A citation-based method for searching scientific literature

Iris M Bakkeren, Adriana Kater-Kuipers, Eline M Bunnik, Attie T J I Go, Aad Tibben, Inez D de Beaufort, Robert-Jan H Galjaard, Sam R Riedijk. J Genet Couns 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity



Ethics of routine: a critical analysis of the concept of 'routinisation' in prenatal screening.
Adriana Kater-Kuipers, Inez D de Beaufort, Robert-Jan H Galjaard, Eline M Bunnik. J Med Ethics 2018
12
66

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
19
66

Rethinking autonomy in the context of prenatal screening decision-making.
Elisa García, Danielle R M Timmermans, Evert van Leeuwen. Prenat Diagn 2008
38
66

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
122
66

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.
Dick Oepkes, G C Lieve Page-Christiaens, Caroline J Bax, Mireille N Bekker, Catia M Bilardo, Elles M J Boon, G Heleen Schuring-Blom, Audrey B C Coumans, Brigitte H Faas, Robert-Jan H Galjaard,[...]. Prenat Diagn 2016
78
66


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
64
66

Attitudes of mothers of children with down syndrome towards noninvasive prenatal testing.
Gregory Kellogg, Leah Slattery, Louanne Hudgins, Kelly Ormond. J Genet Couns 2014
43
66

The value of non-invasive prenatal testing: preferences of Canadian pregnant women, their partners, and health professionals regarding NIPT use and access.
Stanislav Birko, Vardit Ravitsky, Charles Dupras, Jessica Le Clerc-Blain, Marie-Eve Lemoine, Aliya O Affdal, Hazar Haidar, Anne-Marie Laberge. BMC Pregnancy Childbirth 2019
10
66

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
48
33

Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012.
E Mersy, L J M Smits, L A A P van Winden, C E M de Die-Smulders, A D C Paulussen, M V E Macville, A B C Coumans, S G M Frints. Hum Reprod Update 2013
43
33

NIPT in a clinical setting: an analysis of uptake in the first months of clinical availability.
Joanne B Taylor, Valerie Y Chock, Louanne Hudgins. J Genet Couns 2014
32
33

A new era in noninvasive prenatal testing.
Stephanie Morain, Michael F Greene, Michelle M Mello. N Engl J Med 2013
58
33


Public viewpoints on new non-invasive prenatal genetic tests.
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
29
33

Prenatal counseling for congenital anomaly tests: parental preferences and perceptions of midwife performance.
L Martin, S Van Dulmen, E Spelten, A De Jonge, P De Cock, E Hutton. Prenat Diagn 2013
22
33

Midwives' views on appropriate antenatal counselling for congenital anomaly tests: do they match clients' preferences?
Linda Martin, Eileen K Hutton, Evelien R Spelten, Janneke T Gitsels-van der Wal, Sandra van Dulmen. Midwifery 2014
19
33

UK NHS pilot study on cell-free DNA testing in screening for fetal trisomies: factors affecting uptake.
M M Gil, G Giunta, E A Macalli, L C Poon, K H Nicolaides. Ultrasound Obstet Gynecol 2015
22
33

Offering a choice between NIPT and invasive PND in prenatal genetic counseling: the impact of clinician characteristics on patients' test uptake.
Sanne L van der Steen, Diewertje Houtman, Iris M Bakkeren, Robert-Jan H Galjaard, Marike G Polak, Jan J Busschbach, Aad Tibben, Sam R Riedijk. Eur J Hum Genet 2019
6
33

The impact of ethical beliefs on decisions about prenatal screening tests: searching for justification.
Elisa García, Danielle R M Timmermans, Evert van Leeuwen. Soc Sci Med 2008
47
33

Low uptake of the combined test in The Netherlands--which factors contribute?
Merel Bakker, Erwin Birnie, Eva Pajkrt, Caterina Maddalena Bilardo, Rosalinde Johanna Maria Snijders. Prenat Diagn 2012
46
33

The role of non-directiveness in genetic counseling.
Fuat S Oduncu. Med Health Care Philos 2002
19
33

Antenatal counselling for congenital anomaly tests: an exploratory video-observational study about client-midwife communication.
Linda Martin, Eileen K Hutton, Janneke T Gitsels-van der Wal, Evelien R Spelten, Fleur Kuiper, Monique T R Pereboom, Sandra van Dulmen. Midwifery 2015
8
33

