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Research Output

2019

Growth, health, and motor development of 5-year-old children born after preimplantation genetic diagnosis

Heijligers, M., Peeters, A., van Montfoort, A., Nijsten, J., Janssen, E., Gunnewiek, F. K., de Rooy, R., van Golde, R., Coonen, E., Meijer-Hoogeveen, M., Broekmans, F., van der Hoeven, M., Arens, Y. & de Die-Smulders, C., Jun 2019, In : Fertility and Sterility. 111, 6, p. 1151-1158 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

2018

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

The cognitive and socio-emotional development of 5-year-old children born after PGD

Heijligers, M., Verheijden, L. M. M., Jonkman, L. M., van der Sangen, M., Meijer-Hoogeveen, M., Arens, Y., van der Hoeven, M. A. & de Die-Smulders, C. E. M., Nov 2018, In : Human Reproduction. 33, 11, p. 2150–2157 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

2015

Recurrent miscarriage in translocation carriers: no differences in clinical characteristics between couples who accept and couples who decline PGD

De Krom, G., Arens, Y. H. J. M., Coonen, E., Van Ravenswaaij-Arts, C. M. A., Meijer-Hoogeveen, M., Evers, J. L. H., Van Golde, R. J. T. & De Die-Smulders, C. E. M., Feb 2015, In : Human Reproduction. 30, 2, p. 484-489

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)
2014

Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of I-Ks, but preserved cAMP-dependent up-regulation

Spätjens, R., Bebarova, M., Seyen, S. R. M., Lentink, V., Jongbloed, R. J., Arens, Y. H. J. M., Heijman, J. & Volders, P. G. A., 1 Oct 2014, In : Cardiovascular Research. 104, 1, p. 216-225

Research output: Contribution to journalArticleAcademicpeer-review

2 Citations (Scopus)
2011

Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects

Breckpot, J., Thienpont, B., Arens, Y., Tranchevent, L. C., Vermeesch, J. R., Moreau, Y., Gewillig, M. & Devriendt, K., 2011, In : Cytogenetic and Genome Research. 135, 3-4, p. 251-259

Research output: Contribution to journalArticleAcademicpeer-review

Exercise related ventricular arrhythmias are related to cardiac fibrosis in hypertrophic cardiomyopathy mutation carriers

van Rijsingen, I. A. W., Bekkers, S. C. A. M., Schalla, S., Hermans-van Ast, J. F., Snoep, G., Alzand, B. S. N., Arens, Y. H. J. M., van den Wijngaard, A., Crijns, H. J. G. M. & Pinto, Y. M., Apr 2011, In : Netherlands Heart Journal. 19, 4, p. 168-174

Research output: Contribution to journalArticleAcademicpeer-review

Expanding the Spectrum of FOXC1 and PITX2 Mutations and Copy Number Changes in Patients with Anterior Segment Malformations

D'haene, B., Meire, F., Claerhout, I., Kroes, H. Y., Plomp, A., Arens, Y. H., de Ravel, T., Casteels, I., De Jaegere, S., Hooghe, S., Wuyts, W., van den Ende, J., Roulez, F., Veenstra-Knol, H. E., Oldenburg, R. A., Giltay, J., Verheij, J. B. G. M., de Faber, J-T., Menten, B., De Paepe, A. & 3 others, Kestelyn, P., Leroy, B. P. & De Baere, E., Jan 2011, In : Investigative Ophthalmology & Visual Science. 52, 1, p. 324-333

Research output: Contribution to journalArticleAcademicpeer-review

Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy

Christiaans, I., Birnie, E., Bonsel, G. J., Mannens, M. M. A. M., Michels, M., Majoor-Krakauer, D., Dooijes, D., van Tintelen, J. P., Van den Berg, M. P., Volders, P. G. A., Arens, Y. H., van den Wijngaard, A., Atsma, D. E., Helderman-van den Enden, A. T. J. M., Houweling, A. C., de Boer, K., van der Smagt, J. J., Hauer, R. N. W., Marcelis, C. L. M., Timmermans, J. & 2 others, van Langen, I. M. & Wilde, A. A. M., May 2011, In : European Heart Journal. 32, 9, p. 1161-1170

Research output: Contribution to journalArticleAcademicpeer-review

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

van den Wijngaard, A., Volders, P., van Tintelen, J. P., Jongbloed, J. D. H., van den Berg, M. P., Deprez, R. H. L., Mannens, M. M. A. M., Hofmann, N., van Slegtenhorst, M., Dooijes, D., Michels, M., Arens, Y., Jongbloed, R. & Smeets, B. J. M., Aug 2011, In : Netherlands Heart Journal. 19, 7-8, p. 344-351

Research output: Contribution to journalArticleAcademicpeer-review

2010

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria Impact of New Task Force Criteria

Cox, M. G. P. J., van der Smagt, J. J., Noorman, M., Wiesfeld, A. C. P., Volders, P. G. A., van Langen, I. M., Atsma, D. E., Dooijes, D., Houweling, A. C., Loh, P., Jordaens, L. J. L. M., Arens, Y., Cramer, M. J., Doevendans, P. A., van Tintelen, J. P., Wilde, A. A. M. & Hauer, R. N. W., Apr 2010, In : Circulation-Arrhythmia and Electrophysiology. 3, 2, p. 126-133

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

2001
Open Access
File
209 Downloads (Pure)
2000

Trisomy 7p: report of 2 patients and literature review

Arens, Y. H. J. M., Toutain, A., Engelen, J. J. M., Offermans, J. P. M., Hamers, A. J. H., Schrander, J. J. P., Pulles-Heintzberger, C. F. M. & Schrander-Stumpel, C. T. R. M., 1 Jan 2000, In : Genetic Counseling. 11, 4, p. 347-354 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Scopus)