A citation-based method for searching scientific literature

Gabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, Angela Fenwick, Anneke Lucassen. BMC Med Ethics 2017
Times Cited: 33







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



Times Cited
  Times     Co-cited
Similarity


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
216
21

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
994
21

Experiences with obtaining informed consent for genomic sequencing.
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am J Med Genet A 2015
74
21

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
15



Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
49
12



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
136
12

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
62
12

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
78
12

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
41
12

Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical research.
Sandi Dheensa, Angela Fenwick, Shiri Shkedi-Rafid, Gillian Crawford, Anneke Lucassen. Genet Med 2016
53
12


The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
146
9



"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
40
9

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
9

DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.
Patricia Birch, S Adam, N Bansback, R R Coe, J Hicklin, A Lehman, K C Li, J M Friedman. J Genet Couns 2016
27
11

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
50
9

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
408
9

Known unknowns: building an ethics of uncertainty into genomic medicine.
Ainsley J Newson, Samantha J Leonard, Alison Hall, Clara L Gaff. BMC Med Genomics 2016
54
9


Genetic information: a joint account?
Michael Parker, Anneke M Lucassen. BMJ 2004
78
9

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients.
T Rigter, C J A van Aart, M W Elting, Q Waisfisz, M C Cornel, L Henneman. Clin Genet 2014
31
9


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
42
9

Patient-centered informed consent in surgical practice.
James L Bernat, Lynn M Peterson. Arch Surg 2006
96
9

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
8
37

Genetic counselling in the era of genomic medicine.
Christine Patch, Anna Middleton. Br Med Bull 2018
42
9

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet Med 2017
52
9

Empty ethics: the problem with informed consent.
Oonagh Corrigan. Sociol Health Illn 2003
175
9

Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?
Edward S Dove, Vicky Chico, Michael Fay, Graeme Laurie, Anneke M Lucassen, Emily Postan. J Med Ethics 2019
19
15

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
38
9

Beyond individualism: Is there a place for relational autonomy in clinical practice and research?
Edward S Dove, Susan E Kelly, Federica Lucivero, Mavis Machirori, Sandi Dheensa, Barbara Prainsack. Clin Ethics 2017
58
9

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.
Holly K Tabor, Benjamin E Berkman, Sara Chandros Hull, Michael J Bamshad. Am J Med Genet A 2011
95
9


An investigation of patients' motivations for their participation in genetics-related research.
N Hallowell, S Cooke, G Crawford, A Lucassen, M Parker, C Snowdon. J Med Ethics 2010
72
6

The UK's 100,000 Genomes Project: manifesting policymakers' expectations.
Gabrielle Natalie Samuel, Bobbie Farsides. New Genet Soc 2017
24
8


Men's experiences of antenatal screening: a metasynthesis of the qualitative research.
Sandi Dheensa, Alison Metcalfe, Robert Alan Williams. Int J Nurs Stud 2013
36
6


Supporting patient autonomy: the importance of clinician-patient relationships.
Vikki A Entwistle, Stacy M Carter, Alan Cribb, Kirsten McCaffery. J Gen Intern Med 2010
205
6

Interpretations of informed choice in antenatal screening: a cross-cultural, Q-methodology study.
Shenaz Ahmed, Louise D Bryant, Zahra Tizro, Darren Shickle. Soc Sci Med 2012
22
9

Noninvasive prenatal testing goes global.
Subhashini Chandrasekharan, Mollie A Minear, Anthony Hung, Megan Allyse. Sci Transl Med 2014
78
6


Distinguishing research from clinical care in cancer genetics: theoretical justifications and practical strategies.
Nina Hallowell, Sarah Cooke, Gill Crawford, Anneke Lucassen, Michael Parker. Soc Sci Med 2009
30
6

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur J Hum Genet 2016
121
6


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.