A citation-based method for searching scientific literature

G Terrenoire. J Med Ethics 1992
Times Cited: 24







List of co-cited articles
57 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
347
25

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
20

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
317
20






Testing children for genetic predispositions: is it in their best interest?
D E Hoffmann, E A Wulfsberg. J Law Med Ethics 1995
40
12

Genes and discrimination.
B J Culliton. Nat Med 1995
6
50

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
12



Genetic testing for children and adolescents. Who decides?
D C Wertz, J H Fanos, P R Reilly. JAMA 1994
203
12




Attitudes toward presymptomatic testing in Huntington disease.
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
127
12


Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform.
Bartha Maria Knoppers, Denise Avard, Karine Sénécal, Ma'n H Zawati. Eur J Hum Genet 2014
46
12

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
181
12


Uptake of presymptomatic predictive testing for Huntington's disease.
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
180
12

Genetic discrimination and the law.
M R Natowicz, J K Alper, J S Alper. Am J Hum Genet 1992
83
8



Genetic counseling for families with inherited susceptibility to breast and ovarian cancer.
B B Biesecker, M Boehnke, K Calzone, D S Markel, J E Garber, F S Collins, B L Weber. JAMA 1993
249
8

Parental guilt: The part played by the clinical geneticist.
A Chapple, C May, P Campion. J Genet Couns 1995
19
10

Huntington disease and the abuse of genetics.
P S Harper. Am J Hum Genet 1992
20
10

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
103
8


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
8




Predictive genetic testing in children.
Fiona H Richards, Roslyn J Tassicker, Jennifer G R Kromberg, Barbara M Singaram. Med J Aust 2002
5
40



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
8

Understanding the low uptake of presymptomatic DNA testing for Huntington's disease.
A Tibben, M F Niermeijer, R A Roos, M Vegter van de Vlis, P G Frets, G J van Ommen, J J van de Kamp, F Verhage. Lancet 1992
32
8





Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.
Donald B Bailey, Debra Skinner, Arlene M Davis, Ian Whitmarsh, Cynthia Powell. Pediatrics 2008
72
8


Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
157
8

We screen newborns, don't we?: realizing the promise of public health genomics.
James P Evans, Jonathan S Berg, Andrew F Olshan, Terry Magnuson, Barbara K Rimer. Genet Med 2013
44
8


Newborn screening technology: proceed with caution.
Jeffrey R Botkin, Ellen Wright Clayton, Norman C Fost, Wylie Burke, Thomas H Murray, Mary Ann Baily, Benjamin Wilfond, Alfred Berg, Lainie Friedman Ross. Pediatrics 2006
100
8


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.