  | 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 |
 | Vanderheyden, I., BULK, S., & Jouret, F. (July 2024). Solitary kidney in a patient with Pallister-Hall syndrome. Kidney International, 106 (1), 155. doi:10.1016/j.kint.2024.01.026 Peer Reviewed verified by ORBi |
Chatelain, C., KUKOR, L., BULK, S., Bours, V., & Docampo Martínez, E. (12 April 2024). SKI missense variant c.539C>T p.(Thr180Met), a recurrent variant in Shprintzen-Goldberg syndrome: a case report and review of literature [Poster presentation]. Annual Symposium : Single cells, to care or not to care?, Leuven, Belgium. |
  | Harvengt, J., Docampo Martínez, E., Jacquinet, A., Alkan, S., Martin, M., Debray, F.-G., BULK, S., & Bours, V. (12 April 2024). New paradigms in clinical geneticist practice in the era of emerging therapies: examples of two pediatric syndromes [Poster presentation]. BESHG Annual Symposium 2024. Peer reviewed |
 | Mouraux, C., FOUQUET, C., Artesi, M., Durkin, K., Dideberg, V., BULK, S., & Depierreux, F. (2024). Homozygous pathogenic MYH3 variant associated with arthrogryposis and lingual dystonia [Poster presentation]. BeSHG annual symposium 2024, Belgium. Editorial reviewed |
 | Lorquet, S., Chatelain, C., Laterre, M., FUDVOYE, J., SENTERRE, A., Vanwynsberghe, A., DEBERG, M., Gatot, J.-S., Bulk, S., & Harvengt, J. (January 2024). Cas clinique : Mise au point diagnostique d’une discordance de sexe fœtal à l’ère du IPT génomique : illustration clinique et recommandation pratique. Revue Médicale de Liège, 79 (1). Editorial Reviewed verified by ORBi |
 | Fouquet, C., Leroi, N., Coupier, J., Docampo Martínez, E., Bulk, S., & Bours, V. (17 March 2023). Discordancy in interpretation of a BRCA1 variant in the Belgian population [Poster presentation]. BeSHG Annual Meeting 2023. |
Chatelain, C., Harvengt, J., Leroy, P. (Other coll.), CABERG, J.-H. (Other coll.), Debray, F.-G. (Other coll.), BULK, S. (Other coll.), & Bours, V. (Other coll.). (17 March 2023). Missense variant c.593A>G p.(Lys198Arg) in CSNK2A1, a recurrent variant in Okur-Chung neurodevelopmental syndrome: a case report and review of literature [Poster presentation]. Annual Meeting : To DNA and beyond, Charleroi, Belgium. |
 | 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 Peer Reviewed verified by ORBi |
 | Levaux, J., Farhat, N., VAN CASTEREN, L., BULK, S., & Seghaye, M.-C. (26 August 2022). Cerebral Seizures in an Adolescent with Jervell and Lange-Nielsen Syndrome: It May Not Be Epilepsy. Clinics and Practice, 12 (5), 677-685. doi:10.3390/clinpract12050070 Peer Reviewed verified by ORBi |
 | Kukor, L., BERTOLI, S., CREVECOEUR, J., Bours, V., & BULK, S. (21 April 2022). What does a Genetic Counsellor do in the University Hospital of Liège ? [Poster presentation]. BeSHG/NVHG Annual Genetics Symposium 2022. |
 | Marangoni, M., Smits, G., Ceysens, G., Costa, E., Coulon, R., Daelemans, C., De Coninck, C., Derisbourg, S., Gajewska, K., Garofalo, G., Gounongbe, C., Guizani, M., Holoye, A., Houba, C., Makhoul, J., Norgaard, C., Regnard, C., Romée, S., Soto, J., ... Migeotte, I. (February 2022). Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohorts. Genetics in Medicine, 24 (2), 344 - 363. doi:10.1016/j.gim.2021.09.016 Peer Reviewed verified by ORBi |
 | GALOPIN, C., Denoo, X., JAMBLIN, P., Delbecque, K., BULK, S., Chantraine, F., & Nisolle, M. (February 2021). Lethal metatropic dwarfism: a case report. European Gynecology and Obstetrics, 3 (1), 37-39. Peer reviewed |
