A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



Concerns About Justification for Fetal Genome Sequencing.
Jeffrey R Botkin, Leslie P Francis, Nancy C Rose. Am J Bioeth 2017
7
71

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet. Med. 2013
105
16

Prenatal Whole Genome Sequencing: An Argument for Professional Self-Regulation.
Benjamin E Berkman, Michelle Bayefsky. Am J Bioeth 2017
4
100


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet. Med. 2013
16

Serious genetic disorders: can or should they be defined?
Dorothy C Wertz, Bartha Maria Knoppers. Am. J. Med. Genet. 2002
42
12


Generating a taxonomy for genetic conditions relevant to reproductive planning.
Diane M Korngiebel, Carmit K McMullen, Laura M Amendola, Jonathan S Berg, James V Davis, Marian J Gilmore, Cary O Harding, Patricia Himes, Gail P Jarvik, Tia L Kauffman,[...]. Am. J. Med. Genet. A 2016
15
20

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
75

Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy.
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
6
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
75


Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur. J. Hum. Genet. 2015
102
12

Prenatal screening: an ethical agenda for the near future.
Antina de Jong, Guido M W R de Wert. Bioethics 2015
28
12

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat. Diagn. 2018
77
12




Racial/ethnic disparities in obstetric outcomes and care: prevalence and determinants.
Allison S Bryant, Ayaba Worjoloh, Aaron B Caughey, A Eugene Washington. Am. J. Obstet. Gynecol. 2010
278
8

Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.
David N Cooper, Michael Krawczak, Constantin Polychronakos, Chris Tyler-Smith, Hildegard Kehrer-Sawatzki. Hum. Genet. 2013
240
8

Fetal privacy and confidentiality.
J R Botkin. Hastings Cent Rep 1995
15
13



Mandating Moral Reflection?
Jessica Mozersky, Pamela Sankar. Am J Bioeth 2017
2
100


Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N. Engl. J. Med. 2015
288
8

Prenatal whole genome sequencing: just because we can, should we?
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
30
8

Cell-free fetal DNA testing: who is driving implementation?
Jessica Mozersky, Michael T Mennuti. Genet. Med. 2013
11
18

Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
24
8

Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.
Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Gradus van den Berg, Hazar Haidar, François Rousseau.  2016
14
14


Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat. Diagn. 2016
20
10

Known unknowns: building an ethics of uncertainty into genomic medicine.
Ainsley J Newson, Samantha J Leonard, Alison Hall, Clara L Gaff. BMC Med Genomics 2016
26
8

Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat. Diagn. 2015
27
8

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
47
8


Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.
Michelle J Bayefsky, Amina White, Paul Wakim, Sara Chandros Hull, David Wasserman, Stephanie Chen, Benjamin E Berkman. Prenat. Diagn. 2016
12
16


Advances in prenatal screening: the ethical dimension.
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat. Rev. Genet. 2011
68
8


Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange.  2014
22
9

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
617
8

Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels.
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS ONE 2014
36
8

"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening.
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
27
8

Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, Frances L Lynch, Jacob A Reiss, Marian J Gilmore, Patricia Himes, Tia L Kauffman, James V Davis, Gail P Jarvik,[...]. Am. J. Med. Genet. A 2016
15
13

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet. Med. 2016
204
8


Risks, values, and decision making surrounding pregnancy.
Anne Drapkin Lyerly, Lisa M Mitchell, Elizabeth M Armstrong, Lisa H Harris, Rebecca Kukla, Miriam Kuppermann, Margaret Olivia Little. Obstet Gynecol 2007
58
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.