A citation-based method for searching scientific literature

Antina de Jong, Guido M W R de Wert. Bioethics 2015
Times Cited: 38







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



Times Cited
  Times     Co-cited
Similarity



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
142
31

Disability rights critique of prenatal genetic testing: reflections and recommendations.
Erik Parens, Adrienne Asch. Ment Retard Dev Disabil Res Rev 2003
78
26

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
72
26


Prenatal screening: current practice, new developments, ethical challenges.
Antina de Jong, Idit Maya, Jan M M van Lith. Bioethics 2015
30
26

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
81
21

Will the introduction of non-invasive prenatal diagnostic testing erode informed choices? An experimental study of health care professionals.
Ananda van den Heuvel, Lyn Chitty, Elizabeth Dormandy, Ainsley Newson, Zuzana Deans, Sophie Attwood, Shelley Haynes, Theresa M Marteau. Patient Educ Couns 2010
79
21

Non-invasive prenatal testing: ethics and policy considerations.
Meredith Vanstone, Carol King, Barbra de Vrijer, Jeff Nisker. J Obstet Gynaecol Can 2014
28
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
21



An offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis.
Dagmar Schmitz, Christian Netzer, Wolfram Henn. Nat Rev Genet 2009
35
20


ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
Anthony R Gregg, S J Gross, R G Best, K G Monaghan, K Bajaj, B G Skotko, B H Thompson, M S Watson. Genet Med 2013
177
15


Non-invasive prenatal testing: a review of international implementation and challenges.
Megan Allyse, Mollie A Minear, Elisa Berson, Shilpa Sridhar, Margaret Rote, Anthony Hung, Subhashini Chandrasekharan. Int J Womens Health 2015
150
15

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
51
15


Challenging the rhetoric of choice in prenatal screening.
Victoria Seavilleklein. Bioethics 2009
43
13

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
241
13

Non-invasive prenatal testing: ethical issues explored.
Antina de Jong, Wybo J Dondorp, Christine E M de Die-Smulders, Suzanne G M Frints, Guido M W R de Wert. Eur J Hum Genet 2010
93
13

Ethical aspects arising from non-invasive fetal diagnosis.
Ainsley J Newson. Semin Fetal Neonatal Med 2008
57
13

Prenatal whole genome sequencing: just because we can, should we?
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
36
13


Women's Experiences of Publicly Funded Non-Invasive Prenatal Testing in Ontario, Canada: Considerations for Health Technology Policy-Making.
Meredith Vanstone, Karima Yacoub, Mita Giacomini, Danielle Hulan, Sarah McDonald. Qual Health Res 2015
26
19

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
315
13

Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands.
Carla Geertruida van El, Toine Pieters, Martina Cornel. J Community Genet 2012
20
20

Informed decision making in the context of prenatal screening.
Matthijs van den Berg, Danielle R M Timmermans, Leo P ten Kate, John M G van Vugt, Gerrit van der Wal. Patient Educ Couns 2006
91
10

Update on procedure-related risks for prenatal diagnosis techniques.
Ann Tabor, Zarko Alfirevic. Fetal Diagn Ther 2010
227
10


Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.
Rossa W K Chiu, K C Allen Chan, Yuan Gao, Virginia Y M Lau, Wenli Zheng, Tak Y Leung, Chris H F Foo, Bin Xie, Nancy B Y Tsui, Fiona M F Lun,[...]. Proc Natl Acad Sci U S A 2008
570
10

Non-invasive prenatal testing for aneuploidy: current status and future prospects.
P Benn, H Cuckle, E Pergament. Ultrasound Obstet Gynecol 2013
194
10

Explaining variation in Down's syndrome screening uptake: comparing the Netherlands with England and Denmark using documentary analysis and expert stakeholder interviews.
Neeltje M T H Crombag, Ynke E Vellinga, Sandra A Kluijfhout, Louise D Bryant, Pat A Ward, Rita Iedema-Kuiper, Peter C J I Schielen, Jozien M Bensing, Gerard H A Visser, Ann Tabor,[...]. BMC Health Serv Res 2014
47
10


Noninvasive prenatal testing for aneuploidy-ready for prime time?
Lyn S Chitty, Melissa Hill, Helen White, David Wright, Stephen Morris. Am J Obstet Gynecol 2012
55
10


Public viewpoints on new non-invasive prenatal genetic tests.
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
30
13


Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus.
Y M Dennis Lo, K C Allen Chan, Hao Sun, Eric Z Chen, Peiyong Jiang, Fiona M F Lun, Yama W Zheng, Tak Y Leung, Tze K Lau, Charles R Cantor,[...]. Sci Transl Med 2010
587
10

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
392
10

Commercial landscape of noninvasive prenatal testing in the United States.
Ashwin Agarwal, Lauren C Sayres, Mildred K Cho, Robert Cook-Deegan, Subhashini Chandrasekharan. Prenat Diagn 2013
73
10

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.
Glenn E Palomaki, Cosmin Deciu, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Louis M Neveux, Mathias Ehrich, Dirk van den Boom, Allan T Bombard, Wayne W Grody,[...]. Genet Med 2012
365
10

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.
M M Gil, M S Quezada, R Revello, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2015
299
10

Responsible implementation of expanded carrier screening.
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C Cornel, Carla G van El, Francesca Forzano, Alison Hall, Heidi C Howard, Sandra Janssens, Hülya Kayserili,[...]. Eur J Hum Genet 2016
127
10



Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.
Anne Andermann, Ingeborg Blancquaert, Sylvie Beauchamp, Véronique Déry. Bull World Health Organ 2008
431
10

Why abortion is immoral.
Don Marquis. J Philos 1989
109
10

The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians.
Ruth M Farrell, Patricia K Agatisa, Mary Beth Mercer, Ariane G Mitchum, Marissa B Coleridge. Prenat Diagn 2016
27
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.