 | Faundes, V., Goh, S., Akilapa, R., Bezuidenhout, H., Bjornsson, H. T., Bradley, L., Brady, A. F., Brischoux-Boucher, E., Brunner, H., BULK, S., Canham, N., Cody, D., Dentici, M. L., Digilio, M. C., Elmslie, F., Fry, A. E., Gill, H., Hurst, J., Johnson, D., ... Banka, S. (2021). Clinical delineation, sex differences, and genotype-phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2. Genetics in Medicine. doi:10.1038/s41436-021-01119-8 Peer Reviewed verified by ORBi |
 | DOCAMPO MARTINEZ, E., MARTIN, M., GANGOLF, M., HARVENGT, J., BULK, S., SEGERS, K., LEROI, N., LETE, C., PALMARICCIOTTI, V., Freire Chadrina, M., LAMBERT, F., & Bours, V. (2021). Hérédité et cancer. Revue Médicale de Liège, 76 (5-6), 327-336. Peer reviewed |
 | 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 Peer Reviewed verified by ORBi |
 | HARVENGT, J., ALKAN, S., Florkin, B., BULK, S., & Bours, V. (June 2020). POP1-Skeletal dysplasias : description of two new families [Poster presentation]. European Human Genetics Virtual Conference 2020. |
 | Ebrahimi-Fakhari, D., Teinert, J., Behne, R., Wimmer, M., D'Amore, A., Eberhardt, K., Brechmann, B., Ziegler, M., Jensen, D. M., Nagabhyrava, P., Geisel, G., Carmody, E., Shamshad, U., Dies, K. A., Yuskaitis, C. J., Salussolia, C. L., Ebrahimi-Fakhari, D., Pearson, T. S., Saffari, A., ... Sahin, M. (2020). Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia. Brain: a Journal of Neurology, 143 (10), 2929-2944. doi:10.1093/brain/awz307 Peer Reviewed verified by ORBi |
 | Muys, J., Jacquemyn, Y., Blaumeiser, B., Bourlard, L., Brison, N., BULK, S., Chiarappa, P., De Leener, A., De Rademaeker, M., Désir, J., Destrée, A., Devriendt, K., Dheedene, A., Duquenne, A., Fieuw, A., Fransen, E., GATOT, J.-S., JAMAR, M., Janssens, S., ... Janssens, K. (2020). Prenatally detected copy number variants in a national cohort: A postnatal follow-up study. Prenatal Diagnosis. doi:10.1002/pd.5751 Peer Reviewed verified by ORBi |
BULK, S., & Lumaka Zola, A. (22 November 2019). Preconceptional carrier screening in Belgium [Paper presentation]. 42nd Scientific Meeting Begian Society for Reproductive Medicine (BSRM), Antwerp, Belgium. |
 | HARVENGT, J., Boros, E., BULK, S., & Bours, V. (15 March 2019). COL1A2 mutation in a case of isolated short stature [Poster presentation]. 19th Annual Meeting of the Belgian Society of Human Genetics, Liège, Belgium. |
 | Westra, D., Schouten, M. I., Stunnenberg, B. C., Kusters, B., Saris, C. G. J., Erasmus, C. E., van Engelen, B. G., BULK, S., Verschuuren-Bemelmans, C. C., Gerkes, E. H., de Geus, C., van der Zwaag, P. A., Chan, S., Chung, B., Barge-Schaapveld, D. Q. C. M., Kriek, M., Sznajer, Y., van Spaendonck-Zwarts, K., van der Kooi, A. J., ... Voermans, N. C. (2019). Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service. Journal of Neuromuscular Diseases, 6 (2), 241-258. doi:10.3233/JND-180376 Peer Reviewed verified by ORBi |
 | Bachmann, C., Noreen, F., Voermans, N. C., Schär, P. L., Vissing, J., Fock, J. M., BULK, S., Kusters, B., Moore, S. A., Beggs, A. H., Mathews, K. D., Meyer, M., Genetti, C. A., Meola, G., Cardani, R., Mathews, E., Jungbluth, H., Muntoni, F., Zorzato, F., & Treves, S. (2019). Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies. Human Mutation. doi:10.1002/humu.23745 Peer Reviewed verified by ORBi |
