A citation-based method for searching scientific literature

S Adam, S Wiggins, P Whyte, M Bloch, M H Shokeir, H Soltan, W Meschino, A Summers, O Suchowersky, J P Welch. J Med Genet 1993
Times Cited: 75







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



Times Cited
  Times     Co-cited
Similarity


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
26



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
25

Uptake of presymptomatic predictive testing for Huntington's disease.
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
181
20


Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987-1997).
A Maat-Kievit, M Vegter-van der Vlis, M Zoeteweij, M Losekoot, A van Haeringen, H Kanhai, R Roos. Prenat Diagn 1999
33
45

Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.
Gerry Evers-Kiebooms, Kurt Nys, Peter Harper, Moniek Zoeteweij, Alexandra Dürr, Gioia Jacopini, Christos Yapijakis, Sheila Simpson. Eur J Hum Genet 2002
58
25

Exclusion testing in pregnancy for Huntington's disease.
A Tyler, O W Quarrell, L P Lazarou, A L Meredith, P S Harper. J Med Genet 1990
27
51

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
84
18

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
18


The prenatal exclusion test for Huntington's disease: experience in the west of Scotland, 1986-1993.
J L Tolmie, H R Davidson, H M May, K McIntosh, J S Paterson, B Smith. J Med Genet 1995
19
68

Attitudes toward presymptomatic testing in Huntington disease.
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
127
16



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
183
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
114
16

Prenatal testing for Huntington's disease: a European collaborative study.
Sheila A Simpson, Moniek W Zoeteweij, Kurt Nys, Peter Harper, Alexandra Dürr, Gioia Jacopini, Christos Yapijakis, Gerry Evers-Kiebooms. Eur J Hum Genet 2002
32
34




The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutation.
Marleen Decruyenaere, Gerry Evers-Kiebooms, Andrea Boogaerts, Kristien Philippe, Koen Demyttenaere, René Dom, Wim Vandenberghe, Jean-Pierre Fryns. Eur J Hum Genet 2007
53
18

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
12

Identification of the breast cancer susceptibility gene BRCA2.
R Wooster, G Bignell, J Lancaster, S Swift, S Seal, J Mangion, N Collins, S Gregory, C Gumbs, G Micklem. Nature 1995
12

Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas.
P R Braude, G M De Wert, G Evers-Kiebooms, R A Pettigrew, J P Geraedts. Prenat Diagn 1998
36
25

Proceed with care: direct predictive testing for Huntington disease.
C M Benjamin, S Adam, S Wiggins, J L Theilmann, T T Copley, M Bloch, F Squitieri, W McKellin, S Cox, S A Brown. Am J Hum Genet 1994
81
10





Self-selection in predictive testing for Huntington's disease.
A M Codori, R Hanson, J Brandt. Am J Med Genet 1994
115
10

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
M van Slegtenhorst, R de Hoogt, C Hermans, M Nellist, B Janssen, S Verhoef, D Lindhout, A van den Ouweland, D Halley, J Young,[...]. Science 1997
10

Germ-line mutational analysis of the TSC2 gene in 90 tuberous-sclerosis patients.
K S Au, J A Rodriguez, J L Finch, K A Volcik, E S Roach, M R Delgado, E Rodriguez, H Northrup. Am J Hum Genet 1998
94
10


Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos.
K Sermon, V Goossens, S Seneca, W Lissens, A De Vos, M Vandervorst, A Van Steirteghem, I Liebaers. Prenat Diagn 1998
89
10



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
61
13

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
9

Genetic testing for children and adolescents. Who decides?
D C Wertz, J H Fanos, P R Reilly. JAMA 1994
204
9

Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making.
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, J J Cassiman, T Cloostermans, K Demyttenaere, R Dom, J P Fryns, H Van den Berghe. J Med Genet 1996
104
9


Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.
I M van der Steenstraten, A Tibben, R A Roos, J J van de Kamp, M F Niermeijer. Am J Hum Genet 1994
104
9


A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients.
J M Young, M W Burley, S J Jeremiah, D Jeganathan, R Ekong, J P Osborne, S Povey. Ann Hum Genet 1998
39
17

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.
R Niehues, M Hasilik, G Alton, C Körner, M Schiebe-Sukumar, H G Koch, K P Zimmer, R Wu, E Harms, K Reiter,[...]. J Clin Invest 1998
296
9

Molecular genetics of familial spastic paraplegia: a multitude of responsible genes.
H Kobayashi, C A Garcia, G Alfonso, H G Marks, E P Hoffman. J Neurol Sci 1996
46
15

Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes.
A R Zinn, R K Alagappan, L G Brown, I Wool, D C Page. Mol Cell Biol 1994
76
9

Chromosomal in situ suppression hybridization after Giemsa banding.
M Klever, C Grond-Ginsbach, H Scherthan, T M Schroeder-Kurth. Hum Genet 1991
88
9


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.