A citation-based method for searching scientific literature

Sarah A Walser, Allison Werner-Lin, Rebecca Mueller, Victoria A Miller, Sawona Biswas, Barbara A Bernhardt. Per Med 2017
Times Cited: 10







List of co-cited articles
19 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
947
50

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
70
40

Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing.
Allison Werner-Lin, Judith L M McCoyd, Barbara A Bernhardt. J Genet Couns 2016
16
30

"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
39
30

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
90
20

Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results.
Courtney Berrios, Cynthia A James, Karen Raraigh, Juli Bollinger, Brittney Murray, Crystal Tichnell, Carolyn D Applegate, Amanda L Bergner. J Genet Couns 2018
12
20

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
Brooke L Levenseller, Danielle J Soucier, Victoria A Miller, Diana Harris, Laura Conway, Barbara A Bernhardt. J Genet Couns 2014
54
20

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
20

Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings.
Amanda L Bergner, Juli Bollinger, Karen S Raraigh, Crystal Tichnell, Brittney Murray, Carrie Lynn Blout, Aida Bytyci Telegrafi, Cynthia A James. Am J Med Genet A 2014
29
20

The Genetic Counseling Video Project (GCVP): models of practice.
D Roter, L Ellington, L Hamby Erby, S Larson, W Dudley. Am J Med Genet C Semin Med Genet 2006
80
20


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
20

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
186
20

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
40
20

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
38
20

"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result.
Stina Lou, Kirsten Lomborg, Celine Lewis, Sam Riedijk, Olav Bjørn Petersen, Ida Vogel. Acta Obstet Gynecol Scand 2020
9
22

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.
Shiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, Diana Wellesley, Anneke M Lucassen. Prenat Diagn 2016
23
20


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
53
20


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
59
10

'Cancer doesn't have an age': genetic testing and cancer risk management in BRCA1/2 mutation-positive women aged 18-24.
Allison Werner-Lin, Lindsey M Hoskins, Maya H Doyle, Mark H Greene. Health (London) 2012
31
10

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
863
10

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Daniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, Maximilian Er Weiss, Julia Köster, Anett Marais, Omid Paknia, Rolf Schröder, Jose Maria Garcia-Aznar, Martin Werber,[...]. Eur J Hum Genet 2017
194
10

Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.
Candice Cornelis, Aad Tibben, Wybo Dondorp, Mieke van Haelst, Annelien L Bredenoord, Nine Knoers, Marcus Düwell, Ineke Bolt, Marieke van Summeren. Eur J Hum Genet 2016
13
10

The nuanced negative: Meanings of a negative diagnostic result in clinical exome sequencing.
Debra Skinner, Kelly A Raspberry, Martha King. Sociol Health Illn 2016
36
10

Was it worth it? Patients' perspectives on the perceived value of genomic-based individualized medicine.
Colin Me Halverson, Kristin E Clift, Jennifer B McCormick. J Community Genet 2016
31
10

Effects of racial and ethnic group and health literacy on responses to genomic risk information in a medically underserved population.
Kimberly A Kaphingst, Jewel D Stafford, Lucy D'Agostino McGowan, Joann Seo, Christina R Lachance, Melody S Goodman. Health Psychol 2015
26
10

Perceived ambiguity as a barrier to intentions to learn genome sequencing results.
Jennifer M Taber, William M P Klein, Rebecca A Ferrer, Paul K J Han, Katie L Lewis, Leslie G Biesecker, Barbara B Biesecker. J Behav Med 2015
35
10

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
47
10

How do research participants perceive "uncertainty" in genome sequencing?
Barbara B Biesecker, William Klein, Katie L Lewis, Tyler C Fisher, Martha Frances Wright, Leslie G Biesecker, Paul K Han. Genet Med 2014
50
10


Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, Randi Zinberg, Melissa Wasserstein, Andrew Kasarskis, George A Diaz, Eric E Schadt. Eur J Hum Genet 2017
39
10

"Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing.
Debra Skinner, Myra I Roche, Karen E Weck, Kelly A Raspberry, A Katherine M Foreman, Natasha T Strande, Jonathan S Berg, James P Evans, Gail E Henderson. Genet Med 2018
21
10

Participant use and communication of findings from exome sequencing: a mixed-methods study.
Katie L Lewis, Gillian W Hooker, Philip D Connors, Travis C Hyams, Martha F Wright, Samantha Caldwell, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2016
47
10

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
J A Anderson, M S Meyn, C Shuman, R Zlotnik Shaul, L E Mantella, M J Szego, S Bowdin, N Monfared, R Z Hayeems. J Med Ethics 2017
34
10

Associations between relationship support and psychological reactions of participants and partners to BRCA1 and BRCA2 testing in a clinic-based sample.
Sharon Manne, Janet Audrain, Marc Schwartz, David Main, Clinton Finch, Caryn Lerman. Ann Behav Med 2004
35
10

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
10

Narrating troubling experiences.
Linda C Garro. Transcult Psychiatry 2003
17
10

Clinical Decision-Making in Patients with Variant of Uncertain Significance in BRCA1 or BRCA2 Genes.
Jessemae L Welsh, Tanya L Hoskin, Courtney N Day, Abigail S Thomas, Jodie A Cogswell, Fergus J Couch, Judy C Boughey. Ann Surg Oncol 2017
39
10


The Hawthorne Effect: a randomised, controlled trial.
Rob McCarney, James Warner, Steve Iliffe, Robbert van Haselen, Mark Griffin, Peter Fisher. BMC Med Res Methodol 2007
814
10

The usefulness of whole-exome sequencing in routine clinical practice.
Alejandro Iglesias, Kwame Anyane-Yeboa, Julia Wynn, Ashley Wilson, Megan Truitt Cho, Edwin Guzman, Rebecca Sisson, Claire Egan, Wendy K Chung. Genet Med 2014
139
10

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
Holly K Tabor, Jacquie Stock, Tracy Brazg, Margaret J McMillin, Karin M Dent, Joon-Ho Yu, Jay Shendure, Michael J Bamshad. Am J Med Genet A 2012
83
10

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist,[...]. Lancet Respir Med 2015
211
10

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Robert C Green, Katrina A B Goddard, Gail P Jarvik, Laura M Amendola, Paul S Appelbaum, Jonathan S Berg, Barbara A Bernhardt, Leslie G Biesecker, Sawona Biswas, Carrie L Blout,[...]. Am J Hum Genet 2016
100
10

Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?
Deborah Cragun, Courtney Scherr, Lucia Camperlengo, Susan T Vadaparampil, Tuya Pal. Genet Test Mol Biomarkers 2016
11
10


Public attitudes toward ancillary information revealed by pharmacogenetic testing under limited information conditions.
Susanne B Haga, Julianne M O'Daniel, Genevieve M Tindall, Isaac R Lipkus, Robert Agans. Genet Med 2011
43
10

Genetics patients' perspectives on clinical genomic testing.
Michelle L McGowan, Allison Glinka, Janelle Highland, George Asaad, Richard R Sharp. Per Med 2013
29
10


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.