 | Ebetiuc, I., BULK, S., & LEROY, P. (2019). L'heterotopie nodulaire periventriculaire. Un cas pediatrique. Revue Médicale de Liège, 74 (7-8), 388-390. |
 | BARREA, C., VAESSEN, S., BULK, S., HARVENGT, J., & Misson, J.-P. (2018). Phenotype-genotype correlation in children with neurofibromatosis type 1. Neuropediatrics. doi:10.1055/s-0037-1620239 Peer Reviewed verified by ORBi |
 | BERTOLI, S., VAN CASTEREN, L., Bours, V., & BULK, S. (16 February 2018). The cardiogenetics consultation : an inventorisation of the Liege population [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |
 | HARVENGT, J., Schierloh, U., BULK, S., & PIERQUIN, G. (16 February 2018). Post axial polydactyly : isolated symptom or part of a syndrome. A case of BBS8 with two novel molecular anomalies [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |
 | D'OTREPPE DE BOUVETTE, S., Lombet, J., Tebache, M., CABERG, J.-H., & BULK, S. (16 February 2018). Another case of Galloway-Mowat syndrome associated with a biallelic mutation of the OSGEP gene [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |
 | ALKAN, S., LEROY, P., & BULK, S. (16 February 2018). Confirmation of an association between CTNNB1 mutations and hyperekplexia [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |
 | KUKOR, L., BERTOLI, S., Bours, V., BULK, S., & DOCAMPO MARTINEZ, E. (16 February 2018). Ehlers-Danlos syndrome in the University Hospital of Liege [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |
 | Muys, J., Blaumeiser, B., Jacquemyn, Y., Bandelier, C., Brison, N., BULK, S., Chiarappa, P., COURTENS, W., De Leener, A., De Rademaeker, M., Desir, J., Destree, A., Devriendt, K., Dheedene, A., Fieuw, A., Fransen, E., GATOT, J.-S., Holmgren, P., JAMAR, M., ... Janssens, K. (2018). The BElgian PREnatal MicroArray (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations. Prenatal Diagnosis. doi:10.1002/pd.5373 Peer Reviewed verified by ORBi |
 | PIERQUIN, G., & BULK, S. (January 2018). Pseudarthose de l'avant-bras chez une patiente atteinte de neurofibromatose [Poster presentation]. 9ème Assises de Génétique Humaine et Médicale, Nantes, France. |
 | Van Damme, T., Pang, X., Guillemyn, B., Gulberti, S., Syx, D., De Rycke, R., Kaye, O., de Die-Smulders, C. E. M., Pfundt, R., Kariminejad, A., Nampoothiri, S., PIERQUIN, G., BULK, S., Larson, A. A., Chatfield, K. C., Simon, M., Legrand, A., Gerard, M., Symoens, S., ... Malfait, F. (2018). Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome. Human Molecular Genetics, 27 (20), 3475-3487. doi:10.1093/hmg/ddy234 Peer Reviewed verified by ORBi |
 | HARVENGT, J., SAGOT, C., Decortis, T., Damry, N., Rondia, CABERG, J.-H., Bours, V., & BULK, S. (27 May 2017). A tale of two anomalies. A paternal duplication and a maternal deletion of 15q13 [Poster presentation]. European Human Genetics Conference, Copenhague, Denmark. |
 | BULK, S., & PIERQUIN, G. (04 February 2016). Dysmorphology Quiz [Paper presentation]. Dysmorphology Meeting. |
 | PIERQUIN, G., CABERG, J.-H., & BULK, S. (03 February 2016). Microdélétions et duplications 22q11.22 distales [Poster presentation]. 8èmes Assises de Génétique Humaine et Médicale, Lyon, France. |
 | Magotteaux, S., BULK, S., FARHAT, N., SAKALIHASAN, N., Defraigne, J.-O., & Seghaye, M.-C. (2016). Le syndrome de Marfan chez l'enfant et l'adolescent : cas clinique. Revue Médicale de Liège, 71 (7-8), 342-348. Peer reviewed |
