Publications and communications of François Boemer

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

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

Renaud, B., Kruse, C., François, A.-C., Boemer, F., Gustin, P., & Votion, D. (11 July 2023). On the edge of equine atypical myopathy: A first large‐scale report of subclinical Hypoglycin A poisoning in horses. Journal of Veterinary Pharmacology and Therapeutics, 46 (1), 83. doi:10.1111/jvp.13278

Tangeraas, T., Constante, J. R., Backe, P. H., Oyarzábal, A., Neugebauer, J., Weinhold, N., Boemer, F., Debray, F.-G., Ozturk-Hism, B., Evren, G., Tuba, E. F., Ummuhan, O., Footitt, E., Davison, J., Martinez, C., Bueno, C., Machado, I., Rodríguez-Pombo, P., Al-Sannaa, N., ... García-Cazorla, A. (03 July 2023). BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening. Brain: a Journal of Neurology, 146 (7), 3003 - 3013. doi:10.1093/brain/awad010

Bonhomme, M., Patarin, F., Kruse, C., François, A.-C., Renaud, B., Couroucé, A., Richard, E. A., Leleu, C., Boemer, F., Toquet, M.-P., Seignot, J., Wouters, C., & Votion, D. (July 2023). Characterisation of high-intensity exercise during training using an untargeted metabolomics approach in thoroughbred flat racehorses [Poster presentation]. 4th ECVSMR Scientific Meeting, Maisons-Alfort, France.

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., Gonon Rodrigues 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

Dangouloff, T., MOURAUX, C., Piazzon, F., Mashhadizadeh, D., Hovhannesyan, K., Helou, L., Gonon Rodrigues 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.

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.

Wouters, C., Voz, M., Boemer, F., Joris, M., & Votion, D. (15 December 2022). Zebrafish larvae model to screen for the risk of Acer pseudoplatanus intoxication in grazing animals [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.

BOEMER, F. (12 November 2021). Spinal Muscular Atrophy Survey of European (and overseas) Screening Laboratory Experience [Paper presentation]. ISNS 2021.

BOULANGER, M., BOEMER, F., COENEN, R., LUIS, G., & DEBOIS, D. (10 November 2021). Newborn Screening for Endocrine Disorders: Belgian Experience with ZenTech s.a. devices [Poster presentation]. ISNS 2021.

ROUSSEAU, A.-F., schmitz, S., COLSON, C., FARRAUTO, L., MINGUET, P., CAVALIER, E., Misset, B., & BOEMER, F. (November 2021). Etude du profil en acylcarnitines après séjour prolongé aux soins intensifs [Poster presentation]. Journées Francophones de Nutrition, Lille, France.

BOEMER, F. (06 October 2021). Newborn Screening of Duchenne Muscular Dystrophy Specifically Targeting Deletions Amenable to Exon-skipping Therapy [Paper presentation]. APHL 2021 Newborn Screening Symposium, online, United States.

BOEMER, F. (27 August 2021). Experiencia belga en el Tamizaje Neonatal de las Hemoglobinopatias: 14 años de experiencia con espectrometria de masas [Paper presentation]. Simposio Internacional de Tamizaje Neonatal.

BOEMER, F. (07 August 2021). Experiencia belga en el Tamizaje Neonatal de las Hemoglobinopatias: 14 años de experiencia con espectrometria de masas [Paper presentation]. Simposio de Tamizaje Neonatal 2021.

BOEMER, F. (20 May 2021). Aminoacidopathies : Aspects cliniques et analytiques [Paper presentation]. Formation Continue de Biologie Clinique.

BOEMER, F. (08 April 2021). Métodos de laboratorio para el cribado neonatal de atrofia muscular espinal y experiencia de implantación de un estudio piloto en Bélgica [Paper presentation]. Sociedad Española de Medicina de Laboratorio.

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.

BOEMER, F. (19 March 2021). Improving safety of Fluoro-Pyrimidine treatment based on assessment of Dihydropyrimidine Dehydrogenase activity [Paper presentation]. BOPP days.

