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Schoos Roland

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Main Referenced Co-authors
Boemer, François  (13)
Bours, Vincent  (6)
Koulischer, Lucien  (4)
Verloes, Alain  (4)
Deberg, Michelle  (3)
Main Referenced Keywords
aTRAQ (2); Mass spectrometry (2); Neonatal screening (2); acylcarnitines (1); Amino acids (1);
Main Referenced Unit & Research Centers
FARAH - Fundamental and Applied Research for Animals and Health - ULiège (1)
Main Referenced Disciplines
Genetics & genetic processes (11)
Public health, health care sciences & services (2)
Endocrinology, metabolism & nutrition (1)
Hematology (1)
Laboratory medicine & medical technology (1)

Publications (total 17)

The most downloaded
146 downloads
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 https://hdl.handle.net/2268/138074

The most cited

121 citations (OpenAlex)

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 https://hdl.handle.net/2268/138064

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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.

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

Verloes, A., Gillerot, Y., Van Maldergem, L., Schoos, R., Herens, C., Jamar, M., Dideberg, V., Lesenfants, S., & Koulischer, L. (January 2001). Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test? European Journal of Human Genetics, 9 (1), 1-4. doi:10.1038/sj.ejhg.5200575
Peer Reviewed verified by ORBi

Schoos, R., Verloes, A., Bourguignon, J.-P., & Koulischer, L. (May 1998). Les programmes de dépistage systématique en néonatologie. Aspects pharmaco-économiques. Revue Médicale de Liège, 53 (5), 311-5.
Peer reviewed

Verloes, A., Schoos, R., Herens, C., Vintens, A., & Koulischer, L. (January 1995). A Prenatal Trisomy 21 Screening Program Using Alpha-Fetoprotein, Human Chorionic Gonadotropin, and Free Estriol Assays on Maternal Dried Blood. American Journal of Obstetrics and Gynecology, 172 (1, Pt 1), 167-74. doi:10.1016/0002-9378(95)90108-6
Peer Reviewed verified by ORBi

Koulischer, L., Schoos, R., Verloes, A., & Herens, C. (December 1991). Le dépistage prénatal de la trisomie 21 sur sérum maternel. Mise au point. Revue Médicale de Liège, 46 (12), 625-32.
Peer reviewed

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