A citation-based method for searching scientific literature

Emma C Hitchcock, Causes Study, Alison M Elliott. Mol Genet Genomic Med 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


The importance of genetic counselling in genome-wide sequencing.
Alison M Elliott, Jan M Friedman. Nat Rev Genet 2018
23
50

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
14
50

Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.
Lotte Krabbenborg, L E L M Vissers, J Schieving, T Kleefstra, E J Kamsteeg, J A Veltman, M A Willemsen, S Van der Burg. J Genet Couns 2016
46
50

Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.
Allyn McConkie Rosell, Loren D M Pena, Kelly Schoch, Rebecca Spillmann, Jennifer Sullivan, Stephen R Hooper, Yong-Hui Jiang, Nicolas Mathey-Andrews, David B Goldstein, Vandana Shashi. J Genet Couns 2016
57
50



Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project.
Stacey Pereira, Jill Oliver Robinson, Amanda M Gutierrez, Devan K Petersen, Rebecca L Hsu, Caroline H Lee, Talia S Schwartz, Ingrid A Holm, Alan H Beggs, Robert C Green,[...]. Pediatrics 2019
17
50

Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project.
Casie A Genetti, Talia S Schwartz, Jill O Robinson, Grace E VanNoy, Devan Petersen, Stacey Pereira, Shawn Fayer, Hayley A Peoples, Pankaj B Agrawal, Wendi N Betting,[...]. Genet Med 2019
29
50

New developmental syndromes: Understanding the family experience.
Cara N Inglese, Alison M Elliott, Anna Lehman. J Genet Couns 2019
13
50

Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.
Emma E Smith, Christèle du Souich, Nick Dragojlovic, Alison M Elliott. J Genet Couns 2019
15
50

Moving Forward on Consent Practices in Australia.
Rebekah E McWhirter, Lisa Eckstein. J Bioeth Inq 2018
7
25

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
88
25


Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
Xin Li, Rachel Nusbaum, Constance Smith-Hicks, Leila Jamal, Shannan Dixon, Sonal Mahida. J Genet Couns 2019
10
25

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
25


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
25

The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders.
Nick Dragojlovic, Clara D M van Karnebeek, Aisha Ghani, Dallas Genereaux, Ellen Kim, Patricia Birch, Alison M Elliott, Jan M Friedman, Larry D Lynd. Genet Med 2020
17
25

Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research.
Amy Corneli, Emily Namey, Monique P Mueller, Jenae Tharaldson, Steve Sortijas, Thomas Grey, Jeremy Sugarman. J Empir Res Hum Res Ethics 2017
17
25

Simplifying informed consent for biorepositories: stakeholder perspectives.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. Genet Med 2010
37
25

Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions.
Shelin Adam, Patricia H Birch, Rachel R Coe, Nick Bansback, Adrian L Jones, Mary B Connolly, Michelle K Demos, Eric B Toyota, Matthew J Farrer, Jan M Friedman. J Genet Couns 2018
10
25

From the Patient Perspective, Consent Forms Fall Short of Providing Information to Guide Decision Making.
Christine J Manta, Jacqueline Ortiz, Benjamin W Moulton, Seema S Sonnad. J Patient Saf 2021
15
25

Development of a consent resource for genomic data sharing in the clinical setting.
Erin Rooney Riggs, Danielle R Azzariti, Annie Niehaus, Scott R Goehringer, Erin M Ramos, Laura Lyman Rodriguez, Bartha Knoppers, Heidi L Rehm, Christa Lese Martin. Genet Med 2019
9
25

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
25


The challenge of consent in clinical genome-wide testing.
Katherine Burke, Angus Clarke. Arch Dis Child 2016
16
25

Challenges to informed consent for exome sequencing: A best-worst scaling experiment.
Rachel H Gore, John F P Bridges, Julie S Cohen, Barbara B Biesecker. J Genet Couns 2019
3
33

IRB perspectives on the return of individual results from genomic research.
Lynn G Dressler, Sondra Smolek, Roselle Ponsaran, Janell M Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric Juengst, Georgia L Wiesner. Genet Med 2012
51
25

The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia.
Alison M Elliott, Christèle du Souich, Shelin Adam, Nick Dragojlovic, Clara van Karnebeek, Tanya N Nelson, Anna Lehman, Larry D Lynd, Jan M Friedman. Mol Genet Genomic Med 2018
15
25


Paving the way to a more effective informed consent process: Recommendations from the Clinical Trials Transformation Initiative.
Jennifer Lentz, Michele Kennett, Jane Perlmutter, Annemarie Forrest. Contemp Clin Trials 2016
38
25

How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.
Sandi Dheensa, Gillian Crawford, Claire Salter, Michael Parker, Angela Fenwick, Anneke Lucassen. Fam Cancer 2018
7
25

The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
47
25


Public participation in genomics research in the Netherlands: validating a measurement scale.
Anne M Dijkstra, Jan M Gutteling, J A A Swart, Nicolien F Wieringa, Henny J van Derwindt, Erwin R Seydel. Public Underst Sci 2012
8
25

"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
38
25

The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.
Nick Dragojlovic, Alison M Elliott, Shelin Adam, Clara van Karnebeek, Anna Lehman, Jill C Mwenifumbo, Tanya N Nelson, Christèle du Souich, Jan M Friedman, Larry D Lynd. Genet Med 2018
46
25


Views of clinical trial participants on the readability and their understanding of informed consent documents.
Rita Somers, Cornelius Van Staden, Francois Steffens. AJOB Empir Bioeth 2017
5
25

Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
80
25


Prioritizing diversity in human genomics research.
Lucia A Hindorff, Vence L Bonham, Lawrence C Brody, Margaret E C Ginoza, Carolyn M Hutter, Teri A Manolio, Eric D Green. Nat Rev Genet 2018
151
25

Variation among Consent Forms for Clinical Whole Exome Sequencing.
Sara A Fowler, Carol J Saunders, Mark A Hoffman. J Genet Couns 2018
11
25

Model consent clauses for rare disease research.
Minh Thu Nguyen, Jack Goldblatt, Rosario Isasi, Marlene Jagut, Anneliene Hechtelt Jonker, Petra Kaufmann, Laetitia Ouillade, Fruszina Molnar-Gabor, Mahsa Shabani, Eric Sid,[...]. BMC Med Ethics 2019
5
25

Perspectives of IRB chairs on the informed consent process.
Eugene I Kane, Joseph J Gallo. AJOB Empir Bioeth 2017
9
25

Randomization to standard and concise informed consent forms: development of evidence-based consent practices.
Mary E Enama, Zonghui Hu, Ingelise Gordon, Pamela Costner, Julie E Ledgerwood, Christine Grady. Contemp Clin Trials 2012
31
25

Readability of informed consent forms for whole-exome and whole-genome sequencing.
Emilia Niemiec, Danya F Vears, Pascal Borry, Heidi Carmen Howard. J Community Genet 2018
12
25


The evolution of consent forms for research: a quarter century of changes.
Ilene Albala, Margaret Doyle, Paul S Appelbaum. IRB 2010
45
25



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.