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

Meiouet, F., Kabbaj, S. E., DEBRAY, F.-G., & BOEMER, F. (2021). Diagnostic et suivi de la phénylcétonurie par LC-MS-MS au Maroc. Annales de Biologie Clinique. doi:10.1684/abc.2021.1619

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. (14 January 2021). L'expérience wallonne du dépistage néonatal de l'amyotrophie spinale [Paper presentation]. Révision de la Loi de Bioéthique en 2021 et ses implications en génétique, France.

BECKERS, P., CABERG, J.-H., DIDEBERG, V., Dangouloff, T., den Dunnen, J. T., BOURS, V., Servais, L., & BOEMER, F. (2021). Newborn Screening of Duchenne Muscular Dystrophy Specifically Targeting Deletions Amenable to Exon-skipping Therapy [Poster presentation]. European Human Genetics Conference - ESHG.

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

Coughlin, C. R. N., Tseng, L. A., Abdenur, J. E., Ashmore, C., BOEMER, F., Bok, L. A., Boyer, M., Buhas, D., Clayton, P. T., Das, A., Dekker, H., Evangeliou, A., Feillet, F., Footitt, E. J., Gospe, S. M. J., Hartmann, H., Kara, M., Kristensen, E., Lee, J., ... van Karnebeek, C. D. M. (2021). Consensus guidelines for the diagnosis and management of pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency. Journal of Inherited Metabolic Disease. doi:10.1002/jimd.12332

Dangouloff, T., Boemer, F., & Servais, L. (2021). Newborn screening of neuromuscular diseases. Neuromuscular disorders : NMD. 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 : official journal of the American College of Medical Genetics, 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

Wouters, C., Toquet, M.-P., Renaud, B., François, A.-C., Fortier-Guillaume, J., Marcillaud-Pitel, C., BOEMER, F., De Tullio, P., Richard, E., & Votion, D. (2021). Metabolomic Signatures Discriminate Horses with Clinical Signs of Atypical Myopathy from Healthy Co-grazing Horses. Journal of Proteome Research. doi:10.1021/acs.jproteome.1c00225

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., BOEMER, F., CABERG, J.-H., & Servais, L. (2020). Correspondence on: “Discrepancy in Spinal Muscular Atrophy Incidence findings in newborn screening programs: the influence of carrier screening?” by Kay et al. Genetics in Medicine. doi:10.1038/s41436-020-0887-1

NEEMA UFOYMUNGU, Y., JUAKALI SIHALIKYOLO, J. J., Marini Djang'Eing'A, R., KATENGA BOSUNGA, G., Avohou, T. H., LEDUC, S., BOEMER, F., & BATINA AGASA, S. (2020). Performance of Sickle SCAN® in the Screening of Sickle Cell Disease in Kisangani Pregnant Women and Attitude towards Results. Open Journal of Blood Diseases. doi:10.4236/ojbd.2020.102003

BOEMER, F. (06 March 2020). (S)un (M)ay (A)rise on SMA: the newborn screening experience in Southern Belgium [Paper presentation]. BeSHG, Bruxelles, Belgium.

TEBANDITE KASAI, E., BOEMER, F., Marini Djang'Eing'A, R., KADIMA NTOKAMUNDA, J., BATINA AGASA, S., NGBONDA DAULY, N., & ALWORONG'A OPARA, J.-P. (2020). Systematic Screening of Neonatal Sickle Cell Disease with HemoTypeSCTM Kit-Test: Case Study and Literature Review. Open Journal of Blood Diseases. doi:10.4236/ojbd.2020.101002

Dangouloff, T., BOEMER, F., DIDEBERG, V., CABERG, J.-H., & Servais, L. (2020). Reader response: Discrepancy in redetermination of SMN2 copy numbers in children with SMA [letter to the editor]. American Academy of Neurology. doi:10.1212/WNL.0000000000009907

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

BOEMER, F. (17 December 2019). Underivatized Method for the Newborn Screening of Aminoacids, Acylcarnitines and LPC’s [Paper presentation]. Mass Spectrometry in Laboratory Medicine, Bruxelles, Belgium.

