A citation-based method for searching scientific literature

Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Elfride De Baere, Ignaas Devisch. BMC Med Ethics 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
71

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
42

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
42

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
42

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
28

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
28

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations.
Pascal Pujol, Pierre Vande Perre, Laurence Faivre, Damien Sanlaville, Carole Corsini, Bernard Baertschi, Michèle Anahory, Dominique Vaur, Sylviane Olschwang, Nadem Soufir,[...]. Eur J Hum Genet 2018
13
28

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
28

1 in 38 individuals at risk of a dominant medically actionable disease.
Lonneke Haer-Wigman, Vyne van der Schoot, Ilse Feenstra, Anneke T Vulto-van Silfhout, Christian Gilissen, Han G Brunner, Lisenka E L M Vissers, Helger G Yntema. Eur J Hum Genet 2019
28
28


Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
157
28

Point-counterpoint. Ethics and genomic incidental findings.
Amy L McGuire, Steven Joffe, Barbara A Koenig, Barbara B Biesecker, Laurence B McCullough, Jennifer S Blumenthal-Barby, Timothy Caulfield, Sharon F Terry, Robert C Green. Science 2013
130
28

Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.
Julie C Sapp, Jennifer J Johnston, Kate Driscoll, Alexis R Heidlebaugh, Ane Miren Sagardia, D Nadine Dogbe, Kendall L Umstead, Erin Turbitt, Ilias Alevizos, Jeffrey Baron,[...]. Am J Hum Genet 2018
18
28

Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
13
28

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics.
Guido de Wert, Wybo Dondorp, Angus Clarke, Elisabeth M C Dequeker, Christophe Cordier, Zandra Deans, Carla G van El, Florence Fellmann, Ros Hastings, Sabine Hentze,[...]. Eur J Hum Genet 2021
13
28

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
28

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
70
28

Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
F Houdayer, O Putois, M L Babonneau, H Chaumet, L Joly, C Juif, C C Michon, S Staraci, E Cretin, S Delanoue,[...]. Eur J Med Genet 2019
8
28

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
14

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
14

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
50

The Use of Forensic DNA Phenotyping in Predicting Appearance and Biogeographic Ancestry.
Peter M Schneider, Barbara Prainsack, Manfred Kayser. Dtsch Arztebl Int 2019
24
14



Next generation sequencing and its applications in forensic genetics.
Claus Børsting, Niels Morling. Forensic Sci Int Genet 2015
180
14

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
14

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
14

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
16

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
14

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
14

Social and ethical aspects of forensic genetics: A critical review.
R Williams, M Wienroth. Forensic Sci Rev 2017
12
14

Next-generation DNA sequencing.
Jay Shendure, Hanlee Ji. Nat Biotechnol 2008
14

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

Technological innovations in forensic genetics: social, legal and ethical aspects.
Matthias Wienroth, Niels Morling, Robin Williams. Recent Adv DNA Gene Seq 2014
12
14

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
20


Introduction: the challenge of incidental findings.
Susan M Wolf. J Law Med Ethics 2008
37
14


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
14

Why genomics researchers are sometimes morally required to hunt for secondary findings.
Julian J Koplin, Julian Savulescu, Danya F Vears. BMC Med Ethics 2020
5
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
14



Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.
Kathleen McGlone West, Erika Blacksher, Wylie Burke. JAMA 2017
39
14


p53 and Me.
Shekinah N C Elmore. N Engl J Med 2018
4
25

Patients-in-waiting: Living between sickness and health in the genomics era.
Stefan Timmermans, Mara Buchbinder. J Health Soc Behav 2010
143
14

Analysis of laboratory reporting practices using a quality assessment of a virtual patient.
Danya F Vears, Martin Elferink, Marjolein Kriek, Pascal Borry, Koen L van Gassen. Genet Med 2021
2
50

Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
Katrina A Andrews, David B Ascher, Douglas Eduardo Valente Pires, Daniel R Barnes, Lindsey Vialard, Ruth T Casey, Nicola Bradshaw, Julian Adlard, Simon Aylwin, Paul Brennan,[...]. J Med Genet 2018
81
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.