Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review

Por Timman, R, Stijnen, T, Tibben, A
Publicado em 2004

Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics

Por Riedijk, S., Oudesluijs, G., Tibben, A.
Publicado em 2012

Psychological studies in Huntington's disease: making up the balance

Por Duisterhof, M., Trijsburg, R., Niermeijer, M., Roos, R., Tibben, A.
Publicado em 2001

A Decade of Genetic Counseling in Frontotemporal Dementia Affected Families: Few Counseling Requests and much Familial Opposition to Testing

Por Riedijk, S. R., Niermeijer, M. F. N., Dooijes, D., Tibben, A.
Publicado em 2009

Predicting adaptation to presymptomatic DNA testing for late onset disorders: who will experience distress? Rotterdam Leiden Genetics Workgroup.

Por DudokdeWit, A C, Tibben, A, Duivenvoorden, H J, Niermeijer, M F, Passchier, J
Publicado em 1998

Behavioural complaints in participants who underwent predictive testing for Huntington's disease

Por Witjes-Ane, M, Zwinderman, A, Tibben, A, van Ommen, G-J B, Roos, R
Publicado em 2002

Dilemmas in counselling females with the fragile X syndrome

Por de Vries, B. B A, van den Boer-van, ... H. M A, Niermeijer, M., Tibben, A.
Publicado em 1999

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

Por van der Steenstraten, I. M., Tibben, A., Roos, R. A., van de Kamp, J. J., Niermeijer, M. F.
Publicado em 1994

Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease.

Por Tibben, A, Stevens, M, de Wert, G M, Niermeijer, M F, van Duijn, C M, van Swieten, J C
Publicado em 1997

DNA testing for fragile X syndrome: implications for parents and family.

Por van Rijn, M A, de Vries, B B, Tibben, A, van den Ouweland, A M, Halley, D J, Niermeijer, M F
Publicado em 1997

Intelligence indices in people with a high/low risk for developing Huntington's disease.

Por de Boo, G M, Tibben, A, Lanser, J B, Jennekens-Schinkel, A, Hermans, J, Vegter-van der Vlis, M, Roos, R A
Publicado em 1997

New problems in testing for Huntington's disease: the issue of intermediate and reduced penetrance alleles

Por MAAT-KIEVIT, A., LOSEKOOT, M., DEN BERG, H. V. D. B.-V., VAN OMMEN, G.-J., NIERMEIJER, M., BREUNING, M., TIBBEN, A.
Publicado em 2001

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup.

Por DudokdeWit, A C, Tibben, A, Duivenvoorden, H J, Frets, P G, Zoeteweij, M W, Losekoot, M, van Haeringen, A, Niermeijer, M F, Passchier, J
Publicado em 1997

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation

Por Wagner, A, Tops, C, Wijnen, J, Zwinderman, K, van der Meer, C, Kets, M, Niermeijer, M, Klijn, J, Tibben, A, Vasen, H, Meijers-Heijboer, H
Publicado em 2002

Screening for the fragile X syndrome among the mentally retarded: a clinical study

Por de Vries, B. B A, Mohkamsing, S., van den Ouweland, A. M W, Mol, E., Gelsema, K., van Rijn, M., Tibben, A., Halley, D., Duivenvoorden, H., Oostra, B., Niermeijer, M.
Publicado em 1999

Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks?

Por Lodder, L, Frets, P, Trijsburg, R, Meijers-Heijboer, E, Klijn, J, Duivenvoorden, H, Tibben, A, Wagner, A, van der Meer, C A, Devilee, P, Cornelisse, C, Niermeijer, M, m other
Publicado em 1999

Impact of screening for breast cancer in high-risk women on health-related quality of life

Por Rijnsburger, A J, Essink-Bot, M L, van Dooren, S, Borsboom, G J J M, Seynaeve, C, Bartels, C C M, Klijn, J G M, Tibben, A, de Koning, H J
Publicado em 2004

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Por Rizzu, P, Van Swieten, J C, Joosse, M, Hasegawa, M, Stevens, M, Tibben, A, Niermeijer, M F, Hillebrand, M, Ravid, R, Oostra, B A, Goedert, M, van Duijn, C M, Heutink, P
Publicado em 1999

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group.

Por de Vries, B B, van den Ouweland, A M, Mohkamsing, S, Duivenvoorden, H J, Mol, E, Gelsema, K, van Rijn, M, Halley, D J, Sandkuijl, L A, Oostra, B A, Tibben, A, Niermeijer, M F
Publicado em 1997

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents’ Experiences

Por van der Steen, S. L., Riedijk, S. R., Verhagen-Visser, J., Govaerts, L. C. P., Srebniak, M. I., Van Opstal, D., Joosten, M., Knapen, M. F. C. M., Tibben, A., Diderich, K. E. M., Galjaard, R. J. H.
Publicado no J Genet Couns (2016)