 | Uwineza, A., BULK, S., CABERG, J.-H., & PIERQUIN, G. (06 March 2015). A new case of microdeletion 14q32.3 [Poster presentation]. 15th Belgium Society of Human Genetics Meeting, Charleroi, Belgium. |
| BULK, S., Decortis, T., Rondia, G., CABERG, J.-H., & Bours, V. (06 March 2015). A tale of two anomalies. A paternal duplication and a maternal deletion of 15q13 [Poster presentation]. 15th Belgium Society of Human Genetics Meeting, Charleroi, Belgium. |
BULK, S., PIERQUIN, G., GAILLEZ, S., GATOT, J.-S., CABERG, J.-H., & Bours, V. (07 February 2014). Evaluation of the distal 22q11 deletion syndrome. A highly variable phenotype [Poster presentation]. 14th Belgium Society of Human Genetics Meeting. |
 | Vanakker, O., Vilain, C., Janssens, K., Van der Aa, N., Smits, G., Bandelier, C., Blaumeiser, B., BULK, S., CABERG, J.-H., De Leener, A., De Rademaeker, M., de Ravel, T., Desir, J., Destree, A., Dheedene, A., GAILLEZ, S., Grisart, B., Hellin, A.-C., Janssens, S., ... Devriendt, K. (2014). Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges. European Journal of Medical Genetics, 57 (4), 151-6. doi:10.1016/j.ejmg.2014.02.002 Peer Reviewed verified by ORBi |
 | Beunders, G., Voorhoeve, E., Golzio, C., Pardo, L. M., Rosenfeld, J. A., Talkowski, M. E., Simonic, I., Lionel, A. C., Vergult, S., Pyatt, R. E., van de Kamp, J., Nieuwint, A., Weiss, M. M., Rizzu, P., Verwer, L. E. N. I., van Spaendonk, R. M. L., Shen, Y., Wu, B.-L., Yu, T., ... Sistermans, E. A. (2013). Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. American Journal of Human Genetics, 92 (2), 210-20. doi:10.1016/j.ajhg.2012.12.011 Peer Reviewed verified by ORBi |
 | Stalpers, X. L., Verrips, A., Poll-The, B. T., Cobben, J.-M., Snoeck, I. N., de Coo, I. F. M., Brooks, A., BULK, S., Gooskens, R., Fock, A., Verschuuren-Bemelmans, C., Sinke, R. J., de Visser, M., & Lemmink, H. H. (2013). Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in The Netherlands. Neuromuscular Disorders, 23 (6), 461-8. doi:10.1016/j.nmd.2013.03.002 Peer Reviewed verified by ORBi |
 | Postma, A. V., Alders, M., Sylva, M., Bilardo, C. M., Pajkrt, E., van Rijn, R. R., Schulte-Merker, S., BULK, S., Stefanovic, S., Ilgun, A., Barnett, P., Mannens, M. M. A. M., Moorman, A. F. M., Oostra, R. J., & van Maarle, M. C. (2013). Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal. Journal of Medical Genetics. doi:10.1136/jmedgenet-2013-102001 Peer Reviewed verified by ORBi |
 | Rijkaart, D. C., Berkhof, J., van Kemenade, F. J., Coupe, V. M. H., Rozendaal, L., Heideman, D. A. M., Verheijen, R. H. M., BULK, S., Verweij, W., Snijders, P. J. F., & Meijer, C. J. L. M. (2012). HPV DNA testing in population-based cervical screening (VUSA-Screen study): results and implications. British Journal of Cancer, 106 (5), 975-81. doi:10.1038/bjc.2011.581 Peer Reviewed verified by ORBi |
 | Rijkaart, D. C., Berkhof, J., van Kemenade, F. J., Coupe, V. M. H., Hesselink, A. T., Rozendaal, L., Heideman, D. A. M., Verheijen, R. H., BULK, S., Verweij, W. M., Snijders, P. J. F., & Meijer, C. J. L. M. (2012). Evaluation of 14 triage strategies for HPV DNA-positive women in population-based cervical screening. International Journal of Cancer, 130 (3), 602-10. doi:10.1002/ijc.26056 Peer Reviewed verified by ORBi |
 | Rapcencu, A. E., Lindhout, D., & BULK, S. (2012). Frequently asked questions on epilepsy, pregnancy and lactation: a EURAP-NL report. Seizure: the Journal of the British Epilepsy Association, 21 (8), 606-9. doi:10.1016/j.seizure.2012.06.011 Peer Reviewed verified by ORBi |
