[Genetic risk of mental illness: what do we know and how do we communicate this?]

Autor: J R, Zinkstok, M Z, van der Horst, R P H, Wouters, C M, Aalfs, J J, Luykx

Publikováno v: Tijdschrift voor psychiatrie. 64(5)

Insights from psychiatric genetics research and large international psychiatric genetics consortia are promising but still remain outside the realm of clinical practice.brAIM: To provide an overview of developments in the field of psychiatric genetic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b9dbfd15ff6f8bbf0c2a2a6196bbb382
https://pubmed.ncbi.nlm.nih.gov/35735035

Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer

Autor: F. G. J. Kallenberg, C. M. Aalfs, F. O. The, C. A. Wientjes, A. C. Depla, M. W. Mundt, P. M. M. Bossuyt, E. Dekker

Publikováno v: Familial Cancer
Familial Cancer, 17(3), 371-380. Springer Netherlands
Familial cancer, 17(3), 371-380. Springer Netherlands

Identifying a hereditary colorectal cancer (CRC) syndrome or familial CRC (FCC) in a CRC patient may enable the patient and relatives to enroll in surveillance protocols. As these individuals are insufficiently recognized, we evaluated an online fami

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f53cb8271b22c2fd26362709dab1ba91
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85029708142&origin=inward

[Making better use of the clinical geneticist's expertise; treating physician could request a DNA test for most cancer patients]

Autor: C M, Aalfs, A M, Westermann, C G, van El

Publikováno v: Nederlands tijdschrift voor geneeskunde. 161

Eight university medical centres in the Netherlands have established clinical genetic services. Patients receive intensive, and therefore costly, genetic counselling before genetic testing takes place. In recent years the number of patients referred

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::08ab2812540ca53a47dc9acf4400d4a9
https://pubmed.ncbi.nlm.nih.gov/28589870

Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008

Autor: M C, van Rij, P A M, de Koning Gans, C M, Aalfs, M, Elting, P F, Ippel, J A, Maat-Kievit, S, Vermeer, C C, Verschuuren-Bemelmans, M J, van Belzen, R D M, Belfroid, M, Losekoot, J P M, Geraedts, R A C, Roos, A, Tibben, C E M, de Die-Smulders, E K, Bijlsma

Publikováno v: Clinical genetics. 85(1)

This study aims to give an overview of the number of prenatal tests for Huntington's disease (HD), test results, and pregnancy outcomes in the Netherlands between 1998 and 2008 and to compare them with available data from the period 1987 to 1997. A t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0853d680886b60aa117b7f854f362c8d
https://pubmed.ncbi.nlm.nih.gov/23350614

Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics

Autor: C M, Aalfs, E D, Mollema, F J, Oort, J C J M, de Haes, N J, Leschot, E M A, Smets

Publikováno v: Clinical genetics. 66(2)

Reproductive genetic counseling for a familial genetic risk factor preferably takes place before conception. However, of the women with a family history of genetic conditions who attend our department of clinical genetics, about 10-20% attend for the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3ca58c1bdef244613a2e7c8ab19b80ac
https://pubmed.ncbi.nlm.nih.gov/15253761