A citation-based method for searching scientific literature

Leigh Jackson, Lesley Goldsmith, Anita O'Connor, Heather Skirton. Am J Med Genet A 2012
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity


One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants.
Fiona Alice Miller, Robin Zoe Hayeems, Li Li, Jessica Peace Bytautas. Eur J Hum Genet 2012
17
11

Medicine. Reestablishing the researcher-patient compact.
Isaac S Kohane, Kenneth D Mandl, Patrick L Taylor, Ingrid A Holm, Daniel J Nigrin, Louis M Kunkel. Science 2007
100
5

Human genome sequencing in health and disease.
Claudia Gonzaga-Jauregui, James R Lupski, Richard A Gibbs. Annu Rev Med 2012
255
5


Introduction: the challenge of incidental findings.
Susan M Wolf. J Law Med Ethics 2008
36
5

Incidental findings in genetics research using archived DNA.
Ellen Wright Clayton. J Law Med Ethics 2008
42
5

Clinical assessment incorporating a personal genome.
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
461
5

Consumer perceptions of direct-to-consumer personalized genomic risk assessments.
Cinnamon S Bloss, Laura Ornowski, Elana Silver, Michele Cargill, Vance Vanier, Nicholas J Schork, Eric J Topol. Genet Med 2010
88
5

Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screening.
F A Miller, R Z Hayeems, Y Bombard, J Little, J C Carroll, B Wilson, J Allanson, M Paynter, J P Bytautas, R Christensen,[...]. J Med Ethics 2009
19
10


The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository.
Erin D Harris, Sonja I Ziniel, Jonathan G Amatruda, Catherine M Clinton, Sarah K Savage, Patrick L Taylor, Noelle L Huntington, Robert C Green, Ingrid A Holm. Genet Med 2012
38
5


Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
Sarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, Peter N Ray, Stephen W Scherer. Pediatr Res 2009
48
5

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.
T Schwarzbraun, A C Obenauf, A Langmann, U Gruber-Sedlmayr, K Wagner, M R Speicher, P M Kroisel. J Med Genet 2009
31
6

The return of individual research findings in paediatric genetic research.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. J Med Ethics 2011
47
5

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
155
5

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
79
5

The Deciphering Developmental Disorders (DDD) study.
Helen V Firth, Caroline F Wright. Dev Med Child Neurol 2011
86
5

Incidental findings in human subjects research: what do investigators owe research participants?
Franklin G Miller, Michelle M Mello, Steven Joffe. J Law Med Ethics 2008
70
5

Return of "accurate" and "actionable" results: yes!
Bartha Maria Knoppers, Claude Laberge. Am J Bioeth 2009
18
11

Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies.
Katrina A B Goddard, Evelyn P Whitlock, Jonathan S Berg, Marc S Williams, Elizabeth M Webber, Jennifer A Webster, Jennifer S Lin, Kasmintan A Schrader, Doug Campos-Outcalt, Kenneth Offit,[...]. Genet Med 2013
33
6

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
81
5

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton. Genet Med 2009
146
5

Ethical issues in genetic counseling: a comparison of M.S. counselor and medical geneticist perspectives.
Deborah F Pencarinha, Nora K Bell, Janice G Edwards, Robert G Best. J Genet Couns 1992
35
5

Disclosure of misattributed paternity: issues involved in the discovery of unsought information.
Linda Wright, Susan MacRae, Debra Gordon, Esther Elliot, David Dixon, Susan Abbey, Robert Richardson. Semin Dial 2002
29
6

The Rapid Assessment of Physical Activity (RAPA) among older adults.
Tari D Topolski, James LoGerfo, Donald L Patrick, Barbara Williams, Julie Walwick, Marsha B Patrick. Prev Chronic Dis 2006
348
5

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
331
5

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
343
5


The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases.
William A Gahl, Thomas C Markello, Camilo Toro, Karin Fuentes Fajardo, Murat Sincan, Fred Gill, Hannah Carlson-Donohoe, Andrea Gropman, Tyler Mark Pierson, Gretchen Golas,[...]. Genet Med 2012
180
5

Survey of US public attitudes toward pharmacogenetic testing.
S B Haga, J M O'Daniel, G M Tindall, I R Lipkus, R Agans. Pharmacogenomics J 2012
95
5

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
5

Detection of clinically relevant copy number variants with whole-exome sequencing.
Joep de Ligt, Philip M Boone, Rolph Pfundt, Lisenka E L M Vissers, Todd Richmond, Joel Geoghegan, Kathleen O'Moore, Nicole de Leeuw, Christine Shaw, Han G Brunner,[...]. Hum Mutat 2013
78
5

Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada?
Ma'n H Zawati, David Parry, Adrian Thorogood, Minh Thu Nguyen, Kym M Boycott, David Rosenblatt, Bartha Maria Knoppers. J Med Genet 2014
20
10

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
55
5

Processes and factors involved in decisions regarding return of incidental genomic findings in research.
Robert Klitzman, Brigitte Buquez, Paul S Appelbaum, Abby Fyer, Wendy K Chung. Genet Med 2014
22
9

Researcher and institutional review board chair perspectives on incidental findings in genomic research.
Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Nancy Downing, Laura Shinkunas, Debra Brandt, Christian Simon. Genet Test Mol Biomarkers 2012
26
7




Latent class analysis in medical research.
A K Formann, T Kohlmann. Stat Methods Med Res 1996
81
5

Incidental findings from clinical sequencing in Greece: reporting experts' attitudes.
E G Gourna, N Armstrong, S E Wallace. J Community Genet 2014
5
40

Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland).
Anna Middleton, Chris Patch, Jennifer Wiggins, Kathy Barnes, Gill Crawford, Caroline Benjamin, Anita Bruce. Eur J Hum Genet 2014
20
10



Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care.
Fiona A Miller, Robin Z Hayeems, Jessica P Bytautas, Philippe L Bedard, Scott Ernst, Hal Hirte, Sebastien Hotte, Amit Oza, Albiruni Razak, Stephen Welch,[...]. Eur J Hum Genet 2014
59
5

The evaluation of genetic tests.
Ron L Zimmern, Mark Kroese. J Public Health (Oxf) 2007
30
6


Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
49
5

A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs.
Debra S Brandt, Laura Shinkunas, Stephen L Hillis, Sandra E Daack-Hirsch, Martha Driessnack, Nancy R Downing, Megan F Liu, Lisa L Shah, Janet K Williams, Christian M Simon. J Genet Couns 2013
22
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.