 | Lombardi, M. P., BULK, S., Celli, J., Lampe, A., Gabbett, M. T., Ousager, L. B., van der Smagt, J. J., Soller, M., Stattin, E.-L., Mannens, M. A. M. M., Smigiel, R., & Hennekam, R. C. (2011). Mutation update for the PORCN gene. Human Mutation, 32 (7), 723-8. doi:10.1002/humu.21505 Peer Reviewed verified by ORBi |
 | de Leeuw, N., BULK, S., Green, A., Jaeckle-Santos, L., Baker, L. A., Zinn, A. R., Kleefstra, T., van der Smagt, J. J., Vianne Morgante, A. M., de Vries, B. B. A., van Bokhoven, H., & de Brouwer, A. P. M. (2010). UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients. American Journal of Medical Genetics. Part A, 152A (12), 3084-90. doi:10.1002/ajmg.a.33743 Peer Reviewed verified by ORBi |
 | Rijkaart, D. C., Berkhof, J., van Kemenade, F. J., Rozendaal, L., Verheijen, R. H. M., BULK, S., Herreilers, M. E., Verweij, W. M., Snijders, P. J. F., & Meijer, C. J. L. M. (2010). Comparison of HPV and cytology triage algorithms for women with borderline or mild dyskaryosis in population-based cervical screening (VUSA-screen study). International Journal of Cancer, 126 (9), 2175-81. doi:10.1002/ijc.24891 Peer Reviewed verified by ORBi |
 | Wegner, I., Edelbroek, P. M., BULK, S., & Lindhout, D. (2009). Lamotrigine kinetics within the menstrual cycle, after menopause, and with oral contraceptives. Neurology, 73 (17), 1388-93. doi:10.1212/WNL.0b013e3181bd8295 Peer Reviewed verified by ORBi |
 | van den Broek, T., BULK, S., Pruijs, J. E. H., & Beek, F. J. A. (2009). Radiological "bone within a bone" appearance with atraumatic fractures. Postgraduate Medical Journal, 85 (1008), 514. doi:10.1136/pgmj.2008.075382 Peer Reviewed verified by ORBi |
 | BULK, S., Rozendaal, L., Zielinski, G. D., Berkhof, J., Daalmeijer, N. C. F., Snijders, P. J. F., van Kemenade, F. J., & Meijer, C. J. L. M. (2008). High-risk human papillomavirus is present in cytologically false-negative smears: an analysis of "normal" smears preceding CIN2/3. Journal of Clinical Pathology, 61 (3), 385-9. doi:10.1136/jcp.2006.045948 Peer Reviewed verified by ORBi |
 | Bulkmans, N. W. J., Berkhof, J., Rozendaal, L., van Kemenade, F. J., Boeke, A. J. P., BULK, S., Voorhorst, F. J., Verheijen, R. H. M., van Groningen, K., Boon, M. E., Ruitinga, W., van Ballegooijen, M., Snijders, P. J. F., & Meijer, C. J. L. M. (2007). Human papillomavirus DNA testing for the detection of cervical intraepithelial neoplasia grade 3 and cancer: 5-year follow-up of a randomised controlled implementation trial. The Lancet, 370 (9601), 1764-72. doi:10.1016/S0140-6736(07)61450-0 Peer Reviewed verified by ORBi |
 | BULK, S., Berkhof, J., Rozendaal, L., Fransen Daalmeijer, N. C., Gok, M., de Schipper, F. A., van Kemenade, F. J., Snijders, P. J. F., & Meijer, C. J. L. M. (2007). The contribution of HPV18 to cervical cancer is underestimated using high-grade CIN as a measure of screening efficiency. British Journal of Cancer, 96 (8), 1234-6. doi:10.1038/sj.bjc.6603693 Peer Reviewed verified by ORBi |
 | Bulkmans, N. W. J., Berkhof, J., BULK, S., Bleeker, M. C. G., van Kemenade, F. J., Rozendaal, L., Snijders, P. J. F., & Meijer, C. J. L. M. (2007). High-risk HPV type-specific clearance rates in cervical screening. British Journal of Cancer, 96 (9), 1419-24. doi:10.1038/sj.bjc.6603653 Peer Reviewed verified by ORBi |