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.
Rachèl V van Schendel, G C Lieve Page-Christiaens, Lean Beulen, Catia M Bilardo, Marjon A de Boer, Audrey B C Coumans, Brigitte H Faas, Irene M van Langen, Klaske D Lichtenbelt, Merel C van Maarle,[...]. Prenat Diagn 2016
27
33

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
29
33

The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing.
Sam Riedijk, Karin E M Diderich, Sanne L van der Steen, Lutgarde C P Govaerts, Marieke Joosten, Maarten F C M Knapen, Femke A T de Vries, Diane van Opstal, Aad Tibben, Robert-Jan H Galjaard. J Clin Med 2014
17
33


Changing to NIPT as a first-tier screening test and future perspectives: opinions of health professionals.
Saskia Tamminga, Rachèl V van Schendel, Wieke Rommers, Caterina M Bilardo, Eva Pajkrt, Wybo J Dondorp, Merel van Maarle, Martina C Cornel, Lidewij Henneman. Prenat Diagn 2015
19
33

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
163
33

The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.
Antina de Jong, Wybo J Dondorp, Anja Krumeich, Julie Boonekamp, Jan M M van Lith, Guido M W R de Wert. J Community Genet 2013
17
33

Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening.
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
102
33

Social influence and the collective dynamics of opinion formation.
Mehdi Moussaïd, Juliane E Kämmer, Pantelis P Analytis, Hansjörg Neth. PLoS One 2013
44
33

People who influence women's decisions and preferred sources of information about prenatal testing for birth defects.
Alice M Jaques, Robin J Bell, Lyndsey Watson, Jane L Halliday. Aust N Z J Obstet Gynaecol 2004
17
33

Determinants of first trimester combined test participation within the central region of the Netherlands.
Neeltje M T H Crombag, Peter C J I Schielen, Chantal W Hukkelhoven, Rita Iedema, Jozien M Bensing, Gerard H A Visser, Philip Stoutenbeek, Maria P H Koster. Prenat Diagn 2015
10
33

Supporting Women's Autonomy in Prenatal Testing.
Josephine Johnston, Ruth M Farrell, Erik Parens. N Engl J Med 2017
9
33



Non-invasive prenatal testing for single gene disorders: exploring the ethics.
Zuzana Deans, Melissa Hill, Lyn S Chitty, Celine Lewis. Eur J Hum Genet 2013
26
33

Our children are not a diagnosis: the experience of parents who continue their pregnancy after a prenatal diagnosis of trisomy 13 or 18.
Jennifer Guon, Benjamin S Wilfond, Barbara Farlow, Tracy Brazg, Annie Janvier. Am J Med Genet A 2014
65
33

What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?
Rachèl V van Schendel, Adriana Kater-Kuipers, Elsbeth H van Vliet-Lachotzki, Wybo J Dondorp, Martina C Cornel, Lidewij Henneman. J Genet Couns 2017
23
33


Facilitating informed choice about non-invasive prenatal testing (NIPT): a systematic review and qualitative meta-synthesis of women's experiences.
Alexandra Cernat, Chante De Freitas, Umair Majid, Forum Trivedi, Caroline Higgins, Meredith Vanstone. BMC Pregnancy Childbirth 2019
15
33

Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation.
Kasper Gadsbøll, Olav B Petersen, Vincent Gatinois, Heather Strange, Bo Jacobsson, Ronald Wapner, Joris R Vermeesch, Ida Vogel. Acta Obstet Gynecol Scand 2020
15
33

Fathers' Worries During Pregnancy: A Qualitative Content Analysis of Reddit.
Pamela D Pilkington, Holly Rominov. J Perinat Educ 2017
4
33

How the public uses social media wechat to obtain health information in china: a survey study.
Xingting Zhang, Dong Wen, Jun Liang, Jianbo Lei. BMC Med Inform Decis Mak 2017
81
33

Health and social media: perfect storm of information.
Luis Fernández-Luque, Teresa Bau. Healthc Inform Res 2015
47
33

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
33


How to Peddle Hope: An Analysis of YouTube Patient Testimonials of Unproven Stem Cell Treatments.
Bethany Hawke, Alexandra R Przybylo, Danielle Paciulli, Timothy Caulfield, Amy Zarzeczny, Zubin Master. Stem Cell Reports 2019
15
33


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.