLoS ONE. doi:10.1371/journal.pone.0047770

REENAERS, C., DELWAIDE, J., GERARD, C., Bastens, B., Bataille, C., BOEMER, F., Servais, B., BELAICHE, J., DE ROOVER, A., DETRY, O., HONORE, P., Meurisse, M., Rentier, B., & VAIRA, D. (2004). HCV genotype 5: an easy to treat population. Acta Gastro-Enterologica Belgica, 67, 15.