A citation-based method for searching scientific literature

Jessica Mozersky, Pamela Sankar. Am J Bioeth 2017
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity




Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy.
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
7
100



Concerns About Justification for Fetal Genome Sequencing.
Jeffrey R Botkin, Leslie P Francis, Nancy C Rose. Am J Bioeth 2017
7
100

Prenatal Whole Genome Sequencing: An Argument for Professional Self-Regulation.
Benjamin E Berkman, Michelle Bayefsky. Am J Bioeth 2017
4
50

Beneficence In Utero: A Framework for Restricted Prenatal Whole-Genome Sequencing to Respect and Enhance the Well-Being of Children.
W Kevin Conley Ii, Douglas C McAdams, G Kevin Donovan, Kevin T FitzGerald. Am J Bioeth 2017
4
50

A Brave New World of Bespoke Babies?
Tom Shakespeare. Am J Bioeth 2017
2
50

Dr. Pangloss's Clinic: Prenatal Whole Genome Sequencing and a Return to Reality.
Megan Allyse, James P Evans, Marsha Michie. Am J Bioeth 2017
4
50


Defining and redefining the scope and goals of genetic counseling.
Robert G Resta. Am J Med Genet C Semin Med Genet 2006
41
50

Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease.
Yvonne Bombard, JoAnne Palin, Jan M Friedman, Gerry Veenstra, Susan Creighton, Joan L Bottorff, Michael R Hayden. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2012
24
50


'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care.
Angus J Clarke, David N Cooper, Michael Krawczak, Chris Tyler-Smith, Helen M Wallace, Andrew O M Wilkie, Frances Lucy Raymond, Ruth Chadwick, Nick Craddock, Ros John,[...]. Hum. Genomics 2012
4
50

Carrier testing in children and adolescents.
Danya F Vears, Sylvia A Metcalfe. Eur J Med Genet 2015
3
50

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol. 2011
210
50

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, Denise Avard, Bartha M Knoppers, Martina C Cornel, Pascal Borry. Nat. Rev. Genet. 2009
14
50


"Testing times, challenging choices": an Australian study of prenatal genetic counseling.
Jan M Hodgson, Lynn H Gillam, Margaret A Sahhar, Sylvia A Metcalfe. J Genet Couns 2010
21
50

"It was the missing piece": adolescent experiences of predictive genetic testing for adult-onset conditions.
Cara Mand, Lynn Gillam, Rony E Duncan, Martin B Delatycki. Genet. Med. 2013
20
50





Professional ambivalence: accounts of ethical practice in childhood genetic testing.
Michael Arribas-Ayllon, Srikant Sarangi, Angus Clarke. J Genet Couns 2009
13
50

Variations in male-female infant ratios among births to Canadian- and Indian-born mothers, 1990-2011: a population-based register study.
Marcelo L Urquia, Joel G Ray, Susitha Wanigaratne, Rahim Moineddin, Patricia J O'Campo.  2016
9
50


Clinician integrity and limits to patient autonomy.
John Lantos, Ann Marie Matlock, David Wendler. JAMA 2011
25
50







Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat. Rev. Genet. 2015
76
50

Problems assessing uptake of Huntington disease predictive testing and a proposed solution.
Roslyn J Tassicker, Betty Teltscher, M Kaye Trembath, Veronica Collins, Leslie J Sheffield, Edmond Chiu, Lyle Gurrin, Martin B Delatycki. Eur. J. Hum. Genet. 2009
35
50


Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease.
Cynthia A James, Neil A Holtzman, Donald W Hadley. Am J Med Genet C Semin Med Genet 2003
17
50

He was my son, not a dying baby.
Pauline Thiele. J Med Ethics 2010
12
50


An informatics approach to analyzing the incidentalome.
Jonathan S Berg, Michael Adams, Nassib Nassar, Chris Bizon, Kristy Lee, Charles P Schmitt, Kirk C Wilhelmsen, James P Evans. Genet. Med. 2013
97
50




Nondirectiveness and genetic counseling.
Gerhard Wolff, Christine Jung. J Genet Couns 1995
32
50



Family communication matters: the impact of telling relatives about unclassified variants and uninformative DNA-test results.
Joël Vos, Anna M Jansen, Fred Menko, Christi J van Asperen, Anne M Stiggelbout, Aad Tibben. Genet. Med. 2011
26
50

Is nondirectiveness possible within the context of antenatal screening and testing?
Clare Williams, Priscilla Alderson, Bobbie Farsides. Soc Sci Med 2002
64
50


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.