A citation-based method for searching scientific literature

Liza-Marie Johnson, Kayla V Hamilton, Jessica M Valdez, Esther Knapp, Justin N Baker, Kim E Nichols. Expert Rev Mol Diagn 2017
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Overcoming challenges to meaningful informed consent for whole genome sequencing in pediatric cancer research.
Jennifer A Oberg, Julia L Glade Bender, Elizabeth G Cohn, Marilyn Morris, Jenny Ruiz, Wendy K Chung, Paul S Appelbaum, Andrew L Kung, Jennifer M Levine. Pediatr Blood Cancer 2015
18
45

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
36

Germline Mutations in Predisposition Genes in Pediatric Cancer.
Jinghui Zhang, Michael F Walsh, Gang Wu, Michael N Edmonson, Tanja A Gruber, John Easton, Dale Hedges, Xiaotu Ma, Xin Zhou, Donald A Yergeau,[...]. N Engl J Med 2015
539
27

Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors.
Laurence B McCullough, Melody J Slashinski, Amy L McGuire, Richard L Street, Christine M Eng, Richard A Gibbs, D William Parsons, Sharon E Plon. Pediatr Blood Cancer 2016
25
27

Communicating and understanding the purpose of pediatric phase I cancer trials.
Melissa K Cousino, Stephen J Zyzanski, Amy D Yamokoski, Rebecca A Hazen, Justin N Baker, Robert B Noll, Susan R Rheingold, J Russell Geyer, Stewart C Alexander, Dennis Drotar,[...]. J Clin Oncol 2012
50
27

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.
Anita Villani, Ari Shore, Jonathan D Wasserman, Derek Stephens, Raymond H Kim, Harriet Druker, Bailey Gallinger, Anne Naumer, Wendy Kohlmann, Ana Novokmet,[...]. Lancet Oncol 2016
235
18

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
259
18

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
D Williams Parsons, Angshumoy Roy, Yaping Yang, Tao Wang, Sarah Scollon, Katie Bergstrom, Robin A Kerstein, Stephanie Gutierrez, Andrea K Petersen, Abhishek Bavle,[...]. JAMA Oncol 2016
232
18

Balancing research interests and patient interests: a qualitative study into the intertwinement of care and research in paediatric oncology.
Sara A S Dekking, Rieke van der Graaf, Marijke C Kars, Auke Beishuizen, Martine C de Vries, Johannes J M van Delden. Pediatr Blood Cancer 2015
15
18

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
32
18

Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study.
Barbara C Worst, Cornelis M van Tilburg, Gnana Prakash Balasubramanian, Petra Fiesel, Ruth Witt, Angelika Freitag, Miream Boudalil, Christopher Previti, Stephan Wolf, Sabine Schmidt,[...]. Eur J Cancer 2016
154
18

Practical communication guidance to improve phase 1 informed consent conversations and decision-making in pediatric oncology.
Liza-Marie Johnson, Angela C Leek, Dennis Drotar, Robert B Noll, Susan R Rheingold, Eric D Kodish, Justin N Baker. Cancer 2015
23
18


Differences in parent-provider concordance regarding prognosis and goals of care among children with advanced cancer.
Abby R Rosenberg, Liliana Orellana, Tammy I Kang, J Russell Geyer, Chris Feudtner, Veronica Dussel, Joanne Wolfe. J Clin Oncol 2014
52
18

Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.
Liza-Marie Johnson, Jessica M Valdez, Emily A Quinn, April D Sykes, Rose B McGee, Regina Nuccio, Stacy J Hines-Dowell, Justin N Baker, Chimene Kesserwan, Kim E Nichols,[...]. Cancer 2017
32
18

Precision medicine in pediatric oncology: Lessons learned and next steps.
Rajen J Mody, John R Prensner, Jessica Everett, D Williams Parsons, Arul M Chinnaiyan. Pediatr Blood Cancer 2017
38
18

Precision medicine in pediatric oncology.
Suzanne J Forrest, Birgit Geoerger, Katherine A Janeway. Curr Opin Pediatr 2018
46
18

Perspective on Precision Medicine in Oncology.
Tali M Johnson. Pharmacotherapy 2017
6
33

Multidisciplinary molecular tumour board: a tool to improve clinical practice and selection accrual for clinical trials in patients with cancer.
Christian Rolfo, Paolo Manca, Roberto Salgado, Peter Van Dam, Amelie Dendooven, Jose Ferri Gandia, Annemie Rutten, Willem Lybaert, Joanna Vermeij, Thomas Gevaert,[...]. ESMO Open 2018
36
18

Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
76
18

Key Lessons Learned from Moffitt's Molecular Tumor Board: The Clinical Genomics Action Committee Experience.
Todd C Knepper, Gillian C Bell, J Kevin Hicks, Eric Padron, Jamie K Teer, Teresa T Vo, Nancy K Gillis, Neil T Mason, Howard L McLeod, Christine M Walko. Oncologist 2017
38
18


Matching up.
Shraddha Chakradhar. Nat Med 2018
2
100

Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur J Hum Genet 2018
31
18

Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process.
Karine Sénécal, Vasiliki Rahimzadeh, Bartha M Knoppers, Conrad V Fernandez, Denise Avard, Daniel Sinnett. Genome 2015
15
18

Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform.
Bartha Maria Knoppers, Denise Avard, Karine Sénécal, Ma'n H Zawati. Eur J Hum Genet 2014
46
18

Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition.
Jessica M Valdez, Kim E Nichols, Chimene Kesserwan. Br J Haematol 2017
38
9

Addressing the ethical challenges in genetic testing and sequencing of children.
Ellen Wright Clayton, Laurence B McCullough, Leslie G Biesecker, Steven Joffe, Lainie Friedman Ross, Susan M Wolf. Am J Bioeth 2014
71
9

How families communicate about HNPCC genetic testing: findings from a qualitative study.
Susan K Peterson, Beatty G Watts, Laura M Koehly, Sally W Vernon, Walter F Baile, Wendy K Kohlmann, Ellen R Gritz. Am J Med Genet C Semin Med Genet 2003
110
9

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol 2011
251
9

Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences.
Alison Metcalfe, Gill Plumridge, Jane Coad, Andrew Shanks, Paramjit Gill. Eur J Hum Genet 2011
66
9

Adolescents and genetic testing: what do they think about it?
Asaff Harel, Dianne Abuelo, Alessandra Kazura. J Adolesc Health 2003
24
9

Communicating genetic information in families--a review of guidelines and position papers.
Laura E Forrest, Martin B Delatycki, Loane Skene, MaryAnne Aitken. Eur J Hum Genet 2007
85
9

Parent decision-making around the genetic testing of children for germline TP53 mutations.
Melissa A Alderfer, Kristin Zelley, Robert B Lindell, Ana Novokmet, Phuong L Mai, Judy E Garber, Deepika Nathan, Sarah Scollon, Nicolette M Chun, Andrea F Patenaude,[...]. Cancer 2015
31
9


The psychological impact of genetic information on children: a systematic review.
Claire E Wakefield, Lucy V Hanlon, Katherine M Tucker, Andrea F Patenaude, Christina Signorelli, Jordana K McLoone, Richard J Cohn. Genet Med 2016
52
9

Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.
Chantal R M Lammens, Neil K Aaronson, Anja Wagner, Rolf H Sijmons, Margreet G E M Ausems, Annette H J T Vriends, Mariëlle W G Ruijs, Theo A M van Os, Liesbeth Spruijt, Encarna B Gómez García,[...]. J Clin Oncol 2010
73
9

Childhood predictive genetic testing for Li-Fraumeni syndrome.
D G Evans, P Lunt, T Clancy, R Eeles. Fam Cancer 2010
17
9



Should Genetic Testing be Offered for Children? The Perspectives of Adolescents and Emerging Adults in Families with Li-Fraumeni Syndrome.
Melissa A Alderfer, Robert B Lindell, Claire I Viadro, Kristin Zelley, Jessica Valdez, Belinda Mandrell, Carol A Ford, Kim E Nichols. J Genet Couns 2017
21
9


Genetic testing for cancer predisposition.
C Eng, H Hampel, A de la Chapelle. Annu Rev Med 2001
82
9


Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank.
Carmen Radecki Breitkopf, Gloria M Petersen, Susan M Wolf, Kari G Chaffee, Marguerite E Robinson, Deborah R Gordon, Noralane M Lindor, Barbara A Koenig. J Law Med Ethics 2015
21
9

Communication of genetic test results to family and health-care providers following disclosure of research results.
Kristi D Graves, Pamela S Sinicrope, Mary Jane Esplen, Susan K Peterson, Christi A Patten, Jan Lowery, Frank A Sinicrope, Sandra K Nigon, Joyce Borgen, Sherri Sheinfeld Gorin,[...]. Genet Med 2014
26
9

Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research.
Alison Metcalfe, Jane Coad, Gill M Plumridge, Paramjit Gill, Peter Farndon. Eur J Hum Genet 2008
89
9


The return of individual research findings in paediatric genetic research.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. J Med Ethics 2011
48
9



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.