Yvonne Arens

Research output

Research output per year 2000 2011 2022

• 15 Article
• 1 Chapter
• 1 Doctoral Thesis

Research output per year

Research output per year

Search results

• 2022

  Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals

  Van der Schoot, V., Haer-Wigman, L., Feenstra, I., Tammer, F., Oerlemans, A. J. M., Van Koolwijk, M. P. A., Van Agt, F., Arens, Y. H. J. M., Brunner, H. G., Vissers, L. E. L. M. & Yntema, H. G., Feb 2022, In: European Journal of Human Genetics. 30, 2, p. 170-177 8 p.

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
• 2021

  The impact of unsolicited findings in clinical exome sequencing, a qualitative interview study

  van der Schoot, V., Viellevoije, S. J., Tammer, F., Brunner, H. G., Arens, Y., Yntema, H. G. & Oerlemans, A. J. M., Jun 2021, In: European Journal of Human Genetics. 29, 6, p. 930-939 10 p.

  Research output: Contribution to journal › Article › Academic › peer-review
• 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 journal › Article › Academic › peer-review

  Open Access
• 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 journal › Article › Academic › peer-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 journal › Article › Academic › peer-review

  Open Access

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• 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 journal › Article › Academic › peer-review
• 2014

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

  Spätjens, R. L. H., 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 journal › Article › Academic › peer-review

  Open Access
• 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 journal › Article › Academic › peer-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 journal › Article › Academic › peer-review

  Open Access

• 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 othersKestelyn, P., Leroy, B. P. & De Baere, E., Jan 2011, In: Investigative Ophthalmology & Visual Science. 52, 1, p. 324-333

  Research output: Contribution to journal › Article › Academic › peer-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 othersvan Langen, I. M. & Wilde, A. A. M., May 2011, In: European Heart Journal. 32, 9, p. 1161-1170

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access

• 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 journal › Article › Academic › peer-review

  Open Access
• 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 journal › Article › Academic › peer-review

  Open Access

• 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 othersvan 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 Sept 2010, In: European Journal of Human Genetics. 18, 9, p. 999-1005

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
• 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 journal › Article › Academic › peer-review