A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
39



Predictive testing for Huntington's disease with use of a linked DNA marker.
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
156
26

Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk.
M Huggins, M Bloch, S Wiggins, S Adam, O Suchowersky, M Trew, M Klimek, C R Greenberg, M Eleff, L P Thompson. Am J Med Genet 1992
182
26


Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's disease.
J Brandt, K A Quaid, S E Folstein, P Garber, N E Maestri, M H Abbott, P R Slavney, M L Franz, L Kasch, H H Kazazian. JAMA 1989
124
22

The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing.
S Wiggins, P Whyte, M Huggins, S Adam, J Theilmann, M Bloch, S B Sheps, M T Schechter, M R Hayden. N Engl J Med 1992
348
22

Uptake of presymptomatic predictive testing for Huntington's disease.
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
181
22


Attitudes toward presymptomatic testing in Huntington disease.
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
127
20


Attitudes of persons at risk for Huntington disease toward predictive testing.
S Kessler, T Field, L Worth, H Mosbarger. Am J Med Genet 1987
159
16

Recommendations for the predictive genetic test in Huntington's disease.
R MacLeod, A Tibben, M Frontali, G Evers-Kiebooms, A Jones, A Martinez-Descales, R A Roos. Clin Genet 2013
117
16








On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program.
A Tibben, P G Frets, J J van de Kamp, M F Niermeijer, M Vegtervan der Vlis, R A Roos, H G Rooymans, G J van Ommen, F Verhage. Am J Med Genet 1993
95
11

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
816
11


DNA-testing for Huntington's disease in The Netherlands: a retrospective study on psychosocial effects.
A Tibben, M Vegter-van der Vlis, M I Skraastad, P G Frets, J J van der Kamp, M F Niermeijer, G J van Ommen, R A Roos, H G Rooijmans, D Stronks. Am J Med Genet 1992
74
11

Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program.
A Tibben, P G Frets, J J van de Kamp, M F Niermeijer, M Vegter-van der Vlis, R A Roos, G J van Ommen, H J Duivenvoorden, F Verhage. Am J Med Genet 1993
83
11

Self-selection in predictive testing for Huntington's disease.
A M Codori, R Hanson, J Brandt. Am J Med Genet 1994
114
9



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
161
9


A highly polymorphic locus very tightly linked to the Huntington's disease gene.
J J Wasmuth, J Hewitt, B Smith, D Allard, J L Haines, D Skarecky, E Partlow, M R Hayden. Nature 1988
155
9

Problems in genetic prediction for Huntington's disease.
M J Morris, A Tyler, L Lazarou, L Meredith, P S Harper. Lancet 1989
41
12

Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention.
A Tibben, H J Duivenvoorden, M Vegter-van der Vlis, M F Niermeijer, P G Frets, J J van de Kamp, R A Roos, H G Rooijmans, F Verhage. Am J Med Genet 1993
74
9




Long-term outcome of presymptomatic testing in Huntington disease.
Marcela Gargiulo, Séverine Lejeune, Marie-Laure Tanguy, Khadija Lahlou-Laforêt, Anne Faudet, David Cohen, Josué Feingold, Alexandra Durr. Eur J Hum Genet 2009
63
9

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
9




Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.
A Goate, M C Chartier-Harlin, M Mullan, J Brown, F Crawford, L Fidani, L Giuffra, A Haynes, N Irving, L James. Nature 1991
7

The clinical introduction of genetic testing for Alzheimer disease. An ethical perspective.
S G Post, P J Whitehouse, R H Binstock, T D Bird, S K Eckert, L A Farrer, L M Fleck, A D Gaines, E T Juengst, H Karlinsky,[...]. JAMA 1997
144
7




Discrimination as a consequence of genetic testing.
P R Billings, M A Kohn, M de Cuevas, J Beckwith, J S Alper, M R Natowicz. Am J Hum Genet 1992
319
7

Psychological distress in the 5-year period after predictive testing for Huntington's disease.
Marleen Decruyenaere, Gerry Evers-Kiebooms, Trees Cloostermans, Andrea Boogaerts, Koen Demyttenaere, René Dom, Jean Pierre Fryns. Eur J Hum Genet 2003
84
7



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.