van Langen IM - Search Results

1

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.

van der Meij KRM, Sistermans EA, Macville MVE, Stevens SJC, Bax CJ, Bekker MN, Bilardo CM, Boon EMJ, Boter M, Diderich KEM, de Die-Smulders CEM, Duin LK, Faas BHW, Feenstra I, Haak MC, Hoffer MJV, den Hollander NS, Hollink IHIM, Jehee FS, Knapen MFCM, Kooper AJA, van Langen IM, Lichtenbelt KD, Linskens IH, van Maarle MC, Oepkes D, Pieters MJ, Schuring-Blom GH, Sikkel E, Sikkema-Raddatz B, Smeets DFCM, Srebniak MI, Suijkerbuijk RF, Tan-Sindhunata GM, van der Ven AJEM, van Zelderen-Bhola SL, Henneman L, Galjaard RH, Van Opstal D, Weiss MM; Dutch NIPT Consortium. van der Meij KRM, et al. Among authors: van zelderen bhola sl, van maarle mc, van langen im, van der ven ajem, van opstal d. Am J Hum Genet. 2019 Dec 5;105(6):1091-1101. doi: 10.1016/j.ajhg.2019.10.005. Epub 2019 Nov 7. Am J Hum Genet. 2019. PMID: 31708118 Free PMC article.

2

High distress in parents whose children undergo predictive testing for long QT syndrome.

Hendriks KS, Grosfeld FJ, Wilde AA, van den Bout J, van Langen IM, van Tintelen JP, ten Kroode HF. Hendriks KS, et al. Among authors: van den bout j, van langen im, van tintelen jp. Community Genet. 2005;8(2):103-13. doi: 10.1159/000084778. Community Genet. 2005. PMID: 15925886

3

Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy.

Christiaans I, Birnie E, Bonsel GJ, Wilde AA, van Langen IM. Christiaans I, et al. Among authors: van langen im. Eur J Hum Genet. 2008 Oct;16(10):1201-7. doi: 10.1038/ejhg.2008.92. Epub 2008 May 14. Eur J Hum Genet. 2008. PMID: 18478037

4

A new mutation for Huntington disease following maternal transmission of an intermediate allele.

Semaka A, Kay C, Belfroid RD, Bijlsma EK, Losekoot M, van Langen IM, van Maarle MC, Oosterloo M, Hayden MR, van Belzen MJ. Semaka A, et al. Among authors: van belzen mj, van maarle mc, van langen im. Eur J Med Genet. 2015 Jan;58(1):28-30. doi: 10.1016/j.ejmg.2014.11.005. Epub 2014 Nov 20. Eur J Med Genet. 2015. PMID: 25464109

5

Maximising the efficiency of clinical screening programmes: balancing predictive genetic testing with a right not to know.

Schuurman AG, van der Kolk DM, Verkerk MA, Birnie E, Ranchor AV, Plantinga M, van Langen IM. Schuurman AG, et al. Among authors: van langen im, van der kolk dm. Eur J Hum Genet. 2015 Sep;23(9):1124-8. doi: 10.1038/ejhg.2014.269. Epub 2015 Jan 7. Eur J Hum Genet. 2015. PMID: 25564039 Free PMC article.

6

A group approach to genetic counselling of cardiomyopathy patients: satisfaction and psychological outcomes sufficient for further implementation.

Otten E, Birnie E, Ranchor AV, van Tintelen JP, van Langen IM. Otten E, et al. Among authors: van langen im, van tintelen jp. Eur J Hum Genet. 2015 Nov;23(11):1462-7. doi: 10.1038/ejhg.2015.10. Epub 2015 Feb 4. Eur J Hum Genet. 2015. PMID: 25649380 Free PMC article.

7

Telegenetics use in presymptomatic genetic counselling: patient evaluations on satisfaction and quality of care.

Otten E, Birnie E, Ranchor AV, van Langen IM. Otten E, et al. Among authors: van langen im. Eur J Hum Genet. 2016 Apr;24(4):513-20. doi: 10.1038/ejhg.2015.164. Epub 2015 Jul 15. Eur J Hum Genet. 2016. PMID: 26173963 Free PMC article.

8

Online genetic counseling from the providers' perspective: counselors' evaluations and a time and cost analysis.

Otten E, Birnie E, Ranchor AV, van Langen IM. Otten E, et al. Among authors: van langen im. Eur J Hum Genet. 2016 Aug;24(9):1255-61. doi: 10.1038/ejhg.2015.283. Epub 2016 Jan 20. Eur J Hum Genet. 2016. PMID: 26785833 Free PMC article.

9

Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.

Plantinga M, Birnie E, Abbott KM, Sinke RJ, Lucassen AM, Schuurmans J, Kaplan S, Verkerk MA, Ranchor AV, van Langen IM. Plantinga M, et al. Among authors: van langen im. Eur J Hum Genet. 2016 Oct;24(10):1417-23. doi: 10.1038/ejhg.2016.43. Epub 2016 May 11. Eur J Hum Genet. 2016. PMID: 27165008 Free PMC article.

10

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.

van Schendel RV, Page-Christiaens GC, Beulen L, Bilardo CM, de Boer MA, Coumans AB, Faas BH, van Langen IM, Lichtenbelt KD, van Maarle MC, Macville MV, Oepkes D, Pajkrt E, Henneman L; Dutch NIPT Consortium. van Schendel RV, et al. Among authors: van maarle mc, van langen im. Prenat Diagn. 2016 Dec;36(12):1091-1098. doi: 10.1002/pd.4941. Epub 2016 Nov 16. Prenat Diagn. 2016. PMID: 27739584 Free PMC article.

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