A citation-based method for searching scientific literature

M R Hayden, J Goldblatt, G Wallis, I M Winship, P Beighton. S Afr Med J 1987
Times Cited: 4







List of co-cited articles
6 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


The high frequency of juvenile Huntington's chorea in South Africa.
M R Hayden, J M MacGregor, D S Saffer, P H Beighton. J Med Genet 1982
25
50


The prevalence of Huntington's chorea in South Africa.
M R Hayden, J M MacGregor, P H Beighton. S Afr Med J 1980
58
50

The origin of Huntington's chorea in the Afrikaner population of South Africa.
M R Hayden, H C Hopkins, M Macrea, P H Beighton. S Afr Med J 1980
31
50


The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.
S E Andrew, Y P Goldberg, B Kremer, H Telenius, J Theilmann, S Adam, E Starr, F Squitieri, B Lin, M A Kalchman. Nat Genet 1993
793
50

De novo expansion of a CAG repeat in a Japanese patient with sporadic Huntington's disease.
M Watanabe, A Satoh, M Kanemoto, N Ohkoshi, S Shoji. J Neurol Sci 2000
7
25

The Huntington's chorea register of Tanzania.
E M Scrimgeour. East Afr Med J 1982
6
25

Huntington's disease confirmed by genetic testing in five African families.
E Silber, J Kromberg, J A Temlett, A Krause, D Saffer. Mov Disord 1998
15
25

Huntington's disease in a Coloured family.
D S Saffer, D C Nathan, P A Kahle, B Steingo. S Afr Med J 1974
9
25


Huntington disease in black African populations.
E M Scrimgeour, S A Simpson. Hum Genet 1992
6
25

Social perspectives in Huntington's chorea.
M R Hayden, R Ehrlich, H Parker, S J Ferera. S Afr Med J 1980
45
25

Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg.
J G Kromberg, A Krause, A B Spurdle, J A Temlett, M Lucas, D Rodseth, G Stevens, T Jenkins. S Afr Med J 1999
9
25


[Huntington disease in Burkina Faso].
J Kaboré, A Ouédraogo. Rev Neurol (Paris) 2000
4
25

A South African mixed ancestry family with Huntington disease-like 2: clinical and genetic features.
Soraya Bardien, Fatima Abrahams, Himla Soodyall, Lize van der Merwe, Jacquie Greenberg, Tinus Brink, Jonathan Carr. Mov Disord 2007
29
25

Huntington's disease in a Sudanese family from Khartoum.
E M Scrimgeour, Y Samman, D J Brock. Hum Genet 1995
7
25

Huntington's chorea in a black Rhodesian family.
B L Samuels, M Gelfand. S Afr Med J 1978
14
25


Hereditary neurodegenerative disorders in Nigerian Africans.
A B Aiyesimoju, B O Osuntokun, O Bademosi, A O Adeuja. Neurology 1984
38
25

Junctophilins: a novel family of junctional membrane complex proteins.
H Takeshima, S Komazaki, M Nishi, M Iino, K Kangawa. Mol Cell 2000
458
25

Huntington disease in Maryland: clinical aspects of racial variation.
S E Folstein, G A Chase, W E Wahl, A M McDonnell, M F Folstein. Am J Hum Genet 1987
93
25

A short test of mental status: description and preliminary results.
E Kokmen, J M Naessens, K P Offord. Mayo Clin Proc 1987
284
25

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.
S E Holmes, E O'Hearn, A Rosenblatt, C Callahan, H S Hwang, R G Ingersoll-Ashworth, A Fleisher, G Stevanin, A Brice, N T Potter,[...]. Nat Genet 2001
191
25

Huntington's disease in Tanzania.
E M Scrimgeour. J Med Genet 1981
14
25

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.
B Kremer, P Goldberg, S E Andrew, J Theilmann, H Telenius, J Zeisler, F Squitieri, B Lin, A Bassett, E Almqvist. N Engl J Med 1994
420
25

