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BULK Saskia

Unilab > Clinique de génétique

Consultation Génétique

See author's contact details
Main Referenced Co-authors
Bours, Vincent  (12)
Meijer, C. J. L. M. (9)
Rozendaal, L. (9)
Caberg, Jean-Hubert  (8)
Harvengt, Julie  (8)
Main Referenced Keywords
Humans (28); Female (24); Adult (19); Middle Aged (18); Male (9);
Main Referenced Disciplines
Genetics & genetic processes (53)
Cardiovascular & respiratory systems (3)
Pediatrics (3)
Reproductive medicine (gynecology, andrology, obstetrics) (2)
Neurology (1)

Publications (total 61)

The most downloaded
600 downloads
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 https://hdl.handle.net/2268/264339

The most cited

548 citations (Scopus®)

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 https://hdl.handle.net/2268/181851

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.

Mouraux, C., FOUQUET, C., Artesi, M., Durkin, K., BULK, S., & Depierreux, F. (2024). Homozygous pathogenic MYH3 variant associated with arthrogryposis and lingual dystonia [Poster presentation]. BeSHG annual symposium 2024, Belgium.
Peer reviewed

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., 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
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 : official journal of the American College of Medical Genetics. doi:10.1038/s41436-021-01119-8
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

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

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
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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
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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
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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

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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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Lemstra, A. W., van Meegen, M. T., Vreyling, J. P., Meijerink, P. H., Jansen, G. H., BULK, S., Baas, F., & van Gool, W. A. (2000). 14-3-3 testing in diagnosing Creutzfeldt-Jakob disease: a prospective study in 112 patients. Neurology, 55 (4), 514-6. doi:10.1212/WNL.55.4.514
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