If you made any changes in Pure these will be visible here soon.

Research Output 2000 2019

  • 55 Article
  • 2 Comment/Letter to the editor
  • 1 Review article
  • 1 Doctoral Thesis
2019

Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time

Coenen, M. J. H., Paulussen, A. D. C., Breuer, M., Lindhout, M., Tserpelis, D. C. J., Steyls, A., Bierau, J. & van den Bosch, B. J. C., 2019, In : Current Therapeutic Research-Clinical and Experimental. 90, p. 1-7 7 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Metabolic events in HIV-infected patients using abacavir are associated with erythrocyte inosine triphosphatase activity

Peltenburg, N. C., Bierau, J., Schippers, J. A., Lowe, S. H., Paulussen, A. D. C., van den Bosch, B. J. C., Leers, M. P. G., Andrinopoulou, E-R., Bakker, J. A. & Verbon, A., Jan 2019, In : Journal of Antimicrobial Chemotherapy. 74, 1, p. 157-164 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing

Masset, H., Esteki, M. Z., Dimitriadou, E., Dreesen, J., Debrock, S., Derhaag, J., Derks, K., Destouni, A., Drusedau, M., Meekels, J., Melotte, C., Peeraer, K., Tsuiko, O., van Uum, C., Allemeersch, J., Devogelaere, B., Francois, K. O., Happe, S., Lorson, D., Richards, R. L. & 7 others, Theuns, J., Brunner, H., de Die-Smulders, C., Voet, T., Paulussen, A., Coonen, E. & Vermeesch, J. R., Aug 2019, In : Human Reproduction. 34, 8, p. 1608-1619 12 p.

Research output: Contribution to journalArticleAcademicpeer-review

New insights into minor splicing-a transcriptomic analysis of cells derived from TALS patients

Cologne, A., Benoit-Pilven, C., Besson, A., Putoux, A., Campan-Fournier, A., Bober, M. B., De Die-Smulders, C. E. M., PAULUSSEN, A. D. C., Pinson, L., Toutain, A., Roifman, C. M., Leutenegger, A-L., Mazoyer, S., Edery, P. & Lacroix, V., Sep 2019, In : Rna-A Publication of the Rna Society. 25, 9, p. 1130-1149 20 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
2018

Erythrocyte Inosine triphosphatase activity: A potential biomarker for adverse events during combination antiretroviral therapy for HIV

Peltenburg, N. C., Bierau, J., Bakker, J. A., Schippers, J. A., Lowe, S. H., Paulussen, A. D. C., van den Bosch, B. J. C., Leers, M. P. G., Hansen, B. E. & Verbon, A., 12 Jan 2018, In : PLOS ONE. 13, 1, 14 p., e0191069.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications

Hovinga, I. C. L. K., Giltay, J. C., van der Crabben, S. N., Steyls, A., van der Kamp, H. J. & Paulussen, A. D. C., 1 Sep 2018, In : Clinical Endocrinology. 89, 3, p. 378-380 3 p.

Research output: Contribution to journalComment/Letter to the editorAcademicpeer-review

Mutation-specific effects in germline transmission of pathogenic mtDNA variants

Otten, A. B. C., Sallevelt, S. C. E. H., Carling, P. J., Dreesen, J. C. F. M., Drusedau, M., Spierts, S., Paulussen, A. D. C., de Die-Smulders, C. E. M., Herbert, M., Chinnery, P. F., Samuels, D. C., Lindsey, P. & Smeets, H. J. M., 1 Jul 2018, In : Human Reproduction. 33, 7, p. 1331-1341 11 p.

