A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
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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
410
23

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
468
23

Family history and DNA analysis in patients with suspected Huntington's disease.
S Siesling, M Vegter-van de Vlis, M Losekoot, R D Belfroid, J A Maat-Kievit, H P Kremer, R A Roos. J Neurol Neurosurg Psychiatry 2000
20
70

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
778
22


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
797
20

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence.
F Squitieri, S E Andrew, Y P Goldberg, B Kremer, N Spence, J Zeisler, K Nichol, J Theilmann, J Greenberg, J Goto. Hum Mol Genet 1994
144
20

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.
Y P Goldberg, B Kremer, S E Andrew, J Theilmann, R K Graham, F Squitieri, H Telenius, S Adam, A Sajoo, E Starr. Nat Genet 1993
221
19

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.
D C Rubinsztein, J Leggo, R Coles, E Almqvist, V Biancalana, J J Cassiman, K Chotai, M Connarty, D Crauford, A Curtis,[...]. Am J Hum Genet 1996
339
19

A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
D R Langbehn, R R Brinkman, D Falush, J S Paulsen, M R Hayden. Clin Genet 2004
509
19

CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup.
Simon C Warby, Alexandre Montpetit, Anna R Hayden, Jeffrey B Carroll, Stefanie L Butland, Henk Visscher, Jennifer A Collins, Alicia Semaka, Thomas J Hudson, Michael R Hayden. Am J Hum Genet 2009
131
19

HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.
Simon C Warby, Henk Visscher, Jennifer A Collins, Crystal N Doty, Catherine Carter, Stefanie L Butland, Anna R Hayden, Ichiro Kanazawa, Colin J Ross, Michael R Hayden. Eur J Hum Genet 2011
97
19

Incidence and prevalence of Huntington's disease in Olmsted County, Minnesota (1950 through 1989).
E Kokmen, F S Ozekmekçi, C M Beard, P C O'Brien, L T Kurland. Arch Neurol 1994
30
36

Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population.
Y P Goldberg, C T McMurray, J Zeisler, E Almqvist, D Sillence, F Richards, A M Gacy, J Buchanan, H Telenius, M R Hayden. Hum Mol Genet 1995
98
17


Huntington's disease: from molecular pathogenesis to clinical treatment.
Christopher A Ross, Sarah J Tabrizi. Lancet Neurol 2011
851
17

Prevalence of adult Huntington's disease in the UK based on diagnoses recorded in general practice records.
Stephen J W Evans, Ian Douglas, Michael D Rawlins, Nancy S Wexler, Sarah J Tabrizi, Liam Smeeth. J Neurol Neurosurg Psychiatry 2013
96
17

The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.
Tamara Pringsheim, Katie Wiltshire, Lundy Day, Jonathan Dykeman, Thomas Steeves, Nathalie Jette. Mov Disord 2012
254
17

The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.
R R Brinkman, M M Mezei, J Theilmann, E Almqvist, M R Hayden. Am J Hum Genet 1997
252
15

Late-onset Huntington's disease: a clinical and molecular study.
C M James, G D Houlihan, R G Snell, J P Cheadle, P S Harper. Age Ageing 1994
37
27

A polymorphic DNA marker genetically linked to Huntington's disease.
J F Gusella, N S Wexler, P M Conneally, S L Naylor, M A Anderson, R E Tanzi, P C Watkins, K Ottina, M R Wallace, A Y Sakaguchi. Nature 1983
15

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.
R G Snell, J C MacMillan, J P Cheadle, I Fenton, L P Lazarou, P Davies, M E MacDonald, J F Gusella, P S Harper, D J Shaw. Nat Genet 1993
577
15


Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.
B Kremer, E Almqvist, J Theilmann, N Spence, H Telenius, Y P Goldberg, M R Hayden. Am J Hum Genet 1995
110
14


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
14


De novo expansion of a (CAG)n repeat in sporadic Huntington's disease.
R H Myers, M E MacDonald, W J Koroshetz, M P Duyao, C M Ambrose, S A Taylor, G Barnes, J Srinidhi, C S Lin, W L Whaley. Nat Genet 1993
195
14

Neuropsychiatric aspects of Huntington's disease.
J S Paulsen, R E Ready, J M Hamilton, M S Mega, J L Cummings. J Neurol Neurosurg Psychiatry 2001
257
14

Huntington's disease.
Francis O Walker. Lancet 2007
14

Huntington disease: natural history, biomarkers and prospects for therapeutics.
Christopher A Ross, Elizabeth H Aylward, Edward J Wild, Douglas R Langbehn, Jeffrey D Long, John H Warner, Rachael I Scahill, Blair R Leavitt, Julie C Stout, Jane S Paulsen,[...]. Nat Rev Neurol 2014
493
14

Huntington disease: genetics and epidemiology.
P M Conneally. Am J Hum Genet 1984
168
12

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
12

Increased rate of suicide among patients with Huntington's disease.
M Schoenfeld, R H Myers, L A Cupples, B Berkman, D S Sax, E Clark. J Neurol Neurosurg Psychiatry 1984
157
12



Differences in duration of Huntington's disease based on age at onset.
T Foroud, J Gray, J Ivashina, P M Conneally. J Neurol Neurosurg Psychiatry 1999
129
12


Technical standards and guidelines for Huntington disease testing.
Nicholas T Potter, Elaine B Spector, Thomas W Prior. Genet Med 2004
55
14

Origins and evolution of Huntington disease chromosomes.
S E Andrew, M R Hayden. Neurodegeneration 1995
21
38

Huntington's disease in Hong Kong Chinese: epidemiology and clinical picture.
C M Chang, Y L Yu, K Y Fong, M T Wong, Y W Chan, T H Ng, C M Leung, V Chan. Clin Exp Neurol 1994
18
44


DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland.
F Laccone, U Engel, E Holinski-Feder, M Weigell-Weber, K Marczinek, D Nolte, D J Morris-Rosendahl, C Zühlke, K Fuchs, H Weirich-Schwaiger,[...]. Neurology 1999
60
11

Huntington disease phenocopy is a familial prion disease.
R C Moore, F Xiang, J Monaghan, D Han, Z Zhang, L Edström, M Anvret, S B Prusiner. Am J Hum Genet 2001
86
11



Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses.
S S Chong, E Almqvist, H Telenius, L LaTray, K Nichol, B Bourdelat-Parks, Y P Goldberg, B R Haddad, F Richards, D Sillence,[...]. Hum Mol Genet 1997
82
11


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.