M Bloch, M Fahy, S Fox, M R Hayden. Am J Med Genet 1989
Times Cited: 137
Times Cited: 137
A Tibben, H J Duivenvoorden, M F Niermeijer, M Vegter-van der Vlis, R A Roos, F Verhage. Psychosom Med 1994
Times Cited: 59
Times Cited: 59
List of shared articles
Times cited
More appreciation of life or regretting the test? Experiences of living as a mutation carrier of Huntington's disease.
Anette Hagberg, The-Hung Bui, Elisabeth Winnberg. J Genet Couns 2011
Anette Hagberg, The-Hung Bui, Elisabeth Winnberg. J Genet Couns 2011
Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba.
Milena Paneque, Carolina Lemos, Karell Escalona, Lizandra Prieto, Rubén Reynaldo, Mercedes Velázquez, Judith Quevedo, Nieves Santos, Luis Enrique Almaguer, Luis Velázquez,[...]. J Genet Couns 2007
Milena Paneque, Carolina Lemos, Karell Escalona, Lizandra Prieto, Rubén Reynaldo, Mercedes Velázquez, Judith Quevedo, Nieves Santos, Luis Enrique Almaguer, Luis Velázquez,[...]. J Genet Couns 2007
Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review.
R Timman, T Stijnen, A Tibben. J Med Genet 2004
R Timman, T Stijnen, A Tibben. J Med Genet 2004
Psychological effect of genetic testing for Huntington's disease: an update of the literature.
B Meiser, S Dunn. West J Med 2001
B Meiser, S Dunn. West J Med 2001
Presymptomatic testing in myotonic dystrophy: genetic counselling approaches.
S Fokstuen, J Myring, C Evans, P S Harper. J Med Genet 2001
S Fokstuen, J Myring, C Evans, P S Harper. J Med Genet 2001
Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy.
J Amiel, V Raclin, J M Jouannic, N Morichon, H Hoffman-Radvanyi, M Dommergues, J Feingold, A Munnich, J P Bonnefont. J Med Genet 2001
J Amiel, V Raclin, J M Jouannic, N Morichon, H Hoffman-Radvanyi, M Dommergues, J Feingold, A Munnich, J P Bonnefont. J Med Genet 2001
Psychological studies in Huntington's disease: making up the balance.
M Duisterhof, R W Trijsburg, M F Niermeijer, R A Roos, A Tibben. J Med Genet 2001
M Duisterhof, R W Trijsburg, M F Niermeijer, R A Roos, A Tibben. J Med Genet 2001
A novel 3' mutation in the APC gene in a family presenting with a desmoid tumour.
D Eccles, J Harvey, A Bateman, F Ross. J Med Genet 2001
D Eccles, J Harvey, A Bateman, F Ross. J Med Genet 2001
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family.
M Montera, F Piaggio, C Marchese, V Gismondi, A Stella, N Resta, L Varesco, G Guanti, C Mareni. J Med Genet 2001
M Montera, F Piaggio, C Marchese, V Gismondi, A Stella, N Resta, L Varesco, G Guanti, C Mareni. J Med Genet 2001
Evidence of somatic mosaicism for a MECP2 mutation in females with Rett syndrome: diagnostic implications.
V Bourdon, C Philippe, T Bienvenu, B Koenig, M Tardieu, J Chelly, P Jonveaux. J Med Genet 2001
V Bourdon, C Philippe, T Bienvenu, B Koenig, M Tardieu, J Chelly, P Jonveaux. J Med Genet 2001
Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disorders.
A Imamura, N Shimozawa, Y Suzuki, Z Zhang, T Tsukamoto, T Orii, T Osumi, N Kondo. J Med Genet 2001
A Imamura, N Shimozawa, Y Suzuki, Z Zhang, T Tsukamoto, T Orii, T Osumi, N Kondo. J Med Genet 2001
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX).
I Kobayashi, R Shiari, M Yamada, N Kawamura, M Okano, A Yara, A Iguchi, N Ishikawa, T Ariga, Y Sakiyama,[...]. J Med Genet 2001
I Kobayashi, R Shiari, M Yamada, N Kawamura, M Okano, A Yara, A Iguchi, N Ishikawa, T Ariga, Y Sakiyama,[...]. J Med Genet 2001
Maternal uniparental isodisomy 11q13qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13qter.
D Kotzot, B Röthlisberger, M Riegel, A Schinzel. J Med Genet 2001
D Kotzot, B Röthlisberger, M Riegel, A Schinzel. J Med Genet 2001
High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample.
M Ehrlich, F Tsien, D Herrera, V Blackman, J Roggenbuck, C M Tuck-Muller. J Med Genet 2001
M Ehrlich, F Tsien, D Herrera, V Blackman, J Roggenbuck, C M Tuck-Muller. J Med Genet 2001
Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child.
B Röthlisberger, T Zerova, D Kotzot, T I Buzhievskaya, D Balmer, A Schinzel. J Med Genet 2001
B Röthlisberger, T Zerova, D Kotzot, T I Buzhievskaya, D Balmer, A Schinzel. J Med Genet 2001
Sponastrime dysplasia: presentation in infancy.
A C Offiah, M Lees, R M Winter, C M Hall. J Med Genet 2001
A C Offiah, M Lees, R M Winter, C M Hall. J Med Genet 2001
Psychological impact of genetic testing for Huntington's disease: an update of the literature.
B Meiser, S Dunn. J Neurol Neurosurg Psychiatry 2000
B Meiser, S Dunn. J Neurol Neurosurg Psychiatry 2000
Who Is at Risk for Psychological Distress in Genetic Testing Programs for Hereditary Cancer Disorders?
F J Grosfeld, C J Lips, F A Beemer, H F Ten Kroode. J Genet Couns 2000
F J Grosfeld, C J Lips, F A Beemer, H F Ten Kroode. J Genet Couns 2000
Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: comparing questionnaire results with in-depth interviews. Rotterdam/Leiden Genetics Workgroup.
A C DudokdeWit, A Tibben, H J Duivenvoorden, M F Niermeijer, J Passchier, R W Trijsburg. Am J Med Genet 1998
A C DudokdeWit, A Tibben, H J Duivenvoorden, M F Niermeijer, J Passchier, R W Trijsburg. Am J Med Genet 1998
Course of distress experienced by persons at risk for an autosomal dominant inheritable disorder participating in a predictive testing program: an explorative study. Rotterdam/Leiden Genetics Workgroup.
A C Dudok deWit, H J Duivenvoorden, J Passchier, M F Niermeijer, A Tibben. Psychosom Med 1998
A C Dudok deWit, H J Duivenvoorden, J Passchier, M F Niermeijer, A Tibben. Psychosom Med 1998
Preparing for presymptomatic DNA testing for early onset Alzheimer's disease/cerebral haemorrhage and hereditary Pick disease.
A Tibben, M Stevens, G M de Wert, M F Niermeijer, C M van Duijn, J C van Swieten. J Med Genet 1997
A Tibben, M Stevens, G M de Wert, M F Niermeijer, C M van Duijn, J C van Swieten. J Med Genet 1997