Research output: Contribution to journalArticleAcademicpeer-review

New mutations and an updated database for the patched-1 (PTCH1) gene

Reinders, M. G., van Hout, A. F., Cosgun, B., Paulussen, A. D., Leter, E. M., Steijlen, P. M., Mosterd, K., van Geel, M. & Gille, J. J., May 2018, In : Molecular genetics & genomic medicine. 6, 3, p. 409-415 7 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014

Heijligers, M., Van Montfoort, A., Meijer-Hoogeveen, M., Broekmans, F., Bouman, K., Homminga, I., Dreesen, J., Paulussen, A., Engelen, J., Coonen, E., Van der Schoot, V., van Deursen-Luijten, M., Muntjewerff, N., Peeters, A., van Golde, R., van der Hoeven, M., Arens, Y. & de Die-Smulders, C., Nov 2018, In : Journal of Assisted Reproduction and Genetics. 35, 11, p. 1995-2002 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome

Gielen, R-J. C. A. M., Reinders, M. G. H. C., Koillinen, H. K., Paulussen, A. D. C., Mosterd, K. & van Geel, M., 1 Sep 2018, In : Journal of Human Genetics. 63, 9, p. 965-969 5 p.

Research output: Contribution to journalArticleAcademicpeer-review

2017
Open Access

BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD

Derks-Smeets, I. A. P., van Tilborg, T. C., van Montfoort, A., Smits, L., Torrance, H. L., Meijer-Hoogeveen, M., Broekmans, F., Dreesen, J. C. F. M., Paulussen, A. D. C., Tjan-Heijnen, V. C. G., Homminga, I., van den Berg, M. M. J., Ausems, M. G. E. M., de Rycke, M., de Die-Smulders, C. E. M., Verpoest, W. & van Golde, R., Nov 2017, In : Journal of Assisted Reproduction and Genetics. 34, 11, p. 1475-1482 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
Open Access

PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy

Sallevelt, S. C. E. H., Dreesen, J. C. F. M., Druesedau, M., Hellebrekers, D. M. E. I., Paulussen, A. D. C., Coonen, E., Van Golde, R. J. T., Geraedts, J. P. M., Gianaroli, L., Magli, M. C., Zeviani, M., Smeets, H. J. M. & de Die-Smulders, C. E. M., Mar 2017, In : Human Reproduction. 32, 3, p. 698-703 6 p.

Research output: Contribution to journalArticleAcademicpeer-review

Postzygotic mosaicism in basal cell naevus syndrome

Reinders, M. G. H. C., Boersma, H. J., Leter, E. M., Vreeburg, M., Paulussen, A. D. C., Arits, A. H. M. M., Roemen, G. M. J. M., Speel, E. J. M., Steijlen, P. M., van Geel, M. & Mosterd, K., Jul 2017, In : British Journal of Dermatology. 177, 1, p. 249-252 4 p.

Research output: Contribution to journalArticleAcademicpeer-review

2016
5 Citations (Scopus)

Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers

Claes, G. R. F., van Tienen, F. H. J., Lindsey, P., Krapels, I. P. C., van den Enden, A., Hoos, M., Barrois, Y. E. G., Janssen, J., Paulussen, A. D. C., Sels, J-W. E. M., Kuijpers, S. H. H., van Tintelen, J. P., van den Berg, M. P., Heesen, W. F., Garcia-Pavia, P., Perrot, A., Christiaans, I., Salemink, S., Marcelis, C. L. M., Smeets, B. & 3 others, Brunner, H. G., Volders, P. G. A. & van den Wijngaard, A., 14 Jun 2016, In : European Heart Journal. 37, 23, p. 1815-1822

Research output: Contribution to journalArticleAcademicpeer-review

Inosine Triphosphate Pyrophosphohydrolase Expression: Decreased in Leukocytes of HIV-Infected Patients Using Combination Antiretroviral Therapy

Peltenburg, N. C., Leers, M. P. G., Bakker, J. A., Lowe, S. H., Vroemen, W. H. M., Paulussen, A. D. C., van den Bosch, B. J. C., Bierau, J. & Verbon, A., 1 Dec 2016, In : Jaids-journal of Acquired Immune Deficiency Syndromes. 73, 4, p. 390-395 6 p.