 | BULK, S., Bulkmans, N. W. J., Berkhof, J., Rozendaal, L., Boeke, A. J. P., Verheijen, R. H. M., Snijders, P. J. F., & Meijer, C. J. L. M. (2007). Risk of high-grade cervical intra-epithelial neoplasia based on cytology and high-risk HPV testing at baseline and at 6-months. International Journal of Cancer, 121 (2), 361-7. doi:10.1002/ijc.22677 Peer Reviewed verified by ORBi |
 | BULK, S., Berkhof, J., Bulkmans, N. W. J., Zielinski, G. D., Rozendaal, L., van Kemenade, F. J., Snijders, P. J. F., & Meijer, C. J. L. M. (2006). Preferential risk of HPV16 for squamous cell carcinoma and of HPV18 for adenocarcinoma of the cervix compared to women with normal cytology in The Netherlands. British Journal of Cancer, 94 (1), 171-5. doi:10.1038/sj.bjc.6602915 Peer Reviewed verified by ORBi |
 | Berkhof, J., Bulkmans, N. W. J., Bleeker, M. C. G., BULK, S., Snijders, P. J. F., Voorhorst, F. J., & Meijer, C. J. L. M. (2006). Human papillomavirus type-specific 18-month risk of high-grade cervical intraepithelial neoplasia in women with a normal or borderline/mildly dyskaryotic smear. Cancer Epidemiology, Biomarkers and Prevention, 15 (7), 1268-73. doi:10.1158/1055-9965.EPI-05-0764 Peer Reviewed verified by ORBi |
 | Bulkmans, N. W. J., BULK, S., Ottevanger, M. S., Rozendaal, L., Hellenberg, S. M., van Kemenade, F. J., Snijders, P. J. F., Boeke, A. J. P., & Meijer, C. J. L. M. (2006). Implementation of human papillomavirus testing in cervical screening without a concomitant decrease in participation rate. Journal of Clinical Pathology, 59 (11), 1218-20. doi:10.1136/jcp.2005.031690 Peer Reviewed verified by ORBi |
 | BULK, S., Visser, O., Rozendaal, L., Verheijen, R. H. M., & Meijer, C. J. L. M. (2005). Cervical cancer in the Netherlands 1989-1998: Decrease of squamous cell carcinoma in older women, increase of adenocarcinoma in younger women. International Journal of Cancer, 113 (6), 1005-9. doi:10.1002/ijc.20678 Peer Reviewed verified by ORBi |
 | BULK, S., Van Kemenade, F. J., Rozendaal, L., & Meijer, C. J. L. M. (2004). The Dutch CISOE-A framework for cytology reporting increases efficacy of screening upon standardisation since 1996. Journal of Clinical Pathology, 57 (4), 388-93. doi:10.1136/jcp.2003.011841 Peer Reviewed verified by ORBi |
 | van der Meer, I. M., Brouwers, G.-J., BULK, S., Leebeek, F. W. G., van der Kuip, D. A. M., Hofman, A., Witteman, J. C. M., & Gomez Garcia, E. B. (2004). Genetic variability of von Willebrand factor and risk of coronary heart disease: the Rotterdam Study. British Journal of Haematology, 124 (3), 343-7. doi:10.1046/j.1365-2141.2003.04776.x Peer Reviewed verified by ORBi |
 | BULK, S., Visser, O., Rozendaal, L., Verheijen, R. H. M., & Meijer, C. J. L. M. (2003). Incidence and survival rate of women with cervical cancer in the Greater Amsterdam area. British Journal of Cancer, 89 (5), 834-9. doi:10.1038/sj.bjc.6601157 Peer Reviewed verified by ORBi |
 | Brouwers, G. J., Vos, H. L., Leebeek, F. W., BULK, S., Schneider, M., Boffa, M., Koschinsky, M., van Tilburg, N. H., Nesheim, M. E., Bertina, R. M., & Gomez Garcia, E. B. (2001). A novel, possibly functional, single nucleotide polymorphism in the coding region of the thrombin-activatable fibrinolysis inhibitor (TAFI) gene is also associated with TAFI levels. Blood, 98 (6), 1992-3. doi:10.1182/blood.V98.6.1992 Peer Reviewed verified by ORBi |
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