A citation-based method for searching scientific literature

Saskia C Sanderson, Sabrina A Suckiel, Micol Zweig, Erwin P Bottinger, Ethylin Wang Jabs, Lynne D Richardson. Genet Med 2016
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity


Effects of informed consent for individual genome sequencing on relevant knowledge.
K A Kaphingst, F M Facio, M-R Cheng, S Brooks, H Eidem, A Linn, B B Biesecker, L G Biesecker. Clin Genet 2012
76
25

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
25

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018
40
16

Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
22

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
118
12

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
43
12


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
53
12

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
12

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
19
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
761
12

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
96
12

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
31
12

Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study.
Saskia C Sanderson, Michael A Diefenbach, Randi Zinberg, Carol R Horowitz, Margaret Smirnoff, Micol Zweig, Samantha Streicher, Ethylin Wang Jabs, Lynne D Richardson. J Community Genet 2013
37
9

Relationship between public attitudes toward genomic studies related to medicine and their level of genomic literacy in Japan.
Izumi Ishiyama, Akiko Nagai, Kaori Muto, Akiko Tamakoshi, Minori Kokado, Kyoko Mimura, Tetsuro Tanzawa, Zentaro Yamagata. Am J Med Genet A 2008
32
9

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
108
9

Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
44
9

Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Hum Genet 2014
85
9

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
75
9




Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
230
9


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
975
9


How Well Do Customers of Direct-to-Consumer Personal Genomic Testing Services Comprehend Genetic Test Results? Findings from the Impact of Personal Genomics Study.
Jenny E Ostergren, Michele C Gornick, Deanna Alexis Carere, Sarah S Kalia, Wendy R Uhlmann, Mack T Ruffin, Joanna L Mountain, Robert C Green, J Scott Roberts. Public Health Genomics 2015
44
9

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
42
9

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
96
9

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
687
9

Development of a measure of genome sequencing knowledge for young people: The kids-KOGS.
Celine Lewis, Bao S Loe, Chris Sidey-Gibbons, Christine Patch, Lyn S Chitty, Saskia C Sanderson. Clin Genet 2019
3
100

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
125
9

Increasing genomic literacy among adolescents.
Maya Sabatello, Ying Chen, Saskia C Sanderson, Wendy K Chung, Paul S Appelbaum. Genet Med 2019
5
60

Development of the Knowledge of Genome Sequencing (KOGS) questionnaire.
Saskia C Sanderson, Bao Sheng Loe, Maddie Freeman, Camila Gabriel, Danielle C Stevenson, Chris Gibbons, Lyn Chitty, Celine Lewis. Patient Educ Couns 2018
4
75

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
108
9

Effect of a computer-based decision aid on knowledge, perceptions, and intentions about genetic testing for breast cancer susceptibility: a randomized controlled trial.
Michael J Green, Susan K Peterson, Maria Wagner Baker, Gregory R Harper, Lois C Friedman, Wendy S Rubinstein, David T Mauger. JAMA 2004
216
9

Development and evaluation of a general information leaflet for women with a family history of breast cancer.
Anne A J Andermann, Joan Austoker, Eila K Watson, Anneke M Lucassen, James Mackay. J Cancer Educ 2002
6
33

Validation of a decisional conflict scale.
A M O'Connor. Med Decis Making 1995
6

Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era.
Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
42
6

A measure of informed choice.
T M Marteau, E Dormandy, S Michie. Health Expect 2001
432
6

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Jason L Vassy, Denise M Lautenbach, Heather M McLaughlin, Sek Won Kong, Kurt D Christensen, Joel Krier, Isaac S Kohane, Lindsay Z Feuerman, Jennifer Blumenthal-Barby, J Scott Roberts,[...]. Trials 2014
96
6

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
24
8

Patient satisfaction with health care decisions: the satisfaction with decision scale.
M Holmes-Rovner, J Kroll, N Schmitt, D R Rovner, M L Breer, M L Rothert, G Padonu, G Talarczyk. Med Decis Making 1996
380
6

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry.
C R Horowitz, N S Abul-Husn, S Ellis, M A Ramos, R Negron, M Suprun, R E Zinberg, T Sabin, D Hauser, N Calman,[...]. Contemp Clin Trials 2016
24
8

Development and validation of a Breast Cancer Genetic Counseling Knowledge Questionnaire.
Joel Erblich, Karen Brown, Youngmee Kim, Heiddis B Valdimarsdottir, Barbara E Livingston, Dana H Bovbjerg. Patient Educ Couns 2005
43
6

The influence of health care policies and health care system distrust on willingness to undergo genetic testing.
Katrina Armstrong, Mary Putt, Chanita Hughes Halbert, David Grande, Jerome Sanford Schwartz, Kaijun Liao, Noora Marcus, Mirar Bristol Demeter, Judy Shea. Med Care 2012
30
6

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet Med 2013
81
6

Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research.
Julia Wynn, Josue Martinez, Jimmy Duong, Yuan Zhang, Jo Phelan, Abby Fyer, Robert Klitzman, Paul S Appelbaum, Wendy K Chung. J Genet Couns 2015
13
15


Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.
Christopher H Wade, Beth A Tarini, Benjamin S Wilfond. Annu Rev Genomics Hum Genet 2013
42
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.