A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Prenatal Whole Genome Sequencing: An Argument for Professional Self-Regulation.
Benjamin E Berkman, Michelle Bayefsky. Am J Bioeth 2017
8
75

Concerns About Justification for Fetal Genome Sequencing.
Jeffrey R Botkin, Leslie P Francis, Nancy C Rose. Am J Bioeth 2017
8
75


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
129
17

Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy.
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
9
55


Serious genetic disorders: can or should they be defined?
Dorothy C Wertz, Bartha Maria Knoppers. Am J Med Genet 2002
47
14

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
136
14

Prenatal screening: an ethical agenda for the near future.
Antina de Jong, Guido M W R de Wert. Bioethics 2015
34
14

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
14

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
130
14


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
16
18

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



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


Mandating Moral Reflection?
Jessica Mozersky, Pamela Sankar. Am J Bioeth 2017
5
60

Prenatal whole genome sequencing: just because we can, should we?
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
36
10

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. Appl Clin Genet 2016
21
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
27
11

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
42
10

Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat Diagn 2015
32
10

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
50
10


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
14
21

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
80
10

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
294
10

Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues.
Mollie A Minear, Stephanie Alessi, Megan Allyse, Marsha Michie, Subhashini Chandrasekharan. Annu Rev Genomics Hum Genet 2015
48
10

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
10


Noninvasive Prenatal Whole Genome Sequencing: Pregnant Women's Views and Preferences.
Haley K Sullivan, Michelle Bayefsky, Paul G Wakim, Kathi Huddleston, Barbara B Biesecker, Sara Chandros Hull, Benjamin E Berkman. Obstet Gynecol 2019
10
30



Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
212
7


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
350
7

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
302
7

Fetal privacy and confidentiality.
J R Botkin. Hastings Cent Rep 1995
24
8


A Brave New World of Bespoke Babies?
Tom Shakespeare. Am J Bioeth 2017
3
66


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
372
7


Cell-free fetal DNA testing: who is driving implementation?
Jessica Mozersky, Michael T Mennuti. Genet Med 2013
12
16

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
35
7



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
47
7


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.