BOEMER, F. (07 December 2019). Guthrie 3.0 [Paper presentation]. Groupement Belge des Pédiatres de langue Française : congrès d'hiver, Gembloux, Belgium.

BOEMER, F. (15 November 2019). (S)un (M)ay (A)rise on SMA The newborn screening program in Southern Belgium [Paper presentation]. Royal Belgian Society of Laboratory Medicine.

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. (27 September 2019). 40 ans de dépistage prénatal d'aneuploïdies [Paper presentation]. Corata.

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.

BOEMER, F. (27 June 2019). (S)un (M)ay (A)rise on SMA: Quand les nouveaux traitements de la SMA bouleversent les paradigmes [Paper presentation]. Formation Continue - Biologie Clinique.

BOEMER, F. (2019). Association of SMA neonatal screening with other screening tests. Neuromuscular Disorders.

BOEMER, F. (2019). In-house techniques for SMA screening test: validation. Neuromuscular Disorders.

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.

Votion, D., BOEMER, F., Marcillaud-Pitel, C., Jourdan, M., CELLO, C., François, A.-C., Renaud, B., Toquet, M. P., Cassart, D., Detilleux, J., & Richard, E. (March 2019). Point sur les outils diagnostiques et pronostiques de la myopathie atypique. Pratique Vétérinaire Équine, 201, 12-19.

Boemer, F., CABERG, J.-H., Dideberg, V., DARDENNE, D., Bours, V., Hiligsmann, M., Dangouloff, T., & Servais, L. (2019). Newborn screening for SMA in Southern Belgium. Neuromuscular Disorders. doi:10.1016/j.nmd.2019.02.003

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

Cesarini Latorre, C., Votion, D., BOEMER, F., cerri, S., Lefère, L., Palmers, K., van Loon, G., Amory, H., Daube, G., & Taminiau, B. (09 November 2018). Correlation between faecal microbiota and serum levels of Hypoglycin A and MCPA-carnitine in horses with atypical myopathy [Paper presentation]. 11th European College of Equine Internal Medicine congress.

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

Wimmer-Scherr, C., Votion, D., BOEMER, F., Cerri, S., Lefère, L., Palmers, K., van Loon, G., Amory, H., Daube, G., Taminiau, B., & Cesarini Latorre, C. (2018). Atypical Myopathy: is there a relationship between serum hypoglycin A and MCPACarnitin levels and the composition of faecal microbiota? In Proceedings 5th FARAH-Day (pp. 29).

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.

Boboli, E., BOEMER, F., Donneau, A.-F., Streel, S., & SEGHAYE, M.-C. (June 2018). Cystic fibrosis newborn screening: a Belgian experience [Poster presentation]. 41st European Cystic Fibrosis Conference, Belgrade, Serbia.

Bunert, C., Langer, S., Votion, D., BOEMER, F., Müller, A., Ternes, K., & Liesegang, A. (2018). Atypical myopathy in Père David’s deer (Elaphurus davidianus) associated with ingestion of hypoglycin A. Journal of Animal Science. doi:10.1093/jas/sky200

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

Habyarimana, J. B. A., Baise, E., Douny, C., Weber, M., BOEMER, F., De Tullio, P., Franck, T., Marcillaud-Pitel, C., Frederich, M., Mouithys-Mickalad, A., Richard, E., Scippo, M.-L., Votion, D., & Gustin, P. (2017). Development of an HPTLC method for determination of hypoglycin A in aqueous extracts of seedlings and samaras of Acer species. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/212226. doi:10.1101/148262

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

Marcillaud-Pitel, C., Baise, E., BOEMER, F., Habyarimana, J. B. A., Gustin, P., CELLO, C., Douny, C., Richard, E., Toquet, M.-P., Detilleux, J., Amory, H., Weber, M., Guez, A., & Votion, D. (2017). Point sur les travaux de recherche sur la myopathie atypique et leurs impacts sur la filière: quoi de neuf ? In Proceeding de la 43ème Journée de la Recherche équine (pp. 27-35).

