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



J Buxton, P Shelbourne, J Davies, C Jones, T Van Tongeren, C Aslanidis, P de Jong, G Jansen, M Anvret, B Riley. Nature 1992
Times Cited: 569




List of shared articles



Times cited

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 R√∂thlisberger, 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

Molecular genetics of Huntington's disease.
J F Gusella, M E MacDonald, C M Ambrose, M P Duyao. Arch Neurol 1993
103

Molecular genetics in neurology.
J B Martin. Ann Neurol 1993
37

Trinucleotide repeat length instability and age of onset in Huntington's disease.
M Duyao, C Ambrose, R Myers, A Novelletto, F Persichetti, M Frontali, S Folstein, C Ross, M Franz, M Abbott. Nat Genet 1993
799