A citation-based method for searching scientific literature

Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity



"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
7

Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin. Perinatol. 2016
27
7

Attitudes of European Geneticists Regarding Expanded Carrier Screening.
Sandra Janssens, Davit Chokoshvili, Danya Vears, Anne De Paepe, Pascal Borry. J Obstet Gynecol Neonatal Nurs 2017
12
16

Content analysis: method, applications, and issues.
B Downe-Wamboldt. Health Care Women Int 1992
591
4


The changing landscape of carrier screening: expanding technology and options?.
Michelle L McGowan, Deborah Cho, Richard R Sharp. Health Matrix Clevel 2013
14
14

Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur. J. Hum. Genet. 2016
33
6

Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape.
Kim C A Holtkamp, Evelien M Vos, Tessel Rigter, Phillis Lakeman, Lidewij Henneman, Martina C Cornel. BMC Health Serv Res 2017
10
20

Comparison of participant information and informed consent forms of five European studies in genetic isolated populations.
Deborah Mascalzoni, A Cecile J W Janssens, Alison Stewart, Peter Pramstaller, Ulf Gyllensten, Igor Rudan, Cornelia M van Duijn, James F Wilson, Harry Campbell, Ruth M C Quillan. Eur. J. Hum. Genet. 2010
23
8

Informed consent for human genetic and genomic studies: a systematic review.
A Khan, B J Capps, M Y Sum, C N Kuswanto, K Sim. Clin. Genet. 2014
19
10

The emerging need for family-centric initiatives for obtaining consent in personal genome research.
Jusaku Minari, Harriet Teare, Colin Mitchell, Jane Kaye, Kazuto Kato. Genome Med 2014
11
18

Defining and managing incidental findings in genetic and genomic practice.
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J. Med. Genet. 2014
34
5

Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
36
5

Should you profit from your genome?
Jessica L Roberts, Stacey Pereira, Amy L McGuire. Nat. Biotechnol. 2017
10
20

Mining electronic health records: towards better research applications and clinical care.
Peter B Jensen, Lars J Jensen, Søren Brunak. Nat. Rev. Genet. 2012
432
4

From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
78
4

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol. 2006
194
4

Open sharing of genomic data: Who does it and why?
Tobias Haeusermann, Bastian Greshake, Alessandro Blasimme, Darja Irdam, Martin Richards, Effy Vayena. PLoS ONE 2017
25
8


Precision medicine: Beyond the inflection point.
Sam Hawgood, India G Hook-Barnard, Theresa C O'Brien, Keith R Yamamoto. Sci Transl Med 2015
50
4

Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
21
9

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat. Biotechnol. 2015
81
4

Digital drug safety surveillance: monitoring pharmaceutical products in twitter.
Clark C Freifeld, John S Brownstein, Christopher M Menone, Wenjie Bao, Ross Filice, Taha Kass-Hout, Nabarun Dasgupta. Drug Saf 2014
114
4

Ethical endgames: broad consent for narrow interests; open consent for closed minds.
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
16
12

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
33
6


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
21
9

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
15
13

Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet. Med. 2010
116
4




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
592
4

Towards a European consensus for reporting incidental findings during clinical NGS testing.
Jayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, Conny van Ravenswaaij-Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon-Thomsen, Philippos Patsalis, Joris Vermeesch,[...]. Eur. J. Hum. Genet. 2015
50
4

Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.
Gabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, Angela Fenwick, Anneke Lucassen. BMC Med Ethics 2017
18
11


A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet. Med. 2016
159
4

The 'thousand-dollar genome': an ethical exploration.
Wybo J Dondorp, Guido M W R de Wert. Eur. J. Hum. Genet. 2013
30
6

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.
Hussein Daoud, Stephanie M Luco, Rui Li, Eric Bareke, Chandree Beaulieu, Olga Jarinova, Nancy Carson, Sarah M Nikkel, Gail E Graham, Julie Richer,[...]. CMAJ 2016
41
4

Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet. Med. 2018
54
4

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Sarah E Soden, Carol J Saunders, Laurel K Willig, Emily G Farrow, Laurie D Smith, Josh E Petrikin, Jean-Baptiste LePichon, Neil A Miller, Isabelle Thiffault, Darrell L Dinwiddie,[...]. Sci Transl Med 2014
274
4


Reframing Consent for Clinical Research: A Function-Based Approach.
Neal W Dickert, Nir Eyal, Sara F Goldkind, Christine Grady, Steven Joffe, Bernard Lo, Franklin G Miller, Rebecca D Pentz, Robert Silbergleit, Kevin P Weinfurt,[...]. Am J Bioeth 2017
45
4

Factors influencing health insurers' decisions to cover new genetic technologies.
M M Schoonmaker, B A Bernhardt, N A Holtzman. Int J Technol Assess Health Care 2000
15
6


Billing for medical genetics and genetic counseling services: a national survey.
Tabitha A Harrison, Debra Lochner Doyle, Caroline McGowan, Leslie Cohen, Elizabeth Repass, Ruthann B Pfau, Trish Brown. J Genet Couns 2010
16
6

Population studies: return of research results and incidental findings Policy Statement.
Bartha Maria Knoppers, Mylène Deschênes, Ma'n H Zawati, Anne Marie Tassé. Eur. J. Hum. Genet. 2013
62
2




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.