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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 3
2005 5
2006 1
2007 4
2008 4
2009 1
2010 4
2011 5
2012 4
2013 2
2014 3
2015 2
2016 5
2017 6
2018 6
2019 4
2020 1
2021 4
2022 2
2023 2
2024 3

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61 results

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Page 1
Liquid biopsy: state of reproductive medicine and beyond.
Schobers G, Koeck R, Pellaers D, Stevens SJC, Macville MVE, Paulussen ADC, Coonen E, van den Wijngaard A, de Die-Smulders C, de Wert G, Brunner HG, Zamani Esteki M. Schobers G, et al. Among authors: paulussen adc. Hum Reprod. 2021 Oct 18;36(11):2824-2839. doi: 10.1093/humrep/deab206. Hum Reprod. 2021. PMID: 34562078 Free PMC article. Review.
Preimplantation genetic testing for Neurofibromatosis type 1: more than 20 years of clinical experience.
Vernimmen V, Paulussen ADC, Dreesen JCFM, van Golde RJ, Zamani Esteki M, Coonen E, van Buul-van Zwet ML, Homminga I, Derijck AAHA, Brandts L, Stumpel CTRM, de Die-Smulders CEM. Vernimmen V, et al. Among authors: paulussen adc. Eur J Hum Genet. 2023 Aug;31(8):918-924. doi: 10.1038/s41431-023-01404-x. Epub 2023 Jun 19. Eur J Hum Genet. 2023. PMID: 37337089 Free PMC article.
Genome sequencing as a generic diagnostic strategy for rare disease.
Schobers G, Derks R, den Ouden A, Swinkels H, van Reeuwijk J, Bosgoed E, Lugtenberg D, Sun SM, Corominas Galbany J, Weiss M, Blok MJ, Olde Keizer RACM, Hofste T, Hellebrekers D, de Leeuw N, Stegmann A, Kamsteeg EJ, Paulussen ADC, Ligtenberg MJL, Bradley XZ, Peden J, Gutierrez A, Pullen A, Payne T, Gilissen C, van den Wijngaard A, Brunner HG, Nelen M, Yntema HG, Vissers LELM. Schobers G, et al. Among authors: paulussen adc. Genome Med. 2024 Feb 14;16(1):32. doi: 10.1186/s13073-024-01301-y. Genome Med. 2024. PMID: 38355605 Free PMC article.
Facioscapulohumeral muscular dystrophy-Reproductive counseling, pregnancy, and delivery in a complex multigenetic disease.
Vincenten SCC, Van Der Stoep N, Paulussen ADC, Mul K, Badrising UA, Kriek M, Van Der Heijden OWH, Van Engelen BGM, Voermans NC, De Die-Smulders CEM, Lassche S. Vincenten SCC, et al. Among authors: paulussen adc. Clin Genet. 2022 Feb;101(2):149-160. doi: 10.1111/cge.14031. Epub 2021 Aug 1. Clin Genet. 2022. PMID: 34297364 Free PMC article. Review.
Pharmacogenomics and acquired long QT syndrome.
Aerssens J, Paulussen AD. Aerssens J, et al. Among authors: paulussen ad. Pharmacogenomics. 2005 Apr;6(3):259-70. doi: 10.1517/14622416.6.3.259. Pharmacogenomics. 2005. PMID: 16013957 Review.
Preimplantation Genetic Testing for Monogenic Kidney Disease.
Snoek R, Stokman MF, Lichtenbelt KD, van Tilborg TC, Simcox CE, Paulussen ADC, Dreesen JCMF, van Reekum F, Lely AT, Knoers NVAM, de Die-Smulders CEM, van Eerde AM. Snoek R, et al. Among authors: paulussen adc. Clin J Am Soc Nephrol. 2020 Sep 7;15(9):1279-1286. doi: 10.2215/CJN.03550320. Epub 2020 Aug 27. Clin J Am Soc Nephrol. 2020. PMID: 32855195 Free PMC article.
Genetic basis of drug-induced arrhythmias.
Vos MA, Paulussen AD. Vos MA, et al. Among authors: paulussen ad. Ann Med. 2004;36 Suppl 1:35-40. doi: 10.1080/17431380410032634. Ann Med. 2004. PMID: 15176422 Review.
Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012.
Mersy E, Smits LJ, van Winden LA, de Die-Smulders CE; South-East Netherlands NIPT Consortium; Paulussen AD, Macville MV, Coumans AB, Frints SG. Mersy E, et al. Among authors: paulussen ad. Hum Reprod Update. 2013 Jul-Aug;19(4):318-29. doi: 10.1093/humupd/dmt001. Epub 2013 Feb 8. Hum Reprod Update. 2013. PMID: 23396607 Review.
61 results