A citation-based method for searching scientific literature

G J Meissen, R H Myers, C A Mastromauro, W J Koroshetz, K W Klinger, L A Farrer, P A Watkins, J F Gusella, E D Bird, J B Martin. N Engl J Med 1988
Times Cited: 154







List of shared articles



Times cited

Genetic counseling and testing for Huntington's disease: A historical review.
Martha A Nance. Am J Med Genet B Neuropsychiatr Genet 2017
13

Genetic testing for Huntington disease.
Kimberly A Quaid. Handb Clin Neurol 2017
5

22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction Consortium.
Sheharyar S Baig, Mark Strong, Elisabeth Rosser, Nicola V Taverner, Ruth Glew, Zosia Miedzybrodzka, Angus Clarke, David Craufurd, Oliver W Quarrell. Eur J Hum Genet 2016
30

Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Maria Elisa Alonso, Adriana Ochoa, Ana Luisa Sosa, Yaneth Rodríguez, Mireya Chávez, Catherine Boll, Petra Yescas, Rosario Macías, Astrid Rasmussen. Genet Test Mol Biomarkers 2009
16


Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
S Creighton, E W Almqvist, D MacGregor, B Fernandez, H Hogg, J Beis, J P Welch, C Riddell, R Lokkesmoe, M Khalifa,[...]. Clin Genet 2003
113


Presymptomatic testing in myotonic dystrophy: genetic counselling approaches.
S Fokstuen, J Myring, C Evans, P S Harper. J Med Genet 2001
11

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
5

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
42

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
6

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
43

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
15

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
3

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
84



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
26

Sponastrime dysplasia: presentation in infancy.
A C Offiah, M Lees, R M Winter, C M Hall. J Med Genet 2001
6