Jos Dreesen

Research output

Research output per year 2012 2017 2018 2019 2020 2023 2024

• 17 Article
• 1 Chapter
• 1 Preprint

Research output per year

Research output per year

Search results

• Preprint

  Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing

  Janssen, A. E. J., Koeck, R. M., Essers, R., van Dijk, W., Drusedau, M., Meekels, J., Yaldiz, B., van de Vorst, M., Cao, P., de Koning, B., Hellebrekers, D. M. E. I., Stevens, S. J. C., Sun, S. M., Heijligers, M., de Munnik, S. A., van Uum, C. M. J., Achten, J., Hamers, L., Naghdi, M., Vissers, L. E. L. M., & 9 othersvan Golde, R. J. T., de Wert, G., Dreesen, J. C. F. M., de Die-Smulders, C., Coonen, E., Brunner, H. G., van den Wijngaard, A., Paulussen, A. D. C. & Zamani Esteki, M., 8 Dec 2023, 32 p.

  Research output: Working paper / Preprint › Preprint
• Chapter

  Selecting the right embryo in mitochondrial disorders

  Sallevelt, S. C. E. H., Dreesen, J. C. F. M., De Coo, I. F. M., de Die-Smulders, C. E. M. & Smeets, H. J. M., 2015, Screening the Single Euploid Embryo, Molecular Genetics in Reproductive Medicine. Springer, p. 231 246 p.

  Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic
• Article

  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 journal › Article › Academic › peer-review

  Open Access

• Clinical Guideline for Preimplantation Genetic Testing in Inherited Cardiac Diseases

  Verdonschot, J. A. J., Hellebrekers, D. M. E. I., van Empel, V. P. M., Heijligers, M., de Munnik, S., Coonen, E., Dreesen, J. C. M. F., van den Wijngaard, A., Brunner, H. G., Zamani Esteki, M., Heymans, S. R. B., de Die-Smulders, C. E. M. & Paulussen, A. D. C., 22 Mar 2024, In: Circulation: Genomic and Precision Medicine. 17, 2, E004416.

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

  Open Access

• Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing

  van Dijk, W., Derks, K., Drüsedau, M., Meekels, J., Koeck, R., Essers, R., Dreesen, J., Coonen, E., de Die-Smulders, C., Stevens, S. J. C., Brunner, H. G., van den Wijngaard, A., Paulussen, A. D. C. & Zamani Esteki, M., 31 Oct 2022, In: Human Reproduction. 37, 11, p. 2700-2708 9 p.

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

  Open Access

• ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders

  Carvalho, F., Moutou, C., Dimitriadou, E., Dreesen, J., Giménez, C., Goossens, V., Kakourou, G., Vermeulen, N., Zuccarello, D., De Rycke, M. & ESHRE PGT-M Working Group, 2020, In: Human reproduction open. 2020, 3, p. 1-18 18 p., 018.

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

  Open Access

• 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 journal › Article › Academic › peer-review

  Open Access

• 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 othersTheuns, 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 journal › Article › Academic › peer-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 journal › Article › Academic › peer-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 journal › Article › Academic › peer-review

  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 journal › Article › Academic › peer-review

  Open Access

• Präimplantationsdiagnostik in den Niederlanden

  Translated title of the contribution: Preimplantation genetic diagnosis (PGD) in the NetherlandsGeraedts, 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 journal › Article › Academic › peer-review

  Open Access

• Preimplantation genetic diagnosis for mitochondrial DNA mutations: analysis of one blastomere suffices

  Sallevelt, S. C. E. H., Dreesen, J. C. F. M., Coonen, E., Paulussen, A. D. C., Hellebrekers, D. M. E. I., de Die-Smulders, C. E. M., Smeets, H. J. M. & Lindsey, P., Oct 2017, In: Journal of Medical Genetics. 54, 10, p. 693-697 5 p.

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

• Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success

  Sallevelt, S. C. E. H., Dreesen, J. C. F. M., Drüsedau, M., Spierts, S., Coonen, E., van Tienen, F. H. J., van Golde, R. J. T., de Coo, I. F. M., Geraedts, J. P. M., de Die-Smulders, C. E. M. & Smeets, H. J. M., Feb 2013, In: Journal of Medical Genetics. 50, 2, p. 125-132 8 p.

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

• Preimplantation Genetic Testing for Monogenic Kidney Disease

  Snoek, R., Stokman, M. F., Lichtenbelt, K. D., van Tilborg, T. C., Simcox, C. E., Paulussen, A. D. C., Dreesen, J. C. M. F., van Reekum, F., Lely, A. T., Knoers, N. V. A. M., de Die-Smulders, C. E. M. & van Eerde, A. M., 7 Sept 2020, In: Clinical journal of the American Society of Nephrology. 15, 9, p. 1279-1286 8 p.

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

  Open Access

• Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas

  van der Schoot, V., Dondorp, W., Dreesen, J. C. F. M., Coonen, E., Paulussen, A. D. C., de Wert, G. & de Die-Smulders, C. E. M., Jun 2019, In: Human Reproduction. 34, 6, p. 1146-1154 9 p.

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

  Open Access

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• Preimplantation genetic testing for Neurofibromatosis type 1: more than 20 years of clinical experience

  Vernimmen, V., Paulussen, A. D. C., Dreesen, J. C. F. M., van Golde, R. J. J., Esteki, M. Z., Coonen, E., van Buul-van Zwet, M. L. L., Homminga, I., Derijck, A. A. H. A., Brandts, L., Stumpel, C. T. R. M. & de Die-Smulders, C. E. M., Aug 2023, In: European Journal of Human Genetics. 31, 8, p. 918-924 7 p.

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

  Open Access

• Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss

  Essers, R., Lebedev, I. N., Kurg, A., Fonova, E. A., Stevens, S. J. C., Koeck, R. M., von Rango, U., Brandts, L., Deligiannis, S. P., Nikitina, T. V., Sazhenova, E. A., Tolmacheva, E. N., Kashevarova, A. A., Fedotov, D. A., Demeneva, V. V., Zhigalina, D. I., Drozdov, G. V., Al-Nasiry, S., Macville, M. V. E., van den Wijngaard, A., & 6 othersDreesen, J., Paulussen, A., Hoischen, A., Brunner, H. G., Salumets, A. & Zamani Esteki, M., Dec 2023, In: Nature Medicine. 29, 12, p. 3233-3242 10 p.

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

  Open Access

• SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

  van Uum, C. M. J., Stevens, S. J. C., Dreesen, J. C. F. M., Drusedau, M., Smeets, H. J., Hollanders-Crombach, B., de Die-Smulders, C. E. M., Geraedts, J. P. M., Engelen, J. J. M. & Coonen, E., Sept 2012, In: European Journal of Human Genetics. 20, 9, p. 938-944

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

  Open Access