Research output: Contribution to journalArticleAcademicpeer-review

Präimplantationsdiagnostik in den Niederlanden

Geraedts, J., Coonen, E., Dreesen, J., Paulussen, A. & de Die-Smulders, C., Dec 2016, In : Medizinische Genetik. 28, 3, p. 310–319 9 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
1 Citation (Scopus)

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

Paulussen, A. D. C., Steyls, A., Vanoevelen, J., van Tienen, F. H. J., Krapels, I. P. C., Claes, G. R. F., Chocron, S., Velter, C., Tan-Sindhunata, G. M., Lundin, C., Valenzuela, I., Nagy, B., Bache, I., Maroun, L. L., Avela, K., Brunner, H. G., Smeets, H. J. M., Bakkers, J. & van den Wijngaard, A., Dec 2016, In : European Journal of Human Genetics. 24, 12, p. 1783-1791

Research output: Contribution to journalArticleAcademicpeer-review

Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome

Putoux, A., Alqahtani, A., Pinson, L., Paulussen, A. D. C., Michel, J., Besson, A., Mazoyer, S., Borg, I., Nampoothiri, S., Vasiljevic, A., Uwineza, A., Boggio, D., Champion, F., de Die-Smulders, C. E., Gardeitchik, T., van Putten, W. K., Perez, M. J., Musizzano, Y., Razavi, F., Drunat, S. & 7 others, Verloes, A., Hennekam, R., Guibaud, L., Alix, E., Sanlaville, D., Lesca, G. & Edery, P., Dec 2016, In : Clinical Genetics. 90, 6, p. 550-555

Research output: Contribution to journalArticleAcademicpeer-review

2015

Cell-Free RNA Is a Reliable Fetoplacental Marker in Noninvasive Fetal Sex Determination

Mersy, E., Faas, B. H. W., Spierts, S., Houben, L. M. H., Macville, M. V. E., Frints, S. G. M., Paulussen, A. D. C. & Veltman, J. A., Dec 2015, In : Clinical Chemistry. 61, 12, p. 1515-1523

Research output: Contribution to journalArticleAcademicpeer-review

2014
29 Citations (Scopus)

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

Natesan, S. A., Bladon, A. J., Coskun, S., Qubbaj, W., Prates, R., Munne, S., Coonen, E., Dreesen, J. C. F. M., Stevens, S. J. C., Paulussen, A. D. C., Stock-Myer, S. E., Wilton, L. J., Jaroudi, S., Wells, D., Brown, A. P. C. & Handyside, A. H., Nov 2014, In : Genetics in Medicine. 16, 11, p. 838-845

Research output: Contribution to journalArticleAcademicpeer-review

4 Citations (Scopus)
198 Downloads (Pure)

Hereditary breast and ovarian cancer and reproduction: an observational study on the suitability of preimplantation genetic diagnosis for both asymptomatic carriers and breast cancer survivors

Derks - Smeets, I. A. P., de Die-Smulders, C. E. M., Mackens, S., van Golde, R., Paulussen, A. D., Dreesen, J., Tournaye, H., Verdyck, P., Tjan-Heijnen, V. C. G., Meijer-Hoogeveen, M., de Greve, J., Geraedts, J., de Rycke, M., Bonduelle, M. & Verpoest, W. M., Jun 2014, In : Breast Cancer Research and Treatment. 145, 3, p. 673-681 9 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access
File
8 Citations (Scopus)

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers

Drusedau, M., Dreesen, J. C., Derks-Smeets, I., Coonen, E., van Golde, R., van Echten-Arends, J., Kastrop, P. M. M., Blok, M. J., Gomez-Garcia, E., Geraedts, J. P., Smeets, H. J., de Die-Smulders, C. E. & Paulussen, A. D., Dec 2013, In : European Journal of Human Genetics. 21, 12, p. 1361-1368

Research output: Contribution to journalArticleAcademicpeer-review

2012
11 Citations (Scopus)

A Patient With a Mild Holoprosencephaly Spectrum Phenotype and Heterotaxy and a 1.3 Mb Deletion Encompassing GLI2

Kevelam, S. H. G., van Harssel, J. J. T., van der Zwaag, B., Smeets, H. J. M., Paulussen, A. D. C. & Lichtenbelt, K. D., Jan 2012, In : American Journal of Medical Genetics Part A. 158A, 1, p. 166-173

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)

Erythrocyte Inosine Triphosphatase Activity Is Decreased in HIV-Seropositive Individuals

Bierau, J., Bakker, J. A., Schippers, J. A., Grashorn, J. A. C., Lindhout, M., Lowe, S. H., Paulussen, A. D. C. & Verbon, A., 17 Jan 2012, In : PLOS ONE. 7, 1, e30175.

