A citation-based method for searching scientific literature

Emilia Niemiec, Pascal Borry, Wim Pinxten, Heidi Carmen Howard. Hum Mutat 2016
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
31
42

Ethical issues in consumer genome sequencing: Use of consumers' samples and data.
Emilia Niemiec, Heidi Carmen Howard. Appl Transl Genom 2016
25
28

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
235
28


Informed choice in direct-to-consumer genetic testing (DTCGT) websites: a content analysis of benefits, risks, and limitations.
Amanda Singleton, Lori Hamby Erby, Kathryn V Foisie, Kimberly A Kaphingst. J Genet Couns 2012
39
28


The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues.
Stuart Hogarth, Gail Javitt, David Melzer. Annu Rev Genomics Hum Genet 2008
153
28

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
28

Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
14

Stakeholder views on returning research results.
Susanne B Haga, Jennifer Q Zhao. Adv Genet 2013
12
14

Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection.
Antina de Jong, Wybo J Dondorp, Merryn V E Macville, Christine E M de Die-Smulders, Jan M M van Lith, Guido M W R de Wert. Hum Genet 2014
26
14

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
37
14

Letting the genome out of the bottle--will we get our wish?
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N Engl J Med 2008
258
14

Criteria for fairly allocating scarce health-care resources to genetic tests: which matter most?
Wolf H Rogowski, Scott D Grosse, Jörg Schmidtke, Georg Marckmann. Eur J Hum Genet 2014
20
14

Prenatal whole-genome sequencing--is the quest to know a fetus's future ethical?
Ilana R Yurkiewicz, Bruce R Korf, Lisa Soleymani Lehmann. N Engl J Med 2014
19
14


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
14

Public perspectives on returning genetics and genomics research results.
J O'Daniel, S B Haga. Public Health Genomics 2011
55
14


The best possible child.
Michael Parker. J Med Ethics 2007
37
14

Generic consent for genetic screening.
S Elias, G J Annas. N Engl J Med 1994
111
14

The new genetics and informed consent: differentiating choice to preserve autonomy.
Eline M Bunnik, Antina de Jong, Niels Nijsingh, Guido M W R de Wert. Bioethics 2013
35
14

Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat Diagn 2015
32
14




Genetic information: a joint account?
Michael Parker, Anneke M Lucassen. BMJ 2004
71
14

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
14



Prenatal exome sequencing for fetuses with structural abnormalities: the next step.
S C Hillman, D Willams, K J Carss, D J McMullan, M E Hurles, M D Kilby. Ultrasound Obstet Gynecol 2015
35
14


Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
363
14



Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
240
14

Return of results: not that complicated?
James P Evans, Barbra B Rothschild. Genet Med 2012
48
14

Imposing genetic diversity.
Robert Sparrow. Am J Bioeth 2015
20
14

Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
40
14

Cell-free fetal DNA: the new tool in fetal medicine.
T R Everett, L S Chitty. Ultrasound Obstet Gynecol 2015
17
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


Evolving applications of microarray analysis in prenatal diagnosis.
Melissa S Savage, Mirella J Mourad, Ronald J Wapner. Curr Opin Obstet Gynecol 2011
29
14

An offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis.
Dagmar Schmitz, Christian Netzer, Wolfram Henn. Nat Rev Genet 2009
35
14




Genome sequencing: a systematic review of health economic evidence.
Martin Frank, Anne Prenzler, Roland Eils, J-Matthias Graf von der Schulenburg. Health Econ Rev 2013
35
14

Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
85
14


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.