A citation-based method for searching scientific literature

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

Times Cited
  Times     Co-cited

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.