Research output: Contribution to journalArticleAcademicpeer-review

7 Citations (Scopus)

Genetics of maximally attained lung function: A role for leptin?

van den Borst, B., Souren, N. Y. P., Loos, R. J., Paulussen, A. D. C., Derom, C., Schols, A. M. W. J. & Zeegers, M. P. A., 1 Jan 2012, In : Respiratory Medicine. 106, 2, p. 235-242 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog

Solomon, B. D., Bear, K. A., Wyllie, A., Keaton, A. A., Dubourg, C., David, V., Mercier, S., Odent, S., Hehr, U., Paulussen, A., Clegg, N. J., Delgado, M. R., Bale, S. J., Lacbawan, F., Ardinger, H. H., Aylsworth, A. S., Bhengu, N. L., Braddock, S., Brookhyser, K., Burton, B. & 25 others, Gaspar, H., Grix, A., Horovitz, D., Kanetzke, E., Kayserili, H., Lev, D., Nikkel, S. M., Norton, M., Roberts, R., Saal, H., Schaefer, G. B., Schneider, A., Smith, E. K., Sowry, E., Spence, M. A., Shalev, S. A., Steiner, C. E., Thompson, E. M., Winder, T. L., Balog, J. Z., Hadley, D. W., Zhou, N., Pineda-Alvarez, D. E., Roessler, E. & Muenke, M., Jul 2012, In : Journal of Medical Genetics. 49, 7, p. 473-479

Research output: Contribution to journalArticleAcademicpeer-review

22 Citations (Scopus)

Therapeutic drug monitoring of thiopurine metabolites in adult thiopurine tolerant IBD patients on maintenance therapy.

Gilissen, L. P., Wong, D. R., Engels, L. G. B., Bierau, J., Bakker, J. A., Paulussen, A. D. C., Romberg-Camps, M., Stronkhorst, A., Bus, P., Bos, L. P., Hooymans, P. M., Stockbrügger, R. W., Neef, C. K. & Masclee, A. A. M., 1 Jan 2012, In : Journal of Crohn's & Colitis. 6, 6, p. 698-707

Research output: Contribution to journalArticleAcademicpeer-review

2011
4 Citations (Scopus)

Association between the IL6 -174G/C SNP and maximally attained lung function

van den Borst, B., Souren, N. Y., Gielen, M. J. F., Loos, R. J., Paulussen, A. D. C., Derom, C., Schols, A. M. W. J. & Zeegers, M. P. A., Feb 2011, In : Thorax. 66, 2, p. 179 1 p.

Research output: Contribution to journalComment/Letter to the editorAcademicpeer-review

MLL2 Mutation Spectrum in 45 Patients with Kabuki Syndrome

Paulussen, A. D. C., Stegmann, A. P. A., Blok, M. J., Tserpelis, D., Posma-Velter, C., Detisch, Y., Smeets, E. E. J. G. L., Wagemans, A. M. A., Schrander, J. J. P., van den Boogaard, M. J. H., van der Smagt, J. J., van Haeringen, A., Stolte-Dijkstra, I., Kerstjens-Frederikse, W. S., Mancini, G. M. S., Wessels, M. W., Hennekam, R. C. M., Vreeburg, M., Geraedts, J., de Ravel, T. & 4 others, Fryns, J-P., Smeets, H. J. T., Devriendt, K. & Schrander-Stumpel, C. T. R. M., Feb 2011, In : Human Mutation. 32, 2, p. E2018-E2025

