A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
63





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
48

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
45




Predictive testing for Huntington's disease: risk perception, reasons for testing and psychological profile of test applicants.
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, J J Cassiman, T Cloostermans, K Demyttenaere, R Dom, J P Fryns, H Van den Berghe. Genet Couns 1995
69
45

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
45

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
45


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
42



Testing for Huntington's disease with support for all parties.
A Tibben, M Vegter-vd Vlis, M F vd Niermeijer, J J Kamp, R A Roos, H G Rooijmans, P G Frets, F Verhage. Lancet 1990
42
42

Psychological effects of presymptomatic DNA testing for Huntington's disease in the Dutch program.
A Tibben, H J Duivenvoorden, M F Niermeijer, M Vegter-van der Vlis, R A Roos, F Verhage. Psychosom Med 1994
59
39

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
39



The measurement of pessimism: the hopelessness scale.
A T Beck, A Weissman, D Lester, L Trexler. J Consult Clin Psychol 1974
39

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
39

ICF syndrome: a new case and review of the literature.
D F Smeets, U Moog, C M Weemaes, G Vaes-Peeters, G F Merkx, J P Niehof, G Hamers. Hum Genet 1994
88
36


Non-participation in predictive testing for Huntington's disease: individual decision-making, personality and avoidant behaviour in the family.
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, T Cloostermans, J J Cassiman, K Demyttenaere, R Dom, J P Fryns, H Van den Berghe. Eur J Hum Genet 1997
52
36


Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse.
M E Brunkow, E W Jeffery, K A Hjerrild, B Paeper, L B Clark, S A Yasayko, J E Wilkinson, D Galas, S F Ziegler, F Ramsdell. Nat Genet 2001
36



A Japanese family of X-linked auto-immune enteropathy with haemolytic anaemia and polyendocrinopathy.
N Satake, M Nakanishi, M Okano, K Tomizawa, A Ishizaka, K Kojima, M Onodera, T Ariga, A Satake, Y Sakiyama. Eur J Pediatr 1993
65
36

Unstable DNA sequence in myotonic dystrophy.
H G Harley, S A Rundle, W Reardon, J Myring, S Crow, J D Brook, P S Harper, D J Shaw. Lancet 1992
182
36

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene.
G L Xu, T H Bestor, D Bourc'his, C L Hsieh, N Tommerup, M Bugge, M Hulten, X Qu, J J Russo, E Viegas-Péquignot. Nature 1999
838
36

Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects.
L L Field, R Tobias, W P Robinson, R Paisey, S Bain. Am J Hum Genet 1998
45
36

Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.
N Shimozawa, Z Zhang, Y Suzuki, A Imamura, T Tsukamoto, T Osumi, Y Fujiki, T Orii, P G Barth, R J Wanders,[...]. Biochem Biophys Res Commun 1999
46
36

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.
J Buxton, P Shelbourne, J Davies, C Jones, T Van Tongeren, C Aslanidis, P de Jong, G Jansen, M Anvret, B Riley. Nature 1992
574
36

Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1.
R Dufourcq-Lagelouse, N Lambert, M Duval, G Viot, E Vilmer, A Fischer, M Prieur, G de Saint Basile. Eur J Hum Genet 1999
50
36

Sponastrime dysplasia. A radiologic-pathologic correlation.
R S Lachman, H Stoss, J Spranger. Pediatr Radiol 1989
28
42


Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.
B E Reuber, E Germain-Lee, C S Collins, J C Morrell, R Ameritunga, H W Moser, D Valle, S J Gould. Nat Genet 1997
179
36

Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.
A U López-Gutiérrez, L Riba, M L Ordoñez-Sánchez, S Ramírez-Jiménez, M Cerrillo-Hinojosa, M T Tusié-Luna. J Med Genet 1998
38
36

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.
T Ashizawa, M Anvret, M Baiget, J M Barceló, H Brunner, A M Cobo, B Dallapiccola, R G Fenwick, U Grandell, H Harley. Am J Hum Genet 1994
116
36

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.
P Shelbourne, R Winqvist, E Kunert, J Davies, J Leisti, H Thiele, H Bachmann, J Buxton, B Williamson, K Johnson. Hum Mol Genet 1992
117
36

Sponastrime dysplasia: five new cases and review of nine previously published cases.
L O Langer, R K Beals, S LaFranchi, C I Scott, J J Sockalosky. Am J Med Genet 1996
25
48

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders.
H Portsteffen, A Beyer, E Becker, C Epplen, A Pawlak, W H Kunau, G Dodt. Nat Genet 1997
122
36

Predictive genetic testing: psychological factors.
P M Salkovskis, K A Rimes. J Psychosom Res 1997
39
36


DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
C M Tuck-Muller, A Narayan, F Tsien, D F Smeets, J Sawyer, E S Fiala, O S Sohn, M Ehrlich. Cytogenet Cell Genet 2000
171
36

Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes.
T Yorifuji, J Muroi, M Kawai, A Uematsu, H Sasaki, T Momoi, M Kaji, C Yamanaka, K Furusho. J Med Genet 1998
35
36


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.