When is it not Huntington's disease?
J M Heckmann, A Bryer, L J Greenberg. S Afr Med J 2001
1
100



Expansion of a (CAG)n repeat region in a sporadic case of HD.
A Bozza, S Malagù, E Calzolari, A Novelletto, M Pavoni, L del Senno. Acta Neurol Scand 1995
12
25

Huntington's disease in black kindreds in South Carolina.
H H Wright, C N Still, R K Abramson. Arch Neurol 1981
23
25

Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease.
C Zuccato, A Ciammola, D Rigamonti, B R Leavitt, D Goffredo, L Conti, M E MacDonald, R M Friedlander, V Silani, M R Hayden,[...]. Science 2001
921
25

Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan.
Saeid Morovvati, Masanori Nakagawa, Mitsuhiro Osame, Ali Karami. Arch Med Res 2008
13
25

Triplet repeats and DNA repair: germ cell and somatic cell instability in transgenic mice.
Irina V Kovtun, Craig Spiro, Cynthia T McMurray. Methods Mol Biol 2004
11
25

DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.
C K Wang, Y R Wu, W L Hwu, C M Chen, L S Ro, S T Chen, K Gwinn-Hardy, C C Yang, R M Wu, T F Chen,[...]. Eur Neurol 2004
15
25

A systematic review of the treatment studies in Huntington's disease since 1990.
Raphael M Bonelli, Peter Hofmann. Expert Opin Pharmacother 2007
55
25

Huntington's chorea.
P Beighton, M R Hayden. S Afr Med J 1981
9
25

A study of potential interactive genetic factors in Huntington's disease.
Peter K Panegyres, John Beilby, Max Bulsara, Katina Toufexis, Cathy Wong. Eur Neurol 2006
14
25

Juvenile onset Huntington disease resulting from a very large maternal expansion.
F A Nahhas, J Garbern, K M Krajewski, B B Roa, G L Feldman. Am J Med Genet A 2005
28
25

Huntington disease: DNA analysis in Brazilian population.
S Raskin, N Allan, H A Teive, F Cardoso, M S Haddad, G Levi, R Boy, J Lerena Junior, V S Sotomaior, M Janzen-Dück,[...]. Arq Neuropsiquiatr 2000
20
25

Huntington's disease as caused by 34 CAG repeats.
Jürgen Andrich, Larissa Arning, Stefan Wieczorek, Peter H Kraus, Ralf Gold, Carsten Saft. Mov Disord 2008
37
25

Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.
D C Rubinsztein, W Amos, J Leggo, S Goodburn, R S Ramesar, J Old, R Bontrop, R McMahon, D E Barton, M A Ferguson-Smith. Nat Genet 1994
116
25

Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease.
M A Nance, V Mathias-Hagen, G Breningstall, M J Wick, R C McGlennen. Neurology 1999
77
25

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain.
M DiFiglia, E Sapp, K O Chase, S W Davies, G P Bates, J P Vonsattel, N Aronin. Science 1997
25

Mechanisms of neurodegeneration in Huntington's disease.
Joana M Gil, Ana Cristina Rego. Eur J Neurosci 2008
299
25

Factors associated with HD CAG repeat instability in Huntington disease.
V C Wheeler, F Persichetti, S M McNeil, J S Mysore, S S Mysore, M E MacDonald, R H Myers, J F Gusella, N S Wexler. J Med Genet 2007
80
25

Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset.
Nancy S Wexler, Judith Lorimer, Julie Porter, Fidela Gomez, Carol Moskowitz, Edith Shackell, Karen Marder, Graciela Penchaszadeh, Simone A Roberts, Javier Gayán,[...]. Proc Natl Acad Sci U S A 2004
476
25

The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation.
Maria do Carmo Costa, Paula Magalhães, Laura Guimarães, Patrícia Maciel, Jorge Sequeiros, Alda Sousa. J Hum Genet 2006
22
25

Origins and evolution of Huntington disease chromosomes.
S E Andrew, M R Hayden. Neurodegeneration 1995
21
25


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.