Research output: Contribution to journalArticleAcademicpeer-review

THE EFFECT OF ITPA POLYMORPHISMS ON THE ENZYME KINETIC PROPERTIES OF HUMAN ERYTHROCYTE INOSINE TRIPHOSPHATASE TOWARD ITS SUBSTRATES ITP AND 6-THIO-ITP

Bakker, J. A., Lindhout, M., Habets, D. D. J., van den Wijngaard, A., Paulussen, A. D. C. & Bierau, J., 2011, In : Nucleosides Nucleotides & Nucleic Acids. 30, 11, p. 839-849

Research output: Contribution to journalArticleAcademicpeer-review

2010
12 Citations (Scopus)

Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection

van Harssel, J. J., van Roozendaal, C. E., Detisch, Y., Brandao, R. D., Paulussen, A. D. C., Zeegers, M. P. A., Blok, M. J. & Gomez Garcia, E. B., Jun 2010, In : Familial Cancer. 9, 2, p. 193-201 9 p.

Research output: Contribution to journalArticleAcademicpeer-review

Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

Solomon, B. D., Lacbawan, F., Mercier, S., Clegg, N. J., Delgado, M. R., Rosenbaum, K., Dubourg, C., David, V., Olney, A. H., Wehner, L-E., Hehr, U., Bale, S. J., Paulussen, A., Smeets, H. J. T., Hardisty, E., Tylki-Szymanska, A., Pronicka, E., Clemens, M., McPherson, E., Hennekam, R. C. M. & 21 others, Hahn, J., Stashinko, E., Levey, E., Wieczorek, D., Roeder, E., Schell-Apacik, C. C., Booth, C. W., Thomas, R. L., Kenwrick, S., Cummings, D. A. T., Bous, S. M., Keaton, A. A., Balog, J. Z., Hadley, D. W., Zhou, N., Long, R., Velez, J. I., Pineda-Alvarez, D. E., Odent, S., Roessler, E. & Muenke, M., Aug 2010, In : Journal of Medical Genetics. 47, 8, p. 513-524

Research output: Contribution to journalArticleAcademicpeer-review

The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes

Paulussen, A. D. C., Schrander-Stumpel, C. T. R. M., Tserpelis, D. C. J., Spee, M. K. M., Stegmann, A. P. A., Mancini, G. M. S., Brooks, A. S., Collee, M. J., Maat-Kievit, A., Simon, M. E. H., van Bever, Y., Stolte-Dijkstra, I., Kerstjens-Frederikse, W. S., Herkert, J. C., van Essen, A. J., Lichtenbelt, K. D., van Haeringen, A., Kwee, M. L., Lachmeijer, A. M. A., Tan-Sindhunata, G. M. B. & 7 others, van Maarle, M. C., Arens, Y. H. J. M., Smeets, E. E. J. G. L., de Die-Smulders, C. E. M., Engelen, J. J. M., Smeets, H. J. M. & Herbergs, J., 10 Sep 2010, In : European Journal of Human Genetics. 18, 9, p. 999-1005

Research output: Contribution to journalArticleAcademicpeer-review

2009
7 Citations (Scopus)

Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors.

Souren, N. Y., Paulussen, A. D., Steyls, A., Loos, R. J., Brandao, R. D., Gielen, M. J., Smeets, H. J., Beunen, G., Fagard, R., Derom, C., Vlietinck, R. F. M., Geraedts, J. P. & Zeegers, M. P., 1 Jan 2009, In : International Journal of Obesity. 33, 9, p. 962-970

Research output: Contribution to journalArticleAcademicpeer-review

2008
6 Citations (Scopus)

Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses

Souren, N. Y., Zeegers, M. P., Janssen, R. G., Steyls, A., Gielen, M., Loos, R. J., Beunen, G., Fagard, R., Stassen, A. P., Aerssens, J., Derom, C., Vlietinck, R. & Paulussen, A. D., 1 Jan 2008, In : Twin Research and Human Genetics. 11, 5, p. 505-16

Research output: Contribution to journalArticleAcademicpeer-review

Common SNPs in LEP and LEPR associated with birth weight and type 2 diabetes-related metabolic risk factors in twins

Souren, N. Y., Paulussen, A. D., Steyls, A., Loos, R. J., Stassen, A. P., Gielen, M., Smeets, H. J., Beunen, G., Fagard, R., Derom, C., Vlietinck, R., Geraedts, J. P. & Zeegers, M. P., 20 May 2008, In : International Journal of Obesity. 32, p. 1233-1239

Research output: Contribution to journalArticleAcademicpeer-review

25 Citations (Scopus)

Modeling genetic and environmental factors to increase heritability and ease the identification of candidate genes for birth weight: a twin study.