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

BOEMER, F., Detilleux, J., Baise, E., CELLO, C., Amory, H., Marcillaud-Pitel, C., Richard, E., & Votion, D. (2016). Vivra, ne vivra pas ? Comment définir le pronostic de survie des cas de myopathie atypique ? In Journée AVEF (Association des Vétérinaires Equins Français) (pp. 150-151).

Detemmerman, L., BOEMER, F., SEGERS, K., & Olivier, S. (12 May 2016). Molecular detection of single nucleotide polymorphisms on whole blood without DNA extraction [Poster presentation]. International Society for Laboratory Hematology, Milan, Italy.

DETEMMERMAN, L., BOEMER, F., & OLIVIER, S. (February 2016). Diagnosis of sickle cell disease by innovative PCR without DNA extraction [Poster presentation]. First Joint Meeting of the BeSHG/NVHG, Leuven, Belgium.

Baise, E., Habyarimana, J. B. A., Amory, H., BOEMER, F., Douny, C., Gustin, P., Marcillaud-Pitel, C., Patarin, F., Weber, M., & Votion, D. (2016). Samaras and seedlings of Acer pseudoplatanus are potential sources of hypoglycin A intoxication in atypical myopathy without necessarily inducing clinical signs. Equine Veterinary Journal. doi:10.1111/evj.12499

BOEMER, F., DEBERG, M., SCHOOS, R., CABERG, J.-H., GAILLEZ, S., Dugauquier, C., Delbecque, K., François, A., Maton, P., Demonceau, N., Senterre, G., Ferdinandusse, S., & DEBRAY, F.-G. (2016). Diagnostic pitfall in antenatal manifestations of CPT II deficiency. Clinical Genetics. doi:10.1111/cge.12593

Høffer, S. E., Votion, D., Anderberg, M., BOEMER, F., Nautrup Olsen, S., & Van Galen, G. (2016). Atypical myopathy in Denmark confirmed with the aTRAQ Assay. Journal of Equine Veterinary Science, 47, 77-79. doi:10.1016/j.jevs.2016.08.010

Lemieux, H., BOEMER, F., Van Galen, G., Serteyn, D., Amory, H., Baise, E., Cassart, D., van Loon, G., Marcillaud-Pitel, C., & Votion, D. (2016). Mitochondrial function is altered in horse atypical myopathy. Mitochondrion, 30, 35-41. doi:10.1016/j.mito.2016.06.005

De Ridder, T., BOEMER, F., Baise, E., Amory, H., & Votion, D. (16 October 2015). Identification of a new prognostic tool for atypical myopathy [Paper presentation]. 2nd FARAH-Day, Liège 1 (Sart Tilman), Belgium.

Ernoult, O., Baise, E., BOEMER, F., Gustin, P., Habyarimana, J. B. A., Weber, M., & Votion, D. (16 October 2015). Atypical myopathy: a preliminary study to identify the site of hypoglycin A metabolism [Paper presentation]. 2nd FARAH-Day, Liège 1 (Sart Tilman), Belgium.

BOEMER, F., DEBERG, M., SCHOOS, R., Baise, E., Amory, H., Gault, G., Carlier, J., Gaillard, Y., Marcillaud-Pitel, C., & Votion, D. (2015). Quantification of hypoglycin A in serum using aTRAQ((R)) assay. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 997, 75-80. doi:10.1016/j.jchromb.2015.06.004

BOEMER, F., SCHOOS, R., & DEBERG, M. (2015). Quantification of physiological aminoacids using aTRAQ kit: evaluation and implementation of new markers. Annales de Biologie Clinique, 73 (4), 427-442. doi:10.1684/abc.2015.1066

DEBRAY, F.-G., Stumpfig, C., Vanlander, A. V., DIDEBERG, V., Josse, C., CABERG, J.-H., BOEMER, F., Bours, V., Stevens, R., Seneca, S., Smet, J., Lill, R., & van Coster, R. (2015). Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy. Journal of Inherited Metabolic Disease. doi:10.1007/s10545-015-9857-1

Habyarimana, J. B. A., BOEMER, F., Amory, H., Baise, E., Carlier, J., De Tullio, P., Douny, C., Gault, G., Gustin, P., Fanck, T., Frederich, M., Marcillaud-Pitel, C., Richard, E., Patarin, F., Weber, M., & Votion, D. (2015). Les nouveaux outils de diagnostic et de pronostic de la myopathie atypique. In Proceeding de la 41ème Journée de la Recherche équine.

