A citation-based method for searching scientific literature

Julian J Koplin, Julian Savulescu, Danya F Vears. BMC Med Ethics 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
106
40

Social and ethical aspects of forensic genetics: A critical review.
R Williams, M Wienroth. Forensic Sci Rev 2017
12
40

The duty to warn at-risk relatives-The experience of genetic counselors and medical geneticists.
Tabitha J Perry, Samantha I Patton, Meagan B Farmer, Christina B Hurst, Gerald McGwin, Nathaniel H Robin. Am J Med Genet A 2020
2
100

Technological innovations in forensic genetics: social, legal and ethical aspects.
Matthias Wienroth, Niels Morling, Robin Williams. Recent Adv DNA Gene Seq 2014
12
40

Should doctors have a legal duty to warn relatives of their genetic risks?
Anna Middleton, Richard Milne, Lauren Robarts, Jonathan Roberts, Christine Patch. Lancet 2019
5
40


Next generation sequencing and its applications in forensic genetics.
Claus Børsting, Niels Morling. Forensic Sci Int Genet 2015
180
40

Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration.
Katarzyna Michaud, Florence Fellmann, Hugues Abriel, Jacques S Beckmann, Patrice Mangin, Bernice S Elger. Swiss Med Wkly 2009
28
40



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
842
40

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
40

Incidental findings in the use of DNA to identify human remains: an ethical assessment.
Lisa S Parker, Alex John London, Jay D Aronson. Forensic Sci Int Genet 2013
9
20

The genetics of skin, hair, and eye color variation and its relevance to forensic pigmentation predictive tests.
O Maroñas, J Söchtig, Y Ruiz, C Phillips, Á Carracedo, M V Lareu. Forensic Sci Rev 2015
13
20

Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study.
Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Elfride De Baere, Ignaas Devisch. BMC Med Ethics 2020
7
20

The Use of Forensic DNA Phenotyping in Predicting Appearance and Biogeographic Ancestry.
Peter M Schneider, Barbara Prainsack, Manfred Kayser. Dtsch Arztebl Int 2019
24
20


Disclosing incidental findings in genetics contexts: a review of the empirical ethical research.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Med Genet 2013
29
20

Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussions.
Gabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, Kris Dierickx. Med Health Care Philos 2015
6
20

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
92
20

Management of Incidental Findings in the Era of Next-generation Sequencing.
Heather L Blackburn, Bradley Schroeder, Clesson Turner, Craig D Shriver, Darrell L Ellsworth, Rachel E Ellsworth. Curr Genomics 2015
26
20

Next-generation DNA sequencing.
Jay Shendure, Hanlee Ji. Nat Biotechnol 2008
20

Postmortem medicolegal genetic diagnostics also require reporting guidance.
Antti Sajantila, Bruce Budowle. Eur J Hum Genet 2016
5
20


Introduction: the challenge of incidental findings.
Susan M Wolf. J Law Med Ethics 2008
37
20


HIrisPlex-S system for eye, hair, and skin color prediction from DNA: Massively parallel sequencing solutions for two common forensically used platforms.
Krystal Breslin, Bailey Wills, Arwin Ralf, Marina Ventayol Garcia, Magdalena Kukla-Bartoszek, Ewelina Pospiech, Ana Freire-Aradas, Catarina Xavier, Sabrina Ingold, Maria de La Puente,[...]. Forensic Sci Int Genet 2019
16
20

Managing unsolicited findings in genomics: A qualitative interview study with cancer patients.
R M Bijlsma, R H P Wouters, H Wessels, A M May, M G E M Ausems, E E Voest, A L Bredenoord. Psychooncology 2018
10
20

Defining and redefining the scope and goals of genetic counseling.
Robert G Resta. Am J Med Genet C Semin Med Genet 2006
49
20


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
203
20

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
119
20

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
206
20

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
819
20



Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Joon-Ho Yu, Paul S Appelbaum, Kyle B Brothers, Steven Joffe, Tia L Kauffman, Barbara A Koenig, Anya Er Prince, Sarah Scollon, Susan M Wolf, Barbara A Bernhardt,[...]. Per Med 2019
5
20


Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry. Eur J Hum Genet 2018
32
20

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
59
20

Searching for secondary findings: considering actionability and preserving the right not to know.
Bertrand Isidor, Sophie Julia, Pascale Saugier-Veber, Paul-Loup Weil-Dubuc, Stéphane Bézieau, Eric Bieth, Jean-Paul Bonnefont, Arnold Munnich, Franck Bourdeaut, Catherine Bourgain,[...]. Eur J Hum Genet 2019
8
20

An ethical framework for genetic counseling in the genomic era.
Leila Jamal, Will Schupmann, Benjamin E Berkman. J Genet Couns 2020
8
20

The 'thousand-dollar genome': an ethical exploration.
Wybo J Dondorp, Guido M W R de Wert. Eur J Hum Genet 2013
36
20

Reconceptualizing Autonomy for Bioethics.
Lisa Dive, Ainsley J Newson. Kennedy Inst Ethics J 2018
10
20

Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
567
20

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
20

Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.
Tanya Dwarte, Kristine Barlow-Stewart, Rosie O'Shea, Marcel E Dinger, Bronwyn Terrill. J Genet Couns 2019
3
33

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.
Erin Turbitt, Paola P Chrysostomou, Holly L Peay, Alexis R Heidlebaugh, Lawrence M Nelson, Barbara B Biesecker. Eur J Hum Genet 2018
7
20

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
52
20

Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.
Christel Thauvin-Robinet, Julien Thevenon, Sophie Nambot, Julian Delanne, Paul Kuentz, Ange-Line Bruel, Aline Chassagne, Elodie Cretin, Aurore Pelissier, Chritine Peyron,[...]. Eur J Hum Genet 2019
7
20


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.