Gielen, M. J. F., Lindsey, P., Derom, C., Smeets, H. J., Souren, N. Y. P., Paulussen, A., Derom, R. & Nijhuis, J. G., 1 Jan 2008, In : Behavior Genetics. 38, 1, p. 44-54

Research output: Contribution to journalArticleAcademicpeer-review

26 Citations (Scopus)

Twin-specific intrauterine 'growth' charts based on cross-sectional birthweight data.

Gielen, M., Lindsey, P. J., Derom, C., Loos, R. J. F., Souren, N. Y. P., Paulussen, A. D., Zeegers, M. P. A., Derom, R., Vlietinck, R. F. M. & Nijhuis, J. G., 1 Jan 2008, In : Twin Research and Human Genetics. 11, 2, p. 224-235

Research output: Contribution to journalArticleAcademicpeer-review

2007
62 Citations (Scopus)

Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities.

Souren, N. Y. P., Paulussen, A., Loos, R. J. F., Gielen, M. J., Beunen, G., Fagard, R., Derom, C., Vlietinck, R. F. M. & Zeegers, M. P. A., 1 Jan 2007, In : Diabetologia. 50, 10, p. 2107-2116

Research output: Contribution to journalArticleAcademicpeer-review

49 Citations (Scopus)

Does occupational exposure to PAHs, diesel and aromatic amines interact with smoking and metabolic genetic polymorphisms to increase the risk on bladder cancer?; The Belgian case control study on bladder cancer risk

Kellen, E., Zeegers, M. P. A., Paulussen, A. D. C., Vlietinck, R. F. M., Vlem, E. V., Veulemans, H. & Buntinx, F., 1 Jan 2007, In : Cancer Letters. 245, 1-2, p. 51-60

Research output: Contribution to journalArticleAcademicpeer-review

2006
51 Citations (Scopus)
32 Citations (Scopus)

Two functionally relevant polymorphisms in the human progesterone receptor gene (+331 G/A and progins) and the predisposition for breast and/or ovarian cancer

Romano, A., Lindsey, P. J., Fischer, D. C., Delvoux, B., Paulussen, A. D., Janssen, R. G. J. H. & Kieback, D. G., 1 Jan 2006, In : Gynecologic Oncology. 101, 2, p. 287-297

Research output: Contribution to journalArticleAcademicpeer-review

2005
18 Citations (Scopus)

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency

Paulussen, A. D., Raes, A., Jongbloed, R. J. E., Gilissen, R. A., Wilde, A. A., Snyders, D. J., Smeets, H. J. & Aerssens, J. M. M. R., 1 Jan 2005, In : Cardiovascular Research. 67, 3, p. 467-475

Research output: Contribution to journalArticleAcademicpeer-review

15 Citations (Scopus)

Influence of the endothelial nitric oxide synthase gene on conventional and ambulatory blood pressure: sib-pair analysis and haplotype study

Persu, A., Vinck, W. J., El Khattabi, O., Janssen, R. G. J. H., Paulussen, A. D. C., Devuyst, O., Vlietinck, R. F. M. & Fagard, R. H., 1 Jan 2005, In : Journal of Hypertension. 23, 4, p. 759-765

Research output: Contribution to journalArticleAcademicpeer-review

29 Citations (Scopus)

Pharmacogenomics and acquired long QT syndrome

Aerssens, J. M. M. R. & Paulussen, A. D., 1 Jan 2005, In : Pharmacogenomics. 6, 3, p. 259-270

Research output: Contribution to journalArticleAcademicpeer-review