Ketelslegers, O., Eyskens, F., BOEMER, F., Bours, V., Minon, J.-M., & Gulbis, B. (2015). Epidemiological data on sickle cell disease in Belgium. Belgian Journal of Hematology, 6 (4), 135-141.

McKenzie, R. K., Hill, F. I., Habyarimana, J. B. A., BOEMER, F., & Votion, D. (2015). Detection of hypoglycin A in the seeds of sycamore (Acer pseudoplatanus) and box elder (A. negundo) in New Zealand; the toxin associated with cases of equine atypical myopathy. New Zealand Veterinary Journal, 1-17. doi:10.1080/00480169.2015.1123123

Yahyaoui, R., Rueda, Dayaldasani, A., & BOEMER, F. (2015). Falsos positivos de C5-carnitina elevada en cribado neonatal: A que son debidos? Medicina Clinica. doi:10.1016/j.medcli.2014.03.011

BOEMER, F. (11 December 2014). Cystic Fibrosis screening by simultaneous ELISA for IRT1 and PAP proteins. A pilot study [Paper presentation]. Second Nationale Conference on Research and Education - Personalized Medicine, Lublin, Poland.

BOEMER, F. (October 2014). 6-Years Experience of NBS for Hemoglobin Disorders using TMS [Paper presentation]. 9th ISNS European Neonatal Screening Regional Meeting, Birmingham, United Kingdom.

BOEMER, F., SCHOOS, R., de HALLEUX, V., Kalenga, M., & DEBRAY, F.-G. (2014). Surprising causes of C5-carnitine false positive results in newborn screening. Molecular Genetics and Metabolism, 111 (1), 52-4. doi:10.1016/j.ymgme.2013.11.005

Debray, F.-G., Seneca, S., GONCE, M., Vancampenhaut, K., Bianchi, E., BOEMER, F., WEEKERS, L., Smet, J., & Van Coster, R. (2014). Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene. Mitochondrion. doi:10.1016/j.mito.2014.06.003

RAMAEKERS, V., Thony, B., Sequeira, J. M., Ansseau, M., Philippe, P., BOEMER, F., Bours, V., & Quadros, E. V. (2014). Folinic acid treatment for schizophrenia associated with folate receptor autoantibodies. Molecular Genetics and Metabolism, 113 (4), 307-14. doi:10.1016/j.ymgme.2014.10.002

Munlemvo Mavanga, N., BOEMER, F., SEIDEL, L., Nkebolo Malafu, A., GOTHOT, A., & GERARD, C. (06 November 2013). BLOOD GROUPS, HEMOGLOBIN PHENOTYPES AND CLINICAL DISORDERS OF CONSANGUINEOUS YANSI POPULATION. World Journal of Hematology, 2 (4), 109-114.

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

BOEMER, F., SCHOOS, R., ACQUAVIVA, C., VIANEY-SABAN, C., WEEKERS, L., & DEBRAY, F.-G. (September 2013). HETEROGENOUS CLINICAL AND LABORATORY PRESENTATIONS IN MAD DEFICIENCY [Poster presentation]. 12th International Congress of Inborn Errors of Metabolism, Barcelona, Spain.

