A citation-based method for searching scientific literature

Allison Werner-Lin, Lori Zaspel, Mae Carlson, Rebecca Mueller, Sarah A Walser, Ria Desai, Barbara A Bernhardt. Am J Med Genet A 2018
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
49
36


Adolescent and Parental Attitudes About Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences.
Michelle L McGowan, Cynthia A Prows, Melissa DeJonckheere, William B Brinkman, Lisa Vaughn, Melanie F Myers. J Empir Res Hum Res Ethics 2018
16
27

Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact.
J Wynn, R Ottman, J Duong, A L Wilson, P Ahimaz, J Martinez, R Rabin, E Rosen, R Webster, C Au,[...]. Clin Genet 2018
24
27

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
220
27

The importance of genetic counselling in genome-wide sequencing.
Alison M Elliott, Jan M Friedman. Nat Rev Genet 2018
22
27

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
27

"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
16
18


Distress among women receiving uninformative BRCA1/2 results: 12-month outcomes.
Suzanne C O'Neill, Christine Rini, Rachel E Goldsmith, Heiddis Valdimarsdottir, Lawrence H Cohen, Marc D Schwartz. Psychooncology 2009
71
18

Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance.
Ilana Solomon, Elizabeth Harrington, Gillian Hooker, Lori Erby, Jennifer Axilbund, Heather Hampel, Kara Semotiuk, Amie Blanco, William M P Klein, Francis Giardiello,[...]. J Genet Couns 2017
30
18

Disclosure of cardiac variants of uncertain significance results in an exome cohort.
T A Lawal, K L Lewis, J J Johnston, A R Heidlebaugh, D Ng, F G Gaston-Johansson, W M P Klein, B B Biesecker, L G Biesecker. Clin Genet 2018
9
22

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
18

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
18

Giving adolescents a voice: the types of genetic information adolescents choose to learn and why.
Josie Pervola, Melanie F Myers, Michelle L McGowan, Cynthia A Prows. Genet Med 2019
11
18

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
157
18

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
Anath C Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S Reuter, S Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam,[...]. Genet Med 2018
192
18

Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review.
B C McGill, C E Wakefield, J Vetsch, K Barlow-Stewart, N A Kasparian, A F Patenaude, M-A Young, R J Cohn, K M Tucker. Clin Genet 2019
14
18

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
18

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS.
Clare Turnbull, Richard H Scott, Ellen Thomas, Louise Jones, Nirupa Murugaesu, Freya Boardman Pretty, Dina Halai, Emma Baple, Clare Craig, Angela Hamblin,[...]. BMJ 2018
176
18

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
49
18

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
18

Predictive testing of eighteen year olds: counseling challenges.
Clara L Gaff, Elly Lynch, Lesley Spencer. J Genet Couns 2006
22
18

Experience with genetic counseling: the adolescent perspective.
Amanda Pichini, Cheryl Shuman, Karen Sappleton, Miriam Kaufman, David Chitayat, Riyana Babul-Hirji. J Genet Couns 2016
10
20



Adolescents' preferences regarding disclosure of incidental findings in genomic sequencing that are not medically actionable in childhood.
Sophia B Hufnagel, Lisa J Martin, Amy Cassedy, Robert J Hopkin, Armand H Matheny Antommaria. Am J Med Genet A 2016
18
18

The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine.
S C Bowdin, R Z Hayeems, N Monfared, R D Cohn, M S Meyn. Clin Genet 2016
25
18

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
98
18

Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
13
18


Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?
Jan M Friedman, Yvonne Bombard, Martina C Cornel, Conrad V Fernandez, Anne K Junker, Sharon E Plon, Zornitza Stark, Bartha Maria Knoppers. Genet Med 2019
24
18

Validation of a decision regret scale.
Jamie C Brehaut, Annette M O'Connor, Timothy J Wood, Thomas F Hack, Laura Siminoff, Elisa Gordon, Deb Feldman-Stewart. Med Decis Making 2003
614
18

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
41
18

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Stephen F Kingsmore, Julie A Cakici, Michelle M Clark, Mary Gaughran, Michele Feddock, Sergey Batalov, Matthew N Bainbridge, Jeanne Carroll, Sara A Caylor, Christina Clarke,[...]. Am J Hum Genet 2019
79
18


New developmental syndromes: Understanding the family experience.
Cara N Inglese, Alison M Elliott, Anna Lehman. J Genet Couns 2019
13
18

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
18




Social networks--the future for health care delivery.
Frances Griffiths, Jonathan Cave, Felicity Boardman, Justin Ren, Teresa Pawlikowska, Robin Ball, Aileen Clarke, Alan Cohen. Soc Sci Med 2012
57
9

Life after BRCA1/2 testing: family communication and support issues.
Tiffani A DeMarco, Wendy C McKinnon. Breast Dis 2006
22
9

Catalysts towards cancer risk management action: A longitudinal study of reproductive-aged women with BRCA1/2 mutations.
Allison Werner-Lin, Anne L Ersig, Rebecca Mueller, Jennifer L Young, Lindsey M Hoskins, Ria Desai, Mark H Greene. J Psychosoc Oncol 2018
7
14

Understanding health behavior change among couples: an interdependence and communal coping approach.
Megan A Lewis, Colleen M McBride, Kathryn I Pollak, Elaine Puleo, Rita M Butterfield, Karen M Emmons. Soc Sci Med 2006
305
9


Unpacking the blockers: understanding perceptions and social constraints of health communication in hereditary breast ovarian cancer (HBOC) susceptibility families.
June A Peters, Regina Kenen, Lindsey M Hoskins, Laura M Koehly, Barry Graubard, Jennifer T Loud, Mark H Greene. J Genet Couns 2011
23
9


Experiencing the cancer of a loved one influences decision-making for breast cancer prevention.
Tasleem J Padamsee, Anna Muraveva, Lisa D Yee, Celia E Wills, Electra D Paskett. J Health Psychol 2020
6
16



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.