Votion, D., Van Galen, G., Sweetan, BOEMER, F., De Tullio, P., Dopagne, C., Lefere, L., Mouithys-Mickalad, A., Patarin, F., Rouxhet, S., van Loon, G., Serteyn, D., Sponseller, B., & Valber, S. (2013). Identification of methylenecyclopropyl acetic acid in serum of European horses with atypical myopathy. Equine Veterinary Journal. doi:10.1111/evj.12117

Marquardt, G., Currier, R., McHugh, D. M. S., Gavrilov, D., Magera, M. J., Matern, D., Oglesbee, D., Raymond, K., Rinaldo, P., Smith, E. H., Tortorelli, S., Willis, S. A., Rocha, H., Vilarinho, L., John, C., Lim, J., Caldwell, S. G., Tomashitis, K., Castĩeiras Ramos, D. E., ... Sesser, D. E. (July 2012). Enhanced interpretation of newborn screening results without analyte cutoff values. Genetics in Medicine, 14 (7), 648-655. doi:10.1038/gim.2012.2

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

McHugh, D., Cameron, C. A., Abdenur, J. E., Abdulrahman, M., Adair, O., Al Nuaimi, S. A., Åhlman, H., Allen, J. J., Antonozzi, I., Archer, S., Au, S., Auray-Blais, C., Baker, M., Bamforth, F., Beckmann, K., Pino, G. B., Berberich, S. L., Binard, R., & BOEMER, F. (March 2011). Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project. Genetics in Medicine, 13 (3), 230-54. doi:10.1097/GIM.0b013e31820d5e67

BOEMER, F., Cornet, Y., LIBIOULLE, C., SEGERS, K., Bours, V., & SCHOOS, R. (2011). 3-years experience review of neonatal screening for hemoglobin disorders using tandem mass spectrometry. Clinica Chimica Acta, 412 (15-16), 1476-9. doi:10.1016/j.cca.2011.04.031

BOEMER, F. (April 2009). Newborn Screening for Sickle Cell Disease using Tandem Mass Spectrometry [Paper presentation]. ISNS European Regional Meeting, Prague, Czechia.

BOEMER, F. (2009). Dépistage Néonatal de la Drépanocytose: Nouvelles Méthodologies [Doctoral thesis, ULiège - Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/170274

Boemer, F., Bours, V., Schoos, R., Hubert, P., & Rozet, E. (2009). Analytical validation based on total error measurement and cut-off interpretation of a neonatal screening TSH-immunoassay. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 877, 2412-2417. doi:10.1016/j.jchromb.2008.11.004

Boemer, F., Ketelslegers, O., Minon, J.-M., Bours, V., & Schoos, R. (2008). Newborn Screening for Sickle Cell Disease Using Tandem Mass Spectrometry. Clinical Chemistry, 54 (12), 2036-2041. doi:10.1373/clinchem.2008.106369

Mutesa, L., Muganga, N., Lissens, W., Boemer, F., Schoos, R., Pierquin, G., & Bours, V. (December 2007). Molecular Analysis in Two Siblings African Patients with Severe Form of Hunter Syndrome: Identification of a Novel (P.Y54x) Nonsense Mutation. Journal of Tropical Pediatrics, 53 (6), 434-7. doi:10.1093/tropej/fmm056

BOEMER, F. (2007). Neonatal screening of hemoglobinopathies on dried blood.

Mutesa, L., Boemer, F., Ngendahayo, L., Rulisa, S., Rusingiza, E., Cwinya-Ay, N., Mazina, D., Kariyo, P., Bours, V., & Schoos, R. (2007). Neonatal screening for sickle cell disease in Central Africa: a study of 1825 newborns with a new enzyme-linked immunosorbent assay test. Journal of Medical Screening, 14 (3), 113-116. doi:10.1258/096914107782066211

Boemer, F., Vanbellinghen, J.-F., Bours, V., & Schoos, R. (2006). Screening for sickle cell disease on dried blood: a new approach evaluated on 27,000 Belgian newborns. Journal of Medical Screening, 13 (3), 132-136. doi:10.1258/096914106778440644

BOEMER, F. (2005). Screening for hemoglobinopathies on dried blood spot by ELISA : 2 years experience on 30,000 newborns.

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.

Boemer, F., Cielniaszek, N., Paulus, J.-M., & Gothot, A. (2002). Evaluation of the Hycel Diagnostics Diana-5 Hematology Analyzer. Laboratory Hematology, 8, 126-133.